You are here: vision-research.eu » People » Research Groups » Greece » Petersen, Michael

Department of Genetics

Group consists of Clinical Genetics (3 MDs), Cytogenetics (1 PhD, 2 techs), Molecular Genetics (2 PhDs).

Methodology

  • Mutation detection by DGGE and DNA sequencing
  • SNP analysis by RT-PCR

Scientific Cooperations

  • Cooperation 1
    Dept. of Ophthalmology, University of Ioannina, Greece
  • Cooperation 2
    Dept. of Ophthalmology, University of Athens, Greece
  • Cooperation 3
    Dept. of Ophthalmology, General Hospital of Larissa, Greece
  • Cooperation 4
    Casey Eye Institute, Oregon Health Sciences University, Portland, OR, USA
  • Cooperation 5
    Center for Eye Research Australia, University of Melbourne, Australia

Group Leader

Michael Bjorn Petersen
[more information]

Contact

“Aghia Sophia” Children’s Hospital

Department of Genetics
Institute of Child Health

Thivon & Livadeias
Doxiadis Building
GR-11527 Athens
Greece

Phone: +30 210 7467789
Fax: +30 210 7700111

Email:
mpetersen[at]ich.gr

Website:
www.ich.gr

Current Research Projects

  • Project 1
    MYOC mutations in Greek POAG patients.
  • Project 2
    CYP1B1 mutations in Greek patients with buphthalmos.
  • Project 3
    Genetic association study in Greek patients with pseudoexfoliation.
  • Project 4
    Genetic association study in Greek patients with ARMD.
  • Project 5
    Database of rare disorders (Orphanet Greece).

Research Groups

People

Related Research Groups

age-related macular degeneration
Oops, an error occurred! Code: 201906170219101b49fa02
disease gene mapping
Oops, an error occurred! Code: 201906170219106335e21f
gene microarray
Oops, an error occurred! Code: 20190617021910ddcab064
genetics
Oops, an error occurred! Code: 20190617021910ed5e8b16
glaucoma
Oops, an error occurred! Code: 2019061702191020b2973f
Leber congenital amaurosis
Oops, an error occurred! Code: 201906170219108528fd2e
linkage analysis
Oops, an error occurred! Code: 2019061702191022cd7db0
macular dystrophy, inherited
Oops, an error occurred! Code: 201906170219101e4ca581
molecular diagnostics
Oops, an error occurred! Code: 201906170219102e694b34
retinal degenerations: hereditary
Oops, an error occurred! Code: 20190617021910ba8b152a
mutation detection
Oops, an error occurred! Code: 20190617021910f87af88b
linkage mapping
Oops, an error occurred! Code: 20190617021910f84bde26
ARMD
Oops, an error occurred! Code: 20190617021910d0ac43d2
buphthalmos
Oops, an error occurred! Code: 2019061702191065b879ba