Forbes Manson

4.1k citations

61 papers · 2.6k indexed · h-index 26

Molecular Biology top 5%
Ophthalmology top 0.5%
Genetics top 2%
Cell Biology top 5%
Radiology, Nuclear Medicine and Imaging top 5%

Co-authors: Graeme C. Black Alan F. Wright Jill Urquhart Stephen K. Chapman Gillian Reid Thomas Meitinger Alan Lennon Peter de Nully Brown
Topics: Retinal Development and Disorders (25 papers)Photosynthetic Processes and Mechanisms (8 papers)Retinal Diseases and Treatments (7 papers)
Cited by: Ophthalmology Molecular Biology Genetics
Journals: Proceedings of the National Academy of Sciences Nature Genetics Biochemistry
Partner nations: United Kingdom United States Germany

In The Last Decade

Forbes Manson

59 papers receiving 2.6k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Tadalafil Rescues the p.M325T Mutant of Best1 Chloride Channel 2023 ·Molecules ·(unknown),Jim Warwicker,Sally Freeman,Forbes Manson	0
2	Restoration of mutant bestrophin-1 expression, localisation and function in a polarised epithelial cell model 2016 ·Disease Models & Mechanisms ·Carolina Uggenti,(unknown),(unknown),Steven J. Thomson,(unknown),Richard A. Baines,Eileithyia Swanton,Forbes Manson	18
3	MiR-204 is responsible for inherited retinal dystrophy associated with ocular coloboma 2015 ·Proceedings of the National Academy of Sciences ·Iván Conte,Kristen D. Hadfield,Sara Barbato,Sabrina Carrella,Mariateresa Pizzo,(unknown),Annamaria Carissimo,Marianthi Karali,Louise F. Porter,Jill Urquhart,(unknown),James O’Sullivan,Forbes Manson,Stephan C. F. Neuhauss,Sandro Banfi,Graeme C. Black	84
4	Bruch’s membrane abnormalities in PRDM5-related brittle cornea syndrome 2015 ·Orphanet Journal of Rare Diseases ·Louise F. Porter,Roberto Gallego‐Pinazo,(unknown),(unknown),Nicoletta Zoppi,Marina Colombi,Cecilia Giunta,R E Bonshek,Forbes Manson,Graeme C. Black	20
5	A role for repressive complexes and H3K9 di-methylation in PRDM5-associated brittle cornea syndrome 2015 ·Human Molecular Genetics ·Louise F. Porter,Giorgio Giacomo Galli,(unknown),J. Selley,David Knight,Nursel Elçioğlu,(unknown),(unknown),Hanka Venselaar,Anders H. Lund,R E Bonshek,Graeme C. Black,Forbes Manson	16
6	Disease-causing mutations associated with four bestrophinopathies exhibit disparate effects on the localization, but not the oligomerization, of Bestrophin-1 2014 ·Experimental Eye Research ·Adiv A. Johnson,(unknown),(unknown),Paolo Tammaro,Forbes Manson,Lihua Y. Marmorstein,Alan D. Marmorstein	34
7	ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components 2013 ·Molecular Genetics and Metabolism ·Marianne Rohrbach,Helen Spencer,Louise F. Porter,Emma Burkitt‐Wright,Céline Bürer,Andreas Janecke,Madhura Bakshi,David Sillence,Hailah Al‐Hussain,Matthias R. Baumgartner,Beat Steinmann,Graeme C. Black,Forbes Manson,Cecilia Giunta	58
8	Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies) 2012 ·European Journal of Human Genetics ·Simon Ramsden,Alice E. Davidson,Bart P. Leroy,Anthony T. Moore,Andrew R. Webster,Graeme C. Black,Forbes Manson	2
9	Focus on Molecules: Lens intrinsic membrane protein (LIM2/MP20) 2011 ·Experimental Eye Research ·Geoffrey J. Maher,Graeme C. Black,Forbes Manson	8
10	The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1 2009 ·The American Journal of Human Genetics ·Dan Hanson,Philip Murray,Amit Sud,Samia A. Temtamy,Mona Aglan,Andrea Superti‐Furga,Sue Holder,Jill Urquhart,Emma Hilton,Forbes Manson,Peter Scambler,Graeme C. Black,Peter Clayton	81
11	Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome 2008 ·Human Mutation ·May Tassabehji,Zhi Fang,Emma Hilton,Julie McGaughran,Zhongming Zhao,Charles E. de Bock,Emma Howard,(unknown),Dian Donnai,Ashish D. Diwan,Forbes Manson,(unknown),Raymond A. Clarke	148
