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Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa Duncan, Laramie; Yilmaz, Zeynep; Gaspar, Helena; Walters, Raymond; ... Bulik, Cynthia M 2017
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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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Comparative Genomics of Community-Associated Methicillin-Resistant Staphylococcus aureus Shows the Emergence of Clone ST8-USA300 in Geneva, Switzerland Von Dach, Elodie; Diene, Seydina Mouhamadou; Fankhauser-Rodriguez, Carolina Maria; Schrenzel, Jacques; ... Francois, Patrice 2016
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Assessing allele-specific expression across multiple tissues from RNA-seq read data Pirinen, Matti; Lappalainen, Tuuli Emilia; Zaitlen, Noah A; Dermitzakis, Emmanouil; ... Rivas, Manuel A 2015
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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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Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing Gutierrez Arcelus, Maria; Ongen, Halit; Lappalainen, Tuuli Emilia; Montgomery, Stephen; ... Dermitzakis, Emmanouil 2015
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Towards the identification of a genetic basis for Landau-Kleffner syndrome Conroy, Judith; McGettigan, Paul A; McCreary, Dara; Shah, Naisha; ... King, Mary D 2014
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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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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration van der Zee, Julie 2014
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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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Identification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data Waszak, Sebastian M; Kilpinen, Leena Helena; Gschwind, Andreas R; Orioli, Andrea; ... Deplancke, Bart 2014
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Predicting stroke through genetic risk functions: the CHARGE Risk Score Project Ehret, Georg Benedikt 2014
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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
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First evidence of a polygenic susceptibility to pain in a pediatric cohort Mamie, Chantal; Rebsamen, Michela; Morris, Michael Andréw; Morabia, Alfredo 2013
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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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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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Transcriptome and genome sequencing uncovers functional variation in humans Lappalainen, Tuuli Emilia; Giger, Thomas; Padioleau, Ismael; Ongen, Halit; ... Dermitzakis, Emmanouil 2013
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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
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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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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
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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
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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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An integrated encyclopedia of DNA elements in the human genome ENCODE Project Consortium 2012
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Identification of VPS35 mutations replicated in French families with Parkinson disease Lesage, S; Condroyer, C; Klebe, S; Honoré, A; ... Brice, A 2012
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An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium 2012
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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
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Epidemiology and virulence insights from MRSA and MSSA genome analysis Lazarevic, Vladimir; Beaume, Marie-Emilie; Corvaglia, Anna; Hernandez, David; ... Francois, Patrice 2011
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Replication of association between a SCN1A splice variant and febrile seizures Le Gal, François; Trachsler-Salzmann, Annick; Crespel, Arielle; Malafosse, Alain 2011
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IL28B polymorphisms predict reduction of HCV RNA from the first day of therapy in chronic hepatitis C. Bochud, Pierre-Yves; Bibert, Stéphanie; Negro, Francesco; Haagmans, B; ... Lagging, M 2011
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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
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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
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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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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
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Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes Strawbridge, Rona J 2011
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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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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study Ross, Owen A 2011
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Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice Fokstuen, Siv; Munoz, Analia; Melacini, Paola; Iliceto, Sabino; ... Blouin, Jean-Louis 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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Genome-wide pharmacogenetics of antidepressant response in the GENDEP project Uher, Rudolf; Perroud, Nader Ali; Ng, Mandy Y. M.; Hauser, Joanna; ... McGuffin, Peter 2010
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A map of human genome variation from population-scale sequencing 1000 Genomes Project Consortium 2010
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Tissue biomarker development in a multicentre trial context: a feasibility study on the PETACC3 stage II and III colon cancer adjuvant treatment trial Bosman, Fred T.; Yan, Pu; Tejpar, Sabine; Fiocca, Roberto; ... Roth, Arnaud 2009
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Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms Ibáñez, Pablo; Lesage, Suzanne; Janin, Sabine; Lohmann, Ebba; ... Brice, Alexis 2009
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Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry Benjamin, Emelia J.; Ehret, Georg Benedikt 2009
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Common genetic variation and the control of HIV-1 in humans Fellay, Jacques; Ge, Dongliang 2009
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CNVs and genetic medicine (excitement and consequences of a rediscovery) Beckmann, J. S.; Sharp, A. J.; Antonarakis, Stylianos 2008
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Glutathione S-transferase genotype increases risk of progression from bronchial hyperresponsiveness to asthma in adults Imboden, Medea; Rochat, Thierry; Brutsche, M.; Schindler, Christian; ... Probst-Hensch, Nicole M. 2008
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PPARG by dietary fat interaction influences bone mass in mice and humans Ackert-Bicknell, Cheryl L.; Demissie, Serkalem; Marín de Evsikova, Caralina; Hsu, Yi-Hsiang; ... Rosen, Clifford J. 2008
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Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations Schwabe, Georg C.; Hoffmann, Katrin; Loges, Niki Tomas; Birker, Daniel; ... Bartoloni, Lucia 2008
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Conserved noncoding sequences are selectively constrained and not mutation cold spots Drake, J. A.; Bird, Christine; Nemesh, James; Thomas, D. J.; ... Hirschhorn, J. N. 2006
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Association of the connexin36 gene with juvenile myoclonic epilepsy Mas, Christophe; Taske, N.; Deutsch, Samuel; Guipponi, Michel; ... Meda, Paolo 2004
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