Brenna Boyd
Impact in
-
- Prenatal Screening and Diagnostics
-
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
-
- Congenital heart defects research 1
- Genetics, Bioinformatics, and Biomedical Research 1
- RNA Research and Splicing 1
- Genetics 2
- BRCA gene mutations in cancer 1
- Genomic variations and chromosomal abnormalities 1
- Genomics and Rare Diseases 1
- Co-authors
- Catherine H. Sillari (1 shared paper)Emily Glanton (1 shared paper)Jennefer N. Kohler (1 shared paper)Shruti Marwaha (1 shared paper)Yajuan J. Liu (1 shared paper)He Fang (1 shared paper)Diane Allingham‐Hawkins (1 shared paper)Gregory J. Fischer (1 shared paper)
- Journals
- American Journal of Medical Genetics Part A (1 paper)Journal of Genetic Counseling (1 paper)
- Partner nations
- United States
In The Last Decade
Brenna Boyd
2 papers receiving 5 citations
Peers
Comparison fields: 5 of 10
- Pediatrics, Perinatology and Child Health 3
- Genetics 4
- Cancer Research 1
- Psychiatry and Mental health 1
- Neurology 1
Countries citing papers authored by Brenna Boyd
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
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-authors
The 10 scholars most cited alongside Brenna Boyd, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
About Brenna Boyd
Brenna Boyd is a scholar working on Molecular Biology, Genetics, Infectious Diseases, Organic Chemistry and Surgery, having authored 2 papers that have together received 6 indexed citations. Recurring topics across this work include Congenital heart defects research (1 paper), Genetics, Bioinformatics, and Biomedical Research (1 paper), RNA Research and Splicing (1 paper), BRCA gene mutations in cancer (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (3 citations), Genetics (4 citations), Cancer Research (1 citation), Psychiatry and Mental health (1 citation) and Neurology (1 citation). Brenna Boyd has collaborated with scholars based in United States. Frequent co-authors include Catherine H. Sillari, Emily Glanton, Jennefer N. Kohler, Shruti Marwaha, Yajuan J. Liu, He Fang, Diane Allingham‐Hawkins, Gregory J. Fischer, Siwu Peng and Fuki M. Hisama. Their work appears in journals such as American Journal of Medical Genetics Part A and Journal of Genetic Counseling.
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.