PuSH - HMGU Publikationen https://push-zb.helmholtz-munich.de PuSH - Publikationen-Server des Helmholtz Zentrums München de-de <![CDATA[Li, J.* et al. Single-cell atlas of the transcriptome and chromatin accessibility in the human retina. Nat. Genet. 58, 418–433 (2026)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=76709&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=76709&la=de Thu, 12 Mar 2026 00:00:00 +0000 <![CDATA[Li, J.* et al. Author Correction: Single-cell atlas of the transcriptome and chromatin accessibility in the human retina. Nat. Genet. 58, 673–674 (2026)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=77036&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=77036&la=de Tue, 31 Mar 2026 00:00:00 +0000 <![CDATA[Soremekun, O. et al. Linking the plasma proteome to genetics in individuals from continental Africa provides insights into type 2 diabetes pathogenesis. Nat. Genet. 58, 39–46 (2026)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=76523&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=76523&la=de Mon, 02 Mar 2026 00:00:00 +0000 <![CDATA[Yépez, V.A.* et al. Author Correction: The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease. Nat. Genet. 58:231 (2026)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=76514&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=76514&la=de Thu, 12 Feb 2026 00:00:00 +0000 <![CDATA[Birk, S. et al. Quantitative characterization of cell niches in spatially resolved omics data. Nat. Genet. 57, 897–909 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73719&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73719&la=de Fri, 09 May 2025 00:00:00 +0000 <![CDATA[Fatumo, S.* et al. KidneyGenAfrica, a pan-African partnership to deliver research and training excellence in genomics of kidney disease. Nat. Genet. 57, 2079–2082 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75494&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75494&la=de Fri, 17 Oct 2025 00:00:00 +0000 <![CDATA[Guo, W.* et al. A barley pan-transcriptome reveals layers of genotype-dependent transcriptional complexity. Nat. Genet. 57, 441-450 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73284&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73284&la=de Tue, 01 Apr 2025 00:00:00 +0000 <![CDATA[Lammi, V.* et al. Genome-wide association study of long COVID. Nat. Genet. 57, 1402–1417 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74779&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74779&la=de Mon, 02 Jun 2025 00:00:00 +0000 <![CDATA[Lazarescu, O.* et al. Human subcutaneous and visceral adipocyte atlases uncover classical and nonclassical adipocytes and depot-specific patterns. Nat. Genet. 57, 413-426 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73177&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73177&la=de Tue, 25 Mar 2025 00:00:00 +0000 <![CDATA[Nava, C.* et al. Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption. Nat. Genet., DOI: 10.1038/s41588-025-02184-4 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74588&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74588&la=de Wed, 21 May 2025 00:00:00 +0000 <![CDATA[Roselli, C.* et al. Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases. Nat. Genet. 57, 539-547 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73599&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73599&la=de Wed, 09 Apr 2025 00:00:00 +0000 <![CDATA[Schmidt, A.* et al. Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings. Nat. Genet., DOI: 10.1038/s41588-025-02271-6 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75016&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75016&la=de Thu, 26 Jun 2025 00:00:00 +0000 <![CDATA[Tejada Lapuerta, A. et al. Causal machine learning for single-cell genomics. Nat. Genet. 57, 797–808 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73921&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73921&la=de Wed, 02 Apr 2025 00:00:00 +0000 <![CDATA[Tomaz da Silva, P.* et al. Nucleotide dependency analysis of genomic language models detects functional elements. Nat. Genet. 57, 2589-2602 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75751&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75751&la=de Tue, 14 Oct 2025 00:00:00 +0000 <![CDATA[van der Laan, C.M.* et al. Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes. Nat. Genet. 57, 2427-2435 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75583&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75583&la=de Tue, 21 Oct 2025 00:00:00 +0000 <![CDATA[van der Laan, C.M.* et al. Publisher Correction: Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes. Nat. Genet. 57:2604 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75669&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75669&la=de Wed, 22 Oct 2025 00:00:00 +0000 <![CDATA[Xu, Q.* et al. An integrated transcriptomic cell atlas of human endoderm-derived organoids. Nat. Genet. 57, 1201–1212 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74539&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74539&la=de Wed, 14 May 2025 00:00:00 +0000 <![CDATA[Yépez, V.A.* et al. The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease. Nat. Genet. 57, 2361-2370 (2025)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75538&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75538&la=de Mon, 20 Oct 2025 00:00:00 +0000 <![CDATA[Clarke, B.* et al. Integration of variant annotations using deep set networks boosts rare variant association testing. Nat. Genet., DOI: 10.1038/s41588-024-01919-z (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71840&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71840&la=de Tue, 29 Oct 2024 00:00:00 +0000 <![CDATA[García-Marín, L.M.* et al. Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries. Nat. Genet. 56, 2333–2344 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71997&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71997&la=de Wed, 30 Oct 2024 00:00:00 +0000 <![CDATA[Garg, V.* et al. Unlocking plant genetics with telomere-to-telomere genome assemblies. Nat. Genet., 1788–1799 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71301&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71301&la=de Tue, 30 Jul 2024 00:00:00 +0000 <![CDATA[Keaton, J.M.* et al. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits. Nat. Genet. 56, 778-791 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70632&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70632&la=de Tue, 11 Jun 2024 00:00:00 +0000 <![CDATA[Kentistou, K.A.* et al. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nat. Genet. 56, 1763-1764 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71102&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71102&la=de Mon, 22 Jul 2024 00:00:00 +0000 <![CDATA[Kentistou, K.A.* et al. Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nat. Genet. 56, 1397–1411 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71030&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71030&la=de Wed, 17 Jul 2024 00:00:00 +0000 <![CDATA[Meng, X.* et al. Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference. Nat. Genet. 56, 222-233 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68998&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68998&la=de Mon, 08 Apr 2024 00:00:00 +0000 <![CDATA[Rayner, N.W. ; Park, Y.-C. ; Fuchsberger, C.* ; Barysenska, A. & Zeggini, E. Toward GDPR compliance with the Helmholtz Munich genotype imputation server. Nat. Genet., DOI: 10.1038/s41588-024-02012-1 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72380&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72380&la=de Wed, 27 Nov 2024 00:00:00 +0000 <![CDATA[Schmidt, A.* et al. Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings. Nat. Genet. 56, 1644–1653 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71268&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=71268&la=de Wed, 24 Jul 2024 00:00:00 +0000 <![CDATA[Schormair, B. et al. Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nat. Genet. 56, 1090-1099 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70809&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70809&la=de Tue, 18 Jun 2024 00:00:00 +0000 <![CDATA[Shrine, N.* et al. Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Nat. Genet. 56, 1032-1033 (2024)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70533&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70533&la=de Fri, 07 Jun 2024 00:00:00 +0000 <![CDATA[An, U.* et al. Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries. Nat. Genet. 55, 2269-2276 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68783&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68783&la=de Tue, 28 Nov 2023 00:00:00 +0000 <![CDATA[Dahl, A.* et al. Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorder. Nat. Genet. 55, 2082-2093 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68786&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68786&la=de Tue, 28 Nov 2023 00:00:00 +0000 <![CDATA[Lagou, V.* et al. GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification. Nat. Genet. 55, 1448-1461 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68305&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68305&la=de Wed, 18 Oct 2023 00:00:00 +0000 <![CDATA[Rahmioglu, N.* et al. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nat. Genet. 55, 423-436 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67729&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67729&la=de Fri, 06 Oct 2023 00:00:00 +0000 <![CDATA[Shrine, N.* et al. Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Nat. Genet. 55, 410-422 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67730&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67730&la=de Fri, 06 Oct 2023 00:00:00 +0000 <![CDATA[Shrine, N.* et al. Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk (Nature Genetics, (2023), 55, 3, (410-422), 10.1038/s41588-023-01314-0). Nat. Genet. 55, 1778-1779 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68216&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68216&la=de Wed, 18 Oct 2023 00:00:00 +0000 <![CDATA[Wagner, N.* et al. Aberrant splicing prediction across human tissues. Nat. Genet. 55, 861-870 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67775&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67775&la=de Fri, 06 Oct 2023 00:00:00 +0000 <![CDATA[Williamson, A.* et al. Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Nat. Genet. 55, 973-983 (2023)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67838&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67838&la=de Fri, 06 Oct 2023 00:00:00 +0000 <![CDATA[Aragam, K.G.* et al. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants. Nat. Genet. 54, 1803-1815 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66938&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66938&la=de Thu, 15 Dec 2022 00:00:00 +0000 <![CDATA[Barc, J.* et al. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nat. Genet. 54, 232-239 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64546&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64546&la=de Tue, 26 Apr 2022 00:00:00 +0000 <![CDATA[Barc, J.* et al. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nat. Genet. 54:735 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65040&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65040&la=de Wed, 06 Jul 2022 00:00:00 +0000 <![CDATA[Bellenguez, C.* et al. New insights into the genetic etiology of Alzheimer's disease and related dementias. Nat. Genet. 54, 412-436 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66506&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66506&la=de Fri, 28 Oct 2022 00:00:00 +0000 <![CDATA[Byun, J.* et al. Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. Nat. Genet. 54, 1167-1177 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65843&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65843&la=de Mon, 29 Aug 2022 00:00:00 +0000 <![CDATA[Hawe, J. et al. Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function. Nat. Genet. 54, 18–29 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64018&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64018&la=de Tue, 08 Feb 2022 00:00:00 +0000 <![CDATA[Eumorphia Consortium (Hrabě de Angelis, M. ; Wurst, W. ; Abe, K. ; Beckers, J. ; Busch, D.H. ; Dalke, C. ; Gailus-Durner, V. ; Fuchs, H. ; Graw, J. ; Hölter, S.M. ; Kallnik, M. ; Lengger, C. ; Pedersen, V. ; Puk, O. ; Vogt Weisenhorn, D.M. ; Wagner, S.) & Quintanilla-Fend, L. EMPReSS: Standardized phenotype screens for functional annotation of the mouse genome (vol 37, pg 1155, 2005). Nat. Genet. 54, 358-360 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64476&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64476&la=de Fri, 22 Apr 2022 00:00:00 +0000 <![CDATA[Hsieh, T.C.* et al. GestaltMatcher facilitates rare disease matching using facial phenotype descriptors. Nat. Genet. 54, 349-357 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64310&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64310&la=de Fri, 22 Apr 2022 00:00:00 +0000 <![CDATA[Hu, B.* et al. Origin and function of activated fibroblast states during zebrafish heart regeneration. Nat. Genet. 54, 1227-1237 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65758&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65758&la=de Thu, 03 Nov 2022 00:00:00 +0000 <![CDATA[Mahajan, A.* et al. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. Nat. Genet. 54, 560-572 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65002&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65002&la=de Wed, 06 Jul 2022 00:00:00 +0000 <![CDATA[Nakatani, T. et al. DNA replication fork speed underlies cell fate changes and promotes reprogramming. Nat. Genet. 54, 318–327 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64507&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64507&la=de Fri, 22 Apr 2022 00:00:00 +0000 <![CDATA[Okbay, A.* et al. Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals. Nat. Genet. 54, 437-449 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65061&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65061&la=de Tue, 24 May 2022 00:00:00 +0000 <![CDATA[Schork, A.J.* ; Peterson, R.E.* ; Dahl, A.* ; Cai, N. & Kendler, K.S.* Indirect paths from genetics to education. Nat. Genet. 54, 372-373 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64757&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64757&la=de Fri, 22 Apr 2022 00:00:00 +0000 <![CDATA[Schork, A.J.* ; Peterson, R.E.* ; Dahl, A.* ; Cai, N. & Kendler, K.S.* Author Correction: Indirect paths from genetics to education (Nature Genetics, (2022), 54, 4, (372-373), 10.1038/s41588-021-00999-5). Nat. Genet., DOI: 10.1038/s41588-022-01092-1 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64979&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64979&la=de Mon, 30 May 2022 00:00:00 +0000 <![CDATA[Wang, Z.* et al. Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Nat. Genet. 54, 1332–1344 (2022)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66168&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66168&la=de Wed, 19 Oct 2022 00:00:00 +0000 <![CDATA[Birling, M.C.* et al. A resource of targeted mutant mouse lines for 5,061 genes. Nat. Genet. 53, 416-419 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61787&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61787&la=de Wed, 14 Apr 2021 00:00:00 +0000 <![CDATA[Bonder, M.J.* et al. Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics. Nat. Genet. 53, 313-321 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61449&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61449&la=de Tue, 27 Apr 2021 00:00:00 +0000 <![CDATA[Chen, J.* et al. The trans-ancestral genomic architecture of glycemic traits. Nat. Genet. 53, 840-860 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62216&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62216&la=de Wed, 07 Jul 2021 00:00:00 +0000 <![CDATA[Cousin, M.A.* et al. Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome. Nat. Genet. 53, 1006-1021 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62430&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62430&la=de Tue, 03 Aug 2021 00:00:00 +0000 <![CDATA[Lotta, L.A.* et al. A cross-platform approach identifies genetic regulators of human metabolism and health. Nat. Genet. 53, 54-64 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60943&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60943&la=de Mon, 08 Feb 2021 00:00:00 +0000 <![CDATA[Rabanus-Wallace, M.T.* et al. Chromosome-scale genome assembly provides insights into rye biology, evolution and agronomic potential. Nat. Genet. 53, 564-573 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61706&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61706&la=de Tue, 25 May 2021 00:00:00 +0000 <![CDATA[Rühlemann, M.C.* et al. Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. Nat. Genet. 53, 147–155 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61090&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61090&la=de Mon, 08 Feb 2021 00:00:00 +0000 <![CDATA[Surendran, P.* et al. Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (Nature Genetics, (2020), 52, 12, (1314-1332), 10.1038/s41588-020-00713-x). Nat. Genet., DOI: 10.1038/s41588-021-00832-z (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61642&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61642&la=de Tue, 27 Apr 2021 00:00:00 +0000 <![CDATA[Tadros, R.* et al. Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Nat. Genet. 53, 128-134 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61211&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61211&la=de Wed, 14 Apr 2021 00:00:00 +0000 <![CDATA[Võsa, U.* et al. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. Nat. Genet. 53, 1300-1310 (2021)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62962&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62962&la=de Thu, 14 Oct 2021 00:00:00 +0000 <![CDATA[Bryois, J.* et al. Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease. Nat. Genet. 52, 482-493 (2020)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=59077&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=59077&la=de Thu, 04 Jun 2020 00:00:00 +0000 <![CDATA[Cai, N. et al. Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Nat. Genet. 52, 437-447 (2020)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58773&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58773&la=de Mon, 06 Apr 2020 00:00:00 +0000 <![CDATA[Haberer, G. et al. European maize genomes highlight intraspecies variation in repeat and gene content. Nat. Genet. 52, 950-957 (2020)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=59786&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=59786&la=de Mon, 05 Oct 2020 00:00:00 +0000 <![CDATA[Schlosser, P.* et al. Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans. Nat. Genet. 52, 167-176 (2020)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58739&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58739&la=de Wed, 01 Apr 2020 00:00:00 +0000 <![CDATA[Surendran, P.* et al. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Nat. Genet. 52, 1314–133 (2020)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60613&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60613&la=de Wed, 16 Dec 2020 00:00:00 +0000 <![CDATA[Szabo, Q.* et al. Regulation of single-cell genome organization into TADs and chromatin nanodomains. Nat. Genet. 52, 1151-1157 (2020)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60339&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60339&la=de Fri, 13 Nov 2020 00:00:00 +0000 <![CDATA[Bentley, A.R.* et al. Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Nat. Genet. 51, 636-648 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55838&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55838&la=de Fri, 12 Apr 2019 00:00:00 +0000 <![CDATA[Demontis, D.* et al. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nat. Genet. 51, 63–75 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54899&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54899&la=de Tue, 11 Dec 2018 00:00:00 +0000 <![CDATA[Justice, A.E.* et al. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Nat. Genet. 