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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
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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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 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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 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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 The effect of the Neolithic expansion on European molecular diversity Currat, Mathias; Excoffier, Laurent Georges Louis 2005
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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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 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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 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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 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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 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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 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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 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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 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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 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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 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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 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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 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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 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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 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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