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Anne-Louise Leutenegger
Anne-Louise Leutenegger
NeuroDiderot, Inserm U1141
Verified email at inserm.fr - Homepage
Title
Cited by
Cited by
Year
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
11992008
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
6812006
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
4042016
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
3592017
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
3082003
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
2392011
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
2352005
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
1562005
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
1332016
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
1002000
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
872011
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
792002
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
762016
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
752015
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
742015
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
682011
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
682007
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
662006
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
612010
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
562014
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Articles 1–20