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	Title	Authors / Editors	Date
unige:45219	A map of human genome variation from population-scale sequencing	1000 Genomes Project Consortium	2010
unige:32728	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
unige:26871	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
unige:21098	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
unige:90264	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
unige:32170	Analysis of case-control association studies with known risk variants	Zaitlen, Noah; Pasaniuc, Bogdan; Patterson, Nick; Pollack, Samuela; ... Price, Alkes L	2012
unige:25737	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
unige:21036	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
unige:21005	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
unige:21077	BRD2 and TAP-1 genes and juvenile myoclonic epilepsy	Layouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed	2010
unige:90266	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
unige:24045	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
unige:107726	Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies	Masnada, Silvia; Hedrich, Ulrike B S; Gardella, Elena; Korff, Christian; ... Rubboli, Guido	2017
unige:34655	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
unige:32175	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
unige:21124	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
unige:88476	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
unige:55178	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
unige:138252	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
unige:116553	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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