Runs of homozygosity in European populations R McQuillan, AL Leutenegger, R Abdel-Rahman, CS Franklin, M Pericic, ... The American Journal of Human Genetics 83 (3), 359-372, 2008 | 1224 | 2008 |
LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs S Lesage, A Dürr, M Tazir, E Lohmann, AL Leutenegger, S Janin, P Pollak, ... New England Journal of Medicine 354 (4), 422-423, 2006 | 683 | 2006 |
Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... The American Journal of Human Genetics 98 (3), 500-513, 2016 | 415 | 2016 |
Variation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis B Marin, F Boumédiene, G Logroscino, P Couratier, MC Babron, ... International journal of epidemiology 46 (1), 57-74, 2017 | 368 | 2017 |
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 | 313 | 2003 |
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 |
G2019S LRRK2 mutation in French and North African families with Parkinson's disease S Lesage, P Ibanez, E Lohmann, P Pollak, F Tison, M Tazir, ... Annals of Neurology: Official Journal of the American Neurological …, 2005 | 236 | 2005 |
LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century S Lesage, AL Leutenegger, P Ibanez, S Janin, E Lohmann, A Dürr, ... The American Journal of Human Genetics 77 (2), 330-332, 2005 | 156 | 2005 |
Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin B Marin, G Logroscino, F Boumédiene, A Labrunie, P Couratier, ... European journal of epidemiology 31, 229-245, 2016 | 133 | 2016 |
Segregation analysis of phenotypic components of learning disabilities. I. Nonword memory and digit span EM Wijsman, D Peterson, AL Leutenegger, JB Thomson, KAB Goddard, ... The American Journal of Human Genetics 67 (3), 631-646, 2000 | 100 | 2000 |
Genetics of VEGF serum variation in human isolated populations of cilento: importance of VEGF polymorphisms D Ruggiero, C Dalmasso, T Nutile, R Sorice, L Dionisi, M Aversano, ... PLoS One 6 (2), e16982, 2011 | 87 | 2011 |
Presence of large deletions in kindreds with autism CE Yu, G Dawson, J Munson, I D’Souza, J Osterling, A Estes, ... The American Journal of Human Genetics 71 (1), 100-115, 2002 | 81 | 2002 |
Six novel loci associated with circulating VEGF levels identified by a meta-analysis of genome-wide association studies SH Choi, D Ruggiero, R Sorice, C Song, T Nutile, A Vernon Smith, ... PLoS genetics 12 (2), e1005874, 2016 | 77 | 2016 |
A new F‐box protein 7 gene mutation causing typical Parkinson's disease E Lohmann, AS Coquel, A Honoré, H Gurvit, H Hanagasi, M Emre, ... Movement Disorders 30 (8), 1130-1133, 2015 | 76 | 2015 |
High level of inbreeding in final phase of 1000 Genomes Project S Gazal, M Sahbatou, MC Babron, E Génin, AL Leutenegger Scientific reports 5 (1), 17453, 2015 | 75 | 2015 |
Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us? AL Leutenegger, M Sahbatou, S Gazal, H Cann, E Génin European Journal of Human Genetics 19 (5), 583-587, 2011 | 68 | 2011 |
LRRK2emph exon 41 mutations in sporadic Parkinson disease in Europeans S Lesage, S Janin, E Lohmann, AL Leutenegger, L Leclere, F Viallet, ... Archives of neurology 64 (3), 425-430, 2007 | 68 | 2007 |
Using genomic inbreeding coefficient estimates for homozygosity mapping of rare recessive traits: application to Taybi-Linder syndrome AL Leutenegger, A Labalme, E Génin, A Toutain, E Steichen, ... The American journal of human genetics 79 (1), 62-66, 2006 | 66 | 2006 |
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans S Lesage, E Patin, C Condroyer, AL Leutenegger, E Lohmann, N Giladi, ... Human Molecular Genetics 19 (10), 1998-2004, 2010 | 62 | 2010 |
Inbreeding coefficient estimation with dense SNP data: comparison of strategies and application to HapMap III S Gazal, M Sahbatou, H Perdry, S Letort, E Génin, AL Leutenegger Human heredity 77 (1-4), 49-62, 2014 | 57 | 2014 |