Publications by authors named "Marie-Claude Babron"

33Publications

Strategies for phasing and imputation in a population isolate.

Genet Epidemiol 2018 03 10;42(2):201-213. Epub 2018 Jan 10.

Université Paris-Diderot, Sorbonne Paris Cité, U946, Paris, France.

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http://doi.wiley.com/10.1002/gepi.22109
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http://dx.doi.org/10.1002/gepi.22109DOI Listing
March 2018

High level of inbreeding in final phase of 1000 Genomes Project.

Sci Rep 2015 Dec 2;5:17453. Epub 2015 Dec 2.

INSERM, Genetic variability and human diseases, UMR 946, F-75010 Paris, France.

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http://dx.doi.org/10.1038/srep17453DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667178PMC
December 2015

Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin.

Eur J Epidemiol 2016 Mar 12;31(3):229-45. Epub 2015 Oct 12.

Laboratorio di Malattie Neurologiche, Dipartimento di Neuroscienze, IRCCS Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.

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http://dx.doi.org/10.1007/s10654-015-0090-xDOI Listing
March 2016

A New Correction for Multiple Testing in Gene-Gene Interaction Studies.

Ann Hum Genet 2015 Sep 23;79(5):380-384. Epub 2015 Apr 23.

Inserm, UMR946, Genetic variation and Human diseases, F-75010, Paris, France.

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http://dx.doi.org/10.1111/ahg.12113DOI Listing
September 2015

Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings.

PLoS One 2015 6;10(2):e0117418. Epub 2015 Feb 6.

Institut de Génétique et Développement de Rennes, Equipe Génétique des Pathologies Liées au Développement, Faculté de Médecine, Université de Rennes 1, 35043 Rennes, France; Laboratoire de Génétique Moléculaire et Génomique, CHU Pontchaillou, 35033 Rennes, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0117418PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4319975PMC
February 2016

Genetic variants in DNA repair pathways and risk of upper aerodigestive tract cancers: combined analysis of data from two genome-wide association studies in European populations.

Carcinogenesis 2014 Jul 21;35(7):1523-7. Epub 2014 Mar 21.

Inserm, U946, Genetic Variation and Human, Diseases and Université Paris-Diderot, Sorbonne Paris-Cité, UMRS-946, Paris, F-75010, France, Gustave Roussy, Villejuif, F-94805, France

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https://academic.oup.com/carcin/article-lookup/doi/10.1093/c
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http://dx.doi.org/10.1093/carcin/bgu075DOI Listing
July 2014

FSuite: exploiting inbreeding in dense SNP chip and exome data.

Bioinformatics 2014 Jul 14;30(13):1940-1. Epub 2014 Mar 14.

Inserm, U946, Genetic variability and human diseases, Paris, 75010, Université Paris Sud, Kremlin-Bicêtre, 94270, Fondation Jean Dausset CEPH, Paris, 75010, Université Paris-Diderot, UMR 946, Institut Universitaire d'Hématologie, Paris, 75475, Inserm, U1078, Génétique, Génomique fonctionnelle et Biotechnologies, Brest, 29218 and Centre Hospitalier Régional Universitaire de Brest, Brest, 29200, France Inserm, U946, Genetic variability and human diseases, Paris, 75010, Université Paris Sud, Kremlin-Bicêtre, 94270, Fondation Jean Dausset CEPH, Paris, 75010, Université Paris-Diderot, UMR 946, Institut Universitaire d'Hématologie, Paris, 75475, Inserm, U1078, Génétique, Génomique fonctionnelle et Biotechnologies, Brest, 29218 and Centre Hospitalier Régional Universitaire de Brest, Brest, 29200, France.

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http://dx.doi.org/10.1093/bioinformatics/btu149DOI Listing
July 2014

Comparative power of family-based association strategies to detect disease-causing variants under two-locus models.

Genet Epidemiol 2012 Dec 9;36(8):848-55. Epub 2012 Aug 9.

INSERM, UMR-S946, Fondation Jean Dausset-CEPH, Paris, France; Univ Paris-Diderot, PRES Sorbonne Paris Cité, Institut Universitaire d'Hématologie, UMR-S946, Paris, France.

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http://doi.wiley.com/10.1002/gepi.21672
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http://dx.doi.org/10.1002/gepi.21672DOI Listing
December 2012

Could inbred cases identified in GWAS data succeed in detecting rare recessive variants where affected sib-pairs have failed?

Hum Hered 2012 11;74(3-4):142-52. Epub 2013 Apr 11.

Inserm UMR-946, Genetic Variability and Human Diseases, Paris, France.

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http://dx.doi.org/10.1159/000346790DOI Listing
October 2013

Genetic association and gene-environment interaction: a new method for overcoming the lack of exposure information in controls.

Am J Epidemiol 2011 Jan 17;173(2):225-35. Epub 2010 Nov 17.

Université Paris-Sud, Le Kremlin Bicêtre, France.

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http://dx.doi.org/10.1093/aje/kwq352DOI Listing
January 2011

The ordered transmission disequilibrium test: detection of modifier genes.

Genet Epidemiol 2009 Jan;33(1):1-5

INSERM U535, BP 1000, F-94817 Villejuif, France.

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http://dx.doi.org/10.1002/gepi.20348DOI Listing
January 2009

An ordered subset approach to including covariates in the transmission disequilibrium test.

BMC Proc 2007 18;1 Suppl 1:S77. Epub 2007 Dec 18.

Center for Craniofacial and Dental Genetics, Cellomics Suite 500, 100 Technology Drive, University of Pittsburgh School of Dental Medicine, Pittsburgh, Pennsylvania 15219, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367525PMC
http://dx.doi.org/10.1186/1753-6561-1-s1-s77DOI Listing
December 2009

On the choice of linkage statistics.

BMC Proc 2007 18;1 Suppl 1:S102. Epub 2007 Dec 18.

INSERM U535, F-94817 Villejuif, France.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367543PMC
http://dx.doi.org/10.1186/1753-6561-1-s1-s102DOI Listing
December 2009

Detection of susceptibility loci by genome-wide linkage analysis.

BMC Genet 2005 Dec 30;6 Suppl 1:S18. Epub 2005 Dec 30.

INSERM U535, 94817 Villejuif Cedex, Villejuif, France.

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http://dx.doi.org/10.1186/1471-2156-6-S1-S18DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866769PMC
December 2005

Impact of the diagnosis definition on linkage detection.

BMC Genet 2005 Dec 30;6 Suppl 1:S140. Epub 2005 Dec 30.

Hôpital Paul Brousse, Bâtiment Leriche, B.P. 1000, 94817 Villejuif Cedex, France.

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http://bmcgenet.biomedcentral.com/articles/10.1186/1471-2156
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http://dx.doi.org/10.1186/1471-2156-6-S1-S140DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866795PMC
December 2005

Genetic analysis of multiple sclerosis in Europeans: French data.

J Neuroimmunol 2003 Oct;143(1-2):74-8

Laboratoire d'Immunologie, UPRES EA 1257 (IFR97), Faculté de Médecine, 2 Avenue du Pr Léon Bernard CS 34317, 35043 Rennes Cedex, France.

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http://dx.doi.org/10.1016/j.jneuroim.2003.08.015DOI Listing
October 2003