Michał Witt

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe

Thilo Dörk, Milan Maçek, Frauke Mekus et al. · Human Genetics · 2000 · 146 citations

Life Sciences, Genetics, Molecular Genetics +11

Impact of SNPs on methylation readouts by Illumina Infinium HumanMethylation450 BeadChip Array: implications for comparative population studies

Patrycja Daca‐Roszak, Aleksandra Pfeifer, Jadwiga Żebracka‐Gala et al. · BMC Genomics · 2015 · 90 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

<i>RPGR</i> mutations might cause reduced orientation of respiratory cilia

Zuzanna Bukowy‐Bieryłło, Ewa Ziętkiewicz, Niki T. Loges et al. · Pediatric Pulmonology · 2012 · 86 citations

Life Sciences, Genetics, Molecular Genetics +16

Primary ciliary dyskinesia: genes, candidate genes and chromosomal regions.

Maciej Geremek, Michał Witt · PubMed · 2004 · 80 citations

Medicine, Molecular Genetics, Neurology +10

Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects

Alina Wojda, Ewa Ziętkiewicz, Michał Witt · Mutagenesis · 2007 · 78 citations · Full text

Life Sciences, Cell Biology, Genetics +17