Brian Paul Chadwick
Impact in
- Physiology top 2%
- Molecular Biology top 5%
- Genomics and Chromatin Dynamics
- Epigenetics and DNA Methylation
- RNA Research and Splicing
- RNA modifications and cancer
- CRISPR and Genetic Engineering
Papers in
- Genetics 27
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 16
- Genetics and Neurodevelopmental Disorders 7
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- Genomics and Chromatin Dynamics 24
- Epigenetics and DNA Methylation 7
- RNA modifications and cancer 7
- RNA Research and Splicing 6
- Co-authors
- Huntington F. Willard (6 shared papers)Anna‐Maria Frischauf (5 shared papers)Anna-Maria Frischauf (2 shared papers)Taiping Chen (1 shared paper)Yi Zhang (1 shared paper)En Li (1 shared paper)Jia Fang (1 shared paper)Parimal Majumder (2 shared papers)
- Journals
- Chromosome Research (5 papers)Chromosoma (5 papers)Genomics (5 papers)Mammalian Genome (4 papers)The Journal of Cell Biology (3 papers)
- Partner nations
- United StatesUnited KingdomIsrael
In The Last Decade
Brian Paul Chadwick
58 papers receiving 3.3k citations
Peers
Comparison fields: 5 of 158
- Physiology 209
- Molecular Biology 2.5k
- Genetics 934
- Cellular and Molecular Neuroscience 322
- Plant Science 642
Countries citing papers authored by Brian Paul Chadwick
This map shows the geographic impact of Brian Paul Chadwick'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 Brian Paul Chadwick with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brian Paul Chadwick more than expected).
Fields of papers citing papers by Brian Paul Chadwick
This network shows the impact of papers produced by Brian Paul Chadwick. 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 Brian Paul Chadwick. The network helps show where Brian Paul Chadwick may publish in the future.
Co-authors
The 25 scholars most cited alongside Brian Paul Chadwick, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 58 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 496 | |
| 2 | 2012 | 264 | |
| 3 | 2004 | 205 | |
| 4 | 2016 | 192 | |
| 5 | 2004 | 190 | |
| 6 | 1995 | 189 | |
| 7 | 2001 | 152 | |
| 8 | 2008 | 152 | |
| 9 | 2001 | 147 | |
| 10 | 1998 | 103 | |
| 11 | 2003 | 100 | |
| 12 | 1999 | 96 | |
| 13 | 2002 | 89 | |
| 14 | 2016 | 67 | |
| 15 | 2012 | 64 | |
| 16 | 1997 | 63 | |
| 17 | 2007 | 62 | |
| 18 | 2001 | 56 | |
| 19 | 1997 | 52 | |
| 20 | 2000 | 50 |
About Brian Paul Chadwick
Brian Paul Chadwick is a scholar working on Genetics, Molecular Biology, Plant Science, Cellular and Molecular Neuroscience and Physiology, having authored 58 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (24 papers), Chromosomal and Genetic Variations (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (16 papers), Epigenetics and DNA Methylation (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), RNA modifications and cancer (7 papers), Hereditary Neurological Disorders (6 papers) and RNA Research and Splicing (6 papers). The work is most often cited by research in Physiology (209 citations), Molecular Biology (2.5k citations), Genetics (934 citations), Cellular and Molecular Neuroscience (322 citations) and Plant Science (642 citations). Brian Paul Chadwick has collaborated with scholars based in United States, United Kingdom and Israel. Frequent co-authors include Huntington F. Willard, Anna‐Maria Frischauf, Anna-Maria Frischauf, Taiping Chen, Yi Zhang, En Li, Jia Fang, Parimal Majumder, Jeremy M. Boss and Deanna C. Tremblay. Their work appears in journals such as Chromosome Research, Chromosoma, Genomics, Mammalian Genome and The Journal of Cell Biology.
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.