Maimuna Paul
Affiliations: | 2019- | Baylor College of Medicine, Houston, TX |
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| Paul MS, Michener SL, Pan H, et al. (2024) A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3. American Journal of Human Genetics. 111: 96-118 |
| Paul MS, Michener SL, Pan H, et al. (2023) Rare variants in cause delayed development, intellectual disability, autism, and epilepsy. Medrxiv : the Preprint Server For Health Sciences |
| Paul MS, Duncan AR, Genetti CA, et al. (2023) Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy. American Journal of Human Genetics. 110: 548 |
| Paul MS, Duncan AR, Genetti CA, et al. (2022) Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy. American Journal of Human Genetics |
| Singh A, Paul MS, Dutta D, et al. (2019) Regulation of notch signaling by a chromatin modeling protein Hat-trick. Development (Cambridge, England) |
| Singh A, Dutta D, Paul MS, et al. (2018) ---Pleiotropic Functions of the Chromodomain-Containing Protein Hat-trick During Oogenesis in Drosophila melanogaster. G3 (Bethesda, Md.) |