Anna R. Duncan

RAPGEF5 Regulates Nuclear Translocation of β-Catenin

John N. Griffin, Florencia Del Viso, Anna R. Duncan et al. · Developmental Cell · 2017 · 94 citations · Full text

Transcriptional Regulation, Signaling Pathway, Molecular Regulation +3

Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores

Steven E. Boyden, Lane J. Mahoney, Genri Kawahara et al. · Neurogenetics · 2012 · 82 citations · Full text

Mitochondrial Myopathy, Rare Diseases, Murine Megf10 +13

Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders

Anna R. Duncan, Maya M. Polovitskaya, Héctor Gaitán‐Peñas et al. · The American Journal of Human Genetics · 2021 · 43 citations · Full text

Neurodevelopmental Disorders, Molecular Neuroscience, Developmental Biology +10

Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects

Anna R. Duncan, Antonio Vitobello, Stephan C. Collins et al. · The American Journal of Human Genetics · 2020 · 29 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +10

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy

Maimuna Sali Paul, Anna R. Duncan, Casie A. Genetti et al. · The American Journal of Human Genetics · 2022 · 29 citations · Full text

Neurodevelopmental Disorders, Mendelian Disorder, Genetic Disorder +8