Dr. Vinodh Narayanan, MD is a board certified neurologist in Phoenix, Arizona. He is currently licensed to practice medicine in Arizona. He is affiliated with St. Joseph's Hospital and Medical Center, Maricopa Integrated Health System, and HonorHealth Scottsdale Shea Medical Center.
Education & Training
HonorHealth Scottsdale Shea Medical Center
St. Joseph's Hospital and Medical Center
Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish.
Siekierska, A.,Stamberger, H.,Deconinck, T.,Oprescu, S. N.,Partoens, M.,Zhang, Y.,Sourbron, J.,Adriaenssens, E.,Mullen, P.,Wiencek, P.,Hardies, K.,Lee, J. S.,Giong, H. K.,Distelmaier, F.,Elpeleg, O.,Helbig, K. L.,Hersh, J.,Isikay, S.,Jordan, E.,Karaca, E.,Kecskes, A.,Lupski, J. R.,Kovacs-Nagy, R.,May, P.,Narayanan, V.,Pendziwiat, M.,Ramsey, K.,Rangasamy, S.,Shinde, D. N.,Spiegel, R.,Timmerman, V.,von Spiczak, S.,Helbig, I.,Weckhuysen, S.,Francklyn, C.,Antonellis, A.,de Witte, P.,De Jonghe, P.
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature.
Am. J. Med. Genet. A
Hemati, P.,Revah-Politi, A.,Bassan, H.,Petrovski, S.,Bilancia, C. G.,Ramsey, K.,Griffin, N. G.,Bier, L.,Cho, M. T.,Rosello, M.,Lynch, S. A.,Colombo, S.,Weber, A.,Haug, M.,Heinzen, E. L.,Sands, T. T.,Narayanan, V.,Primiano, M.,Aggarwal, V. S.,Millan, F.,Sattler-Holtrop, S. G.,Caro-Llopis, A.,Pillar, N.,Baker, J.,Freedman, R.,Kroes, H. Y.,Sacharow, S.,Stong, N.,Lapunzina, P.,Schneider, M. C.,Mendelsohn, N. J.,Singleton, A.,Loik Ramey, V.,Wou, K.,Kuzminsky, A.,Monfort, S.,Weiss, M.,Doyle, S.,Iglesias, A.,Martinez, F.,Mckenzie, F.,Orellana, C.,van Gassen, KLI.,Palomares, M.,Bazak, L.,Lee, A.,Bircher, A.,Basel-Vanagaite, L.,Hafström, M.,Houge, G.,Goldstein, D. B.,Anyane-Yeboa, K.
De novo variant in KIF26B is associated with pontocerebellar hypoplasia with infantile spinal muscular atrophy.
Am. J. Med. Genet. A
Wojcik, M. H.,Okada, K.,Prabhu, S. P.,Nowakowski, D. W.,Ramsey, K.,Balak, C.,Rangasamy, S.,Brownstein, C. A.,Schmitz-Abe, K.,Cohen, J. S.,Fatemi, A.,Shi, J.,Grant, E. P.,Narayanan, V.,Ho, H. H.,Agrawal, P. B.
"A de novo splice-site mutation in CASK causes FG syndrome-4 and congenital nystagmus"
American Journal of Medical Genetics, Part A
Dunn P, Prigatano GP, Szelinger S, et al
"An Atypical presentation of ACAD9 deficiency: Diagnosis by whole exome sequencing broadens the phenotypic spectrum and alters treatment approach"
Molecular Genetics and Metabolism Reports
Aintablian HK, Narayanan V, Belnap N, Ramsey K, Grebe T
Neurodegeneration associated with WDR45 mutation in a brother and sister: BPAN (beta-propeller protein-associated neurodegeneration) due to maternal gonadal mosaicism.
Annual Meeting of the American College of Medical Genetics
Szelinger S, et al
Missense mutations of DST (encoding dystonin) cause neonatal feeding difficulty, hypotonia, dystonia, choreoathetosis and hypoalgesia.
Annual Meeting of the Child Neurology Society
Narayanan V, Ramsey K, Narayanan M, Rangasamy S, Szelinger S, Corneveaux JJ, Schrauwen I, Siniard A, Kurdoglu A, Richholt R, de Both M, Swaminathan S, Huentelman M, Craig D
Congenital Myasthenia Syndrome: Uniparental disomy of chromosome 2 and homozygous mutation of GFPT1.
Annual Meeting of the American Society of Human Genetics
Rangasamy S, Szelinger S, Ramsey K, Krate J, Corneveaux JJ, Schrauwen I, Siniard A, Kurdoglu A, Richholt R, de Both M, Swaminathan S, Huentelman M, Craig D, Narayanan V
Swaiman's Pediatric Neurology: Principles and Practice
Rangasamy S, Narayanan M, Schrauwen I, Muotri A, Narayanan V
"Reduced Neuronal Size and mTOR pathway activity in the Mecp2 A140V Rett syndrome mouse model"
Rangasamy S, Olfers SL, Gerald B, Hilbert A, Svejda S, Narayanan V
Researchers Link Sisters' Paralysis to an 'Extremely Rare' Genetic Variant
ScienceDaily · November 15, 2019
...der group of more than 150 other pediatric patients enrolled under our research protocol," said Dr. Vinodh Narayanan, the Center's Medical Director and one of the study's authors. Using these precision medicine techn...
Gene Linked to Physical and Intellectual Disabilities Identified
Neuroscience News · August 16, 2019
...ere led to the discovery of a new neurodevelopmental syndrome caused by mutation of DDX6,” said Dr. Vinodh Narayanan, Medical Director of the Center, and another of the study’s senior authors. “We expect that the ins...
The Power of Precision Medicine, Personalized Care & A Brave Kid: Beorn’s Story
3BL Media · October 24, 2017
Beorn and Stephanie Rankin and their son, Beorn, talk with Dr. Vinodh Narayanan. As part of our work with TGen, we learn about remarkable young patients, and their families with e...