12	Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination 2007 ·Human Molecular Genetics ·Emma Hilton,Forbes Manson,Jill Urquhart,Jennifer J. Johnston,Anne Slavotinek,Peter Hedera,Eva‐Lena Stattin,Ann Nordgren,Leslie G. Biesecker,Graeme C. Black	40
13	Evidence of Genetic Heterogeneity in MRCS (Microcornea, Rod-Cone Dystrophy, Cataract, and Posterior Staphyloma) Syndrome 2006 ·American Journal of Ophthalmology ·Michel Michaelides,Jill Urquhart,Graham E. Holder,Marie Restori,(unknown),Forbes Manson,Graeme C. Black	18
14	Inherited eye disease: cause and late effect 2005 ·Trends in Molecular Medicine ·Forbes Manson,Dorothy Trump,Andrew Read,Graeme C. Black	1
15	Mutations of VMD2 Splicing Regulators Cause Nanophthalmos and Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) 2004 ·Investigative Ophthalmology & Visual Science ·(unknown),Bart P. Leroy,Niki Hart‐Holden,B. A. Lafaut,Bart Loeys,Ludwine Messiaen,Rahat Perveen,M. Ashwin Reddy,Shomi S. Bhattacharya,Elias I. Traboulsi,Diana Baralle,Jean‐Jacques De Laey,Bernard Puech,Philippe Kestelyn,Anthony T. Moore,Forbes Manson,Graeme C. Black	163
16	Delineation of Cohen Syndrome Following a Large-Scale Genotype-Phenotype Screen 2004 ·The American Journal of Human Genetics ·Juha Kolehmainen,Robert N. Wilkinson,Anna-Elina Lehesjoki,Kate Chandler,Satu Kivitie‐Kallio,Jill Clayton‐Smith,(unknown),(unknown),Anne Saarinen,Jabbar Khan,Varda Gross‐Tsur,Elias I. Traboulsi,Mette Warburg,Jean‐Pierre Fryns,Reijo Norio,Graeme C. Black,Forbes Manson	69
17	Colocalization of RPGR, RPGRIP, and Microtubules in Different Cytoskeletal Systems in the Outer Segments of Rods and Cones 2002 ·Investigative Ophthalmology & Visual Science ·(unknown),A. F. Wright,Forbes Manson	1
18	A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3) 1996 ·Nature Genetics ·A Meindl,Katherine L. Dry,Karin A. Herrmann,Forbes Manson,Alfredo Ciccodicola,(unknown),Maria Raquel Santos Carvalho,Helene Achatz,Heide Hellebrand,Alan Lennon,Carmela Migliaccio,Keith Porter,Eberhart Zrenner,Alan C. Bird,Marcelle Jay,Birgit Lorenz,B Wittwer,Michele D’Urso,Thomas Meitinger,Alan F. Wright	391
19	On the lack of coordination between protein folding and flavin insertion in Escherichia coli for flavocytochrome b₂ mutant forms Y254L and D282N 1995 ·Protein Science ·Muriel Gondry,Kim Le,Florence Lederer,Forbes Manson,(unknown),(unknown),F. Scott Mathews	11
20	Identification of a novel gene, ETX1, from Xp21.1, a candidate gene for X-linked retinitis pigmentosa (RP3) 1995 ·Human Molecular Genetics ·Katherine L. Dry,Micheala A. Aldred,(unknown),(unknown),Forbes Manson,(unknown),Jane Prosser,(unknown),Alan Lennon,Kate Thomson,(unknown),David M. Kurnit,Alan C. Bird,Marcelle Jay,Anthony P. Monaco,Alan F. Wright	23

About Forbes Manson

Forbes Manson is a scholar working on Ophthalmology, Cell Biology and Molecular Biology, having authored 61 papers that have together received 2.6k indexed citations. Recurring topics across this work include Retinal Development and Disorders (25 papers), Photosynthetic Processes and Mechanisms (8 papers) and Retinal Diseases and Treatments (7 papers). The work is most often cited by research in Ophthalmology (776 citations), Molecular Biology (2.0k citations) and Genetics (746 citations). Forbes Manson has collaborated with scholars based in United Kingdom, United States and Germany. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Biochemistry.

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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