Cyril Chapman

2.0k total citations
19 papers, 564 citations indexed

About

Cyril Chapman is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Cyril Chapman has authored 19 papers receiving a total of 564 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Molecular Biology and 4 papers in Oncology. Recurrent topics in Cyril Chapman's work include BRCA gene mutations in cancer (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Mitochondrial Function and Pathology (3 papers). Cyril Chapman is often cited by papers focused on BRCA gene mutations in cancer (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Mitochondrial Function and Pathology (3 papers). Cyril Chapman collaborates with scholars based in United Kingdom, New Zealand and China. Cyril Chapman's co-authors include Neil Pearce, Allan H. Smith, Eamonn R. Maher, Tania R. Gunn, Farida Latif, Matthew Jackson, John Elston, Mohammed A. Hannan, Elena G. Bochukova and Eimear Dunne and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, JNCI Journal of the National Cancer Institute and Clinical Cancer Research.

In The Last Decade

Cyril Chapman

19 papers receiving 537 citations

Peers

Cyril Chapman

GENET

CMN

PPCH

Jacob A. Reiss United States

Diane Allingham‐Hawkins Canada

Hyon J. Kim South Korea

Gayle Patel United States

María‐Isabel Tejada Spain

M Stefanova Germany

Moran Gal Israel

Huw Dorkins United Kingdom

J. Kunze Germany

Violetta Anastasiadou Cyprus

Jacob A. Reiss United States

Cyril Chapman

514 ×1.6

GENET

273 ×1.1

64 ×0.8

CMN

143 ×1.9

PPCH

45 ×0.6

Citations per year, relative to Cyril Chapman Cyril Chapman (= 1×) peers Jacob A. Reiss

Countries citing papers authored by Cyril Chapman

Since Specialization

Citations

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

Fields of papers citing papers by Cyril Chapman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cyril Chapman

This figure shows the co-authorship network connecting the top 25 collaborators of Cyril Chapman. A scholar is included among the top collaborators of Cyril Chapman 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 Cyril Chapman. Cyril Chapman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

Manchanda, Ranjit, K Loggenberg, Saskia C. Sanderson, et al.. (2014). Population Testing for Cancer Predisposing BRCA1/BRCA2 Mutations in the Ashkenazi-Jewish Community: A Randomized Controlled Trial. JNCI Journal of the National Cancer Institute. 107(1). 379–379. 139 indexed citations

Whitworth, James W., Cyril Chapman, Kai Ren Ong, et al.. (2014). A clinical and genetic analysis of multiple primary cancer referrals to genetics services. European Journal of Human Genetics. 23(5). 581–587. 16 indexed citations

Albada, Akke, Julie Werrett, Sandra van Dulmen, et al.. (2011). Breast cancer genetic counselling referrals: how comparable are the findings between the UK and the Netherlands?. Journal of Community Genetics. 2(4). 233–247. 8 indexed citations

Metcalfe, Alison, et al.. (2009). Cancer genetic predisposition: information needs of patients irrespective of risk level. Familial Cancer. 8(4). 403–412. 17 indexed citations

Shuib, Salwati, Dominic McMullan, Eleanor Rattenberry, et al.. (2009). Microarray based analysis of 3p25‐p26 deletions (3p‐ syndrome). American Journal of Medical Genetics Part A. 149A(10). 2099–2105. 76 indexed citations

Woodward, Emma R., Christopher J. Ricketts, Sophie Gad, et al.. (2008). Familial Non-VHL Clear Cell (Conventional) Renal Cell Carcinoma: Clinical Features, Segregation Analysis, and Mutation Analysis of FLCN. Clinical Cancer Research. 14(18). 5925–5930. 47 indexed citations

Wilson, Sue, Sheila Greenfield, Helen Pattison, et al.. (2006). Prevalence of the use of cancer related self-tests by members of the public: a community survey. BMC Cancer. 6(1). 215–215. 5 indexed citations

Rose, Peter W., Michael Murphy, Marcus R. Munafò, et al.. (2004). Improving the ascertainment of families at high risk of colorectal cancer: a prospective GP register study.. PubMed. 54(501). 267–71. 11 indexed citations

Christie, Paul T., M. Andrew Nesbit, Cyril Chapman, et al.. (2001). Mutational Analysis in X-Linked Spondyloepiphyseal Dysplasia Tarda1. The Journal of Clinical Endocrinology & Metabolism. 86(7). 3233–3236. 17 indexed citations

10.

Németh, Andrea H., Elena G. Bochukova, Eimear Dunne, et al.. (2000). Autosomal Recessive Cerebellar Ataxia with Oculomotor Apraxia (Ataxia-Telangiectasia–Like Syndrome) Is Linked to Chromosome 9q34. The American Journal of Human Genetics. 67(5). 1320–1326. 64 indexed citations

11.

Németh, Andrea H., Elena G. Bochukova, Eimear Dunne, et al.. (2000). Autosomal Recessive Cerebellar Ataxia with Oculomotor Apraxia (Ataxia‐Telangiectasia–Like Syndrome) Is Linked to Chromosome 9q34. The American Journal of Human Genetics. 67(5). 1320–1326. 15 indexed citations

12.

Robertson, Stephen P., Tania R. Gunn, Bruce G. Allen, Cyril Chapman, & D. M. O. Becroft. (1997). Are Melnick-Needles syndrome and oto-palato-digital syndrome type II allelic? Observations in a four-generation kindred. American Journal of Medical Genetics. 71(3). 341–347. 32 indexed citations

13.

Hon, Kam‐Lun Ellis, Cyril Chapman, & Tania R. Gunn. (1995). Family with partial monosomy 10p and trisomy 10p. American Journal of Medical Genetics. 56(2). 136–140. 14 indexed citations

14.

Chapman, Cyril, et al.. (1992). Fragile site Xq27.3 in a family without mental retardation. Clinical Genetics. 41(1). 33–35. 11 indexed citations

15.

Chapman, Cyril. (1990). A visual interface to computer programs for linkage analysis. American Journal of Medical Genetics. 36(2). 155–160. 10 indexed citations

16.

Smythe, R H, et al.. (1984). Direct intrachromosomal duplication of 16q and heritable fragile site fra (10) (q25) in the same patient. American Journal of Medical Genetics. 19(3). 507–513. 11 indexed citations

17.

Smythe, R H, et al.. (1983). Familial paracentric inversion of 1p. American Journal of Medical Genetics. 14(4). 629–634. 14 indexed citations

18.

Smith, Allan H., et al.. (1982). Congenital Defects and Miscarriages among New Zealand 2,4,5-T Sprayers. Archives of Environmental Health An International Journal. 37(4). 197–200. 54 indexed citations

19.

Chapman, Cyril, et al.. (1975). Galactosaemia: Estimated live birth incidence in New Zealand. Human Genetics. 28(1). 79–82. 3 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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