Werner Temmel

Association of Complement Factor H Y402H Gene Polymorphism with Different Subtypes of Exudative Age-Related Macular Degeneration

Beate J. Wegscheider, Martin Weger, Wilfried Renner et al. · Ophthalmology · 2007 · 87 citations

Medicine, Genetics, Ophthalmology +12

Hyperhomocyst(e)inemia and MTHFR C677T genotypes in patients with central retinal vein occlusion

Martin Weger, Olaf Stanger, Hannes Deutschmann et al. · Graefe s Archive for Clinical and Experimental Ophthalmology · 2002 · 61 citations

Medicine, Genetics, Ophthalmology +5

Role of Thrombophilic Gene Polymorphisms in Branch Retinal Vein Occlusion

Martin Weger, Wilfried Renner, Iris Steinbrugger et al. · Ophthalmology · 2005 · 55 citations

Medicine, Genetics, Hematology +11

Hyperhomocyst(e)inemia, but not methylenetetrahydrofolate reductase C677T mutation, as a risk factor in branch retinal vein occlusion

Martin Weger, Olaf Stanger, Hannes Deutschmann et al. · Ophthalmology · 2002 · 45 citations

Medicine, Genetics, Ophthalmology +12

Methylenetetrahydrofolatereductase (MTHFR) 677C>T polymorphism and open angle glaucoma.

Georg Mossböck, Martin Weger, Christoph Faschinger et al. · PubMed · 2006 · 33 citations

Life Sciences, Genetics, Ophthalmology +16