C. Rasberry

619 total citations
15 papers, 536 citations indexed

About

C. Rasberry is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, C. Rasberry has authored 15 papers receiving a total of 536 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Molecular Biology and 4 papers in Reproductive Medicine. Recurrent topics in C. Rasberry's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genetic Syndromes and Imprinting (4 papers) and Epigenetics and DNA Methylation (4 papers). C. Rasberry is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genetic Syndromes and Imprinting (4 papers) and Epigenetics and DNA Methylation (4 papers). C. Rasberry collaborates with scholars based in United Kingdom, France and United States. C. Rasberry's co-authors include B.M. Cattanach, E.P. Evans, P. Avner, Marie‐Christine Simmler, Claire Rougeulle, Simon Ball, Carolyn M. Hustad, Robert M. Kovatch, Jo Peters and William L. Perry and has published in prestigious journals such as Nature Genetics, Genetics and Human Molecular Genetics.

In The Last Decade

C. Rasberry

15 papers receiving 521 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
C. Rasberry United Kingdom	11	383	361	52	50	48	15	536
Karen Fancher United States	7	563 1.5×	151 0.4×	53 1.0×	41 0.8×	58 1.2×	8	698
L. A. Caston United States	7	482 1.3×	241 0.7×	32 0.6×	87 1.7×	20 0.4×	7	651
Gregor Schlüter Germany	13	246 0.6×	186 0.5×	67 1.3×	151 3.0×	37 0.8×	25	486
Harry W. Goodall United Kingdom	11	403 1.1×	137 0.4×	37 0.7×	47 0.9×	47 1.0×	12	592
Andrew Fedoriw United States	12	681 1.8×	294 0.8×	24 0.5×	35 0.7×	126 2.6×	14	764
M. Lutz Germany	10	475 1.2×	185 0.5×	37 0.7×	11 0.2×	38 0.8×	10	542
Sandra S. de Vries Netherlands	7	612 1.6×	209 0.6×	36 0.7×	53 1.1×	26 0.5×	7	773
Bruno Passet France	14	494 1.3×	133 0.4×	83 1.6×	27 0.5×	77 1.6×	45	666
Victor De Leon United States	9	672 1.8×	246 0.7×	81 1.6×	234 4.7×	38 0.8×	14	920
Aurélie Dipietromaria France	13	295 0.8×	301 0.8×	49 0.9×	155 3.1×	28 0.6×	13	531

Countries citing papers authored by C. Rasberry

Since Specialization

Citations

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

Fields of papers citing papers by C. Rasberry

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Rasberry

This figure shows the co-authorship network connecting the top 25 collaborators of C. Rasberry. A scholar is included among the top collaborators of C. Rasberry based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with C. Rasberry. C. Rasberry is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Tevendale, Maxine, Marie Watkins, C. Rasberry, B.M. Cattanach, & Anne C. Ferguson‐Smith. (2006). Analysis of mouse conceptuses with uniparental duplication/deficiency for distal chromosome 12: comparison with chromosome 12 uniparental disomy and implications for genomic imprinting. Cytogenetic and Genome Research. 113(1-4). 215–222. 24 indexed citations

Cattanach, B.M., Jo Peters, Simon Ball, & C. Rasberry. (2000). Two imprinted gene mutations: three phenotypes. Human Molecular Genetics. 9(15). 2263–2273. 47 indexed citations

Banerjee, Subhasis, Prim B. Singh, C. Rasberry, & B.M. Cattanach. (2000). Embryonic inheritance of the chromatin organisation of the imprinted H19 domain in mouse spermatozoa. Mechanisms of Development. 90(2). 217–226. 10 indexed citations

Cattanach, B.M., C.V. Beechey, C. Rasberry, Janet Jones, & D.G. Papworth. (1996). Time of initiation and site of action of the mouse chromosome 11 imprinting effects. Genetics Research. 68(1). 35–43. 25 indexed citations

Hustad, Carolyn M., William L. Perry, Linda D. Siracusa, et al.. (1995). Molecular genetic characterization of six recessive viable alleles of the mouse agouti locus.. Genetics. 140(1). 255–265. 108 indexed citations

Cattanach, B.M. & C. Rasberry. (1994). Enhanced specific-locus mutation response of 101/H male mice to single, acute X-irradiation. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 311(1). 77–84. 7 indexed citations

Cattanach, B.M., et al.. (1993). Large deletions and other gross forms of chromosome imbalance compatible with viability and fertility in the mouse. Nature Genetics. 3(1). 56–61. 68 indexed citations

Simmler, Marie‐Christine, B.M. Cattanach, C. Rasberry, Claire Rougeulle, & P. Avner. (1993). Mapping the murine Xce locus with (CA)n repeats. Mammalian Genome. 4(9). 523–530. 91 indexed citations

Capel, Blanche, C. Rasberry, Julian Dyson, et al.. (1993). Deletion of Y chromosome sequences located outside the testis determining region can cause XY female sex reversal. Nature Genetics. 5(3). 301–307. 87 indexed citations

10.

Cattanach, B.M., C. Rasberry, E.P. Evans, et al.. (1991). 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. 56(3-4). 137–143. 25 indexed citations

11.

Cattanach, B.M., C. Rasberry, M. D. Burtenshaw, & E.P. Evans. (1990). Illegitimate pairing of the X and Y chromosomes in Sxr mice. Genetics Research. 56(2-3). 121–128. 10 indexed citations

12.

Cattanach, B.M., J. Peters, & C. Rasberry. (1989). Induction of specific locus mutations in mouse spermatogonial stem cells by combined chemical X-ray treatments. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 212(1). 91–101. 8 indexed citations

13.

Jones, Janet, Josephine Peters, C. Rasberry, & B.M. Cattanach. (1989). X-inactivation of theStslocus in the mouse: an anomaly of the dosage compensation mechanism. Genetics Research. 53(3). 193–199. 16 indexed citations

14.

Jones, J. B., J. Peters, C. Rasberry, & B.M. Cattanach. (1989). X-inactivation of the Sts locus in the mouse: an anomaly of the dosage compensation mechanism. Trends in Genetics. 5. 322–322. 1 indexed citations

15.

Cattanach, B.M. & C. Rasberry. (1987). 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. 51(6). 985–996. 9 indexed citations

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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