Brandon Wilk

Also affiliated with University of Alabama at Birmingham, National Human Genome Research Institute, Institut thématique Génétique, génomique et bioinformatique, National Institutes of Health Clinical Center

Biochemistry, Genetics and Molecular BiologyMedicineComputer Science

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 5 papers. Top paper: “Applying whole-genome sequencing in relation to phenotype and outcomes in siblings with cystic fibrosis”.

Applying whole-genome sequencing in relation to phenotype and outcomes in siblings with cystic fibrosis

Molecular Case Studies(2020)10.1101/mcs.a004531

N/A

0DataRank · unranked

11 citations

Andrew T. Braun, Philip M. Farrell, Anita Laxova, Donna M. Brown, James Holt +5 more

Genetic factors help explain the variable responses of young children with cystic fibrosis to vitamin D supplements

Clinical Nutrition ESPEN(2022)10.1016/j.clnesp.2022.07.018

N/A

0DataRank · unranked

11 citations

Jie Song, Qiongshi Lu, Sangita G. Murali, Manavalan Gajapathy, Brandon Wilk +4 more

Ten simple rules for using public biological data for your research

PLoS Computational Biology(2023)10.1371/journal.pcbi.1010749

N/A

0DataRank · unranked

6 citations

Jordan H. Whitlock, Elizabeth J. Wilk, Angelina Uno-Antonison, Brandon Wilk, Manavalan Gajapathy +6 more

DITTO: An Explainable Machine-Learning Model for Transcript-Specific Variant Pathogenicity Prediction

Preprints.org(2024)10.20944/preprints202404.0837.v1

N/A

0DataRank · unranked

2 citations

Brandon Wilk, Manavalan Gajapathy, Elizabeth A. Worthey, Tarun Karthik Kumar Mamidi

An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser

Genome Medicine(2025)10.1186/s13073-025-01546-1

N/A

0DataRank · unranked

8 citations

Shruti Marwaha, Alistair Ward, Shilpa N. Kobren, Jennefer N. Carter, Undiagnosed Diseases Network +94 more