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European Journal of Human Genetics : EJHG|March 2, 2012
Diagnosis by sequencing: correction of misdiagnosis from FSHD2 to LGMD2A by whole-exome analysisAndreas Leidenroth, Hanne Sørmo Sorte, Gregor Gilfillan, et al.
Biochimica Et Biophysica Acta|January 24, 2007
RNAPol-ChIP analysis of transcription from FSHD-linked tandem repeats and satellite DNAVassilios Alexiadis, Mary E Ballestas, Cecilia Sanchez, et al.
Epigenetics|March 3, 2018
Developmentally linked human DNA hypermethylation is associated with down-modulation, repression, and upregulation of transcriptionCarl Baribault, Kenneth C Ehrlich, V K Chaithanya Ponnaluri, et al.
Chromosoma|April 28, 2005
Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cellsDavid Gisselsson, Chunbo Shao, Cathy M Tuck-Muller, et al.
Epigenomes|December 22, 2022
Promoter-Adjacent DNA Hypermethylation Can Downmodulate Gene Expression: <i>TBX15</i> in the Muscle LineageKenneth C Ehrlich, Michelle Lacey, Carl Baribault, et al.
Epigenomes|February 23, 2024
Epigenetics of Genes Preferentially Expressed in Dissimilar Cell Populations: Myoblasts and CerebellumMelanie Ehrlich, Kenneth C Ehrlich, Michelle Lacey, et al.
Plos One|November 19, 2011
DNA replication timing is maintained genome-wide in primary human myoblasts independent of D4Z4 contraction in FSH muscular dystrophyBenjamin D Pope, Koji Tsumagari, Dana Battaglia, et al.
Epigenetics|March 28, 2014
Notch signaling genes: myogenic DNA hypomethylation and 5-hydroxymethylcytosineJolyon Terragni, Guoqiang Zhang, Zhiyi Sun, et al.
Epigenetics|December 3, 2016
Association of 5-hydroxymethylation and 5-methylation of DNA cytosine with tissue-specific gene expressionV K Chaithanya Ponnaluri, Kenneth C Ehrlich, Guoqiang Zhang, et al.
Human Molecular Genetics|September 25, 2003
Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4qGuanchao Jiang, Fan Yang, Petra G M van Overveld, et al.
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