Monika Ołdak

M34T and V37I mutations in <i>GJB2</i> associated hearing impairment: Evidence for pathogenicity and reduced penetrance

Agnieszka Pollak, Agata Skórka, Małgorzata Mueller‐Malesińska et al. · American Journal of Medical Genetics Part A · 2007 · 104 citations

Human Papillomavirus Type 8 Interferes with a Novel C/EBPβ-Mediated Mechanism of Keratinocyte CCL20 Chemokine Expression and Langerhans Cell Migration

Tanya Sperling, Monika Ołdak, Barbara Walch‐Rückheim et al. · PLoS Pathogens · 2012 · 78 citations · Full text

Immune Regulation, Immunology, Pathology +24

Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation.

Jacek P. Szaflik, Monika Ołdak, Radosław Maksym et al. · PubMed · 2008 · 71 citations

Novel neuro-audiological findings and further evidence for TWNK involvement in Perrault syndrome

Monika Ołdak, Dominika Oziębło, Agnieszka Pollak et al. · Journal of Translational Medicine · 2017 · 51 citations · Full text

Mutation analysis of mitochondrial 12S rRNA gene in Polish patients with non-syndromic and aminoglycoside-induced hearing loss

Małgorzata Rydzanicz, Maciej Wróbel, Agnieszka Pollak et al. · Biochemical and Biophysical Research Communications · 2010 · 48 citations

Mendelian Disorder, Mitochondrial Biogenesis, Mitochondrial Function +9