Vinodh Narayanan

5.3k total citations
67 papers, 2.3k citations indexed

About

Vinodh Narayanan is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Vinodh Narayanan has authored 67 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 25 papers in Genetics and 13 papers in Cellular and Molecular Neuroscience. Recurrent topics in Vinodh Narayanan's work include Genetics and Neurodevelopmental Disorders (19 papers), RNA Research and Splicing (9 papers) and Autism Spectrum Disorder Research (7 papers). Vinodh Narayanan is often cited by papers focused on Genetics and Neurodevelopmental Disorders (19 papers), RNA Research and Splicing (9 papers) and Autism Spectrum Disorder Research (7 papers). Vinodh Narayanan collaborates with scholars based in United States, Spain and China. Vinodh Narayanan's co-authors include Carl F. Lagenaur, Peihua Jiang, Gülay Alper, Yimin Yan, Sampathkumar Rangasamy, Santosh R. D’Mello, Eric P. Hoffman, Sinan Çomu, Adam A. Rosenberg and Mathew Jones and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Neuron.

In The Last Decade

Vinodh Narayanan

64 papers receiving 2.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Vinodh Narayanan United States 25 1.2k 749 418 399 398 67 2.3k
Bert van der Zwaag Netherlands 23 1.2k 1.1× 704 0.9× 372 0.9× 161 0.4× 200 0.5× 44 2.2k
Tayfun Özçelık Türkiye 30 1.5k 1.3× 859 1.1× 541 1.3× 405 1.0× 172 0.4× 59 3.1k
Roderick T. Bronson United States 7 1.6k 1.4× 815 1.1× 218 0.5× 315 0.8× 115 0.3× 7 3.0k
Lina Basel‐Vanagaite Israel 32 1.9k 1.6× 1.4k 1.9× 468 1.1× 167 0.4× 245 0.6× 111 3.6k
Kimberly A. Aldinger United States 25 1.3k 1.1× 613 0.8× 344 0.8× 147 0.4× 365 0.9× 48 2.3k
Patrick Edery France 33 2.4k 2.1× 1.6k 2.1× 304 0.7× 205 0.5× 171 0.4× 117 4.5k
A. Micheil Innes Canada 33 2.0k 1.8× 1.1k 1.5× 353 0.8× 190 0.5× 105 0.3× 113 3.5k
Marlène Rio France 33 2.2k 1.9× 1.7k 2.2× 237 0.6× 225 0.6× 197 0.5× 112 3.5k
Kerstin Kutsche Germany 32 2.3k 2.0× 1.3k 1.8× 358 0.9× 242 0.6× 177 0.4× 118 3.6k
Pascale Saugier-Véber France 28 1.1k 1.0× 672 0.9× 437 1.0× 89 0.2× 85 0.2× 82 2.3k

Countries citing papers authored by Vinodh Narayanan

Since Specialization
Citations

This map shows the geographic impact of Vinodh Narayanan's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Vinodh Narayanan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vinodh Narayanan more than expected).

Fields of papers citing papers by Vinodh Narayanan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vinodh Narayanan. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Vinodh Narayanan. The network helps show where Vinodh Narayanan may publish in the future.

