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

James P. Cook

University of Liverpool

ORCID: 0000-0001-9927-5394

Also affiliated with King's College Hospital NHS Foundation Trust, Genomics England, King's College Hospital

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
8.5Author 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.

Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank

The Lancet Respiratory Medicine(2015)10.1016/s2213-2600(15)00283-0
Top 2%
7.7DataRank
Top 2%438 citations

Nick Shrine, Suzanne Miller, Victoria E. Jackson, Ioanna Ntalla, María Soler Artigas +39 more

Papers

Driven by 13 papers — median percentile 87. Top paper: “Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank”.

Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank

The Lancet Respiratory Medicine(2015)10.1016/s2213-2600(15)00283-0
Top 2%
7.7DataRank
Top 2%438 citations

Nick Shrine, Suzanne Miller, Victoria E. Jackson, Ioanna Ntalla, María Soler Artigas +39 more

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

Nature Genetics(2020)10.1038/s41588-020-00713-x
N/A
3.7DataRank · unranked
242 citations

Elena V. Feofanova, Najim Lahrouchi, Ioanna Ntalla, Savita Karthikeyan, James P. Cook +94 more

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

Nature Genetics(2024)10.1038/s41588-024-01714-w
N/A
2.4DataRank · unranked
193 citations

Zoha Kamali, Tian Xie, Ahmad Vaez, Ariel Williams, Slavina B. Goleva +95 more

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Nature Genetics(2022)10.1038/s41588-022-01058-3
N/A
0.994DataRank · unranked
754 citations

Cassandra N. Spracklen, Weihua Zhang, Maggie C. Y. Ng, Lauren E. Petty, Hidetoshi Kitajima +95 more

The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

Nature Genetics(2023)10.1038/s41588-023-01323-z
N/A
0.853DataRank · unranked
293 citations

Sally Mortlock, Marzieh Ghiasi, Peter Möller, Lilja Stefánsdóttir, Geneviève Galarneau +95 more

The Genomics of Heart Failure: Design and Rationale of the HERMES Consortium

ESC Heart Failure(2021)10.1002/ehf2.13517
Top 24%
0.829DataRank
Top 24%22 citations

Sonia Shah, Honghuang Lin, Tomasz Czuba, Albert Henry, Daniel I. Swerdlow +95 more

Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes

Human Molecular Genetics(2022)10.1093/hmg/ddac050
N/A
0.730DataRank · unranked
129 citations

Gunn-Helen Moen, Maria Carolina Borges, Teresa Ferreira, James P. Cook, Catherine Allard +68 more

Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts

The Lancet Respiratory Medicine(2020)10.1016/s2213-2600(20)30101-6
N/A
0.727DataRank · unranked
126 citations

Phuwanat Sakornsakolpat, Nick Shrine, Brian D. Hobbs, Dawn L. DeMeo, Catherine John +82 more

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

Kidney International(2022)10.1016/j.kint.2022.05.021
N/A
0.601DataRank · unranked
54 citations

Humaira Rasheed, Alexander Teumer, Laurent F. Thomas, Sarah E. Graham, Garðar Sveinbjörnsson +94 more

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

Nature Communications(2022)10.1038/s41467-022-32821-z
N/A
0.596DataRank · unranked
52 citations

Najim Lahrouchi, Aaron Isaacs, ThuyVy Duong, Luisa Foco, Farah Ahmed +95 more

Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

Nature Communications(2022)10.1038/s41467-022-33222-y
N/A
0.170DataRank · unranked
2 citations

Netta Mäkinen, Holly R. Harris, Nilüfer Rahmioğlu, Outi Uimari, James P. Cook +54 more

Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

Nature(2024)10.1038/s41586-024-07019-6
N/A
0DataRank · unranked
537 citations

Konstantinos Hatzikotoulas, Lorraine Southam, Henry J. Taylor, Xianyong Yin, Kimberly Lorenz +95 more

Functional validity, role, and implications of heavy alcohol consumption genetic loci

Science Advances(2020)10.1126/sciadv.aay5034
N/A
0DataRank · unranked
76 citations

James P. Cook, Hélène Choquet, Eric Jorgenson, Jie Yin, Tarja Kinnunen +4 more