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 TitleAuthors / EditorsDate
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Human pancreatic islet three-dimensional chromatin architecture provides insights into the genetics of type 2 diabetes Miguel-Escalada, Irene; Bonàs-Guarch, Silvia; Cebola, Inês; Ponsa-Cobas, Joan; ... Ferrer, Jorge 2019
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Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation Gamazon, Eric R.; Segrè, Ayellet V.; van de Bunt, Martijn; Wen, Xiaoquan; ... Ardlie, Kristin G. 2018
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De novo variants in neurodevelopmental disorders with epilepsy Heyne, Henrike O; Singh, Tarjinder; Stamberger, Hannah; Abou Jamra, Rami; ... Lemke, Johannes R 2018
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Evangelou, Evangelos; Warren, Helen R; Mosen-Ansorena, David; Mifsud, Borbala; ... Caulfield, Mark J 2018
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Polymer physics predicts the effects of structural variants on chromatin architecture Bianco, Simona; Lupiáñez, Darío G; Chiariello, Andrea M; Annunziatella, Carlo; ... Nicodemi, Mario 2018
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Dynamic 3D chromatin architecture contributes to enhancer specificity and limb morphogenesis Kragesteen, Bjørt K; Spielmann, Malte; Visel, Axel; Mundlos, Stefan; Andrey, Guillaume 2018
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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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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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Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation Hoffmann, Thomas J; Ehret, Georg Benedikt; Nandakumar, Priyanka; Ranatunga, Dilrini; ... Risch, Neil 2017
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Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci Liu, Chunyu; Kraja, Aldi T; Smith, Jennifer A; Brody, Jennifer A; ... Chasman, Daniel I 2016
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The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals Ehret, Georg Benedikt; Ferreira, Teresa; Morris, Andrew P; Newton-Cheh, Christopher; Munroe, Patricia B 2016
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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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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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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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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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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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