Biblio

Found 3 results
Filters: Author is Meili, Fabian  [Clear All Filters]
2021
Meili F, Wei WJ, Sin W-C, Meyers WM, Dascalu I, Callaghan DB, Rogic S, Pavlidis P, Haas K.  2021.  Multi-parametric analysis of 57 SYNGAP1 variants reveal impacts on GTPase signaling, localization, and protein stability.. Am J Hum Genet. 108(1):148-162.
2020
Post KL, Belmadani M, Ganguly P, Meili F, Dingwall R, McDiarmid TA, Meyers WM, Herrington C, Young BP, Callaghan DB et al..  2020.  Multi-model functionalization of disease-associated PTEN missense mutations identifies multiple molecular mechanisms underlying protein dysfunction.. Nat Commun. 11(1):2073.
McDiarmid TA, Belmadani M, Liang J, Meili F, Mathews EA, Mullen GP, Hendi A, Wong W-R, Rand JB, Mizumoto K et al..  2020.  Systematic phenomics analysis of autism-associated genes reveals parallel networks underlying reversible impairments in habituation.. Proc Natl Acad Sci U S A. 117(1):656-667.