C.V. Beechey

4.3k citations

90 papers · 3.3k · h-index 29

Impact in

Genetics top 0.5%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Pediatrics, Perinatology and Child Health top 0.5%
- Prenatal Screening and Diagnostics

Papers in

Genetics 61
- Genetic Syndromes and Imprinting 38
- Genomic variations and chromosomal abnormalities 15
- Animal Genetics and Reproduction 9
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
Molecular Biology 48
- Epigenetics and DNA Methylation 32

Co-authors: B.M. Cattanach (15 shared papers)A.G. Searle (38 shared papers)Christine M. Williamson (11 shared papers)Jo Peters (10 shared papers)Gavin Kelsey (7 shared papers)Josephine Peters (9 shared papers)Simon Ball (12 shared papers)M. Azim Surani (2 shared papers)
Journals: Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis (13 papers)Genetics Research (8 papers)Cytogenetic and Genome Research (7 papers)Mammalian Genome (6 papers)Genomics (4 papers)
Partner nations: United Kingdom United States Japan

In The Last Decade

C.V. Beechey

84 papers receiving 3.2k citations

Peers

Replace Michael Brandeis with:

Michael Brandeis Israel

J. Richard Chaillet United States

Sébastien A. Smallwood United Kingdom

M Prieur France

Andràs Páldi France

Hiroyuki Sasaki Japan

Rebecca J. Oakey United Kingdom

Julia Arand Germany

Alexandre Wagschal France

Seiichi Matsui Japan

C.V. Beechey relative to Michael Brandeis Israel Michael Brandeis's profile →

Citations per field

00.5×2×2.9×

Michael Brandeis · 1×

×2.7 2k/898

GENET

×2.4 931/394

PPCH

×0.8 2k/3k

MB

×2.2 261/119

CR

×2.9 146/51

RM

Citations per year

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Countries citing papers authored by C.V. Beechey

Since Specialization

Citations

This map shows the geographic impact of C.V. Beechey'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 C.V. Beechey with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C.V. Beechey more than expected).

Fields of papers citing papers by C.V. Beechey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C.V. Beechey. 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 C.V. Beechey. The network helps show where C.V. Beechey may publish in the future.

