P. Pearson

14.5k total citations · 1 hit paper
209 papers, 10.7k citations indexed

About

P. Pearson is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, P. Pearson has authored 209 papers receiving a total of 10.7k indexed citations (citations by other indexed papers that have themselves been cited), including 128 papers in Molecular Biology, 101 papers in Genetics and 30 papers in Plant Science. Recurrent topics in P. Pearson's work include Genomic variations and chromosomal abnormalities (40 papers), Chromosomal and Genetic Variations (28 papers) and Muscle Physiology and Disorders (22 papers). P. Pearson is often cited by papers focused on Genomic variations and chromosomal abnormalities (40 papers), Chromosomal and Genetic Variations (28 papers) and Muscle Physiology and Disorders (22 papers). P. Pearson collaborates with scholars based in Netherlands, United States and United Kingdom. P. Pearson's co-authors include Martin Bobrow, Egbert Bakker, G.J.B. van Ommen, Kay E. Davies, Peter Devilee, Canio G. Vosa, Johan T. den Dunnen, Martin C. Wapenaar, Marten H. Hofker and Stephen T. Reeders and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

P. Pearson

208 papers receiving 10.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

1985 518 citations Stephen T. Reeders, M.H. Breuning et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
P. Pearson Netherlands	55	6.3k	4.7k	1.4k	901	843	209	10.7k
Ethylin Wang Jabs United States	58	8.6k 1.4×	7.9k 1.7×	644 0.5×	696 0.8×	538 0.6×	243	14.7k
Christine M. Distèche United States	67	10.6k 1.7×	6.9k 1.5×	2.3k 1.7×	833 0.9×	409 0.5×	226	17.3k
Veronica van Heyningen United Kingdom	64	12.3k 2.0×	5.0k 1.1×	680 0.5×	836 0.9×	735 0.9×	212	15.9k
Egbert Bakker Netherlands	62	7.2k 1.2×	4.1k 0.9×	558 0.4×	898 1.0×	1.4k 1.7×	246	12.3k
Orsetta Zuffardi Italy	56	6.8k 1.1×	7.3k 1.6×	2.2k 1.6×	1.6k 1.8×	1.1k 1.3×	324	12.2k
Gudrun Rappold Germany	53	5.9k 0.9×	5.1k 1.1×	1.1k 0.8×	431 0.5×	472 0.6×	216	10.0k
Mary F. Lyon United Kingdom	59	8.6k 1.4×	7.6k 1.6×	2.0k 1.4×	778 0.9×	311 0.4×	232	14.3k
S. Steven Potter United States	60	9.2k 1.5×	3.0k 0.6×	741 0.5×	637 0.7×	368 0.4×	166	12.4k
Cynthia C. Morton United States	73	8.7k 1.4×	2.9k 0.6×	600 0.4×	867 1.0×	1.2k 1.4×	281	18.9k
Jean‐Pierre Fryns Belgium	46	4.9k 0.8×	5.7k 1.2×	818 0.6×	1.3k 1.4×	470 0.6×	255	9.1k

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

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20 of 20 papers shown

Jorge, Alexander A.L., Lucilene Arilho Ribeiro, Fernando Kok, et al.. (2021). Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses. American Journal of Medical Genetics Part A. 185(8). 2335–2344. 2 indexed citations

Gorab, Eduardo & P. Pearson. (2017). Thiazole Orange as an Alternative to Antibody Binding for Detecting Triple-helical DNA in Heterochromatin of Drosophila and Rhynchosciara. Journal of Histochemistry & Cytochemistry. 66(3). 143–154. 1 indexed citations

Bakker, S C, Jan K. Buitelaar, Lodewijk A. Sandkuijl, et al.. (2003). A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q. The American Journal of Human Genetics. 72(5). 1251–1260. 168 indexed citations

Belzen, Martine J. van, Chris J. Mulder, P. Pearson, Roderick H.J. Houwen, & Cisca Wijmenga. (2001). The tissue transglutaminase gene is not a primary factor predisposing to celiac disease. The American Journal of Gastroenterology. 96(12). 3337–3340. 11 indexed citations

