Forbes Manson

4.1k total citations
61 papers, 2.6k citations indexed

About

Forbes Manson is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Forbes Manson has authored 61 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 16 papers in Genetics and 14 papers in Ophthalmology. Recurrent topics in Forbes Manson's work include Retinal Development and Disorders (25 papers), Photosynthetic Processes and Mechanisms (8 papers) and Retinal Diseases and Treatments (7 papers). Forbes Manson is often cited by papers focused on Retinal Development and Disorders (25 papers), Photosynthetic Processes and Mechanisms (8 papers) and Retinal Diseases and Treatments (7 papers). Forbes Manson collaborates with scholars based in United Kingdom, United States and Germany. Forbes Manson's co-authors include Graeme C. Black, Alan F. Wright, Jill Urquhart, Stephen K. Chapman, Gillian Reid, Thomas Meitinger, Alan Lennon, Peter de Nully Brown, I. D. Millar and Bart P. Leroy and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Biochemistry.

In The Last Decade

Forbes Manson

59 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Forbes Manson United Kingdom 26 2.0k 776 746 430 332 61 2.6k
Gennadiy Moiseyev United States 27 2.2k 1.1× 1.1k 1.5× 187 0.3× 294 0.7× 261 0.8× 55 2.5k
Motokazu Tsujikawa Japan 35 1.3k 0.6× 1.8k 2.3× 395 0.5× 310 0.7× 1.8k 5.4× 102 3.6k
Stephanie A. Hagstrom United States 24 1.3k 0.7× 1.6k 2.1× 207 0.3× 313 0.7× 1.1k 3.2× 73 2.8k
Charlotte Andrieu‐Soler France 25 1.7k 0.8× 233 0.3× 230 0.3× 651 1.5× 190 0.6× 43 2.4k
Sikha Ghosh United States 21 1.1k 0.5× 288 0.4× 155 0.2× 492 1.1× 171 0.5× 38 1.8k
Chio Oka Japan 20 1.1k 0.5× 337 0.4× 181 0.2× 150 0.3× 227 0.7× 45 2.0k
Hisashi Takeda Japan 20 825 0.4× 563 0.7× 209 0.3× 311 0.7× 362 1.1× 42 1.6k
Xianjun Zhu China 22 1.2k 0.6× 398 0.5× 175 0.2× 211 0.5× 115 0.3× 106 1.7k
Bruce A. Pfeffer United States 22 1.2k 0.6× 666 0.9× 93 0.1× 238 0.6× 266 0.8× 33 1.6k
Seongjin Seo United States 24 2.2k 1.1× 62 0.1× 1.7k 2.2× 467 1.1× 219 0.7× 47 3.0k

Countries citing papers authored by Forbes Manson

Since Specialization
Citations

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

Fields of papers citing papers by Forbes Manson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Forbes Manson

This figure shows the co-authorship network connecting the top 25 collaborators of Forbes Manson. A scholar is included among the top collaborators of Forbes Manson 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 Forbes Manson. Forbes Manson 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.
Warwicker, Jim, et al.. (2023). Tadalafil Rescues the p.M325T Mutant of Best1 Chloride Channel. Molecules. 28(8). 3317–3317.
2.
Uggenti, Carolina, et al.. (2016). Restoration of mutant bestrophin-1 expression, localisation and function in a polarised epithelial cell model. Disease Models & Mechanisms. 9(11). 1317–1328. 18 indexed citations
3.
Conte, Iván, Kristen D. Hadfield, Sara Barbato, et al.. (2015). MiR-204 is responsible for inherited retinal dystrophy associated with ocular coloboma. Proceedings of the National Academy of Sciences. 112(25). E3236–45. 84 indexed citations
4.
Porter, Louise F., Roberto Gallego‐Pinazo, Nicoletta Zoppi, et al.. (2015). Bruch’s membrane abnormalities in PRDM5-related brittle cornea syndrome. Orphanet Journal of Rare Diseases. 10(1). 145–145. 20 indexed citations
5.
Porter, Louise F., Giorgio Giacomo Galli, J. Selley, et al.. (2015). A role for repressive complexes and H3K9 di-methylation in PRDM5-associated brittle cornea syndrome. Human Molecular Genetics. 24(23). 6565–6579. 16 indexed citations
6.
7.
Rohrbach, Marianne, Helen Spencer, Louise F. Porter, et al.. (2013). ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components. Molecular Genetics and Metabolism. 109(3). 289–295. 58 indexed citations
8.
Ramsden, Simon, Alice E. Davidson, Bart P. Leroy, et al.. (2012). Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies). European Journal of Human Genetics. 20(5). 4–4. 2 indexed citations
9.
Maher, Geoffrey J., Graeme C. Black, & Forbes Manson. (2011). Focus on Molecules: Lens intrinsic membrane protein (LIM2/MP20). Experimental Eye Research. 103. 115–116. 8 indexed citations
10.
Hanson, Dan, Philip Murray, Amit Sud, et al.. (2009). The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1. The American Journal of Human Genetics. 84(6). 801–806. 81 indexed citations
11.
Tassabehji, May, Zhi Fang, Emma Hilton, et al.. (2008). Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome. Human Mutation. 29(8). 1017–1027. 148 indexed citations
12.
Hilton, Emma, Forbes Manson, Jill Urquhart, et al.. (2007). Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination. Human Molecular Genetics. 16(14). 1773–1782. 40 indexed citations
13.
Michaelides, Michel, Jill Urquhart, Graham E. Holder, et al.. (2006). Evidence of Genetic Heterogeneity in MRCS (Microcornea, Rod-Cone Dystrophy, Cataract, and Posterior Staphyloma) Syndrome. American Journal of Ophthalmology. 141(2). 418–420. 18 indexed citations
14.
Manson, Forbes, Dorothy Trump, Andrew Read, & Graeme C. Black. (2005). Inherited eye disease: cause and late effect. Trends in Molecular Medicine. 11(10). 449–455. 1 indexed citations
15.
Leroy, Bart P., Niki Hart‐Holden, B. A. Lafaut, et al.. (2004). Mutations of VMD2 Splicing Regulators Cause Nanophthalmos and Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC). Investigative Ophthalmology & Visual Science. 45(10). 3683–3683. 163 indexed citations
16.
Kolehmainen, Juha, Robert N. Wilkinson, Anna-Elina Lehesjoki, et al.. (2004). Delineation of Cohen Syndrome Following a Large-Scale Genotype-Phenotype Screen. The American Journal of Human Genetics. 75(1). 122–127. 69 indexed citations
17.
Wright, A. F., et al.. (2002). Colocalization of RPGR, RPGRIP, and Microtubules in Different Cytoskeletal Systems in the Outer Segments of Rods and Cones. Investigative Ophthalmology & Visual Science. 43(13). 3739–3739. 1 indexed citations
18.
Meindl, A, Katherine L. Dry, Karin A. Herrmann, et al.. (1996). A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3). Nature Genetics. 13(1). 35–42. 391 indexed citations
19.
20.
Dry, Katherine L., Micheala A. Aldred, Forbes Manson, et al.. (1995). Identification of a novel gene, ETX1, from Xp21.1, a candidate gene for X-linked retinitis pigmentosa (RP3). Human Molecular Genetics. 4(12). 2347–2353. 23 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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