Sruti Rayaprolu, Ph.D.

Affiliations: 
Neurology Emory University School of Medicine, Atlanta, GA, United States 
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"Sruti Rayaprolu"
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Publications

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Moloney C, Rayaprolu S, Howard J, et al. (2018) Analysis of spinal and muscle pathology in transgenic mice overexpressing wild-type and ALS-linked mutant MATR3. Acta Neuropathologica Communications. 6: 137
Rayaprolu S, Seven YB, Howard J, et al. (2018) Partial loss of ATP13A2 causes selective gliosis independent of robust lipofuscinosis. Molecular and Cellular Neurosciences
Moloney C, Rayaprolu S, Howard J, et al. (2017) Retraction Note: Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotype. Acta Neuropathologica Communications. 5: 97
Moloney C, Rayaprolu S, Howard J, et al. (2016) Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotype. Acta Neuropathologica Communications. 4: 122
Rayaprolu S, D'Alton S, Crosby K, et al. (2016) Heterogeneity of Matrin 3 in the developing and aging murine central nervous system. The Journal of Comparative Neurology
Hassan A, Heckman MG, Ahlskog JE, et al. (2015) Association of Parkinson disease age of onset with DRD2, DRD3 and GRIN2B polymorphisms. Parkinsonism & Related Disorders
Labbé C, Ogaki K, Lorenzo-Betancor O, et al. (2015) Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies. Neurology
Rajput A, Ross JP, Bernales CQ, et al. (2015) VPS35 and DNAJC13 disease-causing variants in essential tremor. European Journal of Human Genetics : Ejhg. 23: 887-8
Heckman MG, Schottlaender L, Soto-Ortolaza AI, et al. (2014) LRRK2 exonic variants and risk of multiple system atrophy. Neurology. 83: 2256-61
Ogaki K, Fujioka S, Heckman MG, et al. (2014) Analysis of COQ2 gene in multiple system atrophy. Molecular Neurodegeneration. 9: 44
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