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.
Research
Latest papers
Traffic Jams in the Brain: How Kinesin Dysfunction Shapes Neurodevelopmental Disorders.
Current issues in molecular biology · 2026
The contribution of de novo coding mutations to meningomyelocele.
Nature · 2025
Planar cell polarity zebrafish models of congenital scoliosis reveal underlying defects in notochord morphogenesis.
Development (Cambridge, England) · 2024 · senior author
Latest funding
- $2,000,000
ICanCME : Interdisciplinary Canadian Collaborative Myalgic Encephalomyelitis Research Network.
CIHR · 2024 · Co-investigator
- $757,350
Investigating the role of notochord defects in the etiopathogenesis of congenital scoliosis
CIHR · 2024 · Nominated PI
- $100,000
Investigating the role of notochord defects in the etiopathogenesis of congenital scoliosis
CIHR · 2022 · Nominated PI
23 publications.
Traffic Jams in the Brain: How Kinesin Dysfunction Shapes Neurodevelopmental Disorders.
Shams Nosrati MS, Doustmohammadi M, Dostmohammadi A, Kakavand Hamidi A, Boogari M, Hoseini Tavassol Z, Khosravinejat S, Asgari M, Shafiei M, Nemati AH, Romano F, Capra V, Sterlini B, Darbalaei M, Salehi M, Omrani MD, Zara F, Kibar Z, Miyamoto T, Scala M
The contribution of de novo coding mutations to meningomyelocele.
Ha YJ, Nisal A, Tang I, Lee C, Jhamb I, Wallace C, Howarth R, Schroeder S, Vong KI, Meave N, Jiwani F, Barrows C, Lee S, Jiang N, Patel A, Bagga K, Banka N, Friedman L, Blanco FA, Yu S, Rhee S, Jeong HS, Plutzer I, Major MB, Benoit B, Poüs C, Heffner C, Kibar Z, Bot GM, Northrup H, Au KS, Strain M, Ashley-Koch AE, Finnell RH, Le JT, Meltzer HS, Araujo C, Machado HR, Stevenson RE, Yurrita A, Mumtaz S, Ahmed A, Khara MH, Mutchinick OM, Medina-Bereciartu JR, Hildebrandt F, Melikishvili G, Marwan AI, Capra V, Noureldeen MM, Salem AMS, Issa MY, Zaki MS, Xu L, Lee JE, Shin D, Alkelai A, Shuldiner AR, Kingsmore SF, Murray SA, Gee HY, Miller WT, Tolias KF, Wallingford JB, Spina Bifida Sequencing Consortium, Kim S, Gleeson JG
Planar cell polarity zebrafish models of congenital scoliosis reveal underlying defects in notochord morphogenesis.
Wang M, Zhao S, Shi C, Guyot MC, Liao M, Tauer JT, Willie BM, Cobetto N, Aubin CÉ, Küster-Schöck E, Drapeau P, Zhang J, Wu N, Kibar Z
Risk of meningomyelocele mediated by the common 22q11.2 deletion.
Vong KI, Lee S, Au KS, Crowley TB, Capra V, Martino J, Haller M, Araújo C, Machado HR, George R, Gerding B, James KN, Stanley V, Jiang N, Alu K, Meave N, Nidhiry AS, Jiwani F, Tang I, Nisal A, Jhamb I, Patel A, Patel A, McEvoy-Venneri J, Barrows C, Shen C, Ha YJ, Howarth R, Strain M, Ashley-Koch AE, Azam M, Mumtaz S, Bot GM, Finnell RH, Kibar Z, Marwan AI, Melikishvili G, Meltzer HS, Mutchinick OM, Stevenson DA, Mroczkowski HJ, Ostrander B, Schindewolf E, Moldenhauer J, Zackai EH, Emanuel BS, Garcia-Minaur S, Nowakowska BA, Stevenson RE, Zaki MS, Northrup H, McNamara HK, Aldinger KA, Phelps IG, Deng M, Glass IA, Spina Bifida Sequencing Consortium‡, Morrow B, McDonald-McGinn DM, Sanna-Cherchi S, Lamb DJ, Gleeson JG
A new murine Rpl5 (uL18) mutation provides a unique model of variably penetrant Diamond-Blackfan anemia.
Yu L, Lemay P, Ludlow A, Guyot MC, Jones M, Mohamed FF, Saroya GA, Panaretos C, Schneider E, Wang Y, Myers G, Khoriaty R, Li Q, Franceschi R, Engel JD, Kaartinen V, Rothstein TL, Justice MJ, Kibar Z, Singh SA
Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention.
Larrivée-Vanier S, Magne F, Hamdoun E, Petryk A, Kibar Z, Van Vliet G, Deladoëy J
Update on the Role of the Non-Canonical Wnt/Planar Cell Polarity Pathway in Neural Tube Defects.
Wang M, Marco P, Capra V, Kibar Z
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis.
