World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

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

Arthur A.B. Bergen publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Arthur A.B. Bergen sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 189 publications — 46th percentile

46% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Arthur A.B. Bergen D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Arthur A.B. Bergen sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 67 D-Index — 43rd percentile

43% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

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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