Brandon J. Cushman

989 total citations
3 papers, 158 citations indexed

About

Brandon J. Cushman is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Brandon J. Cushman has authored 3 papers receiving a total of 158 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 1 paper in Genetics and 1 paper in Immunology. Recurrent topics in Brandon J. Cushman's work include Genomics and Phylogenetic Studies (2 papers), Genomics and Rare Diseases (1 paper) and Protein Tyrosine Phosphatases (1 paper). Brandon J. Cushman is often cited by papers focused on Genomics and Phylogenetic Studies (2 papers), Genomics and Rare Diseases (1 paper) and Protein Tyrosine Phosphatases (1 paper). Brandon J. Cushman collaborates with scholars based in United States, Switzerland and Cuba. Brandon J. Cushman's co-authors include Heidi L. Rehm, Marina T. DiStefano, Sarah E. Hemphill, Karen Eilbeck, Steven M. Harrison, Danielle R. Azzariti, Andrew R. Grant, Mitchell W. Dillon, Heather Mason‐Suares and Martin Zenker and has published in prestigious journals such as Human Mutation and Journal of Molecular Diagnostics.

In The Last Decade

Brandon J. Cushman

3 papers receiving 157 citations

Peers

Countries citing papers authored by Brandon J. Cushman

Since Specialization

Citations

This map shows the geographic impact of Brandon J. Cushman'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 J. Cushman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brandon J. Cushman more than expected).

Fields of papers citing papers by Brandon J. Cushman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brandon J. Cushman. 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 J. Cushman. The network helps show where Brandon J. Cushman may publish in the future.

Co-authorship network of co-authors of Brandon J. Cushman

This figure shows the co-authorship network connecting the top 25 collaborators of Brandon J. Cushman. A scholar is included among the top collaborators of Brandon J. Cushman 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 J. Cushman. Brandon J. Cushman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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3 of 3 papers shown

#	Work	Indexed citations
1	Curating Clinically Relevant Transcripts for the Interpretation of Sequence Variants 2018 ·Journal of Molecular Diagnostics ·Marina T. DiStefano, Sarah E. Hemphill, Brandon J. Cushman, Mark Bowser, Elizabeth Hynes, Andrew R. Grant, Rebecca K. Siegert, Andrea M. Oza, Michael Gonzalez, Sami S. Amr, Heidi L. Rehm, Ahmad Abou Tayoun	18
2	ClinVar Miner: Demonstrating utility of a Web-based tool for viewing and filtering ClinVar data 2018 ·Human Mutation ·(unknown), Sarah E. Hemphill, (unknown), Brandon J. Cushman, Marina T. DiStefano, Danielle R. Azzariti, Steven M. Harrison, Heidi L. Rehm, Karen Eilbeck	79
3	Assessing the gene–disease association of 19 genes with the RASopathies using the ClinGen gene curation framework 2018 ·Human Mutation ·Andrew R. Grant, Brandon J. Cushman, Hélène Cavé, Mitchell W. Dillon, Bruce D. Gelb, Karen W. Gripp, Jennifer A. Lee, Heather Mason‐Suares, Katherine A. Rauen, Marco Tartaglia, Lisa M. Vincent, Martin Zenker	61

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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