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

Saquib A. Lakhani

Cedars-Sinai Medical Center

ORCID: 0000-0003-3235-3460

Also affiliated with Yale Cancer Center, Yale University

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 6%percentile
0.176Author 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.

A retrospective cohort analysis of the Yale pediatric genomics discovery program

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62918
Top 67%
0.176DataRank
Top 67%2 citations

Lauren Jeffries, E. Vincent S. Faustino, Weizhen Ji, Emily K. Mis, Monica Konstantino +15 more

Papers

Driven by 12 papers — median percentile 33. Top paper: “A retrospective cohort analysis of the Yale pediatric genomics discovery program”.

A retrospective cohort analysis of the Yale pediatric genomics discovery program

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62918
Top 67%
0.176DataRank
Top 67%2 citations

Lauren Jeffries, E. Vincent S. Faustino, Weizhen Ji, Emily K. Mis, Monica Konstantino +15 more

Human autoinflammatory disease reveals ELF4 as a transcriptional regulator of inflammation

Nature Immunology(2021)10.1038/s41590-021-00984-4
N/A
0DataRank · unranked
108 citations

Molly L. Bucklin, Mengting Zhao, Timothy J. Maher, Andrew J. Rice, Weizhen Ji +13 more

Expansion of NEUROD2 phenotypes to include developmental delay without seizures

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62064
N/A
0DataRank · unranked
11 citations

Annalisa G. Sega, Rebecca Signer, Tracy Cartwright, Weizhen Ji, Julián A. Martínez-Agosto +12 more

Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta

Genetics in Medicine(2023)10.1016/j.gim.2023.100856
N/A
0DataRank · unranked
9 citations

Nicolas Chassaing, Nicola Ragge, Felix Boschann, Angelina My-Hoa Ngu, Elisabeth Meloche +49 more

A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorder

Journal of Clinical Investigation(2024)10.1172/jci174824
N/A
0DataRank · unranked
28 citations

Hartmut Cuny, Ella MMA Martin, Delicia Z Sheng, Kavitha R. Iyer, Stephanie Portelli +34 more

“Deficiency in ELF4, X-Linked”: a Monogenic Disease Entity Resembling Behçet’s Syndrome and Inflammatory Bowel Disease

Journal of Clinical Immunology(2024)10.1007/s10875-023-01610-8
N/A
0DataRank · unranked
15 citations

Shannon K. O’Connor, Marat Kribis, Molly L. Bucklin, Dinesh Babu Uthaya Kumar, Paul Tyler +25 more

CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow

Life Science Alliance(2024)10.26508/lsa.202402708
N/A
0DataRank · unranked
6 citations

Irmak Sakin, Stephen Viviano, Gülten Tuncel, Stephanie Marie Aguilera, Gizem Goles +15 more

Genetic profile of progressive myoclonic epilepsy in Mali reveals novel findings

Frontiers in Neurology(2024)10.3389/fneur.2024.1455467
N/A
0DataRank · unranked
1 citations

Salia Bamba, Seybou Hassane Diallo, Weizhen Ji, M Dembélé, Abdoulaye Yalcouyé +18 more

Mass spectrometry combined with machine learning identifies novel protein signatures as demonstrated with multisystem inflammatory syndrome in children

Scientific Reports(2025)10.1038/s41598-025-20684-5
N/A
0DataRank · unranked
1 citations

Haiyan Zheng, Benjamin Richlin, Christian Suarez, Sunanda Gaur, Elizabeth Ricciardi +20 more

Combining Mass Spectrometry with Machine Learning to Identify Novel Protein Signatures: The Example of Multisystem Inflammatory Syndrome in Children

medRxiv(2025)10.1101/2025.04.17.25325767
N/A
0DataRank · unranked
0 citations

Haiyan Zheng, Benjamin Richlin, Christian Suarez, Sunanda Gaur, Elizabeth Ricciardi +20 more

Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

Human Molecular Genetics(2020)10.1093/hmg/ddaa050
N/A
0DataRank · unranked
42 citations

Athina Ververi, Ana Beleza‐Meireles, Weizhen Ji, Emily K. Mis, Quinten Patterson +25 more

Trio exome analysis is a valuable tool for genetic diagnosis of epilepsy in Mali

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103449
N/A
0DataRank · unranked
0 citations

Lauren Jeffries, Salimata Diarra, Karamoko Nimaga, Amadou Touré, Modibo K. Goita +28 more