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Jacqueline Levilliers

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Catherine Dodé; Luis Teixeira; Jacqueline Levilliers; Corinne Fouveaut; Philippe Bouchard; Marie-Laure Kottler; James Lespinasse; Anne Lienhardt-Roussie; Michèle Mathieu; Alexandre Moerman; Graeme Morgan; Arnaud Murat; Jean-Edmont Toublanc; Slawomir Wolczynski; Marc Delpech; Christine Petit; Jacques Young; Jean-Pierre Hardelin
Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.
Jean-Pierre Hardelin; Françoise Denoyelle; Jacqueline Levilliers; Marie-Christine Simmler; Christine Petit
[Hereditary deafness: molecular genetics].
Catherine Dodé; Jacqueline Levilliers; Jean-Michel Dupont; Anne De Paepe; Nathalie Le Dû; Nadia Soussi-Yanicostas; Roney Coimbra; Sedigheh Delmaghani; Sylvie Compain-Nouaille; Françoise Baverel; Christophe Pêcheux; Dominique Le Tessier; Corinne Cruaud; Marc Delpech; Frank Speleman; Stefan Vermeulen; Andrea Amalfitano; Yvan Bachelot; Philippe Bouchard; Sylvie Cabrol; Jean-Claude Carel; Henriette A Delemarre-Van De Waal; Barbara Goulet-Salmon; Marie-Laure Kottler; Odile Richard; Franco Sanchez-Franco; Robert Saura; Jacques Young; Christine Petit; Jean-Pierre Hardelin
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

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All Publications

2006: Catherine Dodé; Luis Teixeira; Jacqueline Levilliers; Corinne Fouveaut; Philippe Bouchard; Marie-Laure Kottler; James Lespinasse; Anne Lienhardt-Roussie; Michèle Mathieu; Alexandre Moerman; Graeme Morgan; Arnaud Murat; Jean-Edmont Toublanc; Slawomir Wolczynski; Marc Delpech; Christine Petit; Jacques Young; Jean-Pierre Hardelin
Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.
PLoS genetics 2006;2(10):e175.
2004: Jean-Pierre Hardelin; Françoise Denoyelle; Jacqueline Levilliers; Marie-Christine Simmler; Christine Petit
[Hereditary deafness: molecular genetics].
Médecine sciences : M/S 2004;20(3):311-6.
2003: Catherine Dodé; Jacqueline Levilliers; Jean-Michel Dupont; Anne De Paepe; Nathalie Le Dû; Nadia Soussi-Yanicostas; Roney Coimbra; Sedigheh Delmaghani; Sylvie Compain-Nouaille; Françoise Baverel; Christophe Pêcheux; Dominique Le Tessier; Corinne Cruaud; Marc Delpech; Frank Speleman; Stefan Vermeulen; Andrea Amalfitano; Yvan Bachelot; Philippe Bouchard; Sylvie Cabrol; Jean-Claude Carel; Henriette A Delemarre-Van De Waal; Barbara Goulet-Salmon; Marie-Laure Kottler; Odile Richard; Franco Sanchez-Franco; Robert Saura; Jacques Young; Christine Petit; Jean-Pierre Hardelin
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.
Nature genetics 2003;33(4):463-5.
2001: Christine Petit; Jacqueline Levilliers; Jean-Pierre Hardelin
Molecular genetics of hearing loss.
Annual review of genetics 2001;35():589-646.
2000: Jean-Pierre Hardelin; Nadia Soussi-Yanicostas; O Ardouin; Jacqueline Levilliers; Christine Petit
Kallmann syndrome.
Advances in oto-rhino-laryngology 2000;56():268-74.
2000: Françoise Denoyelle; Dominique Weil; Jacqueline Levilliers; Christine Petit
DFNA3.
Advances in oto-rhino-laryngology 2000;56():78-83.
1998: Nadia Soussi-Yanicostas; Catherine Faivre-Sarrailh; Jean-Pierre Hardelin; Jacqueline Levilliers; Geneviève ROUGON; Christine Petit
Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific manner.
