Dominant Mutations in KAT6A Cause Intellectual Disability with Recognizable Syndromic Features

Genome sequencing identifies major causes of severe intellectual disability

Christian Gilissen, Jayne Y. Hehir‐Kwa, Djie Tjwan Thung et al. · Nature · 2014 · 1.1K citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein

Julian Borrow, Vincent P. Stanton, J. Michael Andresen et al. · Nature Genetics · 1996 · 777 citations

Life Sciences, Molecular Biology, Molecular Genetics +11

Activation of AML1‐mediated transcription by MOZ and inhibition by the MOZ–CBP fusion protein

Issay Kitabayashi · The EMBO Journal · 2001 · 232 citations · Full text

Medicine, Genetics, Molecular Biology +10

MOZ is essential for maintenance of hematopoietic stem cells

Takuo Katsumoto, Yukiko Aikawa, Atsushi Iwama et al. · Genes & Development · 2006 · 217 citations · Full text

Life Sciences, Developmental Biology, Genetics +17

Whole-Exome-Sequencing Identifies Mutations in Histone Acetyltransferase Gene KAT6B in Individuals with the Say-Barber-Biesecker Variant of Ohdo Syndrome

Jill Clayton‐Smith, James O’Sullivan, Sarah B. Daly et al. · The American Journal of Human Genetics · 2011 · 184 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9