David R. Crosslin

Also affiliated with University of New Orleans, Tula University

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 100%percentile

0Author DataRank

Indexed papers

4in 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 4 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 →

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

An atlas of genetic variation for linking pathogen-induced cellular traits to human disease

10.1101/202325

Top 51%

0.345DataRank

Top 51%9 citations

Kelly J. Pittman, Jeffrey R. Barker, Raul E. Salinas, Ian B. Stanaway, Graham D. Williams +16 more

Papers

Driven by 28 papers — median percentile 0. Top paper: “A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects”.

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects

Human Genetics(2014)10.1007/s00439-013-1355-7

N/A

5.1DataRank · unranked

148 citations

Joshua C. Denny, Keyue Ding, Hayan Jouni, David R. Crosslin, Mariza de Andrade +15 more

Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

Nature Medicine(2024)10.1038/s41591-024-02796-z

N/A

4.8DataRank · unranked

196 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Joshua Arias, Gillian M. Belbin +73 more

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Genetics in Medicine(2023)10.1016/j.gim.2023.100006

N/A

2.6DataRank · unranked

121 citations

Aimee Allworth, Harris T. Bland, Pedro J. Caraballo, Rex L. Chisholm, Ellen Wright Clayton +95 more

Genome-wide polygenic score to predict chronic kidney disease across ancestries

Nature Medicine(2022)10.1038/s41591-022-01869-1

N/A

0.764DataRank · unranked

162 citations

Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru +34 more

A genome-wide association study of polycystic ovary syndrome identified from electronic health records

American Journal of Obstetrics and Gynecology(2020)10.1016/j.ajog.2020.04.004

N/A

0.698DataRank · unranked

104 citations

Kevin Ho, Jacob M. Keaton, Dustin N. Hartzel, Felix R. Day, Anne E. Justice +15 more

A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgz326

N/A

0.626DataRank · unranked

64 citations

Ky’Era V. Actkins, Jennifer A. Pacheco, Anna O. Basile, Robert J. Carroll, David R. Crosslin +66 more

The polygenic architecture of left ventricular mass mirrors the clinical epidemiology

Scientific Reports(2020)10.1038/s41598-020-64525-z

N/A

0.442DataRank · unranked

18 citations

Rebecca T. Levinson, Eric Farber‐Eger, Todd L. Edwards, Jacklyn N. Hellwege, Adriana M. Hung +20 more

Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid

Human Genetics(2022)10.1007/s00439-022-02442-z

N/A

0.406DataRank · unranked

14 citations

Jacklyn N. Hellwege, Yanfei Zhang, Eric S. Torstenson, Gail P. Jarvik, Ozan Dikilitas +10 more

An atlas of genetic variation for linking pathogen-induced cellular traits to human disease

10.1101/202325

Top 51%

0.345DataRank

Top 51%9 citations

Kelly J. Pittman, Jeffrey R. Barker, Raul E. Salinas, Ian B. Stanaway, Graham D. Williams +16 more

Neptune: an environment for the delivery of genomic medicine

Genetics in Medicine(2021)10.1038/s41436-021-01230-w

N/A

0.330DataRank · unranked

8 citations

Victoria Yi, David R. Murdock, Sara E. Kalla, Tsung-Jung Wu, Aniko Sabo +93 more

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

medRxiv(2023)10.1101/2023.05.25.23290535

N/A

0.330DataRank · unranked

8 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Josh Arias, Gillian M. Belbin +71 more

Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

Scientific Reports(2023)10.1038/s41598-023-45649-4

N/A

0.281DataRank · unranked

3 citations

Taryn O. Hall, Dana C. Crawford, Robb Rowley, Benjamin A. Satterfield, Rongling Li +21 more

Hemochromatosis risk genotype is not associated with colorectal cancer or age at its diagnosis

Human Genetics and Genomics Advances(2020)10.1016/j.xhgg.2020.100010

N/A

0.269DataRank · unranked

5 citations

Xiaoliang Wang, Pierre Fontanillas, Esther Kim, Sirisak Chanprasert, Allan Gordon +55 more

