Chris Bennett

Deletion 9p and sex reversal.

Chris Bennett, Zoe Docherty, S. Robb et al. · Journal of Medical Genetics · 1993 · 168 citations · Full text

Cytogenetics, Genetics, Deletion 9P +18

A mutation update on the LDS-associated genes<i>TGFB2/3</i>and<i>SMAD2/3</i>

Dorien Schepers, Giada Tortora, Hiroko Morisaki et al. · Human Mutation · 2018 · 160 citations · Full text

Germline <i><scp>SMARCE1</scp></i> mutations predispose to both spinal and cranial clear cell meningiomas

Miriam J. Smith, Andrew J. Wallace, Chris Bennett et al. · The Journal of Pathology · 2014 · 132 citations

Novel mutations and deletions of the KIT (steel factor receptor) gene in human piebaldism.

Kazuhiko Ezoe, Stuart A. Holmes, L. Ho et al. · PubMed · 1995 · 111 citations

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

Anne O’Donnell‐Luria, Lynn Pais, Víctor Faúndes et al. · The American Journal of Human Genetics · 2019 · 97 citations · Full text

Neurodevelopmental Disorders, Developmental Biology, Heterozygous Variants +8