Scott E. Hickey

Scott E. Hickey's research centers on clinical and molecular genetics, particularly identifying and characterizing rare genetic syndromes that cause developmental disabilities, craniofacial differences (such as cleft palate), and congenital heart defects. This work often involves describing new disease-causing gene variants and their associated clinical features to improve diagnosis, and also touches on genomic sequencing technology and methods for detecting genetic variation.

Publication output has grown from a handful of papers per year in 2017-2019 to a steadier pace of roughly 8-11 papers annually from 2021 onward, suggesting a generally increasing to stable level of activity over the past decade.

Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026