Publications
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, “Retinal function and preclinical risk traits in children and adolescents at genetic risk of schizophrenia and bipolar disorder.”, Prog Neuropsychopharmacol Biol Psychiatry, vol. 112, p. 110432, 2022.
, “Exploring polypharmacy with artificial intelligence: data analysis protocol.”, BMC Med Inform Decis Mak, vol. 21, no. 1, p. 219, 2021.
, “A multimodal attempt to follow-up linkage regions using RNA expression, SNPs and CpG methylation in schizophrenia and bipolar disorder kindreds.”, Eur J Hum Genet, vol. 28, no. 4, pp. 499-507, 2020.
, “Detection of rare disease variants in extended pedigrees using RVS.”, Bioinformatics, 2018.
, “Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants.”, Genet Epidemiol, 2018.
, “Polygenic risk scores distinguish patients from non-affected adult relatives and from normal controls in schizophrenia and bipolar disorder multi-affected kindreds.”, Am J Med Genet B Neuropsychiatr Genet, vol. 177, no. 3, pp. 329-336, 2018.
, “Post-immunisation fever and the antibody response to measles-containing vaccines.”, Epidemiol Infect, pp. 1-9, 2018.
, “Referential Choices in a Collaborative Storytelling Task: Discourse Stages and Referential Complexity Matter.”, Front Psychol, vol. 9, p. 176, 2018.
, “Association between expression of inflammatory markers in normal breast tissue and mammographic density among premenopausal and postmenopausal women.”, Menopause, vol. 24, no. 5, pp. 524-535, 2017.
, “Association between local inflammation and breast tissue age-related lobular involution among premenopausal and postmenopausal breast cancer patients.”, PLoS One, vol. 12, no. 8, p. e0183579, 2017.
, “The interaction of GSK3B and FXR1 genotypes may influence the mania and depression dimensions in mood disorders.”, J Affect Disord, vol. 213, pp. 172-177, 2017.
, “Reduced antibody response to infant measles vaccination: effects based on type and timing of the first vaccine dose persist after the second dose.”, Clin Infect Dis, 2017.
, “Whole exome association of rare deletions in multiplex oral cleft families.”, Genet Epidemiol, vol. 41, no. 1, pp. 61-69, 2017.
, “Development of a molecular test of Paget's disease of bone.”, Bone, vol. 84, pp. 213-21, 2016.
, “Disinfection by-products exposure and intra-uterine growth restriction: Do genetic polymorphisms of CYP2E1or deletion of GSTM1 or GSTT1 modify the association?”, Environ Int, vol. 92-93, pp. 220-31, 2016.
, “When Is an Endophenotype Useful to Detect Association to a Disease? Exploring the Relationships between Disease Status, Endophenotype and Genetic Polymorphisms.”, Hum Hered, vol. 81, no. 1, pp. 11-25, 2016.
, “Estimating genetic effect sizes under joint disease-endophenotype models in presence of gene-environment interactions.”, Front Genet, vol. 6, p. 248, 2015.
, “A genome-wide association study of suicidal behavior.”, Am J Med Genet B Neuropsychiatr Genet, vol. 168, no. 7, pp. 557-63, 2015.
, “A genome-wide copy number variant study of suicidal behavior.”, PLoS One, vol. 10, no. 5, p. e0128369, 2015.
, “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.
, “Extension of the generalized disequilibrium test to polytomous phenotypes and two-locus models.”, Front Genet, vol. 5, p. 258, 2014.
, “Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.”, Bioinformatics, vol. 30, no. 15, pp. 2189-96, 2014.
, “Plasma polychlorinated biphenyl and organochlorine pesticide concentrations in dementia: the Canadian Study of Health and Aging.”, Environ Int, vol. 69, pp. 141-7, 2014.
, “Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.”, Genetics, vol. 197, no. 3, pp. 1039-44, 2014.
, “Follow-up of a major psychosis linkage site in 13q13-q14 reveals significant association in both case-control and family samples.”, Biol Psychiatry, vol. 74, no. 6, pp. 444-50, 2013.