Journal of cell science 1998;111 ( Pt 19)():2953-65.
1998: Jean-Pierre Hardelin; Nadia Soussi-Yanicostas; Jacqueline Levilliers; V Kalatzis; S Abdelhak; Martine Cohen-Salmon; Christine Petit
Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndrome.
Advances in nephrology from the Necker Hospital 1998;28():419-28.
1998: Catherine Dodé; Dominique Weil; Jacqueline Levilliers; F Crozet; H Chaïb; F Levi-Acobas; P Guilford; Christine Petit
Sequence characterization of a newly identified human alpha-tubulin gene (TUBA2).
Genomics 1998;47(1):125-30.
1996: Nadia Soussi-Yanicostas; Jean-Pierre Hardelin; M M Arroyo-Jimenez; O Ardouin; R Legouis; Jacqueline Levilliers; François Traincard; Jean-Michel Betton; L Cabanié; Christine Petit
Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system.
Journal of cell science 1996;109 ( Pt 7)():1749-57.
1995: P Guilford; Catherine Dodé; F Crozet; Stéphane Blanchard; H Chaïb; Jacqueline Levilliers; F Levi-Acobas; Dominique Weil; Jean Weissenbach; D Cohen
A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C).
Genomics 1995;29(1):163-9.
1995: I Wang; Dominique Weil; Jacqueline Levilliers; Nabeel A Affara; ALBERT DE LA CHAPELLE; Christine Petit
Prevalence and molecular analysis of two hot spots for ectopic recombination leading to XX maleness.
Genomics 1995;28(1):52-8.
1995: Brunella Franco; Germana Meroni; Giancarlo Parenti; Jacqueline Levilliers; L Bernard; Marinella Gebbia; L Cox; P Maroteaux; L Sheffield; G A Rappold; G Andria; C Petit; A Ballabio
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy.
Cell 1995;81(1):15-25.
1995: I Wang; Brunella Franco; GB Ferrero; A Craig Chinault; Jean Weissenbach; I Chumakov; D Le Paslier; Jacqueline Levilliers; A Klink; G A Rappold; A Ballabio; C Petit
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1).
Genomics 1995;26(2):229-38.
1995: Dominique Weil; Stéphane Blanchard; Josseline Kaplan; P Guilford; F Gibson; J Walsh; Philomena Mburu; A Varela; Jacqueline Levilliers; M D Weston
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Nature 1995;374(6517):60-1.
1994: H Chaïb; Geneviève Lina-Granade; P Guilford; H Plauchu; Jacqueline Levilliers; A Morgon; Christine Petit
A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval.
Human molecular genetics 1994;3(12):2219-22.
1994: C Vincent; V Kalatzis; S Compain; Jacqueline Levilliers; R Slim; F Graia; M L Pereira; A Nivelon; Marie-Françoise Croquette; Didier Lacombe
A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene.
Human molecular genetics 1994;3(10):1859-66.
1994: P Guilford; S Ben Arab; Stéphane Blanchard; Jacqueline Levilliers; Jean Weissenbach; A Belkahia; Christine Petit
A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.
Nature genetics 1994;6(1):24-8.
1993: Dominique Weil; Marie-France Portnoï; Jacqueline Levilliers; I Wang; M Mathieu; Jean-Louis Taillemite; M Meier; B Boudailliez; Christine Petit
A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata.
Human molecular genetics 1993;2(11):1853-6.
1993: R Legouis; Martine Cohen-Salmon; I del Castillo; Jacqueline Levilliers; L Capy; J P Mornow; Christine Petit
Characterization of the chicken and quail homologues of the human gene responsible for the X-linked Kallmann syndrome.
Genomics 1993;17(2):516-8.
1993: R Slim; D Le Paslier; S Compain; Jacqueline Levilliers; P Ougen; A Billault; S J Donohue; David Klein; L Mintz; Alain BERNHEIM
Construction of a yeast artificial chromosome contig spanning the pseudoautosomal region and isolation of 25 new sequence-tagged sites.
