Peter Little
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Hemoglobinopathies and Related Disorders
- Molecular Biology top 5%
- Genomics and Chromatin Dynamics
- Epigenetics and DNA Methylation
- Fibroblast Growth Factor Research
- RNA and protein synthesis mechanisms
- RNA Research and Splicing
Papers in
-
- Renal and related cancers 9
- RNA and protein synthesis mechanisms 9
- Genomics and Chromatin Dynamics 9
- RNA Research and Splicing 8
- Epigenetics and DNA Methylation 8
- CRISPR and Genetic Engineering 7
- Genetics 29
- Genetic Syndromes and Imprinting 8
- Co-authors
- Caroline J. Formstone (4 shared papers)Sally H. Cross (2 shared papers)Aravinda Chakravarti (1 shared paper)Takashi Sügimura (3 shared papers)Kiyoshi Miyagawa (2 shared papers)Stuart H. Orkin (1 shared paper)Corinne D. Boehm (1 shared paper)Haig H. Kazazian (1 shared paper)
- Journals
- Genomics (12 papers)Nature (10 papers)Genome Research (5 papers)Proceedings of the National Academy of Sciences (5 papers)Mammalian Genome (4 papers)
- Partner nations
- United KingdomAustraliaUnited States
In The Last Decade
Peter Little
79 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 142
- Genetics 663
- Molecular Biology 1.6k
- Genetics 158
- Cell Biology 201
- Pediatrics, Perinatology and Child Health 202
Countries citing papers authored by Peter Little
This map shows the geographic impact of Peter Little'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 Peter Little with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Little more than expected).
Fields of papers citing papers by Peter Little
This network shows the impact of papers produced by Peter Little. 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 Peter Little. The network helps show where Peter Little may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Little, 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 81 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1987 | 235 | |
| 2 | 1993 | 155 | |
| 3 | 1982 | 148 | |
| 4 | 1992 | 115 | |
| 5 | 2003 | 112 | |
| 6 | 2007 | 88 | |
| 7 | 1987 | 82 | |
| 8 | 2001 | 74 | |
| 9 | 1997 | 73 | |
| 10 | 1990 | 65 | |
| 11 | 1986 | 62 | |
| 12 | 1997 | 58 | |
| 13 | 1982 | 55 | |
| 14 | 1988 | 54 | |
| 15 | 1985 | 52 | |
| 16 | 1998 | 51 | |
| 17 | 1979 | 48 | |
| 18 | 1995 | 46 | |
| 19 | 1987 | 45 | |
| 20 | 2016 | 44 |
About Peter Little
Peter Little is a scholar working on Molecular Biology, Genetics, Plant Science, Pediatrics, Perinatology and Child Health and Cellular and Molecular Neuroscience, having authored 81 papers that have together received 2.3k indexed citations. Recurring topics across this work include Renal and related cancers (9 papers), RNA and protein synthesis mechanisms (9 papers), Genomics and Chromatin Dynamics (9 papers), RNA Research and Splicing (8 papers), Epigenetics and DNA Methylation (8 papers), Genetic Syndromes and Imprinting (8 papers), Prenatal Screening and Diagnostics (7 papers) and CRISPR and Genetic Engineering (7 papers). The work is most often cited by research in Genetics (663 citations), Molecular Biology (1.6k citations), Genetics (158 citations), Cell Biology (201 citations) and Pediatrics, Perinatology and Child Health (202 citations). Peter Little has collaborated with scholars based in United Kingdom, Australia and United States. Frequent co-authors include Caroline J. Formstone, Sally H. Cross, Aravinda Chakravarti, Takashi Sügimura, Kiyoshi Miyagawa, Stuart H. Orkin, Corinne D. Boehm, Haig H. Kazazian, Rohan B. H. Williams and Hideo Sakamoto. Their work appears in journals such as Genomics, Nature, Genome Research, Proceedings of the National Academy of Sciences and Mammalian Genome.
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.