Megha Desai

p66α–MBD2 coiled-coil interaction and recruitment of Mi-2 are critical for globin gene silencing by the MBD2–NuRD complex

Merlin Nithya Gnanapragasam, J.N. Scarsdale, Maria L. Amaya et al. · Proceedings of the National Academy of Sciences · 2011 · 143 citations · Full text

Mi2β-mediated silencing of the fetal γ-globin gene in adult erythroid cells

Maria L. Amaya, Megha Desai, Merlin Nithya Gnanapragasam et al. · Blood · 2013 · 110 citations

An intrinsically disordered region of methyl-CpG binding domain protein 2 (MBD2) recruits the histone deacetylase core of the NuRD complex

Megha Desai, Heather Webb, Leander M. Sinanan et al. · Nucleic Acids Research · 2015 · 92 citations · Full text

Nurd Complex, Mbd2-nurd Complex, Epigenetic Change +18

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

Francesca Clementina Radio, Kaifang Pang, Andrea Ciolfi et al. · The American Journal of Human Genetics · 2021 · 80 citations · Full text

Down Syndrome, Deletion Syndrome, Developmental Biology +11

Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability

Benjamin Cogné, Sophie Ehresmann, Éliane Beauregard‐Lacroix et al. · The American Journal of Human Genetics · 2019 · 51 citations · Full text

Neurodevelopmental Disorders, Chromatin, Syndromic Autism +11