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

Himanshu Goel

Jagannath University

ORCID: 0000-0001-6448-6618

Also affiliated with IMS Unison University, Hunter Genetics, University of Newcastle Australia

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 3%percentile
1.5Author DataRank

Indexed papers

5in 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 5 indexed papers 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.

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases

medRxiv(2023)10.1101/2023.06.06.23290887
Top 32%
0.614DataRank
Top 32%25 citations

Alexander Hustinx, Shahida Moosa, Hannah Klinkhammer, Elaine Marchi, Pilar Caro +95 more

Papers

Driven by 11 papers — median percentile 41. Top paper: “GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases”.

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases

medRxiv(2023)10.1101/2023.06.06.23290887
Top 32%
0.614DataRank
Top 32%25 citations

Alexander Hustinx, Shahida Moosa, Hannah Klinkhammer, Elaine Marchi, Pilar Caro +95 more

Modulating effects of FGF12 variants on NaV1.2 and NaV1.6 being associated with developmental and epileptic encephalopathy and Autism spectrum disorder: A case series

EBioMedicine(2022)10.1016/j.ebiom.2022.104234
N/A
0.515DataRank · unranked
30 citations

Manuela Pendziwiat, Tatjana Bierhals, Himanshu Goel, Niklas Schwarz, Amelie van der Ven +8 more

Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals

Journal of Medical Genetics(2024)10.1136/jmg-2023-109702
Top 38%
0.503DataRank
Top 38%16 citations

Milou G. P. Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling, Elizabeth E. Palmer +12 more

Exome sequencing efficacy and phenotypic expansions involving esophageal atresia/tracheoesophageal fistula plus

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62976
N/A
0.385DataRank · unranked
12 citations

Jaynee Chauhan, Katrina Prescott, Aliza Imam, Alison Kraus, Ana Beleza‐Meireles +48 more

A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome

Scientific Reports(2023)10.1038/s41598-023-40037-4
N/A
0.269DataRank · unranked
5 citations

Shotaro Kishikawa, Vijay Gupta, Natalia T. Leach, Yiping Shen, Oana Moldovan +14 more

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases

Research Square(2024)10.21203/rs.3.rs-4438861/v1
Top 59%
0.261DataRank
Top 59%4 citations

Hellen Lesmann, Alexander Hustinx, Shahida Moosa, Elaine Marchi, Maria del Pilar Caro Martin +95 more

The ClinGen Syndromic Disorders Gene Curation Expert Panel: Assessing the Clinical Validity of 111 Gene-Disease Relationships

medRxiv(2024)10.1101/2024.11.19.24317561
Top 78%
0.104DataRank
Top 78%1 citations

Vanessa Gitau, Alicia B. Byrne, Pamela Ajuyah, Marie Balzotti, Jonathan S. Berg +58 more

The ClinGen Syndromic Disorders Gene Curation Expert Panel: Assessing the clinical validity of 111 gene-disease relationships

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103429
Top 100%
0DataRank
Top 100%0 citations

Vanessa Gitau, Alicia B. Byrne, Pamela Ajuyah, Marie Balzotti, Jonathan S. Berg +58 more

A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome

Research Square(2023)10.21203/rs.3.rs-2572736/v1
N/A
0DataRank · unranked
1 citations

Shotaro Kishikawa, Vijay Gupta, Natalia T. Leach, Yiping Shen, Oana Moldovan +14 more

Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome

npj Genomic Medicine(2024)10.1038/s41525-024-00413-z
N/A
0DataRank · unranked
5 citations

Anne Hebert, Maaike Bastiaansen, Laura Rabaut, Jarl Bastianen, Nele Boeckx +41 more

Modulating effects of FGF12 variants on Na V 1.2 and Na V 1.6 associated with Developmental and Epileptic Encephalopathy and Autism Spectrum Disorder

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.03.471090
N/A
0DataRank · unranked
2 citations

Manuela Pendziwiat, Tatjana Bierhals, Himanshu Goel, Niklas Schwarz, Amelie van der Ven +6 more