| 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 | 540 | 2015 |
| 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 | 178 | 2020 |
| 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 | 149 | 2019 |
| 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 | 54 | 2013 |
| 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 | 48 | 2017 |
| 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 | 34 | 2020 |
| 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 | 30 | 2022 |
| 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 | 21 | 2021 |
| 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, ... | 13 | 2019 |
| 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 | 6 | 2023 |
| Genetics and Epigenetics of ASD BA Mojarad, F Qaiser, RKC Yuen Neurodevelopmental Pediatrics: Genetic and Environmental Influences, 293-307, 2023 | 2 | 2023 |
| 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 | 2 | 2023 |
| 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 |
| 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 |
Gagan D. GuptaToronto Metropolitan University在 torontomu.ca 的电子邮件经过验证
