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Véronique David

Research Profile

Disorders

Physiology

Anatomy

Chromosomes, Human, Pair 6

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Genes, MHC Class I

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Sandra Mercier; Sylvie Odent; Leslie Ratié; Véronique David; Isabelle Gicquel; Valérie Dupé
NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos.
Sandra Mercier; Laurent Pasquier; Chloé Quélin; Leslie Ratié; Lucie Rochard; Marion Belleguic; Claude Bendavid; Boris Campillo-Gimenez; Véronique David; Christèle Dubourg; Valérie Dupé; Nicolas Garcelon; Isabelle Gicquel; Sophie Jaillard; Philippe Loget; Sylvie Odent
New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.
Caroline Le Lan; Annick Mosser; Martine Ropert; Lénaïck Detivaud; Véronique Loustaud-Ratti; Denis Vital-Durand; Laurent Roget; Edouard Bardou-Jacquet; Bruno Turlin; Véronique David; Olivier Loréal; Yves Deugnier; Pierre Brissot; Anne-Marie Jouanolle
Sex and acquired cofactors determine phenotypes of ferroportin disease.

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All Publications

2013: Sandra Mercier; Sylvie Odent; Leslie Ratié; Véronique David; Isabelle Gicquel; Valérie Dupé
NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos.
Disease models & mechanisms 2013;6(2):537-43.
2011: Sandra Mercier; Laurent Pasquier; Chloé Quélin; Leslie Ratié; Lucie Rochard; Marion Belleguic; Claude Bendavid; Boris Campillo-Gimenez; Véronique David; Christèle Dubourg; Valérie Dupé; Nicolas Garcelon; Isabelle Gicquel; Sophie Jaillard; Philippe Loget; Sylvie Odent
New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.
Journal of medical genetics 2011;48(11):752-60.
2011: Caroline Le Lan; Annick Mosser; Martine Ropert; Lénaïck Detivaud; Véronique Loustaud-Ratti; Denis Vital-Durand; Laurent Roget; Edouard Bardou-Jacquet; Bruno Turlin; Véronique David; Olivier Loréal; Yves Deugnier; Pierre Brissot; Anne-Marie Jouanolle
Sex and acquired cofactors determine phenotypes of ferroportin disease.
Gastroenterology 2011;140(4):1199-1207.e1-2.
2011: Sylvie Jaillard; Philippe Loget; Josette Lucas; Christèle Dubourg; Gwenaelle Le Bouar; Florence Demurger; Isabelle Bertorello; Véronique David; Patrice Poulain; Sylvie Odent; Marc-Antoine Belaud-Rotureau
Terminal 6.9 Mb deletion of chromosome 15q, associated with a structurally abnormal X chromosome in a patient with congenital diaphragmatic hernia and heart defect.
European journal of medical genetics 2011;54(2):186-8.
2011: Christèle Dubourg; Damien Sanlaville; Martine Doco-Fenzy; Cédric Le Caignec; Chantal Missirian; Sylvie Jaillard; Caroline Schluth-Bolard; Emilie Landais; Odile Boute; Nicole Philip; Annick Toutain; Albert David; P Edery; Anne Moncla; Dominique Martin-Coignard; Catherine Vincent-Delorme; Isabelle Mortemousque; Bénédicte Duban-Bedu; Sèverine Drunat; Mylène Beri; Jean Mosser; Sylvie Odent; Véronique David; Joris Andrieux
Clinical and molecular characterization of 17q21.31 microdeletion syndrome in 14 French patients with mental retardation.
European journal of medical genetics 2011;54(2):144-51.
2011: Karine Morcel; Tanguy Watrin; Laurent Pasquier; Lucie Rochard; Cédric Le Caignec; Christèle Dubourg; Philippe Loget; Bernard-Jean Paniel; Sylvie Odent; Véronique David; Isabelle Pellerin; Claude Bendavid; Daniel Guerrier
Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci.
Orphanet journal of rare diseases 2011;6():9.
