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 TitleAuthors / EditorsDate
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A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A. Lane, Jérôme; Boehlen, Françoise 2013
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A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium McKay, James D 2011
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A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease Krüger, Rejko; Sharma, Manu 2011
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A map of human genome variation from population-scale sequencing 1000 Genomes Project Consortium 2010
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A multi-SNP locus-association method reveals a substantial fraction of the missing heritability Ehret, Georg Benedikt; Lamparter, David; Hoggart, Clive J.; Whittaker, John C.; ... Kutalik, Zoltán 2012
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A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease Holmans, Peter; Moskvina, Valentina; Jones, Lesley; Sharma, Manu; ... Morris, Huw R 2013
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A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study Peters, Ulrike; North, Kari E; Sethupathy, Praveen; Buyske, Steve; ... Kooperberg, Charles 2013
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A two-stage meta-analysis identifies several new loci for Parkinson's disease French Parkinson's Disease Genetics Study Group 2011
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An integrated encyclopedia of DNA elements in the human genome ENCODE Project Consortium 2012
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An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis Marchetti, Giovanna; Girelli, Domenico; Zerbinati, Carlotta; Lunghi, Barbara; ... Martinelli, Nicola 2015
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An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium 2012
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An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits Hsu, Yi-Hsiang; Zillikens, M Carola; Wilson, Scott G.; Farber, Charles R.; ... Kiel, D. P. 2010
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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 genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study International Consortium for Blood Pressure Genome-Wide Association Studies 2011
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Cigarette smoking reduces DNA methylation levels at multiple genomic loci but the effect is partially reversible upon cessation Tsaprouni, Loukia G; Yang, Tsun-Po; Bell, Jordana; Dick, Katherine J; ... Deloukas, Panos 2014
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Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression Trudu, Matteo; Janas, Sylvie; Lanzani, Chiara; Debaix, Huguette; ... Rampoldi, Luca 2013
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Contribution of genome-wide significant single-nucleotide polymorphisms and antiretroviral therapy to dyslipidemia in HIV-infected individuals: a longitudinal study Rotger, Margalida; Bayard, Cornelia; Taffe, Patrick; Martinez, Raquel; ... Tarr, P. E. 2009
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Discovery and refinement of loci associated with lipid levels Global Lipids Genetics Consortium 2013
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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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Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome Nikolaev, Sergey Igorievich; Santoni, Federico; Vannier, Anne; Falconnet, Emilie; ... Antonarakis, Stylianos 2013
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Extensive natural variation for cellular hydrogen peroxide release is genetically controlled Attar Cohen, Homa; Bedard, Karen; Migliavacca Voeffray, Eugenia Linda; Gagnebin, Maryline; ... Antonarakis, Stylianos 2012
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Extent, causes, and consequences of small RNA expression variation in human adipose tissue Parts, Leopold; Hedman, Åsa K; Keildson, Sarah; Knights, Andrew J; ... Lindgren, Cecilia M 2012
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Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program Simino, Jeannette; Shi, Gang; Kume, Rezart; Schwander, Karen; ... Rao, Dabeeru C 2011
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Follow-up study of the GIGYF2 gene in French families with Parkinson's disease Lesage, Suzanne; Condroyer, Christel; Lohman, Ebba; Troiano, André; ... Brice, Alexis 2010
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From expression QTLs to personalized transcriptomics Montgomery, Stephen; Dermitzakis, Emmanouil 2011
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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
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Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent Powell, Joseph E; Henders, Anjali K; McRae, Allan F; Wright, Margaret J; ... Visscher, Peter M 2012
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Genetic implication of a novel thiamine transporter in human hypertension International Consortium for Blood Pressure Genome-Wide Association Studies 2014
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Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian family Layouni, Samia; Salzmann, Annick; Guipponi, Michel; Mouthon, Dominique; ... Malafosse, Alain 2010
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Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis Tansey, Katherine E; Guipponi, Michel; Perroud, Nader Ali; Bondolfi, Guido; ... Uher, Rudolf 2012
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Genetic studies of body mass index yield new insights for obesity biology Locke, Adam E; Kahali, Bratati; Berndt, Sonja I; Justice, Anne E; ... Mach, François 2015
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Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study Hou, Liping; Heilbronner, Urs; Degenhardt, Franziska; Kelsoe, John R; ... Schulze, Thomas G 2016
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Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study Rauch, Andri; Kutalik, Zoltan; Descombes, Patrick; Cai, Tao; ... Bochud, Pierre-Yves 2010
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Genetics. Life after GWA studies Dermitzakis, Emmanouil; Clark, A. G. 2009
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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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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
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Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population Saad, Mohamad; Lesage, Suzanne; Saint-Pierre, Aude; Corvol, Jean-Christophe; ... Brice, Alexis 2011
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Genome-wide association study identifies a common variant associated with risk of endometrial cancer Montgomery, Stephen; Dermitzakis, Emmanouil 2011
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Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma Chambers, John C; Zhang, Weihua; Sehmi, Joban; Li, Xinzhong; ... Kavousi, Maryam 2011
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Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection Patin, Etienne; Kutalik, Zoltán; Guergnon, Julien; Bibert, Stéphanie; ... Abel, Laurent 2012
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Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior Cornelis, Marilyn C; Kacprowski, Tim; Menni, Cristina; Gustafsson, Stefan; ... Ingelsson, E 2016
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Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele Radhakrishna, Uppala; Nath, Swapan K; McElreavey, Ken; Ratnamala, Uppala; ... Butler, Merlin G 2012
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Genome-wide profiling of blood pressure in adults and children Taal, Hendrik R; Verwoert, Germaine C; Demirkan, Ayse; Janssens, A Cecile J W; ... van Duijn, Cornelia 2012
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Genomic determinants of the efficiency of internal ribosomal entry sites of viral and cellular origin Kazadi, Kayole; Loeuillet, Corinne; Deutsch, Samuel; Ciuffi, Angela; ... Telenti, Amalio 2008
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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
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High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms Kurki, Mitja I; Gaál, Emília Ilona; Kettunen, Johannes; Lappalainen, Tuuli Emilia; ... Jääskeläinen, Juha E 2014
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Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans GTEx Consortium 2015
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Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals Arking, Dan E; Junttila, M. Juhani; Goyette, Philippe; Huertas-Vazquez, Adriana; ... Newton-Cheh, Christopher 2011
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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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Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts Borel, Christelle; Deutsch Escalante, Samuel; Letourneau, Audrey; Migliavacca Voeffray, Eugenia Linda; ... Antonarakis, Stylianos 2011
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