Concepedia

Megan R. Vanstone

MR

Statistics

Publications

7

Citations

1.1K

H-Index

7

Active since

2013

Affiliations

University of Ottawa(Current)

Children's Hospital of Eastern Ontario

McGill University and Génome Québec Innovation Centre

McGill University

University of Washington

Megan R. Vanstone is an author at University of Ottawa specializing in genetics, life sciences, and genetic disorders.

Publications per year

2013–2017

7

Publications

7

International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases

Kym M. Boycott, Ana Rath, Jessica X. Chong et al. · The American Journal of Human Genetics · 2017 · 453 citations · Full text

, , +14

Mutations in PIK3R1 Cause SHORT Syndrome

David A. Dyment, Amanda Smith, Diana Alcantara et al. · The American Journal of Human Genetics · 2013 · 197 citations · Full text

, , +16

A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis

Yee Him Cheung, Tenzin Gayden, Philippe M. Campeau et al. · The American Journal of Human Genetics · 2013 · 171 citations · Full text

, , +6

De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome

Ghayda Mirzaa, David Parry, Andrew E. Fry et al. · Nature Genetics · 2014 · 151 citations · Full text

, , +10

SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases

Karine Choquet, Martine Tétreault, Sharon Yang et al. · European Journal of Human Genetics · 2015 · 59 citations · Full text

, , +12

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