| 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 |