HISTOIRES D'IDENTITÉ (GÉNÉTIQUE) = (HI)STORIES OF (GENETIC) IDENTITYLEUTENEGGER, Anne-Louise; DARLU, Pierre.Bulletins et mémoires de la Société d'anthropologie de Paris. 2009, Vol 21, Num 3-4, pp 215-221, issn 0037-8984, 7 p.Article

LRRK2, un gène de la famille ROCO impliquée dans la maladie de Parkinson = LRRK2 : a gene belonging to the ROCO family is implicated in the Parkinson's diseaseLESAGE, Suzanne; LEUTENEGGER, Anne-Louise; BRICE, Alexis et al.MS. Médecine sciences. 2005, Vol 21, Num 12, pp 1015-1017, issn 0767-0974, 3 p.Article

Développement embryonnaire précoce: Un grand rôle pour un petit ARN = Extreme microcephaly and growth retardation caused by mutations in a non-coding RNA component of the minor spliceosomeEDERY, Patrick; ALIX, Eudeline; CLERGET-DARPOUX, Françoise et al.MS. Médecine sciences. 2012, Vol 28, Num 2, pp 130-133, issn 0767-0974, 4 p.Article

Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us?LEUTENEGGER, Anne-Louise; SAHBATOU, Mourad; GAZAL, Steven et al.European journal of human genetics. 2011, Vol 19, Num 5, pp 583-587, issn 1018-4813, 5 p.Article

Runs of Homozygosity in European PopulationsMCQUILLAN, Ruth; LEUTENEGGER, Anne-Louise; MACLEOD, Andrew K et al.American journal of human genetics. 2008, Vol 83, Num 3, pp 359-372, issn 0002-9297, 14 p.Article

A novel locus for autosomal dominant uncomplicated hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3HANEIN, Sylvain; DÜRR, Alexandra; BRICE, Alexis et al.Human genetics. 2007, Vol 122, Num 3-4, pp 261-273, issn 0340-6717, 13 p.Article

Juvenile-onset parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1LEUTENEGGER, Anne-Louise; SALIH, Mustafa A. M; IBANEZ, Pablo et al.Archives of neurology (Chicago). 2006, Vol 63, Num 9, pp 1257-1261, issn 0003-9942, 5 p.Article

Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNAEDERY, Patrick; MARCAILLOU, Charles; JOUK, Pierre-Simon et al.Science (Washington, D.C.). 2011, Vol 332, Num 6026, pp 240-243, issn 0036-8075, 4 p.Article

G2019S LRRK2 mutation in French and North African families with Parkinson's diseaseLESAGE, Suzanne; IBANEZ, Pablo; DURR, Alexandra et al.Annals of neurology. 2005, Vol 58, Num 5, pp 784-787, issn 0364-5134, 4 p.Article

Presence of large deletions in kindreds with autismYU, Chang-En; DAWSON, Geraldine; SPENCE, M. Anne et al.American journal of human genetics. 2002, Vol 71, Num 1, pp 100-115, issn 0002-9297Article