Boissel S, Fallet-Bianco C, Chitayat D, Kremer V, Nassif C, Rypens F, Delrue MA, Dal Soglio D, Oligny LL, Patey N, Flori E, Cloutier M, Dyment D, Campeau P, Karalis A, Nizard S, Fraser WD, Audibert F, Lemyre E, Rouleau GA, Hamdan FF, Kibar Z, Michaud JL
A genome-wide association study identifies candidate loci associated to syringomyelia secondary to Chiari-like malformation in Cavalier King Charles Spaniels.
Ancot F, Lemay P, Knowler SP, Kennedy K, Griffiths S, Cherubini GB, Sykes J, Mandigers PJJ, Rouleau GA, Rusbridge C, Kibar Z
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.
Hamdan FF, Myers CT, Cossette P, Lemay P, Spiegelman D, Laporte AD, Nassif C, Diallo O, Monlong J, Cadieux-Dion M, Dobrzeniecka S, Meloche C, Retterer K, Cho MT, Rosenfeld JA, Bi W, Massicotte C, Miguet M, Brunga L, Regan BM, Mo K, Tam C, Schneider A, Hollingsworth G, Deciphering Developmental Disorders Study, FitzPatrick DR, Donaldson A, Canham N, Blair E, Kerr B, Fry AE, Thomas RH, Shelagh J, Hurst JA, Brittain H, Blyth M, Lebel RR, Gerkes EH, Davis-Keppen L, Stein Q, Chung WK, Dorison SJ, Benke PJ, Fassi E, Corsten-Janssen N, Kamsteeg EJ, Mau-Them FT, Bruel AL, Verloes A, Õunap K, Wojcik MH, Albert DVF, Venkateswaran S, Ware T, Jones D, Liu YC, Mohammad SS, Bizargity P, Bacino CA, Leuzzi V, Martinelli S, Dallapiccola B, Tartaglia M, Blumkin L, Wierenga KJ, Purcarin G, O'Byrne JJ, Stockler S, Lehman A, Keren B, Nougues MC, Mignot C, Auvin S, Nava C, Hiatt SM, Bebin M, Shao Y, Scaglia F, Lalani SR, Frye RE, Jarjour IT, Jacques S, Boucher RM, Riou E, Srour M, Carmant L, Lortie A, Major P, Diadori P, Dubeau F, D'Anjou G, Bourque G, Berkovic SF, Sadleir LG, Campeau PM, Kibar Z, Lafrenière RG, Girard SL, Mercimek-Mahmutoglu S, Boelman C, Rouleau GA, Scheffer IE, Mefford HC, Andrade DM, Rossignol E, Minassian BA, Michaud JL
ICanCME : Interdisciplinary Canadian Collaborative Myalgic Encephalomyelitis Research Network.
Principal investigators: Moreau, Alain; Al Batran, Rami; Boomer, Kirsten; Brochiero, Emmanuelle; Edgell, Heather; Gignac, Monique A; Huynh, Thao T; Karamchandani, Jason; Kerr, Kathleen J; McGinn, Carrie A; Piche, Alain; Poirier, Sabrina; Pouliot, Marc; Raj, Satish R; Robertson, Hilary
Keywords: Biomarkers; Canadian Database And Management Platform; Chronic Fatigue Syndrome; Integrated Transdisciplinary Team; Mobile Health Monitoring Tools; Myalgic Encephalomyelitis; Patient Oriented Care; Vascular Instability And Sleep Disturbances
Investigating the role of notochord defects in the etiopathogenesis of congenital scoliosis
Principal investigators: Kibar, Zoha
Keywords: Candidate Gene Approach; Congenital Scoliosis; Human Cohorts; Immunohistochemical Studies; Notochord Development; Planar Cell Polarity; Spine Formation; Zebrafish Model
Investigating the role of notochord defects in the etiopathogenesis of congenital scoliosis
Principal investigators: Kibar, Zoha
Keywords: Congenital Scoliosis; Human Cohort; Immunohistochemical Studies; Notochord; Planar Cell Polarity; Re-Sequencing Analyses; Spine Formation; Zebrafish Model
Multimode determination of gene transcription and metabolic labeling
Principal investigators: Tremblay, André
Molecular crosstalk between apical-basal polarity and planar cell polarity in axon guidance
Principal investigators: Kibar, Zoha
De novo mutations in birth defects.
