About Dr. Narayanan
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.
Qualifications and Experience
Education & Training
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Certifications
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Medical Licenses
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Work Experience
Child Neurologist
APNNA - Arizona Pediatric Neurology and Neurogenetics Associates
Phoenix, AZ
2011 - Present
Medical Director, Center for Rare Childhood Disorders
The Translational Genomics Research Institut
Phoenix, AZ
Present
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Hospital Affiliations
HonorHealth Scottsdale Shea Medical Center
Current Affiliation
Scottsdale, AZ
St. Joseph's Hospital and Medical Center
Current Affiliation
Phoenix, AZ
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Professional Memberships
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Publications
PubMed
Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish.
Nature communications
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., Giong, H., 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.
2/14/2019
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature.
American journal of medical genetics. Part 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., Ramey, V. L., Wou, K., Kuzminsky, A., Monfort, S., Weiss, M., Doyle, S., Iglesias, A., Martinez, F., Mckenzie, F., Orellana, C., van Gassen, K. L., Palomares, M., Bazak, L., Lee, A., Bircher, A., Basel-Vanagaite, L., Hafstrm, M., Houge, G., , Goldstein, D. B., Anyane-Yeboa, K.
9/9/2018
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.
8/29/2018
Journal Article
"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
1/1/2017
Lecture
Abstract
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
1/1/2015
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
1/1/2014
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
1/1/2014
Book Chapter
Other
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