Brian P. Chadwick

Tissue-Specific Expression of a Splicing Mutation in the Gene Causes Familial Dysautonomia

Susan A. Slaugenhaupt, Anat Blumenfeld, Sandra Gill et al. · The American Journal of Human Genetics · 2001 · 593 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

A unified phylogeny-based nomenclature for histone variants

Paul B. Talbert, Kami Ahmad, Geneviève Almouzni et al. · Epigenetics & Chromatin · 2012 · 339 citations · Full text

Deletion of <i>DXZ4</i> on the human inactive X chromosome alters higher-order genome architecture

Emily M. Darrow, Miriam Huntley, Olga Dudchenko et al. · Proceedings of the National Academy of Sciences · 2016 · 281 citations · Full text

Genetics, Genomic Mechanism, Molecular Biology +17

Ring1b-mediated H2A Ubiquitination Associates with Inactive X Chromosomes and Is Involved in Initiation of X Inactivation

Jia Fang, Taiping Chen, Brian P. Chadwick et al. · Journal of Biological Chemistry · 2004 · 240 citations · Full text

Histone Modifications, Inactive X Chromosomes, Epigenetic Change +21

Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome

Brian P. Chadwick, Huntington F. Willard · Proceedings of the National Academy of Sciences · 2004 · 233 citations

Histone Modifications, Epigenetic Change, Genetics +20