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	Title	Authors / Editors	Date
unige:29852	Analysis of TAP2 and HLA-DP gene polymorphism in psoriasis	Fakler, J. W.; Schmitt-Egenolf, M.; Vejbaesya, S.; Boehncke, Wolf-Henning; ... Eiermann, T. H.	1994
unige:13227	Human genetic affinities for Y-chromosome P49a,f/TaqI haplotypes show strong correspondence with linguistics	Poloni, Estella S.; Semino, O.; Passarino, G.; Santachiara-Benerecetti, A S.; ... Excoffier, Laurent Georges Louis	1997
unige:8934	Deletion of the fibrogen alpha-chain gene (FGA) causes congenital afibrogenemia	Neerman Arbez, Marguerite; Honsberger, A.; Antonarakis, Stylianos; Morris, Michael Andréw	1999
unige:2010	A worldwide analysis of AG molecular diversity inferred from serology	Sanchez-Mazas, Alicia; Bütler-Brunner, E.; Bütler, R.; Calderón, R.; ... Langaney, André	2001
unige:1630	DNA sequence variability of IGHG3 alleles associated to the main G3m haplotypes in human populations	Dard, Patricia; Lefranc, Marie-Paule; Osipova, Ludmilla; Sanchez-Mazas, Alicia	2001
unige:2011	African diversity from the HLA point of view: influence of genetic drift, geography, linguistics, and natural selection	Sanchez-Mazas, Alicia	2001
unige:45715	Pig hematopoietic cell chimerism in baboons conditioned with a nonmyeloablative regimen and CD154 blockade	Buehler, Leo Hans; Awwad, M; Treter, S; Chang, Q; ... Cooper, D K	2002
unige:2119	Molecular analysis of the beta-globin gene cluster in the Niokholo Mandenka population reveals a recent origin of the beta(S) Senegal mutation	Currat, Mathias; Trabuchet, Guy; Rees, David; Perrin, Pascale; ... Excoffier, Laurent Georges Louis	2002
unige:26597	Tau and neurofilaments in a family with frontotemporal dementia unlinked to chromosome 17q21-22	Savioz, Armand; Riederer, Beat M; Heutink, Peter; Rizzu, Patrizia; ... Leuba, Geneviève	2003
unige:2130	Genetic structure of Mediterranean populations revealed by Y-chromosome haplotype analysis	Quintana-Murci, Lluís; Veitia, Reiner; Fellous, Marc; Semino, Ornella; Poloni, Estella S.	2003
unige:151024	A new DR7-DQ8 haplotype resulting from a recombination between the DQA1 and DQB1 loci in a leukemic patient of Caucasoid origin	Tiercy, Jean-Marie; Villard, Jean	2004
unige:8887	Association of the connexin36 gene with juvenile myoclonic epilepsy	Mas, Christophe; Taske, N.; Deutsch, Samuel; Guipponi, Michel; ... Meda, Paolo	2004
unige:1981	GM haplotype diversity of 82 populations over the world suggests a centrifugal model of human migrations	Dugoujon, Jean-Michel; Hazout, Serge; Loirat, France; Mourrieras, Bruno; ... Sanchez-Mazas, Alicia	2004
unige:1965	Population samples and genotyping technology	Mack, S. J.; Sanchez-Mazas, Alicia; Single, R. M.; Meyer, D.; ... Erlich, H.A.	2007
unige:114069	H1 haplotype of the MAPT gene is associated with lower regional gray matter volume in healthy carriers	Canu, Elisa; Boccardi, Marina; Ghidoni, Roberta; Benussi, Luisa; ... Frisoni, Giovanni	2009
unige:45179	Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms	Ibáñez, Pablo; Lesage, Suzanne; Janin, Sabine; Lohmann, Ebba; ... Brice, Alexis	2009
unige:114066	The CST3 B haplotype is associated with frontotemporal lobar degeneration	Benussi, L; Ghidoni, R; Galimberti, D; Boccardi, Marina; ... Binetti, G	2010
unige:45219	A map of human genome variation from population-scale sequencing	1000 Genomes Project Consortium	2010
unige:32884	Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans	Lesage, Suzanne; Patin, Etienne; Condroyer, Christel; Leutenegger, Anne-Louise; ... Brice, Alexis	2010
unige:45216	An integrated map of genetic variation from 1,092 human genomes	1000 Genomes Project Consortium	2012

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