Ľudevít Kádaši

A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics

Clint Mizzi, Eleni Dalabira, Judit Kumuthini et al. · PLoS ONE · 2016 · 155 citations · Full text

Medicine, Pharmacology, Clinical Pharmacology +16

Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on ‘black bone disease’ in Italy

Martina Nemethova, Ján Radvánszky, Ľudevít Kádaši et al. · European Journal of Human Genetics · 2015 · 102 citations · Full text

Medicine, Genetics, Molecular Genetics +13

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

Life Sciences, Genetics, Molecular Genetics +14

Reconstructing Roma History from Genome-Wide Data

Priya Moorjani, Nick Patterson, Po‐Ru Loh et al. · PLoS ONE · 2013 · 73 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

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 · 59 citations

Life Sciences, Genetics, Molecular Genetics +12