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
Maricopa Integrated Health System
St. Joseph's Hospital and Medical Center
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.
Short-term safety of mTOR inhibitors in infants and very young children with tuberous sclerosis complex (TSC): Multicentre clinical experience.
Eur. J. Paediatr. Neurol.
Krueger, D. A.,Capal, J. K.,Curatolo, P.,Devinsky, O.,Ess, K.,Tzadok, M.,Koenig, M. K.,Narayanan, V.,Ramos, F.,Jozwiak, S.,de Vries, P.,Jansen, A. C.,Wong, M.,Mowat, D.,Lawson, J.,Bruns, S.,Franz, D. N.
"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
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...