Allan J. Richards

4.3k citations

81 papers · 2.9k indexed · h-index 30

Immunology and Allergy top 1%
- Cell Adhesion Molecules Research 24
Genetics top 0.5%
- Connective tissue disorders research 60
- Dermatological and Skeletal Disorders 17
Ophthalmology top 1%
- Intraocular Surgery and Lenses 8
Cell Biology top 2%
- Skin and Cellular Biology Research 9
Rheumatology top 2%
Radiology, Nuclear Medicine and Imaging
- Retinal and Macular Surgery 12
Cancer Research
- Protease and Inhibitor Mechanisms 7
Pediatrics, Perinatology and Child Health
- Child Abuse and Related Trauma 6

Co-authors: Martin P. Snead F M Pope Arabella Poulson John D. Scott Annie McNinch A C Nicholls P Narcisi John R.W. Yates
Cited by: Immunology and Allergy Genetics Ophthalmology
Journals: Nature Genetics (1 paper)Blood (2 papers)Ophthalmology (3 papers)
Partner nations: United Kingdom United States Netherlands

In The Last Decade

Allan J. Richards

78 papers receiving 2.8k citations

Peers

Countries citing papers authored by Allan J. Richards

Since Specialization

Citations

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

Fields of papers citing papers by Allan J. Richards

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Allan J. Richards. 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 Allan J. Richards. The network helps show where Allan J. Richards may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Allan J. Richards, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Allan J. Richards Line = papers co-authored together Allan J. Richards links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Peripapillary Hyperreflective Ovoid Mass-Like Structures in Stickler Syndrome Ophthalmology Retina ·Tasneem Khatib,Antoine Safi,Thomas Nixon,Stelios Georgoulas,Giovanni Montesano,Howard Martin,Allan J. Richards,Annie McNinch,Arabella Poulson,Philip Alexander,Martin P. Snead	2024	1
2	Retinal detachment in Type IX collagen recessive Stickler syndrome Eye ·Daniel Maghsoudi,Thomas Nixon,Howard Martin,Allan J. Richards,Annie McNinch,Philip Alexander,Arabella Poulson,Martin P. Snead	2024	0
3	Legg-Calve-Perthes’ disease: an opportunity to prevent blindness? Archives of Disease in Childhood ·Aijing Wang,Thomas Nixon,Howard Martin,Allan J. Richards,Annie McNinch,Philip Alexander,Rathin Pujari,Peter Bale,Nicholas Shenker,P.W.P. Bearcroft,Senjah Brown,Adrian Blackwell,Arabella Poulson,Martin P. Snead	2023	0
4	Bilateral giant retinal tears in Osteogenesis Imperfecta BMC Medical Genetics ·Paolo Scollo,Martin P. Snead,Allan J. Richards,Rebecca C. Pollitt,Catherine DeVile	2018	11
5	Bone morphogenetic protein 4 (BMP4) loss-of-function variant associated with autosomal dominant Stickler syndrome and renal dysplasia European Journal of Human Genetics ·Thomas Nixon,Allan J. Richards,Laura K. Towns,Gavin Fuller,Stephen Abbs,Philip Alexander,Annie McNinch,Richard Sandford,Martin P. Snead	2018	23
6	Posterior Vitreous Detachment and the Posterior Hyaloid Membrane Ophthalmology ·Gregory Fincham,Sean James,Carl Spickett,Michael Hollingshead,Christopher Thrasivoulou,Arabella Poulson,Annie McNinch,Allan J. Richards,David Snead,G. Astrid Limb,Martin P. Snead	2017	30
7	Splicing analysis of unclassified variants in COL2A1 and COL11A1 identifies deep intronic pathogenic mutations European Journal of Human Genetics ·Allan J. Richards,Annie McNinch,John C. Whittaker,Becky Treacy,Kim Oakhill,Arabella Poulson,Martin P. Snead	2011	29
8	Significant ocular findings are a feature of heritable bone dysplasias resulting from defects in type II collagen British Journal of Ophthalmology ·Sarah Meredith,Allan J. Richards,P.W.P. Bearcroft,A. V Pouson,Martin P. Snead	2007	22
9	Vitreous phenotype: A key diagnostic sign in Stickler syndrome types 1 and 2 complicated by double heterozygosity American Journal of Medical Genetics Part A ·Alan Ang,Tsiang Ung,Narman Puvanachandra,Louise C. Wilson,F M Howard,Michael Ryalls,Allan J. Richards,Sarah Meredith,Maureen Laidlaw,Arabella Poulson,John D. Scott,Martin P. Snead	2007	12
