المؤلفون: Dizier, Marie-Hélène, Margaritte-Jeannin, Patricia, Pain, Lucile, Sarnowski, Chloé, Brossard, Myriam, Mohamdi, Hamida, Lavielle, Nolwenn, Babron, Marie-Claude, Just, Jocelyne, Lathrop, Mark, Laprise, Catherine, Bouzigon, Emmanuelle, Demenais, Florence, Nadif, Rachel

المساهمون: Variabilité Génétique et Maladies Humaines (U946), Institut Universitaire d'Hématologie (IUH), Université Paris Diderot - Paris 7 (UPD7)-Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM), Université Paris Diderot - Paris 7 (UPD7), Département des Sciences Fondamentales Chicoutimi (DSF), Université du Québec à Chicoutimi (UQAC), CHU Trousseau APHP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Department of Human Genetics Montréal, McGill University = Université McGill Montréal, Canada, Vieillissement et Maladies chroniques : approches épidémiologique et de santé publique (VIMA), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut National de la Santé et de la Recherche Médicale (INSERM)

المصدر: ISSN: 0040-6376 ; Thorax ; https://inserm.hal.science/inserm-02939798Test ; Thorax, 2019, 74 (3), pp.254-260. ⟨10.1136/thoraxjnl-2018-211797⟩.

مصطلحات موضوعية: ATP, BHR, ETS, FBAT, GxE interaction, asthma, [SDV]Life Sciences [q-bio], [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30282721; inserm-02939798; https://inserm.hal.science/inserm-02939798Test; https://inserm.hal.science/inserm-02939798/documentTest; https://inserm.hal.science/inserm-02939798/file/thoraxjnl-20186211797-maintext-unmarked-final.pdfTest; PUBMED: 30282721

الإتاحة: https://doi.org/10.1136/thoraxjnl-2018-211797Test
https://inserm.hal.science/inserm-02939798Test
https://inserm.hal.science/inserm-02939798/documentTest
https://inserm.hal.science/inserm-02939798/file/thoraxjnl-20186211797-maintext-unmarked-final.pdfTest

المؤلفون: Marin, Benoît, Logroscino, Giancarlo, Boumédiene, Farid, Labrunie, Anaïs, Couratier, Philippe, Babron, Marie-Claude, Leutenegger, Anne Louise, Preux, Pierre Marie, Beghi, Ettore

المصدر: European Journal of Epidemiology, 2016 Jan 01. 31(3), 229-245.

الوصول الحر: https://www.jstor.org/stable/44851757Test

المؤلفون: Marin, Benoît, Boumé diene, Farid, Logroscino, Giancarlo, Couratier, Philippe, Babron, Marie-Claude, Leutenegger, Anne Louise, Copetti, Massimilano, Preux, Pierre-Marie, Beghi, Ettore

المساهمون: Marin, Benoît, Boumé diene, Farid, Logroscino, Giancarlo, Couratier, Philippe, Babron, Marie-Claude, Leutenegger, Anne Louise, Copetti, Massimilano, Preux, Pierre-Marie, Beghi, Ettore

مصطلحات موضوعية: Amyotrophic lateral sclerosi, Epidemiology, Ethnic group, Incidence

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27185810; volume:46; issue:1; firstpage:57; lastpage:74; numberofpages:18; journal:INTERNATIONAL JOURNAL OF EPIDEMIOLOGY; http://hdl.handle.net/11586/214283Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85019750088; http://ije.oxfordjournals.orgTest/

الإتاحة: https://doi.org/10.1093/ije/dyw061Test
http://hdl.handle.net/11586/214283Test
http://ije.oxfordjournals.orgTest/

المؤلفون: Dizier, Marie-Hélène, Margaritte-Jeannin, Patricia, Pain, Lucile, Sarnowski, Chloé, Brossard, Myriam, Mohamdi, Hamida, Lavielle, Nolwenn, Babron, Marie-Claude C, Just, Jocelyne, Lathrop, Mark, Laprise, Catherine, Bouzigon, Emmanuelle, Demenais, Florence, Nadif, Rachel

المساهمون: Canada Research Chairs on genetic determinants of asthma, Fondation pour la Recherche Médicale, European Commission, Ministère de l’Education Nationale, de l’Enseignement Superieur et de la Recherche, Agence Nationale de la Recherche, Région Ile de France

المصدر: Thorax ; volume 74, issue 3, page 254-260 ; ISSN 0040-6376 1468-3296

الإتاحة: https://doi.org/10.1136/thoraxjnl-2018-211797Test

المؤلفون: Herzig, Anthony, Francis, Nutile, Teresa, Babron, Marie-Claude, Ciullo, Marina, Bellenguez, Céline, Leutenegger, Anne-Louise

المساهمون: Variabilité Génétique et Maladies Humaines (U946), Institut Universitaire d'Hématologie (IUH), Université Paris Diderot - Paris 7 (UPD7)-Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM), Université Sorbonne Paris Cité (USPC), Institute of Genetics and Biophysics "A. Buzzati Traverso" Naples, Italy, National Research Council of Italy, Istituto Neurologico Mediterraneo (NEUROMED I.R.C.C.S.), Università degli Studi di Roma "La Sapienza" = Sapienza University Rome (UNIROMA)-University of Naples Federico II = Università degli studi di Napoli Federico II, Facteurs de Risque et Déterminants Moléculaires des Maladies liées au Vieillissement - U 1167 (RID-AGE), Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille), Excellence Laboratory LabEx DISTALZ, ESGI—The research leading to these results has received funding from the Seventh Framework Programme FP7/2007‐2013 under grant agreement no. 262055. A.F.H. was funded by an international Ph.D. fellowship from Sorbonne Paris Cité (convention HERZI15RDXMTSPC1LIETUE)., We address special thanks to the people of Campora for their participation in the study. We kindly thank the European Genome‐phenome Archive at the European Bioinformatics Institute for making available the UK10K imputation panel (EGAD00001000776) and HRC imputation panel (EGAD00001002729) for the use in our simulation study. We also thank the two anonymous reviewers for their comments that greatly improved the manuscript., European Project: 262055,EC:FP7:INFRA,FP7-INFRASTRUCTURES-2010-1,ESGI(2011)

المصدر: ISSN: 0741-0395.

مصطلحات موضوعية: genotyping errors, linkage disequilibrium, identity by descent, founder effect, study specific panel, MESH: Algorithms, MESH: Chromosomes, Human, Pair 10/genetics, MESH: Male, MESH: Models, Genetic, MESH: Pedigree, MESH: Phenotype, MESH: Research Design, MESH: Software, MESH: Female, MESH: Founder Effect, MESH: Genetics, Population, MESH: Genome, Human/genetics, MESH: Haplotypes/genetics, MESH: Humans, MESH: Italy, MESH: Linkage Disequilibrium/genetics, [SDV.GEN]Life Sciences [q-bio]/Genetics

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/29319195; info:eu-repo/grantAgreement/EC/FP7/262055/EU/European Sequencing and Genotyping Infrastructure/ESGI; inserm-01645064; https://inserm.hal.science/inserm-01645064Test; https://inserm.hal.science/inserm-01645064/documentTest; https://inserm.hal.science/inserm-01645064/file/HERZIG_Article_HAL_INSERM.pdfTest; PUBMED: 29319195

الإتاحة: https://doi.org/10.1002/gepi.22109Test
https://inserm.hal.science/inserm-01645064Test
https://inserm.hal.science/inserm-01645064/documentTest
https://inserm.hal.science/inserm-01645064/file/HERZIG_Article_HAL_INSERM.pdfTest

المؤلفون: Génin, Emmanuelle, Sahbatou, Mourad, Gazal, Steven, Babron, Marie-Claude, Perdry, Hervé, Leutenegger, Anne-Louise

المصدر: Human Heredity, 2012 Jan 01. 74(3/4), 142-152.

الوصول الحر: https://www.jstor.org/stable/48513925Test

المؤلفون: Marin, Benoît, Boumédiene, Farid, Logroscino, Giancarlo, Couratier, Philippe, Babron, Marie-Claude, Leutenegger, Anne Louise, Copetti, Massimilano, Preux, Pierre-Marie, Beghi, Ettore

المصدر: International Journal of Epidemiology ; page dyw061 ; ISSN 0300-5771 1464-3685

مصطلحات موضوعية: General Medicine, Epidemiology

الإتاحة: https://doi.org/10.1093/ije/dyw061Test
http://academic.oup.com/ije/article-pdf/46/1/57/13733106/dyw061.pdfTest

المؤلفون: Forabosco, Paola, Neuhausen, Susan L., Greco, Luigi, Naluai, Åsa Torinsson, Wijmenga, Cisca, Saavalainen, Päivi, Houlston, Richard S., Ciclitira, Paul J., Babron, Marie-Claude, Lewis, Cathryn M.

المصدر: Human Heredity, 2009 Jan 01. 68(4), 223-230.

الوصول الحر: https://www.jstor.org/stable/48513161Test

المؤلفون: Gazal, Steven, Gosset, Simon, Verdura, Edgard, Bergametti, Françoise, Guey, Stéphanie, Babron, Marie-Claude, Tournier-Lasserve, Elisabeth

المصدر: European Journal of Human Genetics ; volume 24, issue 4, page 581-586 ; ISSN 1018-4813 1476-5438

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1038/ejhg.2015.143Test
http://www.nature.com/articles/ejhg2015143.pdfTest
http://www.nature.com/articles/ejhg2015143Test

المؤلفون: Gazal, Steven, Sahbatou, Mourad, Babron, Marie-Claude, Génin, Emmanuelle, Leutenegger, Anne-Louise

المصدر: Scientific Reports ; volume 5, issue 1 ; ISSN 2045-2322

مصطلحات موضوعية: Multidisciplinary

الإتاحة: https://doi.org/10.1038/srep17453Test
https://www.nature.com/articles/srep17453Test
https://www.nature.com/articles/srep17453.pdfTest