Associated Papers
ZMYND11 Restrains KMT2A to Enable a Neuronal Developmental Program.
Greben AW et al.
Biorxiv : the Preprint Server for Biology, 2025
41279818 (PubMed )
Supplement: media-1.pdf
ZMYND11 functions in bimodal regulation of latent genes and brain-like splicing to safeguard corticogenesis.
Chang X et al.
Nature Communications, 2025
Probing the biological consequences of a previously undescribed de novo mutation of ZMYND11 in a schizophrenia patient by CRISPR genome editing and induced pluripotent stem cell based in vitro disease-modeling.
Tordai C et al.
Schizophrenia Research, 2024
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Wang T et al.
Nature Communications, 2020
33004838 (PubMed )
Supplement: 41467_2020_18723_MOESM10_ESM.xlsx › Supplementary_Data_8
ZMYND11-related syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum.
Yates TM et al.
Human Mutation, 2020
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