Co-authorship network of co-authors of Vinodh Narayanan

This figure shows the co-authorship network connecting the top 25 collaborators of Vinodh Narayanan. A scholar is included among the top collaborators of Vinodh Narayanan based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Vinodh Narayanan. Vinodh Narayanan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ramsey, Keri, et al.. (2024). Family and caregiver perspectives on gene therapy for Rett syndrome. SHILAP Revista de lepidopterología. 2. 100045–100045. 2 indexed citations
2.
Belnap, Newell, Keri Ramsey, Alon Abraham, et al.. (2024). Expanded carrier screening for inherited genetic disease using exome and genome sequencing. Journal of Genetic Counseling. 34(2). e1964–e1964.
3.
Ramsey, Keri, Marcus Naymik, Jennifer L. Sloan, et al.. (2024). Duchenne Muscular Dystrophy in Two Half-Brothers Due to Inherited 306 Kb Inverted Insertion of 10p15.1 into Intron 44 of the Dp427m Transcript of the DMD Gene. International Journal of Molecular Sciences. 25(22). 11922–11922.
4.
Hernández, Ciria C., Ningning Hu, Wangzhen Shen, et al.. (2023). GABRG2 Variants Associated with Febrile Seizures. Biomolecules. 13(3). 414–414. 11 indexed citations
5.
Belnap, Newell, Marcus Naymik, Jennifer L. Sloan, et al.. (2023). Snyder-Robinson syndrome presenting with learning disability, epilepsy, and osteoporosis: A novel SMS gene variant. SHILAP Revista de lepidopterología. 2. 100017–100017. 2 indexed citations
6.
Wongkittichote, Parith, Tae‐Ik Choi, Dwight D. Koeberl, et al.. (2022). Expanding allelic and phenotypic spectrum of ZC4H2‐related disorder: A novel hypomorphic variant and high prevalence of tethered cord. Clinical Genetics. 103(2). 167–178. 5 indexed citations
7.
Abruzzo, Todd, René van den Berg, Sudhakar Vadivelu, et al.. (2022). Arterioectatic Spinal Angiopathy of Childhood: Clinical, Imaging, Laboratory, Histologic, and Genetic Description of a Novel CNS Vascular Pathology. American Journal of Neuroradiology. 43(7). 1060–1067. 2 indexed citations
8.
Domínguez, Isabel, J. M. Cruz-Gamero, Sampathkumar Rangasamy, et al.. (2021). Okur-Chung neurodevelopmental syndrome-linked CK2α variants have reduced kinase activity. Human Genetics. 140(7). 1077–1096. 15 indexed citations
9.
Narayanan, Vinodh, et al.. (2021). A novel insertion mutation in atlastin 1 is associated with spastic quadriplegia, increased membrane tethering, and aberrant conformational switching. Journal of Biological Chemistry. 298(1). 101438–101438. 6 indexed citations
10.
Ramsey, Keri, Newell Belnap, Szabolcs Szelinger, et al.. (2017). Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results. Seminars in Pediatric Neurology. 26. 28–32. 9 indexed citations
11.
Ma, Luyao, Wu Chen, Jin Yu, et al.. (2014). Electrophysiological Phenotypes of MeCP2 A140V Mutant Mouse Model. CNS Neuroscience & Therapeutics. 20(5). 420–428. 12 indexed citations
12.
Rangasamy, Sampathkumar, Santosh R. D’Mello, & Vinodh Narayanan. (2013). Epigenetics, Autism Spectrum, and Neurodevelopmental Disorders. Neurotherapeutics. 10(4). 742–756. 78 indexed citations
13.
Dastidar, Somasish Ghosh, Farah Bardai, Chi Ma, et al.. (2012). Isoform-Specific Toxicity of Mecp2 in Postmitotic Neurons: Suppression of Neurotoxicity by FoxG1. Journal of Neuroscience. 32(8). 2846–2855. 61 indexed citations
14.
Otero‐Millan, Jorge, Xoana G. Troncoso, Michael B. McCamy, et al.. (2010). Simultaneous recordings of ocular microtremor and fixational microsaccades with a piezoelectric sensor and a commercial video tracking system. Journal of Vision. 10(7). 506–506. 1 indexed citations
15.
Halperin, Rebecca F., et al.. (2006). Cognitive dysfunction in NFI knock-out mice may result from altered vesicular trafficking of APP/DRD3 complex. BMC Neuroscience. 7(1). 22–22. 17 indexed citations
16.
Narayanan, Vinodh. (2003). Tuberous sclerosis complex: genetics to pathogenesis. Pediatric Neurology. 29(5). 404–409. 80 indexed citations
17.
Alper, Gülay & Vinodh Narayanan. (2003). Friedreich’s ataxia. Pediatric Neurology. 28(5). 335–341. 135 indexed citations
18.
Narayanan, Vinodh, et al.. (1998). Mutation analysis of the M6b gene in patients with Rett syndrome. American Journal of Medical Genetics. 78(2). 165–168. 16 indexed citations
19.
Çomu, Sinan, Vinodh Narayanan, & Michael J. Giuliani. (1996). Episodic ataxia and myokymia syndrome: A new mutation of potassium channel gene Kv1.1. Annals of Neurology. 40(4). 684–687. 48 indexed citations
20.
Yan, Yimin, Vinodh Narayanan, & Carl F. Lagenaur. (1996). Expression of members of the proteolipid protein gene family in the developing murine central nervous system. The Journal of Comparative Neurology. 370(4). 465–478. 56 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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