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American Journal of Human Genetics|December 20, 2011
Mutations in EZH2 cause Weaver syndromeWilliam T Gibson, Rebecca L Hood, Shing Hei Zhan, et al.Clinical Epigenetics|December 21, 2022
Transient Polycomb activity represses developmental genes in growing oocytesEllen G Jarred, Zhipeng Qu, Tesha Tsai, et al.Developmental Cell|March 10, 2023
Activation of β-catenin in mesenchymal progenitors leads to muscle mass lossNasim Kajabadi, Marcela Low, Erik Jacques, et al.Transplant Infectious Disease : an Official Journal of the Transplantation Society|June 26, 2020
COVID-19 in recent heart transplant recipients: Clinicopathologic features and early outcomesBrian Lima, Gregory T Gibson, Sirish Vullaganti, et al.Orphanet Journal of Rare Diseases|August 26, 2015
Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumoursSarah F Barclay, Casey M Rand, Lauren A Borch, et al.Plos One|May 2, 2015
Vasoactive intestinal polypeptide promotes intestinal barrier homeostasis and protection against colitis in miceXiujuan Wu, Victoria S Conlin, Vijay Morampudi, et al.Nature Chemistry|March 14, 2026
Spontaneous trisulfide metathesis in polar aprotic solventsHarshal D Patel, Alfrets D Tikoalu, James N Smith, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|June 2, 2018
The Jamaican Haemophilia Registry: Describing the burden of diseaseG Wharfe, L Buchner-Daley, T Gibson, et al.Human Mutation|December 24, 2015
Weaver Syndrome-Associated EZH2 Protein Variants Show Impaired Histone Methyltransferase Function In VitroAna S A Cohen, Damian B Yap, M E Suzanne Lewis, et al.American Journal of Medical Genetics. Part A|June 7, 2014
Somatic mosaicism for the p.His1047Arg mutation in PIK3CA in a girl with mesenteric lipomatosisAna S A Cohen, Katelin N Townsend, Qing-San Xiang, et al.Pageof 68