Brandon Wilk

456 total citations
9 papers, 146 citations indexed

About

Brandon Wilk is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Brandon Wilk has authored 9 papers receiving a total of 146 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Brandon Wilk's work include Genomics and Rare Diseases (3 papers), Cystic Fibrosis Research Advances (2 papers) and Cancer Genomics and Diagnostics (2 papers). Brandon Wilk is often cited by papers focused on Genomics and Rare Diseases (3 papers), Cystic Fibrosis Research Advances (2 papers) and Cancer Genomics and Diagnostics (2 papers). Brandon Wilk collaborates with scholars based in United States. Brandon Wilk's co-authors include Melissa A. Wilk, Joseph Carroll, Elizabeth A. Worthey, Robert F. Cooper, Christopher S. Langlo, Gordana Raca, Jennifer Laffin, David Dimmock, Edythe A. Strand and Lawrence D. Shriberg and has published in prestigious journals such as BMC Bioinformatics, Vision Research and PLoS Computational Biology.

In The Last Decade

Brandon Wilk

8 papers receiving 145 citations

Peers

Brandon Wilk

MB

GENET

OPHTH

DEP

CN

Avinash M. Veerappa India

Emma McCann United Kingdom

Martha Schatz United States

Mark Lathrop France

Lucy Raymond United Kingdom

Kristen Kocher United States

Branka Stirn Kranjc Slovenia

Joseph Bursztyn France

Arthur W. Grix United States

Ke Ning United States

Avinash M. Veerappa India

Brandon Wilk

148 ×2.5

MB

112 ×2.3

GENET

3 ×0.1

OPHTH

24 ×0.6

DEP

17 ×0.5

CN

Citations per year, relative to Brandon Wilk Brandon Wilk (= 1×) peers Avinash M. Veerappa

Countries citing papers authored by Brandon Wilk

Since Specialization

Citations

This map shows the geographic impact of Brandon Wilk's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Brandon Wilk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brandon Wilk more than expected).

Fields of papers citing papers by Brandon Wilk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brandon Wilk. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Brandon Wilk. The network helps show where Brandon Wilk may publish in the future.

Co-authorship network of co-authors of Brandon Wilk

This figure shows the co-authorship network connecting the top 25 collaborators of Brandon Wilk. A scholar is included among the top collaborators of Brandon Wilk based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Brandon Wilk. Brandon Wilk is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

1.

Wilk, Brandon, et al.. (2023). Ten simple rules for using public biological data for your research. PLoS Computational Biology. 19(1). e1010749–e1010749. 2 indexed citations

2.

Wilk, Brandon, et al.. (2023). QuaC: A Pipeline Implementing Quality Control BestPractices for Genome Sequencing and Exome Sequencing Data. The Journal of Open Source Software. 8(90). 5313–5313.

3.

Lai, HuiChuan J., Qiongshi Lu, Sangita G. Murali, et al.. (2022). Genetic factors help explain the variable responses of young children with cystic fibrosis to vitamin D supplements. Clinical Nutrition ESPEN. 51. 367–376. 9 indexed citations

4.

Wilk, Melissa A., Andrew T. Braun, Philip M. Farrell, et al.. (2020). Applying whole-genome sequencing in relation to phenotype and outcomes in siblings with cystic fibrosis. Molecular Case Studies. 6(1). a004531–a004531. 9 indexed citations

5.

Holt, James, Brandon Wilk, Camille L. Birch, et al.. (2019). VarSight: prioritizing clinically reported variants with binary classification algorithms. BMC Bioinformatics. 20(1). 496–496. 11 indexed citations

6.

Wilk, Melissa A., Robert F. Cooper, Brandon Wilk, Christopher S. Langlo, & Joseph Carroll. (2016). Modeling the Relationship Between Foveal Cone Density and Outer Segment Length. Investigative Ophthalmology & Visual Science. 57(12). 1 indexed citations

7.

Wilk, Melissa A., Brandon Wilk, Christopher S. Langlo, Robert F. Cooper, & Joseph Carroll. (2016). Evaluating outer segment length as a surrogate measure of peak foveal cone density. Vision Research. 130. 57–66. 50 indexed citations

8.

Worthey, Elizabeth A., Gordana Raca, Jennifer Laffin, et al.. (2013). Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech. Journal of Neurodevelopmental Disorders. 5(1). 29–29. 62 indexed citations

9.

Worthey, Elizabeth A., David Bick, David Dimmock, et al.. (2012). Clinical diagnostic whole genome sequencing in a paediatric population: experience from our WGS genetics clinic. BMC Proceedings. 6(S6). 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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