Year |
Citation |
Score |
2023 |
Tuncay IO, DeVries D, Gogate A, Kaur K, Kumar A, Xing C, Goodspeed K, Seyoum-Tesfa L, Chahrour MH. The genetics of autism spectrum disorder in an East African familial cohort. Cell Genomics. 3: 100322. PMID 37492102 DOI: 10.1016/j.xgen.2023.100322 |
0.599 |
|
2022 |
Tuncay IO, Parmalee NL, Khalil R, Kaur K, Kumar A, Jimale M, Howe JL, Goodspeed K, Evans P, Alzghoul L, Xing C, Scherer SW, Chahrour MH. Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants. Npj Genomic Medicine. 7: 13. PMID 35190550 DOI: 10.1038/s41525-022-00284-2 |
0.611 |
|
2020 |
El Hayek L, Tuncay IO, Nijem N, Russell J, Ludwig S, Kaur K, Li X, Anderton P, Tang M, Gerard A, Heinze A, Zacher P, Alsaif HS, Rad A, Hassanpour K, et al. mutations identified in autism spectrum disorder using forward genetics. Elife. 9. PMID 33350388 DOI: 10.7554/eLife.56883 |
0.627 |
|
2019 |
Cheon S, Kaur K, Nijem N, Tuncay IO, Kumar P, Dean M, Juusola J, Guillen-Sacoto MJ, Bedoukian E, Ierardi-Curto L, Kaplan P, Schaefer GB, Mishra P, Chahrour MH. The ubiquitin ligase UBE3B, disrupted in intellectual disability and absent speech, regulates metabolic pathways by targeting BCKDK. Proceedings of the National Academy of Sciences of the United States of America. 116: 3662-3667. PMID 30808755 DOI: 10.1073/pnas.1818751116 |
0.518 |
|
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