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 TitleAuthors / EditorsDate
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 A map of human genome variation from population-scale sequencing 1000 Genomes Project Consortium 2010
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 A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family Levrat, Emmanuel; Aboukhamis, Imad; De Moerloose, Philippe; Farho, Jaafar; ... Neerman Arbez, Marguerite 2011
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 A predictive clinical-genetic model of tissue plasminogen activator response in acute ischemic stroke del Río-Espínola, Alberto; Fernández-Cadenas, Israel; Giralt, Dolors; Quiroga, Adoracion; ... Montaner, Joan 2012
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 ADME pharmacogenetics: investigation of the pharmacokinetics of the antiretroviral agent lopinavir coformulated with ritonavir Lubomirov, Rubin; di Iulio, J.; Fayet, A.; Colombo, Sara; ... Telenti, A. 2010
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 Allelic mapping bias in RNA-sequencing is not a major confounder in eQTL studies Panousis, Nikolaos; Gutierrez Arcelus, Maria; Dermitzakis, Emmanouil; Lappalainen, Tuuli Emilia 2014
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 Analysis of case-control association studies with known risk variants Zaitlen, Noah; Pasaniuc, Bogdan; Patterson, Nick; Pollack, Samuela; ... Price, Alkes L 2012
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 Association of a common vitamin D-binding protein polymorphism with inflammatory bowel disease Eloranta, Jyrki J; Wenger, Christa; Mwinyi, Jessica; Hiller, Christian; ... Kullak-Ublick, Gerd A 2011
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 Association of AKT1 gene variants and protein expression in both schizophrenia and bipolar disorder Karege, Félicien; Perroud, Nader Ali; Schurhoff, F.; Meary, A.; ... Malafosse, Alain 2010
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 Association of STR polymorphisms in CMA1 and IL-4 with asthma and atopy: the SAPALDIA cohort Hersberger, Martin; Thun, Gian-Andri; Imboden, Medea; Brandstatter, Anita; ... Probst-Hensch, Nicole 2010
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 BRD2 and TAP-1 genes and juvenile myoclonic epilepsy Layouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed 2010
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 Cis and trans effects of human genomic variants on gene expression Bryois, Julien; Buil Demur, Alfonso Alberto; Evans, David M; Kemp, John P; ... Dermitzakis, Emmanouil 2014
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 Clinical and genetic correlates of suicidal ideation during antidepressant treatment in a depressed outpatient sample Perroud, Nader Ali; Bondolfi, Guido; Uher, Rudolf; Gex-Fabry, Marianne; ... Kosel, Markus Mathaus 2011
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 Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies Masnada, Silvia; Hedrich, Ulrike B S; Gardella, Elena; Korff, Christian; ... Rubboli, Guido 2017
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 Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion Klopocki, Eva; Lohan, Silke; Doelken, Sandra C; Stricker, Sigmar; ... Mundlos, Stefan 2012
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 Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population Bell, Jordana T; Tsai, Pei-Chien; Yang, Tsun-Po; Pidsley, Ruth; ... Deloukas, Panos 2012
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 European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset Mathieu, Flavie; Dizier, Marie-Helene; Etain, Bruno; Jamain, Stephane; ... Bellivier, Frank 2010
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 Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes Prasad, Rashmi B; Lessmark, Anna; Almgren, Peter; Kovacs, Györgyi; ... Groop, Leif 2016
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 EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations Eggens, Veerle Rc; Barth, Peter G; Niermeijer, Jikke-Mien F; Berg, Jonathan N; ... Baas, Frank 2014
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 Gene-diet interactions associated with complex trait variation in an advanced intercross outbred mouse line Vorobyev, Artem; Gupta, Yask; Sezin, Tanya; Koga, Hiroshi; ... Ludwig, Ralf J 2019
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 Genome-wide and candidate gene approaches of clopidogrel efficacy using pharmacodynamic and clinical end points-Rationale and design of the International Clopidogrel Pharmacogenomics Consortium (ICPC) International Clopidogrel Pharmacogenomics Consortium 2018
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