Associated Papers
Functional analysis of human EED variants using Drosophila.
Cyrus SS et al.
Genetics, 2025
EED related overgrowth: First report of multiple members in a single family.
Goel H et al.
American Journal of Medical Genetics. Part A, 2024
The engagement of histone lysine methyltransferases with nucleosomes: structural basis, regulatory mechanisms, and therapeutic implications.
Li Y et al.
Protein & Cell, 2023
PRC2-complex related dysfunction in overgrowth syndromes: A review of EZH2, EED, and SUZ12 and their syndromic phenotypes.
Cyrus S et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2019
Three additional patients with EED-associated overgrowth: potential mutation hotspots identified?
Spellicy CJ et al.
Journal of Human Genetics, 2019
EED and EZH2 constitutive variants: A study to expand the Cohen-Gibson syndrome phenotype and contrast it with Weaver syndrome.
Griffiths S et al.
American Journal of Medical Genetics. Part A, 2019
Novel de novo mutation affecting two adjacent aminoacids in the EED gene in a patient with Weaver syndrome.
Smigiel R et al.
Journal of Human Genetics, 2018
Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome.
Imagawa E et al.
Human Mutation, 2017
EED-associated overgrowth in a second male patient.
Cohen AS et al.
Journal of Human Genetics, 2016
Select a paper to view details