51, 452–469 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55567&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55567&la=de Wed, 27 Feb 2019 00:00:00 +0000 <![CDATA[Karlsson Linnér, R.* et al. Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Nat. Genet. 51, 245-257 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55312&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55312&la=de Mon, 11 Mar 2019 00:00:00 +0000 <![CDATA[Kunkle, B.W.* et al. Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nat. Genet. 51, 414-430 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55740&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55740&la=de Tue, 26 Mar 2019 00:00:00 +0000 <![CDATA[Kunkle, B.W.* et al. Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (Nature Genetics, (2019), 51, 3, (414-430), 10.1038/s41588-019-0358-2). Nat. Genet. 51, 1423-1424 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56759&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56759&la=de Mon, 30 Sep 2019 00:00:00 +0000 <![CDATA[Lane, J.M.* et al. Biological and clinical insights from genetics of insomnia symptoms. Nat. Genet. 51, 387-393 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55580&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55580&la=de Fri, 22 Mar 2019 00:00:00 +0000 <![CDATA[Maccaferri, M.* et al. Durum wheat genome highlights past domestication signatures and future improvement targets. Nat. Genet. 51, 885–895 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55825&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55825&la=de Fri, 12 Apr 2019 00:00:00 +0000 <![CDATA[Malik, R.* et al. Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (Nature Genetics, (2018), 50, 4, (524-537), 10.1038/s41588-018-0058-3). Nat. Genet. (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56353&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56353&la=de Thu, 27 Jun 2019 00:00:00 +0000 <![CDATA[Pont, C.* et al. Tracing the ancestry of modern bread wheats. Nat. Genet. 51, 905-911 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55977&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55977&la=de Tue, 14 May 2019 00:00:00 +0000 <![CDATA[Sakornsakolpat, P.* et al. Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. Nat. Genet. 51, 494-505 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55601&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55601&la=de Mon, 18 Mar 2019 00:00:00 +0000 <![CDATA[Satizabal, C.L.* et al. Genetic architecture of subcortical brain structures in 38,851 individuals. Nat. Genet. 51, 1624-1636 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=57169&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=57169&la=de Fri, 25 Oct 2019 00:00:00 +0000 <![CDATA[Shrine, N.* et al. New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Nat. Genet. 51, 481-493 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55581&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55581&la=de Tue, 19 Mar 2019 00:00:00 +0000 <![CDATA[Shrine, N.* et al. Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries (Nature Genetics, (2019), 51, 3, (481-493), 10.1038/s41588-018-0321-7). Nat. Genet., DOI: 10.1038/s41588-019-0438-3 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56099&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56099&la=de Wed, 22 May 2019 00:00:00 +0000 <![CDATA[Tachmazidou, I.* et al. Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. Nat. Genet. 51, 230-236 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55359&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55359&la=de Fri, 15 Mar 2019 00:00:00 +0000 <![CDATA[Tin, A.* et al. Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Nat. Genet. 51, 1459-1474 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=57010&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=57010&la=de Mon, 07 Oct 2019 00:00:00 +0000 <![CDATA[Warrington, N.M.* et al. Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. Nat. Genet. 51, 804-814 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55978&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55978&la=de Tue, 14 May 2019 00:00:00 +0000 <![CDATA[Watson, H.J.* et al. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nat. Genet. 51, 1207-1214 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56579&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56579&la=de Thu, 01 Aug 2019 00:00:00 +0000 <![CDATA[Wuttke, M.* et al. A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nat. Genet. 51, 957-972 (2019)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56203&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56203&la=de Thu, 06 Jun 2019 00:00:00 +0000 <![CDATA[Demenais, F.* et al. Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Nat. Genet. 50, 42-53 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52592&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52592&la=de Mon, 25 Dec 2017 00:00:00 +0000 <![CDATA[Evangelou, E.* et al. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nat. Genet. 50, 1412-1425 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54333&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54333&la=de Mon, 01 Oct 2018 00:00:00 +0000 <![CDATA[Evangelou, E.* et al. Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x). Nat. Genet., DOI: 10.1038/s41588-018-0297-3 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54757&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54757&la=de Thu, 22 Nov 2018 00:00:00 +0000 <![CDATA[Fernandes-Rosa, F.L.* et al. A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism. Nat. Genet. 50, 355-361 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52889&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52889&la=de Fri, 18 May 2018 00:00:00 +0000 <![CDATA[Klarin, D.* et al. Genetics of blood lipids among similar to 300,000 multi-ethnic participants of the Million Veteran Program. Nat. Genet. 50, 1514-1523 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54689&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54689&la=de Tue, 13 Nov 2018 00:00:00 +0000 <![CDATA[Lee, J.J.* et al. Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Nat. Genet. 52, 1112-1121 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54051&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54051&la=de Fri, 03 Aug 2018 00:00:00 +0000 <![CDATA[Mahajan, A.* et al. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Nat. Genet. 50, 559-571 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53544&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53544&la=de Fri, 18 May 2018 00:00:00 +0000 <![CDATA[Mahajan, A.* et al. Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps. Nat. Genet. 50, 1505-1513 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54688&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54688&la=de Tue, 13 Nov 2018 00:00:00 +0000 <![CDATA[Malik, R.* et al. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nat. Genet. 50, 524-537 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53263&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53263&la=de Thu, 03 May 2018 00:00:00 +0000 <![CDATA[Marti-Renom, M.A.* et al. Challenges and guidelines toward 4D nucleome data and model standards. Nat. Genet. 50, 1352-1358 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54447&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54447&la=de Fri, 19 Oct 2018 00:00:00 +0000 <![CDATA[Roselli, C.* et al. Multi-ethnic genome-wide association study for atrial fibrillation. Nat. Genet. 50, 1225–1233 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53830&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53830&la=de Thu, 12 Jul 2018 00:00:00 +0000 <![CDATA[Tedja, M.S.* et al. Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Nat. Genet. 50, 834-848 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53578&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53578&la=de Tue, 19 Jun 2018 00:00:00 +0000 <![CDATA[Turcot, V.* et al. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat. Genet. 50, 26-41 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52673&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52673&la=de Wed, 31 Jan 2018 00:00:00 +0000 <![CDATA[Turcot, V.* et al. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (vol 50, pg 765, 2017). Nat. Genet. 50, 764-768 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53335&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53335&la=de Mon, 04 Jun 2018 00:00:00 +0000 <![CDATA[Waage, J.* et al. Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nat. Genet. 50, 1072–1080 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53957&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53957&la=de Thu, 19 Jul 2018 00:00:00 +0000 <![CDATA[Waage, J.* et al. Author correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nat. Genet. 50:1343 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54137&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54137&la=de Wed, 12 Sep 2018 00:00:00 +0000 <![CDATA[Zierer, J. et al. The fecal metabolome as a functional readout of the gut microbiome. Nat. Genet. 50, 790-795 (2018)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53577&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53577&la=de Wed, 27 Jun 2018 00:00:00 +0000 <![CDATA[Christophersen, I.E.* et al. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat. Genet. 49, 946-952 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51375&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51375&la=de Mon, 03 Jul 2017 00:00:00 +0000 <![CDATA[Day, F.R.* et al. Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nat. Genet. 49, 834-841 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50976&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50976&la=de Wed, 14 Jun 2017 00:00:00 +0000 <![CDATA[Ferreira, M.A.* et al. Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Nat. Genet. 49, 1752-1757 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52237&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52237&la=de Thu, 16 Nov 2017 00:00:00 +0000 <![CDATA[Hammerschlag, A.R.* et al. Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Nat. Genet. 