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	Title	Authors / Editors	Date
unige:32743	SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertension	Won, Joong-Ho; Ehret, Georg Benedikt; Chakravarti, Aravinda; Olshen, Richard A	2011
unige:34661	Network-guided analysis of genes with altered somatic copy number and gene expression reveals pathways commonly perturbed in metastatic melanoma	Valsesia, Armand; Rimoldi, Donata; Martinet, Danielle; Ibberson, Mark; ... Stevenson, Brian J	2011
unige:25698	Replication of association between a SCN1A splice variant and febrile seizures	Le Gal, François; Trachsler-Salzmann, Annick; Crespel, Arielle; Malafosse, Alain	2011
unige:45209	A two-stage meta-analysis identifies several new loci for Parkinson's disease	French Parkinson's Disease Genetics Study Group	2011
unige:45211	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies	Nalls, Michael A; Plagnol, Vincent; Hernandez, Dena G; Sharma, Manu; ... Wood, Nicholas W	2011
unige:45216	An integrated map of genetic variation from 1,092 human genomes	1000 Genomes Project Consortium	2012
unige:31211	Polymorphism in multidrug resistance-associated protein gene 3 is associated with outcomes in childhood acute lymphoblastic leukemia	Ansari Djaberi, Marc Georges; Sauty, G; Labuda, M; Gagné, V; ... Krajinovic, M	2012
unige:28410	Consistency between cross-sectional and longitudinal SNP: blood lipid associations	Costanza, Michael C; Beer-Borst, Sigrid; James, Richard William; Gaspoz, Jean-Michel; Morabia, Alfredo	2012
unige:27166	A genetic validation study reveals a role of vitamin D metabolism in the response to interferon-alfa-based therapy of chronic hepatitis C.	Lange, Christian M; Bibert, Stéphanie; Kutalik, Zoltan; Burgisser, Philippe; ... Moradpour, Darius	2012
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:37818	An integrated encyclopedia of DNA elements in the human genome	ENCODE Project Consortium	2012
unige:45205	Identification of VPS35 mutations replicated in French families with Parkinson disease	Lesage, S; Condroyer, C; Klebe, S; Honoré, A; ... Brice, A	2012
unige:34328	Transcriptome and genome sequencing uncovers functional variation in humans	Lappalainen, Tuuli Emilia; Giger, Thomas; Padioleau, Ismael; Ongen, Halit; ... Dermitzakis, Emmanouil	2013
unige:34640	Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity	Esko, Tõnu; Mezzavilla, Massimo; Nelis, Mari; Borel, Christelle; Antonarakis, Stylianos	2013
unige:43643	Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls	Brenner, Darren R; Brennan, Paul; Boffetta, Paolo; Amos, Christopher I; ... Hung, Rayjean J	2013
unige:40637	Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations	Franceschini, Nora	2013
unige:35220	First evidence of a polygenic susceptibility to pain in a pediatric cohort	Mamie, Chantal; Rebsamen, Michela; Morris, Michael Andréw; Morabia, Alfredo	2013
unige:90281	Gene expression changes with age in skin, adipose tissue, blood and brain	Glass, Daniel; Viñuela, Ana; Davies, Matthew N; Ramasamy, Adaikalavan; ... Spector, Tim D	2013
unige:33603	The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism	Klebe, Stephan; Golmard, Jean-Louis; Nalls, Michael A; Saad, Mohamad; ... Corvol, Jean-Christophe	2013
unige:94193	Association of adenosine receptor gene polymorphisms and in vivo adenosine A1 receptor binding in the human brain	Hohoff, Christa; Garibotto, Valentina; Elmenhorst, David; Baffa, Anna; ... Bauer, Andreas	2014

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