Zrenner Lab

Pathophysiology of Vision

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Ditta Zobor

First nameDitta
Present position and titleMD, FEBO
Specialist in Ophthalmology

Business address

Institute of Ophthalmic Research
Centre for Ophthalmology,
University of Tübingen
Elfriede-Aulhorn-Straße 7
72076 Tübingen

Phone: +49 (0)7071 29-80733
Fax: +49 (0)7071 29-5361
E-mail: ditta.zobor[at]med.uni-tuebingen.de

Academic Education

Year Degree University Field of study
2010 FEBO (fellow of the European Board of Ophthalmology) European Board of Ophthalmology Ophthalmology
2010 Specialization University of Tübingen Ophthalmology
2004 MD Semmelweis University Budapest, Hungary Human Medicine

Professional Experience

Period Institution Position Discipline
Since 03/2011 University of Tübingen, Institute of Ophthalmic Research Specialist in Ophthalmology Ophthalmology
07/2010-02/2011 Neuhann Private Practice in Munich, Germany Specialist in Ophthalmology Ophthalmology
09/2005-06/2010 University of Tübingen, University Eye Hospital Tübingen Research fellow and resident Ophthalmology
10/2004-11/2006 University Eye Clinic Budapest, Semmelweis University, Budapest, Hungary Resident in Ophthalmology Ophthalmology

Additional information

2010-2011Speaker of the Centre for Rare Eye Diseases Tübingen
2010Fellow of the European Board of Ophthalmology (FEBO),DOG (Deutsche Ophthalmologische Gesellschaft) award for excellent exam 
Since 2006several travel grants from the ARVO and ISCEV Committes
2004Dr.med. (summa cum laude) Semmelweis University, Budapest, Hungary
2003Scholarship of the  Ministry of Education, Republic of Hungary
2002Leonardo and Erasmus Scholarships, research work in the Histology Lab of the University Eye Clinic Freiburg, Germany

Major Publications

  1. Kitiratschky VB, Nagy D, Zabel T, Zrenner E, Wissinger B, Kohl S, Jägle H. Cone and cone-rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation. Br J Ophthalmol. 2008 Aug;92(8):1086-91. PubMed PMID: 18653602.
  2. Nagy D, Schönfisch B, Zrenner E, Jägle H. Long-term follow-up of retinitis pigmentosa patients with multifocal electroretinography. Invest Ophthalmol Vis Sci. 2008 Oct;49(10):4664-71. Epub 2008 Jun 19. PubMed PMID: 18566474.
  3. Becirovic E, Ebermann I, Nagy D, Zrenner E, Seeliger MW, Bolz HJ. Usher syndrome type 1 due to missense mutations on both CDH23 alleles: investigation of mRNA splicing. Hum Mutat. 2008 Mar;29(3):452. PubMed PMID: 18273900.
  4. Zobor D, Zrenner E. [Retinitis pigmentosa - a review. Pathogenesis, guidelines for diagnostics and perspectives]. Ophthalmologe. 2012 May;109(5):501-14;quiz 515. German. PubMed PMID: 22581051.
  5. Wissinger B, Schaich S, Baumann B, Bonin M, Jägle H, Friedburg C, Varsányi B,  Hoyng CB, Dollfus H, Heckenlively JR, Rosenberg T, Rudolph G, Kellner U, Salati R, Plomp A, De Baere E, Andrassi-Darida M, Sauer A, Wolf C, Zobor D, Bernd A, Leroy BP, Enyedi P, Cremers FP, Lorenz B, Zrenner E, Kohl S. Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response. Hum Mutat. 2011 Dec;32(12):1398-406. doi: 10.1002/humu.21580. Epub 2011 Sep 12. PubMed PMID: 21882291.
  6. Zobor D, Kaufmann DH, Weckerle P, Sauer A, Wissinger B, Wilhelm H, Kohl S. Cone-rod dystrophy associated with amelogenesis imperfecta in a child with neurofibromatosis type 1. Ophthalmic Genet. 2012 Mar;33(1):34-8. Epub 2011 Jul 5. PubMed PMID: 21728811.
  7. Jägle H, Zobor D, Brauns T. Accommodation limits induced optical defocus in defocus experiments. Doc Ophthalmol. 2010 Oct;121(2):103-9. Epub 2010 Jun 11. PubMed PMID: 20544259.
  8. Perrault I, Estrada-Cuzcano A, Lopez I, Kohl S, Li S, Testa F, Zekveld-VroonR, Wang X, Pomares E, Andorf J, Aboussair N, Banfi S, Delphin N, den HollanderAI, Edelson C, Florijn R, Jean-Pierre M, Leowski C, Megarbane A, Villanueva C,Flores B, Munnich A, Ren H, Zobor D, Bergen A, Chen R, Cremers FP,Gonzalez-Duarte R, Koenekoop RK, Simonelli F, Stone E, Wissinger B, Zhang Q,Kaplan J, Rozet JM. Union Makes Strength: A Worldwide Collaborative Genetic andClinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineatethe Associated Phenotype. PLoS One. 2013;8(1):e51622. doi:10.1371/journal.pone.0051622. Epub 2013 Jan 7. PubMed PMID: 23308101; PubMedCentral PMCID: PMC3538699.
  9. Zobor D, Kohl S, Wissinger B, Zrenner E, Jägle H. Rod and cone function inpatients with KCNV2 retinopathy. PLoS One. 2012;7(10):e46762. doi:10.1371/journal.pone.0046762. Epub 2012 Oct 15. PubMed PMID: 23077521; PubMedCentral PMCID: PMC3471896.
  10. Dominik Fischer M*, Zobor D*, Keliris GA, Shao Y, Seeliger MW, Haverkamp S,Jägle H, Logothetis NK, Smirnakis SM. Detailed functional and structuralcharacterization of a macular lesion in a rhesus macaque. Doc Ophthalmol. 2012Aug 26. [Epub ahead of print] PubMed PMID: 22923360.