49, 1584-1592 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51290&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51290&la=de Mon, 17 Jul 2017 00:00:00 +0000 <![CDATA[Howson, J.M.M.* et al. Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms. Nat. Genet. 49, 1113-1119 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51513&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51513&la=de Mon, 17 Jul 2017 00:00:00 +0000 <![CDATA[Iturbide Martinez De Albeniz, A. & Torres-Padilla, M.E. Starting embryonic transcription for the first time. Nat. Genet. 49, 820-821 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51197&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51197&la=de Wed, 28 Jun 2017 00:00:00 +0000 <![CDATA[Jachowicz, J.W. et al. LINE-1 activation after fertilization regulates global chromatin accessibility in the early mouse embryo. Nat. Genet. 49, 1502–1510 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51763&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51763&la=de Wed, 13 Sep 2017 00:00:00 +0000 <![CDATA[Liu, D.J.* et al. Exome-wide association study of plasma lipids in >300,000 individuals. Nat. Genet. 49, 1758-1766 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52501&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52501&la=de Wed, 13 Dec 2017 00:00:00 +0000 <![CDATA[Lu, X.* et al. Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease. Nat. Genet. 49, 1722–1730 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52531&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52531&la=de Thu, 28 Dec 2017 00:00:00 +0000 <![CDATA[McKay, J.D.* et al. Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Nat. Genet. 49, 1126-1132 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51291&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51291&la=de Fri, 14 Jul 2017 00:00:00 +0000 <![CDATA[Meehan, T.F.* et al. Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. Nat. Genet. 49, 1231-1238 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51406&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51406&la=de Thu, 20 Jul 2017 00:00:00 +0000 <![CDATA[Melin, B.S.* et al. Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Nat. Genet. 49, 789-794 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51129&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51129&la=de Tue, 30 May 2017 00:00:00 +0000 <![CDATA[Rodriguez-Terrones, D. et al. A molecular roadmap for the emergence of early-embryonic-like cells in culture. Nat. Genet. 50, 106-119 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52572&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52572&la=de Wed, 27 Dec 2017 00:00:00 +0000 <![CDATA[Wain, L.V.* et al. Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. Nat. Genet. 49, 416-425 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50656&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50656&la=de Thu, 09 Mar 2017 00:00:00 +0000 <![CDATA[Warren, H.R.* et al. Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Nat. Genet. 49, 403-415 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50660&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50660&la=de Thu, 09 Mar 2017 00:00:00 +0000 <![CDATA[Barban, N.* et al. Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat. Genet. 48, 1462-1472 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49857&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49857&la=de Wed, 02 Nov 2016 00:00:00 +0000 <![CDATA[Ehret, G.B.* et al. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nat. Genet. 48, 1171-1184 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49464&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49464&la=de Wed, 28 Sep 2016 00:00:00 +0000 <![CDATA[Gormley, P.* et al. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat. Genet. 48, 856-866 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48926&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48926&la=de Tue, 05 Jul 2016 00:00:00 +0000 <![CDATA[Huypens, P. et al. Epigenetic germline inheritance of diet-induced obesity and insulin resistance. Nat. Genet. 48, 497-499 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48106&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48106&la=de Wed, 16 Mar 2016 00:00:00 +0000 <![CDATA[Kenna, K.P.* et al. NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. Nat. Genet. 48, 1037-1042 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49167&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49167&la=de Mon, 01 Aug 2016 00:00:00 +0000 <![CDATA[McCarthy, S.* et al. A reference panel of 64,976 haplotypes for genotype imputation. Nat. Genet. 48, 1279-1283 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49370&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49370&la=de Tue, 06 Sep 2016 00:00:00 +0000 <![CDATA[Okbay, A.* et al. Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nat. Genet. 48, 624-633 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48420&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48420&la=de Wed, 20 Apr 2016 00:00:00 +0000 <![CDATA[Pradeepa, M.M.* et al. Histone H3 globular domain acetylation identifies a new class of enhancers. Nat. Genet. 48, 681-686 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48826&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48826&la=de Mon, 27 Jun 2016 00:00:00 +0000 <![CDATA[Surendran, P.* et al. Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nat. Genet. 48, 1151-1161 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49787&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49787&la=de Mon, 24 Oct 2016 00:00:00 +0000 <![CDATA[van Rheenen, W.* et al. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nat. Genet. 48, 1043-1048 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49166&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49166&la=de Mon, 01 Aug 2016 00:00:00 +0000 <![CDATA[Witteveen, J.S.* et al. Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity. Nat. Genet. 48, 877-887 (2016)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49153&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49153&la=de Fri, 29 Jul 2016 00:00:00 +0000 <![CDATA[Chen, Y.-C.* et al. Transcriptional regulator PRDM12 is essential for human pain perception. Nat. Genet. 47, 803-808 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44968&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44968&la=de Wed, 27 May 2015 00:00:00 +0000 <![CDATA[Chen, Y.-C.* et al. Corrigendum: Transcriptional regulator PRDM12 is essential for human pain perception. Nat. Genet. 47, 962 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46502&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46502&la=de Wed, 05 Aug 2015 00:00:00 +0000 <![CDATA[Day, F.R.* et al. Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nat. Genet. 47, 1294-1303 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47210&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47210&la=de Fri, 06 Nov 2015 00:00:00 +0000 <![CDATA[Debette, S.* et al. Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection. Nat. Genet. 47, 78-83 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42826&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42826&la=de Wed, 26 Nov 2014 00:00:00 +0000 <![CDATA[Gaulton, K.J.* et al. Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. Nat. Genet. 47, 1415-1425 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47226&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47226&la=de Tue, 08 Dec 2015 00:00:00 +0000 <![CDATA[Goyette, P.* et al. High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis. Nat. Genet. 47, 172-179 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46312&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46312&la=de Wed, 15 Jul 2015 00:00:00 +0000 <![CDATA[Hrabě de Angelis, M. et al. Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics. Nat. Genet. 47, 969-978 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46429&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46429&la=de Wed, 29 Jul 2015 00:00:00 +0000 <![CDATA[Kato, N.* et al. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Nat. Genet. 47, 1282-1293 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46925&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46925&la=de Wed, 07 Oct 2015 00:00:00 +0000 <![CDATA[Kohl, S.* et al. Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia. Nat. Genet. 47, 757-765 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=45069&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=45069&la=de Wed, 03 Jun 2015 00:00:00 +0000 <![CDATA[Moutsianas, L.* et al. Class II HLA interactions modulate genetic risk for multiple sclerosis. Nat. Genet. 47, 1107-1113 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46978&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46978&la=de Wed, 14 Oct 2015 00:00:00 +0000 <![CDATA[CARDIoGRAMplusC4D Consortium (Nikpay, M.* ; Goel, A.* ; Won, H.* ; Hall, L.M.* ; Willenborg, C.* ; Kanoni, S.* ; Saleheen, D.* ; Gieger, C. ; Meitinger, T. ; Peters, A. ; Watkins, H.* ; Kathiresan, S.* ; MacPherson, R.*) A comprehensive 1000 genomes–based genome-wide association meta-analysis of coronary artery disease. Nat. Genet. 47, 1121-1130 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46918&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46918&la=de Wed, 07 Oct 2015 00:00:00 +0000 <![CDATA[Paternoster, L.* et al. Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. Nat. Genet. 47, 1449-1456 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47689&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47689&la=de Fri, 13 Nov 2015 00:00:00 +0000 <![CDATA[Reincke, M.* et al. Mutations in the deubiquitinase gene USP8 cause Cushing's disease. Nat. Genet. 47, 31-38 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42923&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42923&la=de Wed, 10 Dec 2014 00:00:00 +0000 <![CDATA[Surakka, I.* et al. The impact of low-frequency and rare variants on lipid levels. Nat. Genet. 47, 589-597 (2015)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44834&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44834&la=de Wed, 13 May 2015 00:00:00 +0000 <![CDATA[Arking, D.E.* et al. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat. Genet. 46, 826-836 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31665&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31665&la=de Wed, 25 Jun 2014 00:00:00 +0000 <![CDATA[Flannick, J.* et al. Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. Nat. Genet. 46, 357-363 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=43127&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=43127&la=de Wed, 31 Dec 2014 00:00:00 +0000 <![CDATA[DIAGRAM Consortium (Gieger, C. ; Grallert, H. ; Illig, T. ; Klopp, N. ; Müller-Nurasyid, M. ; Peters, A.) et al. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat. Genet. 46, 234-244 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=30792&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=30792&la=de Tue, 18 Mar 2014 00:00:00 +0000 <![CDATA[Loth, D.W.* et al. Genome-wide association analysis identifies six new loci associated with forced vital capacity. Nat. Genet. 46, 669-677 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31623&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31623&la=de Tue, 17 Jun 2014 00:00:00 +0000 <![CDATA[Shin, S.Y.* et al. An atlas of genetic influences on human blood metabolites. Nat. Genet. 46, 543-550 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31272&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31272&la=de Wed, 14 May 2014 00:00:00 +0000 <![CDATA[Walsh, K.M.* et al. Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk. Nat. Genet. 46, 731-735 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31817&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31817&la=de Mon, 28 Jul 2014 00:00:00 +0000 <![CDATA[Wang, M.* et al. The genome sequence of African rice (Oryza glaberrima) and evidence for independent domestication. Nat. Genet. 46, 982-988 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31850&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31850&la=de Thu, 31 Jul 2014 00:00:00 +0000 <![CDATA[Wood, A.R.* et al. Defining the role of common variation in the genomic and biological architecture of adult human height. Nat. Genet. 46, 1173-1186 (2014)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=32470&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=32470&la=de Sun, 05 Oct 2014 00:00:00 +0000 <![CDATA[AMD Gene Consortium et al. Seven new loci associated with age-related macular degeneration. Nat. Genet. 45, 433-439 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23761&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23761&la=de Thu, 11 Apr 2013 00:00:00 +0000 <![CDATA[Global Lipids Genetics Consortium et al. Discovery and refinement of loci associated with lipid levels. Nat. Genet. 45, 1274-1283 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28110&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28110&la=de Wed, 06 Nov 2013 00:00:00 +0000 <![CDATA[Agarwala, V.* ; Flannick, J.* ; Sunyaev, S.R.* ; GoT2D Consortium (Gieger, C. ; Grallert, H. ; Hrabě de Angelis, M. ; Huth, C. ; Kriebel, J. ; Meisinger, C. ; Meitinger, T. ; Müller-Nurasyid, M. ; Peters, A. ; Rathmann, W. ; Ried, J.S. ; Strauch, K. ; Strom, T.M.) & Altshuler, D.* Evaluating empirical bounds on complex disease genetic architecture. Nat. Genet. 45, 1418-1427 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=43141&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=43141&la=de Wed, 31 Dec 2014 00:00:00 +0000 <![CDATA[Anttila, V.* et al. Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nat. Genet. 45, 912-917 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=26605&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=26605&la=de Mon, 12 Aug 2013 00:00:00 +0000 <![CDATA[Berndt, S.I.* et al. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat. Genet. 45, 501-512 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24392&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24392&la=de Wed, 15 May 2013 00:00:00 +0000 <![CDATA[Beuschlein, F.* et al. Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension. Nat. Genet. 45, 440-444 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24036&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24036&la=de Mon, 22 Apr 2013 00:00:00 +0000 <![CDATA[Bezzina, C.R.* et al. Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. Nat. Genet. 45, 1044-1049 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=26023&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=26023&la=de Mon, 29 Jul 2013 00:00:00 +0000 <![CDATA[Bønnelykke, K.* et al. Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization. Nat. Genet. 45, 902-906 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=25677&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=25677&la=de Mon, 08 Jul 2013 00:00:00 +0000 <![CDATA[Cappello, S. et al. Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development. Nat. Genet. 45, 1300-1308 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=27509&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=27509&la=de Thu, 26 Sep 2013 00:00:00 +0000 <![CDATA[Codd, V.* et al. Identification of seven loci affecting mean telomere length and their association with disease. Nat. Genet. 45, 422-427 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23763&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23763&la=de Thu, 11 Apr 2013 00:00:00 +0000 <![CDATA[Deloukas, P.* et al. Large-scale association analysis identifies new risk loci for coronary artery disease. Nat. Genet. 45, 25-35 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22409&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22409&la=de Fri, 01 Feb 2013 00:00:00 +0000 <![CDATA[den Hoed, M.* et al. Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat. Genet. 45, 621-631 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24955&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24955&la=de Mon, 24 Jun 2013 00:00:00 +0000 <![CDATA[Do, R.* et al. Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat. Genet. 45, 1345-1352 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=27901&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=27901&la=de Thu, 24 Oct 2013 00:00:00 +0000 <![CDATA[Ellinghaus, D.* et al. High-density genotyping study identifies four new susceptibility loci for atopic dermatitis. Nat. Genet. 45, 808-812 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=26132&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=26132&la=de Wed, 31 Jul 2013 00:00:00 +0000 <![CDATA[Garcia-Closas, M.* et al. Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Nat. Genet. 45, 392-398 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24235&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24235&la=de Fri, 03 May 2013 00:00:00 +0000 <![CDATA[Hoff, S.* et al. ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3. Nat. Genet. 45, 951-956 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=26162&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=26162&la=de Wed, 31 Jul 2013 00:00:00 +0000 <![CDATA[Horikoshi, M.* et al. New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Nat. Genet. 45, 76-82 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=11861&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=11861&la=de Wed, 23 Jan 2013 00:00:00 +0000 <![CDATA[International Multiple Sclerosis Genetics Consortium (Illig, T. ; Lichtner, P.) et al. Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat. Genet. 45, 1353-1360 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28290&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28290&la=de Tue, 19 Nov 2013 00:00:00 +0000 <![CDATA[Kornblum, C.* et al. Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease. Nat. Genet. 45, 214-219 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22963&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22963&la=de Fri, 01 Mar 2013 00:00:00 +0000 <![CDATA[Köttgen, A.* et al. Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat. Genet. 45, 145-154 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=11719&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=11719&la=de Mon, 31 Dec 2012 00:00:00 +0000 <![CDATA[Liu, J.Z.* et al. Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Nat. Genet. 45, 670-675 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=25510&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=25510&la=de Fri, 05 Jul 2013 00:00:00 +0000 <![CDATA[Michailidou, K.* et al. Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Nat. Genet. 45, 353-361 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24242&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24242&la=de Fri, 03 May 2013 00:00:00 +0000 <![CDATA[Verhoeven, V.J.M.* et al. Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat. Genet. 45, 314-318 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23614&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23614&la=de Thu, 28 Mar 2013 00:00:00 +0000 <![CDATA[Westra, H.J.* et al. Systematic identification of trans eQTLs as putative drivers of known disease associations. Nat. Genet. 45, 1238-1243 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=27485&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=27485&la=de Thu, 26 Sep 2013 00:00:00 +0000 <![CDATA[Bonnefond, A.* et al. Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes. Nat. Genet. 44, 297-301 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28629&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28629&la=de Wed, 11 Dec 2013 00:00:00 +0000 <![CDATA[Bradfield, J.P.* et al. A genome-wide association meta-analysis identifies new childhood obesity loci. Nat. Genet. 44, 526-531 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7531&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7531&la=de Thu, 14 Jun 2012 00:00:00 +0000 <![CDATA[Cho, Y.S.* et al. Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. Nat. Genet. 44, 67-72 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7219&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7219&la=de Fri, 02 Mar 2012 00:00:00 +0000 <![CDATA[Ellinor, P.T.* et al. Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat. Genet. 44, 670-675 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7994&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7994&la=de Mon, 23 Jul 2012 00:00:00 +0000 <![CDATA[Freilinger, T.