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Christine Bétard

Observed names: C BETARD, C Betard, C Bétard, C. Betard, C. Bétard, Christine Betard
Observed institutions: Centre National de la Recherche Scientifique, Institut national de recherche en sciences et technologies du numérique, Université de Bordeaux, Inserm, Institut Pasteur, Université de Bourgogne, Collège de France, Montreal General Hospital, Institut Pasteur de Lille, McGill University Health Centre, King Saud University, IQVIA (United Kingdom), Centre Hospitalier Universitaire de Bordeaux, Centre National de Recherche en Génomique Humaine, Institut de génétique et de biologie moléculaire et cellulaire, Sorbonne Paris Cité, Centre hospitalier universitaire de Québec, Assistance Publique – Hôpitaux de Paris, Hôpital Européen Georges-Pompidou, Bordeaux Population Health, CHU Dijon Bourgogne, McGill Genome Centre, Hôtel-Dieu de Québec, Institut Bergonié, Hôpitaux Universitaires de Strasbourg, Montreal Clinical Research Institute, King Fahad Hospital Hufūf, Centre de Recherche Épidémiologie et Statistique, Centre d'Investigation Clinique Plurithématique de Bordeaux, Université Paris Descartes, SISTM: Statistics In System biology and Translational Medicine, Pathologie vasculaire et endocrinologie rénale, McGill University, Université de Montréal
OpenAlex ID: A5107845130
Molecular scanning of the human PPARα gene: association of the L162V mutation with hyperapobetalipoproteinemia
2000 · Marie-Claude Vohl, Pierre Lepage, et al. · Journal of Lipid Research · 176
Safety and immunogenicity of a two-dose heterologous Ad26.ZEBOV and MVA-BN-Filo Ebola vaccine regimen in adults in Europe (EBOVAC2): a randomised, observer-blind, participant-blind, placebo-controlled, phase 2 trial
2020 · Andrew J Pollard, Odile Launay, et al. · The Lancet Infectious Diseases · 164
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Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithium
2001 · G Turecki, P Grof, et al. · Molecular Psychiatry · 164
Shwachman-Diamond Syndrome with Exocrine Pancreatic Dysfunction and Bone Marrow Failure Maps to the Centromeric Region of Chromosome 7
2001 · Sharan Goobie, Maja Popovic, et al. · The American Journal of Human Genetics · 144
Distribution of brain cytochrome oxidase activity in various neurodegenerative diseases
1995 · Pierre Chagnon, Christine Bétard, et al. · Neuroreport · 111
Apo E allele frequencies in Alzheimerʼs disease, Lewy body dementia, Alzheimerʼs disease with cerebrovascular disease and vascular dementia
1994 · Christine Bétard, Yves Robitaille, et al. · Neuroreport · 81
Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14
2006 · B Etain, F Mathieu, et al. · Molecular Psychiatry · 76
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Mapping of Familial Thoracic Aortic Aneurysm/Dissection With Patent Ductus Arteriosus to 16p12.2–p13.13
2005 · Philippe Khau Van Kien, Flavie Mathieu, et al. · Circulation · 72
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Identification of a second “French Canadian” LDL receptor gene deletion and development of a rapid method to detect both deletions
1989 · Yuanhong MA, Christine Bétard, et al. · Clinical Genetics · 71
Safety and immunogenicity of 2-dose heterologous Ad26.ZEBOV, MVA-BN-Filo Ebola vaccination in healthy and HIV-infected adults: A randomised, placebo-controlled Phase II clinical trial in Africa
2021 · Houreratou Barry, Gaudensia Mutua, et al. · PLoS Medicine · 68
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Safety and immunogenicity of 2-dose heterologous Ad26.ZEBOV, MVA-BN-Filo Ebola vaccination in children and adolescents in Africa: A randomised, placebo-controlled, multicentre Phase II clinical trial
2022 · Zacchaeus Anywaine, Houreratou Barry, et al. · PLoS Medicine · 65
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Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French Canadians
1992 · Christine Bétard, A. M. Kessling, et al. · Human Genetics · 64
Patterns of association between genetic variability in apolipoprotein (apo) B, apo AI-CIII-AIV, and cholesterol ester transfer protein gene regions and quantitative variation in lipid and lipoprotein traits: influence of gender and exogenous hormones.
1992 · A Kessling, S Ouellette, et al. · PubMed · 63
Homozygosity mapping of Marinesco–Sjögren syndrome to 5q31
2003 · C Lagier-Tourenne, L Tranebjærg, et al. · European Journal of Human Genetics · 62
A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23
2007 · M. Gribaa, M. Salih, et al. · Brain · 49
Characterization of two polymorphic sites in the human kinin B1 receptor gene
1998 · D R Bachvarov, M Landry, et al. · Journal of the American Society of Nephrology · 48
Homozygosity mapping of a third Joubert syndrome locus to 6q23
2004 · C Lagier-Tourenne, E Boltshauser, et al. · Journal of Medical Genetics · 42
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Localization of a Recessive Gene for North American Indian Childhood Cirrhosis to Chromosome Region 16q22—and Identification of a Shared Haplotype
2000 · Christine Bétard, Andrée Rasquin-Weber, et al. · The American Journal of Human Genetics · 42
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Genome-wide scan linkage analysis for Parkinson’s disease: the European genetic study of Parkinson’s disease
2004 · M Martinez, A Brice, et al. · Journal of Medical Genetics · 40
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Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families
2004 · Emmanuelle Bouzigon, Marie-Hélène Dizier, et al. · Human Molecular Genetics · 40
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Association between human African trypanosomiasis and the IL6 gene in a Congolese population
2006 · David Courtin, Jacqueline Milet, et al. · Infection Genetics and Evolution · 39
Genome screen in the French EGEA study: detection of linked regions shared or not shared by allergic rhinitis and asthma
2005 · M -H Dizier, E Bouzigon, et al. · Genes and Immunity · 36
Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease
2005 · Maria Martinez, Alexis Brice, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 32
Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay (ARSACS): High-Resolution Physical and Transcript Map of the Candidate Region in Chromosome Region 13q11
1999 · James C. Engert, Carole Doré, et al. · Genomics · 32
Response to HMG CoA reductase inhibitors in heterozygous familial hypercholesterolemia due to the 10-kb deletion ("French Canadian mutation") of the LDL receptor gene.
1994 · L Karayan, S Qiu, et al. · Arteriosclerosis and Thrombosis A Journal of Vascular Biology · 31
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Works count: 38
Citation count: 1,943
H-index: 25
I10-index: 31
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