Alan F. Wright

72.0k citations

227 papers · 11.9k indexed · 2 hit papers · h-index 58

Ophthalmology top 0.1%
- Retinal Diseases and Treatments 37
Genetics top 0.2%
- Genetic Associations and Epidemiology 36
- Genetic and Kidney Cyst Diseases 17
- Genetic Mapping and Diversity in Plants and Animals 14
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 13
Molecular Biology top 0.5%
- Retinal Development and Disorders 68
- Retinoids in leukemia and cellular processes 17
- RNA regulation and disease 15
Nephrology top 1%
Radiology, Nuclear Medicine and Imaging top 0.5%

Co-authors: Igor Rudan Caroline Hayward Anthony J. Swerdlow Minouk J. Schoemaker Craig Higgins Patricia A. Jacobs Andrew D. Carothers Xinhua Shu
Cited by: Ophthalmology Genetics Molecular Biology
Journals: Investigative Ophthalmology & Visual Science (15 papers)Human Molecular Genetics (14 papers)Journal of Medical Genetics (8 papers)
Partner nations: United Kingdom United States Croatia

In The Last Decade

Alan F. Wright

224 papers receiving 11.6k citations

Hit Papers

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Peers

Countries citing papers authored by Alan F. Wright

Since Specialization

Citations

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

Fields of papers citing papers by Alan F. Wright

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alan F. Wright. 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 Alan F. Wright. The network helps show where Alan F. Wright may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Alan F. Wright, 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 Alan F. Wright Line = papers co-authored together Alan F. Wright links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	1979P phase I trial of pembrolizumab in HIV-associated Kaposi sarcoma (KS) Annals of Oncology ·Kathryn Lurain,Ramya Ramaswami,Irene Ekwede,Rebecca Geer,Gaurav Goyal,Manoj Menon,Thomas Odeny,Elad Sharon,Michael J. Wagner,Chi‐Chuan Wang,Nina Bhardwaj,Maher Abdul‐Hay,Judith C. Kaiser,Alan F. Wright,Robert Yarchoan,Steven P. Fling,Qiang Lü,Thomas S. Uldrick	2023	2
2	Assessment of the sensitivity of ²H MR spectroscopy measurements of [2,3‐²H₂]fumarate metabolism for detecting tumor cell death NMR in Biomedicine ·Friederike Hesse,Alan F. Wright,王雄彪,Felix Kreis,Kevin M. Brindle	2023	4
3	Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits PLoS Genetics ·Andrew D. Bretherick,Oriol Canela‐Xandri,Peter K. Joshi,David W. Clark,Konrad Rawlik,Thibaud Boutin,Yanni Zeng,Carmen Amador,Pau Navarro,Igor Rudan,Alan F. Wright,Harry Campbell,Véronique Vitart,Caroline Hayward,James F. Wilson,Albert Tenesa,Chris P. Ponting,J. Kenneth Baillie,Chris Haley	2020	21
4	Using Haplotype Mapping to Uncover the Missing Heritability: A Simulation Study Proceedings of the World Congress on Genetics Applied to Livestock Production ·Masoud Shirali,Ricardo Pong‐Wong,Sara Knott,Caroline Hayward,Véronique Vitart,Igor Rudan,Harry Campbell,Nick Hastie,Alan F. Wright,Pau Navarro,Chris Haley	2014	0
5	Effect of protein intake and weight gain velocity on body fat mass at 6 months of age: The EU Childhood Obesity Programme International Journal of Obesity ·(unknown),Joaquín Escribano,Verónica Luque,Natàlia Ferré,Enno Littmann,Berthold Koletzko,Veit Grote,Hans Demmelmair,Les Bluck,Alan F. Wright,Ricardo Closa‐Monasterolo	2012	91
6	Knockdown of the Zebrafish Ortholog of the Retinitis Pigmentosa 2 ( RP2 ) Gene Results in Retinal Degeneration Investigative Ophthalmology & Visual Science ·Xinhua Shu,Zhiqiang Zeng,Philippe Gautier,Alan Lennon,Milica Gakovic,Michael E. Cheetham,E. Elizabeth Patton,Alan F. Wright	2011	30
7	Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways: Figure 1 Journal of Medical Genetics ·Giorgia Girotto,Nicola Pirastu,Rossella Sorice,Ginevra Biino,Harry Campbell,Pio D’Adamo,N D Hastie,Teresa Nutile,Ozren Polašek,Laura Portas,Igor Rudan,Sheila Ulivi,Tatijana Zemunik,Alan F. Wright,Marina Ciullo,Caroline Hayward,Mario Pirastu,Paolo Gasparini	2011	59
8	The Predisposing Pathology and Clinical Characteristics in the Scottish Retinal Detachment Study Ophthalmology ·Danny Mitry,Jaswinder Singh,David Yorston,M. A. Rehman Siddiqui,Alan F. Wright,Brian W. Fleck,Harry Campbell,David G. Charteris	2011	100
9	The Epidemiology and Socioeconomic Associations of Retinal Detachment in Scotland: A Two-Year Prospective Population-Based Study Investigative Ophthalmology & Visual Science ·Danny Mitry,David G. Charteris,David Yorston,M. A. Rehman Siddiqui,Harry Campbell,Anna Grobelny,Brian W. Fleck,Alan F. Wright,Jaswinder Singh	2010	136
