P. Pearson

2.8k total citations
50 papers, 1.6k citations indexed

About

P. Pearson is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, P. Pearson has authored 50 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in P. Pearson's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chromosomal and Genetic Variations (5 papers). P. Pearson is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chromosomal and Genetic Variations (5 papers). P. Pearson collaborates with scholars based in Netherlands, United Kingdom and United States. P. Pearson's co-authors include K.K. Kidd, H.F. Willard, Peter Devilee, Robert Robbins, A. Bowcock, Tim Kievits, Nina W. Matheson, M.H. Skolnick, J.-L. Mandel and R.K. Track and has published in prestigious journals such as Science, The Lancet and Nucleic Acids Research.

In The Last Decade

P. Pearson

49 papers receiving 1.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
P. Pearson Netherlands 21 879 710 276 144 109 50 1.6k
W. Roy Breg United States 18 1.1k 1.2× 815 1.1× 238 0.9× 149 1.0× 154 1.4× 26 2.0k
H F Willard United States 22 1.2k 1.4× 804 1.1× 545 2.0× 124 0.9× 168 1.5× 28 1.8k
Shaun S. Abeysinghe United Kingdom 8 1.4k 1.6× 845 1.2× 185 0.7× 57 0.4× 186 1.7× 8 2.1k
Digamber S. Borgaonkar United States 20 1.1k 1.3× 955 1.3× 268 1.0× 226 1.6× 257 2.4× 66 2.4k
Karen Duran Netherlands 21 755 0.9× 575 0.8× 137 0.5× 136 0.9× 150 1.4× 28 1.4k
Barbara K. Goodman United States 25 811 0.9× 360 0.5× 109 0.4× 124 0.9× 146 1.3× 48 1.5k
Elena Prigmore United Kingdom 18 742 0.8× 758 1.1× 225 0.8× 164 1.1× 131 1.2× 27 1.4k
Elizabeth Roeder United States 21 1.2k 1.3× 972 1.4× 158 0.6× 346 2.4× 50 0.5× 37 1.9k
Simone Schuffenhauer Germany 23 1.0k 1.2× 964 1.4× 181 0.7× 308 2.1× 84 0.8× 42 1.7k
Christine Steinhoff Germany 25 1.4k 1.6× 322 0.5× 111 0.4× 66 0.5× 189 1.7× 34 2.1k

Countries citing papers authored by P. Pearson

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of P. Pearson

This figure shows the co-authorship network connecting the top 25 collaborators of P. Pearson. A scholar is included among the top collaborators of P. Pearson based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with P. Pearson. P. Pearson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Bakker, S C, Mechteld L.C. Hoogendoorn, Judith Hendriks, et al.. (2006). The PIP5K2A and RGS4 genes are differentially associated with deficit and non‐deficit schizophrenia. Genes Brain & Behavior. 6(2). 113–119. 53 indexed citations
2.
Roelofs, Helene, A. H. Zwinderman, Hans C. van Houwelingen, et al.. (2005). Studying the biological and technical sources of variation in telomere length of individual chromosomes. Cytometry Part A. 65A(1). 35–39. 3 indexed citations
3.
Giltay, Jacques C., et al.. (1999). Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISH. Cytogenetic and Genome Research. 84(1-2). 67–72. 45 indexed citations
4.
White, Julia A., P.J. McAlpine, Stylianos E. Antonarakis, et al.. (1997). NOMENCLATURE. Genomics. 45(2). 468–471. 69 indexed citations
5.
Pearson, P., et al.. (1992). The GDBTM Human Genome Data Base Anno 1992. Nucleic Acids Research. 20(suppl). 2201–2206. 93 indexed citations
6.
Pearson, P., et al.. (1991). The Human Genome Initiative—Do Databases Reflect Current Progress?. Science. 254(5029). 214–215. 13 indexed citations
7.
Pearson, P.. (1991). The genome data base (GDB)--a human gene mapping repository. Nucleic Acids Research. 19(suppl). 2237–2239. 32 indexed citations
8.
Williamson, R., A. Bowcock, K.K. Kidd, et al.. (1991). Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 24 of 27). Cytogenetic and Genome Research. 58(3-4). 1790–1800. 1 indexed citations
9.
Williamson, R., A. Bowcock, K.K. Kidd, et al.. (1991). Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 16 of 27). Cytogenetic and Genome Research. 58(3-4). 1685–1705. 1 indexed citations
10.
Kievits, Tim, J.G. Dauwerse, J. Wiegant, et al.. (1990). Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization. Cytogenetic and Genome Research. 53(2-3). 134–136. 137 indexed citations
11.
Wapenaar, Martin C., Tim Kievits, P. Meera Khan, P. Pearson, & G.J.B. van Ommen. (1990). Isolation and characterization of cell hybrids containing human Xp-chromosome fragments. Cytogenetic and Genome Research. 54(1-2). 10–14. 6 indexed citations
12.
Devilee, Peter, et al.. (1990). Loss of heterozygosity on 17p in human breast carcinomas: defining the smallest common region of deletion. Cytogenetic and Genome Research. 53(1). 52–54. 25 indexed citations
13.
Kidd, K.K., A. Bowcock, J. Schmidtke, et al.. (1989). Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 622-643. Cytogenetic and Genome Research. 51(1-4). 622–643. 197 indexed citations
14.
Bröcker-Vriends, A, E Briët, H. H. H. Kanhai, et al.. (1988). First trimester prenatal diagnosis of haemophilia A: Two years' experience. Prenatal Diagnosis. 8(6). 411–421. 8 indexed citations
15.
Arveiler, Benoı̂t, I. Oberlé, Anne Vincent, et al.. (1988). Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.. PubMed. 42(2). 380–9. 48 indexed citations
16.
Bakker, Egbert, et al.. (1987). Two additional RFLPs at the D4S10 locus, useful for Huntington's disease (HD)-family studies. Nucleic Acids Research. 15(21). 9100–9100. 12 indexed citations
17.
Reeders, Stephen T., M.H. Breuning, G. CORNEY, et al.. (1986). Two Genetic Markers Closely Linked to Adult Polycystic Kidney Disease on Chromosome 16. The Journal of Urology. 136(4). 987–987. 13 indexed citations
18.
Willard, H.F., M.H. Skolnick, P. Pearson, & J.-L. Mandel. (1985). Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques (Part 1 of 5). Cytogenetic and Genome Research. 40(1-4). 360–385. 74 indexed citations
19.
Cavalli‐Sforza, L. L., P. Pearson, H H Kazazian, et al.. (1982). Workshop on DNA polymorphisms.. PubMed. 103 Pt A. 79–81. 1 indexed citations
20.

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.

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