Rhian Gwilliam

53.8k total citations
19 papers, 797 citations indexed

About

Rhian Gwilliam is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Genetics. According to data from OpenAlex, Rhian Gwilliam has authored 19 papers receiving a total of 797 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Radiology, Nuclear Medicine and Imaging and 5 papers in Genetics. Recurrent topics in Rhian Gwilliam's work include Corneal surgery and disorders (5 papers), Fungal and yeast genetics research (4 papers) and Corneal Surgery and Treatments (2 papers). Rhian Gwilliam is often cited by papers focused on Corneal surgery and disorders (5 papers), Fungal and yeast genetics research (4 papers) and Corneal Surgery and Treatments (2 papers). Rhian Gwilliam collaborates with scholars based in United Kingdom, United States and Czechia. Rhian Gwilliam's co-authors include Panos Deloukas, Neil D. Ebenezer, Petra Lišková, Yik Ying Teo, Dominic Kwiatkowski, Kerrin S. Small, Taane G. Clark, Michael Inouye, Keith J. Edwards and Gary Barker and has published in prestigious journals such as Blood, Bioinformatics and PLoS ONE.

In The Last Decade

Rhian Gwilliam

18 papers receiving 776 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rhian Gwilliam United Kingdom 12 307 301 214 209 99 19 797
Arata Shimada Japan 12 157 0.5× 81 0.3× 292 1.4× 7 0.0× 23 0.2× 19 617
Zenaida P. Lopez-Dee United States 8 64 0.2× 277 0.9× 383 1.8× 13 0.1× 6 0.1× 11 595
Yuxiang Huang United States 13 22 0.1× 47 0.2× 194 0.9× 82 0.4× 124 1.3× 18 527
Brenda Alvarado‐Sánchez Mexico 11 69 0.2× 40 0.1× 103 0.5× 20 0.1× 7 0.1× 17 619
Alice Y. Kim United States 11 14 0.0× 191 0.6× 124 0.6× 484 2.3× 630 6.4× 22 1.0k
Muhammad Farooq Sabar Pakistan 11 70 0.2× 114 0.4× 123 0.6× 8 0.0× 8 0.1× 59 355
A. Collé France 11 30 0.1× 23 0.1× 73 0.3× 19 0.1× 18 0.2× 22 394
Markus Irgang Germany 9 428 1.4× 43 0.1× 302 1.4× 8 0.0× 2 0.0× 9 749
Kenji Tanaka Japan 11 25 0.1× 71 0.2× 224 1.0× 35 0.2× 34 0.3× 44 458

Countries citing papers authored by Rhian Gwilliam

Since Specialization
Citations

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

Fields of papers citing papers by Rhian Gwilliam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rhian Gwilliam

