Suzanne Broadgate

668 total citations
25 papers, 423 citations indexed

About

Suzanne Broadgate is a scholar working on Molecular Biology, Ophthalmology and Cell Biology. According to data from OpenAlex, Suzanne Broadgate has authored 25 papers receiving a total of 423 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 13 papers in Ophthalmology and 4 papers in Cell Biology. Recurrent topics in Suzanne Broadgate's work include Retinal Development and Disorders (16 papers), Retinal Diseases and Treatments (12 papers) and Connexins and lens biology (3 papers). Suzanne Broadgate is often cited by papers focused on Retinal Development and Disorders (16 papers), Retinal Diseases and Treatments (12 papers) and Connexins and lens biology (3 papers). Suzanne Broadgate collaborates with scholars based in United Kingdom, Australia and Singapore. Suzanne Broadgate's co-authors include Stephanie Halford, Susan M. Downes, Jing Yu, Tomoko Iwata, Francesca Pellicano, Louise Ocaka, Richard Holt, Jonathan D. Cooper, M. Tartaglia and Rachel E. Thomson and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Ophthalmology.

In The Last Decade

Suzanne Broadgate

22 papers receiving 413 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Suzanne Broadgate United Kingdom 10 351 177 87 57 49 25 423
Shinichiro Takezawa Japan 7 452 1.3× 137 0.8× 94 1.1× 30 0.5× 131 2.7× 8 545
Pietro Farinelli Sweden 9 461 1.3× 171 1.0× 96 1.1× 68 1.2× 107 2.2× 13 508
Cristina Martínez-Fernández de la Cámara United Kingdom 16 500 1.4× 265 1.5× 106 1.2× 23 0.4× 97 2.0× 25 582
Esther Pomares Spain 14 413 1.2× 176 1.0× 89 1.0× 70 1.2× 61 1.2× 30 489
Stefan Kustermann Germany 5 339 1.0× 131 0.7× 21 0.2× 32 0.6× 118 2.4× 6 378
Rachayata Dharmat United States 6 270 0.8× 88 0.5× 66 0.8× 31 0.5× 65 1.3× 6 318
Julie E. Smith United States 9 524 1.5× 280 1.6× 65 0.7× 98 1.7× 161 3.3× 10 623
J D Lindsey United States 7 133 0.4× 292 1.6× 21 0.2× 84 1.5× 62 1.3× 7 500
Eric Weh United States 11 219 0.6× 266 1.5× 100 1.1× 33 0.6× 22 0.4× 22 486

