Peter Lees Pearson
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Neurogenetic and Muscular Disorders Research
- Molecular Biology top 1%
- Muscle Physiology and Disorders
- Genomics and Chromatin Dynamics
Papers in
- Genetics 95
- Genomic variations and chromosomal abnormalities 36
- Genetics and Neurodevelopmental Disorders 19
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 18
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- Muscle Physiology and Disorders 26
- RNA modifications and cancer 15
- CRISPR and Genetic Engineering 14
- DNA and Nucleic Acid Chemistry 14
- Co-authors
- Martin Bobrow (9 shared papers)Egbert Bakker (26 shared papers)G.J.B. van Ommen (20 shared papers)Kay Elizabeth Davies (10 shared papers)Peter Devilee (7 shared papers)Canio Giuseppe Vosa (2 shared papers)Johan T. den Dunnen (8 shared papers)Martin C. Wapenaar (9 shared papers)
- Journals
- Human Genetics (27 papers)Nucleic Acids Research (13 papers)Journal of Medical Genetics (12 papers)Genomics (9 papers)Nature (8 papers)
- Partner nations
- NetherlandsUnited StatesUnited Kingdom
In The Last Decade
Peter Lees Pearson
208 papers receiving 10.7k citations
Peter Lees Pearson's Hit Papers
Peers
Comparison fields: 5 of 150
- Genetics 4.6k
- Molecular Biology 6.5k
- Genetics 874
- Reproductive Medicine 529
- Pediatrics, Perinatology and Child Health 914
Countries citing papers authored by Peter Lees Pearson
This map shows the geographic impact of Peter Lees 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 Peter Lees Pearson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Lees Pearson more than expected).
Fields of papers citing papers by Peter Lees Pearson
This network shows the impact of papers produced by Peter Lees 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 Peter Lees Pearson. The network helps show where Peter Lees Pearson may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Lees 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
Showing the 20 most-cited of 222 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16 Hit paper breakdown → | 1985 | 578 |
| 2 | Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications. | 1989 | 461 |
| 3 | 1970 | 399 | |
| 4 | 1983 | 331 | |
| 5 | 1986 | 320 | |
| 6 | 1985 | 312 | |
| 7 | 1993 | 273 | |
| 8 | 2001 | 248 | |
| 9 | 1984 | 241 | |
| 10 | 1972 | 220 | |
| 11 | Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes. | 1988 | 213 |
| 12 | 1985 | 198 | |
| 13 | 2003 | 198 | |
| 14 | 2006 | 198 | |
| 15 | 1989 | 183 | |
| 16 | 1988 | 179 | |
| 17 | 1987 | 173 | |
| 18 | 1988 | 173 | |
| 19 | 1989 | 170 | |
| 20 | 1987 | 168 |
About Peter Lees Pearson
Peter Lees Pearson is a scholar working on Genetics, Molecular Biology, Plant Science, Genetics and Cellular and Molecular Neuroscience, having authored 222 papers that have together received 11.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (36 papers), Chromosomal and Genetic Variations (28 papers), Muscle Physiology and Disorders (26 papers), Genetics and Neurodevelopmental Disorders (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers), RNA modifications and cancer (15 papers), CRISPR and Genetic Engineering (14 papers) and DNA and Nucleic Acid Chemistry (14 papers). The work is most often cited by research in Genetics (4.6k citations), Molecular Biology (6.5k citations), Genetics (874 citations), Reproductive Medicine (529 citations) and Pediatrics, Perinatology and Child Health (914 citations). Peter Lees Pearson has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Martin Bobrow, Egbert Bakker, G.J.B. van Ommen, Kay Elizabeth Davies, Peter Devilee, Canio Giuseppe Vosa, Johan T. den Dunnen, Martin C. Wapenaar, Marten H. Hofker and Stephen T. Reeders. Their work appears in journals such as Human Genetics, Nucleic Acids Research, Journal of Medical Genetics, Genomics and Nature.
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.