Jonathan J. Wilde

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

Matthew A. Deardorff, Masashige Bando, Ryuichiro Nakato et al. · Nature · 2012 · 563 citations · Full text

Mendelian Disorder, Cohesin Acetylation Cycle, Genetic Disorder +8

RAD21 Mutations Cause a Human Cohesinopathy

Matthew A. Deardorff, Jonathan J. Wilde, Melanie Albrecht et al. · The American Journal of Human Genetics · 2012 · 267 citations · Full text

Rad21 Mutations Cause, Genetic Disorder, Genetics +4

Microcephaly disease gene Wdr62 regulates mitotic progression of embryonic neural stem cells and brain size

Jian-Fu Chen, Ying Zhang, Jonathan J. Wilde et al. · Nature Communications · 2014 · 151 citations · Full text

Developmental Biology, Brain Development, Medicine +12

Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance

Frank J. Kaiser, Morad Ansari, Diana Braunholz et al. · Human Molecular Genetics · 2014 · 146 citations · Full text

Genetics, Immunodeficiencies, Genetic Epidemiology +27

Efficient embryonic homozygous gene conversion via RAD51-enhanced interhomolog repair

Jonathan J. Wilde, Tomomi Aida, Ricardo C.H. del Rosario et al. · Cell · 2021 · 78 citations · Full text

Genetics, Molecular Biology, Genetic Engineering +3