Marko Hawlina

Genotyping microarray (gene chip) for the<i>ABCR</i>(<i>ABCA4</i>) gene

Kaie Jaakson, Jana Zernant, Maigi Külm et al. · Human Mutation · 2003 · 238 citations

ISCEV standard for clinical pattern electroretinography—2007 update

Graham E. Holder, Mitchell Brigell, Marko Hawlina et al. · Documenta Ophthalmologica · 2007 · 144 citations · Full text

Phenotypic Variation in Enhanced S-cone Syndrome

Isabelle Audo, Michel Michaelides, Anthony G. Robson et al. · Investigative Ophthalmology & Visual Science · 2008 · 121 citations

Abnormal fundus autofluorescence in relation to retinal function in patients with retinitis pigmentosa

Petra Popović, Martina Jarc-Vidmar, Marko Hawlina · Graefe s Archive for Clinical and Experimental Ophthalmology · 2005 · 116 citations

Ocular Disease, Retina, Ophthalmology +7

An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

Crystel Bonnet, Zied Riahi, Sandra Chantot‐Bastaraud et al. · European Journal of Human Genetics · 2016 · 106 citations · Full text