| The ubiquitin ligase UBE3B, disrupted in intellectual disability and absent speech, regulates metabolic pathways by targeting BCKDK S Cheon, K Kaur, N Nijem, IO Tuncay, P Kumar, M Dean, J Juusola, ... Proceedings of the National Academy of Sciences 116 (9), 3662-3667, 2019 | 38 | 2019 |
| KDM5A mutations identified in autism spectrum disorder using forward genetics L El Hayek, IO Tuncay, N Nijem, J Russell, S Ludwig, K Kaur, X Li, ... Elife 9, e56883, 2020 | 35 | 2020 |
| Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants IO Tuncay, NL Parmalee, R Khalil, K Kaur, A Kumar, M Jimale, JL Howe, ... npj Genomic Medicine 7 (1), 13, 2022 | 20 | 2022 |
| The genetics of autism spectrum disorder in an East African familial cohort IO Tuncay, D DeVries, A Gogate, K Kaur, A Kumar, C Xing, K Goodspeed, ... Cell Genomics 3 (7), 2023 | 4 | 2023 |
| Target-enhanced whole-genome sequencing (TE-WGS) shows clinical validity equivalent to commercially available targeted oncology panel S Lee, J Roh, JS Park, IO Tuncay, W Lee, JA Kim, BBL Oh, JY Shin, ... medRxiv, 2023.12. 20.23300156, 2023 | 3 | 2023 |
| Characterizing the genomic landscapes of breast and lung tumors using cost-effective whole genome sequencing H Benjamin, I Soifer, D Shem-Tov, M Levy, IO Tuncay, BL Oh, JY Shin, ... Cancer Research 84 (6_Supplement), 2946-2946, 2024 | | 2024 |
| Investigation of Rare Genetic Variation in Autism Spectrum Disorder by Genomic Screens IO Tuncay | | 2022 |
| Genetics of Autism Spectrum Disorder: Searching for the Rare to Explain the Common IO Tuncay, MH Chahrour Encyclopedia of Behavioral Neuroscience, 2nd Edition 1, 299-306, 2022 | | 2022 |
| Identification and characterization of exonic variants related with familial essential tremor İO Tuncay PQDT-Global, 2017 | | 2017 |
Maria ChahrourThe University of Texas Southwestern Medical Center at Dallas在 utsouthwestern.edu 的电子邮件经过验证