2010: Sylvie Jaillard; Séverine Drunat; Claude Bendavid; Azzedine Aboura; Amandine Etcheverry; Hubert Journel; Andrée Delahaye; Laurent Pasquier; Dominique Bonneau; Annick Toutain; Lydie Burglen; Agnès Guichet; Eva Pipiras; Brigitte Gilbert-Dussardier; Brigitte Benzacken; Dominique Martin-Coignard; Catherine Henry; Albert David; Josette Lucas; Jean Mosser; Véronique David; Sylvie Odent; Alain Verloes; Christèle Dubourg
Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.
European journal of medical genetics 2010;53(2):66-75.
2010: Daniel E Pineda-Alvarez; Christèle Dubourg; Véronique David; Erich Roessler; Maximilian Muenke
Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients.
American journal of medical genetics. Part C, Seminars in medical genetics 2010;154C(1):93-101.
2009: Sophie Jaillard; Christèle Dubourg; M Gérard-Blanluet; A Delahaye; Laurent Pasquier; C Dupont; C Henry; A-C Tabet; J Lucas; A Aboura; Véronique David; B Benzacken; Sylvie Odent; E Pipiras
2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?
Journal of medical genetics 2009;46(12):847-55.
2009: Erich Roessler; Kenia B El-Jaick; Christèle Dubourg; Jorge I Vélez; Benjamin D Solomon; Daniel E Pineda-Alvarez; Felicitas Lacbawan; Nan Zhou; Maia V Ouspenskaia; Aimée Paulussen; Hubert J Smeets; Ute Hehr; Claude Bendavid; Sherri Bale; Sylvie Odent; Véronique David; Maximilian Muenke
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.
Human mutation 2009;30(10):E921-35.
2009: Marie-Laure Island; Anne-Marie Jouanolle; Annick Mosser; Yves Deugnier; Véronique David; Pierre Brissot; Olivier Loréal
A new mutation in the hepcidin promoter impairs its BMP response and contributes to a severe phenotype in HFE related hemochromatosis.
Haematologica 2009;94(5):720-4.
2007: Claude Bendavid; Christèle Dubourg; Laurent Pasquier; Isabelle Gicquel; Simon Le Gallou; Stéphanie Mottier; Marie-Renée Durou; Catherine Henry; Sylvie Odent; Véronique David
MLPA screening reveals novel subtelomeric rearrangements in holoprosencephaly.
Human mutation 2007;28(12):1189-97.
2007: Cédric Le Caignec; Bertrand Isidor; Ulrika de Pontbriand; Véronique David; Marie-Pierre Audrezet; Claude Ferec; Albert David
Third case of paternal isodisomy for chromosome 7 with cystic fibrosis: a new patient presenting with normal growth.
American journal of medical genetics. Part A 2007;143A(22):2696-9.
2007: Guillaume Bouguen; Sylvain Manfredi; Martine Blayau; Catherine Dugast; Bruno Buecher; Dominique Bonneau; Laurent Siproudhis; Véronique David; Jean-François Bretagne
Colorectal adenomatous polyposis Associated with MYH mutations: genotype and phenotype characteristics.
Diseases of the colon and rectum 2007;50(10):1612-7.
2007: Olivier Loréal; Martine Ropert; Annick Mosser; Valérie Déhais; Yves Deugnier; Véronique David; Pierre Brissot; Anne-Marie Jouanolle
[Pathophysiology and genetics of classic HFE (type 1) hemochromatosis].
Presse médicale (Paris, France : 1983) 2007;36(9 Pt 2):1271-7.
2007: Michel Roussey; A Le Bihannic; Virginie Scotet; Marie-Pierre Audrezet; Martine Blayau; M Dagorne; Véronique David; Eric Deneuville; J L Giniès; M Laurans; Valérie Moisan-Petit; Gilles Rault; P Vigneron; Claude Férec
Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutations.
Journal of inherited metabolic disease 2007;30(4):613.
2007: Christèle Dubourg; Claude Bendavid; Laurent Pasquier; Catherine Henry; Sylvie Odent; Véronique David
Holoprosencephaly.
Orphanet journal of rare diseases 2007;2():8.
