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

Ashwin Dalal

Nizam's Institute of Medical Sciences

ORCID: 0000-0001-5929-745X

Also affiliated with Dr. Reddy's Foundation, Centre for DNA Fingerprinting and Diagnostics

Biochemistry, Genetics and Molecular BiologyMedicine

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 4%percentile
0.853Author 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 →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

A data set of variants derived from 1455 clinical and research exomes is efficient in variant prioritization for early‐onset monogenic disorders in Indians

Human Mutation(2021)10.1002/humu.24172
Top 24%
0.853DataRank
Top 24%51 citations

Anju Shukla, Neerja Gupta, Gandham SriLakshmi Bhavani, Samarth Kulshrestha, Aneek Das Bhowmik +11 more

Papers

Driven by 8 papers — median percentile 76. Top paper: “A data set of variants derived from 1455 clinical and research exomes is efficient in variant prioritization for early‐onset monogenic disorders in Indians”.

A data set of variants derived from 1455 clinical and research exomes is efficient in variant prioritization for early‐onset monogenic disorders in Indians

Human Mutation(2021)10.1002/humu.24172
Top 24%
0.853DataRank
Top 24%51 citations

Anju Shukla, Neerja Gupta, Gandham SriLakshmi Bhavani, Samarth Kulshrestha, Aneek Das Bhowmik +11 more

Further evidence of affected females with a heterozygous variant in FGF13 causing X-linked developmental and epileptic encephalopathy 90

European Journal of Medical Genetics(2021)10.1016/j.ejmg.2021.104403
N/A
0.416DataRank · unranked
15 citations

Purvi Majethia, Shrikiran Aroor, Shahyan Siddiqui, Ashwin Dalal, Anju Shukla +1 more

Duchenne Muscular Dystrophy from Brain to Muscle: The Role of Brain Dystrophin Isoforms in Motor Functions

Journal of Clinical Medicine(2023)10.3390/jcm12175637
N/A
0.396DataRank · unranked
13 citations

Lakmal Gonawala, Pyara Ratnayake, Dhammika Amaratunga, Yetrib Hathout, Chandra Mohan +5 more

Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders

medRxiv(2022)10.1101/2022.02.15.22270795
N/A
0.373DataRank · unranked
11 citations

Mana M. Mehrjouy, Ryan L. Collins, Mads Bak, Olga Dudchenko, Harrison Brand +95 more

Serum metabolomic signatures of patients with rare neurogenetic diseases: an insight into potential biomarkers and treatment targets

Frontiers in Molecular Neuroscience(2025)10.3389/fnmol.2024.1482999
N/A
0DataRank · unranked
2 citations

Lakmal Gonawala, Pyara Ratnayake, Darshana Sirisena, Harsha Gunasekara, Athula Dissanayake +8 more

Gene therapy for selected neuromuscular and trinucleotide repeat disorders – An insight to subsume South Asia for multicenter clinical trials

IBRO Neuroscience Reports(2023)10.1016/j.ibneur.2023.01.009
N/A
0DataRank · unranked
10 citations

Lakmal Gonawala, Pyara Ratnayake, Darshana Sirisena, Harsha Gunasekara, Athula Dissanayake +9 more

Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrum

Genetics in Medicine(2023)10.1016/j.gim.2023.100863
N/A
0DataRank · unranked
6 citations

Ashish R. Deshwar, Harsha Murthy, Daniela D’Agostino, Lucie Dupuis, Balram Gangaram +19 more

Diagnostic outcome of pro bono neurogenetic diagnostic service in Sri Lanka: A wealth creation

European Journal of Human Genetics(2024)10.1038/s41431-023-01525-3
N/A
0DataRank · unranked
4 citations

Nalaka Wijekoon, D.P.S.T.G. Attanayaka, Pyara Ratnayake, Darshana Sirisena, Harsha Gunasekara +8 more