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Evica Rajcan‐Separovic | Researchclopedia

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Evica Rajcan‐Separovic

97

Works

3,786

Citations

33

h-index

58

i10-index

Research Topics

Genomic variations and chromosomal abnormalities Genetics and Neurodevelopmental Disorders Prenatal Screening and Diagnostics

Affiliations

University of British Columbia Hospital2013–2018

Agriculture and Agri-Food Canada1993–1993

University of British Columbia2003–2022

University of Ottawa1995–1995

Washington State University Spokane2003–2003

Top Works

Oligonucleotide Microarray Analysis of Genomic Imbalance in Children with Mental Retardation

Jan M. Friedman,Ágnes Baross,et al.

2006326 citations

Chromosomal and Genetic Variations

Genomics and Rare Diseases

Expression and Genetic Analysis of XIAP-Associated Factor 1 (XAF1) in Cancer Cell Lines

Wai Gin Fong,Peter Liston,et al.

2000211 citations

Disruption at the <i>PTCHD1</i> Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability

Abdul Noor,Annabel Whibley,et al.

2010194 citations

Non‐muscle myosin heavy chain (MYH9): A new partner fused to ALK in anaplastic large cell lymphoma

Laurence Lamant,Randy D. Gascoyne,et al.

2003132 citations

Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1

Evica Rajcan‐Separovic,Chansonette Harvard,et al.

2006127 citations

Genomic changes detected by array CGH in human embryos with developmental defects

Evica Rajcan‐Separovic,Ying Qiao,et al.

2009117 citations

Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss

Evica Rajcan‐Separovic,Dan Diego‐Álvarez,et al.

2010112 citations

Submicroscopic deletions and duplications in individuals with intellectual disability detected by array‐CGH

Christine Tyson,Chansonette Harvard,et al.

2005107 citations

Autism‐associated familial microdeletion of Xp11.22

Ying Qiao,Xueke Liu,et al.

2008106 citations