Brenna Boyd

606 total citations
2 papers, 6 citations indexed

About

Brenna Boyd is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, Brenna Boyd has authored 2 papers receiving a total of 6 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Genetics and 0 papers in Infectious Diseases. Recurrent topics in Brenna Boyd's work include Genomic variations and chromosomal abnormalities (1 paper), RNA Research and Splicing (1 paper) and Genomics and Rare Diseases (1 paper). Brenna Boyd is often cited by papers focused on Genomic variations and chromosomal abnormalities (1 paper), RNA Research and Splicing (1 paper) and Genomics and Rare Diseases (1 paper). Brenna Boyd collaborates with scholars based in United States. Brenna Boyd's co-authors include Emily Glanton, Shruti Marwaha, Jennefer N. Kohler, Catherine H. Sillari, Fuki M. Hisama, Diane Allingham‐Hawkins, Yajuan J. Liu, He Fang, Siwu Peng and Gregory J. Fischer and has published in prestigious journals such as American Journal of Medical Genetics Part A and Journal of Genetic Counseling.

In The Last Decade

Brenna Boyd

2 papers receiving 5 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Brenna Boyd United States	2	4	3	1	1	1	2	6
Cornelius A. Rietveld Netherlands	2	2 0.5×	2 0.7×				3	4
V. Kartik Chundru United Kingdom	2	4 1.0×		1 1.0×			6	7
Aubrey Annis United States	1	4 1.0×		1 1.0×			2	7
S Viennot France	2	4 1.0×					3	5
Jae Hun Shin South Korea	2	3 0.8×	3 1.0×	2 2.0×			2	10
Jonathan Davitte United States	3	3 0.8×	1 0.3×				3	9
Qingchuan Bao China	2	3 0.8×					3	5
Lucas Richter United States	2	3 0.8×	1 0.3×	1 1.0×			3	4
Mairo Puusepp Estonia	1	3 0.8×		1 1.0×			2	5
Олександра Козак Ukraine	2	3 0.8×					10	6

Countries citing papers authored by Brenna Boyd

Since Specialization

Citations

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

Fields of papers citing papers by Brenna Boyd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brenna Boyd. 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 Brenna Boyd. The network helps show where Brenna Boyd may publish in the future.

Co-authorship network of co-authors of Brenna Boyd

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

All Works

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2 of 2 papers shown

1.

Boyd, Brenna, He Fang, Diane Allingham‐Hawkins, et al.. (2024). Chromosomal translocation resolves a diagnostic odyssey for familial Ruvalcaba syndrome. American Journal of Medical Genetics Part A. 197(1). e63847–e63847. 2 indexed citations

2.

Kohler, Jennefer N., et al.. (2021). Genetic counselor roles in the undiagnosed diseases network research study: Clinical care, collaboration, and curation. Journal of Genetic Counseling. 31(2). 326–337. 4 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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