Vinodh Narayanan, MD

Vinodh Narayanan, MD

Neurology in Phoenix, AZ


 (602) 914-1520

Contact


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Office Hours

Monday:
9:00 am - 5:00 pm
Tuesday:
Closed
Wednesday:
Closed
Thursday:
Closed
Friday:
9:00 am - 5:00 pm
Saturday:
Closed
Sunday:
Closed
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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



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Education & Training

St Louis Children's Hospital
Fellowship, Child Neurology, 1984 - 1986

Washington University - Barnes-Jewish Hospital
Residency, Neurology, 1983 - 1984

Johns Hopkins University
Residency, Pediatrics, 1981 - 1983

Louisiana State University in New Orleans
Class of 1981

Princeton University
MA, Physics, 1976

Washington University
B.S., Physics, 1972

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Certifications

American Board of Pediatrics
Pediatrics

American Board of Psychiatry and Neurology
Neurology with Special Qualification in Child Neurology

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Medical Licenses

AZ State Medical License
2003 - 2020

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Hospital Affiliations

The Translational Genomics Research Institute
Current Affiliation

APNNA - Arizona Pediatric Neurology & Neurogenetics Associates, PLLC
Current Affiliation

Children's Rehabilitative Services
Current Affiliation

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

American Academy of Neurology - AAN
Member

Child Neurology Society
Member

American Neurological Association
Member

American Society of Human Genetics
Member

American College of Medical Genetics and Genomics
Member

Society for Neuroscience
Member

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Publications



PubMed

Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish.
Nat Commun
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.
2/14/2019

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.
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

See All

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

"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
1/1/2017

"A gain-of-function mutation in GRIK2 causes neurodevelopmental deficits"
Neurology Genetics
Guzman YF, Ramsey K, Stolz JR, Craig DW, Huentelman MJ, Narayanan V, Swanson GT
1/1/2017

Lecture

Neurogenomics Approach to the Diagnosis of Neurological Disorders
1/12/2016

Genetics and Epilepsy
1/18/2015
Phoenix Children's Hospital

Rett Syndrome: Bench to Bedside
1/29/2014

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

Swaiman's Pediatric Neurology: Principles and Practice
Rangasamy S, Narayanan M, Schrauwen I, Muotri A, Narayanan V
1/1/2015

Current Management in Child Neurology
Sivakumar, K, and Narayanan, V.
1/1/2005

Current Therapy in Neurological Diseases
Bodensteiner, JB, and Narayanan, V.
1/1/2005

Other

"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
1/1/2016

Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed development, and periventricular white matter hyperintensities.
Narayanan M, Ramsey K, Grebe T et al
1/1/2015

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Press Mentions



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...

Finding the Needle in a Genomic Haystack
Medical Xpress · February 03, 2017
...will lead to improvements, for this patient and many others with rare medical disorders," said Dr. Vinodh Narayanan, Medical Director of TGen's Center for Rare Childhood Disorders, and a co-author of the study. TGen...

First Genetic Mutation Associated with Aicardi Syndrome
ScienceDaily · June 19, 2015
...e a better understanding of the disease biology, and lead to better treatment approaches," said Dr. Vinodh Narayanan, Medical Director of TGen's Center for Rare Childhood Disorders and one of the study's authors. TGe...