All publications
2014
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
2013
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
2012
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
2011
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
2010
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
2008
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
2007
Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects
Wojda A, Zietkiewicz E, Witt M
Mutagenesis. 2007
2006
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
2005
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
2004
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
Mikrojądra w komórkach człowieka - powstawanie, zawartość oraz wykorzystanie diagnostyczne i prognostyczne
Lubka M, Wojda A, Witt M
Postępy Biol Kom. 2004
2003