Mojarad, Bahareh A.
Hospital for Sick Children
4 papers on CoChatORCID 0000-0003-1943-9163
Most cited papers
- Verified
A Dynamic Protein Interaction Landscape of the Human Centrosome-Cilium Interface
Gupta, G. D., Coyaud, É., Gonçalves, J., Mojarad, B. A., Liu, Y., Wu, Q., Gheiratmand, L., Comartin, D., Tkach, J. M., Cheung, S. W. T., et al. (2015) · Cell
Genetic and Kidney Cyst DiseasesBiotin and Related Studies
Cited by 538
- Verified
Genome-wide detection of tandem DNA repeats that are expanded in autism
Trost, B., Engchuan, W., Nguyen, C. M., Thiruvahindrapuram, B., Dolzhenko, E., Backstrom, I., Mirceta, M., Mojarad, B. A., Yin, Y., Dov, A., et al. (2020) · Nature
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 238
- Verified
A large data resource of genomic copy number variation across neurodevelopmental disorders
Zarrei, M., Burton, C. L., Engchuan, W., Young, E. J., Higginbotham, E. J., MacDonald, J. R., Trost, B., Chan, A. J. S., Walker, S., Lamoureux, S., et al. (2019) · npj Genomic Medicine
Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders
Cited by 187
- Verified
Genes and pathways implicated in tetralogy of Fallot revealed by ultra-rare variant burden analysis in 231 genome sequences
Manshaei, R., Merico, D., Reuter, M. S., Engchuan, W., Mojarad, B. A., Chaturvedi, R., Heung, T., Pellecchia, G., Zarrei, M., Nalpathamkalam, T., et al. (2020) · Frontiers in Genetics
Genomics and Rare DiseasesCongenital heart defects research
Cited by 36
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