Countries citing papers authored by Suzanne Broadgate

Since Specialization
Citations

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

Fields of papers citing papers by Suzanne Broadgate

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Suzanne Broadgate

This figure shows the co-authorship network connecting the top 25 collaborators of Suzanne Broadgate. A scholar is included among the top collaborators of Suzanne Broadgate 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 Suzanne Broadgate. Suzanne Broadgate 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.
Street, Duncan, et al.. (2025). Myoclonus-dystonia due to novel mutation in the guanine nucleotide-binding protein (GNB1) gene. Parkinsonism & Related Disorders. 107822–107822.
2.
Pearce, Elizabeth, Sobha Sivaprasad, Suzanne Broadgate, et al.. (2023). Intraretinal Microvascular Abnormalities and Venous Beading Have Different Genetic Profiles in Caucasian Patients with Non-Proliferative Diabetic Retinopathy. Vision. 7(1). 18–18. 1 indexed citations
3.
Shah, Mital, Suzanne Broadgate, Morag Shanks, et al.. (2022). Phenotypic and Genetic Characteristics in a Cohort of Patients with Usher Genes. Genes. 13(8). 1423–1423. 5 indexed citations
4.
Broadgate, Suzanne, et al.. (2021). Whole genome sequencing in a Knobloch syndrome family confirms the molecular diagnosis. Ophthalmic Genetics. 43(2). 201–209.
5.
Broadgate, Suzanne, et al.. (2021). An Overview of the Genetics of ABCA4 Retinopathies, an Evolving Story. Genes. 12(8). 1241–1241. 38 indexed citations
6.
Hudspith, K, Suzanne Broadgate, Morag Shanks, et al.. (2021). Targeted next generation sequencing and family survey enable correct genetic diagnosis in CRX associated macular dystrophy – a case report. BMC Ophthalmology. 21(1). 168–168. 3 indexed citations
7.
Shah, Mital, et al.. (2021). The role of multimodal imaging and vision function testing in ABCA4-related retinopathies and their relevance to future therapeutic interventions. SHILAP Revista de lepidopterología. 13. 3324609280–3324609280. 4 indexed citations
8.
Downes, Susan M., Vicky Tai, Suzanne Broadgate, et al.. (2020). Genetic and Clinical Findings in an Ethnically Diverse Cohort with Retinitis Pigmentosa Associated with Pathogenic Variants in CERKL. Genes. 11(12). 1497–1497. 6 indexed citations
9.
Broadgate, Suzanne, Stephanie Halford, Jasleen K. Jolly, et al.. (2020). Novel Pathogenic Sequence Variants in NR2E3 and Clinical Findings in Three Patients. Genes. 11(11). 1288–1288. 7 indexed citations
10.
Broadgate, Suzanne, Stephanie Halford, Robert E. MacLaren, et al.. (2020). “Genetic and clinical findings in an ethnically diverse retinitis pigmentosa cohort associated with pathogenic variants in EYS”. Eye. 35(5). 1440–1449. 7 indexed citations
11.
Broadgate, Suzanne, Christine A. Kiire, Stephanie Halford, & Victor Chong. (2018). Diabetic macular oedema: under‐represented in the genetic analysis of diabetic retinopathy. Acta Ophthalmologica. 96(A111). 1–51. 10 indexed citations
12.
Holt, Richard, Fabiola Ceroni, Dorine A. Bax, et al.. (2017). New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders. Scientific Reports. 7(1). 7975–7975. 11 indexed citations
13.
Broadgate, Suzanne, Jing Yu, Susan M. Downes, & Stephanie Halford. (2017). Unravelling the genetics of inherited retinal dystrophies: Past, present and future. Progress in Retinal and Eye Research. 59. 53–96. 89 indexed citations
14.
Singh, Mandeep S., Suzanne Broadgate, Ranjana Mathur, et al.. (2016). Hypotrichosis and juvenile macular dystrophy caused by CDH3 mutation: A candidate disease for retinal gene therapy. Scientific Reports. 6(1). 23674–23674. 10 indexed citations
15.
Holt, Richard, Sı̇bel Aylı̇n Uğur İşerı̇, Dorine A. Bax, et al.. (2016). Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders. Human Genetics. 136(1). 119–127. 9 indexed citations
16.
Kiire, Christine A., Suzanne Broadgate, Stephanie Halford, & Victor Chong. (2014). Diabetic macular edema with foveal eversion shows a distinct cytokine profile to other forms of diabetic macular edema in patients with type 2 diabetes. Investigative Ophthalmology & Visual Science. 55(13). 4408–4408. 5 indexed citations
17.
Halford, Stephanie, Gerald Liew, Donna S. Mackay, et al.. (2014). Detailed Phenotypic and Genotypic Characterization of Bietti Crystalline Dystrophy. Ophthalmology. 121(6). 1174–1184. 72 indexed citations
18.
Broadgate, Suzanne, Rachel E. Thomson, Francesca Pellicano, et al.. (2005). FGFR3 regulates brain size by controlling progenitor cell proliferation and apoptosis during embryonic development. Developmental Biology. 279(1). 73–85. 66 indexed citations
19.
Pellicano, Francesca, et al.. (2005). Expression of coiled-coil protein 1, a novel gene downstream of FGF2, in the developing brain. Gene Expression Patterns. 6(3). 285–293. 4 indexed citations
20.
Broadgate, Suzanne, Louise Ocaka, Michelle Gaasenbeek, et al.. (2005). Isolation and characterization of murine Cds (CDP-diacylglycerol synthase) 1 and 2. Gene. 356. 19–31. 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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