* et al. Genome-wide association analysis identifies susceptibility loci for migraine without aura. Nat. Genet. 44, 777-782 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8189&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8189&la=de Thu, 26 Jul 2012 00:00:00 +0000 <![CDATA[Ghoussaini, M.* et al. Genome-wide association analysis identifies three new breast cancer susceptibility loci. Nat. Genet. 44, 312-319 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7255&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7255&la=de Tue, 27 Mar 2012 00:00:00 +0000 <![CDATA[Ikram, M.A.* et al. Common variants at 6q22 and 17q21 are associated with intracranial volume. Nat. Genet. 44, 539-544 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7462&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7462&la=de Tue, 05 Jun 2012 00:00:00 +0000 <![CDATA[Lu, X.* et al. Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease. Nat. Genet. 44, 890-894 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=11162&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=11162&la=de Fri, 30 Nov 2012 00:00:00 +0000 <![CDATA[Manning, A.K.* et al. A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nat. Genet. 44, 659-669 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8453&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8453&la=de Thu, 30 Aug 2012 00:00:00 +0000 <![CDATA[International Stroke Genetics Consortium (Meisinger, C.) & Wellcome Trust Case Control Consortium 2 (WTCCC2) (*) Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nat. Genet. 44, 328-333 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7256&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7256&la=de Tue, 27 Mar 2012 00:00:00 +0000 <![CDATA[Morris, A.P.* et al. Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat. Genet. 44, 981-990 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=10446&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=10446&la=de Thu, 11 Oct 2012 00:00:00 +0000 <![CDATA[Okada, Y.* et al. Meta-analysis identifies multiple loci associated with kidney function-related traits in East Asian populations. Nat. Genet. 44, 904-909 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8432&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8432&la=de Thu, 30 Aug 2012 00:00:00 +0000 <![CDATA[Okada, Y.* et al. Common variants at CDKAL1 and KLF9 are associated with body mass index in East Asian populations. Nat. Genet. 44, 302-306 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28626&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28626&la=de Wed, 11 Dec 2013 00:00:00 +0000 <![CDATA[Paternoster, L.* et al. Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. Nat. Genet. 44, 187-192 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6901&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6901&la=de Sat, 31 Dec 2011 00:00:00 +0000 <![CDATA[Scott, R.A.* et al. Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nat. Genet. 44, 991-1005 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=10445&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=10445&la=de Thu, 11 Oct 2012 00:00:00 +0000 <![CDATA[Stahl, E.A.* et al. Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis. Nat. Genet. 44, 483-489 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7541&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7541&la=de Tue, 19 Jun 2012 00:00:00 +0000 <![CDATA[Stolk, L.* et al. Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat. Genet. 44, 260-268 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7263&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7263&la=de Wed, 28 Mar 2012 00:00:00 +0000 <![CDATA[Taal, H.R.* et al. Common variants at 12q15 and 12q24 are associated with infant head circumference. Nat. Genet. 44, 532-538 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7461&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7461&la=de Tue, 05 Jun 2012 00:00:00 +0000 <![CDATA[Tsoi, L.C.* et al. Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nat. Genet. 44, 1341-1348 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=11504&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=11504&la=de Fri, 28 Dec 2012 00:00:00 +0000 <![CDATA[Turchin, M.C.* et al. Evidence of widespread selection on standing variation in Europe at height-associated SNPs. Nat. Genet. 44, 1015-1019 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28628&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28628&la=de Wed, 11 Dec 2013 00:00:00 +0000 <![CDATA[Wen, W.* et al. Meta-analysis identifies common variants associated with body mass index in east Asians. Nat. Genet. 44, 307-311 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28627&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28627&la=de Wed, 11 Dec 2013 00:00:00 +0000 <![CDATA[Yang, J.* et al. Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nat. Genet. 44, 369-375 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8167&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8167&la=de Tue, 24 Jul 2012 00:00:00 +0000 <![CDATA[Artigas, M.S.* et al. Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nat. Genet. 43, 1082-1090 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4702&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4702&la=de Mon, 07 Nov 2011 00:00:00 +0000 <![CDATA[Bis, J.C.* et al. Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. Nat. Genet. 43, 940-947 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6701&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6701&la=de Mon, 28 Nov 2011 00:00:00 +0000 <![CDATA[Chambers, J.C.* et al. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Nat. Genet. 43, 1131-1138 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6365&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6365&la=de Mon, 12 Dec 2011 00:00:00 +0000 <![CDATA[Heid, I.M. et al. Corrigendum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat. Genet. 43, 1164 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=10431&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=10431&la=de Mon, 08 Oct 2012 00:00:00 +0000 <![CDATA[Hollingworth, P.* et al. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat. Genet. 43, 429-436 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2342&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2342&la=de Thu, 30 Jun 2011 00:00:00 +0000 <![CDATA[Hu, T.T.* et al. The Arabidopsis lyrata genome sequence and the basis of rapid genome size change. Nat. Genet. 43, 476-481 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6255&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6255&la=de Mon, 21 Nov 2011 00:00:00 +0000 <![CDATA[Kilpeläinen, T.O.* et al. Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile. Nat. Genet. 43, 753-760 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6468&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6468&la=de Tue, 06 Sep 2011 00:00:00 +0000 <![CDATA[Kornum, B.R.* et al. Common variants in P2RY11 are associated with narcolepsy. Nat. Genet. 43, 66-71 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4674&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4674&la=de Mon, 24 Jan 2011 00:00:00 +0000 <![CDATA[Melum, E.* et al. Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. Nat. Genet. 43, 17-19 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6299&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6299&la=de Tue, 24 May 2011 00:00:00 +0000 <![CDATA[Purdue, M.P.* et al. Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3. Nat. Genet. 43, 60-65 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6379&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6379&la=de Wed, 22 Jun 2011 00:00:00 +0000 <![CDATA[Schunkert, H.* et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat. Genet. 43, 333-340 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4665&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4665&la=de Tue, 05 Jul 2011 00:00:00 +0000 <![CDATA[Small, K.S.* et al. Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes. Nat. Genet. 43, 561-564 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6769&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6769&la=de Thu, 08 Dec 2011 00:00:00 +0000 <![CDATA[Suhre, K. et al. A genome-wide association study of metabolic traits in human urine. Nat. Genet. 43, 565-571 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6422&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6422&la=de Wed, 27 Jul 2011 00:00:00 +0000 <![CDATA[Wain, L.V.* et al. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat. Genet. 43, 1005-1011 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6662&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6662&la=de Mon, 14 Nov 2011 00:00:00 +0000 <![CDATA[GoDARTS and UKPDS Diabetes Pharmacogenetics Study Group (Zhou, K.* ; Bellenguez, C.* ; Spencer, C.C.* ; Bennett, A.J.* ; Coleman, R.L.* ; Tavendale, R.* ; Hawley, S.A.* ; Donnelly, L.A.* ; Schofield, C.* ; Groves, C.J.* ; Burch, L.* ; Carr, F.* ; Strange, A.* ; Freeman, C.* ; Blackwell, J.M.* ; Bramon, E.* ; Brown, M.A.* ; Casas, J.P.* ; Corvin, A.* ; Craddock, N.* ; Deloukas, P.* ; Dronov, S.* ; Duncanson, A.* ; Edkins, S.* ; Gray, E.* ; Hunt, S.* ; Jankowski, J.* ; Langford, C.* ; Markus, H.S.* ; Mathew, C.G.* ; Plomin, R.* ; Rautanen, A.* ; Sawcer, S.J.* ; Samani, N.J.* ; Trembath, R.* ; Viswanathan, A.C.* ; Wood, N.W* ; Harries, L.W.* ; Hattersley, A.T.* ; Doney, A.S.* ; Colhoun, H.* ; Morris, A.D.* ; Sutherland, C.* ; Hardie, D.G.* ; Peltonen, L.* ; McCarthy, M.I.* ; Holman, R.R.* ; Palmer, C.N.* ; Donnelly, P.* ; Pearson, E.R.*) ; Wellcome Trust Case Control Consortium 2 (WTCCC2) (*) & MAGIC Investigators (Grallert, H. ; Gieger, C. ; Meisinger, C. ; Thorand, B. ; Wichmann, H.-E. ; Illig, T.) Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. Nat. Genet. 43, 117-120 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3971&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3971&la=de Sat, 31 Dec 2011 00:00:00 +0000 <![CDATA[Anttila, V.* et al. Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Nat. Genet. 