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 and email address may be missing. Find their university profile.
Research
Latest papers
Ethanolamine-phosphate on the second mannose is a preferential bridge for some GPI-anchored proteins.
EMBO reports · 2022
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome.
European journal of human genetics : EJHG · 2020
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis.
Genetics in medicine : official journal of the American College of Medical Genetics · 2018
Latest funding
- $120,000
Identification of neuronal processes underlying the fatty acid synthase-related developmental and epileptic encephalopathy
CIHR · 2025 · Supervisor
- $757,350
Investigating the role of notochord defects in the etiopathogenesis of congenital scoliosis
CIHR · 2024 · Co-investigator
- $439,300
Developmental Trajectories in ARID1B-Related Disorders - a Multi-Method Multi-Site Prospective Natural History Study
CIHR · 2023 · Nominated PI
3 publications.
Ethanolamine-phosphate on the second mannose is a preferential bridge for some GPI-anchored proteins.
Ishida M, Maki Y, Ninomiya A, Takada Y, Campeau P, Kinoshita T, Murakami Y
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome.
Drivas TG, Li D, Nair D, Alaimo JT, Alders M, Altmüller J, Barakat TS, Bebin EM, Bertsch NL, Blackburn PR, Blesson A, Bouman AM, Brockmann K, Brunelle P, Burmeister M, Cooper GM, Denecke J, Dieux-Coëslier A, Dubbs H, Ferrer A, Gal D, Bartik LE, Gunderson LB, Hasadsri L, Jain M, Karimov C, Keena B, Klee EW, Kloth K, Lace B, Macchiaiolo M, Marcadier JL, Milunsky JM, Napier MP, Ortiz-Gonzalez XR, Pichurin PN, Pinner J, Powis Z, Prasad C, Radio FC, Rasmussen KJ, Renaud DL, Rush ET, Saunders C, Selcen D, Seman AR, Shinde DN, Smith ED, Smol T, Snijders Blok L, Stoler JM, Tang S, Tartaglia M, Thompson ML, van de Kamp JM, Wang J, Weise D, Weiss K, Woitschach R, Wollnik B, Yan H, Zackai EH, Zampino G, Campeau P, Bhoj E
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
Identification of neuronal processes underlying the fatty acid synthase-related developmental and epileptic encephalopathy
Principal investigators: Hermida Borroto, Maria C
Keywords: Epilepsy; Fatty Acid Synthase; Lipidomics; Mouse Models; Myelination; Neurodegeneration; Neurodevelopmental Disorders; Rare Genetic Syndromes; Single-Cell Transcriptomics; Translational Neuroscience
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
Developmental Trajectories in ARID1B-Related Disorders - a Multi-Method Multi-Site Prospective Natural History Study
Principal investigators: Campeau, Philippe M
Keywords: Arid1b-Related Diseases; Coffin-Siris Syndrome; Epigenetic Diseases; Natural History Study; Neurodevelopmental Disorders
Identifying and understanding a new skeletal dysplasia caused by ERI1 mutations
Principal investigators: Campeau, Philippe M
Keywords: Bone Disease; Genetic Disease; Rna Processing; Skeletal Dysplasia
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
Genetic bone diseases; new genes and new treatments
Principal investigators: Campeau, Philippe M
Keywords: Exome Sequencing; Mendelian Disorders; Skeletal Dysplasia
Role of fibronectin mutations in spondylometaphyseal dysplasia and idiopathic scoliosis.
Principal investigators: Campeau, Philippe M; Reinhardt, Dieter P
Keywords: Fibronectin; Scoliosis; Skeletal Dysplasia
Characterization of a new group of vesicular transport diseases.
Principal investigators: Campeau, Philippe M
Keywords: Deafness; Epilepsy; Mendelian Disorders; Mouse Model; Skeletal Disorder; Tbc1d24; Vesicular Transport
Genetic bone diseases; new genes and new treatments
Principal investigators: Campeau, Philippe M
Keywords: Deafness; Epilepsy; Mendelian Disorders; Mouse Model; Skeletal Disorder; Tbc1d24; Vesicular Transport
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
- Philippe Campeau and Philippe Campeau: 3 shared papers
- 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
- 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 Philippe Campeau: 1 shared paper
- Pediatrics
- Anatomy and Cell Biology
- Computer Science
- 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.
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