D.N. Cooper

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 1%percentile

34.6Author DataRank

Indexed papers

5in 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 5 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.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

Papers

Driven by 31 papers — median percentile 98. Top paper: “Analysis of protein-coding genetic variation in 60,706 humans”.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

Nature Communications(2014)10.1038/ncomms4934

Top 2%

8.3DataRank

Top 2%460 citations

Jonathan Marchini, Peter Donnelly, Gerton Lunter, Jonathan L. Marchini, Simon Myers +364 more

The genetic structure of the Turkish population reveals high levels of variation and admixture

Proceedings of the National Academy of Sciences(2021)10.1073/pnas.2026076118

Top 9%

2.4DataRank

Top 9%98 citations

A. Nazlı Başak, Onur Emre Onat, Kaya Bilgüvar, Jungmin Choi, Yuval Itan +11 more

Lineage-specific accelerated sequences underlying primate evolution

Science Advances(2023)10.1126/sciadv.adc9507

N/A

1.1DataRank · unranked

46 citations

Long Zhou, Jin-Jin Zhang, Shaohong Feng, Mei Hu, D.N. Cooper +5 more

A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes

Science(2012)10.1126/science.1215040

N/A

1.1DataRank · unranked

1321 citations

Suganthi Balasubramanian, Michael G. FitzGerald, Ni Huang, James Morris, Fred R. Hirsch +54 more

Inferring the molecular and phenotypic impact of amino acid variants with MutPred2

Nature Communications(2020)10.1038/s41467-020-19669-x

N/A

1.0DataRank · unranked

830 citations

Jorge Urresti, Jose Lugo-Martinez, Kymberleigh A. Pagel, Guan Ning Lin, Hyun‐Jun Nam +7 more

Effect of predicted protein-truncating genetic variants on the human transcriptome

Science(2015)10.1126/science.1261877

N/A

0.877DataRank · unranked

345 citations

Matti Pirinen, Donald F. Conrad, Monkol Lek, Emily K. Tsang, Konrad J. Karczewski +206 more

Distinct sequence features underlie microdeletions and gross deletions in the human genome

Human Mutation(2021)10.1002/humu.24314

Top 44%

0.421DataRank

Top 44%8 citations

Peter D. Stenson, Edward V. Ball, John A. Tainer, Albino Bacolla, Hildegard Kehrer‐Sawatzki +3 more

Profiling human pathogenic repeat expansion regions by synergistic and multi-level impacts on molecular connections

Human Genetics(2022)10.1007/s00439-022-02500-6

N/A

0DataRank · unranked

1 citations

Ken Chen, Yukai Wang, Edward V. Ball, Peter D. Stenson, Matthew Mort +6 more

Genome-wide detection of human variants that disrupt intronic branchpoints

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.18.488668

N/A

0DataRank · unranked

7 citations

Quentin Philippot, Weicheng Ren, Wei‐Te Lei, Juan Li, Peter D. Stenson +11 more

Genome-wide prediction of pathogenic gain- and loss-of-function variants from ensemble learning of a diverse feature set

Genome Medicine(2023)10.1186/s13073-023-01261-9

N/A

0DataRank · unranked

49 citations

Meltem Ece Kars, Yiming Wu, Çiğdem Sevim Bayrak, Peter D. Stenson, D.N. Cooper +3 more

Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites

Proceedings of the National Academy of Sciences(2023)10.1073/pnas.2314225120

N/A

0DataRank · unranked

19 citations

Matthieu Chaldebas, Masato Ogishi, Fahd Al Qureshah, Khoren Ponsin, Yi Feng +15 more

Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients

Nature Communications(2023)10.1038/s41467-023-37849-3

N/A

0DataRank · unranked

18 citations

Kyle Gettler, Meltem Ece Kars, Mamta Giri, Dalin Li, Çiğdem Sevim Bayrak +26 more

Development of a human genetics-guided priority score for 19,365 genes and 399 drug indications

Nature Genetics(2024)10.1038/s41588-023-01609-2

N/A

0DataRank · unranked

32 citations

Ben Omega Petrazzini, David Stein, Joshua K. Park, Iain S. Forrest, Kyle Gibson +12 more

Expanding drug targets for 112 chronic diseases using a machine learning-assisted genetic priority score

Nature Communications(2024)10.1038/s41467-024-53333-y

N/A

0DataRank · unranked

11 citations

Áine Duffy, Ben Omega Petrazzini, Ha My T. Vy, David Stein, Matthew Mort +8 more

Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa

UNC Libraries(2024)10.17615/k3wp-sy78

N/A

0DataRank · unranked

0 citations

D.N. Cooper, A.P. Reiner, A.P. Morris, Eric Young, Cristina Pomilla +52 more

Critical assessment of missense variant effect predictors on disease-relevant variant data

