Publications
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“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.
, “Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies.”, Genet Epidemiol, vol. 35, no. 3, pp. 182-9, 2011.
, “A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity.”, Hum Hered, vol. 68, no. 4, pp. 231-42, 2009.
, “Using disease symptoms to improve detection of linkage under genetic heterogeneity.”, Genet Epidemiol, vol. 32, no. 5, pp. 476-86, 2008.
, “[The fragile X syndrome: one protein missing and 1001 disoriented mRNAs].”, Med Sci (Paris), vol. 22, no. 1, pp. 41-6, 2006.
, “Identifying SNPs predictive of phenotype using random forests.”, Genet Epidemiol, vol. 28, no. 2, pp. 171-82, 2005.
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