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

Anthony M. Musolf

Merck & Co., Inc., Rahway, NJ, USA (United States)

ORCID: 0000-0002-7290-483X
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 2%percentile
2.7Author 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.

IMI 2021 Yearly Digest

Investigative Ophthalmology & Visual Science(2021)10.1167/iovs.62.5.7
Top 9%
2.5DataRank
Top 9%68 citations

Jost B. Jonas, James S. Wolffsohn, David A. Berntsen, Pauline Cho, Danielle Clarkson-Townsend +20 more

Papers

Driven by 15 papers — median percentile 35. Top paper: “What makes a good prediction? Feature importance and beginning to open the black box of machine learning in genetics”.

What makes a good prediction? Feature importance and beginning to open the black box of machine learning in genetics

Human Genetics(2021)10.1007/s00439-021-02402-z
N/A
3.4DataRank · unranked
127 citations

Emily Holzinger, James D. Malley, Joan E. Bailey-Wilson, Anthony M. Musolf

IMI 2021 Yearly Digest

Investigative Ophthalmology & Visual Science(2021)10.1167/iovs.62.5.7
Top 9%
2.5DataRank
Top 9%68 citations

Jost B. Jonas, James S. Wolffsohn, David A. Berntsen, Pauline Cho, Danielle Clarkson-Townsend +20 more

A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degeneration

EBioMedicine(2023)10.1016/j.ebiom.2023.104551
N/A
0.749DataRank · unranked
33 citations

Samantha Sze‐Yee Lee, Ran Du, Yining Wang, Sander C. M. Kneepkens, Jason Charng +91 more

Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape

Nature Communications(2023)10.1038/s41467-023-43237-8
N/A
0.608DataRank · unranked
26 citations

Hanne Hoskens, Ryan J. Eller, Noah Herrick, Anthony M. Musolf, Cristina M. Justice +15 more

Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428

Scientific Reports(2024)10.1038/s41598-024-58343-w
N/A
0.241DataRank · unranked
4 citations

Cristina M. Justice, Zeynep Erdogan-Yildirim, Seppe Goovaerts, Araceli Cuellar, John R. Shaffer +16 more

Genome-wide linkage search for cancer susceptibility loci in a cohort of non BRCA1/2 families in Sri Lanka

BMC Research Notes(2022)10.1186/s13104-022-06081-5
Top 65%
0.206DataRank
Top 65%2 citations

Anthony M. Musolf, Joan E. Bailey-Wilson, T. Kalum Wetthasinghe, Vajira H. W. Dissanayake, Prabhavi Wijesiriwardhana

Transmission disequilibrium analysis of whole genome data in childhood-onset systemic lupus erythematosus

Genes and Immunity(2023)10.1038/s41435-023-00214-x
N/A
0DataRank · unranked
7 citations

Anthony M. Musolf, Joan E. Bailey-Wilson, Linda T. Hiraki, Earl D. Silverman, Christiaan Scott +6 more

A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall‐cell lung cancer

International Journal of Cancer(2023)10.1002/ijc.34510
N/A
0DataRank · unranked
3 citations

Craig C. Teerlink, Jeff Stevens, Julio C. Facelli, Shamus R. Carr, Kristina Allen-Brady +5 more

Data from Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer

(2023)10.1158/0008-5472.c.6513273.v1
N/A
0DataRank · unranked
0 citations

Claire L. Simpson, Bilal A. Moiz, Claudio W. Pikielny, Candace D. Middlebrooks, Diptasri Mandal +13 more

Entanglement Mapping: A Novel Method to Detect Interacting SNPs in Genome-Wide Studies

(2022)10.1109/cibcb55180.2022.9863029
N/A
0DataRank · unranked
1 citations

Anthony M. Musolf, James D. Malley, Daniel S. Kiser, Dwight Stambolian, Qing Li +2 more

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants

UNC Libraries(2020)10.17615/gd7n-3n77
Top 100%
0DataRank
Top 100%0 citations

Olivier Cussenot, Diptasri Mandal, Nilah M. Ioannidis, Graham G. Giles, Shannon K. McDonnell +36 more

Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer

Cancer Research(2021)10.1158/0008-5472.can-20-3196
N/A
0DataRank · unranked
11 citations

Claire L. Simpson, Bilal A. Moiz, Claudio W. Pikielny, Candace D. Middlebrooks, Diptasri Mandal +13 more

A likely HOXC4 predisposition variant for Chiari malformations

Journal of neurosurgery(2022)10.3171/2022.10.jns22956
N/A
0DataRank · unranked
6 citations

Samuel Cheshier, Jeff Stevens, Julio C. Facelli, Kerry Rowe, John D. Heiss +5 more

Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error

Communications Biology(2020)10.1038/s42003-020-0802-y
N/A
0DataRank · unranked
42 citations

Alfred Pozarickij, Nicholas Y.Q. Tan, Xiaobo Guo, Virginie J. M. Verhoeven, Véronique Vitart +94 more

Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

Communications Biology(2023)10.1038/s42003-022-04323-7
N/A
0DataRank · unranked
10 citations

Annechien E. G. Haarman, Robert Luben, Jue‐Sheng Ong, Karina Patasova, Rolando Hernández Trapero +89 more