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    <title>PuSH - HMGU Publikationen</title>
    <link>https://push-zb.helmholtz-munich.de</link>
    <description>
    PuSH - Publikationen-Server des Helmholtz Zentrums München
    </description>
    <language>de-de</language>

    <item>
      <title><![CDATA[Byun, J.* et al. Genome-wide association study for lung cancer in 6531 African Americans reveals new susceptibility loci. Hum. Mol. Genet. 34, 1227-1237 (2025)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74360&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=74360&amp;la=de</guid>
      <pubDate>Sat, 10 May 2025 00:00:00 +0000</pubDate>
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      <title><![CDATA[Singh, A. ; Bocher, O. &amp; Zeggini, E. Insights into the molecular underpinning of type 2 diabetes complications. Hum. Mol. Genet. 34, 469-480 (2025)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73030&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73030&amp;la=de</guid>
      <pubDate>Thu, 20 Mar 2025 00:00:00 +0000</pubDate>
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    <item>
      <title><![CDATA[Kreitmaier, P. et al. Epigenomic profiling of the infrapatellar fat pad in osteoarthritis. Hum. Mol. Genet. 33:ddad198 (2023)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68768&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68768&amp;la=de</guid>
      <pubDate>Tue, 28 Nov 2023 00:00:00 +0000</pubDate>
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      <title><![CDATA[Lucienne, M.* et al. Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria. Hum. Mol. Genet. 32, 2717-2734 (2023)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68344&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68344&amp;la=de</guid>
      <pubDate>Wed, 18 Oct 2023 00:00:00 +0000</pubDate>
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      <title><![CDATA[Thareja, G.* et al. Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hum. Mol. Genet. 32, 907–916 (2023)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66379&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66379&amp;la=de</guid>
      <pubDate>Thu, 24 Nov 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Aboulmaouahib, B.* et al. First mitochondrial genome wide association study with metabolomics. Hum. Mol. Genet. 31, 3367-3376 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63429&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63429&amp;la=de</guid>
      <pubDate>Thu, 16 Dec 2021 00:00:00 +0000</pubDate>
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      <title><![CDATA[Brunet, T. et al. Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. Hum. Mol. Genet. 31, 2386-2395 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64351&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64351&amp;la=de</guid>
      <pubDate>Tue, 28 Jun 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Castaneda, A.B.* et al. Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues. Hum. Mol. Genet. 31, 1171-1182 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63644&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63644&amp;la=de</guid>
      <pubDate>Mon, 31 Jan 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Cruz, R.* et al. Novel genes and sex differences in COVID-19 severity. Hum. Mol. Genet. 31, 3789-3806 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65563&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65563&amp;la=de</guid>
      <pubDate>Thu, 29 Sep 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Degenhardt, F.* et al. Detailed stratified GWAS analysis for severe COVID-19 in four European populations. Hum. Mol. Genet. 31, 3945-3966 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65771&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65771&amp;la=de</guid>
      <pubDate>Wed, 19 Mar 2025 00:00:00 +0000</pubDate>
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      <title><![CDATA[Gergei, I.* et al. GWAS META-analysis followed by MENDELIAN randomisation revealed potential control mechanisms for circulating α-klotho levels. Hum. Mol. Genet. 31, 792-802 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63034&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63034&amp;la=de</guid>
      <pubDate>Fri, 15 Oct 2021 00:00:00 +0000</pubDate>
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      <title><![CDATA[Katsoula, G. et al. A molecular map of long non-coding RNA expression, isoform switching and alternative splicing in osteoarthritis. Hum. Mol. Genet. 31, 2090-2105 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64263&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64263&amp;la=de</guid>
      <pubDate>Thu, 23 Jun 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Kuhn, T.* et al. Comparative genomic analyses of multiple backcross mouse populations suggest SGCG as a novel potential obesity-modifier gene. Hum. Mol. Genet. 31, 4019-4033 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65658&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65658&amp;la=de</guid>
      <pubDate>Thu, 27 Oct 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Pervjakova, N.* et al. Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes. Hum. Mol. Genet. 31, 3377–3391 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64539&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64539&amp;la=de</guid>
