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“Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.”, Bioinformatics, vol. 30, no. 15, pp. 2189-96, 2014.
, “Evidence for altered basal ganglia-brainstem connections in cervical dystonia.”, PLoS One, vol. 7, no. 2, p. e31654, 2012.
, “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.
, “Differences and similarities in the serotonergic diathesis for suicide attempts and mood disorders: a 22-year longitudinal gene-environment study.”, Mol Psychiatry, vol. 15, no. 8, pp. 831-43, 2010.
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