10	Missense and silent mutations in COL2A1 result in Stickler syndrome but via different molecular mechanisms Human Mutation ·Allan J. Richards,Maureen Laidlaw,Sarah Meredith,Pallavi Shankar,Arabella Poulson,John D. Scott,Martin P. Snead	2007	26
11	Type 1 Stickler syndrome: a histological and ultrastructural study of an untreated globe Eye ·Mary MacRae,Dipika V. Patel,Allan J. Richards,Martin P. Snead,John Tolmie,W. Robert Lee	2005	5
12	Prevalence of mitral valve prolapse in Stickler syndrome American Journal of Medical Genetics Part A ·Nadeem Ahmad,Allan J. Richards,Helen C. Murfett,Leonard M. Shapiro,John D. Scott,John R.W. Yates,Joanne Norton,Martin P. Snead	2002	28
13	Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule Journal of Medical Genetics ·Allan J. Richards,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	2002	28
14	COL2A1 exon 2 mutations: relevance to the Stickler and Wagner syndromes British Journal of Ophthalmology ·Allan J. Richards	2000	97
15	Variation in the Vitreous Phenotype of Stickler Syndrome Can Be Caused by Different Amino Acid Substitutions in the X Position of the Type II Collagen Gly-X-Y Triple Helix The American Journal of Human Genetics ·Allan J. Richards,David Baguley,John R.W. Yates,Carol Lane,Mary Nicol,Peter S. Harper,John D. Scott,Martin P. Snead	2000	84
16	A single base mutation in COL5A2 causes Ehlers-Danlos syndrome type II. Journal of Medical Genetics ·Allan J. Richards,Sophie G. Martin,A C Nicholls,J. B. Harrison,F M Pope,Nigel Burrows	1998	60
17	Clinicopathological Correlations of Compound Heterozygous COL7A1 Mutations in Recessive Dystrophic Epidermolysis Bullosa Journal of Investigative Dermatology ·M. G. S. Dunnill,John A. McGrath,Allan J. Richards,Angela M. Christiano,Jouni Uitto,F M Pope,Robin A.J. Eady	1996	41
18	A novel homozygous point mutation in the collagen VII gene (COL7A1) in two cousins with recessive dystrophic epidermolysis bullosa Human Molecular Genetics ·M. G. S. Dunnill,Allan J. Richards,G. Mllana,F. Mollica,Robin A.J. Eady,F M Pope	1994	28
19	Two new mutations affecting the donor splice site of COL3A1 IVS37 and causing skipping of exon 37 in patients with Ehlers—Danlos syndrome type IV Human Molecular Genetics ·Allan J. Richards,P Narcisi,Carole Ferguson,Jan M. Cobben,F M Pope	1994	7
20	A family with Ehlers — Danlos syndrome type III/articular hypermobility syndrome has a glycine 637 to serine substitution in type III collagen Human Molecular Genetics ·P Narcisi,Allan J. Richards,Stanley D. Ferguson,F M Pope	1994	66

About Allan J. Richards

Allan J. Richards is a scholar working on Immunology and Allergy, Genetics and Cell Biology, having authored 81 papers that have together received 2.9k indexed citations. Recurring topics across this work include Connective tissue disorders research (60 papers), Cell Adhesion Molecules Research (24 papers), Dermatological and Skeletal Disorders (17 papers), Retinal and Macular Surgery (12 papers), Skin and Cellular Biology Research (9 papers), Intraocular Surgery and Lenses (8 papers), Protease and Inhibitor Mechanisms (7 papers) and Child Abuse and Related Trauma (6 papers). The work is most often cited by research in Immunology and Allergy (552 citations), Genetics (1.9k citations) and Ophthalmology (394 citations). Allan J. Richards has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Martin P. Snead, F M Pope, Arabella Poulson, John D. Scott, Annie McNinch, A C Nicholls, P Narcisi, John R.W. Yates, Lionel Bercovitch and Zsolt Urbán. Their work appears in journals such as Nature Genetics, Blood and Ophthalmology.

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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