🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Vinodh Narayanan

Translational Genomics Research Institute

ORCID: 0000-0002-0658-3847
Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile
0Author DataRank

Indexed papers

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 14 papers. Top paper: “Friedreich’s ataxia”.

Friedreich’s ataxia

Pediatric Neurology(2003)10.1016/s0887-8994(03)00004-3
N/A
0.787DataRank · unranked
189 citations

Vinodh Narayanan, Gulay Alper

Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex

Nature Communications(2020)10.1038/s41467-020-17105-8
N/A
0DataRank · unranked
27 citations

Apoorva Bharthur, Morgan Wolfgang, Vinodh Narayanan, Keri Ramsey, Newell Belnap +14 more

Integrated phenotypic and mutational approach defines EBF3-related HADD syndrome genotype-phenotype relationships

medRxiv(2020)10.1101/2020.12.07.20238691
N/A
0DataRank · unranked
1 citations

Aarushi Nayak, Nathan D. Bliss, Vanesa Lerma, Ashley W. LeMaire, Vinodh Narayanan +8 more

Improved methods for RNAseq-based alternative splicing analysis

Scientific Reports(2021)10.1038/s41598-021-89938-2
N/A
0DataRank · unranked
44 citations

Apurva M. Hegde, Jessica D. Lang, Elizabeth A. Raupach, Vinodh Narayanan, Matt Huentelman +13 more

A novel insertion mutation in atlastin 1 is associated with spastic quadriplegia, increased membrane tethering, and aberrant conformational switching

Journal of Biological Chemistry(2021)10.1016/j.jbc.2021.101438
N/A
0DataRank · unranked
10 citations

Peter J. Zeiger, Vinodh Narayanan, Keri Ramsey, Holger Sondermann, Carolyn M. Kelly

Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis

Brain(2022)10.1093/brain/awac145
N/A
0DataRank · unranked
36 citations

Davide Mei, Katalin Kerti‐Szigeti, Sara Pepe, Mary Kay Koenig, Gretchen Von Allmen +48 more

SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance

Human Molecular Genetics(2022)10.1093/hmg/ddac114
N/A
0DataRank · unranked
17 citations

Martina Schaettin, Médéric Jeanne, Veranika Panasenkava, Anne‐Sophie Denommé‐Pichon, Boris Keren +43 more

Damaging de novo missense variants inEEF1A2lead to a developmental and degenerative epileptic‐dyskinetic encephalopathy

Human Mutation(2020)10.1002/humu.24015
N/A
0DataRank · unranked
40 citations

Katherine L. Helbig, Candace T. Myers, Marcello Scala, Robert Huether, Sara A. Lewis +40 more

GABRG2 Variants Associated with Febrile Seizures

Biomolecules(2023)10.3390/biom13030414
N/A
0DataRank · unranked
18 citations

Yan-Wen Shen, Ningning Hu, Wangzhen Shen, Vinodh Narayanan, Keri Ramsey +4 more

Bi-allelic SNAPC4 variants dysregulate global alternative splicing and lead to neuroregression and progressive spastic paraparesis

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.001
N/A
0DataRank · unranked
13 citations

Marie Morimoto, Prashant Sharma, Lyse Ruaud, Newell Belnap, Daniel G. Calame +33 more

An autosomal-dominant childhood-onset disorder associated with pathogenic variants in VCP

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.007
N/A
0DataRank · unranked
8 citations

Jil Daw, Diana Huynh, Mengcheng Wu, Benjamin C. Creekmore, William Burns +30 more

Recurrent p.H119Y variant in MAP2K1 expands the phenotypic spectrum of MAP2K1‐related RASopathy

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63854
N/A
0DataRank · unranked
0 citations

Daniel Wegner, Jennifer Wambach, Kathleen Sisco, Stephen Stone, Jonathan H. Sheehan +6 more

De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies

Genetics in Medicine(2025)10.1016/j.gim.2025.101369
N/A
0DataRank · unranked
4 citations

Lindsay C. Burrage, Sharayu Jangam, Jill A. Rosenfeld, Sandra von Hardenberg, Anke K. Bergmann +92 more

An Integrated Phenotypic and Genotypic Approach Reveals a High‐Risk Subtype Association for EBF3 Missense Variants Affecting the Zinc Finger Domain

Annals of Neurology(2022)10.1002/ana.26359
N/A
0DataRank · unranked
16 citations

Vanesa Lerma, Christina L. Magyar, Jessica M. Pfliger, Aarushi Nayak, Nathan D. Bliss +10 more