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Cell Genomics|July 26, 2023
The genetics of autism spectrum disorder in an East African familial cohortIslam Oguz Tuncay, Darlene DeVries, Ashlesha Gogate, et al.
NPJ Genomic Medicine|October 10, 2025
Whole genome sequencing in adolescent idiopathic scoliosis cohort implicates multiple biological pathwaysIslam Oguz Tuncay, Eun Kyoung Lee, Anxhela Gustafson, et al.
International Journal of Molecular Sciences|November 27, 2025
Cryopreserved Tissue Biospecimens Offer Superior Quality for Whole-Genome Sequencing of Various Cancers Compared to Paired Formalin-Fixed Paraffin-Embedded TissuesKen Dixon, Jeong-Hoon Lee, Ryan Miller, et al.
NPJ Genomic Medicine|February 22, 2022
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variantsIslam Oguz Tuncay, Nancy L Parmalee, Raida Khalil, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 2019
The ubiquitin ligase UBE3B, disrupted in intellectual disability and absent speech, regulates metabolic pathways by targeting BCKDKSolmi Cheon, Kiran Kaur, Nadine Nijem, et al.
Cancer Research and Treatment|September 20, 2024
Target-Enhanced Whole-Genome Sequencing Shows Clinical Validity Equivalent to Commercially Available Targeted Oncology PanelSangmoon Lee, Jin Roh, Jun Sung Park, et al.
Elife|December 22, 2020
KDM5A mutations identified in autism spectrum disorder using forward geneticsLauretta El Hayek, Islam Oguz Tuncay, Nadine Nijem, et al.
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