Publications
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Filters: Keyword is Genetic Linkage [Clear All Filters]
, “On the validity of within-nuclear-family genetic association analysis in samples of extended families.”, Stat Appl Genet Mol Biol, vol. 14, no. 6, pp. 533-49, 2015.
, “Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.”, Bioinformatics, vol. 30, no. 15, pp. 2189-96, 2014.
, “A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity.”, Hum Hered, vol. 68, no. 4, pp. 231-42, 2009.
, “Decomposing the autism phenotype into familial dimensions.”, Am J Med Genet B Neuropsychiatr Genet, vol. 147B, no. 1, pp. 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, pp. 737-44, 2008.
, “Using disease symptoms to improve detection of linkage under genetic heterogeneity.”, Genet Epidemiol, vol. 32, no. 5, pp. 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, pp. 1063-9, 2007.
, “Autosomal dominant macular dystrophy in a large Canadian family.”, Can J Ophthalmol, vol. 38, no. 1, pp. 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, pp. 960-6, 2003.
, “Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.”, Ophthalmology, vol. 109, no. 10, pp. 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, pp. 1006-18, 1995.
