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

Khalid A. Fakhro

Qatar Airways (Qatar)

ORCID: 0000-0002-3150-1276

Also affiliated with Sidra Medical and Research Center, Hamad bin Khalifa University, Weill Cornell Medical College in Qatar

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 4%percentile
0.652Author DataRank

Indexed papers

3in 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 3 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.

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 7 papers — median percentile 46. Top paper: “GA4GH: International policies and standards for data sharing across genomic research and healthcare”.

GA4GH: International policies and standards for data sharing across genomic research and healthcare

Cell Genomics(2021)10.1016/j.xgen.2021.100029
N/A
6.0DataRank · unranked
306 citations

Angela Page, Lindsay Smith, Jeremy Adams, Gil Alterovitz, Lawrence Babb +95 more

Genetic variations influence brain changes in patients with attention-deficit hyperactivity disorder

Translational Psychiatry(2021)10.1038/s41398-021-01473-w
N/A
0.675DataRank · unranked
89 citations

Ajaz A. Bhat, Sheema Hashem, Sabah Nisar, Madeeha Kamal, Najeeb Syed +12 more

Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications

Nature Communications(2024)10.1038/s41467-024-46354-0
N/A
0.568DataRank · unranked
43 citations

Henriette Aksnes, Reza Maroofian, Lauren C. LaMonica, Luís Seabra, Anette Siggervåg +55 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

Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

medRxiv(2022)10.1101/2022.05.05.22274031
Top 65%
0.208DataRank
Top 65%3 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

Equity, diversity, and inclusion at the Global Alliance for Genomics and Health

Cell Genomics(2023)10.1016/j.xgen.2023.100386
N/A
0DataRank · unranked
18 citations

Shakuntala Baichoo, Tiffany Boughtwood, Esmeralda Casas-Silva, Subhashini Chandrasekharan, Sanjay Dave +20 more

Genomic architecture of autism from comprehensive whole-genome sequence annotation

Cell(2022)10.1016/j.cell.2022.10.009
N/A
0DataRank · unranked
280 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more