Ann M. Joseph‐George

University of Toronto CA

Publications

346

Citations

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Data combined from OpenAlex + Semantic Scholar. OA = OpenAlex S2 = Semantic Scholar

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Publication & Citation Trends

Most Cited Works

Genome assembly comparison identifies structural variants in the human genome OA

Razi Khaja, Junjun Zhang, Jeffrey R. MacDonald, Yongshu He, Ann M. Joseph‐George +15 more

Nature Genetics 2006

165

The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants OA

Miriam S. Reuter, Susan Walker, Bhooma Thiruvahindrapuram, J. Andrew Whitney, Iris Cohn +48 more

Canadian Medical Association Journal 2018

Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay OA

Mohammed Uddin, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, Lia D’Abate, Daniele Merico +24 more

Scientific Reports 2016

Warsaw breakage syndrome: Further clinical and genetic delineation OA

Ebba Alkhunaizi, Ranad Shaheen, Sanjay Kumar Bharti, Ann M. Joseph‐George, Karen Chong +11 more

American Journal of Medical Genetics Part A 2018

Stable transmission of an unbalanced chromosome 21 derived from chromoanasynthesis in a patient with a SYNGAP1 likely pathogenic variant OA

Peter Sabatini, Resham Ejaz, Dimitri J. Stavropoulos, Roberto Mendoza‐Londono, Ann M. Joseph‐George

Molecular Cytogenetics 2018

Publications

10 total

The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants PDF

Miriam S. Reuter, Susan Walker, Bhooma Thiruvahindrapuram, J. Andrew Whitney, Iris Cohn et al. - Canadian Medical Association Journal, 2018

Cited by 63 OpenAlex

Warsaw breakage syndrome: Further clinical and genetic delineation PDF

Ebba Alkhunaizi, Ranad Shaheen, Sanjay Kumar Bharti, Ann M. Joseph‐George, Karen Chong et al. - American Journal of Medical Genetics Part A, 2018

Cited by 29 OpenAlex

Stable transmission of an unbalanced chromosome 21 derived from chromoanasynthesis in a patient with a SYNGAP1 likely pathogenic variant PDF

Peter Sabatini, Resham Ejaz, Dimitri J. Stavropoulos, Roberto Mendoza‐Londono, Ann M. Joseph‐George - Molecular Cytogenetics, 2018

Cited by 12 OpenAlex

Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay PDF

Mohammed Uddin, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, Lia D’Abate, Daniele Merico et al. - Scientific Reports, 2016

Cited by 47 OpenAlex

Co-occurrence of 16p13.11 microdeletion and ring chromosome 20 syndrome PDF

Lance H. Rodan, Maria Zak, James Stavropoulos, Ann M. Joseph‐George, Berge A. Minassian - Neurology Genetics, 2016

Cited by 1 OpenAlex

PGD for a carrier of an intrachromosomal insertion using aCGH

Claire Jones, Elena Kolomietz, Georges Maire, M. Vlasschaert, Ann M. Joseph‐George et al. - Systems Biology in Reproductive Medicine, 2014

Cited by 6 OpenAlex

MuLV-related endogenous retroviral elements and <i>Flt3</i> participate in aberrant end-joining events that promote B-cell leukemogenesis PDF

Radia Marie Johnson, Eniko Papp, Ildiko Grandal, Paul E. Kowalski, Lauryl M. J. Nutter et al. - Genes & Development, 2014

Cited by 4 OpenAlex

MuLV-related endogenous retroviral elements and Flt3 participate in aberrant end-joining events that promote B-cell leukemogenesis OA

Radia M. Johnson, E. Papp, Ildiko Grandal, P. Kowalski, L. Nutter - Genes & Development, 2014

Cited by 5 Semantic Scholar

Euchromatic 9q13-q21 duplication variants are tandem segmental amplifications of sequence reciprocal to 9q13-q21 deletions

Ann M. Joseph-George, Yongshu He, C. Marshall, Raymond C C Wong, J. MacDonald - Journal of Medical Genetics, 2011

Cited by 11 Semantic Scholar

Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder

Melissa T Carter, S. Nikkel, Bridget A. Fernandez, C. Marshall, A. Noor - Clinical Genetics, 2011

Cited by 73 Semantic Scholar

Research Topics

Genomic variations and chromosomal abnormalities (7) Genomics and Rare Diseases (4) Congenital heart defects research (3) Prenatal Screening and Diagnostics (2) Genetics and Neurodevelopmental Disorders (2)

Frequent Co-Authors

Stephen W. Scherer

4 joint publications

Dimitri J. Stavropoulos

3 joint publications

Jeffrey R. MacDonald

2 joint publications

John Wei

2 joint publications

Mary Shago

2 joint publications

Susan Walker

2 joint publications

Affiliations

University of Toronto

CA 2018 - 2006

Hospital for Sick Children

CA 2018 - 2005

Laboratory of Molecular Genetics

PL 2014 - 2014

SickKids Foundation

CA 2018 - 2005

Toronto Centre for Phenogenomics

CA 2018 - 2018

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Ann M. Joseph‐George

Publication & Citation Trends

Most Cited Works

Publications

MuLV-related endogenous retroviral elements and Flt3 participate in aberrant end-joining events that promote B-cell leukemogenesis OA

Research Topics

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