| M34T and V37I mutations in GJB2 associated hearing impairment: Evidence for pathogenicity and reduced penetrance A Pollak, A Skórka, M Mueller‐Malesińska, G Kostrzewa, B Kisiel, ... American journal of medical genetics Part A 143 (21), 2534-2543, 2007 | 124 | 2007 |
| Cervical cancer cell‐derived interleukin‐6 impairs CCR7‐dependent migration of MMP‐9‐expressing dendritic cells J Pahne‐Zeppenfeld, N Schröer, B Walch‐Rückheim, M Oldak, A Gorter, ... International journal of cancer 134 (9), 2061-2073, 2014 | 110 | 2014 |
| The Papillomavirus E2 protein binds to and synergizes with C/EBP factors involved in keratinocyte differentiation D Hadaschik, K Hinterkeuser, M Oldak, HJ Pfister, S Smola-Hess Journal of virology 77 (9), 5253-5265, 2003 | 108 | 2003 |
| Human papillomavirus type 8 interferes with a novel C/EBPβ-mediated mechanism of keratinocyte CCL20 chemokine expression and Langerhans cell migration T Sperling, M Ołdak, B Walch-Rückheim, C Wickenhauser, J Doorbar, ... PLoS pathogens 8 (7), e1002833, 2012 | 91 | 2012 |
| Mutation analysis of mitochondrial 12S rRNA gene in Polish patients with non-syndromic and aminoglycoside-induced hearing loss M Rydzanicz, M Wróbel, A Pollak, W Gawęcki, D Brauze, ... Biochemical and biophysical research communications 395 (1), 116-121, 2010 | 67 | 2010 |
| Molecular activity of sirolimus and its possible application in tuberous sclerosis treatment J Jozwiak, S Jozwiak, M Oldak Medicinal research reviews 26 (2), 160-180, 2006 | 61 | 2006 |
| The human papillomavirus type 8 E2 protein suppresses β4-integrin expression in primary human keratinocytes M Oldak, H Smola, M Aumailley, F Rivero, H Pfister, S Smola-Hess Journal of virology 78 (19), 10738-10746, 2004 | 55 | 2004 |
| Novel neuro-audiological findings and further evidence for TWNK involvement in Perrault syndrome M Ołdak, D Oziębło, A Pollak, I Stępniak, M Lazniewski, U Lechowicz, ... Journal of translational medicine 15, 1-13, 2017 | 44 | 2017 |
| Screening of the General Polish Population for Deafness-Associated Mutations in Mitochondrial 12S rRNA and tRNASer(UCN) Genes M Rydzanicz, M Wróbel, K Cywińska, D Froehlich, W Gawęcki, W Szyfter, ... Genetic testing and molecular biomarkers 13 (2), 167-172, 2009 | 44 | 2009 |
| Clinical aspects of disrupted Hedgehog signaling M Oldakr, T Grzela, M Lazarczyk, J Malejczyk, P Skopinski International journal of molecular medicine 8 (4), 445-452, 2001 | 40 | 2001 |
| Next-generation sequencing of ABCA4: High frequency of complex alleles and novel mutations in patients with retinal dystrophies from Central Europe A Ścieżyńska, D Oziębło, AM Ambroziak, M Korwin, K Szulborski, ... Experimental eye research 145, 93-99, 2016 | 38 | 2016 |
| Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation JP Szaflik, M Ołdak, RB Maksym, A Kamińska, A Pollak, M Udziela, ... Molecular Vision 14, 1713, 2008 | 35 | 2008 |
| Differential regulation of human papillomavirus type 8 by interferon regulatory factors 3 and 7 M Oldak, L Tolzmann, A Wnorowski, MJ Podgórska, S Silling, R Lin, ... Journal of virology 85 (1), 178-188, 2011 | 33 | 2011 |
| Isolation and culture of human primary keratinocytes—a methods review A Ścieżyńska, A Nogowska, M Sikorska, J Konys, A Karpińska, ... Experimental Dermatology 28 (2), 107-112, 2019 | 32 | 2019 |
| Fuchs endothelial corneal dystrophy: strong association with rs613872 not paralleled by changes in corneal endothelial TCF4 mRNA level M Ołdak, E Ruszkowska, M Udziela, D Oziębło, E Bińczyk, A Ścieżyńska, ... BioMed research international 2015, 2015 | 31 | 2015 |
| Novel and De Novo Mutations Extend Association of POU3F4 with Distinct Clinical and Radiological Phenotype of Hearing Loss A Pollak, U Lechowicz, A Kędra, P Stawiński, M Rydzanicz, M Furmanek, ... PloS one 11 (12), e0166618, 2016 | 30 | 2016 |
| Clinical applications for next-generation sequencing U Demkow, R Ploski Academic Press, 2015 | 29 | 2015 |
| Human Papillomavirus Type 8 E2 Protein Unravels JunB/Fra-1 as an Activator of the β4-Integrin Gene in Human Keratinocytes M Oldak, RB Maksym, T Sperling, M Yaniv, H Smola, HJ Pfister, ... Journal of virology 84 (3), 1376-1386, 2010 | 26 | 2010 |
| Phacoemulsification with corneal astigmatism correction with the use of a toric intraocular lens in a case of megalocornea M Rekas, R Pawlik, A Klus, R Rózycki, JP Szaflik, M Oldak Journal of Cataract & Refractive Surgery 37 (8), 1546-1550, 2011 | 25 | 2011 |
| Association of UDP-glucuronosyltransferase 1A9 (UGT1A9) gene polymorphism with kidney allograft function J Pazik, M Oldak, M Dabrowski, Z Lewandowski, E Sitarek, M Podgórska, ... Ann Transplant 16 (4), 69-73, 2011 | 23 | 2011 |
