Jila Dastan

Hospital for Sick Children — Canada

Biochemistry, Genetics and Molecular Biology · Life Sciences

9h-index330citations21works0.02yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(9), Congenital heart defects research(5), Prenatal Screening and Diagnostics(3), Cervical Cancer and HPV Research(2), Chromosomal and Genetic Variations(2)

Publications21 total

Segregating patterns of copy number variations in extended autism spectrum disorder (<scp>ASD</scp>) pedigrees
American Journal of Medical Genetics Part B Neuropsychiatric Genetics·2020· 11 citedOpen Access
Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplication
BMC Medical Genetics·2016· 50 citedOpen Access
Exome sequencing for understanding phenotypic variability in subjects with 16p11.2 CNV
Open Collections·2016Open Access
MG-138 Co-occurrence of cohen syndrome with 16p11.2 duplication: The exome sequencing approach
2015
Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID)
BMC Medical Genetics·2014· 14 citedOpen Access
"Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes
Molecular Cytogenetics·2012· 8 citedOpen Access
"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements
Molecular Cytogenetics·2012· 4 citedOpen Access
First‐trimester screening for chromosomal abnormalities by integrated application of nuchal translucency, nasal bone, tricuspid regurgitation and ductus venosus flow combined with maternal serum free β‐hCG and PAPP‐A: a 5‐year prospective study
Ultrasound in Obstetrics and Gynecology·2011· 51 citedOpen Access
Investigation of QF-PCR Application for Rapid Prenatal Diagnosis of Chromosomal Aneuploidies in Iranian Population.
PubMed·2011· 6 citedOpen Access
Tracing Human Papilloma Virus in Breast Tumors of Iranian Breast Cancer Patients
The Breast Journal·2011· 9 cited
Her2 amplification status in Iranian breast cancer patients: comparison of immunohistochemistry (IHC) and fluorescence in situ hybridisation (FISH).
PubMed·2011· 13 cited
A novel truncating mutation in the E-cadherin gene in the first Iranian family with hereditary diffuse gastric cancer
European Journal of Surgical Oncology·2010· 20 cited
Molecular cytogenetic analysis of urothelial carcinomas using urine samples.
PubMed·2009· 1 cited
Comparative genomic hybridization (CGH) analysis of chromosomal aberrations in Iranian patients with invasive ductal carcinoma breast cancer.
PubMed·2009· 4 cited
MICRODELETION STUDY IN CHILDREN WITH SELECTIVE CONGENITAL HEART DISEASE; AN IRANIAN MULTICENTER STUDY
TSpace·2009· 2 cited
Hematological Indices of Parents in Non-Immune Hydrops Fetalis Pregnancie
SHILAP Revista de lepidopterología·2008Open Access
Chromosomal radiosensitivity in patients with common variable immunodeficiency
Immunobiology·2008· 59 cited
Investigation of RBC Indices and HbA2 Levels in Parents of Beta-Thalassemia Patients: Impacts on Premarital Genetic Counseling
SHILAP Revista de lepidopterología·2007Open Access
Prevalence of human papillomavirus genotypes in women with normal and abnormal cervical cytology in Iran.
PubMed·2007· 71 cited
Combining mammaglobin and carcinoembryonic mRNA markers for early detection of micrometastases from breast cancers--a molecular study of 59 patients.
PubMed·2007· 7 cited
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Frequent Co-authors

Saeed Reza Ghaffari(12), Tayebeh Sabokbar(10), Maryam Rafati(7), Mohammad Ali Mohagheghi(4), Ying Qiao(3), Evica Rajcan‐Separovic(3), M. E. Suzanne Lewis(3), Alireza Mosavi-Jarrahi(3), Abdolvahab Moradi(2), Asghar Aghamohammadi(2), L. Eslamian(2), Shirin Moossavi(2), Chieko Chijiwa(2), Flamingo Tang(2), Mohammad R Ghadirzadeh(2), Yaser Heshmati(2), Homeira Adibi(2), Zarrintaj Keihanidoust(2), Mohammad Reza Eshraghian(2), Azadeh Hoseini(2)