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Lagouge, M.* et al. SLIRP regulates the rate of mitochondrial protein synthesis and protects LRPPRC from degradation. PLoS Genet. 11:e1005423 (2015)
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Mahajan, A.* et al. Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. PLoS Genet. 11:e1004876 (2015)
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Winkler, T.W.* et al. The influence of age and sex on genetic associations with adult body size and shape: A large-scale genome-wide interaction study. PLoS Genet. 11:e1005378 (2015)
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Medici, M.* et al. Identification of novel genetic loci associated with thyroid peroxidase antibodies and clinical thyroid disease. PLoS Genet. 10:e1004123 (2014)
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Qanbari, S.* et al. Classic selective sweeps revealed by massive sequencing in cattle. PLoS Genet. 10:e1004148 (2014)
Cevik, S.* et al. Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain. PLoS Genet. 9:e1003977 (2013)
Evans, D.M* et al. Mining the human phenome using allelic scores that index biological intermediates. PLoS Genet. 9:e1003919 (2013)
Faraco, J.* et al. ImmunoChip study implicates antigen presentation to T cells in narcolepsy. PLoS Genet. 9:e1003270 (2013)
Hancock, D.B.* et al. Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. PLoS Genet. 8:e1003098 (2013)
Krähling, A.M.* et al. CRIS - a novel cAMP-binding protein controlling spermiogenesis and the development of flagellar bending. PLoS Genet. 9:e1003960 (2013)
Müller, T.D. ; Tschöp, M.H. & Hofmann, S.M. Emerging function of fat mass and obesity-associated protein (FTO). PLoS Genet. 9:e1003223 (2013)
O'Seaghdha, C.M.* et al. Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. PLoS Genet. 9:e1003796 (2013)
Occhi, G.* et al. A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype. PLoS Genet. 9:e1003350 (2013)
Randall, J.C.* et al. Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. PLoS Genet. 9:e1003500 (2013)
Schardl, C.L.* et al. Plant-symbiotic fungi as chemical engineers: Multi-genome analysis of the clavicipitaceae reveals dynamics of alkaloid loci. PLoS Genet. 9:e1003323 (2013)
Thun, G.A.* et al. Causal and synthetic associations of variants in the SERPINA gene cluster with alpha1-antitrypsin serum levels. PLoS Genet. 9:e1003585 (2013)
Wredenberg, A.* et al. MTERF3 regulates mitochondrial ribosome biogenesis in invertebrates and mammals. PLoS Genet. 9:e1003178 (2013)
Coviello, A.D.* et al. A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple loci implicated in sex steroid hormone regulation. PLoS Genet. 8:e1002805 (2012)
Dastani, Z.* et al. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: A multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet. 8:e1002607 (2012)
Demirkan, A.* et al. Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. PLoS Genet. 8:e1002490 (2012)
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Nilsson, L.M.* et al. Mouse genetics suggests cell-context dependency for Myc-regulated metabolic enzymes during tumorigenesis. PLoS Genet. 8:e1002573 (2012)
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Amselem, J.* et al. Genomic analysis of the necrotrophic fungal pathogens Sclerotinia sclerotiorum and Botrytis cinerea. PLoS Genet. 7:e1002230 (2011)
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International Parkinson's Disease Genomics Consortium (IPDGC) (Illig, T. ; Lichtner, P.) & Wellcome Trust Case Control Consortium 2 (WTCCC2) (*) A two-stage meta-analysis identifies several new loci for Parkinson's disease. PLoS Genet. 7:e1002142 (2011)
IBC 50K CAD Consortium (Klopp, N. ; Baumert, J.J. ; Peters, A. ; Meisinger, C. ; Gieger, C. ; Döring, A. ; Illig, T. ; Meitinger, T. ; Wichmann, H.-E.) Large-scale gene-centric analysis identifies novel variants for coronary artery disease. PLoS Genet. 7:e1002260 (2011)
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Mittelstraß, K. et al. Discovery of sexual dimorphisms in metabolic and genetic biomarkers. PLoS Genet. 7:e1002215 (2011)
Nalls, M.A.* et al. Multiple loci are associated with white blood cell phenotypes. PLoS Genet. 7:e1002113 (2011)
Nicholson, G.* et al. A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection. PLoS Genet. 7:e1002270 (2011)
Ohlsson, C.* et al. Genetic determinants of serum testosterone concentrations in men. PLoS Genet. 7:e1002313 (2011)
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Speliotes, E.K.* et al. Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. PLoS Genet. 7:e1001324 (2011)
Surakka, I.* et al. A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. PLoS Genet. 7:e1002333 (2011)
Winkelmann, J. et al. Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. PLoS Genet. 7:e1002171 (2011)
Wöhlke, A. et al. A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier. PLoS Genet. 7:e1002304 (2011)
Griciuc, A. et al. Inactivation of VCP/ter94 suppresses retinal pathology caused by misfolded rhodopsin in Drosophila. PLoS Genet. 6:e1001075 (2010)
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Ikram, M.K.* et al. Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genet. 6:e1001184 (2010)
Marzi, C. et al. Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. PLoS Genet. 6:e1001213 (2010)
Meyer, T.E.* et al. Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six loci influencing serum magnesium levels. PLoS Genet. 6:e1001045 (2010)
Naukkarinen, J.* et al. Use of genome-wide expression data to mine the 'Gray Zone' of GWA studies leads to novel candidate obesity genes. PLoS Genet. 6, 1-10:e1000976 (2010)
Padmanabhan, S.* et al. Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension. PLoS Genet. 6, 1-11:e1001177 (2010)
Scherag, A.* et al. Two new loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and German study groups. PLoS Genet. 6:e1000916 (2010)
Segrè, A.V.* et al. Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits. PLoS Genet. 6:e1001058 (2010)
Stark, K.* et al. Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy. PLoS Genet. 6:e1001167 (2010)
Blagodatski, A.* et al. A cis-acting diversification activator both necessary and sufficient for AID-mediated hypermutation. PLoS Genet. 5:e1000332 (2009)
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Hicks, A.A.* et al. Genetic determinants of circulating sphingolipid concentrations in European populations. PLoS Genet. 5:e1000672 (2009)
Kolz, M. et al. Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. PLoS Genet. 5:e1000504 (2009)
Lindgren, C.M.* et al. Genome-wide association scan meta-analysis identifies three loci influencing adiposity and fat distribution. PLoS Genet. 5:e1000508 (2009)
Richards, J.B.* et al. A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. PLoS Genet. 5:e1000768 (2009)
Gieger, C. et al. Genetics meets metabolomics: A genome-wide association study of metabolite profiles in human serum. PLoS Genet. 4:e1000282 (2008)
Hertzano, R.* et al. A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells. PLoS Genet. 4:e1000207 (2008)
Lisse, T.S. et al. ER stress-mediated apoptosis in a new mouse model of Osteogenesis imperfecta. PLoS Genet. 4:e7 (2008)
Spiden, S.L.* et al. The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss. PLoS Genet. 4:e1000238 (2008)
Weidinger, S. et al. Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus. PLoS Genet. 4:e1000166 (2008)
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Perocchi, F.* et al. Assessing systems properties of yeast mitochondria through an interaction map of the organelle. PLoS Genet. 2, 1612-1624:e170 (2006)