Author

Hugo J. Bellen

Institutions: Baylor College of Medicine, Texas Children's Hospital

Observed institutions: Howard Hughes Medical Institute, Baylor College of Medicine, Texas Children's Hospital

OpenAlex ID: A5123193402

A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3

2016 · Hsiao-Tuan Chao, Mariska Davids, et al. · The American Journal of Human Genetics · 115

Bi-allelic variants in the secretory pathway gene SEC16A are associated with a neurodevelopmental disorder

2026 · Mengqi Ma, Xiaowei Lei, et al. · Journal of Clinical Investigation

Uncovering phenotypic expansion in AXIN2-related disorders through precision animal modeling

2026 · Nathalie M. Aceves-Ewing, Denise G. Lanza, et al. · Genetics in Medicine

Works count: 4

Citation count: 115

H-index: 1

I10-index: 1