Rebecca Darlay

2.8k total citations
19 papers, 305 citations indexed

About

Rebecca Darlay is a scholar working on Genetics, Epidemiology and Surgery. According to data from OpenAlex, Rebecca Darlay has authored 19 papers receiving a total of 305 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Epidemiology and 3 papers in Surgery. Recurrent topics in Rebecca Darlay's work include Liver Disease Diagnosis and Treatment (4 papers), Genetic Associations and Epidemiology (3 papers) and Pediatric Urology and Nephrology Studies (3 papers). Rebecca Darlay is often cited by papers focused on Liver Disease Diagnosis and Treatment (4 papers), Genetic Associations and Epidemiology (3 papers) and Pediatric Urology and Nephrology Studies (3 papers). Rebecca Darlay collaborates with scholars based in United Kingdom, Switzerland and Norway. Rebecca Darlay's co-authors include Heather J. Cordell, David Langton, Benedicte A. Lie, John Burn, Stephen C Bourke, Carlos Echevarria, Colin Shepherd, Michael D. Rushton, Louise N. Reynard and Timothy H.J. Goodship and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Rebecca Darlay

18 papers receiving 301 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rebecca Darlay United Kingdom 9 117 68 57 52 51 19 305
Eunhee Han South Korea 11 119 1.0× 26 0.4× 39 0.7× 33 0.6× 70 1.4× 44 387
Franco Gorlero Italy 10 143 1.2× 13 0.2× 20 0.4× 20 0.4× 11 0.2× 24 383
Ashley R. Jackson United States 10 98 0.8× 10 0.1× 30 0.5× 70 1.3× 9 0.2× 33 321
Ángeles Flórez Spain 12 47 0.4× 36 0.5× 43 0.8× 8 0.2× 42 0.8× 85 398
Xiumin Huang China 9 107 0.9× 31 0.5× 29 0.5× 11 0.2× 42 0.8× 19 301
C. B. Andersen Denmark 9 43 0.4× 26 0.4× 119 2.1× 11 0.2× 112 2.2× 16 340
Myda Khalid United States 7 105 0.9× 23 0.3× 39 0.7× 26 0.5× 22 0.4× 13 197
Allan Haynes United States 8 52 0.4× 9 0.1× 28 0.5× 17 0.3× 9 0.2× 14 350
Kyu Rae Kim South Korea 9 62 0.5× 11 0.2× 109 1.9× 26 0.5× 30 0.6× 14 330
Sumir Kumar India 9 53 0.5× 19 0.3× 21 0.4× 6 0.1× 43 0.8× 43 361

Countries citing papers authored by Rebecca Darlay

Since Specialization
Citations

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

Fields of papers citing papers by Rebecca Darlay

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rebecca Darlay

This figure shows the co-authorship network connecting the top 25 collaborators of Rebecca Darlay. A scholar is included among the top collaborators of Rebecca Darlay 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 Rebecca Darlay. Rebecca Darlay 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.
Saluja, Sushant, Rebecca Darlay, Rachel Lennon, Bernard Keavney, & Heather J. Cordell. (2024). Whole -genome survival analysis of 144 286 people from the UK Biobank identifies novel loci associated with blood pressure. Journal of Hypertension. 42(9). 1647–1652.
2.
Vandersteen, Anthony M., Ruwan Weerakkody, David Parry, et al.. (2023). Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome. Journal of Medical Genetics. 61(3). 232–238. 7 indexed citations
3.
Langton, David, TJ Joyce, Stephen P. Rushton, et al.. (2022). The influence of HLA genotype on the development of metal hypersensitivity following joint replacement. SHILAP Revista de lepidopterología. 2(1). 73–73. 14 indexed citations
4.
Darlay, Rebecca, Ruchi Shukla, Misti McCain, et al.. (2021). A PDCD1 Role in the Genetic Predisposition to NAFLD-HCC?. Cancers. 13(6). 1412–1412. 27 indexed citations
5.
Langton, David, Stephen C Bourke, Benedicte A. Lie, et al.. (2021). The influence of HLA genotype on the severity of COVID‐19 infection. HLA. 98(1). 14–22. 89 indexed citations
6.
7.
Darlay, Rebecca, Kristin L. Ayers, George Mells, et al.. (2018). Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitis. PLoS Genetics. 14(12). e1007833–e1007833. 7 indexed citations
8.
Darlow, John M., Rebecca Darlay, Mark G. Dobson, et al.. (2017). Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux. Scientific Reports. 7(1). 14595–14595. 11 indexed citations
9.
Howey, Richard, et al.. (2016). Examination of previously identified associations within the Genetic Analysis Workshop 19 data. BMC Proceedings. 10(S7). 97–101. 1 indexed citations
10.
Liu, Wanqing, Quentin M. Anstee, Xiaoliang Wang, et al.. (2016). Transcriptional regulation of PNPLA3 and its impact on susceptibility to nonalcoholic fatty liver Disease (NAFLD) in humans. Aging. 9(1). 26–40. 13 indexed citations
11.
Rushton, Michael D., Louise N. Reynard, Colin Shepherd, et al.. (2015). Methylation of cartilage DNA is a mediator of genetic risk at several OA susceptibility loci. Osteoarthritis and Cartilage. 23. A71–A72. 1 indexed citations
12.
Mitchell, Anna L., Anette S. B. Wolff, Jolanta U. Weaver, et al.. (2015). Linkage Analysis in Autoimmune Addison’s Disease: NFATC1 as a Potential Novel Susceptibility Locus. PLoS ONE. 10(6). e0123550–e0123550. 8 indexed citations
13.
Rushton, Michael D., Louise N. Reynard, David A. Young, et al.. (2015). Methylation quantitative trait locus analysis of osteoarthritis links epigenetics with genetic risk. Human Molecular Genetics. 24(25). 7432–7444. 46 indexed citations
14.
Darlay, Rebecca, M.J. Stear, Sam Mason, J. E. Smith, & Marie‐Anne Shaw. (2014). The heritability of abortion in pedigree Charollais flocks. Animal Reproduction Science. 149(3-4). 297–304. 1 indexed citations
15.
Wilson, Valerie, Rebecca Darlay, William Wong, et al.. (2013). Genotype/Phenotype Correlations in Complement Factor H Deficiency Arising From Uniparental Isodisomy. American Journal of Kidney Diseases. 62(5). 978–983. 8 indexed citations
16.
Darlow, John M., Mark G. Dobson, Rebecca Darlay, et al.. (2013). A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development. Molecular Genetics & Genomic Medicine. 2(1). 7–29. 17 indexed citations
17.
Anstee, Quentin M., Vlad Ratziu, Heather J. Cordell, et al.. (2013). 72 MAPPING EXPRESSION QUANTITATIVE TRAITS LOCI (eQTL) FOR PNPLA3 GENE IDENTIFIES ADDITIONAL SNPS ASSOCIATED WITH NON-ALCOHOLIC FATTY LIVER DISEASE (NAFLD) INDEPENDENT OF rs738409. Journal of Hepatology. 58. S32–S33. 1 indexed citations
18.
Darlay, Rebecca, et al.. (2011). Novel polymorphisms in ovine immune response genes and their association with abortion. Animal Genetics. 42(5). 535–543. 11 indexed citations
19.
Cordell, Heather J., Rebecca Darlay, Pimphen Charoen, et al.. (2009). Whole-Genome Linkage and Association Scan in Primary, Nonsyndromic Vesicoureteric Reflux. Journal of the American Society of Nephrology. 21(1). 113–123. 42 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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