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Research
Latest papers
Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.
Molecular psychiatry · 2021
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.
Molecular psychiatry · 2021
Differential Allelic Expression of HTR1B in Suicide Victims: Genetic and Epigenetic Effect of the Cis-Acting Variants.
Neuropsychobiology · 2016
Latest funding
- $1,304,325
PTCHD1 in autism and cognition: from function to diagnostics
CIHR · 2024 · Nominated PI
- $1,154,195
Identifying Autosomal Recessive Genes for Intellectual Disability
CIHR · 2017 · Nominated PI
- $1,005,975
PTCHD1 in autism and cognition: from function to phenotype
CIHR · 2017 · Nominated PI
4 publications.
Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.
Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, Shen L, Thai K, Zawistowski M, Zhuang Y, Abecasis G, Akil H, Bergen S, Burmeister M, Chapman S, DelaBastide M, Juréus A, Kang HM, Kwok PY, Li JZ, Levy SE, Monson ET, Moran J, Sobell J, Watson S, Willour V, Zöllner S, Adolfsson R, Blackwood D, Boehnke M, Breen G, Corvin A, Craddock N, DiFlorio A, Hultman CM, Landen M, Lewis C, McCarroll SA, Richard McCombie W, McGuffin P, McIntosh A, McQuillin A, Morris D, Myers RM, O'Donovan M, Ophoff R, Boks M, Kahn R, Ouwehand W, Owen M, Pato C, Pato M, Posthuma D, Potash JB, Reif A, Sklar P, Smoller J, Sullivan PF, Vincent J, Walters J, Neale B, Purcell S, Risch N, Schaefer C, Stahl EA, Zandi PP, Scott LJ
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.
Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, Shen L, Thai K, Zawistowski M, Zhuang Y, Abecasis G, Akil H, Bergen S, Burmeister M, Chapman S, DelaBastide M, Juréus A, Kang HM, Kwok PY, Li JZ, Levy SE, Monson ET, Moran J, Sobell J, Watson S, Willour V, Zöllner S, Adolfsson R, Blackwood D, Boehnke M, Breen G, Corvin A, Craddock N, DiFlorio A, Hultman CM, Landen M, Lewis C, McCarroll SA, Richard McCombie W, McGuffin P, McIntosh A, McQuillin A, Morris D, Myers RM, O'Donovan M, Ophoff R, Boks M, Kahn R, Ouwehand W, Owen M, Pato C, Pato M, Posthuma D, Potash JB, Reif A, Sklar P, Smoller J, Sullivan PF, Vincent J, Walters J, Neale B, Purcell S, Risch N, Schaefer C, Stahl EA, Zandi PP, Scott LJ
Differential Allelic Expression of HTR1B in Suicide Victims: Genetic and Epigenetic Effect of the Cis-Acting Variants.
Bani-Fatemi A, Howe A, Zai C, Kennedy JL, Vincent J, Strauss J, Wong A, De Luca V
Contribution of SHANK3 Mutations to Autism Spectrum Disorder
Moessner R, Marshall CR, Sutcliffe JS, Skaug J, Pinto D, Vincent J, Zwaigenbaum L, Fernandez B, Roberts W, Szatmari P
PTCHD1 in autism and cognition: from function to diagnostics
Principal investigators: Vincent, John B
Keywords: Animal Models; Autism; Cell-Based Models; Diagnostics; Intellectual Disability,; Neuronal Disruption; Protein Function; Therapeutics
Identifying Autosomal Recessive Genes for Intellectual Disability
Principal investigators: Vincent, John B
Keywords: Autism; Autosomal Recessive; Cognitive Deficit; Genetics; Genomics; Homozygosity-By-Descent; Intellectual Disability; Microarray; Next Generation Sequencing
PTCHD1 in autism and cognition: from function to phenotype
Principal investigators: Vincent, John B
Keywords: Animal Models; Autism; Clinical; Diagnostic; Intellectual Disability; Phenotype; Protein Function; Therapeutic
Elucidating the Role of PTCHD1 in Autism and Intellectual Disability
Principal investigators: Vincent, John B
Keywords: Autism Spectrum Disorder; Copy Number Variation; Disease Gene Identification; Mental Retardation; Mouse Model; Mutation Screening; Protein Function
Brain Development and Addiction in Youth and Adulthood: Causes and Consequences
Principal investigators: Paus, Tomas
Keywords: Addiction; Brain Development; Brain Imaging; Genes; Pregnancy; Smoking; Youth
Programming Brains across Generations: How early environment and genes shape the risk of addiction
Principal investigators: Paus, Tomas
Keywords: Addiction; Brain Development; Brain Imaging; Cohorts; Genes; Pregnancy; Smoking; Two-Generational Families; Youth
Identification of Loci and Genes for Autosomal Recessive Mental Retardation and Autism in Consanguineous Pakistani Families
Principal investigators: Vincent, John B
Keywords: Autism; Autosomal Recessive; Disease Gene Identification; Mental Retardation; Mutation Screening; Phenotype
From Chromatin to Neurophysiology to Behaviour: Studies to Understand, and Develop Treatment Strategies For, the Autism-Spectrum Disorder Rett Syndrome
Principal investigators: Eubanks, James H
Keywords: Chromatin Biology; Electrophysiology; Induced Pluripotent Stem Cells; Rett Syndrome; Transgenic Mice; Viral-Mediated Gene Transfer
Investigation of Chromosome X Copy Number Variants in Autism
Principal investigators: Noor, Abdul
Keywords: Autism; Chromosome X; Copy Number Variants
From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.
Frequent collaborators
- Peter Szatmari and Peter Szatmari: 285 shared papers
- John Strauss and Clement Zai: 13 shared papers
- Peter Szatmari and John Strauss: 3 shared papers
- Peter Szatmari and John Strauss: 3 shared papers
- John Strauss and Albert Wong: 3 shared papers
- Albert Wong and Clement Zai: 3 shared papers
- Peter Szatmari and John Vincent: 1 shared paper
- Peter Szatmari and John Vincent: 1 shared paper
- John Strauss and John Vincent: 1 shared paper
- John Vincent and Albert Wong: 1 shared paper
- John Vincent and Clement Zai: 1 shared paper
- Neurosciences
- Epidemiology Division
- Health Research Methods, Evidence, and Impact
- Other
Co-authors at University of Toronto, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
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