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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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Alternative Splicing QTLs in European and African Populations Ongen, Halit; Dermitzakis, Emmanouil 2015
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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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Association of the CD226 Ser(307) variant with systemic sclerosis: evidence of a contribution of costimulation pathways in systemic sclerosis pathogenesis Dieudé, P; Guedj, M; Truchetet, Marie-Elise; Wipff, J; ... Allanore, Y 2011
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Caffeine intake and CYP1A2 variants associated with high caffeine intake protect non-smokers from hypertension Guessous, Idris; Dobrinas, Maria; Kutalik, Zoltán; Pruijm, Menno; ... Bochud, Murielle 2012
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Defining the role of common variation in the genomic and biological architecture of adult human height Wood, Andrew R; Esko, Tonu; Yang, Jian; Vedantam, Sailaja; ... Goddard, Michael E 2014
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Dimorphism of TAP-1 gene in Caucasian with juvenile myoclonic epilepsy and in Tunisian with idiopathic generalized epilepsies Layouni, S.; Chouchane, L.; Malafosse, Alain; Dogui, M. 2010
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Discovery and refinement of loci associated with lipid levels Global Lipids Genetics Consortium 2013
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Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies Nguyen, Khanh-Dung H; Pihur, Vasyl; Ganesh, Santhi K; Rakha, Ankit; ... Chakravarti, Aravinda 2013
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Effects of single genetic variants and polygenic obesity risk scores on disordered eating in adolescents - The HUNT study Sardahaee, Farzaneh Saeedzadeh; Holmen, Turid Lingaas; Micali, Nadia; Kvaløy, Kirsti 2017
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EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants? Lesage, Suzanne; Condroyer, Christel; Klebe, Stephan; Lohmann, Ebba; ... Brice, Alexis 2012
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Epistatic selection between coding and regulatory variation in human evolution and disease Lappalainen, Tuuli Emilia; Montgomery, Stephen; Nica, Alexandra; Dermitzakis, Emmanouil 2011
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Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study Ehret, Georg Benedikt; O'Connor, Ashley A.; Weder, Alan; Cooper, Richard S.; Chakravarti, Aravinda 2009
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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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Genetic differentiation of Yemeni people according to rhesus and Gm polymorphisms Chaabani, H.; Sanchez-Mazas, Alicia; Sallami, S. F. 2000
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Genetic structure of Mediterranean populations revealed by Y-chromosome haplotype analysis Quintana-Murci, Lluís; Veitia, Reiner; Fellous, Marc; Semino, Ornella; Poloni, Estella S. 2003
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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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HLA-DRB1 and HLA-DQB1 allele associations in an Albanian patient population with rheumatoid arthritis: correlations with the specific autoantibody markers and inter-population DRB1 allele frequency variability Prifti-Kurti, Margarita; Nunes, Jose Manuel; Shyti, Erkena; Ylli, Zamira; ... Sulcebe, Genc 2014
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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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Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease Lesage, Suzanne; Anheim, Mathieu; Condroyer, Christel; Pollak, Pierre; ... Brice, Alexis 2011
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Loci influencing blood pressure identified using a cardiovascular gene-centric array Ganesh, Santhi K; Tragante, Vinicius; Guo, Wei 2013
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Maternal and paternal lineages in Albania and the genetic structure of Indo-European populations Belledi, M.; Poloni, Estella S.; Casalotti, R.; Conterio, F.; ... Excoffier, Laurent Georges Louis 2000
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Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations O'Seaghdha, Conall M; Guessous, Idris; Köttgen, Anna; Wallaschofski, Henri; ... Bochud, Murielle 2013
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Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Soranzo, Nicole; Rivadeneira, Fernando; Chinappen-Horsley, Usha; Nica, Alexandra; ... Deloukas, P. 2009
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Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease Lesage, S; Condroyer, C; Lannuzel, A; Lohmann, E; ... Brice, A 2009
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Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequency Sosa, Maria Ximena; Sivakumar, I K Ashok; Maragh, Samantha; Veeramachaneni, Vamsi; ... Chakravarti, Aravinda 2012
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Patterns of cis regulatory variation in diverse human populations Stranger, Barbara E; Montgomery, Stephen; Dima, Antigoni; Parts, Leopold; ... Dermitzakis, Emmanouil 2012
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PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population Méneret, Aurélie; Grabli, David; Depienne, Christel; Gaudebout, Cécile; ... Roze, Emmanuel 2012
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Rare and common regulatory variation in population-scale sequenced human genomes Montgomery, Stephen; Lappalainen, Tuuli Emilia; Gutierrez Arcelus, Maria; Dermitzakis, Emmanouil 2011
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SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxia Marelli, Cecilia; van de Leemput, Joyce; Johnson, Janel O; Tison, Francois; ... Brice, Alexis 2011
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The effect of the Neolithic expansion on European molecular diversity Currat, Mathias; Excoffier, Laurent Georges Louis 2005
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Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations North, Kari E.; Franceschini, Nora; Avery, Christy L.; Baird, Lisa; ... Hunt, Steven C. 2010
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Y-chromosome specific YCAII, DYS19 and YAP polymorphisms in human populations: a comparative study Quintana-Murci, L.; Semino, O.; Poloni, Estella S.; Liu, A.; ... Santachiara-Benerecetti, A S. 1999