Genomics 1993;16(3):691-7.
1993: Jean-Pierre Hardelin; Jacqueline Levilliers; Stéphane Blanchard; J C Carel; M Leutenegger; J P Pinard-Bertelletto; Pierre Bouloux; Christine Petit
Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome.
Human molecular genetics 1993;2(4):373-7.
1993: R Slim; Jacqueline Levilliers; Hermann-Josef Lüdecke; Uwe Claussen; V C Nguyen; N M Gough; B Horsthemke; Christine Petit
A human pseudoautosomal gene encodes the ANT3 ADP/ATP translocase and escapes X-inactivation.
Genomics 1993;16(1):26-33.
1993: Jean-Pierre Hardelin; Jacqueline Levilliers; J Young; M Pholsena; R Legouis; J Kirk; Pierre Bouloux; Christine Petit; G Schaison
Xp22.3 deletions in isolated familial Kallmann's syndrome.
The Journal of clinical endocrinology and metabolism 1993;76(4):827-31.
1993: J M Claverie; Jean-Pierre Hardelin; R Legouis; Jacqueline Levilliers; Lydie Bougueleret; M G Mattei; Christine Petit
Characterization and chromosomal assignment of a human cDNA encoding a protein related to the murine 102-kDa cadherin-associated protein (alpha-catenin).
Genomics 1993;15(1):13-20.
1992: Jean-Pierre Hardelin; Jacqueline Levilliers; I del Castillo; Martine Cohen-Salmon; R Legouis; Stéphane Blanchard; S Compain; Pierre Bouloux; J Kirk; C Moraine
X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(17):8190-4.
1991: R Legouis; Jean-Pierre Hardelin; Jacqueline Levilliers; J M Claverie; S Compain; V Wunderle; P Millasseau; D Le Paslier; D Cohen; D Caterina
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules.
Cell 1991;67(2):423-35.
1991: Pierre Bouloux; Jean-Pierre Hardelin; Patricia B Munroe; J M Kirk; R Legouis; Jacqueline Levilliers; J Hazan; J Weissenbach; C Petit
A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3).
Nucleic acids research 1991;19(19):5453.
1990: Thomas Meitinger; B Heye; C Petit; Jacqueline Levilliers; Astrid Golla; C Moraine; B Dalla Piccola; W G Sippell; Jan Murken; A Ballabio
Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.
American journal of human genetics 1990;47(4):664-9.
1990: Christine Petit; J Melki; Jacqueline Levilliers; F Serville; Jean Weissenbach; P Maroteaux
An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature.
Human genetics 1990;85(2):247-50.
1990: Christine Petit; Jacqueline Levilliers; Jean Weissenbach
Long-range restriction map of the terminal part of the short arm of the human X chromosome.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(10):3680-4.
1990: Christine Petit; Jacqueline Levilliers; F Rouyer; M C Simmler; E Herouin; Jean Weissenbach
Isolation of sequences from Xp22.3 and deletion mapping using sex chromosome rearrangements from human X-Y interchange sex reversals.
Genomics 1990;6(4):651-8.
1990: O Gabriel-Robez; Yves Rumpler; C Ratomponirina; C Petit; Jacqueline Levilliers; Marie-Françoise Croquette; J Couturier
Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X;Y translocation.
Cytogenetics and cell genetics 1990;54(1-2):38-42.
1988: Christine Petit; Jacqueline Levilliers; Jean Weissenbach
Physical mapping of the human pseudo-autosomal region; comparison with genetic linkage map.
The EMBO journal 1988;7(8):2369-76.
1987: Jean Weissenbach; Jacqueline Levilliers; Christine Petit; F Rouyer; M C Simmler
Normal and abnormal interchanges between the human X and Y chromosomes.
Development (Cambridge, England) 1987;101 Suppl():67-74.
1986: F Rouyer; M C Simmler; Gilles Vergnaud; C Johnsson; Jacqueline Levilliers; Christine Petit; Jean Weissenbach
The pseudoautosomal region of the human sex chromosomes.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 1():221-8.