      <pubDate>Tue, 05 Jul 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Png, G. et al. Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Hum. Mol. Genet. 32, 1266-1275 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66664&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66664&amp;la=de</guid>
      <pubDate>Thu, 17 Nov 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Portilla-Fernandez, E.* et al. Genetic and clinical determinants of abdominal aortic diameter: Genome-wide association studies, exome array data and Mendelian randomization study. Hum. Mol. Genet. 31, 3566-3579 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64527&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64527&amp;la=de</guid>
      <pubDate>Tue, 05 Jul 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Riedhammer, K.M.* et al. Suleiman-El-Hattab syndrome: A histone modification disorder caused by TASP1 deficiency. Hum. Mol. Genet. 31, 3083-3094 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65022&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65022&amp;la=de</guid>
      <pubDate>Thu, 15 Sep 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Ahluwalia, T.S.* et al. Genome-wide association study of circulating interleukin 6 levels identifies novel loci. Hum. Mol. Genet. 30, 393-409 (2021)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61192&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61192&amp;la=de</guid>
      <pubDate>Tue, 13 Apr 2021 00:00:00 +0000</pubDate>
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      <title><![CDATA[Lam, D.D. et al. Intronic elements associated with insomnia and restless legs syndrome exhibit cell type-specific epigenetic features contributing to MEIS1 regulation. Hum. Mol. Genet. 31, 1733-1746 (2021)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63785&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63785&amp;la=de</guid>
      <pubDate>Fri, 28 Jan 2022 00:00:00 +0000</pubDate>
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    <item>
      <title><![CDATA[Pott, J.* et al. Meta-GWAS of PCSK9 levels detects two novel loci at APOB and TM6SF2. Hum. Mol. Genet. 31, 999-1011 (2021)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63190&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63190&amp;la=de</guid>
      <pubDate>Tue, 23 Nov 2021 00:00:00 +0000</pubDate>
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      <title><![CDATA[Cai, N. ; Choi, K.W.* &amp; Fried, E.I.* Reviewing the genetics of heterogeneity in depression: Operationalizations, manifestations, and etiologies. Hum. Mol. Genet. 29, R10-R18 (2020)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=59535&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=59535&amp;la=de</guid>
      <pubDate>Thu, 16 Jul 2020 00:00:00 +0000</pubDate>
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      <title><![CDATA[Nag, A.* et al. Genome-wide scan identifies novel genetic loci regulating salivary metabolite levels. Hum. Mol. Genet. 29, 864-875 (2020)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58802&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58802&amp;la=de</guid>
      <pubDate>Wed, 15 Apr 2020 00:00:00 +0000</pubDate>
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      <title><![CDATA[Bradfield, J.P.* et al. A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity. Hum. Mol. Genet. 28, 3327-3338 (2019)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56859&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56859&amp;la=de</guid>
      <pubDate>Wed, 25 Sep 2019 00:00:00 +0000</pubDate>
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      <title><![CDATA[Laaksonen, J.* et al. Discovery of mitochondrial DNA variants associated with genome-wide blood cell gene expression: A population-based mtDNA sequencing study. Hum. Mol. Genet. 28, 1381-1391 (2019)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55937&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55937&amp;la=de</guid>
      <pubDate>Wed, 08 May 2019 00:00:00 +0000</pubDate>
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      <title><![CDATA[Sharapov, S.Z.* et al. Defining the genetic control of human blood plasma N-glycome using genome-wide association study. Hum. Mol. Genet. 28, 2062-2077 (2019)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56209&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56209&amp;la=de</guid>
      <pubDate>Fri, 07 Jun 2019 00:00:00 +0000</pubDate>
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      <title><![CDATA[Sung, Y.J.* et al. A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. Hum. Mol. Genet. 28, 2615-2633 (2019)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56162&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56162&amp;la=de</guid>
      <pubDate>Wed, 29 May 2019 00:00:00 +0000</pubDate>
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      <title><![CDATA[Brockmann, S.J.* et al. CHCHD10 mutations p. R15L and p. G66V cause motoneuron disease by haploinsufficiency. Hum. Mol. Genet. 27, 706-715 (2018)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52699&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52699&amp;la=de</guid>
      <pubDate>Thu, 11 Jan 2018 00:00:00 +0000</pubDate>
