P

Philippe M. Campeau

Centre Hospitalier Universitaire Sainte-Justine

ORCID: 0000-0001-9713-7107

360 papers and 11.2k citations.

PubIndex Score97Top 3%How it's scored

360Publications

11.2kTotal Citations

First publication: 2000First senior author: 2009

Top publicationsby citations

Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders

Erfan Aref‐Eshghi, Jennifer Masters, Frédéric Laumonnier et al.|The American Journal of Human Genetics|2020

Cited by 334

BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells

Davor Lessel, Christian Kubisch, Christina Gehbauer et al.|Brain|2018

Cited by 133

Characterization of Gaucher disease bone marrow mesenchymal stromal cells reveals an altered inflammatory secretome

Philippe M. Campeau, Jacques Galipeau|Blood|2009

Cited by 98

Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities – Support for the role of K(ATP) channels in this condition

Catherine A. Brownstein, Alan H. Beggs, Meghan C. Towne et al.|European Journal of Medical Genetics|2013

Cited by 97

Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay

Keren Machol, Carlos A. Bacino, Justine Rousseau et al.|The American Journal of Human Genetics|2018

Cited by 91

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