B. J. Trask
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 10%
- Genomics and Chromatin Dynamics
- DNA Repair Mechanisms
- RNA Research and Splicing
- Advanced biosensing and bioanalysis techniques
- CRISPR and Genetic Engineering
Papers in
-
- Genomics and Chromatin Dynamics 5
- DNA and Nucleic Acid Chemistry 4
- RNA Research and Splicing 3
- Molecular Biology Techniques and Applications 2
- Genetics 8
- Genomic variations and chromosomal abnormalities 8
- Animal Genetics and Reproduction 2
- Co-authors
- Ger van den Engh (7 shared papers)Hiroki Yokota (4 shared papers)Joe W. Gray (6 shared papers)Rainer K. Sachs (1 shared paper)John E. Hearst (1 shared paper)Ger J. van den Engh (2 shared papers)Chi Ma (1 shared paper)Sean P. Martin (1 shared paper)
- Journals
- Genomics (3 papers)Cytometry (2 papers)Cold Spring Harbor Symposia on Quantitative Biology (2 papers)Nature Genetics (1 paper)Trends in Genetics (1 paper)
- Partner nations
- United StatesNetherlandsNorth Macedonia
In The Last Decade
B. J. Trask
20 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 113
- Genetics 623
- Molecular Biology 1.2k
- Plant Science 485
- Aging 13
- Cancer Research 111
Countries citing papers authored by B. J. Trask
This map shows the geographic impact of B. J. Trask'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 B. J. Trask with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites B. J. Trask more than expected).
Fields of papers citing papers by B. J. Trask
This network shows the impact of papers produced by B. J. Trask. 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 B. J. Trask. The network helps show where B. J. Trask may publish in the future.
Co-authors
The 25 scholars most cited alongside B. J. Trask, 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 | 1991 | 296 | |
| 2 | 1995 | 242 | |
| 3 | 1986 | 217 | |
| 4 | 1992 | 210 | |
| 5 | 1993 | 164 | |
| 6 | 1982 | 89 | |
| 7 | 1997 | 71 | |
| 8 | 1987 | 67 | |
| 9 | 1985 | 59 | |
| 10 | 1997 | 58 | |
| 11 | 1996 | 43 | |
| 12 | 1992 | 37 | |
| 13 | Inheritance of chromosome heteromorphisms analyzed by high-resolution bivariate flow karyotyping. | 1989 | 32 |
| 14 | 1986 | 29 | |
| 15 | 1995 | 25 | |
| 16 | 1995 | 22 | |
| 17 | 1986 | 19 | |
| 18 | 1981 | 18 | |
| 19 | 2000 | 17 | |
| 20 | Analytical cytology applied to detection of prognostically important cytogenetic aberrations: Current status and future directions | 1987 | 1 |
About B. J. Trask
B. J. Trask is a scholar working on Molecular Biology, Genetics, Plant Science, Cellular and Molecular Neuroscience and Cancer Research, having authored 20 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (6 papers), Genomics and Chromatin Dynamics (5 papers), DNA and Nucleic Acid Chemistry (4 papers), RNA Research and Splicing (3 papers), Hereditary Neurological Disorders (2 papers), Animal Genetics and Reproduction (2 papers) and Molecular Biology Techniques and Applications (2 papers). The work is most often cited by research in Genetics (623 citations), Molecular Biology (1.2k citations), Plant Science (485 citations), Aging (13 citations) and Cancer Research (111 citations). B. J. Trask has collaborated with scholars based in United States, Netherlands and North Macedonia. Frequent co-authors include Ger van den Engh, Hiroki Yokota, Joe W. Gray, Rainer K. Sachs, John E. Hearst, Ger J. van den Engh, Chi Ma, Sean P. Martin, Joyce L. Hamlin and Daniel Pinkel. Their work appears in journals such as Genomics, Cytometry, Cold Spring Harbor Symposia on Quantitative Biology, Nature Genetics and Trends in 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.