Annette Payne

4.3k total citations
64 papers, 2.9k citations indexed

About

Annette Payne is a scholar working on Molecular Biology, Ophthalmology and Cell Biology. According to data from OpenAlex, Annette Payne has authored 64 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 12 papers in Ophthalmology and 11 papers in Cell Biology. Recurrent topics in Annette Payne's work include Retinal Development and Disorders (23 papers), Retinal Diseases and Treatments (10 papers) and melanin and skin pigmentation (5 papers). Annette Payne is often cited by papers focused on Retinal Development and Disorders (23 papers), Retinal Diseases and Treatments (10 papers) and melanin and skin pigmentation (5 papers). Annette Payne collaborates with scholars based in United Kingdom, United States and Mexico. Annette Payne's co-authors include Shomi S. Bhattacharya, Alan C. Bird, Shagufta Khaliq, John R. Heckenlively, S. Qasim Mehdi, Xiaohui Liu, Bart P. Leroy, Wenbin Yue, Zidong Wang and David Bessant and has published in prestigious journals such as Nature Genetics, Molecular Cell and Scientific Reports.

In The Last Decade

Annette Payne

62 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Annette Payne United Kingdom 26 1.8k 857 424 384 377 64 2.9k
Terry A. Braun United States 29 2.6k 1.4× 816 1.0× 235 0.6× 371 1.0× 1.6k 4.1× 72 4.2k
Nicholas K. Foreman United States 46 2.9k 1.6× 150 0.2× 212 0.5× 338 0.9× 164 0.4× 242 6.5k
Jonathan L. Haines United States 35 1.6k 0.9× 282 0.3× 469 1.1× 270 0.7× 1.7k 4.5× 66 4.2k
J. Sjöstrand Sweden 36 814 0.4× 881 1.0× 788 1.9× 345 0.9× 135 0.4× 95 3.3k
Alex E. Krill United States 35 1.2k 0.7× 1.5k 1.7× 275 0.6× 192 0.5× 327 0.9× 107 3.2k
Sven Schippling Germany 39 737 0.4× 1.4k 1.6× 315 0.7× 72 0.2× 79 0.2× 117 5.8k
Rivka Carmi Israel 33 2.5k 1.4× 277 0.3× 225 0.5× 379 1.0× 1.9k 5.2× 110 5.2k
Michael J. Denton Australia 23 1.3k 0.7× 585 0.7× 324 0.8× 200 0.5× 203 0.5× 52 2.1k
Joyce Y. Tung United States 20 840 0.5× 174 0.2× 171 0.4× 200 0.5× 1.2k 3.2× 28 3.1k
Michael Kalloniatis Australia 39 2.5k 1.4× 2.7k 3.2× 2.0k 4.8× 202 0.5× 93 0.2× 253 5.6k

Countries citing papers authored by Annette Payne

Since Specialization
Citations

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

Fields of papers citing papers by Annette Payne

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annette Payne

This figure shows the co-authorship network connecting the top 25 collaborators of Annette Payne. A scholar is included among the top collaborators of Annette 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 Annette Payne. Annette 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.
Payne, Annette, et al.. (2025). The Association Between Metabolic Syndrome and the Risk of Endometrial Cancer in Pre- and Post-Menopausal Women: A UK Biobank Study. Journal of Clinical Medicine. 14(3). 751–751. 1 indexed citations
2.
Payne, Annette, Susan Jobling, David C. Hay, et al.. (2022). HIV- 1 lentivirus tethering to the genome is associated with transcription factor binding sites found in genes that favour virus survival. Gene Therapy. 29(12). 720–729. 8 indexed citations
3.
Davies, Julie, Jing Chen, Ryan Pink, et al.. (2015). Orexin receptors exert a neuroprotective effect in Alzheimer’s disease (AD) via heterodimerization with GPR103. Scientific Reports. 5(1). 12584–12584. 58 indexed citations
4.
Ghorbani, Mohammadmersad, Michael Themis, & Annette Payne. (2015). Genome wide classification and characterisation of CpG sites in cancer and normal cells. Computers in Biology and Medicine. 68. 57–66. 3 indexed citations
5.
Panteris, Eleftherios, Stephen Swift, Annette Payne, & Xiaohui Liu. (2007). Mining pathway signatures from microarray data and relevant biological knowledge. Journal of Biomedical Informatics. 40(6). 698–706. 10 indexed citations
6.
Gibbons, Nicola, et al.. (2004). Computer Simulations Improve University Instructional Laboratories. PubMed. 3(4). 263–269. 54 indexed citations
7.
Papaioannou, Myrto, Louise Ocaka, David Bessant, et al.. (2000). An analysis of ABCR mutations in British patients with recessive retinal dystrophies.. PubMed. 41(1). 16–9. 55 indexed citations
8.
Payne, Annette, et al.. (2000). A new locus for autosomal recessive retinitis pigmentosa mapping to chromosome 4q32-34.. UCL Discovery (University College London). 1 indexed citations
9.
Hameed, Abdul, Shagufta Khaliq, M. Ismail, et al.. (2000). A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13.. PubMed. 41(3). 629–33. 51 indexed citations
10.
Bessant, David, Annette Payne, Catherine Plant, et al.. (2000). NRL S50T mutation and the importance of ‘founder effects’ in inherited retinal dystrophies. European Journal of Human Genetics. 8(10). 783–787. 20 indexed citations
11.
Kučinskas, Vaidutis, et al.. (1999). Mutations in the human rhodopsin gene and polymorphisms in peripherin/RDS gene in Lithuanian autosomal dominant retinitis pigmentosa patients. Journal of Applied Genetics. 40(1). 53–61. 1 indexed citations
12.
Hollander, Anneke I. den, Jacoline B. ten Brink, Yvette J.M. de Kok, et al.. (1999). Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12). Nature Genetics. 23(2). 217–221. 377 indexed citations
13.
Bessant, David, Khalid Anwar, Shagufta Khaliq, et al.. (1999). Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32. British Journal of Ophthalmology. 83(8). 919–922. 25 indexed citations
14.
Bessant, David, Shagufta Khaliq, Abdul Hameed, et al.. (1999). Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Human Mutation. 13(1). 83–83. 30 indexed citations
15.
16.
Kučinskas, Vaidutis, et al.. (1999). Molecular Genetic Study of Autosomal Dominant Retinitis pigmentosa in Lithuanian Patients. Human Heredity. 49(2). 71–74. 8 indexed citations
17.
18.
Bessant, David, Shagufta Khaliq, Abdul Hameed, et al.. (1998). A Locus for Autosomal Recessive Congenital Microphthalmia Maps to Chromosome 14q32. The American Journal of Human Genetics. 62(5). 1113–1116. 38 indexed citations
19.
Kelsell, Rosemary E., Kevin Gregory-Evans, Annette Payne, et al.. (1998). Mutations in the Retinal Guanylate Cyclase (RETGC-1) Gene in Dominant Cone-Rod Dystrophy. Human Molecular Genetics. 7(7). 1179–1184. 187 indexed citations
20.
Payne, Annette, et al.. (1996). The prevalence and effect of peripherin/RDS mutations in autosomal dominant pattern dystrophy.. UCL Discovery (University College London). 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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