Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Marie Claude Babron"'
Autor:
Charlotte Mouden, Marie de Tayrac, Christèle Dubourg, Sophie Rose, Wilfrid Carré, Houda Hamdi-Rozé, Marie-Claude Babron, Linda Akloul, Bénédicte Héron-Longe, Sylvie Odent, Valérie Dupé, Régis Giet, Véronique David
Publikováno v:
PLoS ONE, Vol 10, Iss 2, p e0117418 (2015)
Holoprosencephaly (HPE) is a frequent congenital malformation of the brain characterized by impaired forebrain cleavage and midline facial anomalies. Heterozygous mutations in 14 genes have been identified in HPE patients that account for only 30% of
Externí odkaz:
https://doaj.org/article/64dc7400317b48858eaf50a81f960129
Autor:
Marie-Claude Babron, Marie de Tayrac, Douglas N Rutledge, Eleftheria Zeggini, Emmanuelle Génin
Publikováno v:
PLoS ONE, Vol 7, Iss 10, p e46519 (2012)
Although variations in allele frequencies at common SNPs have been extensively studied in different populations, little is known about the stratification of rare variants and its impact on association tests. In this paper, we used Affymetrix 500K gen
Externí odkaz:
https://doaj.org/article/37cd504924654e29ba6f17e8cc339db0
Autor:
Marie-Hélène Dizier, Patricia Margaritte-Jeannin, Miriam F. Moffatt, Jocelyne Just, Catherine Laprise, Valérie Gagné-Ouellet, Myriam Brossard, William O.C.M. Cookson, N. Lavielle, Emmanuelle Bouzigon, Marie-Claude Babron, Florence Demenais, Adrien Etcheto, Mark Lathrop, Chloé Sarnowski
Publikováno v:
Clinical & Experimental Allergy. 48:297-305
Background Genetic studies of eczema have identified many genes, which explain only 14% of the heritability. Missing heritability may be partly due to ignored gene-gene (G-G) interactions. Objective Our aim was to detect new interacting genes involve
Autor:
Marie-Claude Babron, Emmanuelle Bouzigon, Patricia Margaritte-Jeannin, Myriam Brossard, Florence Demenais, Mark Lathrop, Rachel Nadif, Nolwenn Lavielle, Jocelyne Just, Chloé Sarnowski, Marie-Hélène Dizier, Lucile Pain, Catherine Laprise, Hamida Mohamdi
Publikováno v:
Thorax
Thorax, BMJ Publishing Group, 2019, 74 (3), pp.254-260. ⟨10.1136/thoraxjnl-2018-211797⟩
Thorax, BMJ Publishing Group, 2019, 74 (3), pp.254-260. ⟨10.1136/thoraxjnl-2018-211797⟩
BackgroundA positional cloning study of bronchial hyper-responsiveness (BHR) at the 17p11 locus in the French Epidemiological study on the Genetics and Environment of Asthma (EGEA) families showed significant interaction between early-life environmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::558655f209c11794d660bd78072f169e
https://www.hal.inserm.fr/inserm-02939798
https://www.hal.inserm.fr/inserm-02939798
Autor:
Massimiliano Copetti, Farid Boumediene, Marie Claude Babron, Philippe Couratier, Giancarlo Logroscino, Ettore Beghi, Anne-Louise Leutenegger, Benoît Marin, Pierre-Marie Preux
Publikováno v:
International Journal of Epidemiology
International Journal of Epidemiology, Oxford University Press (OUP), 2016
International Journal of Epidemiology, 2016
International Journal of Epidemiology, Oxford University Press (OUP), 2016
International Journal of Epidemiology, 2016
Background To assess the worldwide variation of amyotrophic lateral sclerosis (ALS) incidence, we performed a systematic review and meta-analysis of population-based data published to date. Methods We reviewed Medline and Embase up to June 2015 and i
Autor:
Teresa Nutile, Anthony F. Herzig, Céline Bellenguez, Anne-Louise Leutenegger, Marie Claude Babron, Marina Ciullo
Publikováno v:
Genetic Epidemiology
Genetic Epidemiology, 2017, Epub ahead of print. ⟨10.1002/gepi.22109⟩
Genetic Epidemiology, Wiley, 2017, Epub ahead of print. ⟨10.1002/gepi.22109⟩
