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Polymorphism, single nucleotide
 
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 A catalog of genetic loci associated with kidney function from analyses of a million individuals Wuttke, Matthias; Li, Yong; Li, Man; Sieber, Karsten B.; ... Pattaro, Cristian 2019
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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 testicular germ cell tumor Rapley, Elizabeth A.; Turnbull, Clare; Al Olama, Ali Amin; Dermitzakis, Emmanouil; ... Stratton, Michael R. 2009
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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 single-nucleotide substitution mutator phenotype revealed by exome sequencing of human colon adenomas Nikolaev, Sergey Igorievich; Sotiriou, Sotirios K; Pateras, Ioannis S; Santoni, Federico; ... Halazonetis, Thanos 2012
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 A spectrum of LMX1B mutations in Nail-Patella syndrome: new point mutations, deletion, and evidence of mosaicism in unaffected parents Marini, Monica; Bocciardi, Renata; Gimelli, Stefania; Di Duca, Marco; ... Ravazzolo, Roberto 2010
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 A systematic survey of loss-of-function variants in human protein-coding genes MacArthur, Daniel G; Montgomery, Stephen; Dermitzakis, Emmanouil 2012
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 A whole-genome association study of major determinants for host control of HIV-1 Fellay, Jacques; Shianna, K. V.; Ge, Dongliang; Colombo, Sara; ... Goldstein, D. B. 2007
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 ABCB1 polymorphisms and neuropsychiatric adverse events in oseltamivir-treated children during influenza H1N1/09 pandemia L'Huillier, Arnaud; Ing Lorenzini, Kuntheavy; Crisinel, Pierre-Alex; Rebsamen, Michela; ... Desmeules, Jules Alexandre 2011
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 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
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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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 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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 Anticoagulation orale et pharmacogénétique : perspectives pour la pratique clinique Benusiglio, Patrick Raphaël; Desmeules, Jules Alexandre; De Moerloose, Philippe; Dayer, Pierre 2007
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 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
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 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
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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 hypertension drug target genes with blood pressure and hypertension in 86,588 individuals Johnson, Andrew D; Newton-Cheh, Christopher; Chasman, Daniel I; Ehret, Georg Benedikt; ... Levy, Daniel 2011
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 BRD2 and TAP-1 genes and juvenile myoclonic epilepsy Layouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed 2010
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 BXSB/long-lived is a recombinant inbred strain containing powerful disease suppressor loci Haywood, M. E.; Gabriel, Luisa; Rose, S. J.; Rogers, N. J.; ... Morley, B. J. 2007
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