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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: Ader, Marius; AIBILI; Arden, Geoffrey; Audo, Isabelle; Beattie, Renwick; Berendschot, Tos; Bergen, Arthur; Berger, Wolfgang; Bird, Alan; Cremers, Frans; den Hollander, Anneke; Dias, Aylvin; Enzmann, Volker; Fighting Blindness; Greenwood, John; Grimm, Christian; Hauck, Stefanie; Heiduschka, Peter; Hicks, David; Holz, Frank G.; Humphries, Peter; Inglehearn, Chris; Joachim, Stephanie; Johnsen-Soriano, Siv; Julien, Sylvie; Kennedy, Breandan; Larsen, Michael; Lengyel, Imre; Lotery, Andrew John; Moore, Tony; Navea, Amparo; Pastor, Jose-Carlos; Research Group of Tunde Peto; Sennlaub, Florian; Tsilimbaris, Miltiadis; Riva, Charles; Rubin, Gary; Schmetterer, Leopold; Strauss, Olaf; Sørensen, Torben Lykke; Topouzis, Fotis; Ueffing, Marius; Weber, Bernhard; Wright, Alan; Xu, Heping
disease gene mapping: Cremers, Frans; den Hollander, Anneke; Guggenheim, Jez; Inglehearn, Chris; Kennedy, Breandan; Lotery, Andrew John; Schimpf-Linzenbold, Simone; Zeitz, Christina
gene microarray: Ader, Marius; Bergen, Arthur; Chakravarthy, Usha; Cremers, Frans; Dollfus, Hélène; Hamel, Christian; Hindges, Robert; Jager, Martine; Kennedy, Breandan; Palfi, Arpad; Tsilimbaris, Miltiadis; Vignali, Roberto; Roska, Botond; Schaeffel, Frank
genetics: Audo, Isabelle; Banfi, Sandro; Baraas, Rigmor; Bergen, Arthur; Berger, Wolfgang; Bhattacharya, Shomi; Bujakowska, Kinga; Butterworth, Jacqueline; Calonge, Margarita; Cremers, Frans; den Hollander, Anneke; Grau, Tanja; Graw, Jochen; Guggenheim, Jez; Hamel, Christian; Holz, Frank G.; Inglehearn, Chris; Jager, Martine; Kennedy, Breandan; Lagreze, Wolf; Lotery, Andrew John; MacLaren, Robert; Moore, Tony; Neuhauss, Stephan; O'Driscoll, Ciara; Papageorgiou, Elena; Tsilimbaris, Miltiadis; Rivolta, Carlo; Roepman, Ronald; Schimpf-Linzenbold, Simone; Topouzis, Fotis; Zeitz, Christina
glaucoma: AIBILI; Andrés-Guerrero, Vanessa; Bach, Michael; Bergen, Arthur; Bhattacharya, Shomi; Cordeiro, M Francesca; Cotter, Tom G.; Dakin, Steven; den Hollander, Anneke; Dias, Aylvin; Inglehearn, Chris; Joachim, Stephanie; Kremers, Jan; Lagreze, Wolf; Lotery, Andrew John; Lütjen-Drecoll, Elke; Martin, Keith; Naumann, Gottfried; Papageorgiou, Elena; Research Group of Tunde Peto; Picaud, Serge; Detorakis, Efstathios; Jansonius, Nomdo; Riva, Charles; Schiefer, Ulrich; Schmetterer, Leopold; Skorkovská, Karolína; Thanos, Solon; Topouzis, Fotis; Wilhelm, Barbara; Wissinger, Bernd
Leber congenital amaurosis: Audo, Isabelle; Auricchio, Alberto; Berger, Wolfgang; Cottet, Sandra; Cremers, Frans; den Hollander, Anneke; Kawasaki, Aki; Larsen, Michael; Lorenz, Birgit; Tsilimbaris, Miltiadis; Stieger, Knut; Wijnholds, Jan; Zrenner, Eberhart
linkage analysis: Audo, Isabelle; Berger, Wolfgang; den Hollander, Anneke; O'Driscoll, Ciara; Schimpf-Linzenbold, Simone
macular dystrophy, inherited: Audo, Isabelle; Auricchio, Alberto; Bandello, Francesco; Berger, Wolfgang; Cottet, Sandra; Holz, Frank G.; Langmann, Thomas; Larsen, Michael; Lotery, Andrew John; Moore, Tony; Navea, Amparo; Tsilimbaris, Miltiadis; Weber, Bernhard
molecular diagnostics: Bergen, Arthur; Berger, Wolfgang; Grau, Tanja; Holz, Frank G.; van Heyningen, Veronica; Weber, Bernhard
retinal degenerations: hereditary: Arden, Geoffrey; Audo, Isabelle; Auricchio, Alberto; Bach, Michael; Banfi, Sandro; Baraas, Rigmor; Bergen, Arthur; Bhattacharya, Shomi; Bird, Alan; Bovolenta, Paola; Bujakowska, Kinga; Chadderton, Naomi; Cottet, Sandra; Cremers, Frans; den Hollander, Anneke; Ekström, Per; Graw, Jochen; Hamel, Christian; Inglehearn, Chris; Kennedy, Breandan; Langmann, Thomas; Lorenz, Birgit; Lotery, Andrew John; MacLaren, Robert; O'Driscoll, Ciara; Palfi, Arpad; Paquet-Durand, Francois; Tsilimbaris, Miltiadis; Rivolta, Carlo; Roepman, Ronald; Sahaboglu, Ayse; Sancho-Pelluz, Javier; Schimpf-Linzenbold, Simone; Seeliger, Mathias; Stieger, Knut; Strauss, Olaf; van Veen, Theo; Weber, Bernhard; Wijnholds, Jan; Wissinger, Bernd; Wright, Alan; Zrenner, Eberhart
mutation detection
linkage mapping
ARMD
buphthalmos

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