P. L. Pearson
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Associations and Epidemiology
-
- Genomics and Phylogenetic Studies
Papers in
- Genetics 12
- Genomic variations and chromosomal abnormalities 5
- Animal Genetics and Reproduction 3
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- Prenatal Screening and Diagnostics 5
- Co-authors
- ROBERT J. ROBBINS (2 shared papers)Nina W. Matheson (1 shared paper)Mechteld L.C. Hoogendoorn (2 shared papers)Willem Verduijn (2 shared papers)S C Bakker (2 shared papers)Richard J. Sinke (2 shared papers)Jacques C. Giltay (1 shared paper)Wouter G. van Inzen (1 shared paper)
- Journals
- Cytogenetic and Genome Research (7 papers)Nucleic Acids Research (3 papers)Science (2 papers)Thrombosis and Haemostasis (2 papers)European Journal of Human Genetics (1 paper)
- Partner nations
- NetherlandsUnited KingdomUnited States
In The Last Decade
P. L. Pearson
41 papers receiving 621 citations
Peers
Comparison fields: 5 of 76
- Genetics 258
- Molecular Biology 345
- Hematology 43
- Cellular and Molecular Neuroscience 63
- Neurology 49
Countries citing papers authored by P. L. Pearson
This map shows the geographic impact of P. L. 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 P. L. Pearson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. L. Pearson more than expected).
Fields of papers citing papers by P. L. Pearson
This network shows the impact of papers produced by P. L. 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 P. L. Pearson. The network helps show where P. L. Pearson may publish in the future.
Co-authors
The 25 scholars most cited alongside P. L. 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 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 111 | |
| 2 | 1997 | 76 | |
| 3 | 2004 | 68 | |
| 4 | 1999 | 62 | |
| 5 | 2006 | 60 | |
| 6 | Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families. | 1988 | 47 |
| 7 | 2004 | 42 | |
| 8 | 1986 | 40 | |
| 9 | 1991 | 36 | |
| 10 | 1986 | 14 | |
| 11 | 1987 | 14 | |
| 12 | 1991 | 12 | |
| 13 | 1987 | 12 | |
| 14 | 2008 | 11 | |
| 15 | 2003 | 10 | |
| 16 | 2008 | 9 | |
| 17 | 1985 | 9 | |
| 18 | 1988 | 8 | |
| 19 | 2008 | 5 | |
| 20 | 2008 | 4 |
About P. L. Pearson
P. L. Pearson is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Hematology and Reproductive Medicine, having authored 55 papers that have together received 687 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Genomics and Chromatin Dynamics (4 papers), Chromosomal and Genetic Variations (4 papers), Animal Genetics and Reproduction (3 papers), Cancer-related gene regulation (3 papers), Hemophilia Treatment and Research (3 papers) and CRISPR and Genetic Engineering (2 papers). The work is most often cited by research in Genetics (258 citations), Molecular Biology (345 citations), Hematology (43 citations), Cellular and Molecular Neuroscience (63 citations) and Neurology (49 citations). P. L. Pearson has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include ROBERT J. ROBBINS, Nina W. Matheson, Mechteld L.C. Hoogendoorn, Willem Verduijn, S C Bakker, Richard J. Sinke, Jacques C. Giltay, Wouter G. van Inzen, Jacques M. J. C. Scheres and René S. Kahn. Their work appears in journals such as Cytogenetic and Genome Research, Nucleic Acids Research, Science, Thrombosis and Haemostasis and European Journal of Human 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.