Eva Feráková

Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

Martina Plášilová, Ivaylo Stoilov, Mansoor Sarfarazi et al. · Journal of Medical Genetics · 1999 · 174 citations · Full text

Biology, Cytochrome P450 Molecule, Allelic Variant +13

High Frequency of Alkaptonuria in Slovakia: Evidence for the Appearance of Multiple Mutations in HGO Involving Different Mutational Hot Spots

Andrea Zaťková, Daniel Beltrán Valero de Bernabé, H Poláková et al. · The American Journal of Human Genetics · 2000 · 93 citations · Full text

Biology, Allelic Variant, Mendelian Disorder +7

High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL).

Gabriel Minárik, V. Ferák, Eva Feráková et al. · PubMed · 2003 · 75 citations

Carrier Frequency, Gjb2 Mutation W24x, Mendelian Disorder +13

Linkage of Autosomal Recessive Primary Congenital Glaucoma to the GLC3A Locus in Roms (Gypsies) from Slovakia

Martina Plášilová, Eva Feráková, L Kádasi et al. · Human Heredity · 1998 · 55 citations

High Frequency of Alkaptonuria in Slovakia: Evidence for the Appearance of Multiple Mutations in<i>HGO</i>Involving Different Mutational Hot Spots

Andrea Zaťková, Daniel Beltrán Valero de Bernabé, H Poláková et al. · The American Journal of Human Genetics · 2000 · 34 citations

Biology, Allelic Variant, Multiple Mutations +7