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

Ziad Khan

Baylor College of Medicine

ORCID: 0000-0003-2173-9771

Also affiliated with Abbottabad University of Science and Technology, Baylor Genetics

Biochemistry, Genetics and Molecular BiologyAgricultural and Biological Sciences

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
15.5Author 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.

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x
Top 2%
8.6DataRank
Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

Papers

Driven by 9 papers — median percentile 96. Top paper: “Genomic data in the All of Us Research Program”.

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x
Top 2%
8.6DataRank
Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

Benchmarking challenging small variants with linked and long reads

Cell Genomics(2022)10.1016/j.xgen.2022.100128
Top 4%
4.9DataRank
Top 4%212 citations

Nathan D. Olson, Lindsay Harris, Ziad Khan, Jesse Farek, Medhat Mahmoud +36 more

Benchmarking challenging small variants with linked and long reads

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.24.212712
Top 11%
2.0DataRank
Top 11%60 citations

Nathan D. Olson, Lindsay Harris, Jennifer McDaniel, Ziad Khan, Jesse Farek +37 more

A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus

Nature Genetics(2024)10.1038/s41588-024-01808-5
N/A
0.533DataRank · unranked
34 citations

Giulia Gobbo, Madeline Couse, Egor Dolzhenko, Sathiji Nageshwaran, Warren Cheung +95 more

Sequence analysis in Bos taurus reveals pervasiveness of X–Y arms races in mammalian lineages

Genome Research(2020)10.1101/gr.269902.120
N/A
0DataRank · unranked
50 citations

Helen Skaletsky, Tatyana Pyntikova, Natalia Koutseva, Terje Raudsepp, Laura G. Brown +19 more

Constellation illuminates rare disease genetics

medRxiv(2025)10.1101/2025.10.15.25337675
N/A
0DataRank · unranked
0 citations

Qing Zhang, Xinchang Zheng, Shalini N. Jhangiani, Jacqueline Weir, Jesse Farek +15 more

Exome variant discrepancies due to reference-genome differences

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.05.011
N/A
0DataRank · unranked
66 citations

Moez Dawood, Michael M. Khayat, Jesse Farek, Shalini N. Jhangiani, Ziad Khan +8 more

The SHR/Akr Y chromosome reveals repeated turnover of the rat pseudoautosomal region

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.28.656580
N/A
0DataRank · unranked
1 citations

Helen Skaletsky, Jennifer F. Hughes, Laura G. Brown, Tatyana Pyntikova, Ting-Jan Cho +15 more

Celeste : A cloud-based genomics infrastructure with variant-calling pipeline suited for population-scale sequencing projects

medRxiv(2025)10.1101/2025.04.29.25326690
N/A
0DataRank · unranked
0 citations

Breanna Lee, Victoria Yi, Jesse Farek, Ziad Khan, Sara E. Kalla +12 more