42, 869-873 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=527&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=527&la=de Mon, 18 Oct 2010 00:00:00 +0000 <![CDATA[Bezzina, C.R.* et al. Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction. Nat. Genet. 42, 688-691 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5642&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5642&la=de Fri, 01 Oct 2010 00:00:00 +0000 <![CDATA[Dupuis, J.* et al. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat. Genet. 42, 105-116 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1979&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1979&la=de Wed, 31 Mar 2010 00:00:00 +0000 <![CDATA[Elks, C.E.* et al. Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat. Genet. 42, 1077-1085 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3108&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3108&la=de Fri, 31 Dec 2010 00:00:00 +0000 <![CDATA[Ellinghaus, E.* et al. Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. Nat. Genet. 42, 991-995 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5855&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5855&la=de Thu, 25 Nov 2010 00:00:00 +0000 <![CDATA[Ellinor, P.T.* et al. Common variants in KCNN3 are associated with lone atrial fibrillation. Nat. Genet. 42, 240-244 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1583&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1583&la=de Wed, 30 Jun 2010 00:00:00 +0000 <![CDATA[Franke, A.* et al. Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). Nat. Genet. 42, 292-294 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3237&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3237&la=de Mon, 26 Jul 2010 00:00:00 +0000 <![CDATA[Freathy, R.M.* et al. Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nat. Genet. 42, 430-435 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=933&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=933&la=de Tue, 27 Jul 2010 00:00:00 +0000 <![CDATA[Haack, T.B. et al. Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency. Nat. Genet. 42, 1131-1134 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5495&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5495&la=de Fri, 31 Dec 2010 00:00:00 +0000 <![CDATA[Heid, I.M. et al. Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat. Genet. 42, 949-960 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6083&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6083&la=de Fri, 17 Dec 2010 00:00:00 +0000 <![CDATA[Hüffmeier, U.* et al. Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. Nat. Genet. 42, 996-999 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4350&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4350&la=de Fri, 31 Dec 2010 00:00:00 +0000 <![CDATA[Illig, T. et al. A genome-wide perspective of genetic variation in human metabolism. Nat. Genet. 42, 137-141 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52&la=de Mon, 01 Mar 2010 00:00:00 +0000 <![CDATA[Köttgen, A.* et al. New loci associated with kidney function and chronic kidney disease. Nat. Genet. 42, 376-384 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5849&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5849&la=de Thu, 25 Nov 2010 00:00:00 +0000 <![CDATA[Liu, J.Z.* et al. Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nat. Genet. 42, 436-440 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=957&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=957&la=de Mon, 13 Sep 2010 00:00:00 +0000 <![CDATA[Mangold, E.* et al. Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. Nat. Genet. 42, 24-26 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1736&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1736&la=de Mon, 22 Mar 2010 00:00:00 +0000 <![CDATA[Meindl, A.* et al. Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. Nat. Genet. 42, 410-414 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4194&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4194&la=de Wed, 06 Oct 2010 00:00:00 +0000 <![CDATA[Morelli, G.* et al. Yersinia pestis genome sequencing identifies patterns of global phylogenetic diversity. Nat. Genet. 42, 1140-1143 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4675&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4675&la=de Fri, 31 Dec 2010 00:00:00 +0000 <![CDATA[Pfeufer, A. et al. Genome-wide association study of PR interval. Nat. Genet. 42, 153-159 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65&la=de Wed, 30 Jun 2010 00:00:00 +0000 <![CDATA[Repapi, E.* et al. Genome-wide association study identifies five loci associated with lung function. Nat. Genet. 42, 36-44 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2952&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2952&la=de Thu, 28 Jan 2010 00:00:00 +0000 <![CDATA[Saxena, R.* et al. Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Nat. Genet. 42, 142-148 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1053&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1053&la=de Tue, 30 Mar 2010 00:00:00 +0000 <![CDATA[Sotoodehnia, N.* et al. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nat. Genet. 42, 1068-1076 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3906&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3906&la=de Fri, 31 Dec 2010 00:00:00 +0000 <![CDATA[Speliotes, E.K.* et al. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat. Genet. 42, 937-948 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=817&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=817&la=de Mon, 20 Dec 2010 00:00:00 +0000 <![CDATA[Thorgeirsson, T.E.* et al. Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nat. Genet. 42, 448-453 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1168&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1168&la=de Tue, 27 Jul 2010 00:00:00 +0000 <![CDATA[Voight, B.F.* et al. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat. Genet. 42, 579-589 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5641&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5641&la=de Fri, 01 Oct 2010 00:00:00 +0000 <![CDATA[Yasuno, K.* et al. Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nat. Genet. 42, 420-425 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1166&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1166&la=de Tue, 27 Jul 2010 00:00:00 +0000 <![CDATA[Aulchenko, Y.S.* et al. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat. Genet. 41, 47-55 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2245&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2245&la=de Thu, 09 Jul 2009 00:00:00 +0000 <![CDATA[Benjamin, E.J.* et al. Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nat. Genet. 41, 879-81 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=256&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=256&la=de Thu, 03 Sep 2009 00:00:00 +0000 <![CDATA[Erdmann, J.* et al. New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat. Genet. 41, 280-282 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=984&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=984&la=de Thu, 09 Jul 2009 00:00:00 +0000 <![CDATA[Esparza-Gordillo, J.* et al. A common variant on chromosome 11q13 is associated with atopic dermatitis. Nat. Genet. 41, 596-601 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=519&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=519&la=de Thu, 09 Jul 2009 00:00:00 +0000 <![CDATA[Ganesh, S.K.* et al. Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Nat. Genet. 41, 1191-1198 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1439&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1439&la=de Thu, 31 Dec 2009 00:00:00 +0000 <![CDATA[Ghezzi, D.* et al. SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy. Nat. Genet. 41, 654-656 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1499&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1499&la=de Fri, 11 Sep 2009 00:00:00 +0000 <![CDATA[Gudbjartsson, D.F.* et al. A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. Nat. Genet. 41, 876-878 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=359&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=359&la=de Fri, 04 Dec 2009 00:00:00 +0000 <![CDATA[Gudbjartsson, D.F.* et al. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Nat. Genet. 41, 342-347 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=932&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=932&la=de Thu, 09 Jul 2009 00:00:00 +0000 <![CDATA[Hallmayer, J.* et al. Narcolepsy is strongly associated with the T-cell receptor alpha locus. Nat. Genet. 41, 708-711 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1090&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1090&la=de Thu, 09 Jul 2009 00:00:00 +0000 <![CDATA[Harold, D.* et al. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nat. Genet. 41, 1088-1093 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=90&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=90&la=de Wed, 25 Nov 2009 00:00:00 +0000 <![CDATA[Kathiresan, S.* et al. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat. Genet. 41, 334-341 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1637&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1637&la=de Fri, 04 Sep 2009 00:00:00 +0000 <![CDATA[Lewis, M.A.* et al. An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice. Nat. Genet. 41, 614-618 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=683&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=683&la=de Thu, 09 Jul 2009 00:00:00 +0000 <![CDATA[Newton-Cheh, C.* et al. Genome-wide association study identifies eight loci associated with blood pressure. Nat. Genet. 41, 666-676 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1023&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1023&la=de Thu, 03 Dec 2009 00:00:00 +0000 <![CDATA[Pfeufer, A. et al. Common variants at ten loci modulate the QT interval duration in the QTSCD Study. Nat. Genet. 41, 407-414 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=935&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=935&la=de Thu, 09 Jul 2009 00:00:00 +0000 <![CDATA[Prokopenko, I.* et al. Variants in MTNR1B influence fasting glucose levels. Nat. Genet. 