2007: Claude Bendavid; Laurent Pasquier; Tanguy Watrin; Karine Morcel; Josette Lucas; Isabelle Gicquel; Christèle Dubourg; Catherine Henry; Véronique David; Sylvie Odent; Jean Levêque; Isabelle Pellerin; Daniel Guerrier
Phenotypic variability of a 4q34-->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother.
European journal of medical genetics 2007;50(1):66-72.
2006: Claude Bendavid; Bassem R Haddad; A Griffin; Marjan Huizing; Christèle Dubourg; Isabelle Gicquel; Luciane Cavalli; Laurent Pasquier; Alan L Shanske; R Long; Maia V Ouspenskaia; Sylvie Odent; Felicitas Lacbawan; Véronique David; Maximilian Muenke
Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype.
Journal of medical genetics 2006;43(6):496-500.
2006: Claude Bendavid; Christèle Dubourg; Isabelle Gicquel; Laurent Pasquier; Pascale Saugier-Veber; Marie-Renée Durou; Sylvie Jaillard; Thierry Frébourg; Bassem R Haddad; Catherine Henry; Sylvie Odent; Véronique David
Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genes.
Human genetics 2006;119(1-2):1-8.
2005: Laurent Pasquier; Christèle Dubourg; M Gonzales; Leila Lazaro; Véronique David; Sylvie Odent; Férechté Encha-Razavi
First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutations.
Journal of medical genetics 2005;42(1):e4.
2004: Elisabeth Traiffort; Christèle Dubourg; Hélène Faure; Didier Rognan; Sylvie Odent; Marie-Renée Durou; Véronique David; Martial Ruat
Functional characterization of sonic hedgehog mutations associated with holoprosencephaly.
The Journal of biological chemistry 2004;279(41):42889-97.
2004: Leila Lazaro; Christèle Dubourg; Laurent Pasquier; Franck Le Duff; Martine Blayau; Marie-Renée Durou; Armelle Thomas de la Pintière; Céline Aguilella; Véronique David; Sylvie Odent
Phenotypic and molecular variability of the holoprosencephalic spectrum.
American journal of medical genetics. Part A 2004;129A(1):21-4.
2004: Christèle Dubourg; Leila Lazaro; Laurent Pasquier; Claude Bendavid; Martine Blayau; Franck Le Duff; Marie-Renée Durou; Sylvie Odent; Véronique David
Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
Human mutation 2004;24(1):43-51.
2004: Livia Garavelli; Claudio Zanacca; G Caselli; Giacomo Banchini; Christèle Dubourg; Véronique David; Sylvie Odent; Fiorella Gurrieri; Giovanni Neri
Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehog.
American journal of medical genetics. Part A 2004;127A(1):93-5.
2004: Jean-Yves Le Gall; Anne-Marie Jouanolle; Patricia Fergelot; Jean Mosser; Véronique David
[Genetics of hereditary iron overload].
Bulletin de l'Académie nationale de médecine 2004;188(2):247-62; discussion 262-3.
2004: Karen J Livesey; Victoria L C Wimhurst; K Carter; Mark Worwood; Estelle Cadet; Jacques Rochette; Andrew G Roberts; Jennifer J Pointon; Alison T Merryweather-Clarke; M L Bassett; Anne-Marie Jouanolle; Annick Mosser; Véronique David; J Poulton; Kathryn J H Robson
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.
Journal of medical genetics 2004;41(1):6-10.
2003: Christèle Dubourg; Leila Lazaro; Martine Blayau; Laurent Pasquier; Marie-Renée Durou; Sylvie Odent; Véronique David
[Genetic study of holoprosencephaly].
Annales de biologie clinique 2003;61(6):679-87.
2003: Anne-Marie Jouanolle; Véronique Douabin-Gicquel; Chantal Halimi; Olivier Loréal; Patricia Fergelot; Thierry Delacour; Anne-Sophie de Lajarte-Thirouard; Bruno Turlin; Jean-Yves Le Gall; Estelle Cadet; Jacques Rochette; Véronique David; Pierre Brissot
Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload.
