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Ann M. Joseph‐George
Observed names:
AM Joseph-George,
Ann M Joseph-George,
Ann M. Joseph-George
Institutions:
St. Michael's Hospital,
University Health Network,
University of Toronto,
Hospital for Sick Children,
Centre for Applied Genomics
Observed institutions:
St. Michael's Hospital,
University Health Network,
University of Toronto,
Hospital for Sick Children,
MaRS,
Centre for Applied Genomics
show all 6
OpenAlex ID:
A5041018207
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
2009
·
Bridget A Fernandez
, Wendy Roberts
, et al.
·
Journal of Medical Genetics
·
334
Genome assembly comparison identifies structural variants in the human genome
2006
·
Razi Khaja
, Junjun Zhang
, et al.
·
Nature Genetics
·
166
Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder
2010
·
MT Carter
, SM Nikkel
, et al.
·
Clinical Genetics
·
77
The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants
2018
·
Miriam S. Reuter
, Susan Walker
, et al.
·
Canadian Medical Association Journal
·
61
PDF
Euchromatic 9q13-q21 duplication variants are tandem segmental amplifications of sequence reciprocal to 9q13-q21 deletions
2011
·
Ann M Joseph-George
, Yongshu He
, et al.
·
Journal of Medical Genetics
·
47
Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay
2016
·
Mohammed Uddin
, Giovanna Pellecchia
, et al.
·
Scientific Reports
·
44
PDF
Warsaw breakage syndrome: Further clinical and genetic delineation
2018
·
Ebba Alkhunaizi
, Ranad Shaheen
, et al.
·
American Journal of Medical Genetics Part A
·
34
Stable transmission of an unbalanced chromosome 21 derived from chromoanasynthesis in a patient with a SYNGAP1 likely pathogenic variant
2018
·
Peter J. B. Sabatini
, Resham Ejaz
, et al.
·
Molecular Cytogenetics
·
13
PDF
Complete functional rescue of the ABCA1−/− mouse by human BAC transgenesis
2005
·
Jonathan M. Coutinho
, Roshni R. Singaraja
, et al.
·
Journal of Lipid Research
·
11
Williams-Beuren Syndrome Diagnosis Using Fluorescence In Situ Hybridization
2006
·
Lucy R. Osborne
, Ann M. Joseph-George
, et al.
·
Congenital Heart Disease
·
9
PGD for a carrier of an intrachromosomal insertion using aCGH
2014
·
Claire Ann Jones
, Elena Kolomietz
, et al.
·
Systems Biology in Reproductive Medicine
·
6
PDF
MuLV-related endogenous retroviral elements and Flt3 participate in aberrant end-joining events that promote B-cell leukemogenesis
2014
·
Radia M. Johnson
, Eniko Papp
, et al.
·
Genes & Development
·
4
PDF
Co-occurrence of 16p13.11 microdeletion and ring chromosome 20 syndrome
2016
·
Lance H. Rodan
, Maria Zak
, et al.
·
Neurology Genetics
·
2
PDF
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Works count:
13
Citation count:
808
H-index:
9
I10-index:
9
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