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      <title><![CDATA[Haworth, S.* et al. Consortium-based genome-wide meta-analysis for childhood dental caries traits. Hum. Mol. Genet. 27, 3113-3127 (2018)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53691&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53691&amp;la=de</guid>
      <pubDate>Fri, 29 Jun 2018 00:00:00 +0000</pubDate>
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      <title><![CDATA[Tönjes, A.* et al. Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin. Hum. Mol. Genet. 27, 546-558 (2018)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52913&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52913&amp;la=de</guid>
      <pubDate>Fri, 09 Feb 2018 00:00:00 +0000</pubDate>
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      <title><![CDATA[Vogel, H.* et al. A collective diabetes cross in combination with a computational framework to dissect the genetics of human obesity and Type 2 diabetes. Hum. Mol. Genet. 27, 3099-3112 (2018)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54413&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54413&amp;la=de</guid>
      <pubDate>Mon, 01 Oct 2018 00:00:00 +0000</pubDate>
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      <title><![CDATA[Zaghlool, S.B.* et al. Deep molecular phenotypes link complex disorders and physiological insult to CpG methylation. Hum. Mol. Genet. 27, 1106-1121 (2018)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52721&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52721&amp;la=de</guid>
      <pubDate>Fri, 09 Mar 2018 00:00:00 +0000</pubDate>
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      <title><![CDATA[Cooper, H.M.* et al. ATPase-deficient mitochondrial inner membrane protein ATAD3a disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia. Hum. Mol. Genet. 26, 1432-1443 (2017)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51171&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51171&amp;la=de</guid>
      <pubDate>Wed, 31 May 2017 00:00:00 +0000</pubDate>
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      <title><![CDATA[Dand, N.* et al. Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling. Hum. Mol. Genet. 26, 4301-4313 (2017)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52030&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52030&amp;la=de</guid>
      <pubDate>Tue, 10 Oct 2017 00:00:00 +0000</pubDate>
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      <title><![CDATA[van den Berg, M.* et al. Discovery of novel heart rate-associated loci using the Exome Chip. Hum. Mol. Genet. 26, 2346-2363 (2017)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51372&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51372&amp;la=de</guid>
      <pubDate>Mon, 03 Jul 2017 00:00:00 +0000</pubDate>
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      <title><![CDATA[Bustamante, M.* et al. A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways. Hum. Mol. Genet. 25, 4127-4142 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49327&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49327&amp;la=de</guid>
      <pubDate>Thu, 01 Sep 2016 00:00:00 +0000</pubDate>
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      <title><![CDATA[Cornelis, M.C.* et al. Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior. Hum. Mol. Genet. 25, 5472-5482 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49680&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49680&amp;la=de</guid>
      <pubDate>Fri, 07 Oct 2016 00:00:00 +0000</pubDate>
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      <title><![CDATA[de Vries, P.S.* et al. A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration. Hum. Mol. Genet. 25, 358-370 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47297&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47297&amp;la=de</guid>
      <pubDate>Tue, 08 Dec 2015 00:00:00 +0000</pubDate>
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      <title><![CDATA[Felix, J.F.* et al. Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. Hum. Mol. Genet. 25, 389-403 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47422&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47422&amp;la=de</guid>
      <pubDate>Mon, 07 Dec 2015 00:00:00 +0000</pubDate>
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      <title><![CDATA[Huan, T.* et al. A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smoking. Hum. Mol. Genet. 25, 4611-4623 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49349&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49349&amp;la=de</guid>
      <pubDate>Fri, 02 Sep 2016 00:00:00 +0000</pubDate>
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      <title><![CDATA[Kanoni, S.* et al. Analysis with the exome array identifies multiple new independent variants in lipid loci. Hum. Mol. Genet. 25, 4094-4106 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49185&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49185&amp;la=de</guid>
      <pubDate>Tue, 02 Aug 2016 00:00:00 +0000</pubDate>
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      <title><![CDATA[Kortvely, E.* ; Hauck, S.M. ; Behler, J. ; Ho, N.* &amp; Ueffing, M.* The unconventional secretion of ARMS2. Hum. Mol. Genet. 25, 3143-3151 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48777&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48777&amp;la=de</guid>
      <pubDate>Fri, 10 Jun 2016 00:00:00 +0000</pubDate>
