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Anneke den Hollander

Short CV

1996-2002PhD student, Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands
2002Guest researcher, Telethon Institute of Genetics and Medicine, Naples, Italy
2002-2007Postdoc, Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands
2007-2008Fellow, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston MA, USA
2008-2009Assistant professor, Department of Ophthalmology, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands
2009-currentAssociate professor, Department of Ophthalmology, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands

Memberships

  • Association for Research in Vision and Ophthalmology (ARVO)
  • American Society of Human Genetics (ASHG)
Anneke den Hollander
Anneke den Hollander

Research Group

Genetics of multifactorial eye diseases

Contact

Radboud University Nijmegen Medical Centre

Department of Ophthalmology

Philips van Leydenlaan 15
6525 EX Nijmegen
The Netherlands

Phone: +31-24-3617431
Fax-Number: +31-24-3540488

Email:
a.denhollander[at]antrg.umcn.nl

Website:
www.eugenda.nl

Key Publications

  1. Boon CJF, Klevering BJ, LeRoy BP, Hoyng CB, Keunen JEE & den Hollander AI (2009).
    The spectrum of ocular phenotypes caused by mutations in the BEST1 gene.
    Prog Retin Eye Res 28:187-205.
  2. Boon CJF, Klevering BJ, Hoyng CB, Zonneveld MN, Nabuurs SB, Blokland E, Cremers FPM & den Hollander AI. (2008)
    Basal laminar drusen caused by compound heterozygous variants in the CFH gene.
    Am J Hum Genet 82, 516-523.
  3. Collin RWJ, Littink KW, Klevering BJ, van den Born LI, Koenekoop RK, Zonneveld MN, Blokland EAW, Strom TM, Hoyng CB, den Hollander AI & Cremers FPM (2008).
    Identification of a 2-megabases human orthologue of Drosophila eyes shut/spacemaker that is mutated in patients with retinitis pigmentosa.
    Am J Hum Genet 83, 594-603.
  4. den Hollander AI, Roepman R, Koenekoop RK & Cremers FPM (2008).
    Leber congenital amaurosis: genes, proteins and disease mechanisms.
    Prog Retin Eye Res, 27, 391-419.
  5. den Hollander AI, Koenekoop RK, Mohamed MD, Arts HH, Boldt K, Towns KV, Sedmak T, Beer M, Nagel-Wolfrum K, McKibbin M, Dharmaraj S, Lopez I, Ivings L, Williams GA, Springell K, Woods CG, Jafri H, Rashid Y, Strom TM, van der Zwaag B, Gosens I, Kersten FFJ, van Wijk E, Veltman JA, Zonneveld MN, van Beersum SEC, Maumenee IH, Wolfrum U, Cheetham ME, Ueffing M, Cremers FPM, Inglehearn CF & Roepman R (2007).
    Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.
    Nature Genet 39, 889-895.
  6. den Hollander AI, Koenekoop RK, Yzer S, Lopez I, Arends ML, Voesenek KEJ, Zonneveld MN, Strom TM, Meitinger T, Brunner HG, Hoyng CB, van den Born LI, Rohrschneider K & Cremers FPM (2006).
    Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis.
    Am J Hum Genet 79, 556-561.
  7. den Hollander AI, Heckenlively JR, van den Born LI, de Kok YJM, van der Velde-Visser SD, Kellner U, Jurklies B, van Schooneveld M, Blankenagel A, Rohrschneider K, Wissinger B, Cruysberg JR, Deutman AF, Brunner HG, Apfelstedt-Sylla E, Hoyng CB & Cremers FPM (2001).
    Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homolog 1 (CRB1) gene.
    Am J Hum Genet 69, 198-203.
  8. den Hollander AI, ten Brink JB, de Kok YJM, van Soest S, van den Born LI, van Driel MA, van de Pol DJR, Payne AM, Bhattacharya SS, Kellner U, Hoyng CB, Westerveld A, Brunner HG, Bleeker-Wagemakers EM, Deutman AF, Heckenlively JR, Cremers FPM & Bergen AAB (1999).
    Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12).
    Nature Genet 23, 217-221.
  9. Thiadens AA, den Hollander AI, Roosing S, Nabuurs SB, Zekveld-Vroom RC, Collin RW, De Baere E, Koenekoop RK, van Schooneveld MJ, Strom TM, van Lith-Verhoeven JJ, Lotery AJ, van Moll-Ramirez N, LeRoy BP, van den Born LI, Hoyng CB, Cremers FPM, Klaver CC (2009).
    Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.
    Am J Hum Genet 85, 240-247.
  10. Wang H, den Hollander AI, Moayedi Y, Abulimiti A, Li Y, Collin RW, Hoyng CB, Lopez I, Bray M, Lewis RA, Lupski JR, Mardon G, Koenekoop RK & Chen R (2009).
    SPATA7 is an early onset retinal disease gene.
    Am J Hum Genet 84, 380-387.

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