Common genetic variation in the Angelman syndrome imprinting centre affects the imprinting of chromosome 15

Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith–Wiedemann locus

(2019) Federica Maria Valente et al.   GENETICS IN MEDICINE

Disruption of KCNQ1 prevents methylation of the ICR2 and supports the hypothesis that its transcription is necessary for imprint establishment

(2019) Jasmin Beygo et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains

(2018) David Monk et al.   Epigenetics

Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR

(2018) Keiichiro Joh et al.   Epigenetics & Chromatin

A mouse model of angelman syndrome imprinting defects

(2018) Michael W Lewis et al.   HUMAN MOLECULAR GENETICS

Transcription-driven DNA methylation setting on the mouse Peg3 locus

(2017) Corey L. Bretz et al.   Epigenetics

A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome

(2016) Jasmin Beygo et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Specification and epigenetic programming of the human germ line

(2016) Walfred W. C. Tang et al.   NATURE REVIEWS GENETICS

Angelman syndrome — insights into a rare neurogenetic disorder

(2016) Karin Buiting et al.   Nature Reviews Neurology

Angelman syndrome imprinting center encodes a transcriptional promoter

(2014) Michael W. Lewis et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The Sox Family of Transcription Factors: Versatile Regulators of Stem and Progenitor Cell Fate

(2013) Abby Sarkar et al.   Cell Stem Cell

Transcription Is Required to Establish Maternal Imprinting at the Prader-Willi Syndrome and Angelman Syndrome Locus

(2011) Emily Y. Smith et al.   PLoS Genetics

Transcription is required for establishment of germline methylation marks at imprinted genes

(2009) M. Chotalia et al.   GENES & DEVELOPMENT

Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domain

(2009) Y. Kaufman et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA