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
- Genetics 11
- BRCA gene mutations in cancer 8
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 2
- Forensic and Genetic Research 2
- Neurogenetic and Muscular Disorders Research 1
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- CRISPR and Genetic Engineering 5
- DNA Repair Mechanisms 1
- Co-authors
- Thomas Scholl (11 shared papers)Viatcheslav R. Akmaev (2 shared papers)Elaine A. Sugarman (1 shared paper)Bernice A. Allitto (1 shared paper)Narasimhan Nagan (1 shared paper)Kerry L. Flynn (1 shared paper)Hui Zhu (1 shared paper)Zhaoqing Zhou (1 shared paper)
- Journals
- Journal of Molecular Diagnostics (2 papers)Cancer Research (2 papers)Journal of Clinical Oncology (1 paper)Cancer Epidemiology Biomarkers & Prevention (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- United StatesGermanyHungary
In The Last Decade
Brant C. Hendrickson
15 papers receiving 916 citations
Brant C. Hendrickson's Hit Papers
Peers
Comparison fields: 5 of 60
- Genetics 434
- Genetics 304
- Pathology and Forensic Medicine 156
- Molecular Biology 420
- Cancer Research 77
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 | 462 |
| 2 | 2006 | 136 | |
| 3 | 2007 | 72 | |
| 4 | 2008 | 69 | |
| 5 | 2005 | 52 | |
| 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 | 2003 | 6 | |
| 14 | 2012 | 6 | |
| 15 | 2004 | 1 |
About Brant C. Hendrickson
Brant C. Hendrickson is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Surgery and Genetics, having authored 15 papers that have together received 943 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (8 papers), Genomic variations and chromosomal abnormalities (6 papers), CRISPR and Genetic Engineering (5 papers), Genetic factors in colorectal cancer (3 papers), Genomics and Rare Diseases (2 papers), Forensic and Genetic Research (2 papers), DNA Repair Mechanisms (1 paper) and Neurogenetic and Muscular Disorders Research (1 paper). The work is most often cited by research in Genetics (434 citations), Genetics (304 citations), Pathology and Forensic Medicine (156 citations), Molecular Biology (420 citations) and Cancer Research (77 citations). Brant C. Hendrickson has collaborated with scholars based in United States, Germany and Hungary. Frequent co-authors include Thomas Scholl, Viatcheslav R. Akmaev, Elaine A. Sugarman, Bernice A. Allitto, Narasimhan Nagan, Kerry L. Flynn, Hui Zhu, Zhaoqing Zhou, Elizabeth M. Rohlfs and Thaddeus Judkins. Their work appears in journals such as Journal of Molecular Diagnostics, Cancer Research, Journal of Clinical Oncology, Cancer Epidemiology Biomarkers & Prevention 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.