Principal investigators: Michaud, Jacques L
Keywords: Birth Defects; De Novo Mutation; Next-Generation Sequencing
Identification and characterization of genes predisposing to neural tube defects in humans
Principal investigators: Kibar, Zoha
Keywords: Biochemical Assays; Bioinformatics; Candidate Gene Sequencing; Canonical Wnt Pathway; Genetic Interaction Studies; Mouse Mutant; Neural Tube Defects; Planar Cell Polarity; Whole Exome Sequencing; Zebrafish Model
Molecular crosstalk between apical-basal polarity and planar cell polarity in axon guidance
Principal investigators: Kibar, Zoha
Identification of the gene(s) predisposing to Chiari Malformation I using the Griffon Bruxellois dog model
Principal investigators: Kibar, Zoha
Keywords: Candidate Genes; Chiari Malformation I; Complex Traits; Dog Model; Functional Studies; Genetic Studies; Linkage Disequilibrium Mapping; Malformation Of The Craniovertebral Junction; Mutation Screening; Next Generation Sequencing
CIHR - Quebec Training Network in Perinatal Research
Principal investigators: Fraser, William D; Bujold, Emmanuel; Chaillet, Nils; Gagnon, Robert; Hatem, Marie; Monnier, Patricia O; Muckle, Gina; Murphy, Bruce D; Tremblay, Yves; Williams-Jones, Bryn
Keywords: Environment-Health Interactions; Epidemiology; Knowledge Translation; Network; Perinatal; Training
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
- Myriam Srour and Myriam Srour: 94 shared papers
- Philippe Gros and Elena Torban: 7 shared papers
- Pierre Drapeau and Zoha Kibar: 5 shared papers
- Philippe Gros and Zoha Kibar: 5 shared papers
- Lionel Carmant and Patrick Cossette: 4 shared papers
- Lionel Carmant and Philippe Major: 4 shared papers
- Pierre Drapeau and Philippe Gros: 3 shared papers
- Pierre Drapeau and Patrick Cossette: 3 shared papers
- Philippe Campeau and Philippe Campeau: 3 shared papers
- Elsa Rossignol and Philippe Major: 3 shared papers
- Lionel Carmant and Elsa Rossignol: 2 shared papers
- Philippe Gros and Guillaume Bourque: 2 shared papers
- Zoha Kibar and Myriam Srour: 2 shared papers
- Zoha Kibar and Myriam Srour: 2 shared papers
- Elsa Rossignol and Myriam Srour: 2 shared papers
- Elsa Rossignol and Myriam Srour: 2 shared papers
- Myriam Srour and Philippe Major: 2 shared papers
- Lionel Carmant and Zoha Kibar: 1 shared paper
- Lionel Carmant and Sylvia Stockler: 1 shared paper
- Lionel Carmant and Guillaume Bourque: 1 shared paper
- David Dyment and David Chitayat: 1 shared paper
- David Dyment and Zoha Kibar: 1 shared paper
- David Dyment and Philippe Campeau: 1 shared paper
- David Dyment and Philippe Campeau: 1 shared paper
- Pierre Drapeau and Elena Torban: 1 shared paper
- David Chitayat and Zoha Kibar: 1 shared paper
- David Chitayat and Philippe Campeau: 1 shared paper
- David Chitayat and Philippe Campeau: 1 shared paper
- Zoha Kibar and Elena Torban: 1 shared paper
- Zoha Kibar and Sylvia Stockler: 1 shared paper
- Zoha Kibar and Philippe Campeau: 1 shared paper
- Zoha Kibar and Guillaume Bourque: 1 shared paper
- Zoha Kibar and Elsa Rossignol: 1 shared paper
- Zoha Kibar and Patrick Cossette: 1 shared paper
- Zoha Kibar and Christophe Faure: 1 shared paper
- Zoha Kibar and Philippe Major: 1 shared paper
- Zoha Kibar and Philippe Campeau: 1 shared paper
- Sylvia Stockler and Guillaume Bourque: 1 shared paper
- Neurosciences
- Pediatrics
- Biochemistry
- Computer Science
- Medicine/Nephrology
- Human Genetics
- Anatomy and Cell Biology
- Other
Co-authors at Université de Montréal, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Pierre Drapeau
Neurosciences
5 shared papers, latest 2024
Philippe Gros
Biochemistry
5 shared papers, latest 2011
Myriam Srour
Pediatrics
2 shared papers, latest 2017
Myriam Srour
Faculty
2 shared papers, latest 2017
Philippe Campeau
Pediatrics
1 shared papers, latest 2018
Guillaume Bourque
Human Genetics
1 shared papers, latest 2017
Elsa Rossignol
Neurosciences
1 shared papers, latest 2017
Elena Torban
Medicine/Nephrology
1 shared papers, latest 2007
Christophe Faure
Faculty
1 shared papers, latest 2017
Philippe Major
Neurosciences
1 shared papers, latest 2017
Philippe Campeau
Anatomy and Cell Biology
1 shared papers, latest 2018
Patrick Cossette
Faculty
1 shared papers, latest 2017
Sylvia Stockler
Pediatrics
1 shared papers, latest 2017
Lionel Carmant
Faculty
1 shared papers, latest 2017
David Dyment
Faculty
1 shared papers, latest 2018
David Chitayat
Computer Science
1 shared papers, latest 2018
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