R Elles

798 total citations
21 papers, 530 citations indexed

About

R Elles is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, R Elles has authored 21 papers receiving a total of 530 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Pulmonary and Respiratory Medicine. Recurrent topics in R Elles's work include Prenatal Screening and Diagnostics (5 papers), Genetic Syndromes and Imprinting (3 papers) and BRCA gene mutations in cancer (3 papers). R Elles is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genetic Syndromes and Imprinting (3 papers) and BRCA gene mutations in cancer (3 papers). R Elles collaborates with scholars based in United Kingdom, South Africa and Spain. R Elles's co-authors include Robert Williamson, Bryan D. Young, Kay E. Davies, R Harris, Andrew Read, Meena Niazi, Dulcie V. Coleman, David Horwell, Emilio Rodríguez‐Cerezo and Dolores Ibarreta and has published in prestigious journals such as Nature, New England Journal of Medicine and The Lancet.

In The Last Decade

R Elles

19 papers receiving 495 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R Elles United Kingdom	11	318	302	78	75	37	21	530
Kiyoshi Kikkawa Japan	12	182 0.6×	211 0.7×	56 0.7×	103 1.4×	32 0.9×	27	378
Jack H. Jung Canada	13	218 0.7×	208 0.7×	61 0.8×	83 1.1×	22 0.6×	19	411
Ko–ichiro Yoshiura Japan	12	304 1.0×	251 0.8×	69 0.9×	107 1.4×	31 0.8×	22	505
I. López Pajares Spain	12	286 0.9×	316 1.0×	94 1.2×	106 1.4×	48 1.3×	27	493
Philip N. Mowrey United States	11	162 0.5×	232 0.8×	88 1.1×	134 1.8×	46 1.2×	22	436
B. G. A. ter Haar Netherlands	15	212 0.7×	160 0.5×	39 0.5×	67 0.9×	28 0.8×	20	423
Simona Cavani Italy	16	313 1.0×	393 1.3×	82 1.1×	160 2.1×	23 0.6×	31	692
María Palomares‐Bralo Spain	13	339 1.1×	364 1.2×	55 0.7×	105 1.4×	53 1.4×	38	540
Daniele De Brasi Italy	14	224 0.7×	256 0.8×	48 0.6×	86 1.1×	38 1.0×	44	478
Mildred L. Kistenmacher United States	12	315 1.0×	326 1.1×	119 1.5×	138 1.8×	56 1.5×	17	595

Countries citing papers authored by R Elles

Since Specialization

Citations

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

Fields of papers citing papers by R Elles

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R Elles

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

All Works

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20 of 20 papers shown

Elles, R, et al.. (2020). PRO40 FACTORS ASSOCIATED WITH THE FORMATION OF INHIBITORS IN PATIENTS WITH HEMOPHILIA OF THE SUBSIDIZED REGIME IN COLOMBIA.. Value in Health. 23. S335–S336.

Vermeesch, Joris, et al.. (2010). European external quality assessment (EQA) for Constitutional molecular karyotyping: Experiences from the CEQA/EMQN pilot scheme. European Journal of Human Genetics. 18. 367–368.

Ellison, Gillian, et al.. (2010). Circulating free DNA as a surrogate for tumor material for EGFR and KRAS analysis. Clinical Cancer Research. 16(19_Supplement). PR4–PR4. 1 indexed citations

Wallace, Andrew J., et al.. (2004). Mutation Scanning of the NF2 Gene: An Improved Service Based on Meta-PCR/Sequencing, Dosage Analysis, and Loss of Heterozygosity Analysis. Genetic Testing. 8(4). 368–380. 28 indexed citations

Ibarreta, Dolores, R Elles, Jean‐Jacques Cassiman, Emilio Rodríguez‐Cerezo, & Elisabeth Dequeker. (2004). Towards quality assurance and harmonization of genetic testing services in the European Union. Nature Biotechnology. 22(10). 1230–1235. 37 indexed citations

Elles, R, et al.. (2002). The National Genetics Reference Laboratories. ePrints Soton (University of Southampton). 1 indexed citations

Wallace, Andrew J., et al.. (1999). Meta-PCR: A Novel Method for Creating Chimeric DNA Molecules and Increasing the Productivity of Mutation Scanning Techniques. Genetic Testing. 3(2). 173–183. 5 indexed citations

Lalloo, Fiona, Barbara Bulman, Jenny Varley, et al.. (1998). An evaluation of common breast cancer gene mutations in a population of Ashkenazi Jews.. Journal of Medical Genetics. 35(1). 10–12. 10 indexed citations

Veldhuisen, Barbera, Jasper J. Saris, Simone de Haij, et al.. (1997). A Spectrum of Mutations in the Second Gene for Autosomal Dominant Polycystic Kidney Disease (PKD2). The American Journal of Human Genetics. 61(3). 547–555. 77 indexed citations

10.

Elles, R, et al.. (1990). Recombination or heterogeneity: is there a second locus for adult polycystic kidney disease?. Journal of Medical Genetics. 27(7). 413–417. 6 indexed citations

11.

Ivinson, Adrian J., Andrew Read, R Harris, et al.. (1989). Testing for cystic fibrosis using allelic association.. Journal of Medical Genetics. 26(7). 426–430. 6 indexed citations

12.

Harris, R, R Elles, David Craufurd, et al.. (1989). Molecular genetics in the National Health Service in Britain.. Journal of Medical Genetics. 26(4). 219–225. 13 indexed citations

13.

Super, Maurice, Martin Schwarz, R Elles, et al.. (1987). CLINIC EXPERIENCE OF PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS BY USE OF LINKED DNA PROBES. The Lancet. 330(8562). 782–784. 21 indexed citations

14.

Read, Andrew, L Kerzin-Storrar, R. Mountford, R Elles, & R Harris. (1986). A register based system for gene tracking in Duchenne muscular dystrophy.. Journal of Medical Genetics. 23(6). 581–586. 15 indexed citations

15.

Taylor, G M, et al.. (1985). Expression of HLA class I α chain determinants by human X mouse hybrid T cells is correlated with HLA‐β₂m but not with H‐2. Tissue Antigens. 26(2). 121–131. 2 indexed citations

16.

Elles, R, Robert Williamson, Meena Niazi, Dulcie V. Coleman, & David Horwell. (1984). Absence of Maternal Contamination of Chorionic Villi Used for Fetal-Gene Analysis. Obstetrical & Gynecological Survey. 39(3). 138–138. 2 indexed citations

17.

Pembrey, Marcus, et al.. (1984). Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophy.. Archives of Disease in Childhood. 59(3). 208–216. 23 indexed citations

18.

Elles, R, Robert Williamson, Meena Niazi, Dulcie V. Coleman, & David Horwell. (1983). Absence of Maternal Contamination of Chorionic Villi Used for Fetal-Gene Analysis. New England Journal of Medicine. 308(24). 1433–1435. 48 indexed citations

19.

Davies, Kay E., et al.. (1981). Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry. Nature. 293(5831). 374–376. 217 indexed citations

20.

Elles, R & I. Sutherland. (1980). Purification of specific restriction fragments of human deoxyribonucleic acid by using liquid countercurrent chromatography. Biochemical Society Transactions. 8(2). 173–173. 1 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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