B.M. Cattanach

11.7k citations

136 papers · 9.4k indexed · 3 hit papers · h-index 47

Genetics top 0.1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 41
- Genetic Syndromes and Imprinting 29
- Animal Genetics and Reproduction 19
Reproductive Medicine top 0.5%
- Sperm and Testicular Function 19
Molecular Biology top 1%
- Epigenetics and DNA Methylation 24
- Sexual Differentiation and Disorders 13
Pediatrics, Perinatology and Child Health top 0.5%
- Prenatal Screening and Diagnostics 16
Cancer Research top 5%
- Carcinogens and Genotoxicity Assessment 15

Co-authors: Maggie Kirk C.V. Beechey M. Azim Surani C.E. Pollard Anne C. Ferguson‐Smith J. H. Isaacson E.P. Evans C. Rasberry
Cited by: Genetics Reproductive Medicine Molecular Biology
Journals: Genetics Research (21 papers)Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis (16 papers)Cytogenetic and Genome Research (13 papers)
Partner nations: United Kingdom United States Japan

In The Last Decade

B.M. Cattanach

136 papers receiving 8.9k citations

Hit Papers

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Peers

Countries citing papers authored by B.M. Cattanach

Since Specialization

Citations

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

Fields of papers citing papers by B.M. Cattanach

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by B.M. Cattanach. 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 B.M. Cattanach. The network helps show where B.M. Cattanach may publish in the future.

Co-authorship network

The 25 scholars most cited alongside B.M. Cattanach, 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 B.M. Cattanach Line = papers co-authored together B.M. Cattanach links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A β-Defensin Mutation Causes Black Coat Color in Domestic Dogs Science ·Sophie I. Candille,Christopher B. Kaelin,B.M. Cattanach,Bin Yu,Darren A. Thompson,Matthew A. Nix,Julie A. Kerns,S. M. Schmutz,Glenn L. Millhauser,Gregory S. Barsh	2007	265
2	Two imprinted gene mutations: three phenotypes Human Molecular Genetics ·B.M. Cattanach,Jo Peters,Simon Ball,C. Rasberry	2000	47
3	Investigation of Lung Tumour Induction in BALB/cJ Mice Following Paternal X-irradiation International Journal of Radiation Biology ·B.M. Cattanach,G. Patrick,D.G. Papworth,D.T. Goodhead,Cipriano Urbano Rodríguez,Loren Cobb,Rakesh Mia	1995	48
4	Abstracts of papers presented at the third Mammalian Genetics and Development Workshop held at Birkbeck College, Malet Street, London on 4–6 November 1992 Genetics Research ·Peter Baker,Antony W. Burgess,Ursula Mittwoch,Beatriz Lamas,Pan G,B.M. Cattanach	1993	1
5	Large deletions and other gross forms of chromosome imbalance compatible with viability and fertility in the mouse Nature Genetics ·B.M. Cattanach,Longhua Zou,C. Rasberry,E.P. Evans	1993	68
6	A candidate mouse model for Prader–Willi syndrome which shows an absence of Snrpn expression Nature Genetics ·B.M. Cattanach,Папышева Ольга Виуленовна,E.P. Evans,Longhua Zou,C.V. Beechey,Stuart E. Leff,Camilynn I. Brannan,Neal G. Copeland,Nancy A. Jenkins,Jean-Christophe Robert	1992	150
7	Genetic and molecular evidence of an X-chromosome deletion spanning the tabby (<i>Ta</i>) and testicular feminization (<i>Tfm</i>) loci in the mouse Cytogenetic and Genome Research ·B.M. Cattanach,C. Rasberry,E.P. Evans,Luisa Dandolo,M.C. Simmler,P. Avner	1991	25
8	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
9	Induction of specific locus mutations in mouse spermatogonial stem cells by combined chemical X-ray treatments Mutation research. Fundamental and molecular mechanisms of mutagenesis ·B.M. Cattanach,J. Peters,C. Rasberry	1989	8
10	Genetic Effects of Combined Chemical-X-ray Treatments in Male Mouse Germ Cells International Journal of Radiation Biology and Related Studies in Physics Chemistry and Medicine ·B.M. Cattanach,C. Rasberry	1987	9
11	Location of xce in the mouse x chromosome and effects on pgk-1 expression. Abstr. Genetics Research ·B.M. Cattanach,Theodor Bücher,M. A. Reguero	1982	5
12	Enzyme levels in testis and other tissues of genetically sex-reversed mice Reproduction ·Peter Soyka,Tarun Sehgal,B.M. Cattanach	1979	2
13	Translocation yield from mouse spermatogonial stem cells following unequal-sized X-ray fractionations: Evidence of radiation-induced loss of heterogeneity Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·B.M. Cattanach,Rodolfo de Moraes Peixoto Correio	1979	25
14	Translocation yield from the immature mouse testis and the nature of spermatogonial stem cell heterogeneity Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·B.M. Cattanach,Iain R. Murray,Michele Zanitti	1977	26
15	Sterile period, translocation and specific locus mutation in the mouse following fractionated X-ray treatments with different fractionation intervals Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·B.M. Cattanach,J.K. Vidanarachchi	1974	35
16	Mutagenicity tests with cyclohexylamine in the mouse Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·B.M. Cattanach,K.C. Kouassi	1971	22
17	A search for chromosome aberrations induced in mouse spermatogonia by chemical mutagens Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·B.M. Cattanach,Christie E. Williams	1971	27
18	Ethyl methanesulfonate-induced chromosome breakage in the mouse Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·B.M. Cattanach,C.E. Pollard,J. H. Isaacson	1968	89
19	Induction of paternal sex-chromosome losses and deletions and of autosomal gene mutations by the treatment of mouse post-meiotic germ cells with triethylenemelamine Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·B.M. Cattanach	1967	23
20	Chemically induced mutations in mice Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·B.M. Cattanach	1966	55

About B.M. Cattanach

B.M. Cattanach is a scholar working on Genetics, Reproductive Medicine and Cancer Research, having authored 136 papers that have together received 9.4k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (41 papers), Genetic Syndromes and Imprinting (29 papers), Epigenetics and DNA Methylation (24 papers), Sperm and Testicular Function (19 papers), Animal Genetics and Reproduction (19 papers), Prenatal Screening and Diagnostics (16 papers), Carcinogens and Genotoxicity Assessment (15 papers) and Sexual Differentiation and Disorders (13 papers). The work is most often cited by research in Genetics (5.5k citations), Reproductive Medicine (960 citations) and Molecular Biology (5.9k citations). B.M. Cattanach has collaborated with scholars based in United Kingdom, United States and Japan. Frequent co-authors include Maggie Kirk, C.V. Beechey, M. Azim Surani, C.E. Pollard, Anne C. Ferguson‐Smith, J. H. Isaacson, E.P. Evans, C. Rasberry, Hiroyuki Sasaki and S Hawkes. Their work appears in journals such as Genetics Research, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, Cytogenetic and Genome Research, Nature and Molecular 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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