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      <title><![CDATA[Lamina, C.* et al. A genome-wide association meta-analysis on apolipoprotein A-IV concentrations. Hum. Mol. Genet. 25, 3635-3646 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49085&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49085&amp;la=de</guid>
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    <item>
      <title><![CDATA[Lubbe, S.J.* et al. Additional rare variant analysis in Parkinson&#039;s disease cases with and without known pathogenic mutations: Evidence for oligogenic inheritance. Hum. Mol. Genet. 25, 5483-5489 (2016)]]></title>
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    <item>
      <title><![CDATA[Trifunovic, D.* et al. HDAC inhibition in the cpfl1 mouse protects degenerating cone photoreceptors in vivo. Hum. Mol. Genet. 25, 4462-4472 (2016)]]></title>
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    <item>
      <title><![CDATA[Yang, J.* et al. Catenin delta-1 (CTNND1) phosphorylation controls the mesenchymal to epithelial transition in astrocytic tumors. Hum. Mol. Genet. 25, 4201-4210 (2016)]]></title>
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      <title><![CDATA[Zhang, Y.* ; Xu, H.* &amp; Frishman, D. Genomic determinants of somatic copy number alterations across human cancers. Hum. Mol. Genet. 25, 1019-1030 (2016)]]></title>
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    <item>
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    <item>
      <title><![CDATA[Stambolian, D.* et al. Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Hum. Mol. Genet. 22, 2754-2764 (2013)]]></title>
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    <item>
      <title><![CDATA[Weidinger, S.* et al. A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. Hum. Mol. Genet. 22, 4841-4856 (2013)]]></title>
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    <item>
      <title><![CDATA[Boraska, V.* et al. Genome-wide meta-analysis of common variant differences between men and women. Hum. Mol. Genet. 21, 4805-4815 (2012)]]></title>
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    <item>
      <title><![CDATA[Chasman, D.I.* et al. Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Hum. Mol. Genet. 21, 5329-5343 (2012)]]></title>
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    <item>
      <title><![CDATA[Imamura, M.* et al. A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations. Hum. Mol. Genet. 21, 3042-3049 (2012)]]></title>
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    <item>
      <title><![CDATA[Keller, M.F.* et al. Using genome-wide complex trait analysis to quantify &#039;missing heritability&#039; in Parkinson&#039;s disease. Hum. Mol. Genet. 21, 4996-5009 (2012)]]></title>
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      <title><![CDATA[Mead, S.* et al. Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. Hum. Mol. Genet. 21, 1897-1906 (2012)]]></title>
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    <item>
      <title><![CDATA[Petersen, A.-K. et al. Genetic associations with lipoprotein subfractions provide information on their biological nature. Hum. Mol. Genet. 21, 1433-1443 (2012)]]></title>
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      <title><![CDATA[Rawal, R. et al. Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function. Hum. Mol. Genet. 21, 3275-3282 (2012)]]></title>
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      <title><![CDATA[Siddiq, A.* et al. A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. Hum. Mol. Genet. 21, 5373-5384 (2012)]]></title>
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      <title><![CDATA[Steffens, M.* et al. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. Hum. Mol. Genet. 21, 5359-5372 (2012)]]></title>
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      <title><![CDATA[Thiele, F. et al. Cardiopulmonary dysfunction in the osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms. Hum. Mol. Genet. 21, 3535-3545 (2012)]]></title>
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      <title><![CDATA[Timofeeva, M.N.* et al. Influence of common genetic variation on lung cancer risk: Meta-analysis of 14900 cases and 29485 controls. Hum. Mol. Genet. 21, 4980-4995 (2012)]]></title>
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      <title><![CDATA[Wu, X.* et al. A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23. Hum. Mol. Genet. 21, 456-462 (2012)]]></title>
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      <title><![CDATA[Chapman, G.* ; Sparrow, D.B.* ; Kremmer, E. &amp; Dunwoodie, S.L.* Notch inhibition by the ligand Delta-Like 3 defines the mechanism of abnormal vertebral segmentation in spondylocostal dysostosis. Hum. Mol. Genet. 20, 905-916 (2011)]]></title>
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      <title><![CDATA[Coene, K.L.* et al. The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase. Hum. Mol. Genet. 20, 3592-3605 (2011)]]></title>
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      <title><![CDATA[Perveen, R.* ; Favor, J. ; Jamieson, R.V.* ; Ray, D.W.* &amp; Black, G.C.* A heterozygous c-Maf transactivation domain mutation causes congenital cataract and enhances target gene activation. Hum. Mol. Genet. 16, 1030-1038 (2007)]]></title>
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