Brant C. Hendrickson
Impact in
- Genetics top 2%
- Neurogenetic and Muscular Disorders Research
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Pathology and Forensic Medicine top 10%
- Genetic factors in colorectal cancer
Papers in
-
- CRISPR and Genetic Engineering 6
- Molecular Biology Techniques and Applications 2
- Genetics 11
- BRCA gene mutations in cancer 8
- Genomic variations and chromosomal abnormalities 6
- Forensic and Genetic Research 2
- Genomics and Rare Diseases 2
- Co-authors
- Thomas Scholl (11 shared papers)Viatcheslav R. Akmaev (2 shared papers)Narasimhan Nagan (1 shared paper)Kerry L. Flynn (1 shared paper)Hui Zhu (1 shared paper)Elaine A. Sugarman (1 shared paper)Bernice A. Allitto (1 shared paper)Zhaoqing Zhou (1 shared paper)
- Journals
- Journal of Molecular Diagnostics (2 papers)Cancer Research (2 papers)JAMA (1 paper)Journal of Clinical Oncology (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- United StatesGermanyNorway
In The Last Decade
Brant C. Hendrickson
15 papers receiving 907 citations
Hit Papers
Peers
Comparison fields: 5 of 65
- Genetics 435
- Genetics 317
- Pathology and Forensic Medicine 173
- Molecular Biology 524
- Cancer Research 112
Countries citing papers authored by Brant C. Hendrickson
This map shows the geographic impact of Brant C. Hendrickson'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 Brant C. Hendrickson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brant C. Hendrickson more than expected).
Fields of papers citing papers by Brant C. Hendrickson
This network shows the impact of papers produced by Brant C. Hendrickson. 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 Brant C. Hendrickson. The network helps show where Brant C. Hendrickson may publish in the future.
Co-authors
The 25 scholars most cited alongside Brant C. Hendrickson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens Hit paper breakdown → | 2011 | 457 |
| 2 | 2006 | 135 | |
| 3 | 2007 | 72 | |
| 4 | 2008 | 68 | |
| 5 | 2005 | 51 | |
| 6 | 2005 | 43 | |
| 7 | 2007 | 30 | |
| 8 | 2000 | 19 | |
| 9 | 2005 | 17 | |
| 10 | 2003 | 13 | |
| 11 | Two rare novel polymorphisms in the D8S1179 and D13S317 markers and method to mitigate their impact on human identification. | 2004 | 9 |
| 12 | 2005 | 8 | |
| 13 | 2012 | 6 | |
| 14 | 2003 | 6 | |
| 15 | 2004 | 1 |
About Brant C. Hendrickson
Brant C. Hendrickson is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Plant Science and Surgery, having authored 15 papers that have together received 935 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (8 papers), CRISPR and Genetic Engineering (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Genetic factors in colorectal cancer (3 papers), Forensic and Genetic Research (2 papers), Genomics and Rare Diseases (2 papers), Molecular Biology Techniques and Applications (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Genetics (435 citations), Genetics (317 citations), Pathology and Forensic Medicine (173 citations), Molecular Biology (524 citations) and Cancer Research (112 citations). Brant C. Hendrickson has collaborated with scholars based in United States, Germany and Norway. Frequent co-authors include Thomas Scholl, Viatcheslav R. Akmaev, Narasimhan Nagan, Kerry L. Flynn, Hui Zhu, Elaine A. Sugarman, Bernice A. Allitto, Zhaoqing Zhou, Elizabeth M. Rohlfs and Brian E. Ward. Their work appears in journals such as Journal of Molecular Diagnostics, Cancer Research, JAMA, Journal of Clinical Oncology and European Journal of Human Genetics.
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.