Journal of hepatology 2003;39(2):286-9.
2003: D Siret; G Bretaudeau; Bernard Branger; Alain Dabadie; M Dagorne; Véronique David; Marc de Braekeleer; Valérie Moisan-Petit; G Picherot; Gilles Rault; Véronique Storni; Michel Roussey
Comparing the clinical evolution of cystic fibrosis screened neonatally to that of cystic fibrosis diagnosed from clinical symptoms: a 10-year retrospective study in a French region (Brittany).
Pediatric pulmonology 2003;35(5):342-9.
2003: Céline Aguilella; Christèle Dubourg; Jocelyne Attia-Sobol; Jacqueline Vigneron; Martine Blayau; Laurent Pasquier; Leila Lazaro; Sylvie Odent; Véronique David
Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations.
Human genetics 2003;112(2):131-4.
2001: V Douabin-Gicquel; Nicolas Soriano; H Ferran; F Wojcik; E Palierne; S Tamim; T Jovelin; A T McKie; Jean-Yves Le Gall; Véronique David; Jean Mosser
Identification of 96 single nucleotide polymorphisms in eight genes involved in iron metabolism: efficiency of bioinformatic extraction compared with a systematic sequencing approach.
Human genetics 2001;109(4):393-401.
2001: L Dussaulx-Garin; Martine Blayau; Maël Pagenault; N Le Berre-Heresbach; Jean-Luc Raoul; Jean-Pierre Campion; Véronique David; Jean-François Bretagne
A new mutation of E-cadherin gene in familial gastric linitis plastica cancer with extra-digestive dissemination.
European journal of gastroenterology & hepatology 2001;13(6):711-5.
2001: Christelle Derrien; E Sonnet; Isabelle Gicquel; Jean-Yves Le Gall; Jean-Yves Poirier; Véronique David; Didier Maugendre
Non-hyperfunctioning nodules from multinodular goiters: a minor role in pathogenesis for somatic activating mutations in the TSH-receptor and Gsalpha subunit genes.
Journal of endocrinological investigation 2001;24(5):321-5.
2001: Lúcia Y Brown; Sylvie Odent; Véronique David; Martine Blayau; Christèle Dubourg; C Apacik; M A Delgado; B D Hall; J F Reynolds; A Sommer; D Wieczorek; Stephen A Brown; Maximilian Muenke
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination.
Human molecular genetics 2001;10(8):791-6.
2001: S Sachot; Romain Moirand; Anne-Marie Jouanolle; Jean Mosser; Patricia Fergelot; Yves Deugnier; Pierre Brissot; Jean-Yves Le Gall; Véronique David
Low penetrant hemochromatosis phenotype in eight families: no evidence of modifiers in the MHC region.
Blood cells, molecules & diseases 2001;27(2):518-29.
2000: P Jézéquel; Christèle Dubourg; Dominique Le Lannou; Sylvie Odent; Jean-Yves Le Gall; Martine Blayau; André LE TREUT; Véronique David
Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutations.
Molecular human reproduction 2000;6(12):1063-7.
2000: D Siret; Bernard Branger; Véronique Storni; G Bretaudeau; M Dagorne; Valérie Moisan-Petit; Véronique David; G Picherot; Gilles Rault; Michel Roussey
[Does neonatal screening of cystic fibrosis affect outcome? Comparative study of two cohorts in Britanny and Loire-Atlantique with follow-up after ten years].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2000;7(11):1154-62.
2000: Laurent Pasquier; Christèle Dubourg; Martine Blayau; Leila Lazaro; B Le Marec; Véronique David; Sylvie Odent
A new mutation in the six-domain of SIX3 gene causes holoprosencephaly.
European journal of human genetics : EJHG 2000;8(10):797-800.
2000: Virginie Scotet; Marc de Braekeleer; Michel Roussey; Gilles Rault; Philippe Parent; M Dagorne; Hubert Journel; A Lemoigne; JP Codet; M Catheline; Véronique David; André Chaventré; Ingrid Duguépéroux; C Verlingue; Isabelle Quéré; B Mercier; Marie-Pierre Audrézet; Claude Férec
Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis.
