Recent advances in primary ciliary dyskinesia genetics Kurkowiak M, Ziętkiewicz E, Witt M J Med Genet. 2014 CFTR Mutations Spectrum and the Efficiency of Molecular Diagnostics in Polish Cystic Fibrosis Patients Ziętkiewicz E, Rutkiewicz E, Pogorzelski A, Klimek B, Voelkel K, Witt M PLoS One. 2014 Ciliary genes are down-regulated in bronchial tissue of primary ciliary dyskinesia patients Geremek M, Ziętkiewicz E, Bruinenberg M, Franke L, Pogorzelski A, Wijmenga C, Witt M PLoS One. 2014 BCL11B, FLT3, NOTCH1 and FBXW7 mutation status in T-cell Acute Lymphoblastic Leukemia patients Kraszewska MD, Dawidowska M, Kosmalska M, Sędek Ł, Grzeszczak W, Kowalczyk JR, Szczepański T, Witt M Blood Cells, Molecules and Diseases. 2013 RPGR mutations might cause reduced orientation of respiratory cilia Bukowy-Bieryłło Z, Ziętkiewicz E, Loges NT, Wittmer M, Geremek M, Olbrich H, Fliegauf M, Voelkel K, Rutkiewicz E, Rutland J, Morgan L, Pogorzelski A, Martin J, Haan E, Berger W, Omran H, Witt M Pediatr Pulmonol.. 2012 Mutations in radial spoke head genes and ultrastructural cilia defects in East-European cohort of primary ciliary dyskinesia patients Ziętkiewicz E, Bukowy-Bieryłło Z, Voelkel K, Klimek B, Dmeńska H, Pogorzelski A, Sulikowska-Rowińska A, Rutkiewicz E, Witt M PLoS One. 2012 DNA methylation pattern is altered in childhood T-cell acute lymphoblastic leukemia patients as compared with normal thymic subsets: insights into CpG island methylator phenotype in T-ALL Kraszewska MD, Dawidowska M, Kosmalska M, Sędek L, Grzeszczak W, Szczepański T, Witt M Leukemia. 2012 T-cell acute lymphoblastic leukaemia: recent molecular biology findings Kraszewska MD, Dawidowska M, Szczepanski T, Witt M Br J Haematol. 2012 Immunoglobulin/T-cell receptor gene rearrangements in the diagnostic paradigm of pediatric T-cell acute lymphoblastic leukemia patients Kraszewska MD, Dawidowska M, Kosmalska M, Sędek L, Grzeszczak W, Szczepański T, Witt M Leukemia & Lymphoma. 2012 Current genetic methodologies in the identification of disaster victims and in forensic analysis Ziętkiewicz E, Witt M, Daca P, Zebracka-Gala J, Goniewicz M, Jarząb B, Witt M J Appl Genet.. 2012 In vitro culturing of ciliary respiratory cells--a model for studies of genetic diseases Bukowy Z, Ziętkiewicz E, Witt M J Appl Genet. 2011 Gene expression studies in cells from primary ciliary dyskinesia patients identify 208 potential ciliary genes Geremek M, Bruinenberg M, Ziętkiewicz E, Pogorzelski A, Witt M, Wijmenga C Hum Genet. 2011 Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD) Ziętkiewicz E, Nitka B, Voelkel K, Skrzypczak U, Bukowy Z, Rutkiewicz E, Humińska K, Przystałowska H, Pogorzelski A, Witt M Respir Res. 2010 Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q Geremek M, Schoenmaker F, Zietkiewicz E, Pogorzelski A, Diehl S, Wijmenga C, Witt M Eur J Hum Genet. 2008 Implementation of the standard strategy for identification of Ig/TCR targets for minimal residual disease diagnostics in B-cell precursor ALL pediatric patients: Polish experience Dawidowska M, Jółkowska J, Szczepański T, Derwich K, Wachowiak J, Witt M Arch Immunol Ther Exp (Warsz). 2008 Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects Wojda A, Zietkiewicz E, Witt M Mutagenesis. 2007 Correlation between the level of cytogenetic aberrations in cultured human lymphocytes and the age and gender of donors Wojda A, Zietkiewicz E, Mossakowska M, Pawłowski W, Skrzypczak K, Witt M J Gerontol A Biol Sci Med Sci. 2006 Hematopoietic chimerism after allogeneic stem cell transplantation: a comparison of quantitative analysis by automated DNA sizing and fluorescent in situ hybridization Jólkowska J, Pieczonka A, Strabel T, Boruczkowski D, Wachowiak J, Bader P, Witt M BMC Blood Disord. 2005 Primary ciliary dyskinesia: genes, candidate genes and chromosomal regions Geremek M, Witt M J Appl Genet. 2004 Apparent X-linked primary ciliary dyskinesia associated with retinitis pigmentosa and a hearing loss Krawczyński MR, Dmeńska H, Witt M J Appl Genet. 2004 PCD and RP: X-linked inheritance of both disorders? Krawczyński MR, Witt M Pediatr Pulmonol. 2004 Mikrojądra w komórkach człowieka - powstawanie, zawartość oraz wykorzystanie diagnostyczne i prognostyczne Lubka M, Wojda A, Witt M Postępy Biol Kom. 2004 Manifestations of ageing at the cytogenetic level Wojda A, Witt M J Appl Genet. 2003 The 102-year old woman with translocation (7;12) and infertility in anamnesis Wojda A, Wolnik-Brzozowska D, Lubka M, Mossakowska M, Witt M J Appl Genet. 2003 Cystic fibrosis--a probable cause of Frédéric Chopin's suffering and death Majka L, Goździk J, Witt M J Appl Genet. 2003