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Genetics

D-Index
67
Citations
16772
World Ranking
2527
National Ranking
95

Overview

Arthur A.B. Bergen is affiliated with the University of Amsterdam in the Netherlands. Their research spans multiple fields within the biological and medical sciences, with a significant focus on ocular conditions and molecular biology.

The scientist has published extensively in the areas of biochemistry, genetics, and molecular biology, contributing to 84 publications. Medicine is another major field of study, involving 50 of their works. Within these domains, their subfields of expertise include molecular biology, ophthalmology, cellular and molecular neuroscience, genetics, and radiology, nuclear medicine, and imaging.

Bergen's research principally addresses topics related to retinal health and disease. The main topics of their work are:

  • Retinal Development and Disorders
  • Retinal Diseases and Treatments
  • Photoreceptor and optogenetics research
  • Circadian rhythm and melatonin
  • Glaucoma and retinal disorders
  • Mitochondrial Function and Pathology
  • Retinal Imaging and Analysis

They have published papers in several peer-reviewed journals, with frequent contributions to:

  • International Journal of Molecular Sciences
  • Acta Ophthalmologica
  • Progress in Retinal and Eye Research
  • Ophthalmology Retina
  • Genes

Some of their recent papers include:

  • "Retinitis Pigmentosa: Current Clinical Management and Emerging Therapies," 2023, International Journal of Molecular Sciences
  • "X-Linked Retinoschisis," 2021, Ophthalmology
  • "The retinal pigmentation pathway in human albinism: Not so black and white," 2022, Progress in Retinal and Eye Research
  • "Exploring the choroidal vascular labyrinth and its molecular and structural roles in health and disease," 2021, Progress in Retinal and Eye Research
  • "CRB1-Associated Retinal Dystrophies: A Prospective Natural History Study in Anticipation of Future Clinical Trials," 2021, American Journal of Ophthalmology

Throughout their career, Arthur A.B. Bergen has frequently collaborated with other researchers, including:

  • Jacoline B. ten Brink
  • Camiel J. F. Boon
  • Mary J. van Schooneveld
  • Maria M. van Genderen
  • Carel B. Hoyng

Best Publications

  • Identification of the gene responsible for Best macular dystrophy

    K. Petrukhin;M. J. Koisti;B. Bakall;Wen Li

  • Mutations in ABCC6 cause pseudoxanthoma elasticum.

    A.A. Bergen;A.S. Plomp;E.J. Schuurman;S. Terry

  • The dynamic nature of Bruch's membrane

    J.C. Booij;D.C. Baas;J. Beisekeeva;T.G.M.F. Gorgels

  • Autosomal Recessive Retinitis Pigmentosa and Cone-rod Dystrophy Caused by Splice Site Mutations in the Stargardt's Disease Gene ABCR

    F.P.M. Cremers;T.J.R. van de Pol;M.A. van Driel;A.I. den Hollander

  • Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12).

    A.I. den Hollander;J.B. ten Brink;Y.J.M. de Kok;S. van Soest

  • Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

    Virginie J M Verhoeven;Pirro G Hysi;Robert Wojciechowski;Robert Wojciechowski;Qiao Fan

  • Prevalence of Age-Related Macular Degeneration in Europe: The Past and the Future

    Johanna M. Colijn;Gabriëlle H.S. Buitendijk;Elena Prokofyeva;Dalila Alves

  • Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration.

    Dominiek D. G. Despriet;Caroline C. W. Klaver;Jacqueline C. M. Witteman;Arthur A. B. Bergen

  • Positional cloning of the gene for X-linked retinitis pigmentosa 2

    U. Schwahn;S. Lenzner;J Dong;S. Feil

  • Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

    N.Torben Bech-Hansen;Margaret J. Naylor;Tracy A. Maybaum;Rebecca L. Sparkes

  • Retinitis pigmentosa: defined from a molecular point of view.

    S. van Soest;A. Westerveld;P.T.V.M. de Jong;E.M. Bleeker-Wagemakers

  • Isolation of a candidate gene for Norrie disease by positional cloning.

    Berger W;Meindl A;van de Pol Tj;Cremers Fp

  • Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS)

    J.T. Dendunnen;T. Kraayenbrink;T. Kraayenbrink;M. van Schooneveld;M. van Schooneveld;E. van de Vosse

  • ABCC6–Mediated ATP Secretion by the Liver Is the Main Source of the Mineralization Inhibitor Inorganic Pyrophosphate in the Systemic Circulation—Brief Report

    Robert S. Jansen;Suzanne Duijst;Sunny Mahakena;Daniela Sommer

  • Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

    Maria M.M. van Genderen;Mieke M.M.C. Bijveld;Yvonne Y.B. Claassen;Ralph R.J. Florijn

  • A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.

    Abbas M Solouki;Virginie J M Verhoeven;Cornelia M van Duijn;Annemieke J M H Verkerk

  • ABCC6 prevents ectopic mineralization seen in pseudoxanthoma elasticum by inducing cellular nucleotide release.

    Robert S. Jansen;Aslı Küçükosmanoğlu;Marcel de Haas;Sunny Sapthu

  • Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome

    M. T. Bassi;M. V. Schiaffino;Alessandra Renieri;F. De Nigris

  • A genome-wide association study of optic disc parameters

    Wishal D. Ramdas;Leonieke M. E. van Koolwijk;M. Kamran Ikram;Nomdo M. Jansonius

  • Positional cloning of the gene for x-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1

    R. Roepman;G. Van Duijnhoven;T. Rosenberg;A. J. L. G. Pinckers

Frequent Co-Authors

Caroline C W Klaver
Caroline C W Klaver Erasmus University Rotterdam
Paulus T. V. M. de Jong
Paulus T. V. M. de Jong University of Amsterdam
Frans P.M. Cremers
Frans P.M. Cremers Radboud University
Carel B. Hoyng
Carel B. Hoyng Radboud University
Albert Hofman
Albert Hofman Harvard University
Jan Wijnholds
Jan Wijnholds Leiden University Medical Center
André G. Uitterlinden
André G. Uitterlinden Erasmus University Rotterdam
Maarten Kamermans
Maarten Kamermans Netherlands Institute for Neuroscience
Ben A. Oostra
Ben A. Oostra Erasmus University Rotterdam

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