Lancet 2000;356(9232):789-94.
2000: Agnès Thénié; Magali Orhant; Isabelle Gicquel; Patricia Fergelot; Jean-Yves Le Gall; Véronique David; Jean Mosser
The HFE gene undergoes alternate splicing processes.
Blood cells, molecules & diseases 2000;26(2):155-62.
2000: Lucienne Guenet; Catherine Henry; Bertrand Toutain; Christèle Dubourg; Jean-Yves Le Gall; Véronique David; André LE TREUT
Eukaryotic translation termination factor gene (ETF1/eRF1) maps at D5S500 in a commonly deleted region of chromosome 5q31 in malignant myeloid diseases.
Cytogenetics and cell genetics 2000;88(1-2):82-6.
1999: Alison T Merryweather-Clarke; Jennifer J Pointon; JD Shearman; Kathryn J H Robson; Anne-Marie Jouanolle; Annick Mosser; Véronique David; J Y Le Gall; Halsall David; Terence S Elsey; A Kelly; Timothy M Cox; M Clare; Adrian Bomford; J L Vandwalle; Jacques Rochette; Nicolas Borot; Hélène Coppin; Marie-Paule Roth; E Ryan; John Crowe; Angela Totaro; Paolo Gasparini; Antonella Roetto; Ann P Walker
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium.
Nature genetics 1999;23(3):271.
1999: Véronique David; Anne-Marie Jouanolle; Patricia Fergelot; Pierre Brissot; Yves Deugnier; Jean-Yves Le Gall
[Molecular genetics of hemochromatosis].
Annales d'endocrinologie 1999;60(3):204-9.
1999: Sylvie Odent; T Atti-Bitach; Martine Blayau; M Mathieu; J Aug; A L Delezo de; J Y Gall; B Le Marec; A Munnich; Véronique David; M Vekemans
Expression of the Sonic hedgehog (SHH ) gene during early human development and phenotypic expression of new mutations causing holoprosencephaly.
Human molecular genetics 1999;8(9):1683-9.
1999: Lucienne Guenet; Bertrand Toutain; I Guilleret; B Chauvel; LL Deaven; Jonathan L Longmire; Jean-Yves Le Gall; Véronique David; André LE TREUT
Human release factor eRF1: structural organisation of the unique functional gene on chromosome 5 and of the three processed pseudogenes.
FEBS letters 1999;454(1-2):131-6.
1999: Christèle Dubourg; Sylvie Odent; Patricia Fergelot; Jean-Yves Le Gall; Véronique David; Martine Blayau
Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure. Mutations in brief no. 222. Online.
Human mutation 1999;13(2):173.
1998: Martine Blayau; Sylvie Odent; Christèle Dubourg; Véronique David
FRAXE: the HindIII/OXE20 restriction polymorphism is not a rare variant.
Human genetics 1998;103(5):626-7.
1998: Anne-Marie Jouanolle; G Gandon; Jean-Yves Le Gall; Véronique David
[Genetic hemochromatosis].
Annales de biologie clinique 1998;56 Spec No():31-5.
1998: Anne-Marie Jouanolle; Patricia Fergelot; M L Raoul; G Gandon; M Roussey; Yves Deugnier; J Feingold; Jean-Yves Le Gall; Véronique David
Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?
Annales de génétique 1998;41(4):195-8.
1997: Jean Mosser; N Andrieux; Patricia Fergelot; Isabelle Gicquel; V Lelaure; Francis Galibert; Véronique David
A 1200-kilobase transcription map encompassing the D6S105 locus at 6p21.3.
Genomics 1997;46(3):487-90.
1997: Anne-Marie Jouanolle; Patricia Fergelot; G Gandon; J Yaouanq; Jean-Yves Le Gall; Véronique David
A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.
Human genetics 1997;100(5-6):544-7.
1997: Paul C Adams; M L Campion; G Gandon; J Y LeGall; Véronique David; Anne-Marie Jouanolle
Clinical and family studies in genetic hemochromatosis: microsatellite and HFE studies in five atypical families.
