R. Williamson

2.8k total citations
27 papers, 703 citations indexed

About

R. Williamson is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, R. Williamson has authored 27 papers receiving a total of 703 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Genetics and 3 papers in Plant Science. Recurrent topics in R. Williamson's work include CRISPR and Genetic Engineering (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Chromosomal and Genetic Variations (3 papers). R. Williamson is often cited by papers focused on CRISPR and Genetic Engineering (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Chromosomal and Genetic Variations (3 papers). R. Williamson collaborates with scholars based in United Kingdom, United States and France. R. Williamson's co-authors include David A. Hartley, Dennis Drayna, Giovanna Camerino, Jean‐Louis Mandel, Kelvin J.A. Davies, Rebecca White, Hans Eiberg, Kjeld Schmiegelow, Jan Mohr and Rosemary J. Akhurst and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

R. Williamson

27 papers receiving 646 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R. Williamson United Kingdom 12 341 270 109 105 99 27 703
M.F. Rousseau-Merck France 15 377 1.1× 186 0.7× 81 0.7× 90 0.9× 70 0.7× 29 687
Zeynep Coban‐Akdemir United States 18 544 1.6× 396 1.5× 131 1.2× 41 0.4× 69 0.7× 50 965
Giulia Arrigo Italy 12 339 1.0× 240 0.9× 22 0.2× 121 1.2× 49 0.5× 21 594
Bruno Copin France 14 452 1.3× 260 1.0× 71 0.7× 54 0.5× 147 1.5× 23 922
Michela Barbaro Sweden 22 885 2.6× 596 2.2× 135 1.2× 53 0.5× 78 0.8× 47 1.3k
Lynn Doglio United States 13 423 1.2× 236 0.9× 210 1.9× 55 0.5× 27 0.3× 18 734
J. Barra France 7 635 1.9× 281 1.0× 154 1.4× 88 0.8× 38 0.4× 10 1.1k
Nathalie Allioli France 14 540 1.6× 154 0.6× 96 0.9× 53 0.5× 90 0.9× 19 926
Nisha Padmanabhan United Kingdom 14 457 1.3× 119 0.4× 63 0.6× 48 0.5× 79 0.8× 19 832
Jorge Oliveira Portugal 15 436 1.3× 219 0.8× 25 0.2× 36 0.3× 82 0.8× 56 694

Countries citing papers authored by R. Williamson

Since Specialization
Citations

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

Fields of papers citing papers by R. Williamson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. Williamson

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

All Works

20 of 20 papers shown
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Riley, Brien P. & R. Williamson. (1997). Non-parametric analysis of chromosome 6p24–22 marker data and schizophrenia in southern African Bantu-speaking families. Psychiatric Genetics. 7(3). 131–132. 6 indexed citations
4.
Farrer, Matthew J., Michelle M. Coleman, Lynda Bennett, et al.. (1995). Genetic variation in the COL6A1 region is associated with congenital heart defects in trisomy 21 (Down's syndrome). Annals of Human Genetics. 59(3). 253–269. 37 indexed citations
5.
Twells, Rebecca C.J., Pa‐thai Yenchitsomanus, Rebecca Allotey, et al.. (1994). Autosomal dominant cerebellar ataxia with dementla: evidence for a fourth disease locus. Human Molecular Genetics. 3(1). 177–180. 9 indexed citations
6.
Dow, Eleanor, Susan Gelding, E. ROY SKINNER, et al.. (1994). Genetic Analysis of Glucokinase and the Chromosome 20 Diabetes Susceptibility Locus in Families with Type 2 Diabetes. Diabetic Medicine. 11(9). 856–861. 3 indexed citations
7.
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Farrer, Matthew J., et al.. (1993). Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect.. PubMed. 53(2). 462–71. 13 indexed citations
9.
Williamson, R., A. Bowcock, K.K. Kidd, et al.. (1991). Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 24 of 27). Cytogenetic and Genome Research. 58(3-4). 1790–1800. 1 indexed citations
10.
Williamson, R., A. Bowcock, K.K. Kidd, et al.. (1991). Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 16 of 27). Cytogenetic and Genome Research. 58(3-4). 1685–1705. 1 indexed citations
11.
Williamson, R.. (1991). Polymerase chain reaction. Pathology. 23. 17–17. 10 indexed citations
12.
Williamson, R., A. Bowcock, K.K. Kidd, et al.. (1991). Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 21 of 27). Cytogenetic and Genome Research. 58(3-4). 1764–1767. 1 indexed citations
13.
Tsilfidis, Catherine, A.E. MacKenzie, Gary Shutler, et al.. (1991). D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q.. PubMed. 49(5). 961–5. 12 indexed citations
14.
Ramsay, Michèle, Brandon J. Wainwright, Martin Farrall, et al.. (1990). A new polymorphic locus, D7S411, isolated by cloning from preparative pulse-field gels is close to the mutation causing cystic fibrosis. Genomics. 6(1). 39–47. 11 indexed citations
15.
Duff, Karen, R. Williamson, & Sarah‐Jane Richards. (1990). Expression of genes encoding two chains of the collagen type VI molecule during human fetal heart development. International Journal of Cardiology. 27(1). 128–129. 22 indexed citations
16.
Bonduelle, M, Robert H. Dodd, I. Liebærs, et al.. (1988). Chorionic gonadotrophin-β mRNA, a trophoblast marker, is expressed in human 8-cell embryos derived from tripronucleate zygotes. Human Reproduction. 3(7). 909–914. 117 indexed citations
17.
Williamson, R.. (1988). The molecular genetics of complex inherited diseases.. PubMed. 9. 14–6. 2 indexed citations
18.
Wainwright, Brandon J., Nicholas Lench, Kay E. Davies, et al.. (1987). A human regulatory subunit of type II cAMP-dependent protein kinase localized by its linkage relationship to several cloned chromosome 7q markers. Cytogenetic and Genome Research. 45(3-4). 237–239. 8 indexed citations
19.
Eiberg, Hans, Jan Mohr, Kjeld Schmiegelow, Line Nielsen, & R. Williamson. (1985). Linkage relationships of paraoxonase (PON) with other markers: indication of PON‐cystic fibrosis synteny. Clinical Genetics. 28(4). 265–271. 98 indexed citations
20.
Jackson, James F., et al.. (1976). Chicken globin gene number. Nucleic Acids Research. 3(8). 2019–2026. 5 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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