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

Hamdi Mbarek

Qatar Cardiovascular Research Center

ORCID: 0000-0002-1108-0371

Also affiliated with Qatar Foundation

Biochemistry, Genetics and Molecular BiologyPsychologyMedicine

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 5%percentile
0.444Author 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.

Near-complete Middle Eastern genomes refine autozygosity and enhance disease-causing and population-specific variant discovery

Nature Genetics(2025)10.1038/s41588-025-02173-7
Top 42%
0.444DataRank
Top 42%5 citations

Shabir Moosa, Zenab Siddig, R. Farhad, Haroon Naeem, William T. Harvey +69 more

Papers

Driven by 14 papers — median percentile 58. Top paper: “Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns”.

Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

Nature Communications(2019)10.1038/s41467-019-10461-0
N/A
2.8DataRank · unranked
151 citations

Gökçen Eraslan, Christian M. Page, Jari Lahti, Marius Lahti-Pulkkinen, Esa Hämäläinen +233 more

Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

Nature Human Behaviour(2023)10.1038/s41562-023-01528-6
N/A
1.3DataRank · unranked
59 citations

Felix R. Day, Nicola Barban, Felix C. Tropf, David M. Brazel, Diana van Heemst +92 more

Near-complete Middle Eastern genomes refine autozygosity and enhance disease-causing and population-specific variant discovery

Nature Genetics(2025)10.1038/s41588-025-02173-7
Top 42%
0.444DataRank
Top 42%5 citations

Shabir Moosa, Zenab Siddig, R. Farhad, Haroon Naeem, William T. Harvey +69 more

Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19

medRxiv(2020)10.1101/2020.12.18.20248226
N/A
0DataRank · unranked
10 citations

Guillaume Butler‐Laporte, Ning Shang, Chen Weng, Atlas Khan, Manal Alaamery +44 more

Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

Digital Commons@Becker (Washington University School of Medicine)(2020)10.17615/msaw-3g92
N/A
0DataRank · unranked
0 citations

Patrick Deelen, David J. van Enckevort, Irene Mateo Leach, Gina M. Peloso, Mary F. Feitosa +27 more

Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight

Human Molecular Genetics(2021)10.1093/hmg/ddab121
N/A
0DataRank · unranked
18 citations

Rene Pool, Margot P. van de Weijer, Xu Chen, Eva Krapohl, Scott D. Gordon +29 more

Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.05.003
N/A
0DataRank · unranked
23 citations

Sze Hwee Seet, Michael Maier, Ayşe Gürel, Ricardo Moreno Traspas, Cheryl Lee +67 more

Loss of C2orf69 defines a fatal auto-inflammatory mitochondriopathy in Humans and Zebrafish

medRxiv(2021)10.1101/2021.03.31.21253863
N/A
0DataRank · unranked
0 citations

Sze Hwee Seet, Michael Maier, Ricardo Moreno Traspas, Cheryl Lee, Zhang Shan +42 more

Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

Nature Genetics(2023)10.1038/s41588-023-01314-0
N/A
0DataRank · unranked
190 citations

Abril G. Izquierdo, Jing Chen, Richard Packer, Robert J. Hall, Anna L. Guyatt +95 more

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

Digital Commons@Becker (Washington University School of Medicine)(2020)10.17615/5y99-4w88
N/A
0DataRank · unranked
5 citations

Terho Lehtimäki, P. Eline Slagboom, Albert V. Smith, Dennis O. Mook‐Kanamori, Paul Elliott +93 more

Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity

Human Reproduction(2023)10.1093/humrep/dead247
N/A
0DataRank · unranked
27 citations

Scott D. Gordon, David L Duffy, Nikki Hubers, Sally Mortlock, Jeffrey J. Beck +52 more

Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery: a multi-ancestry study in 10 960 individuals from 9 biobanks

medRxiv(2024)10.1101/2024.09.11.24313458
N/A
0DataRank · unranked
1 citations

Mattia Cordioli, Veronica Tozzo, Sarah Urbut, Kadri Arumäe, Roelof A. J. Smit +27 more

Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery

Nature Medicine(2025)10.1038/s41591-025-03645-3
N/A
0DataRank · unranked
36 citations

Mattia Cordioli, Veronica Tozzo, Sarah Urbut, Kadri Arumäe, Roelof A. J. Smit +27 more

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

UNC Libraries(2020)10.17615/2bje-6g29
N/A
0DataRank · unranked
0 citations

Deborah J. Thompson, Hannes Helgason, Timothy M. Frayling, Hilary K. Finucane, Patrick Sulem +211 more