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bahareh A. Mojarad
bahareh A. Mojarad
University of Toronto
Verified email at wustl.edu
Title
Cited by
Cited by
Year
A dynamic protein interaction landscape of the human centrosome-cilium interface
GD Gupta, É Coyaud, J Gonçalves, BA Mojarad, Y Liu, Q Wu, ...
Cell 163 (6), 1484-1499, 2015
5322015
Genome-wide detection of tandem DNA repeats that are expanded in autism
B Trost, W Engchuan, CM Nguyen, B Thiruvahindrapuram, E Dolzhenko, ...
Nature 586 (7827), 80-86, 2020
1672020
A large data resource of genomic copy number variation across neurodevelopmental disorders
M Zarrei, CL Burton, W Engchuan, EJ Young, EJ Higginbotham, ...
NPJ genomic medicine 4 (1), 26, 2019
1462019
ISL1 protein transduction promotes cardiomyocyte differentiation from human embryonic stem cells
H Fonoudi, M Yeganeh, F Fattahi, Z Ghazizadeh, H Rassouli, M Alikhani, ...
PLoS One 8 (1), e55577, 2013
532013
CEP19 cooperates with FOP and CEP350 to drive early steps in the ciliogenesis programme
BA Mojarad, GD Gupta, M Hasegan, O Goudiam, R Basto, AC Gingras, ...
Open biology 7 (6), 170114, 2017
472017
Genome-wide tandem repeat expansions contribute to schizophrenia risk
BA Mojarad, W Engchuan, B Trost, I Backstrom, Y Yin, ...
Molecular Psychiatry 27 (9), 3692-3698, 2022
282022
Genes and pathways implicated in tetralogy of Fallot revealed by ultra-rare variant burden analysis in 231 genome sequences
R Manshaei, D Merico, MS Reuter, W Engchuan, BA Mojarad, ...
Frontiers in genetics 11, 957, 2020
282020
Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia
BA Mojarad, Y Yin, R Manshaei, I Backstrom, G Costain, T Heung, ...
Translational Psychiatry 11 (1), 84, 2021
202021
A large data resource of genomic copy number variation across neurodevelopmental disorders. NPJ Genom. Med. 4, 26
M Zarrei, CL Burton, W Engchuan, EJ Young, EJ Higginbotham, ...
122019
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data
T Hartley, É Soubry, M Acker, M Osmond, M Couse, MK Gillespie, Y Ito, ...
Clinical genetics 103 (3), 288-300, 2023
52023
Genetics and Epigenetics of ASD
BA Mojarad, F Qaiser, RKC Yuen
Neurodevelopmental Pediatrics: Genetic and Environmental Influences, 293-307, 2023
12023
Clinical whole-genome sequencing and FISH identify two different fusion partners for NUP98 in a patient with acute myeloid leukemia: A case report
BA Mojarad, ZD Crees, MC Schroeder, Z Xiang, J Vader, J Sina, ...
Cancer genetics 280, 1-5, 2024
2024
Profiling PIK3CA variants in disorders of somatic mosaicism
BA Mojarad, PV Hernandez, MJ Evenson, MM Corliss, SL Stein, A Theos, ...
Genetics in Medicine Open 1 (1), 100815, 2023
2023
P515: A somatic pathogenic variant in PTPN11 in a patient with vascular malformation and hemihypertrophy
B Mojarad, S Fishman, K King, B Sisk, J Neidich
Genetics in Medicine Open 1 (1), 2023
2023
105. Clinical whole-genome sequencing identifies NSD3 as the correct fusion partner of NUP98 in a patient with acute myeloid
B Mojarad, Z Crees, M Schroeder, Z Xiang, J Vader, J Sina, J Frater, ...
Cancer Genetics 268, 33-34, 2022
2022
Comparison of PIK3CA Genetic Variation Specific to Disorders of Somatic Mosaicism (DoSM) and Variants Associated with Neoplasms
P Hernandez, B Mojarad, M Evenson, M Corliss, M Schroeder, K Bowling, ...
JOURNAL OF MOLECULAR DIAGNOSTICS 24 (10), S10-S10, 2022
2022
eP378: A 9-year, single-institution retrospective study of chromosomal microarray analysis data obtained from products of conception
B Mojarad, M Zaydman, J Neidich, M Schroeder, Y Cao, K Krysiak, ...
Genetics in Medicine 24 (3), S237-S238, 2022
2022
Clinical Whole-Genome Sequencing Identifies Nsd3 as the Correct Fusion Partner of Nup98 in a Patient with Acute Myeloid Leukemia and T (8; 11)(P11. 2; P15)
BA Mojarad, ZD Crees, MC Schroeder, Z Xiang, J Vader, J Sina, J Frater, ...
Available at SSRN 4223022, 2022
2022
Determination of disease-associated genes and gene-sets in Tetralogy of Fallot
R Manshaei, MS Reuter, BA Mojarad, G Pellecchia, M Zarrei, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1330-1331, 2019
2019
Biogenesis and Function of Human Centriolar Appendages
B Adhamimojarad
University of Toronto (Canada), 2018
2018
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Articles 1–20