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Cancer Genetics|November 27, 2012
SNP array and FISH findings in two pleomorphic hyalinizing angiectatic tumorsArezoo Mohajeri, Lars-Gunnar Kindblom, Vaiyapuri P Sumathi, et al.
Genome Medicine|August 10, 2021
Genome-wide sequencing as a first-tier screening test for short tandem repeat expansionsIndhu-Shree Rajan-Babu, Junran J Peng, Readman Chiu, et al.
European Journal of Human Genetics : EJHG|May 22, 2023
Genetic testing in monogenic early-onset atrial fibrillationBrandon Chalazan, Emma Freeth, Arezoo Mohajeri, et al.
American Journal of Medical Genetics. Part A|February 6, 2026
A Novel Gain-of-Function ITPR1 Variant Associated With a Movement Disorder Characterized by Tremor and DystoniaEmilie T Théberge, Bo Sun, Ruiwu Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 26, 2025
The cost and cost trajectory of genome sequencing and bioinformatics analysis for Indigenous children with suspected rare diseasesMorgan Ehman, Kartik Sharma, Deirdre Weymann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 24, 2025
Disco-Interacting Protein 2 Homolog B CGG Repeat Expansion in Siblings with Neurodevelopmental Disability and Progressive Movement DisorderEmilie T Théberge, Kate Durbano, Diane Demailly, et al.
Genes, Chromosomes & Cancer|June 14, 2013
Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumorArezoo Mohajeri, Johnbosco Tayebwa, Anna Collin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2026
Mutations in VCP cause Adams-Oliver syndrome with or without pulmonary hypertensionAnna Lehman, Sana Ahmed, Arezoo Mohajeri, et al.
Journal of Medical Genetics|June 14, 2023
Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delayArezoo Mohajeri, Maryam Vaseghi-Shanjani, Jill A Rosenfeld, et al.
Journal of Clinical Immunology|April 28, 2025
A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHADHenry Y Lu, Maryam Vaseghi-Shanjani, Avery J Lam, et al.
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