Jeremy Schwartzentruber

Statistics

Publications

112

Citations

19.6K

H-Index

Active since

2008

Affiliations

McGill University and Génome Québec Innovation Centre(Current)

McGill University

Children's Hospital of Eastern Ontario

University of Ottawa

Wellcome Sanger Institute

Jeremy Schwartzentruber is an author at McGill University and Génome Québec Innovation Centre specializing in genetics, life sciences, and molecular genetics.

ORCID

Publications per year

2008–2025

112

Publications

112

Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

Jeremy Schwartzentruber, Andrey Korshunov, Xiao-Yang Liu et al. · Nature · 2012 · 2.7K citations

Medicine, Genetics, Oncology +16

Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma

Dominik Sturm, Hendrik Witt, Volker Hovestadt et al. · Cancer Cell · 2012 · 1.9K citations · Full text

Medicine, Genetics, Molecular Genetics +16

K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas

Dong-Anh Khuong-Quang, Pawel Buczkowicz, Patricia Rakopoulos et al. · Acta Neuropathologica · 2012 · 1K citations · Full text

Medicine, Genetics, Oncology +17

Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma

David Jones, Barbara Hutter, Natalie Jäger et al. · Nature Genetics · 2013 · 835 citations · Full text

Medicine, Oncology, Pathology +10

De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes

Jean-Baptiste Rivière, Ghayda Mirzaa, Brian J. O’Roak et al. · Nature Genetics · 2012 · 753 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

1–5 of 112