Galina N. Filippova

A Single-Cell Atlas of In Vivo Mammalian Chromatin Accessibility

Darren A. Cusanovich, Andrew J. Hill, Delasa Aghamirzaie et al. · Cell · 2018 · 866 citations · Full text

Chromatin, Chromatin Structure, Chromatin Remodeling +10

Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

Richard J.L.F. Lemmers, Rabi Tawil, Lisa M. Petek et al. · Nature Genetics · 2012 · 641 citations · Full text

Rare Diseases, Developmental Biology, Mendelian Disorder +10

An Exceptionally Conserved Transcriptional Repressor, CTCF, Employs Different Combinations of Zinc Fingers To Bind Diverged Promoter Sequences of Avian and Mammalian c-<i>myc</i> Oncogenes

Galina N. Filippova, Sara R. Fagerlie, Elena Klenova et al. · Molecular and Cellular Biology · 1996 · 547 citations · Full text

Diverged Promoter Sequences, Genetics, Gene Characterization +17

CTCF physically links cohesin to chromatin

Eric D. Rubio, David J. Reiss, Piri Welcsh et al. · Proceedings of the National Academy of Sciences · 2008 · 497 citations · Full text

Ctcf-binding Site Distribution, Genetics, Genomic Mechanism +18

Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene

Lauren Snider, Linda N. Geng, Richard J.L.F. Lemmers et al. · PLoS Genetics · 2010 · 479 citations · Full text

Skeletal Muscle Cells, Transcriptional Regulation, Mendelian Disorder +12