H Poláková

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

Analysis of chromosome aberrations and sister-chromatid exchanges in peripheral blood lymphocytes of workers with occupational exposure to the mancozeb-containing fungicide Novozir Mn80

A Jablonická, H Poláková, J Karelová et al. · Mutation Research/Genetic Toxicology · 1989 · 61 citations

Occupational Toxicology, Allergy, Sister-chromatid Exchanges +8

Identification of 11 Novel Homogentisate 1,2 Dioxygenase Variants in Alkaptonuria Patients and Establishment of a Novel LOVD-Based HGD Mutation Database

Andrea Zaťková, Tatiana Sedláčková, Ján Radvánský et al. · JIMD Reports · 2011 · 58 citations · Full text

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