Faculty profile

Patrick Cossette

ResearcherUniversité de Montréal

This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a Université de Montréal directory, so their courses may be missing. Find their university profile.

Patrick Cossette

Researcher

Health Sciences

Université de Montréal

Montreal, Quebec, Canada

Supervision signals

Has led research grants, which requires an independent research appointment. Ask their department whether they supervise graduate students.
5 publications in the last five years, latest in 2025.
Principal investigator on 3 research grants (3 CIHR), most recently in 2015.

These signals come from public records, including CIHR, NSERC and SSHRC funding decisions. Ask the professor or the graduate program whether they are taking new students.

Academic metrics

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Collaborators

Grants

Publications by year

Counts cover the works listed on the university profile; citation counts come from Dimensions.

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Signals and details

Research

Crc

Latest papers

X-Linked Bilateral Polymicrogyria With Epilepsy and Intellectual Disability Associated With a Novel KIF4A Variant.
American journal of medical genetics. Part A · 2025
Unraveling the role of non-coding rare variants in epilepsy.
PloS one · 2023
Novel NALCN variant linked to temporal lobe epilepsy.
American journal of medical genetics. Part A · 2023

All 32 publications

Latest funding

Investigating the role of non-coding variations in epilepsy
CIHR · 2019 · Co-investigator
$436,050
Canada Research Chair Tier 1
CIHR · 2015 · Nominated PI
$1,400,000
The role of mutated GABAA receptors in the pathogenesis of idiopathic generalized epilepsy
CIHR · 2009 · Nominated PI
$658,015

All 5 grants and awards

32 publications.

X-Linked Bilateral Polymicrogyria With Epilepsy and Intellectual Disability Associated With a Novel KIF4A Variant.

Laflamme N, Triassi V, Martineau L, Toffa DH, Létourneau-Guillon L, Laplante A, Cossette P, Samarut É, Tétreault M, Nguyen DK

American journal of medical genetics. Part A2025

DOI: 10.1002/ajmg.a.63860 PMID: 39268972

Unraveling the role of non-coding rare variants in epilepsy.

Girard A, Moreau C, Michaud JL, Minassian B, Cossette P, Girard SL

PloS one2023

DOI: 10.1371/journal.pone.0291935 PMID: 37756314

Novel NALCN variant linked to temporal lobe epilepsy.

Nguyen E, Tétreault M, Toffa DH, Cossette P, Samarut É, Nguyen DK

American journal of medical genetics. Part A2023

DOI: 10.1002/ajmg.a.63209 PMID: 37046053

Usage of Genetic Panels in an Adult Epilepsy Clinic.

Li J, Toffa DH, Lefèbvre M, Tétreault M, Cossette P, Samarut É, Nguyen DK

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques2023

DOI: 10.1017/cjn.2022.49 PMID: 35478072

Assessment of burden and segregation profiles of CNVs in patients with epilepsy.

Moreau C, Tremblay F, Wolking S, Girard A, Laprise C, Hamdan FF, Michaud JL, Minassian BA, Cossette P, Girard SL

Annals of clinical and translational neurology2022

DOI: 10.1002/acn3.51598 PMID: 35678011

Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy.

Buono RJ, Bradfield JP, Wei Z, Sperling MR, Dlugos DJ, Privitera MD, French JA, Lo W, Cossette P, Schachter SC, Basehore H, Lohoff FW, Grant SFA, Ferraro TN, Hakonarson H

Genes2021

DOI: 10.3390/genes12091441 PMID: 34573423

Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy.

Wolking S, Moreau C, McCormack M, Krause R, Krenn M, EpiPGx Consortium, Berkovic S, Cavalleri GL, Delanty N, Depondt C, Johnson MR, Koeleman BPC, Kunz WS, Lerche H, Marson AG, O'Brien TJ, Petrovski S, Sander JW, Sills GJ, Striano P, Zara F, Zimprich F, Sisodiya SM, Girard SL, Cossette P

Annals of clinical and translational neurology2021

DOI: 10.1002/acn3.51374 PMID: 34018700

Increased frequency of proinflammatory CD4 T cells and pathological levels of serum neurofilament light chain in adult drug-resistant epilepsy.

Ouédraogo O, Rébillard RM, Jamann H, Mamane VH, Clénet ML, Daigneault A, Lahav B, Uphaus T, Steffen F, Bittner S, Zipp F, Bérubé A, Lapalme-Remis S, Cossette P, Nguyen DK, Arbour N, Keezer MR, Larochelle C

Epilepsia2021

DOI: 10.1111/epi.16742 PMID: 33140401

Variants in CHRNB2 and CHRNA4 Identified in Patients with Insular Epilepsy.

Cadieux-Dion M, Meneghini S, Villa C, Toffa DH, Wickstrom R, Bouthillier A, Sandvik U, Gustavsson B, Mohamed I, Cossette P, Combi R, Becchetti A, Nguyen DK

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques2020

DOI: 10.1017/cjn.2020.126 PMID: 32536355

Testing association of rare genetic variants with resistance to three common antiseizure medications.

Wolking S, Moreau C, Nies AT, Schaeffeler E, McCormack M, Auce P, Avbersek A, Becker F, Krenn M, Møller RS, Nikanorova M, Weber YG, Weckhuysen S, Cavalleri GL, Delanty N, Depondt C, Johnson MR, Koeleman BPC, Kunz WS, Marson AG, Sander JW, Sills GJ, Striano P, Zara F, Zimprich F, Schwab M, Krause R, Sisodiya SM, Cossette P, Girard SL, Lerche H, EpiPGX Consortium

Epilepsia2020

DOI: 10.1111/epi.16467 PMID: 32141622

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Patrick Cossette

Research

Latest papers

Latest funding

X-Linked Bilateral Polymicrogyria With Epilepsy and&#xa0;Intellectual Disability Associated With a Novel KIF4A Variant.

Unraveling the role of non-coding rare variants in epilepsy.

Novel NALCN variant linked to temporal lobe epilepsy.

Usage of Genetic Panels in an Adult Epilepsy Clinic.

Assessment of burden and segregation profiles of CNVs in patients with epilepsy.

Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy.

Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy.

Increased frequency of proinflammatory CD4 T cells and pathological levels of serum neurofilament light chain in adult drug-resistant epilepsy.

Variants in CHRNB2 and CHRNA4 Identified in Patients with Insular Epilepsy.

Testing association of rare genetic variants with resistance to three common antiseizure medications.

Investigating the role of non-coding variations in epilepsy

Canada Research Chair Tier 1

The role of mutated GABAA receptors in the pathogenesis of idiopathic generalized epilepsy

The role of mutated GABAA receptors in the pathogenesis of idiopathic generalized epilepsy

Epileptogenic zone localization by concurrent electroencephalography and electrical impedance

Frequent collaborators

Lionel Carmant

Pierre Drapeau

Laurent Mottron

Ridha Joober

Ridha Joober

Russell Schachar

Jennifer Crosbie

Catherine Larochelle

Jacob Vorstman

Ekaterina Rogaeva

Myriam Srour

Paul Arnold

Philippe Major

Myriam Srour

Paul Sandor

Paul Arnold

Gustavo Turecki

Nathalie Arbour

Derek Bowie

Guillaume Bourque

Bernard Brais

Elsa Rossignol

Martin Alda

Peter ST GEORGE-HYSLOP

Zoha Kibar

Sylvia Stockler

X-Linked Bilateral Polymicrogyria With Epilepsy and Intellectual Disability Associated With a Novel KIF4A Variant.