Pearson Pl
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
-
- Cancer Genomics and Diagnostics
Papers in
- Genetics 1
- Genomic variations and chromosomal abnormalities 1
- Neurogenetic and Muscular Disorders Research 1
-
- Cancer Genomics and Diagnostics 1
- Co-authors
- Peter Devilee (2 shared papers)Cornelisse Cj (2 shared papers)Pagon Ra (1 shared paper)Uta Francke (1 shared paper)Joseph C. Giacalone (1 shared paper)van Ommen Gj (2 shared papers)Lindgren (1 shared paper)Christine M. Distèche (1 shared paper)
- Journals
- PubMed (7 papers)
- Partner nations
- NetherlandsUnited States
In The Last Decade
Pearson Pl
7 papers receiving 611 citations
Peers
Comparison fields: 5 of 67
- Genetics 221
- Cancer Research 107
- Pathology and Forensic Medicine 109
- Molecular Biology 394
- Genetics 51
Countries citing papers authored by Pearson Pl
This map shows the geographic impact of Pearson Pl'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 Pearson Pl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pearson Pl more than expected).
Fields of papers citing papers by Pearson Pl
This network shows the impact of papers produced by Pearson Pl. 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 Pearson Pl. The network helps show where Pearson Pl may publish in the future.
Co-authors
The 15 scholars most cited alongside Pearson Pl, 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 | Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome. | 1985 | 389 |
| 2 | Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q. | 1991 | 182 |
| 3 | Somatic genetic changes on chromosome 18 in breast carcinomas: is the DCC gene involved? | 1991 | 74 |
| 4 | [Procedure and initial results of presymptomatic DNA studies in Huntington's chorea]. | 1990 | 4 |
| 5 | The behavior of chromosomes. | 1973 | 1 |
| 6 | Restriction fragment length polymorphisms (RFLP's) and their use in mapping the human genome. | 1985 | 1 |
| 7 | Carrier detection and prenatal diagnosis of Duchenne/Becker muscular dystrophy (D/BMD) by DNA-analysis. | 1989 | 1 |
About Pearson Pl
Pearson Pl is a scholar working on Genetics, Cancer Research, Cellular and Molecular Neuroscience, Immunology and Oncology, having authored 7 papers that have together received 652 indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (1 paper), Nuclear Structure and Function (1 paper), interferon and immune responses (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Muscle Physiology and Disorders (1 paper), Cancer-related Molecular Pathways (1 paper), Cytomegalovirus and herpesvirus research (1 paper) and Neurogenetic and Muscular Disorders Research (1 paper). The work is most often cited by research in Genetics (221 citations), Cancer Research (107 citations), Pathology and Forensic Medicine (109 citations), Molecular Biology (394 citations) and Genetics (51 citations). Pearson Pl has collaborated with scholars based in Netherlands and United States. Frequent co-authors include Peter Devilee, Cornelisse Cj, Pagon Ra, Uta Francke, Joseph C. Giacalone, van Ommen Gj, Lindgren, Christine M. Distèche, HD Ochs and J. Hermans. Their work appears in journals such as PubMed.
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.