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

Vamsee Pillalamarri

Johns Hopkins University

ORCID: 0000-0002-3556-8814

Also affiliated with Johns Hopkins Medicine, Genomics (United Kingdom)

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 2%percentile

2.2Author 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 →

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

Consistent RNA sequencing contamination in GTEx and other data sets

Nature Communications(2020)10.1038/s41467-020-15821-9

Top 10%

2.2DataRank

Top 10%93 citations

Stephanie Yang, Rohan Verma, Vamsee Pillalamarri, Dan E. Arking, Avi Z. Rosenberg +3 more

Papers

Driven by 7 papers — median percentile 90. Top paper: “Consistent RNA sequencing contamination in GTEx and other data sets”.

Consistent RNA sequencing contamination in GTEx and other data sets

Nature Communications(2020)10.1038/s41467-020-15821-9

Top 10%

2.2DataRank

Top 10%93 citations

Stephanie Yang, Rohan Verma, Vamsee Pillalamarri, Dan E. Arking, Avi Z. Rosenberg +3 more

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

Nature Genetics(2022)10.1038/s41588-022-01203-y

N/A

1.3DataRank · unranked

55 citations

Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove +94 more

Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality

Nature Communications(2023)10.1038/s41467-023-41785-7

N/A

1.1DataRank · unranked

44 citations

Stephanie L. Battle, Wen Shi, Daniela Puiu, Vamsee Pillalamarri, Jiaqi Xie +21 more

Blood-derived mitochondrial DNA copy number is associated with gene expression across multiple tissues and is predictive for incident neurodegenerative disease

Genome Research(2021)10.1101/gr.269381.120

N/A

0DataRank · unranked

107 citations

Christina A. Castellani, Ryan J. Longchamps, Vamsee Pillalamarri, Brian O’Rourke, Eliseo Güallar +2 more

Blood-derived mitochondrial DNA copy number is associated with gene expression across multiple tissues and is predictive for incident neurodegenerative disease

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.17.209023

N/A

0DataRank · unranked

13 citations

Christina A. Castellani, Ryan J. Longchamps, Vamsee Pillalamarri, Brian O’Rourke, Eliseo Güallar +2 more

Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100147

N/A

0DataRank · unranked

12 citations

Wen Shi, Conrad Say, Stephanie Yang, John Lane, Eliseo Güallar +3 more

Deleterious heteroplasmic mitochondrial mutations increase risk of overall and cancer-specific mortality

medRxiv(2022)10.1101/2022.09.20.22280151

N/A

0DataRank · unranked

2 citations

Yun Soo Hong, Wen Shi, Daniela Puiu, Vamsee Pillalamarri, Nathan Pankratz +5 more