Hepatology (Baltimore, Md.) 1997;26(4):986-90.
1997: Jean Mosser; Anne-Marie Jouanolle; G Gandon; N Andrieux; A Hampe; Véronique David
A YAC contig and an STS map spanning at least 3.9 megabasepairs telomeric to HLA-A.
Immunogenetics 1997;45(6):447-51.
1996: Anne-Marie Jouanolle; G Gandon; Pascal Jézéquel; Martine Blayau; M L Campion; Jacqueline Yaouanq; Jean Mosser; Patricia Fergelot; B Chauvel; P Bouric; G Carn; N Andrieux; I Gicquel; Jean-Yves Le Gall; Véronique David
Haemochromatosis and HLA-H.
Nature genetics 1996;14(3):251-2.
1996: Pascal Jézéquel; B Chauvel; André LE TREUT; Jean-Yves Le Gall; Véronique David; D Le Lannou; Martine Blayau
Identification of a novel mutation in CFTR gene exon 8 (L375F) in a CUAVD phenotype.
Human genetics 1996;97(4):548-9.
1996: L Pichon; G Carn; P Bouric; T Giffon; B Chauvel; M Lepourcelet; Jean Mosser; J Y Legall; Véronique David
Structural analysis of the HLA-A/HLA-F subregion: precise localization of two new multigene families closely associated with the HLA class I sequences.
Genomics 1996;32(2):236-44.
1996: T Giffon; M Lepourcelet; L Pichon; P Jezequel; P Bouric; G Carn; P Pontarotti; J Y Gall; Véronique David
Cloning of a human homologue of the mouse Tctex-5 gene within the MHC class I region.
Immunogenetics 1996;44(5):331-9.
1996: L Pichon; A Hampe; T Giffon; G Carn; J Y Legall; Véronique David
A new non-HLA multigene family associated with the PERB11 family within the MHC class I region.
Immunogenetics 1996;44(4):259-67.
1996: L Pichon; T Giffon; B Chauvel; G Carn; P Bouric; A El Kahloun; J Y Legall; Véronique David
Physical map of the HLA-A/HLA-F subregion and identification of two new coding sequences.
Immunogenetics 1996;43(4):175-81.
1996: G Gandon; Anne-Marie Jouanolle; B Chauvel; V Mauvieux; André LE TREUT; J Feingold; Jean-Yves Le Gall; Véronique David; Jacqueline Yaouanq
Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE).
Human genetics 1996;97(1):103-13.
1995: B Chauvel; I Dorval; Patricia Fergelot; L Pichon; T Giffon; I Gicquel; Jean-Yves Le Gall; Véronique David
A human homologue to the yeast omnipotent suppressor 45 maps 100 kb centromeric to HLA-A.
Immunogenetics 1995;41(6):380-2.
1994: G Gandon; V Lelaure; L Pichon; Anne-Marie Jouanolle; Jean-Yves Le Gall; Véronique David
Dinucleotide repeat polymorphism at the D6S510 locus.
Human molecular genetics 1994;3(7):1210.
1994: A el Kahloun; B Chauvel; V Mauvieux; I Dorval; Anne-Marie Jouanolle; I Gicquel; Jean-Yves Le Gall; Véronique David
Localization of seven new genes around the HLA-A locus.
Advances in experimental medicine and biology 1994;356():319-30.
1993: Jean-Yves Le Gall; Véronique David; Jacqueline Yaouanq; M Périchon; Martine Blayau; Anne-Marie Jouanolle; V Mauvieux; A el Kahloun; B Chauvel; I Dorval
[Molecular genetics of hemochromatosis].
Annales de gastroentérologie et d'hépatologie 1993;29(6):292-8; discussion 298-9.
1993: I Dorval; Sylvie Odent; P Jezequel; H Journel; B Chauvel; A Dabadie; M Roussey; Jean-Yves Le Gall; B Le Marec; Véronique David
Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20.
Human genetics 1993;91(3):254-6.
