Výsledky vyhledávání - Françoise Clerget‐Darpoux

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  1. 1
    Identifying modifier genes of monogenic disease: strategies and difficulties

    Identifying modifier genes of monogenic disease: strategies and difficulties Autor Emmanuelle Génin, Josué Feingold, Françoise Clerget‐Darpoux

    Vydáno 2008
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  2. 2
    Estimation of the Inbreeding Coefficient through Use of Genomic Data

    Estimation of the Inbreeding Coefficient through Use of Genomic Data Autor Anne‐Louise Leutenegger, Bernard Prum, Emmanuelle Génin, Christophe Verny, Arnaud Lemainque, Françoise Clerget‐Darpoux, E. A. Thompson

    Vydáno 2003
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    Artigo
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  3. 3
    New disease gene location and high genetic heterogeneity in idiopathic scoliosis

    New disease gene location and high genetic heterogeneity in idiopathic scoliosis Autor Patrick Edery, Patricia Margaritte‐Jeannin, Bernard Biot, Audrey Labalme, Jean‐Claude Bernard, Joëlle Chastang, Behrouz Kassaï, Marie-Helene Plais, Florina Moldovan, Françoise Clerget‐Darpoux

    Vydáno 2011
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  4. 4
    Meta and pooled analysis of European coeliac disease data

    Meta and pooled analysis of European coeliac disease data Autor Marie‐Claude Babron, Staffan Nilsson, Svetlana Adamovic, Åsa Torinsson Naluai, Jan Wahlström, Henry Ascher, Paul J. Ciclitira, Ludvig M. Sollid, Jukka Partanen, Luigi Greco, Françoise Clerget‐Darpoux

    Vydáno 2003
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  5. 5
    HLA related genetic risk for coeliac disease

    HLA related genetic risk for coeliac disease Autor Mathieu Bourgey, Giuseppe Calcagno, Nadia Tinto, D. Gennarelli, Patricia Margaritte‐Jeannin, Laura Greco, M.G. Limongelli, O. Esposito, C Marano, R Troncone, A. Spampanato, Françoise Clerget‐Darpoux, Lucia Sacchetti

    Vydáno 2007
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  6. 6
    A Gene for Meckel Syndrome Maps to Chromosome 11q13

    A Gene for Meckel Syndrome Maps to Chromosome 11q13 Autor J. Roume, Emmanuelle Génin, Valérie Cormier‐Daire, Hongqi Ma, Blandine Mehaye, Tania Attié‐Bitach, F. Razavi-Encha, Catherine Fallet‐Bianco, Annie Buénerd, Françoise Clerget‐Darpoux, Arnold Münnich, M. Le Merrer

    Vydáno 1998
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  7. 7
    Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis

    Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis Autor Patrice Verpillat, Agnès Camuzat, Didier Hannequin, Catherine Thomas-Antérion, Michèle Puel, Serge Belliard, Bruno Dubois, Mira Didic, Lucette Lacomblez, Olivier Moreaud, Véronique Golfier, Dominique Campion, Alexis Brice, Françoise Clerget‐Darpoux

    Vydáno 2002
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  8. 8
    Validation of the reshaped shared epitope HLA-DRB1 classification in rheumatoid arthritis.

    Validation of the reshaped shared epitope HLA-DRB1 classification in rheumatoid arthritis. Autor Laëtitia Michou, Pascal Croiseau, Élisabeth Petit, Sophie Tézenas du Montcel, Isabelle Lemaire, Céline Pierlot, José Osorio, Wafa Frigui, Sandra Lasbleiz, Patrick Quillet, Thomas Bardin, Bernard Prum, Françoise Clerget‐Darpoux, François Cornélis

    Vydáno 2006
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  9. 9
    Association Between the Extended tau Haplotype and Frontotemporal Dementia

    Association Between the Extended tau Haplotype and Frontotemporal Dementia Autor Patrice Verpillat, Agnès Camuzat, Didier Hannequin, Catherine Thomas-Antérion, Michèle Puel, Serge Belliard, Bruno Dubois, Mira Didic, Bernard‐François Michel, Lucette Lacomblez, Olivier Moreaud, François Sellal, Véronique Golfier, Dominique Campion, Françoise Clerget‐Darpoux, Alexis Brice

    Vydáno 2002
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  10. 10
    Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

    Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum Autor Dominique Campion, Cécile Dumanchin, Didier Hannequin, Bruno Dubois, Serge Belliard, Michèle Puel, Catherine Thomas-Antérion, Agnès Michon, Cosette Martin, Françoise Charbonnier, Grégory Raux, Agnès Camuzat, Christiane Penet, Valérie Mesnage, María Martínez, Françoise Clerget‐Darpoux, Alexis Brice, Thierry Frébourg

    Vydáno 1999
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  11. 11
    Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma

    Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma Autor Anne‐Sophie Jannot, Roubila Meziani, Guylène Bertrand, Bénédicte Gérard, V. Descamps, A. Archimbaud, Catherine Picard, L. Ollivaud, Nicole Basset‐Séguin, Delphine Kérob, Guy Lanternier, Célèste Lebbé, Philippe Saïag, B. Crickx, Françoise Clerget‐Darpoux, Bernard Grandchamp, Nadem Soufir, Melan-Cohort

    Vydáno 2005
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  12. 12
    Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families

    Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families Autor L. Greco, Marie‐Claude Babron, Gino Roberto Corazza, Selvaggia Percopo, R.E.P. Sica, F. Clot, M. C. FULCHIGNONI‐LATAUD, Patrizia Zavattari, Patricia Momigliano‐Richiardi, Giorgio Casari, Paolo Gasparini, Roberto Tosi, Vilma Mantovani, S. De Virgiliis, Giuseppe Iacono, Anna D’Alfonso, Hana Selinger‐Leneman, Arnaud Lemainque, J. L. Serre, Françoise Clerget‐Darpoux

    Vydáno 2001
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  13. 13
    Functional variants of POC5 identified in patients with idiopathic scoliosis

    Functional variants of POC5 identified in patients with idiopathic scoliosis Autor Scott B. Patten, Patricia Margaritte‐Jeannin, Jean‐Claude Bernard, Eudéline Alix, Audrey Labalme, Alicia Besson, Simon Girard, Khaled Fendri, Nicolas Fraisse, Bernard Biot, C. Poizat, Amandine Campan-Fournier, Kariman Abelin-Genevois, V. Cunin, Charlotte Zaouter, Meijiang Liao, Raphaelle Lamy, Gaëtan Lesca, Rita Menassa, Charles Marcaillou, Mélanie Letexier, Damien Sanlaville, J. Bérard, Guy A. Rouleau, Françoise Clerget‐Darpoux, Pierre Drapeau, Florina Moldovan, Patrick Edery

    Vydáno 2015
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  14. 14
    Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome

    Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome Autor Caroline Alby, Kevin Piquand, Céline Huber, André Mégarbané, Amale Ichkou, Marine Legendre, Fanny Pelluard, Ferechté Encha-Ravazi, Georges Abi Tayeh, Bettina Bessières, Salima El Chehadeh-Djebbar, Nicole Laurent, Laurence Faivre, László Sztriha, Melinda Zombor, Hajnalka Szabó, Marion Failler, Meriem Garfa-Traoré, Christine Bole, Patrick Nitschké, Mathilde Nizon, Nadia Elkhartoufi, Françoise Clerget‐Darpoux, Arnold Münnich, Stanislas Lyonnet, Michel Vekemans, Sophie Saunier, Valérie Cormier‐Daire, Tania Attié‐Bitach, Sophie Thomas

    Vydáno 2015
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  15. 15
    Genome Search in Celiac Disease

    Genome Search in Celiac Disease Autor Luigi Greco, Gino Roberto Corazza, Marie‐Claude Babron, Fabienne Clot, Marie-Claude Fulchignoni-Lataud, Selvaggia Percopo, Patrizia Zavattari, F. Bouguerra, Colette Dib, Roberto Tosi, Riccardo Bonfanti, Alessandro Ventura, Wilma Mantavoni, Giuseppe Magazzù, Rosanna Gatti, R Lazzari, Annamaria Giunta, Francesco Perri, Giuseppe Iacono, E Cardi, S. De Virgiliis, F Cataldo, Gianluigi De Angelis, S Musumeci, Roberto Ferrari, Fiorella Balli, Maria Teresa Bardella, Umberto Volta, Carlo Catassi, Giuliano Torre, Jean François Eliaou, Jean Louis Serre, Françoise Clerget‐Darpoux