Genetic epidemiology
42 (2018): 201–213. doi:10.1002/gepi.22109
info:cnr-pdr/source/autori:Herzig, Anthony Francis; Nutile, Teresa; Babron, Marie-Claude; Ciullo, Marina; Bellenguez, Celine; Leutenegger, Anne-Louise et al./titolo:Strategies for phasing and imputation in a population isolate/doi:10.1002%2Fgepi.22109/rivista:Genetic epidemiology (Print)/anno:2018/pagina_da:201/pagina_a:213/intervallo_pagine:201–213/volume:42
Genetic Epidemiology, 2017, Epub ahead of print. ⟨10.1002/gepi.22109⟩
Genetic Epidemiology, Wiley, 2017, Epub ahead of print. ⟨10.1002/gepi.22109⟩
Genetic epidemiology
42 (2018): 201–213. doi:10.1002/gepi.22109
info:cnr-pdr/source/autori:Herzig, Anthony Francis; Nutile, Teresa; Babron, Marie-Claude; Ciullo, Marina; Bellenguez, Celine; Leutenegger, Anne-Louise et al./titolo:Strategies for phasing and imputation in a population isolate/doi:10.1002%2Fgepi.22109/rivista:Genetic epidemiology (Print)/anno:2018/pagina_da:201/pagina_a:213/intervallo_pagine:201–213/volume:42
International audience; In the search for genetic associations with complex traits, population isolates offer the advantage of reduced genetic and environmental heterogeneity. In addition, cost-efficient next-generation association approaches have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::069f1688bc461a7e20bd1a7fd4db4db5
https://www.hal.inserm.fr/inserm-01645064/document
https://www.hal.inserm.fr/inserm-01645064/document
Publikováno v:
Annals of Human Genetics. 79:380-384
Summary A major problem in gene–gene interaction studies in large marker panels is how to correct for multiple testing while accounting for the dependence between marker pairs due to the presence of linkage disequilibrium. The “gold standard” a
Autor:
Alain Sarasin, Endre Anderssen, Valerie Gaborieau, Simone Benhamou, Andres Metspalu, Maiken Bratt Elvestad, John R. McLaughlin, Mark Lathrop, Hans E. Krokan, Marie-Claude Babron, Kristjan Välk, Tõnu Vooder, Rayjean J. Hung, Rémi Kazma, Emmanuelle Génin, John K. Field, Frank Skorpen, Paul Brennan
Publikováno v:
Carcinogenesis. 33:1059-1064
Lung cancer (LC) is the leading cause of cancer-related death worldwide and tobacco smoking is the major associated risk factor. DNA repair is an important process, maintaining genome integrity and polymorphisms in DNA repair genes may contribute to
Autor:
Emmanuelle Génin, Marie-Claude Babron, Steven Gazal, Anne-Louise Leutenegger, Hervé Perdry, Mourad Sahbatou
Publikováno v:
Human Heredity. 74:142-152
To detect fully penetrant rare recessive variants that could constitute Mendelian subentities of complex diseases, we propose a novel strategy, the HBD-GWAS strategy, which can be applied to genome-wide association study (GWAS) data. This strategy fi
Autor:
Lisheng Zhou, Eleftheria Zeggini, Wonkuk Kim, Loubna Jouan, Julie Gauthier, E.E. Marchani, Derek Gordon, Anne-Louise Leutenegger, Ryan D. Hernandez, Ioanna Tachmazidou, I.B. Stanaway, Emmanuelle Génin, Marie-Claude Babron, Jinchuan Xing, Melanie Quintana, Steven Gazal, C.Y.K. Cheung, Alejandro Q. Nato, E.M. Wijsman, Stephen J. Finch, Li Li, Niall Cardin, Druck Reinhardt Druck Basel, Mourad Sahbatou, Anthony M. Musolf, John S. Witte, Deborah A. Nickerson, Dara G. Torgerson, Jennifer L. Asimit, Guy A. Rouleau, Duncan Thomas, H.H. Coon, R. Bernier, M. Cyrus Maher, Françoise Clerget-Darpoux, Lawrence H. Uricchio, N.H. Chapman, Tara C. Matise, Z. Brkanac, Bertram Müller-Myhsok, Fredrick R. Schumacher, Patrick A. Dion, Douglas Londono, Rémi Kazma, K. Ankenman, Satz Mengensatzproduktion, Hervé Perdry, David V. Conti, Jonine L. Bernstein, Graham Casey, Andrew P. Morris
Publikováno v:
Human Heredity. 74:I-IV