| Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis Nature 476 (7359), 214-219, 2011 | 2953 | 2011 |
| Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum D Campion, C Dumanchin, D Hannequin, B Dubois, S Belliard, M Puel, ... The American Journal of Human Genetics 65 (3), 664-670, 1999 | 1102 | 1999 |
| Effects of misspecifying genetic parameters in lod score analysis F Clerget-Darpoux, C Bonaiti-Pellie, J Hochez Biometrics, 393-399, 1986 | 576 | 1986 |
| Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q J Melki, S Abdelhak, P Sheth, MF Bachelot, P Burlet, A Marcadet, J Aicardi, ... Nature 344 (6268), 767-768, 1990 | 498 | 1990 |
| Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant R Sherrington, S Froelich, S Sorbi, D Campion, H Chi, EA Rogaeva, ... Human molecular genetics 5 (7), 985-988, 1996 | 439 | 1996 |
| Mutations of the presenilin I gene in families with early-onset Alzheimer's disease D Campion, JM Flaman, A Brice, D Hannequin, B Dubois, C Martin, ... Human molecular genetics 4 (12), 2373-2377, 1995 | 356 | 1995 |
| Estimation of the inbreeding coefficient through use of genomic data AL Leutenegger, B Prum, E Génin, C Verny, A Lemainque, ... The American Journal of Human Genetics 73 (3), 516-523, 2003 | 311 | 2003 |
| Genome search in celiac disease L Greco, G Corazza, MC Babron, F Clot, MC Fulchignoni-Lataud, ... The American Journal of Human Genetics 62 (3), 669-675, 1998 | 287 | 1998 |
| HLA‐DQ relative risks for coeliac disease in European populations: a study of the European Genetics Cluster on Coeliac Disease P Margaritte‐Jeannin, MC Babron, M Bourgey, AS Louka, F Clot, ... Tissue antigens 63 (6), 562-567, 2004 | 263 | 2004 |
| New classification of HLA–DRB1 alleles supports the shared epitope hypothesis of rheumatoid arthritis susceptibility ST Du Montcel, L Michou, E Petit‐Teixeira, J Osorio, I Lemaire, S Lasbleiz, ... Arthritis & Rheumatism 52 (4), 1063-1068, 2005 | 259 | 2005 |
| More missense in amyloid gene DA Carter, E Desmarais, M Bellis, D Campion, F Clerget-Darpoux, A Brice, ... Nature genetics 2 (4), 255-256, 1992 | 247 | 1992 |
| Association of TALS developmental disorder with defect in minor splicing component U4atac snRNA P Edery, C Marcaillou, M Sahbatou, A Labalme, J Chastang, R Touraine, ... Science 332 (6026), 240-243, 2011 | 242 | 2011 |
| Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex. H Bickeböller, D Campion, A Brice, P Amouyel, D Hannequin, ... American journal of human genetics 60 (2), 439, 1997 | 184 | 1997 |
| HLA related genetic risk for coeliac disease M Bourgey, G Calcagno, N Tinto, D Gennarelli, P Margaritte-Jeannin, ... Gut 56 (8), 1054-1059, 2007 | 168 | 2007 |
| IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations F Weber, B Fontaine, I Cournu-Rebeix, A Kroner, M Knop, S Lutz, ... Genes & Immunity 9 (3), 259-263, 2008 | 167 | 2008 |
| Tyrosine hydroxylase polymorphisms associated with manic-depressive illness M Leboyer, A Malafosse, S Boularand, D Campion, F Gheysen, ... The Lancet 335 (8699), 1219, 1990 | 156 | 1990 |
| Identifying modifier genes of monogenic disease: strategies and difficulties E Génin, J Feingold, F Clerget-Darpoux Human genetics 124, 357-368, 2008 | 145 | 2008 |
| Genetic study of transthyretin amyloid neuropathies: carrier risks among French and Portuguese families V Planté-Bordeneuve, J Carayol, A Ferreira, D Adams, F Clerget-Darpoux, ... Journal of medical genetics 40 (11), e120-e120, 2003 | 145 | 2003 |
| Statistical properties of the allelic and genotypic transmission/disequilibrium test for multiallelic markers H Bickeböller, FO Clerget‐Darpoux Genetic Epidemiology 12 (6), 865-870, 1995 | 139 | 1995 |
| Meta and pooled analysis of European coeliac disease data MC Babron, S Nilsson, S Adamovic, ÅT Naluai, J Wahlström, H Ascher, ... European journal of human genetics 11 (11), 828-834, 2003 | 132 | 2003 |
