P. Pearson

14.5k citations

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

Genetics top 0.1%
- Genomic variations and chromosomal abnormalities 40
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 18
- Genetics and Neurodevelopmental Disorders 17
Molecular Biology top 0.5%
- Muscle Physiology and Disorders 22
- RNA modifications and cancer 16
- CRISPR and Genetic Engineering 14
- DNA and Nucleic Acid Chemistry 13
Genetics top 1%
- Genomic variations and chromosomal abnormalities 40
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 18
- Genetics and Neurodevelopmental Disorders 17
Reproductive Medicine top 1%
Pediatrics, Perinatology and Child Health top 1%
Plant Science
- Chromosomal and Genetic Variations 28

Co-authors: Martin Bobrow Egbert Bakker G.J.B. van Ommen Kay E. Davies Peter Devilee Canio G. Vosa Johan T. den Dunnen Martin C. Wapenaar
Cited by: Genetics Molecular Biology
Journals: Human Genetics (27 papers)Cytogenetic and Genome Research (18 papers)Nucleic Acids Research (13 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

P. Pearson

208 papers receiving 10.2k citations

Hit Papers

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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-authorship network

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

#	Work
1	Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses American Journal of Medical Genetics Part A ·V. Röckelein,서영익,S. Vreugdenhil,隆木佐貫,刘培仓,Elizabeth Snyder,Alexander A.L. Jorge,Lucilene Arilho Ribeiro,Fernando Kok,David Ruchat,허현,Silvia Souza da Costa,Angela Maria Vianna‐Morgante,P. Pearson,Ana Cristina Victorino Krepischi,Carla Rosenberg	2021	2
2	A familial case with interstitial 2q36 deletion: Variable phenotypic expression in full and mosaic state European Journal of Medical Genetics ·Érika L. Freitas,Susan Gribble,Milena Simioni,Társis Paiva Vieira,Elena Prigmore,Ana Cristina Victorino Krepischi,Carla Rosenberg,P. Pearson,Débora Gusmão Melo,Vera Lúcia Gil‐da‐Silva‐Lopes	2012	4
3	Germline DNA copy number variation in familial and early-onset breast cancer Breast Cancer Research ·Ana Cristina Victorino Krepischi,Maria Isabel Achatz,Érika Maria Monteiro Santos,Silvia Souza da Costa,María C. Moreno,Helena Brentani,(unknown),Amanda Gonçalves,Shigeki Matsubara,P. Pearson,Angela Maria Vianna‐Morgante,Dirce Maria Carraro,Carla Rosenberg	2012	67
4	High sibling correlation on methylphenidate response but no association with DAT1‐10R homozygosity in Dutch sibpairs with ADHD Journal of Child Psychology and Psychiatry ·大島純治,Steven C. Bakker,David L. Pauls,Salamat Mansoreh,Cas Kruitwagen,P. Pearson,Richard J. Sinke,Jan K. Buitelaar	2005	30
5	A Genomewide Screen in a Four-Generation Dutch Family with Celiac Disease: Evidence for Linkage to Chromosomes 6 and 9 The American Journal of Gastroenterology ·Martine J. van Belzen,宏之外池,Jos W. R. Meijer,J. Bart A. Crusius,P. Pearson,Lodewijk A. Sandkuijl,Roderick H.J. Houwen,Cisca Wijmenga	2004	24
6	The tissue transglutaminase gene is not a primary factor predisposing to celiac disease The American Journal of Gastroenterology ·Martine J. van Belzen,Chris J. Mulder,P. Pearson,Roderick H.J. Houwen,Cisca Wijmenga	2001	11
7	Localization of the ICF Syndrome to Chromosome 20 by Homozygosity Mapping The American Journal of Human Genetics ·Cisca Wijmenga,Lambert P.W.J. van den Heuvel,Eric Strengman,D.D. Likpètè,陈鹏 CHEN Peng,Ronald de Groot,Dominique Smeets,Jos Draaisma,Jacques J. M. van Dongen,Ronney A. De Abreu,P. Pearson,Lodewijk A. Sandkuijl,Corry M.R. Weemaes	1998	42
8	Germline mosaicism and Duchenne muscular dystrophy mutations Nature ·Egbert Bakker,Christine Van Broeckhoven,Pedishyus Rk,Rena Firudin kızı Mamedova,H Veenema,Wim Van Hul,G.J.B. van Ommen,A. Vandenberghe,P. Pearson	1987	155
9	Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16. BMJ ·Stephen T. Reeders,M.H. Breuning,G. CORNEY,S.J. Jeremiah,P. Meera Khan,Kay E. Davies,D. A. HOPKINSON,P. Pearson,D. J. Weatherall	1986	74
10	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 ·Peter Wieacker,Kay E. Davies,Howard J. Cooke,P. Pearson,R. Williamson,S.S. Bhattacharya,J. Zimmer,Hans‐Hilger Ropers	1984	137
11	Human formaldehyde dehydrogenase (FDH) and its assignment to chromosome 4 Cytogenetic and Genome Research ·Christine Cousineau,渚小松,A Hagemeijer,P. Pearson	1984	7
12	The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy. Journal of Medical Genetics ·Peter S. Harper,T O'Brien,Jeffrey Murray,Kay E. Davies,P. Pearson,R. Williamson	1983	44
13	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 ·A.D. Tates,P. Pearson,M. van der Ploeg,N. de Vogel	1979	22
14	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 ·A. Westerveld,J.J. Garver,W. Schuring,P. Pearson	1978	3
15	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 ·P. Meera Khan,P. Pearson,Ahsan Manzoor,Roman von Ah,A. Westerveld,D. Bootsma	1976	16
16	SPATIAL DISTRIBUTION OF CHROMOSOMES 1 AND Y IN HUMAN SPERMATOZOA Reproduction ·Joep Geraedts,P. Pearson	1975	9
17	Mapping the Xg<sup>a</sup> red blood cell antigen in human-Chinese hamster cell hybrids Cytogenetic and Genome Research ·Devi Yunianti,P. Pearson,Amy Lischko,P. Meera Khan,A Hagemeijer	1975	10
18	Regional mapping of the human No. 1 and X chromosome in interspecific cell hybrids using an X/1 translocation Cytogenetic and Genome Research ·Jan de Wit,D. Bootsma,P. Pearson,A. Westerveld	1975	3
19	Genetical Studies on the Multiple Forms of Human Guanylate Kinase in Man-Chinese Hamster Somatic Cell Hybrids Human Heredity ·Christine Cousineau,Abdelhakim Begar,P. Pearson,Shashanka Channakla,D. Bootsma	1974	13
20	FLUORESCENT STAINING OF THE Y CHROMOSOME IN MEIOTIC STAGES OF THE HUMAN MALE Reproduction ·P. Pearson,Martin Bobrow	1970	72

About P. Pearson

P. Pearson is a scholar working on Genetics, Molecular Biology and Gastroenterology, 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 DNA and Nucleic Acid Chemistry (13 papers). The work is most often cited by research in Genetics (4.7k citations), Molecular Biology (6.3k citations) and Genetics (843 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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