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

Bernard Keavney

Manchester Academic Health Science Centre

ORCID: 0000-0001-9573-0812

Also affiliated with Manchester Royal Infirmary, University of Manchester, British Heart Foundation, Manchester University NHS Foundation Trust, NIHR Manchester Biomedical Research Centre

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

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 →

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.

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

Scientific Reports(2021)10.1038/s41598-021-94021-x
Top 100%
0DataRank
Top 100%0 citations

Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler +21 more

Papers

Driven by 10 papers — median percentile 0. Top paper: “Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney”.

Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney

Nature Genetics(2021)10.1038/s41588-021-00835-w
N/A
2.7DataRank · unranked
68 citations

Xiao Jiang, Xiaoguang Xu, Sushant Saluja, Artur Akbarov, Eddie Cano-Gamez +44 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

Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

Scientific Reports(2020)10.1038/s41598-020-74650-4
N/A
0.955DataRank · unranked
26 citations

Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler +21 more

Hypertension and renin-angiotensin system blockers are not associated with expression of Angiotensin Converting Enzyme 2 (ACE2) in the kidney

medRxiv(2020)10.1101/2020.05.19.20106781
N/A
0.330DataRank · unranked
8 citations

James Eales, David Scannali, Alicja Nazgiewicz, Priscilla R. Prestes, Michelle C. Maier +27 more

Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability

Cell Reports Medicine(2022)10.1016/j.xcrm.2021.100501
N/A
0DataRank · unranked
11 citations

Wenjuan Zhu, Xinxiu Xu, Cullen B. Young, Tuantuan Tan, Amanda M. Smith +32 more

Hypertension and renin-angiotensin system blockers are not associated with expression of angiotensin-converting enzyme 2 (ACE2) in the kidney

European Heart Journal(2020)10.1093/eurheartj/ehaa794
N/A
0DataRank · unranked
55 citations

James Eales, David Scannali, Alicja Nazgiewicz, Priscilla R. Prestes, Michelle C. Maier +28 more

Genetic imputation of kidney transcriptome, proteome and multi-omics illuminates new blood pressure and hypertension targets

Nature Communications(2024)10.1038/s41467-024-46132-y
N/A
0DataRank · unranked
23 citations

Chachrit Khunsriraksakul, James Eales, Sébastien Rubin, David Scannali, Sushant Saluja +34 more

Cardiac imaging of aortic valve area from 26,142 UK Biobank participants reveal novel genetic associations and shared genetic comorbidity with multiple disease phenotypes

medRxiv(2020)10.1101/2020.04.09.20060012
N/A
0DataRank · unranked
3 citations

Catherine Tcheandjieu, Jason Fries, Paroma Varma, Vincent S. Chen, Madalina Fiterau +11 more

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

Genetics in Medicine(2021)10.1038/s41436-021-01212-y
N/A
0DataRank · unranked
17 citations

Najim Lahrouchi, Fernanda M. Bosada, Gregor Dombrowsky, Simon G. Williams, Robert Lesurf +49 more

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

Scientific Reports(2021)10.1038/s41598-021-94021-x
Top 100%
0DataRank
Top 100%0 citations

Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler +21 more