10	Photoreceptor degeneration: genetic and mechanistic dissection of a complex traitbreakdown → Nature Reviews Genetics ·Alan F. Wright,Christina Chakarova,Mai M. Abd El-Aziz,Shomi S. Bhattacharya	2010	488
11	Quantifying the increase in average human heterozygosity due to urbanisation European Journal of Human Genetics ·Igor Rudan,Andrew D. Carothers,Ozren Polašek,Caroline Hayward,Véronique Vitart,Zrinka Biloglav,Ivana Kolčić,Lina Zgaga,Davor Ivanković,Ariana Vorko-Jović,James F. Wilson,James L. Weber,Nick Hastie,Alan F. Wright,Harry Campbell	2008	18
12	Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traits Human Molecular Genetics ·Harry Campbell,Andrew D. Carothers,Igor Rudan,Caroline Hayward,Zrinka Biloglav,Lovorka Barać,Marijana Peričić,Branka Janičijević,Nina Smolej‐Narančić,Ozren Polašek,Ivana Kolčić,James L. Weber,Nicholas D. Hastie,Pavao Rudan,Alan F. Wright	2007	76
13	3000 years of solitude: extreme differentiation in the island isolates of Dalmatia, Croatia European Journal of Human Genetics ·Véronique Vitart,Zrinka Biloglav,Caroline Hayward,Branka Janičijević,Nina Smolej‐Narančić,Lovorka Barać,Marijana Peričić,Irena Martinović Klarić,Tatjana Škarić‐Jurić,Maja Barbalić,Ozren Polašek,Ivana Kolčić,Andrew D. Carothers,Pavao Rudan,Nick Hastie,Alan F. Wright,Harry Campbell,Igor Rudan	2006	51
14	RPGRIP1 mutations in juvenile retinitis pigmentosa: a linkage and mutation study. Investigative Ophthalmology & Visual Science ·I Vălkov,I. López,Maurizio Fossarello,David Mansfield,Alan F. Wright	2004	1
15	Searching for genetic influences on normal cognitive ageing Trends in Cognitive Sciences ·Ian J. Deary,Alan F. Wright,Sarah E. Harris,Lawrence J. Whalley,John M. Starr	2004	58
16	Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate Nature Genetics ·Neena B. Haider,Samuel G. Jacobson,Artur V. Cideciyan,Ruth E. Swiderski,Luan M. Streb,Charles Searby,Gretel Beck,Alexander Dong,David B. Hanna,Susan W. Gorman,David M. Duhl,Rivka Carmi,Jean Bennett,Richard G. Weleber,Gerald A. Fishman,Alan F. Wright,Edwin M. Stone,Val C. Sheffield	2000	374
17	A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3) Nature Genetics ·A Meindl,Katherine L. Dry,Karin A. Herrmann,Forbes Manson,Alfredo Ciccodicola,Yu.F. Berdnychenko,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	1996	391
18	Identification of a novel gene, ETX1, from Xp21.1, a candidate gene for X-linked retinitis pigmentosa (RP3) Human Molecular Genetics ·Katherine L. Dry,Micheala A. Aldred,Yu.F. Berdnychenko,P.P. Balakrishnan,Forbes Manson,Graduate Record Examinations Board,Jane Prosser,Madson Jonhnston Souza Silva,Alan Lennon,Kate Thomson,Leon Rakoš,David M. Kurnit,Alan C. Bird,Marcelle Jay,Anthony P. Monaco,Alan F. Wright	1995	23
19	Adult polycystic kidney disease. BMJ ·Michael L. Watson,A M Macnicol,Alan F. Wright	1990	18
20	Adaptive evolution of G-protein coupled receptor genes. Molecular Biology and Evolution ·Shigeyuki Yokoyama,K E Isenberg,Alan F. Wright	1989	14

About Alan F. Wright

Alan F. Wright is a scholar working on Ophthalmology, Genetics and Nephrology, having authored 227 papers that have together received 11.9k indexed citations. Recurring topics across this work include Retinal Development and Disorders (68 papers), Retinal Diseases and Treatments (37 papers), Genetic Associations and Epidemiology (36 papers), Retinoids in leukemia and cellular processes (17 papers), Genetic and Kidney Cyst Diseases (17 papers), RNA regulation and disease (15 papers), Genetic Mapping and Diversity in Plants and Animals (14 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers). The work is most often cited by research in Ophthalmology (3.0k citations), Genetics (3.6k citations) and Molecular Biology (6.9k citations). Alan F. Wright has collaborated with scholars based in United Kingdom, United States and Croatia. Frequent co-authors include Igor Rudan, Caroline Hayward, Anthony J. Swerdlow, Minouk J. Schoemaker, Craig Higgins, Patricia A. Jacobs, Andrew D. Carothers, Xinhua Shu, Harry Campbell and Alan C. Bird. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Human Molecular Genetics, Journal of Medical Genetics, Human Genetics and European Journal of Human Genetics.

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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