    Vydáno 1998
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  16. 16
    Refining genetic associations in multiple sclerosis

    Refining genetic associations in multiple sclerosis Autor David R. Booth, Robert Heard, Graeme J. Stewart, An Goris, Rita Dobosi, Bénédicte Dubois, Annette Oturai, Helle Bach Søndergaard, Finn Sellebjerg, Janna Saarela, Virpi Leppä, Aarno Palotie, L. Peltonen, B. Fontaine, Isabelle Cournu‐Rebeix, Françoise Clerget‐Darpoux, Marie‐Claude Babron, Frank Weber, Herta Flor, Bertram Müller‐Myhsok, Peter Rieckmann, Antje Kroner, Colin A. Graham, Koen Vandenbroeck, Stanley Hawkins, Sandra D’Alfonso, Laura Bergamaschi, Paola Naldi, Franca Rosa Guerini, Marco Salvetti, Daniela Galimberti, Rogier Q. Hintzen, Cornelia M. van Duijn, Åslaug Rudjord Lorentzen, Elisabeth Gulowsen Celius, Hanne F. Harbo, Anne Spurkland, Francesco Cucca, Maria Giovanna Marrosu, Manuel Comabella, Xavier Montalbán, Pablo Villoslada, Tomas Olsson, Ingrid Kockum, Jan Hillert, Maria Ban, Andrew Walton, S. Sawcer, Alastair Compston, Clive Hawkins, Tania Mihalova, Neil P. Robertson, Gillian Ingram, Philip L. De Jager, David A. Hafler, John D. Rioux, Mark J. Daly, Lisa F. Barcellos, Adrian J. Ivinson, Margaret A. Pericak‐Vance, J. Hoksenberg, Stephen L. Hauser, Jacob L. McCauley, David Sexton, Jonathan L. Haines

    Vydáno 2008
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  17. 17
    Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

    Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis Autor Stephen Sawcer, Garrett Hellenthal, Matti Pirinen, Chris C. A. Spencer, Nikolaos A. Patsopoulos, Loukas Moutsianas, Alexander Dilthey, Zhan Su, Colin Freeman, Sarah Hunt, Sarah Edkins, Emma Gray, David R. Booth, Simon Potter, An Goris, Gavin Band, Annette Oturai, Amy Strange, Janna Saarela, Céline Bellenguez, Bertrand Fontaine, Matthew Gillman, Bernhard Hemmer, Rhian Gwilliam, Frauke Zipp, Alagurevathi Jayakumar, Roland Martinꝉ, Stephen Leslie, Stanley Hawkins, Eleni Giannoulatou, Sandra D’Alfonso, Hannah Blackburn, Filippo Martinelli Boneschi, Jennifer Liddle, Hanne F. Harbo, M. L. Perez, Anne Spurkland, Matthew Waller, Marcin P. Mycko, Michelle Ricketts, Manuel Comabella, Naomi Hammond, Ingrid Kockum, Owen T McCann, Maria Ban, Pamela Whittaker, Anu Kemppinen, Paul A. Weston, Clive Hawkins, Sara Widaa, John Zajicek, Serge Dronov, Neil P. Robertson, Suzannah J. Bumpstead, Lisa F. Barcellos, Rathi Ravindrarajah, Roby Abraham, Lars Alfredsson, Kristin Ardlie, Cristin Aubin, Amie Baker, K. Baker, Sergio E. Baranzini, Laura Bergamaschi, Roberto Bergamaschi, Allan Bernstein, Achim Berthele, Mike Boggild, Jonathan P. Bradfield, David Brassat, Simon Broadley, Dorothea Buck, Helmut Butzkueven, Ruggero Capra, William M. Carroll, Paola Cavalla, Elisabeth Gulowsen Celius, Sabine Cepok, Rosetta Chiavacci, Françoise Clerget‐Darpoux, Katleen Clysters, Gıancarlo Comı, M. Cossburn, Isabelle Cournu‐Rebeix, Mathew Cox, Wendy Cozen, Bruce Cree, Anne H. Cross, Daniele Cusi, Mark J. Daly, Emma Davis, Paul I. W. de Bakker, Marc Debouverie, Marie D’hooghe, Katherine Dixon, Rita Dobosi, Bénédicte Dubois, David Ellinghaus, Irina Elovaara, Federica Esposito

    Vydáno 2011
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