Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants. Human Genetics and Genomics Advances, (3)4:100131, 2022. [PUMA: developmental variant, disease molecular encephalopathy, electrophysiology, Diseases simulations, personalized structural rare dynamics interpretation, epileptic KCNC2, and topic_lifescience DEE, variant Network, Undiagnosed biology,] URL
Identifying digenic disease genes via machine learning in the Undiagnosed Diseases Network. Am. J. Hum. Genet., (108)10:1946--1963, Elsevier BV, October 2021. [PUMA: disease; prediction; disease learning; Network; oligogenic Diseases clinical digenic rare machine topic_lifescience Undiagnosed UDN;]