Publications
Export 11 results:
Filtres: Keyword is Genetic Linkage [Enlever les filtres]
, « On the validity of within-nuclear-family genetic association analysis in samples of extended families. », Stat Appl Genet Mol Biol, vol. 14, nᵒ 6, p. 533-49, 2015.
, « Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. », Bioinformatics, vol. 30, nᵒ 15, p. 2189-96, 2014.
, « A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity. », Hum Hered, vol. 68, nᵒ 4, p. 231-42, 2009.
, « Decomposing the autism phenotype into familial dimensions. », Am J Med Genet B Neuropsychiatr Genet, vol. 147B, nᵒ 1, p. 3-9, 2008.
, « Replication of linkage with bipolar disorder on chromosome 16p in the Eastern Quebec population. », Am J Med Genet B Neuropsychiatr Genet, vol. 147B, nᵒ 6, p. 737-44, 2008.
, « Using disease symptoms to improve detection of linkage under genetic heterogeneity. », Genet Epidemiol, vol. 32, nᵒ 5, p. 476-86, 2008.
, « Possible association of the pro-melanin-concentrating hormone gene with a greater body mass index as a side effect of the antipsychotic olanzapine. », Am J Med Genet B Neuropsychiatr Genet, vol. 144B, nᵒ 8, p. 1063-9, 2007.
, « Autosomal dominant macular dystrophy in a large Canadian family. », Can J Ophthalmol, vol. 38, nᵒ 1, p. 33-40, 2003.
, « [Genetics of schizophrenia and bipolar disorder: recent success of linkage studies with evidence of specific and shared susceptibility loci]. », Med Sci (Paris), vol. 19, nᵒ 10, p. 960-6, 2003.
, « Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation. », Ophthalmology, vol. 109, nᵒ 10, p. 1862-70, 2002.
, « Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome. », Am J Hum Genet, vol. 57, nᵒ 5, p. 1006-18, 1995.
