Faculty profile
Nicholas Barden
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Read how they describe their research on their Université Laval profile.
Latest papers
Gene interactions in depression: pathways out of darkness.
Trends in genetics : TIG · 2007 · senior author
Polymorphisms in the neuronal isoform of tryptophan hydroxylase 2 are associated with bipolar disorder in French Canadian pedigrees.
Psychiatric genetics · 2007 · senior author
Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2006 · first author
Latest funding
- $418,000
Création d'une unité de séquençage et de génotypage à haut débit, axe de recherche en génétique moléculaire des maladies héréditaires de l'adulte
CFI · 1999 · Co-investigator
5 publications.
Gene interactions in depression: pathways out of darkness.
Harvey M, Belleau P, Barden N
Polymorphisms in the neuronal isoform of tryptophan hydroxylase 2 are associated with bipolar disorder in French Canadian pedigrees.
Harvey M, Gagné B, Labbé M, Barden N
Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder.
Barden N, Harvey M, Gagné B, Shink E, Tremblay M, Raymond C, Labbé M, Villeneuve A, Rochette D, Bordeleau L, Stadler H, Holsboer F, Müller-Myhsok B
Analysis of microsatellite markers and single nucleotide polymorphisms in candidate genes for susceptibility to bipolar affective disorder in the chromosome 12Q24.31 region.
Shink E, Harvey M, Tremblay M, Gagné B, Belleau P, Raymond C, Labbé M, Dubé MP, Lafrenière RG, Barden N
Exclusion of non-synonymous SNPs and a polyglutamine tract in SMRT/N-CoR2 as common deleterious mutation for bipolar disorder in the Sagnenay-Lac-St-Jean population.
Shink E, Harvey M, Tremblay M, Raymond C, Labbé M, Gagné B, Barden N
Création d'une unité de séquençage et de génotypage à haut débit, axe de recherche en génétique moléculaire des maladies héréditaires de l'adulte
Principal investigators: Raymond, Vincent
Keywords: biologie moléculaire, génétique, clonage positionnel, maladies héréditaires, génomique, glaucome, psychose maniaco-dépressive, maladie de Paget, dystrophie myotonique, thérapie génique
From public funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998 with their latest competition results, the Canada Foundation for Innovation, Genome Canada, the Canadian Space Agency, Canada Research Chairs, the Fonds de recherche du Québec, Ontario research funding, Michael Smith Health Research BC, the Canadian Cancer Society, Heart & Stroke and Brain Canada.
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Profile data last refreshed on September 27, 2026 from the university directory, publication records and public research funding records.