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 TitleAuthors / EditorsDate
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Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance Lotta, Luca A; Gulati, Pawan; Day, Felix R; Payne, Felicity; ... Scott, Robert A 2017
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Estimating the causal tissues for complex traits and diseases Ongen, Halit; Brown, Andrew Anand; Delaneau, Olivier; Panousis, Nikolaos; ... Dermitzakis, Emmanouil 2017
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Predicting causal variants affecting expression by using whole-genome sequencing and RNA-seq from multiple human tissues Brown, Andrew Anand; Vinuela Rodriguez, Ana; Delaneau, Olivier; Spector, Tim D; ... Dermitzakis, Emmanouil 2017
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Genomic analysis identifies new drivers and progression pathways in skin basal cell carcinoma Bonilla Bustillo, Ximena; Parmentier, Laurent; King, Bryan; Bezrukov, Fedor; ... Nikolaev, Sergey Igorievich 2016
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Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins Buil Demur, Alfonso Alberto; Brown, Andrew Anand; Lappalainen, Tuuli Emilia; Viñuela, Ana; ... Dermitzakis, Emmanouil 2015
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De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy Korff, Christian 2015
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Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization CARe Consortium, COGENT Consortiume, eMERGE Consortium, HRGEN Consortium 2014
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Defining the role of common variation in the genomic and biological architecture of adult human height Wood, Andrew R; Esko, Tonu; Yang, Jian; Vedantam, Sailaja; ... Goddard, Michael E 2014
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Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variants Pasquali, Lorenzo; Gaulton, Kyle J; Rodríguez-Seguí, Santiago A; Mularoni, Loris; ... Ferrer, Jorge 2014
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The common marmoset genome provides insight into primate biology and evolution Worley, Kim C 2014
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Mutations of DEPDC5 cause autosomal dominant focal epilepsies Ishida, Saeko; Picard, Fabienne; Rudolf, Gabrielle; Noé, Eric; ... Baulac, Stéphanie 2013
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Discovery and refinement of loci associated with lipid levels Global Lipids Genetics Consortium 2013
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Cellular genomics for complex traits Dermitzakis, Emmanouil 2012
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Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma Nikolaev, Sergey Igorievich; Rimoldi, Donata; Iseli, Christian; Valsesia, Armand; ... Antonarakis, Stylianos 2012
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Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis Paternoster, Lavinia; Standl, Marie 2012
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Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus Anderson, Beverley H; Kasher, Paul R; Mayer, Josephine 2012
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Mapping cis- and trans-regulatory effects across multiple tissues in twins Nica, Alexandra; Buil Demur, Alfonso Alberto; Dima, Antigoni; Montgomery, Stephen; Dermitzakis, Emmanouil 2012
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KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron Collaboration 2012
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Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes Small, Kerrin S; Hedman, Asa K; Grundberg, Elin; Nica, Alexandra; ... Dermitzakis, Emmanouil 2011
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From expression QTLs to personalized transcriptomics Montgomery, Stephen; Dermitzakis, Emmanouil 2011
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