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

John Lane

University of Minnesota

ORCID: 0000-0002-3582-5825
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 2%percentile
2.8Author DataRank

Indexed papers

2in 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 2 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.

Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

Cell Genomics(2022)10.1016/j.xgen.2021.100084
Top 10%
2.1DataRank
Top 10%82 citations

Matthew P. Conomos, Rebecca Keener, Kruthika Iyer, Joshua S. Weinstock, Lisa R. Yanek +95 more

Papers

Driven by 20 papers — median percentile 81. Top paper: “Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs”.

Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs

Genome Medicine(2020)10.1186/s13073-020-00778-7
N/A
3.0DataRank · unranked
123 citations

Ryan J. Longchamps, Jason A. Sumpter, Charles Newcomb, John Lane, Megan L. Grove +19 more

Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

Cell Genomics(2022)10.1016/j.xgen.2021.100084
Top 10%
2.1DataRank
Top 10%82 citations

Matthew P. Conomos, Rebecca Keener, Kruthika Iyer, Joshua S. Weinstock, Lisa R. Yanek +95 more

Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing’s Disease With or Without an MEN4 Phenotype

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgaa160
N/A
1.4DataRank · unranked
47 citations

Nathan Pankratz, John Lane, Fábio R. Faucz, Margaret F. Keil, Prashant Chittiboina +6 more

Structural variation across 138,134 samples in the TOPMed consortium

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.25.525428
Top 27%
0.737DataRank
Top 27%18 citations

Adam C. English, Ginger Metcalf, Jianzhi Yang, Mark J. P. Chaisson, Nathan Pankratz +82 more

Genetic drivers of Cushing’s disease: Frequency and associated phenotypes

Genetics in Medicine(2022)10.1016/j.gim.2022.08.021
N/A
0.576DataRank · unranked
14 citations

Nathan Pankratz, John Lane, Fábio R. Faucz, Prashant Chittiboina, Denise M. Kay +4 more

Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?

Frontiers in Endocrinology(2020)10.3389/fendo.2020.00433
N/A
0.539DataRank · unranked
13 citations

Laura C. Hernández‐Ramírez, Nancy Portillo, Ana L. Gómez-Gila, Inés Urrutia, Rosa Martı́nez +16 more

Exome sequencing identifies variants in infants with sacral agenesis

Birth Defects Research(2022)10.1002/bdr2.1987
N/A
0.241DataRank · unranked
4 citations

Marcia L. Feldkamp, Nathan Pankratz, John Lane, Denise M. Kay, Kristin M. Conway +21 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

Prediction of venous thromboembolism incidence in the general adult population using two published genetic risk scores

PLoS ONE(2023)10.1371/journal.pone.0280657
N/A
0DataRank · unranked
8 citations

Weihong Tang, Ching-Ping Hong, Wayne D. Rosamond, John Lane, Mary Cushman +2 more

Predicted leukocyte telomere length and risk of myeloid neoplasms

Human Molecular Genetics(2023)10.1093/hmg/ddad126
N/A
0DataRank · unranked
7 citations

Ben Cole, John Lane, John J. Meredith, Erica Langer, Anthony J. Hooten +5 more

Exploratory Study of the Association of Genetic Factors With Recovery of Adrenal Function in Cushing Disease

Journal of the Endocrine Society(2023)10.1210/jendso/bvad046
N/A
0DataRank · unranked
1 citations

Wei Zhang, Nathan Pankratz, John Lane, Prashant Chitiboina, Fábio R. Faucz +4 more

Structural variation across 138,134 samples in the TOPMed consortium

Research Square(2023)10.21203/rs.3.rs-2515453/v1
N/A
0DataRank · unranked
9 citations

Adam C. English, Ginger Metcalf, Jianzhi Yang, Mark J. P. Chaisson, Nathan Pankratz +82 more

Evaluation of mitochondrial DNA copy number estimation techniques

PLoS ONE(2020)10.1371/journal.pone.0228166
N/A
0DataRank · unranked
158 citations

Christina A. Castellani, Stephanie Yang, Charles Newcomb, Jason A. Sumpter, John Lane +8 more

Exome sequencing identifies variants in infants with sacral agenesis

UNC Libraries(2024)10.17615/sevc-bn40
N/A
0DataRank · unranked
0 citations

Faith Pangilinan, Andrew F. Olshan, Richard H. Finnell, Martha M. Werler, Cynthia A. Moore +24 more

Mitochondrial DNA copy number and incident atrial fibrillation

BMC Medicine(2020)10.1186/s12916-020-01715-6
N/A
0DataRank · unranked
40 citations

Traci M. Bartz, Nona Sotoodehnia, Wendy S. Post, Susan R. Heckbert, Álvaro Alonso +12 more

Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program

medRxiv(2020)10.1101/2020.12.09.20246736
N/A
0DataRank · unranked
10 citations

Adrienne M. Stilp, Caitlin McHugh, Shuquan Rao, Deepti Jain, Xiuwen Zheng +74 more

Exome sequencing of child–parent trios with bladder exstrophy: Findings in 26 children

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62439
N/A
0DataRank · unranked
8 citations

Marcia L. Feldkamp, Nathan Pankratz, John Lane, Denise M. Kay, Kristin M. Conway +17 more

Genetic analysis of mitochondrial DNA copy number and associated traits identifies loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation, and reveals a causal association of mitochondrial function with mortality

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.25.428086
N/A
0DataRank · unranked
8 citations

Stephanie Yang, Christina A. Castellani, Wen Shi, John Lane, ML Grove +47 more

Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program

medRxiv(2021)10.1101/2021.12.16.21267871
N/A
0DataRank · unranked
6 citations

Adrienne M. Stilp, Shuquan Rao, Bjarni V. Halldórsson, Doruk Beyter, Jia Wen +54 more

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Nature Communications(2022)10.1038/s41467-022-35354-7
N/A
0DataRank · unranked
18 citations

Adrienne M. Stilp, Shuquan Rao, Bjarni V. Halldórsson, Doruk Beyter, Jia Wen +54 more