Genome-wide polygenic score with APOL1 risk genotypes predicts chronic kidney disease across major continental ancestries

medRxiv(2021)10.1101/2021.10.25.21265398

N/A

0.218DataRank · unranked

2 citations

Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru +33 more

Insights from the largest diverse ancestry sex-specific disease map for genetically predicted height

npj Genomic Medicine(2025)10.1038/s41525-025-00464-w

N/A

0.104DataRank · unranked

1 citations

Elizabeth Litkowski, Mariaelisa Graff, Zhe Wang, Roelof A. J. Smit, Geetha Chittoor +34 more

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

UNC Libraries(2020)10.17615/02rz-mz46

N/A

0DataRank · unranked

0 citations

Jane Ranchalis, Mitzi L. Murray, Ann Katherine M. Foreman, Seema M. Jamal, Andrew D. Johnson +27 more

Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience

UNC Libraries(2023)10.17615/wbfb-8h23

N/A

0DataRank · unranked

2 citations

P. Murali, Fangjing Chen, R. Green, Mark Kvale, David R. Crosslin +15 more

Transformer patient embedding using electronic health records enables patient stratification and progression analysis

npj Digital Medicine(2025)10.1038/s41746-025-01872-z

N/A

0DataRank · unranked

10 citations

Monika E. Grabowska, Iftikhar J. Kullo, Yuan Luo, Jordan W. Smoller, Theresa L. Walunas +5 more

Polygenic risk scores in the clinic: Health-system leaders and primary care providers weigh in

Genetics in Medicine(2025)10.1016/j.gim.2025.101575

N/A

0DataRank · unranked

2 citations

Stephanie M. Fullerton, Betty Cohn, David R. Crosslin, Gail P. Jarvik, Susan Brown Trinidad

Loci identified by a genome‐wide association study of carotid artery stenosis in the eMERGE network

Genetic Epidemiology(2020)10.1002/gepi.22360

N/A

0DataRank · unranked

10 citations

Daniel Seung Kim, David R. Crosslin, Ian B. Stanaway, Elisabeth A. Rosenthal, David Carrell +19 more

Penetrance of breast cancer genes from the eMERGE III Network

10.1101/2021.04.24.21255936

Top 100%

0DataRank

Top 100%0 citations

Julia Wynn, Ning Shang, Cong Liu, Alexander Fedotov, Miranda L.G. Hallquist +24 more

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

UNC Libraries(2020)10.17615/s8sd-h432

Top 100%

0DataRank

Top 100%0 citations

Todd L. Edwards, Jin Li, John M. Starr, Eric Boerwinkle, Yingchang Lu +92 more

Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.09.011

N/A

0DataRank · unranked

112 citations

Kathleen Muenzen, Leslie G. Biesecker, Kevin M. Bowling, Gregory M. Cooper, Michael O. Dorschner +25 more

What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk?

Patient Education and Counseling(2021)10.1016/j.pec.2021.01.001

N/A

0DataRank · unranked

15 citations

Sukh Makhnoon, Brian H. Shirts, Stephanie M. Fullerton, Eric B. Larson, James D. Ralston +5 more

Collaborative Cross Founder Expression Analysis (CCFEA)

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.04.422591

N/A

0DataRank · unranked

0 citations

Reneé C. Ireton, Martin T. Ferris, Kathleen Muenzen, David R. Crosslin, Michael Gale +1 more

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

UNC Libraries(2020)10.17615/m864-xv86

N/A

0DataRank · unranked

0 citations

Lisa R. Yanek, Kjell Nikus, Salman M. Tajuddin, Jussi Hernesniemi, Dawn Waterworth +95 more

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

UNC Libraries(2020)10.17615/a384-d483

N/A

0DataRank · unranked

0 citations

Jerome I. Rotter, Alex P. Reiner, André G. Uitterlinden, Gonçalo R. Abecasis, Digna R. Velez Edwards +95 more

Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100120

N/A

0DataRank · unranked

12 citations

Laura M. Amendola, Tia L. Kauffman, Kathleen F. Mittendorf, Jeannette T. Bensen, Flavia Chen +15 more

David R. Crosslin

Indexed papers

Top data-sharing exemplar

Papers