Author

Julie Sarrazin

Observed institutions: Queen's University, Montreal General Hospital, Kingston General Hospital, Hospital for Sick Children, Centre Hospitalier Universitaire Sainte-Justine, McGill University, Université de Montréal

OpenAlex ID: A5071745540

Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas

1994 · Martin H. Ruttledge, Julie Sarrazin, et al. · Nature Genetics · 568

Human Mitochondrial HMG CoA Synthase: Liver cDNA and Partial Genomic Cloning, Chromosome Mapping to 1p12-p13, and Possible Role in Vertebrate Evolution

1994 · Youssef Boukaftane, Alessandra Duncan, et al. · Genomics · 25

Adenylosuccinate lyase (ADSL) and infantile autism: Absence of previously reported point mutation

1995 · Edward A. Fon, Julie Sarrazin, et al. · American Journal of Medical Genetics · 22

Loss of heterozygosity on chromosome 22 in human gliomas does not inactivate the neurofibromatosis type 2 gene

1996 · David Watkins, Martin H. Ruttledge, et al. · Cancer Genetics and Cytogenetics · 13

Conference on International Research on Food Security, Natural Resource Management and Rural Development

2010 · Gebrelibanos Gebremariam, Sebastien Grenda, et al.

Incidence de virages maniaques chez les patients bipolaires hospitalisés traités avec des antidépresseurs

2009 · Mylène Malenfant, Julie Sarrazin, et al. · Pharmactuel

Locus heterogeneity in autosomal dominant spinocerebellar ataxia: Evidence for the existence of a fifth locus

1994 · Julie Sarrazin, Guy A. Rouleau, et al. · The American Journal of Human Genetics

Works count: 7

Citation count: 628

H-index: 4

I10-index: 4