Charis Eng
Affiliations: | Ohio State University, Columbus, Columbus, OH |
Area:
Genetics, Molecular BiologyGoogle:
"Charis Eng"
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Publications
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| Kang SC, Sarn NB, Venegas J, et al. (2023) Germline PTEN genotype-dependent phenotypic divergence during the early neural developmental process of forebrain organoids. Molecular Psychiatry |
| Dhawan A, Eng C. (2023) Is the gene mutation associated with thrombosis? Cleveland Clinic Journal of Medicine. 90: 661-663 |
| Hitomi M, Venegas J, Kang SC, et al. (2023) Differential cell cycle checkpoint evasion by PTEN germline mutations associated with dichotomous phenotypes of cancer versus autism spectrum disorder. Oncogene |
| Xiong D, Zhao J, Qiu Y, et al. (2023) 3D structural human interactome reveals proteome-wide perturbations by disease mutations. Biorxiv : the Preprint Server For Biology |
| Miller KM, Sbeih F, Contrera K, et al. (2023) Reduced Risk of Corporal Tumors in Patients With Head and Neck Paragangliomas With p.Pro81Leu Mutations. Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery |
| Smith IN, Dawson JE, Eng C. (2023) Comparative Protein Structural Network Analysis Reveals C-Terminal Tail Phosphorylation Structural Communication Fingerprint in -Associated Mutations in Autism and Cancer. The Journal of Physical Chemistry. B |
| Chen JL, Miller DT, Schmidt LS, et al. (2022) Mosaicism in Tumor Suppressor Gene Syndromes: Prevalence, Diagnostic Strategies, and Transmission Risk. Annual Review of Genomics and Human Genetics. 23: 331-361 |
| Brewer T, Yehia L, Bazeley P, et al. (2022) Exome sequencing reveals a distinct somatic genomic landscape in breast cancer from women with germline PTEN variants. American Journal of Human Genetics. 109: 1520-1533 |
| Ramkumar RR, Murthy PB, Nguyen JK, et al. (2020) PTEN Hamartoma Tumor Syndrome: A Case of Renal Cell Carcinoma in a Young Female. Urology |
| Kotsopoulos J, Gronwald J, McCuaig JM, et al. (2020) Breastfeeding and the risk of epithelial ovarian cancer among women with a BRCA1 or BRCA2 mutation. Gynecologic Oncology |