P. Pearson

14.6k citations

211 papers · 11.2k · 1 hit paper · h-index 58

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 127
- Muscle Physiology and Disorders 22
- RNA modifications and cancer 15
- DNA and Nucleic Acid Chemistry 14
- CRISPR and Genetic Engineering 14
Genetics 93
- Genomic variations and chromosomal abnormalities 36
- 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)Canio G. Vosa (2 shared papers)Peter Devilee (7 shared papers)Johan T. den Dunnen (8 shared papers)Martin C. Wapenaar (9 shared papers)
Journals: Human Genetics (27 papers)Nucleic Acids Research (13 papers)Journal of Medical Genetics (12 papers)Genomics (9 papers)Nature (8 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

P. Pearson

199 papers receiving 10.4k citations

P. Pearson's Hit Papers

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A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16 1985 · 568 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 211 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 →	1985	568
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	1989	454
3	Technique for Identifying Y Chromosomes in Human Interphase Nuclei Nature ·P. Pearson, Martin Bobrow, Canio G. Vosa	1970	398
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	1983	323
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	1986	321
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	1985	306
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	1993	261
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	2001	245
9	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	1984	225
10	Staining of Some Specific Regions of Human Chromosomes, particularly the Secondary Constriction of No. 9 Nature New Biology ·Martin Bobrow, K. Madan, P. Pearson	1972	224
11	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	1988	214
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	1985	198
13	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	2003	186
14	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	1989	183
15	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	1988	175
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	2006	173
17	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	1987	169
18	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	1988	168
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	1987	160
20	Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations. Journal of Medical Genetics ·Egbert Bakker, H Veenema, Johan T. den Dunnen, Christine Van Broeckhoven, P.M. Grootscholten, E. J. Bonten, G J van Ommen, P. Pearson	1989	159

About P. Pearson

P. Pearson is a scholar working on Molecular Biology, Genetics, Plant Science, Cellular and Molecular Neuroscience and Genetics, having authored 211 papers that have together received 11.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (36 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 (15 papers), DNA and Nucleic Acid Chemistry (14 papers) and CRISPR and Genetic Engineering (14 papers). The work is most often cited by research in Genetics (4.5k citations), Molecular Biology (6.3k citations), Genetics (826 citations), Reproductive Medicine (525 citations) and Gastroenterology (251 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, Canio G. Vosa, Peter Devilee, Johan T. den Dunnen, Martin C. Wapenaar, Marten H. Hofker and Stephen T. Reeders. Their work appears in journals such as Human Genetics, Nucleic Acids Research, Journal of Medical Genetics, Genomics and Nature.

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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