1993: Jean-Yves Le Gall; Véronique David; Jacqueline Yaouanq; M Périchon; Martine Blayau; Anne-Marie Jouanolle; V Mauvieux; A el Kahloun; B Chauvel; I Dorval
[Molecular genetics of hemochromatosis].
Bulletin de l'Académie nationale de médecine 1993;177(2):187-98; discussion 199-201.
1993: A el Kahloun; B Chauvel; V Mauvieux; I Dorval; Anne-Marie Jouanolle; I Gicquel; Jean-Yves Le Gall; Véronique David
Localization of seven new genes around the HLA-A locus.
Human molecular genetics 1993;2(1):55-60.
1992: Jacqueline Yaouanq; A el Kahloun; Michael J Chorney; Anne-Marie Jouanolle; V Mauvieux; M Perichon; Martine Blayau; Pierre Pontarotti; Jean-Yves Le Gall; Véronique David
Familial screening for genetic haemochromatosis by means of DNA markers.
Journal of medical genetics 1992;29(5):320-2.
1992: A el Kahloun; C Vernet; Anne-Marie Jouanolle; J Boretto; V Mauvieux; Jean-Yves Le Gall; Véronique David; Pierre Pontarotti
A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypes.
Immunogenetics 1992;35(3):183-9.
1991: V Mauvieux; Anne-Marie Jouanolle; A el Kahloun; Martine Blayau; Jean-Yves Le Gall; Véronique David
Dinucleotide repeat polymorphism at the FTHPI locus of chromosome 6.
Nucleic acids research 1991;19(24):6969.
1991: A el Kahloun; Anne-Marie Jouanolle; Michael J Chorney; V Mauvieux; I Gicquel; Pierre Pontarotti; Véronique David
A new polymorphic probe close to HLA-A.
Nucleic acids research 1991;19(18):5100.
1991: V Mauvieux; I Dugast; A el Kahloun; M Perichon; Anne-Marie Jouanolle; J Drysdale; Véronique David
A HindIII RFLP at the FTHP1 locus on chromosome 6.
Nucleic acids research 1991;19(13):3762.
1991: E Zappone; I Dugast; P Papadopoulos; K Theriault; Véronique David; J V LeGall; K Summers; L Powell; J Drysdale
Polymorphism in a ferritin H gene from chromosome 6p.
Human genetics 1991;86(6):557-61.
1990: Véronique David; J Boretto; Anne-Marie Jouanolle; V Mauvieux; A el Khaloun; M Périchon; Martine Blayau; Pierre Pontarotti
Two polymorphisms at the locus D698 defined by a YAC.
Nucleic acids research 1990;18(18):5582.
1990: Anne-Marie Jouanolle; Jacqueline Yaouanq; Martine Blayau; M Périchon; R Fauchet; M P Font; Jean-Yves Le Gall; Véronique David
HLA class I gene polymorphism in genetic hemochromatosis.
Human genetics 1990;85(3):279-82.
1989: Véronique David; P Papadopoulos; Jacqueline Yaouanq; Martine Blayau; L Abel; E Zappone; M Perichon; J Drysdale; Jean-Yves Le Gall; M Simon
Ferritin H gene polymorphism in idiopathic hemochromatosis.
Human genetics 1989;81(2):123-6.
1988: Y Deugnier; Véronique David; G Leray; Martine Blayau; Jean-Yves Le Gall
[Biological markers in hepatocellular carcinoma].
Annales de biologie clinique 1988;46(1):85-8.
1987: M Simon; L Le Mignon; R Fauchet; Jacqueline Yaouanq; Véronique David; Gilles Edan; M Bourel
A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA association.
American journal of human genetics 1987;41(2):89-105.
1986: Véronique David; P Paul; M Simon; Jean-Yves Le Gall; R Fauchet; I Gicquel; I Dugast; L Le Mignon; Jacqueline Yaouanq; D Cohen
DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family.
Human genetics 1986;74(2):113-20.
1983: Véronique David; R Fauchet; H Phengsavath; L Guenet; Jean-Yves Le Gall
Properdin factor B (Bf) polymorphism: subtyping of SS phenotypes.
Human genetics 1983;64(2):189-90.