P. Pearson

2.8k citations

50 papers · 1.6k · h-index 21

Impact in

Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Molecular Biology top 10%
- Genomics and Chromatin Dynamics
- RNA modifications and cancer

Papers in

Molecular Biology 18
- Genomics and Chromatin Dynamics 4
- Cancer-related gene regulation 3
Genetics 13
- Genomic variations and chromosomal abnormalities 5
- Animal Genetics and Reproduction 3

Co-authors: K.K. Kidd (14 shared papers)H.F. Willard (8 shared papers)Peter Devilee (4 shared papers)Robert Robbins (2 shared papers)A. Bowcock (5 shared papers)Tim Kievits (3 shared papers)Nina W. Matheson (1 shared paper)J.-L. Mandel (4 shared papers)
Journals: Cytogenetic and Genome Research (31 papers)Nucleic Acids Research (3 papers)Thrombosis and Haemostasis (2 papers)European Journal of Human Genetics (1 paper)Journal of Medical Genetics (1 paper)
Partner nations: Netherlands United Kingdom United States

In The Last Decade

P. Pearson

49 papers receiving 1.5k citations

Peers

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-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.

Border = papers with P. Pearson Line = papers co-authored together P. Pearson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 622-643 Cytogenetic and Genome Research ·K.K. Kidd, A. Bowcock, J. Schmidtke, R.K. Track, F. Ricciuti, G. Hutchings, A. Bale, P. Pearson, H.F. Willard, Joel Gelernter, L. Giuffra, K. Kubzdela	1989	197
2	Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization Cytogenetic and Genome Research ·Tim Kievits, J.G. Dauwerse, J. Wiegant, Peter Devilee, M.H. Breuning, G.J. Cornelisse, G.J.B. van Ommen, P. Pearson	1990	137
3	Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21 Cytogenetic and Genome Research ·Peter Devilee, Thomas Cremer, P. Eline Slagboom, Egbert Bakker, H. Schöll, H. D. Hager, A. F. G. Stevenson, Cornelisse Cj, P. Pearson	1986	136
4	The GDBTM Human Genome Data Base Anno 1992 Nucleic Acids Research ·P. Pearson, Nina W. Matheson, D.C. Flescher, Robert Robbins	1992	93
5	Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 1 of 27) Cytogenetic and Genome Research ·R. Williamson, A. Bowcock, K.K. Kidd, P. Pearson, J. Schmidtke, P. Ceverha, M. Chipperfield, D.N. Cooper, C. Coutelle, J. Hewitt, K. Klinger, K. Langley, J. Beckmann, M. Tolley, B. Maidak, D. Hewett, C. Linch, G. Maslen	1991	91
6	Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques (Part 1 of 5) Cytogenetic and Genome Research ·H.F. Willard, M.H. Skolnick, P. Pearson, J.-L. Mandel	1985	74
7	NOMENCLATURE Genomics ·Julia A. White, P.J. McAlpine, Stylianos E. Antonarakis, Howard M. Cann, Janan T. Eppig, K S Frazer, J Frézal, Doron Lancet, Joseph Nahmias, P. Pearson, Jo Peters, A. Scott, Hamish S. Scott, N.K. Spurr, C. Talbot, Sue Povey	1997	69
8	The PIP5K2A and RGS4 genes are differentially associated with deficit and non‐deficit schizophrenia Genes Brain & Behavior ·S C Bakker, Mechteld L.C. Hoogendoorn, Judith Hendriks, Kitty F. Verzijlbergen, S. Caron, Willem Verduijn, J.P. Selten, P. Pearson, R.S. Kahn, Richard J. Sinke	2006	53
9	A gross reduction in chiasma formation during meiotic prophase and a defective DNA repair mechanism associated with a case of human male infertility Cytogenetic and Genome Research ·P. Pearson, J. D. Ellis, H.J. Evans	1970	53
10	Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p Cytogenetic and Genome Research ·Johannes G. Dauwerse, Tim Kievits, G.C. Beverstock, D. van der Keur, E.M.E. Smit, Hans W. Wessels, A Hagemeijer, P. Pearson, C.-J.B. van Ommen, M.H. Breaming	1990	51