Human Genetics(2025)10.1007/s00439-025-02732-2

N/A

0DataRank · unranked

21 citations

Ryan Chung, Sindy Li, Chang Li, Kyoungyeul Lee, Junwoo Woo +31 more

Deciphering the digenic architecture of congenital heart disease using trio exome sequencing data

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.01.024

N/A

0DataRank · unranked

8 citations

David Stein, Peter D. Stenson, D.N. Cooper, Wendy K. Chung, Peter J. Gruber +6 more

Expanding the utility of variant effect predictions with phenotype-specific models

Nature Communications(2025)10.1038/s41467-025-66607-w

N/A

0DataRank · unranked

3 citations

Meltem Ece Kars, Baptiste Milisavljevic, Matthew Mort, Peter D. Stenson, Jean-Laurent Casanova +6 more

Development of a genetic priority score to predict drug side effects using human genetic evidence

Nature Communications(2025)10.1038/s41467-025-63762-y

N/A

0DataRank · unranked

1 citations

Robert Chen, David Stein, Joshua K. Park, Matthew Mort, Marie Verbanck +7 more

Disease-specific variant pathogenicity prediction using multimodal biomedical language models

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.09.09.675184

N/A

0DataRank · unranked

0 citations

D.N. Cooper, Haiyuan Yu, Yilin Liu

Predicting interaction-specific protein–protein interaction perturbations by missense variants with MutPred-PPI

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.64898/2025.12.20.695738

N/A

0DataRank · unranked

0 citations

Florent Laval, Georges Coppin, Kerstin Spirohn-Fitzgerald, Maxime Tixhon, Tong Hao +6 more

Role of the Common PRSS1-PRSS2 Haplotype in Alcoholic and Non-Alcoholic Chronic Pancreatitis: Meta- and Re-Analyses

Genes(2020)10.3390/genes11111349

N/A

0DataRank · unranked

17 citations

Emmanuelle Génin, D.N. Cooper, Emmanuelle Masson, Claude Férec, Jian‐Min Chen +1 more

Heritable pattern of oxidized DNA base repair coincides with pre-targeting of repair complexes to open chromatin

Nucleic Acids Research(2020)10.1093/nar/gkaa1120

N/A

0DataRank · unranked

35 citations

Shiladitya Sengupta, Zu Ye, Chunying Yang, Joy Mitra, Ruth B. De-Paula +7 more

Role of the common PRSS1-PRSS2 haplotype in alcoholic and non-alcoholic chronic pancreatitis: meta- and re-analyses

medRxiv(2020)10.1101/2020.10.13.20212365

N/A

0DataRank · unranked

1 citations

Emmanuelle Génin, D.N. Cooper, Emmanuelle Masson, Claude Férec, Jian‐Min Chen +1 more

Identifying novel high-impact rare disease-causing mutations, genes and pathways in exomes of Ashkenazi Jewish inflammatory bowel disease patients

medRxiv(2020)10.1101/2020.07.01.20143750

N/A

0DataRank · unranked

0 citations

Kyle Gettler, Mamta Giri, Dalin Li, Çiğdem Sevim Bayrak, Aayushee Jain +21 more

Identification of discriminative gene-level and protein-level features associated with pathogenic gain-of-function and loss-of-function variants

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.10.007

N/A

0DataRank · unranked

57 citations

David Stein, Aayushee Jain, Kumardeep Chaudhary, Girish N. Nadkarni, Tielman Van Vleck +8 more

DNA Methylation, Deamination, and Translesion Synthesis Combine to Generate Footprint Mutations in Cancer Driver Genes in B-Cell Derived Lymphomas and Other Cancers

Frontiers in Genetics(2021)10.3389/fgene.2021.671866

N/A

0DataRank · unranked

6 citations

Abiel Roche-Lima, Kathrin Tyryshkin, Kelvin Carrasquillo-Carrión, Artem G. Lada, Lennard Y. Poliakov +7 more

Genome-wide detection of human variants that disrupt intronic branchpoints

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2211194119

N/A

0DataRank · unranked

47 citations

Quentin Philippot, Weicheng Ren, Wei‐Te Lei, Juan Li, Peter D. Stenson +11 more

X-CAP improves pathogenicity prediction of stopgain variants

Genome Medicine(2022)10.1186/s13073-022-01078-y

N/A

0DataRank · unranked

4 citations

Peter D. Stenson, D.N. Cooper, Gill Bejerano, Ruchir Rastogi

D.N. Cooper

Indexed papers

Top data-sharing exemplar

Papers