Felicity Payne

19.8k total citations
29 papers, 1.2k citations indexed

About

Felicity Payne is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Felicity Payne has authored 29 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 13 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Felicity Payne's work include Diabetes and associated disorders (6 papers), Immune Cell Function and Interaction (5 papers) and Pancreatic function and diabetes (5 papers). Felicity Payne is often cited by papers focused on Diabetes and associated disorders (6 papers), Immune Cell Function and Interaction (5 papers) and Pancreatic function and diabetes (5 papers). Felicity Payne collaborates with scholars based in United Kingdom, United States and Sweden. Felicity Payne's co-authors include John A. Todd, Inês Barroso, Sarah Nutland, Helen Rance, Bryan J. Barratt, David Clayton, Olov Rolandsson, Paul W. Franks, Frida Renström and Göran Hallmans and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Felicity Payne

28 papers receiving 1.2k citations

Peers

Felicity Payne
Christopher J. Groves United Kingdom
María Eugenia Sáez Spain
Andrew G. Demaine United Kingdom
Nigel W. Rayner United Kingdom
Ratna Dua Puri India
Swarkar Sharma India
Mali Ketzinel‐Gilad Israel
Rachel M. Williams United Kingdom
Sherida E. Tollefsen United States
Regine Bergholdt Denmark
Christopher J. Groves United Kingdom
Felicity Payne
Citations per year, relative to Felicity Payne Felicity Payne (= 1×) peers Christopher J. Groves

Countries citing papers authored by Felicity Payne

Since Specialization
Citations

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

Fields of papers citing papers by Felicity Payne

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Felicity Payne

This figure shows the co-authorship network connecting the top 25 collaborators of Felicity Payne. A scholar is included among the top collaborators of Felicity Payne 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 Felicity Payne. Felicity Payne 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
1.
Welters, Alena, Nadine Bachmann, Carsten Bergmann, et al.. (2023). An expanded clinical spectrum of hypoinsulinaemic hypoketotic hypoglycaemia. Orphanet Journal of Rare Diseases. 18(1). 360–360.
2.
Edgar, Rachel D., Francesca Perrone, Felicity Payne, et al.. (2022). Culture-Associated DNA Methylation Changes Impact on Cellular Function of Human Intestinal Organoids. Cellular and Molecular Gastroenterology and Hepatology. 14(6). 1295–1310. 20 indexed citations
3.
Strisciuglio, Caterina, Felicity Payne, Komal Nayak, et al.. (2021). Disease-associated DNA methylation signatures in esophageal biopsies of children diagnosed with Eosinophilic Esophagitis. Clinical Epigenetics. 13(1). 81–81. 1 indexed citations
4.
Gasparetto, Marco, Felicity Payne, Komal Nayak, et al.. (2020). Transcription and DNA Methylation Patterns of Blood-Derived CD8+ T Cells Are Associated With Age and Inflammatory Bowel Disease But Do Not Predict Prognosis. Gastroenterology. 160(1). 232–244.e7. 35 indexed citations
5.
Rocha, Nuno, Felicity Payne, Isabel Huang‐Doran, et al.. (2017). The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion. Scientific Reports. 7(1). 17593–17593. 24 indexed citations
6.
Chen, Jianhua, Maria Segni, Felicity Payne, et al.. (2015). Truncation of POC1A associated with short stature and extreme insulin resistance. Journal of Molecular Endocrinology. 55(2). 147–158. 22 indexed citations
7.
Payne, Felicity, Rita Colnaghi, Nuno Rocha, et al.. (2014). Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance. Journal of Clinical Investigation. 124(9). 4028–4038. 72 indexed citations
8.
Payne, Felicity, Koini Lim, Amandine Girousse, et al.. (2014). Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease. Proceedings of the National Academy of Sciences. 111(24). 8901–8906. 114 indexed citations
9.
Hussain, Khalid, Benjamin Challis, Nuno Rocha, et al.. (2011). An Activating Mutation of AKT2 and Human Hypoglycemia. Science. 334(6055). 474–474. 114 indexed citations
10.
Fontaine‐Bisson, Bénédicte, Frida Renström, Olov Rolandsson, et al.. (2010). Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population. Diabetologia. 53(10). 2155–2162. 45 indexed citations
11.
Renström, Frida, Felicity Payne, Anna Nordström, et al.. (2009). Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden. Human Molecular Genetics. 18(8). 1489–1496. 184 indexed citations
12.
Franks, Paul W., Olov Rolandsson, S. L. Debenham, et al.. (2008). Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations. Diabetologia. 51(3). 523–523. 3 indexed citations
13.
Franks, Paul W., Olov Rolandsson, S. L. Debenham, et al.. (2007). Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations. Diabetologia. 51(3). 458–463. 90 indexed citations
14.
Cooper, Jason D., Deborah J. Smyth, Rebecca Bailey, et al.. (2007). The candidate genes TAF5L, TCF7, PDCD1 , IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes. BMC Medical Genetics. 8(1). 71–71. 45 indexed citations
15.
Morris, Gerard A. J., Christopher E. Lowe, Jason D. Cooper, et al.. (2006). Polymorphism discovery and association analyses of the interferon genes in type 1 diabetes. BMC Genetics. 7(1). 12–12. 6 indexed citations
16.
Smyth, Deborah J., Joanna M. M. Howson, Felicity Payne, et al.. (2006). Analysis of polymorphisms in 16 genes in type 1 diabetes that have been associated with other immune-mediated diseases. BMC Medical Genetics. 7(1). 20–20. 52 indexed citations
17.
Maier, Lisa M., Joanna M. M. Howson, Neil Walker, et al.. (2006). Association of IL13 with total IgE: Evidence against an inverse association of atopy and diabetes. Journal of Allergy and Clinical Immunology. 117(6). 1306–1313. 52 indexed citations
18.
Burren, Oliver S., Barry Healy, Alexander Lam, et al.. (2004). Development of an integrated genome informatics, data management and workflow infrastructure: A toolbox for the study of complex disease genetics. Human Genomics. 1(2). 98–98. 13 indexed citations
19.
Payne, Felicity & Lynda Jessopp. (2001). NHS Direct: review of activity data for the first year of operation at one site. Journal of Public Health. 23(2). 155–158. 21 indexed citations
20.
Payne, Felicity, et al.. (2001). Patient-perceived benefits of and barriers to using out-of-hours primary care centres. Family Practice. 18(2). 149–155. 18 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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