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

Mariya Shadrina

Child Health and Development Institute

ORCID: 0000-0001-5962-0771

Also affiliated with Icahn School of Medicine at Mount Sinai

Biochemistry, Genetics and Molecular BiologyNeuroscience

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
0.578Author 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 phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank

Nature Communications(2024)10.1038/s41467-024-54678-0
Top 34%
0.578DataRank
Top 34%15 citations

Bharati Jadhav, Paras Garg, Mariya Shadrina, William Lee, Gabrielle Altman +3 more

Papers

Driven by 6 papers — median percentile 66. Top paper: “Burden of Cardiomyopathic Genetic Variation in Lethal Pediatric Myocarditis”.

Burden of Cardiomyopathic Genetic Variation in Lethal Pediatric Myocarditis

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.121.003426
N/A
0.876DataRank · unranked
24 citations

Yingying Tang, Nihir Patel, Zhanna Georgievskaya, Mariya Shadrina, Nori Williams +6 more

A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank

Nature Communications(2024)10.1038/s41467-024-54678-0
Top 34%
0.578DataRank
Top 34%15 citations

Bharati Jadhav, Paras Garg, Mariya Shadrina, William Lee, Gabrielle Altman +3 more

A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 associated with intellectual disability

Nature Genetics(2024)10.1038/s41588-024-01917-1
N/A
0.373DataRank · unranked
11 citations

Paras Garg, Joke J.F.A. van Vugt, Kristina Ibáñez, Delia Gagliardi, William Lee +19 more

A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 as a significant cause of intellectual disability

medRxiv(2023)10.1101/2023.05.03.23289461
N/A
0DataRank · unranked
7 citations

Paras Garg, Joke J.F.A. van Vugt, Kristina Ibáñez, Delia Gagliardi, William Lee +16 more

A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank

medRxiv(2024)10.1101/2024.01.22.24301630
N/A
0DataRank · unranked
6 citations

Bharati Jadhav, Paras Garg, Mariya Shadrina, William Lee, Alejandro Martin-Trujillo +2 more

Efficient identification of de novo mutations in family trios: a consensus-based informatic approach

Life Science Alliance(2025)10.26508/lsa.202403039
N/A
0DataRank · unranked
0 citations

Özem Kalay, Sinem Demirkaya-Budak, Charles A. LeDuc, Wendy K. Chung, Deniz Turgut +9 more