11	Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 1 of 9) Cytogenetic and Genome Research ·P. Pearson, K.K. Kidd, H.F. Willard	1987	50
12	Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 1 of 14) Cytogenetic and Genome Research ·R. Williamson, A. Bowcock, K.K. Kidd, P. Pearson, J. Schmidtke, H.S. Chan, M. Chipperfield, D.N. Cooper, J. Hewitt, F. Lewitter, B. Maidak, M. Quitt, F. Ricciuti, R.K. Track, M. Tolley, S. Trumper, Andrew J. Walley	1990	49
13	Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families. PubMed ·Benoı̂t Arveiler, I. Oberlé, Anne Vincent, Marten H. Hofker, P. Pearson, Jean‐Louis Mandel	1988	48
14	Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISH Cytogenetic and Genome Research ·Jacques C. Giltay, P.M.M. Kastrop, C.H.J. Tiemessen, Wouter G. van Inzen, J. M. J. C. Scheres, P. Pearson	1999	45
15	Genome-Wide Linkage in a Large Dutch Consanguineous Family Maps a Locus for Intracranial Aneurysms to Chromosome 2p13 Stroke ·Yvo B.W.E.M. Roos, Gerard Pals, Patrick Struycken, Gabriël J.E. Rinkel, M. Limburg, Jan C. Pronk, Jan S.P. van den Berg, J.A.F.M. Luijten, P. Pearson, M. Vermeulen, A. Westerveld	2004	40
16	DELETION ON THE X CHROMOSOME DETECTED BY DIRECT DNA ANALYSIS IN ONE OF TWO UNRELATED BOYS WITH GLYCEROL KINASE DEFICIENCY, ADRENAL HYPOPLASIA, AND DUCHENNE MUSCULAR DYSTROPHY The Lancet ·David B. Dunger, Marcus Pembrey, P. Pearson, A. Whitfield, Kay E. Davies, Brian Lake, Donna M. Williams, M J Dillon	1986	37
17	The genome data base (GDB)--a human gene mapping repository Nucleic Acids Research ·P. Pearson	1991	32
18	Cytological assessment of meiotic exchange in a human male with a pericentric inversion of chromosome No. 4 Cytogenetic and Genome Research ·A.G.J.M. van der Linden, P. Pearson, J. J. P. van de Kamp	1975	32
19	Assignment of a gene for glutathione peroxidase (<i>GPX</i><sub>1</sub>) to human chromosome 3 Cytogenetic and Genome Research ·L.M.M. Wijnen, Marry M. van den Heuvel, P. Pearson, P. Meera Khan	1978	31
20	Loss of heterozygosity on 17p in human breast carcinomas: defining the smallest common region of deletion Cytogenetic and Genome Research ·Peter Devilee, Cornelisse Cj, Nel J. Kuipers‐Dijkshoorn, C. Jonker, P. Pearson	1990	25

About P. Pearson

P. Pearson is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Rheumatology, having authored 50 papers that have together received 1.6k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Chromosomal and Genetic Variations (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Genomics and Chromatin Dynamics (4 papers), Hemophilia Treatment and Research (3 papers), Cancer-related gene regulation (3 papers), Animal Genetics and Reproduction (3 papers) and Moyamoya disease diagnosis and treatment (2 papers). The work is most often cited by research in Genetics (710 citations), Molecular Biology (879 citations), Hematology (98 citations), Plant Science (276 citations) and Pediatrics, Perinatology and Child Health (144 citations). P. Pearson has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include K.K. Kidd, H.F. Willard, Peter Devilee, Robert Robbins, A. Bowcock, Tim Kievits, Nina W. Matheson, J.-L. Mandel, M.H. Skolnick and R.K. Track. Their work appears in journals such as Cytogenetic and Genome Research, Nucleic Acids Research, Thrombosis and Haemostasis, European Journal of Human Genetics and Journal of Medical 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.

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