P. Pearson

14.5k citations
209 papers · 10.7k · 1 hit paper · h-index 55

Impact in

  • Genetics top 0.1%
    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Neurogenetic and Muscular Disorders Research
  • Molecular Biology top 0.5%
    • Muscle Physiology and Disorders
    • Genomics and Chromatin Dynamics

Papers in

  • Molecular Biology 128
    • Muscle Physiology and Disorders 22
    • RNA modifications and cancer 16
    • CRISPR and Genetic Engineering 14
  • Genetics 101
    • Genomic variations and chromosomal abnormalities 40
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 18
    • Genetics and Neurodevelopmental Disorders 17
Co-authors
Martin Bobrow (9 shared papers)Egbert Bakker (24 shared papers)G.J.B. van Ommen (20 shared papers)Kay E. Davies (8 shared papers)Peter Devilee (7 shared papers)Canio G. Vosa (2 shared papers)Johan T. den Dunnen (8 shared papers)Martin C. Wapenaar (9 shared papers)
Journals
Human Genetics (27 papers)Cytogenetic and Genome Research (18 papers)Nucleic Acids Research (13 papers)Journal of Medical Genetics (12 papers)Genomics (9 papers)
Partner nations
NetherlandsUnited StatesUnited Kingdom

In The Last Decade

P. Pearson

208 papers receiving 10.2k citations

P. Pearson's Hit Papers

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16 1985 · 518 citations
5180+13+27Years since publication100200300400500
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

  • it has ≥500 total citations;
  • it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
  • it reaches the top citation threshold in at least one of its specific research topics.
  1. 1985 Nature

Peers

P. Pearson
Comparison fields: 5 of 150
  • Genetics 4.7k
  • Molecular Biology 6.3k
  • Genetics 843
  • Reproductive Medicine 599
  • Pediatrics, Perinatology and Child Health 901
Replace Gert Matthijs with:
Gert Matthijs Belgium
Gudrun Rappold Germany
B.M. Cattanach United Kingdom
Egbert Bakker Netherlands
Ethylin Wang Jabs United States
Cynthia C. Morton United States
Eric Legius Belgium
S. Steven Potter United States
Raju Kucherlapati United States
Frank Costantini United States
P. Pearson relative to Gert Matthijs Belgium Gert Matthijs's profile →
Citations per field
00.5×1.5×2.1×
Gert Matthijs · 1×
Citations per year

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

20 of 20 papers shown

Showing the 20 most-cited of 209 papers — load more, or switch the sort, to bring in the rest.

