Annette Payne

4.3k citations
64 papers · 2.9k indexed · h-index 26
Topics
Retinal Development and Disorders (23 papers)Retinal Diseases and Treatments (10 papers)melanin and skin pigmentation (5 papers)

In The Last Decade

Annette Payne

62 papers receiving 2.8k citations

Peers

Annette Payne
Comparison fields: 5 of 157
  • Molecular Biology 1.8k
  • Ophthalmology 857
  • Cellular and Molecular Neuroscience 424
  • Cell Biology 384
  • Genetics 377
Replace Nicholas K. Foreman with:
Nicholas K. Foreman United States
Krisztina Valter Australia
Lea K. Davis United States
Joyce Y. Tung United States
Jonathan L. Haines United States
Takayuki Taniwaki Japan
Terry A. Braun United States
Ben A. Oostra Netherlands
Margaret A. Pericak‐Vance United States
Rivka Carmi Israel
Annette Payne relative to Nicholas K. Foreman United States Nicholas K. Foreman's profile →
Citations per field
00.5×5.7×
Nicholas K. Foreman · 1×
Citations per year

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
#WorkIndexed citations
1 1
2 8
3 58
4 3
5 10
6 54
7
An analysis of ABCR mutations in British patients with recessive retinal dystrophies.
55
8
A new locus for autosomal recessive retinitis pigmentosa mapping to chromosome 4q32-34.
1
9
A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13.
51
10 20
11
Mutations in the human rhodopsin gene and polymorphisms in peripherin/RDS gene in Lithuanian autosomal dominant retinitis pigmentosa patients
1
12 377
13 25
14 30
15 21
16 8
17 188
18 38
19 187
20
The prevalence and effect of peripherin/RDS mutations in autosomal dominant pattern dystrophy.
1

About Annette Payne

Annette Payne is a scholar working on Ophthalmology, Cell Biology and Molecular Biology, having authored 64 papers that have together received 2.9k indexed citations. Recurring topics across this work include Retinal Development and Disorders (23 papers), Retinal Diseases and Treatments (10 papers) and melanin and skin pigmentation (5 papers). The work is most often cited by research in Ophthalmology (857 citations), Molecular Biology (1.8k citations) and Cell Biology (384 citations). Annette Payne has collaborated with scholars based in United Kingdom, United States and Mexico. Frequent 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. Their work appears in journals such as Nature Genetics, Molecular Cell and Scientific Reports.

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026