Nisha Raj

Affiliations: 
2019 Cell Biology Emory University School of Medicine, Atlanta, GA, United States 
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Purcell RH, Sefik E, Werner E, et al. (2023) Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion. Science Advances. 9: eadh0558
Purcell RH, Sefik E, Werner E, et al. (2023) Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion. Biorxiv : the Preprint Server For Biology
Kang Y, Zhou Y, Li Y, et al. (2021) A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies. Nature Neuroscience
Raj N, McEachin ZT, Harousseau W, et al. (2021) Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis. Cell Reports. 35: 108991
McEachin ZT, Parameswaren J, Raj N, et al. (2020) RNA-mediated toxicity in C9orf72 ALS and FTD. Neurobiology of Disease. 105055
Das Sharma S, Pal R, Reddy BK, et al. (2020) Cortical neurons derived from human pluripotent stem cells lacking FMRP display altered spontaneous firing patterns. Molecular Autism. 11: 52
Goering R, Hudish LI, Guzman BB, et al. (2020) FMRP promotes RNA localization to neuronal projections through interactions between its RGG domain and G-quadruplex RNA sequences. Elife. 9
McEachin ZT, Gendron TF, Raj N, et al. (2020) Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36. Neuron
Goering R, Hudish LI, Guzman BB, et al. (2020) Author response: FMRP promotes RNA localization to neuronal projections through interactions between its RGG domain and G-quadruplex RNA sequences Elife
Banerjee A, Ifrim MF, Valdez AN, et al. (2018) Aberrant RNA Translation in Fragile X Syndrome: From FMRP Mechanisms to Emerging Therapeutic Strategies. Brain Research
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