P. Pearson
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
-
- Genomics and Phylogenetic Studies
Papers in
-
- Genomics and Chromatin Dynamics 4
- Cancer-related gene regulation 3
- Genetics 12
- Genomic variations and chromosomal abnormalities 5
- Animal Genetics and Reproduction 3
- Co-authors
- Robert Robbins (2 shared papers)Nina W. Matheson (1 shared paper)Wouter G. van Inzen (1 shared paper)J. M. J. C. Scheres (1 shared paper)Jacques C. Giltay (1 shared paper)P.M.M. Kastrop (1 shared paper)Anne Vincent (1 shared paper)Benoı̂t Arveiler (1 shared paper)
- Journals
- Cytogenetic and Genome Research (6 papers)Nucleic Acids Research (3 papers)Thrombosis and Haemostasis (2 papers)Genomics (1 paper)Cytometry Part A (1 paper)
- Partner nations
- NetherlandsUnited KingdomUnited States
In The Last Decade
P. Pearson
37 papers receiving 541 citations
Peers
Comparison fields: 5 of 75
- Genetics 223
- Molecular Biology 308
- Hematology 42
- Neurology 46
- Reproductive Medicine 23
Countries citing papers authored by P. Pearson
This map shows the geographic impact of P. 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. 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. Pearson more than expected).
Fields of papers citing papers by P. Pearson
This network shows the impact of papers produced by P. 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. Pearson. The network helps show where P. Pearson may publish in the future.
Co-authors
The 25 scholars most cited alongside P. 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 99 | |
| 2 | 1997 | 76 | |
| 3 | 1999 | 64 | |
| 4 | 2006 | 56 | |
| 5 | Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families. | 1988 | 50 |
| 6 | 2004 | 41 | |
| 7 | 1986 | 41 | |
| 8 | 1991 | 36 | |
| 9 | 1987 | 14 | |
| 10 | 1986 | 13 | |
| 11 | 1991 | 13 | |
| 12 | 1987 | 12 | |
| 13 | 2008 | 10 | |
| 14 | 2003 | 9 | |
| 15 | 1985 | 9 | |
| 16 | 2008 | 8 | |
| 17 | 1988 | 8 | |
| 18 | 2008 | 5 | |
| 19 | Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentromeric heterochromatin of chromosomes 13, 21 and 18 | 1986 | 4 |
| 20 | 2008 | 3 |
About P. Pearson
P. Pearson is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Hematology, having authored 50 papers that have together received 600 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (5 papers), Chromosomal and Genetic Variations (4 papers), Genomics and Chromatin Dynamics (4 papers), Hemophilia Treatment and Research (3 papers), Animal Genetics and Reproduction (3 papers), Cancer-related gene regulation (3 papers) and Sperm and Testicular Function (2 papers). The work is most often cited by research in Genetics (223 citations), Molecular Biology (308 citations), Hematology (42 citations), Neurology (46 citations) and Reproductive Medicine (23 citations). P. Pearson has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Robert Robbins, Nina W. Matheson, Wouter G. van Inzen, J. M. J. C. Scheres, Jacques C. Giltay, P.M.M. Kastrop, Anne Vincent, Benoı̂t Arveiler, Marten H. Hofker and Jean‐Louis Mandel. Their work appears in journals such as Cytogenetic and Genome Research, Nucleic Acids Research, Thrombosis and Haemostasis, Genomics and Cytometry Part A.
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.