Co-authors

The 25 scholars most cited alongside C.V. Beechey, 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 C.V. Beechey Line = papers co-authored together C.V. Beechey 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 90 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons Nature Genetics ·Urs Albrecht, James S. Sutcliffe, B.M. Cattanach, C.V. Beechey, Dawna Armstrong, Gregor Eichele, Arthur L. Beaudet	1997	412
2	Embryological and molecular investigations of parental imprinting on mouse chromosome 7 Nature ·Anne C. Ferguson‐Smith, B.M. Cattanach, S. C. Barton, C.V. Beechey, M. Azim Surani	1991	253
3	A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2 Proceedings of the National Academy of Sciences ·Jo Peters, Stephanie F. Wroe, Christine A. Wells, Howard J. Miller, Dorothy Bodle, C.V. Beechey, Christine M. Williamson, Gavin Kelsey	1999	216
4	Autosomal and X-chromosome imprinting Development ·B.M. Cattanach, C.V. Beechey	1990	154
5	A candidate mouse model for Prader–Willi syndrome which shows an absence of Snrpn expression Nature Genetics ·B.M. Cattanach, Jacqueline A. Barr, E.P. Evans, Michael Burtenshaw, C.V. Beechey, Stuart E. Leff, Camilynn I. Brannan, Neal G. Copeland, Nancy A. Jenkins, Janet Jones	1992	149
6	An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus Proceedings of the National Academy of Sciences ·Stephanie F. Wroe, Gavin Kelsey, Judith A. Skinner, Dorothy Bodle, Simon Ball, C.V. Beechey, Josephine Peters, Christine M. Williamson	2000	136
7	Sperm-count, egg-fertilization and dominant lethality after X-irradiation of mice Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·A.G. Searle, C.V. Beechey	1974	130
8	Regulation of alternative polyadenylation by genomic imprinting Genes & Development ·Andrew J. Wood, Reiner Schulz, Kathryn Woodfine, Katarzyna Koltowska, C.V. Beechey, Jo Peters, Déborah Bourc’his, Rebecca J. Oakey	2008	123
9	Genome imprinting phenomena on mouse chromosome 7 Genetics Research ·Antony G. Searle, C.V. Beechey	1990	102
10	Genetic and Functional Analysis of neuronatin in Mice with Maternal or Paternal Duplication of Distal Chr 2 Developmental Biology ·Nobuaki Kikyo, Christine M. Williamson, Rosalind M. John, Sheila C. Barton, C.V. Beechey, Simon Ball, B.M. Cattanach, M. Azim Surani, Josephine Peters	1997	90
11	Uncoupling Antisense-Mediated Silencing and DNA Methylation in the Imprinted Gnas Cluster PLoS Genetics ·Christine M. Williamson, Simon Ball, Claire Dawson, Stuti Mehta, C.V. Beechey, Martin Fray, Lydia Teboul, T. Neil Dear, Gavin Kelsey, Jo Peters	2011	79
12	Genetic imprinting map. C.V. Beechey, B.M. Cattanach, A.G. Searle	1990	76
13	Identification of Imprinted Loci by Methylation-Sensitive Representational Difference Analysis: Application to Mouse Distal Chromosome 2 Genomics ·Gavin Kelsey, Dorothy Bodle, Howard J. Miller, C.V. Beechey, Candice Coombes, Josephine Peters, Christine M. Williamson	1999	74
14	A candidate model for angelman syndrome in the mouse Mammalian Genome ·B.M. Cattanach, J. A. Barr, C.V. Beechey, Joanne E. Martin, Jeffrey L. Noebels, J. B. Jones	1997	72
15	Meiotic disjunction in mouse translocations and the determination of centromere position Genetics Research ·A.G. Searle, C. E. Ford, C.V. Beechey	1971	64
16	The Mouse Murr1 Gene Is Imprinted in the Adult Brain, Presumably Due to Transcriptional Interference by the Antisense-Oriented U2af1-rs1 Gene Molecular and Cellular Biology ·Youdong Wang, Keiichiro Joh, Sadahiko Masuko, Hitomi Yatsuki, Hidenobu Soejima, Akira Nabetani, C.V. Beechey, Satoshi Okinami, Tsunehiro Mukai	2003	64
17	Cytogenetic effects of X-rays and fission neutrons in female mice Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·A.G. Searle, C.V. Beechey	1974	53
18	Linkage analyses of murine immunoglobulin heavy chain and serum prealbumin genes establish their location on chromosome 12 proximal to the T (5;12) 31H breakpoint in band 12F1. Proceedings of the National Academy of Sciences ·T Meo, J. P. Johnson, C.V. Beechey, Sandra J. Andrews, Jo Peters, A.G. Searle	1980	50
19	Glomerular-Specific Imprinting of the Mouse Gsα Gene: How Does This Relate to Hormone Resistance in Albright Hereditary Osteodystrophy? Genomics ·Christine M. Williamson, Julian Schofield, Elizabeth R. Dutton, Adele Seymour, C.V. Beechey, Yvonne H. Edwards, Josephine Peters	1996	50
20	Noncomplementation Phenomena and Their Bearing on Nondisjunctional Effects PubMed ·A.G. Searle, C.V. Beechey	1985	48

About C.V. Beechey

C.V. Beechey is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Reproductive Medicine, having authored 90 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (38 papers), Epigenetics and DNA Methylation (32 papers), Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (15 papers), Sperm and Testicular Function (13 papers), Carcinogens and Genotoxicity Assessment (13 papers), Animal Genetics and Reproduction (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). The work is most often cited by research in Genetics (2.4k citations), Pediatrics, Perinatology and Child Health (931 citations), Molecular Biology (2.4k citations), Cancer Research (261 citations) and Reproductive Medicine (146 citations). C.V. Beechey has collaborated with scholars based in United Kingdom, United States and Japan. Frequent co-authors include B.M. Cattanach, A.G. Searle, Christine M. Williamson, Jo Peters, Gavin Kelsey, Josephine Peters, Simon Ball, M. Azim Surani, James S. Sutcliffe and Urs Albrecht. Their work appears in journals such as Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, Genetics Research, Cytogenetic and Genome Research, Mammalian Genome 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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C.V. Beechey

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