41, 77-81 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=258&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=258&la=de Thu, 09 Jul 2009 00:00:00 +0000 <![CDATA[Simon-Sanchez, J.* et al. Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat. Genet. 41, 1308-1314 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=918&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=918&la=de Thu, 31 Dec 2009 00:00:00 +0000 <![CDATA[Soranzo, N.* et al. A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Nat. Genet. 41, 1182-1190 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=212&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=212&la=de Thu, 03 Dec 2009 00:00:00 +0000 <![CDATA[Tregouet, D.A.* et al. Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat. Genet. 41, 283-285 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1954&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1954&la=de Thu, 09 Jul 2009 00:00:00 +0000 <![CDATA[van Es, M.A.* et al. Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nat. Genet. 41, 1083-1087 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=839&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=839&la=de Fri, 04 Dec 2009 00:00:00 +0000 <![CDATA[Willer, C.J.* et al. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat. Genet. 41, 25-34 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1459&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1459&la=de Thu, 09 Jul 2009 00:00:00 +0000 <![CDATA[Döring, A. et al. SLC2A9 influences uric acid concentrations with pronounced sex-specific effects. Nat. Genet. 40, 430-436 (2008)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2460&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2460&la=de Wed, 18 Jun 2008 00:00:00 +0000 <![CDATA[Lettre, G.* et al. Identification of ten loci associated with height highlights new biological pathways in human growth. Nat. Genet. 40, 584-591 (2008)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4526&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4526&la=de Mon, 15 Sep 2008 00:00:00 +0000 <![CDATA[Loos, R.J.* et al. Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nat. Genet. 40, 768-775 (2008)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4576&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4576&la=de Mon, 15 Sep 2008 00:00:00 +0000 <![CDATA[McGowan, K.A. et al. Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects. Nat. Genet. 40, 963-970 (2008)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1264&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1264&la=de Fri, 29 Aug 2008 00:00:00 +0000 <![CDATA[Schormair, B. et al. PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. Nat. Genet. 40, 946-948 (2008)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=305&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=305&la=de Mon, 13 Oct 2008 00:00:00 +0000 <![CDATA[Zeggini, E.* et al. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat. Genet. 40, 638-645 (2008)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3658&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3658&la=de Tue, 10 Jun 2008 00:00:00 +0000 <![CDATA[den Hollander, A.I.* et al. Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis. Nat. Genet. 39, 889-895 (2007)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=469&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=469&la=de Wed, 24 Oct 2007 00:00:00 +0000 <![CDATA[Horn, C.* et al. Splinkerette PCR for more efficient characterization of gene trap events. Nat. Genet. 39, 933-935 (2007)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1764&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1764&la=de Thu, 30 Aug 2007 00:00:00 +0000 <![CDATA[Winkelmann, J. et al. Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nat. Genet. 39, 1000-1006 (2007)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5822&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5822&la=de Mon, 24 Sep 2007 00:00:00 +0000 <![CDATA[Arking, D.E.* et al. A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat. Genet. 38, 644-651 (2006)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3050&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3050&la=de Wed, 02 Aug 2006 00:00:00 +0000 <![CDATA[Consonni, C.* et al. Conserved requirement for a plant host cell protein in powdery mildew pathogenesis. Nat. Genet. 38, 716-720 (2006)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5699&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5699&la=de Wed, 27 Sep 2006 00:00:00 +0000 <![CDATA[Galy, B.* et al. Iron homeostasis in the brain : Complete iron regulatory protein 2 deficiency without symptomatic neurodegeneration in the mouse. Nat. Genet. 38, 967-969 (2006)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3723&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3723&la=de Fri, 27 Oct 2006 00:00:00 +0000 <![CDATA[Lorenz-Depiereux, B. et al. DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis. Nat. Genet. 38, 1248-1250 (2006)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3254&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3254&la=de Tue, 14 Nov 2006 00:00:00 +0000 <![CDATA[Eumorphia Consortium (Brown, S.D.M. ; Chambon, P. ; Hrabě de Angelis, M. ; Wurst, W. ; Abe, K. ; Beckers, J. ; Busch, D.H. ; Dalke, C. ; Gailus-Durner, V. ; Elvert, R. ; Franz, T. ; Fuchs, H. ; Graw, J. ; Hölter, S.M. ; Jakob, T. ; Kalaydjiev, S. ; Kallnik, M. ; Klempt, M. ; Klingenspor, M. ; Klopstock, T. ; Lengger, C. ; Quintanilla-Martinez, L. ; Pedersen, V. ; Puk, O. ; Schneider, I. ; Vogt Weisenhorn, D.M. ; Wagner, S. ; Wolf, E.) EMPReSS: Standardized phenotype screens for functional annotation of the mouse genome. Nat. Genet. 37, 1155 (2005)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1159&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1159&la=de Thu, 03 Nov 2005 00:00:00 +0000 <![CDATA[Austin, C.P.* & Wurst, W. The Knockout Mouse Project. Nat. Genet. 36, 921-924 (2004)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5204&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5204&la=de Fri, 17 Dec 2004 00:00:00 +0000 <![CDATA[Auwerx, J.* ; Hrabě de Angelis, M. & Wurst, W. The European dimension for the mouse genome mutagenesis program. Nat. Genet. 36, 925-927 (2004)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4288&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4288&la=de Fri, 17 Dec 2004 00:00:00 +0000 <![CDATA[Binder, E.B.* et al. Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment. Nat. Genet. 36, 1319-1325 (2004)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2503&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2503&la=de Thu, 02 Dec 2004 00:00:00 +0000 <![CDATA[Cichon, S.* ; Klopp, N. & Illig, T. Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin. Nat. Genet. 36, 783-785 (2004)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3426&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3426&la=de Fri, 31 Dec 2004 00:00:00 +0000 <![CDATA[Skarnes, W.C.* et al. A public gene trap resource for mouse functional genomics. Nat. Genet. 36, 543-544 (2004)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5067&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5067&la=de Wed, 04 Aug 2004 00:00:00 +0000 <![CDATA[van Raamsdonk, C.D.* ; Fitch, K.R.* ; Fuchs, H. ; Hrabě de Angelis, M. & Barsh, G.S.* Effects of G-protein mutations on skin color. Nat. Genet. 36, 961-968 (2004)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3692&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3692&la=de Mon, 13 Sep 2004 00:00:00 +0000 <![CDATA[Vrontou, S.* et al. Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice. Nat. Genet. 34, 209-214 (2003)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=9716&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=9716&la=de Mon, 29 Sep 2003 00:00:00 +0000 <![CDATA[Vreugde, S.* et al. Beethoven, a mouse model for dominant, progressive hearing loss DFNA36. Nat. Genet. 30, 257-258 (2002)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22372&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22372&la=de Tue, 14 Oct 2003 00:00:00 +0000 <![CDATA[* et al. Mutations in the gene encoding ε-sarcoglycan cause myoclonus-dystonia syndrome. Nat. Genet. 29, 66-69 (2001)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23771&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23771&la=de Mon, 31 Dec 2001 00:00:00 +0000 <![CDATA[Werner, T. The promoter connection. Nat. Genet. 29, 105-106 (2001)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1547&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1547&la=de Fri, 31 Dec 2004 00:00:00 +0000 <![CDATA[Hrabě de Angelis, M. et al. Genome-wide, large-scale production of mutant mice by ENU mutagenesis. Nat. Genet. 25, 444-447 (2000)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22719&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22719&la=de Sun, 31 Dec 2000 00:00:00 +0000 <![CDATA[ADHR Consortium (Lorenz-Depiereux, B. ; Grabowski, M. ; Meitinger, T. ; Strom, T.M.) Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23. Nat. Genet. 26, 345-358 (2000)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23773&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23773&la=de Sun, 31 Dec 2000 00:00:00 +0000 <![CDATA[Vervoort, R.* et al. Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. Nat. Genet. 25, 462-466 (2000)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23798&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23798&la=de Sun, 31 Dec 2000 00:00:00 +0000 <![CDATA[Wiles, M.V.* et al. Establishment of a gene-trap sequence tag library to generate mutant mice from embryonic stem cells. Nat. Genet. 24, 13-14 (2000)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=842&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=842&la=de Fri, 31 Dec 2004 00:00:00 +0000 <![CDATA[Timpl, P.* et al. Impaired stress response and reduced anxiety in mice lacking a functional corticotropin-releasing hormone receptor 1. Nat. Genet. 19, 162-166 (1998)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22868&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22868&la=de Thu, 31 Dec 1998 00:00:00 +0000