A large-scale, consortium-based genomewide association study of asthmaDifferent genes interact with particulate matter and tobacco smoke exposure in affecting lung function decline in the general populationAssociations between nitric oxide synthase genes and exhaled NO-related phenotypes according to asthma statusGenome-wide association study identifies a new melanoma susceptibility locus at 1q21.3Genome-wide association study identifies three new melanoma susceptibility loci.A variant in FTO shows association with melanoma risk not due to BMIAssociation of Forced Vital Capacity with the Developmental Gene NCOR2.CoPE: a collaborative pedigree drawing environment.Using an age-at-onset phenotype with interval censoring to compare methods of segregation and linkage analysis in a candidate region for elevated systolic blood pressure.A two-step multiple-marker strategy for genome-wide association studiesReplication of association between ADAM33 polymorphisms and psoriasis.Gene-environment interactions in asthma and allergic diseases: challenges and perspectives.A linkage study between HLA and cutaneous malignant melanoma or precursor lesions or bothAn epidemiological and genetic study of facial clefting in France. II Segregation analysisNetwork-assisted analysis of GWAS data identifies a functionally-relevant gene module for childhood-onset asthma.Rare missense variants in POT1 predispose to familial cutaneous malignant melanomaGeographical variation in the penetrance of CDKN2A mutations for melanoma.Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study.Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy.The effect on melanoma risk of genes previously associated with telomere length.Genetic and environmental factors in cutaneous malignant melanoma.Effect of 17q21 variants and smoking exposure in early-onset asthma.Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regionsFraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants.Evidence for the segregation of a major gene in human susceptibility/resistance to infection by Schistosoma mansoni.Segregation analysis of congenital glaucoma: approach by two differential models.Further analysis of familial transmission of congenital glaucoma.Detection of major genes for susceptibility to leprosy and its subtypes in a Caribbean island: Desirade island.Interactions between genetic and reproductive factors in breast cancer risk in a French family sample.A common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adultsDetection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers.Genome-wide association study of lung function decline in adults with and without asthma.Transient receptor potential genes, smoking, occupational exposures and cough in adults.Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.Integrated pathway and epistasis analysis reveals interactive effect of genetic variants at TERF1 and AFAP1L2 loci on melanoma risk.Adult onset asthma and interaction between genes and active tobacco smoking: The GABRIEL consortiumGain of power of the general regression model compared to Cochran-Armitage Trend tests: simulation study and application to bipolar disorder.Meta-analysis identifies seven susceptibility loci involved in the atopic marchVitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization study.A general transmission probability model for pedigree data.
P50
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Florence Demenais
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