Nathaniel M. Pearson
Impact in
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic diversity and population structure
-
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
- RNA Research and Splicing
- Genomics and Phylogenetic Studies
Papers in
- Genetics 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genomics and Rare Diseases 2
- Animal Genetics and Reproduction 1
-
- CRISPR and Genetic Engineering 2
- RNA and protein synthesis mechanisms 2
- Co-authors
- Bruce T. Lahn (3 shared papers)Karin Jegalian (1 shared paper)Wenfeng Qian (1 shared paper)Calum J. Maclean (1 shared paper)Jianzhi Zhang (1 shared paper)Wayne H. Knox (2 shared papers)C. Hirlimann (1 shared paper)Wen‐Hsiung Li (1 shared paper)
- Journals
- Optics Letters (2 papers)Blood Advances (1 paper)Gene (1 paper)Journal of Neurology Neurosurgery & Psychiatry (1 paper)Nature Reviews Genetics (1 paper)
- Partner nations
- United StatesUnited KingdomNetherlands
In The Last Decade
Nathaniel M. Pearson
12 papers receiving 589 citations
Peers
Comparison fields: 5 of 83
- Genetics 223
- Molecular Biology 327
- Acoustics and Ultrasonics 3
- Atomic and Molecular Physics, and Optics 93
- Plant Science 103
Countries citing papers authored by Nathaniel M. Pearson
This map shows the geographic impact of Nathaniel M. Pearson'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 Nathaniel M. Pearson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nathaniel M. Pearson more than expected).
Fields of papers citing papers by Nathaniel M. Pearson
This network shows the impact of papers produced by Nathaniel M. Pearson. 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 Nathaniel M. Pearson. The network helps show where Nathaniel M. Pearson may publish in the future.
Co-authors
The 25 scholars most cited alongside Nathaniel M. Pearson, 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 | 2012 | 230 | |
| 2 | 2001 | 159 | |
| 3 | 1988 | 92 | |
| 4 | 1989 | 34 | |
| 5 | 2005 | 32 | |
| 6 | 2003 | 26 | |
| 7 | 2018 | 13 | |
| 8 | 2005 | 12 | |
| 9 | 2021 | 5 | |
| 10 | 2014 | 3 | |
| 11 | 2013 | 2 | |
| 12 | The EUROGEM map of human chromosome 4. | 1994 | 1 |
About Nathaniel M. Pearson
Nathaniel M. Pearson is a scholar working on Genetics, Molecular Biology, Atomic and Molecular Physics, and Optics, Social Psychology and Hematology, having authored 12 papers that have together received 609 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Genomics and Rare Diseases (2 papers), Laser-Matter Interactions and Applications (2 papers), Photorefractive and Nonlinear Optics (2 papers), Advanced Fiber Laser Technologies (2 papers), CRISPR and Genetic Engineering (2 papers), RNA and protein synthesis mechanisms (2 papers) and Animal Genetics and Reproduction (1 paper). The work is most often cited by research in Genetics (223 citations), Molecular Biology (327 citations), Acoustics and Ultrasonics (3 citations), Atomic and Molecular Physics, and Optics (93 citations) and Plant Science (103 citations). Nathaniel M. Pearson has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Bruce T. Lahn, Karin Jegalian, Wenfeng Qian, Calum J. Maclean, Jianzhi Zhang, Wayne H. Knox, C. Hirlimann, Wen‐Hsiung Li, Soojin V. Yi and Ravinder K. Kanda. Their work appears in journals such as Optics Letters, Blood Advances, Gene, Journal of Neurology Neurosurgery & Psychiatry and Nature Reviews 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.