Matthew A. Deardorff

Transcriptional Dysregulation in NIPBL and Cohesin Mutant Human Cells

Zhe Zhang, Katsuhiko Shirahige, Nancy B. Spinner, 2009, PLoS biology.

A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay

Deborah L. Levy, Gregory M. Cooper, Brian L. Browning, 2010, Nature Genetics.

Precision therapy for a new disorder of AMPA receptor recycling due to mutations in ATAD1

Erica Ma, Eric D. Marsh, Neal Sondheimer, 2017, Neurology: Genetics.

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .

HDAC8 mutations in Cornelia de Lange Syndrome affect the cohesin acetylation cycle

Gabriele Gillessen-Kaesbach, Ryuichiro Nakato, Katsuhiko Shirahige, 2012, Nature.