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IFIH1-GCA-KCNH7 locus is not associated with genetic susceptibility to multiple sclerosis in French patientsGenetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patientsCould inbred cases identified in GWAS data succeed in detecting rare recessive variants where affected sib-pairs have failed?FSuite: exploiting inbreeding in dense SNP chip and exome data.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.Meta and pooled analysis of European coeliac disease data.Genetic analysis of multiple sclerosis in Europeans: French data.Impact of the diagnosis definition on linkage detectionDetection of susceptibility loci by genome-wide linkage analysis.Modeling the effect of a genetic factor for a complex trait in a simulated population.Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci.An ordered subset approach to including covariates in the transmission disequilibrium testVariation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis.Rare and low frequency variant stratification in the UK population: description and impact on association tests.HLA-DQ relative risks for coeliac disease in European populations: a study of the European Genetics Cluster on Coeliac Disease.Genome search in celiac disease.Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndrome.IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations.Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings.Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genesApolipoprotein E and Alzheimer disease: genotype-specific risks by age and sexCan whole-exome sequencing data be used for linkage analysis?Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer ConsortiumA second locus for Marfan syndrome maps to chromosome 3p24.2-p25.No effect of the alpha1-antichymotrypsin A allele in Alzheimer's diseaseHigh level of inbreeding in final phase of 1000 Genomes Project.Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin.Susceptibility to coeliac disease in Tunisian children and GM immunoglobulin allotypes.Study of two ectopeptidases in the susceptibility to celiac disease: two newly identified polymorphisms of dipeptidylpeptidase IV.Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations.HLA-associated diseases: a new method for performing linkage analysis with other markers than HLA.Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis.Assessing the effect of multiple linkage tests in complex diseases.On the choice of linkage statistics.Meta-analysis of genome-wide linkage studies in celiac disease.Interactive effect of two candidate genes in a disease: extension of the marker-association-segregation chi(2) method.Cytokines in genetic susceptibility to multiple sclerosis: a candidate gene approach. French Multiple Sclerosis Genetics Group.Manic depressive illness is linked to factor IX in a French pedigree.Genetic association and gene-environment interaction: a new method for overcoming the lack of exposure information in controls.Is a single mutation at the same locus responsible for all affected cases in a large Alzheimer pedigree (FAD4)?
P50
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P50
description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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prefLabel
Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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Marie-Claude Babron
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P106
P21
P31
P496
0000-0002-4100-0299