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

All Works

19 of 19 papers shown
1.
Lišková, Petra, Rhian Gwilliam, Martin Filipec, et al.. (2012). High Prevalence of Posterior Polymorphous Corneal Dystrophy in the Czech Republic; Linkage Disequilibrium Mapping and Dating an Ancestral Mutation. PLoS ONE. 7(9). e45495–e45495. 23 indexed citations
2.
Allen, Alexandra M., Gary Barker, Paul A. Wilkinson, et al.. (2012). Discovery and development of exome‐based, co‐dominant single nucleotide polymorphism markers in hexaploid wheat (Triticum aestivum L.). Plant Biotechnology Journal. 11(3). 279–295. 99 indexed citations
3.
Allen, Alexandra M., Gary Barker, Simon Berry, et al.. (2011). Transcript‐specific, single‐nucleotide polymorphism discovery and linkage analysis in hexaploid bread wheat (Triticum aestivum L.). Plant Biotechnology Journal. 9(9). 1086–1099. 188 indexed citations
4.
Bonaglia, María Clara, Roberto Giorda, Silvana Beri, et al.. (2008). Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversion. European Journal of Human Genetics. 17(4). 426–433. 12 indexed citations
5.
Lišková, Petra, Stephen J. Tuft, Rhian Gwilliam, et al.. (2007). Novel mutations in theZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy. Human Mutation. 28(6). 638–638. 64 indexed citations
6.
Teo, Yik Ying, Michael Inouye, Kerrin S. Small, et al.. (2007). A genotype calling algorithm for the Illumina BeadArray platform. Bioinformatics. 23(20). 2741–2746. 141 indexed citations
7.
Lišková, Petra, Neil D. Ebenezer, Pirro G. Hysi, et al.. (2007). Molecular analysis of the VSX1 gene in familial keratoconus.. PubMed. 13. 1887–91. 44 indexed citations
8.
Jirsová, Kateřina, et al.. (2006). Immunohistochemical characterization of cytokeratins in the abnormal corneal endothelium of posterior polymorphous corneal dystrophy patients. Experimental Eye Research. 84(4). 680–686. 48 indexed citations
9.
Eriksson, Niclas, et al.. (2005). Gamma-glutamyl carboxylase (GGCX) microsatellite and warfarin dosing. Blood. 106(10). 3673–3674. 38 indexed citations
10.
Gwilliam, Rhian, Petra Lišková, Martin Filipec, et al.. (2005). Posterior Polymorphous Corneal Dystrophy in Czech Families Maps to Chromosome 20 and Excludes theVSX1Gene. Investigative Ophthalmology & Visual Science. 46(12). 4480–4480. 50 indexed citations
11.
Aves, Stephen J., Zheng Xiang, M. Lyne, et al.. (2002). The mei3 region of the Schizosaccharomyces pombe genome. Yeast. 19(6). 521–527.
12.
Halford, Stephanie, et al.. (2002). Genomic Organization of Human CDS2 and Evaluation as a Candidate Gene for Corneal Hereditary Endothelial Dystrophy 2 on Chromosome 20p13. Experimental Eye Research. 75(5). 619–623. 4 indexed citations
13.
Moore, Karen, Zheng Xiang, Suzanne M. Hurst, et al.. (2001). Subtelomeric sequence from the right arm ofSchizosaccharomyces pombe chromosome I contains seven permease genes. Yeast. 18(4). 355–361. 7 indexed citations
14.
Revuelta, José Luis, Francisco del Rey, Rhian Gwilliam, et al.. (2001). Analysis of 41 kb of the DNA sequence from the right arm of chromosome II of Schizosaccharomyces pombe. Yeast. 18(12). 1111–1116. 3 indexed citations
15.
Xiang, Zheng, Karen Moore, Valerie Wood, et al.. (2000). Analysis of 114 kb of DNA sequence from fission yeast chromosome 2 immediately centromere-distal tohis5. Yeast. 16(15). 1405–1411. 4 indexed citations
16.
Dunham, Andrew, Alison J. Coffey, S. M. Clegg, et al.. (1999). High-Resolution Landmark Framework for the Sequence-Ready Mapping of Xq23–q26.1. Genome Research. 9(8). 751–762. 1 indexed citations
17.
Bench, Anthony J., Micheala A. Aldred, Sean Humphray, et al.. (1998). A Detailed Physical and Transcriptional Map of the Region of Chromosome 20 That Is Deleted in Myeloproliferative Disorders and Refinement of the Common Deleted Region. Genomics. 49(3). 351–362. 38 indexed citations
18.
Mungall, Andrew J., Carol A. Edwards, Eric Holloway, et al.. (1996). Physical Mapping of Chromosome 6: A Strategy for the Rapid Generation of Sequence-Ready Contigs. DNA sequence. 7(1). 47–49. 7 indexed citations
19.
Dickson, Ian, et al.. (1994). Lumbar vertebral and femoral neck bone mineral density are higher in postmenopausal women with the α2HS-glycoprotein 2 phenotype. Bone and Mineral. 24(3). 181–188. 26 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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