Bakker, Egbert, Christine Van Broeckhoven, H Veenema, et al.. (1987). Germline mosaicism and Duchenne muscular dystrophy mutations. Nature. 329(6139). 554–556. 155 indexed citations

Reeders, Stephen T., M.H. Breuning, G. CORNEY, et al.. (1986). Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16.. BMJ. 292(6524). 851–853. 74 indexed citations

Wieacker, Peter, Kay E. Davies, Howard J. Cooke, et al.. (1984). Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.. PubMed. 36(2). 265–76. 137 indexed citations

Hagemeijer, A, et al.. (1984). Human formaldehyde dehydrogenase (FDH) and its assignment to chromosome 4. Cytogenetic and Genome Research. 38(2). 112–115. 7 indexed citations

Harper, Peter S., T O'Brien, Jeffrey Murray, et al.. (1983). The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy.. Journal of Medical Genetics. 20(4). 252–254. 44 indexed citations

10.

Kingston, Helen, Nick Thomas, P. Pearson, M. Sarfarazi, & Peter S. Harper. (1983). Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.. Journal of Medical Genetics. 20(4). 255–258. 65 indexed citations

11.

Kessel, A.H.M. Geurts van, W. A. M. Boere, Philip G. de Groot, et al.. (1981). Characterization of the Philadelphia chromosome by gene mapping. Cytogenetic and Genome Research. 30(2). 83–91. 35 indexed citations

12.

Tates, A.D., P. Pearson, M. van der Ploeg, & N. de Vogel. (1979). The induction of sex-chromosomal nondisjunction and diploid spermatids following X-irradiation of pre-spermatid stages in the Northern vole Microtus oeconomus. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 61(1). 87–101. 22 indexed citations

13.

Westerveld, A., et al.. (1978). Regional localization of the genes coding for human red cell adenylate kinase, aconitase, and galactose-1-phosphate uridylyltransferase on chromosome 9. Cytogenetic and Genome Research. 22(1-6). 465–467. 3 indexed citations

14.

Pearson, P., et al.. (1978). Gene assignments to the presumptive homologs of human chromosomes 2, 9, 13, 14, and 15 in the Pongidae and Cercopithecoidea. Cytogenetic and Genome Research. 22(1-6). 588–593. 7 indexed citations

15.

Khan, P. Meera, et al.. (1976). Assignment of <i>inosine triphosphatase</i> gene to gorilla chromosome 13 and to human chromosome 20 in primate-rodent somatic cell hybrids. Cytogenetic and Genome Research. 16(1-5). 420–421. 16 indexed citations

16.

Pearson, P., et al.. (1975). Mapping the Xg<sup>a</sup> red blood cell antigen in human-Chinese hamster cell hybrids. Cytogenetic and Genome Research. 14(3-6). 293–295. 10 indexed citations

17.

Geraedts, Joep & P. Pearson. (1975). SPATIAL DISTRIBUTION OF CHROMOSOMES 1 AND Y IN HUMAN SPERMATOZOA. Reproduction. 45(3). 515–517. 9 indexed citations

18.

Wit, Jan de, D. Bootsma, P. Pearson, & A. Westerveld. (1975). Regional mapping of the human No. 1 and X chromosome in interspecific cell hybrids using an X/1 translocation. Cytogenetic and Genome Research. 15(3). 129–137. 3 indexed citations

19.

Pearson, P., et al.. (1974). Genetical Studies on the Multiple Forms of Human Guanylate Kinase in Man-Chinese Hamster Somatic Cell Hybrids. Human Heredity. 24(5-6). 415–423. 13 indexed citations

20.

Pearson, P. & Martin Bobrow. (1970). FLUORESCENT STAINING OF THE Y CHROMOSOME IN MEIOTIC STAGES OF THE HUMAN MALE. Reproduction. 22(1). 177–179. 72 indexed citations

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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