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

Paras Garg

Child Health and Development Institute

ORCID: 0000-0002-7128-1124

Also affiliated with Icahn School of Medicine at Mount Sinai

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
0.578Author 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 16 papers — median percentile 66. Top paper: “A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank”.

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

Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.07.003
N/A
0DataRank · unranked
54 citations

Paras Garg, Lara Tang, Danielle Mendonca, Tess Levy, Mafalda Barbosa +24 more

Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles

PLoS Genetics(2020)10.1371/journal.pgen.1009189
N/A
0DataRank · unranked
43 citations

Nihir Patel, Felix Richter, Bharati Jadhav, Paras Garg, Sarah U. Morton +16 more

Episignatures stratifying ADNP syndrome show modest correlation with phenotype

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.01.014902
N/A
0DataRank · unranked
7 citations

Paras Garg, Lara Tang, Danielle Mendonca, Tess Levy, Mafalda Barbosa +23 more

A survey of rare epigenetic variation in 23,116 human genomes identifies disease-relevant epivariations and novel CGG expansions

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.03.25.007864
N/A
0DataRank · unranked
0 citations

Bharati Jadhav, Oscar L. Rodriguez, Nihir Patel, Alejandro Martin-Trujillo, Miten Jain +8 more

Pervasive cis effects of variation in copy number of large tandem repeats on local epigenetics and gene expression

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.16.423078
N/A
0DataRank · unranked
0 citations

Alejandro Martin-Trujillo, Oscar L. Rodriguez, Scott J Gies, Bharati Jadhav, Andrew J. Sharp +1 more

Pervasive cis effects of variation in copy number of large tandem repeats on local DNA methylation and gene expression

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.03.016
N/A
0DataRank · unranked
47 citations

Alejandro Martin-Trujillo, Oscar L. Rodriguez, Scott J Gies, Elina Hadelia, Bharati Jadhav +4 more

A phenome-wide association study identifies effects of copy-number variation of VNTRs and multicopy genes on multiple human traits

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.04.016
N/A
0DataRank · unranked
25 citations

Bharati Jadhav, William Lee, Oscar L. Rodriguez, Alejandro Martin-Trujillo, Andrew J. Sharp +1 more

Genome-wide evaluation of the effect of short tandem repeat variation on local DNA methylation

Genome Research(2022)10.1101/gr.277057.122
N/A
0DataRank · unranked
30 citations

Paras Garg, Nihir Patel, Bharati Jadhav, Andrew J. Sharp, Alejandro Martin-Trujillo

A phenome-wide association study identifies effects of copy number variation of VNTRs and multicopy genes on multiple human traits

medRxiv(2022)10.1101/2022.01.26.22269891
N/A
0DataRank · unranked
2 citations

Bharati Jadhav, William Lee, Oscar L. Rodriguez, Alejandro Martin-Trujillo, Andrew J. Sharp +1 more

Increased frequency of repeat expansion mutations across different populations

medRxiv(2023)10.1101/2023.07.03.23292162
N/A
0DataRank · unranked
14 citations

Bharati Jadhav, Matteo Zanovello, Delia Gagliardi, Christopher Clarkson, Stefano Facchini +26 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

Increased frequency of repeat expansion mutations across different populations

Nature Medicine(2024)10.1038/s41591-024-03190-5
N/A
0DataRank · unranked
74 citations

Bharati Jadhav, Matteo Zanovello, Delia Gagliardi, Christopher Clarkson, Stefano Facchini +25 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
0DataRank · unranked
11 citations

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

A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.08.019
N/A
0DataRank · unranked
68 citations

Bharati Jadhav, Oscar L. Rodriguez, Nihir Patel, Alejandro Martin-Trujillo, Miten Jain +8 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