#Work
1
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16
Nature ·Stephen T. Reeders, M.H. Breuning, Kay E. Davies, Robert D. Nicholls, Andrew P. Jarman, Douglas R. Higgs, P. Pearson, D. J. Weatherall
Hit paper breakdown →		1985518
2
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.
PubMed ·Johan T. den Dunnen, P.M. Grootscholten, Egbert Bakker, Lau A.J. Blonden, H.B. Ginjaar, Martin C. Wapenaar, H M van Paassen, Christine Van Broeckhoven, P. Pearson, G J van Ommen
1989438
3
Technique for Identifying Y Chromosomes in Human Interphase Nuclei
Nature ·P. Pearson, Martin Bobrow, Canio G. Vosa
1970363
4
Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome
Nucleic Acids Research ·Kay E. Davies, P. Pearson, Peter S. Harper, Jeffrey Murray, T O'Brien, M. Sarfarazi, R. Williamson
1983309
5
Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84
Human Genetics ·Thomas Cremer, J. E. Landegent, Andrea Brückner, H. Schöll, Margit Schardin, H. D. Hager, Peter Devilee, P. Pearson, M. van der Ploeg
1986299
6
PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs
The Lancet ·Egbert Bakker, Nicole Goor, Klaus Wrogemann, Louis M. Kunkel, Wayne A. Fenton, Daniëlle Majoor‐Krakauer, M. G. J. Jahoda, G.J.B. van Ommen, Marten H. Hofker, Jean‐Louis Mandel, Kay E. Davies, H.F. Willard, L. A. Sandkuyl, A.J. van Essen, E. S. Sachs, P. Pearson
1985284
7
Introduction and expression of the 400 kilobase precursor amyloid protein gene in transgenic mice
Nature Genetics ·Bruce T. Lamb, Sangram S. Sisodia, Ann M. Lawler, Hilda H. Slunt, Cheryl A. Kitt, W.G. Kearns, P. Pearson, Donald L. Price, John D. Gearhart
1993229
8
The role of genetic factors in age at natural menopause
Human Reproduction ·Jan Peter de Bruin, H. Bovenhuis, P.A.H. van Noord, P. Pearson, J.A.M. van Arendonk, Egbert R. te Velde, W. W. Kuurman, M. Dorland
2001222
9
Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes.
PubMed ·Peter Devilee, R.F. Thierry, Tim Kievits, Raghu Kolluri, Anton H. N. Hopman, H F Willard, P. Pearson, Cornelisse Cj
1988207
10
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28
Nature ·Siladitya Bhattacharya, Alan F. Wright, John Clayton, W. H. Price, C I Phillips, C. McKeown, Marcelle Jay, Alan C. Bird, P. Pearson, E.M. Southern, H.J. Evans
1984203
11
Staining of Some Specific Regions of Human Chromosomes, particularly the Secondary Constriction of No. 9
Nature New Biology ·Martin Bobrow, K. Madan, P. Pearson
1972197
12
Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy
Human Genetics ·Marten H. Hofker, Martin C. Wapenaar, Nicole Goor, Egbert Bakker, G.J.B. van Ommen, P. Pearson
1985195
13
At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma
Genomics ·Peter Devilee, Marianne van den Broek, Nel Kuipers-Dukshoorn, Rukmini Kolluri, P. Meera Khan, P. Pearson, Cees J. Cornelisse
1989181
14
Duchenne muscular dystrophy
Neurology ·Richard J. Bartlett, Margaret A. Pericak‐Vance, Jin‐Young Koh, Larry H. Yamaoka, J. C. Chen, Wu-Yen Hung, Marcy C. Speer, Martin C. Wapenaar, G.J.B. van Ommen, Egbert Bakker, P. Pearson, R.S. Kandt, Teepu Siddique, J. R. Gilbert, Judith Lee, Marcia Sirotkin-roses, Allen D. Roses
1988170
15
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 ·S C Bakker, Emma M. van der Meulen, Jan K. Buitelaar, Lodewijk A. Sandkuijl, David L. Pauls, A.J. Monsuur, Ruben van 't Slot, Ruud B. Minderaa, W. Boudewijn Gunning, P. Pearson, Richard J. Sinke
2003168
16
Heart Disease Risk Determines Menopausal Age Rather Than the Reverse
Journal of the American College of Cardiology ·Helen S. Kok, Kristel M. van Asselt, Yvonne T. van der Schouw, Ingeborg van der Tweel, Petra H.M. Peeters, Peter W.F. Wilson, P. Pearson, Diederick E. Grobbee
2006163
17
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours
Human Genetics ·Marcel M. A. M. Mannens, Rosalyn Slater, Christa Heyting, Jet Bliek, Jan de Kraker, Jane Coad, P. de Pagter-Holthuizen, P. Pearson
1988161
18
Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels
Nature ·Johan T. den Dunnen, Egbert Bakker, E. G. Klein Breteler, P. Pearson, G.J.B. van Ommen
1987157
19
Germline mosaicism and Duchenne muscular dystrophy mutations
Nature ·Egbert Bakker, Christine Van Broeckhoven, E. J. Bonten, M. J. van de Vooren, H Veenema, Wim Van Hul, G.J.B. van Ommen, A. Vandenberghe, P. Pearson
1987155
20
Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.
PubMed ·Webster K. Cavenee, Robin J. Leach, T. Mohandas, P. Pearson, R. White
1984153

About P. Pearson

P. Pearson is a scholar working on Molecular Biology, Genetics, Plant Science, Pediatrics, Perinatology and Child Health and Cellular and Molecular Neuroscience, having authored 209 papers that have together received 10.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (40 papers), Chromosomal and Genetic Variations (28 papers), Muscle Physiology and Disorders (22 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers), Genetics and Neurodevelopmental Disorders (17 papers), RNA modifications and cancer (16 papers), CRISPR and Genetic Engineering (14 papers) and Prenatal Screening and Diagnostics (13 papers). The work is most often cited by research in Genetics (4.7k citations), Molecular Biology (6.3k citations), Genetics (843 citations), Reproductive Medicine (599 citations) and Pediatrics, Perinatology and Child Health (901 citations). P. Pearson has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent 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. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Nucleic Acids Research, Journal of Medical Genetics and Genomics.

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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