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

Babak Alipanahi

Jefferson Einstein Philadelphia Hospital

ORCID: 0000-0001-8216-7178

Also affiliated with Science Exchange (United States), Palo Alto Institute, BioFire Diagnostics (United States)

Biochemistry, Genetics and Molecular Biology

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 2%percentile
3.0Author 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.

Resource profile and user guide of the Polygenic Index Repository

Nature Human Behaviour(2021)10.1038/s41562-021-01119-3
Top 7%
3.0DataRank
Top 7%184 citations

Casper A.P. Burik, Grant Goldman, Nancy Wang, Hariharan Jayashankar, Michael Bennett +60 more

Papers

Driven by 11 papers — median percentile 93. Top paper: “Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals”.

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Nature Genetics(2022)10.1038/s41588-022-01016-z
N/A
8.1DataRank · unranked
699 citations

Yeda Wu, Nancy Wang, Hariharan Jayashankar, Michael Bennett, Seyed Moeen Nehzati +94 more

Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets

Nature Communications(2021)10.1038/s41467-021-25171-9
N/A
5.0DataRank · unranked
156 citations

Steven Gazal, Po‐Ru Loh, Samuel S. Kim, Nicholas A. Furlotte, Adam Auton +26 more

The effect of LRRK2 loss-of-function variants in humans

Nature Medicine(2020)10.1038/s41591-020-0893-5
N/A
4.9DataRank · unranked
114 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric V. Minikel, Julia K. Goodrich +214 more

Resource profile and user guide of the Polygenic Index Repository

Nature Human Behaviour(2021)10.1038/s41562-021-01119-3
Top 7%
3.0DataRank
Top 7%184 citations

Casper A.P. Burik, Grant Goldman, Nancy Wang, Hariharan Jayashankar, Michael Bennett +60 more

A comprehensive re-assessment of the association between vitamin D and cancer susceptibility using Mendelian randomization

Nature Communications(2021)10.1038/s41467-020-20368-w
N/A
1.9DataRank · unranked
60 citations

Suzanne C. Dixon‐Suen, Xikun Han, Jiyuan An, Rebecca C. Fitzgerald, Matt Buas +61 more

Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/561472
N/A
0.977DataRank · unranked
17 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric Vallabh Minikel, Konrad J. Karczewski +35 more

Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways

Nature Communications(2018)10.1038/s41467-018-03819-3
N/A
0.974DataRank · unranked
660 citations

Abdel Abdellaoui, Masoud Shirali, Jane Hvarregaard Christensen, Riccardo E. Marioni, Gail Davies +40 more

Genome-wide association studies of LRRK2 modifiers of Parkinson's disease

medRxiv(2020)10.1101/2020.12.14.20224378
N/A
0.360DataRank · unranked
10 citations

Babak Alipanahi, Pierre Fontanillas, Tae‐Hwi Schwantes‐An, Jan Aasly, Roy N. Alcalay +55 more

Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

Nature Communications(2022)10.1038/s41467-022-33222-y
N/A
0.170DataRank · unranked
2 citations

Netta Mäkinen, Holly R. Harris, Nilüfer Rahmioğlu, Outi Uimari, James P. Cook +54 more

Leveraging deep-learning on raw spirograms to improve genetic understanding and risk scoring of COPD despite noisy labels

medRxiv(2022)10.1101/2022.09.12.22279863
N/A
0.104DataRank · unranked
1 citations

Babak Behsaz, Babak Alipanahi, Zachary R. McCaw, Davin Hill, Tae‐Hwi Schwantes‐An +7 more

Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease

Annals of Neurology(2021)10.1002/ana.26094
N/A
0DataRank · unranked
50 citations

Babak Alipanahi, Pierre Fontanillas, Tae‐Hwi Schwantes‐An, Jan Aasly, Roy N. Alcalay +56 more