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European Journal of Medical Genetics|November 19, 2013
Oesophageal atresia with tracheoesophageal fistula and anal atresia in a patient with a de novo microduplication in 17q12Robert Smigiel, Carlo Marcelis, Dariusz Patkowski, et al.Oncology Reports|February 10, 2004
Correlation among loss of heterozygosity, promoter methylation and protein expression of MLH1 in larynx cancerRobert Smigiel, Agnieszka Stembalska-Kozlowska, Farhad Mirghomizadeh, et al.Journal of Applied Genetics|May 9, 2024
The analysis of transcriptomic signature of TNBC-searching for the potential RNA-based predictive biomarkers to determine the chemotherapy sensitivityStanislaw Supplitt, Pawel Karpinski, Maria Sasiadek, et al.Leukemia & Lymphoma|September 7, 2018
Bendamustine alone or with rituximab modifies expression of apoptosis-regulating genes and proteins of CLL cells, depending on IGVH mutational statusEwelina Ziolkowska, Dariusz Wolowiec, Pawel Karpinski, et al.Frontiers in Genetics|May 17, 2021
Case Report: Further Delineation of Neurological Symptoms in Young Children Caused by Compound Heterozygous Mutation in the PIEZO2 GeneMagdalena Klaniewska, Maria Jedrzejowska, Malgorzata Rydzanicz, et al.Breast Cancer Research and Treatment|July 30, 2024
Alterations in the expression of homologous recombination repair (HRR) genes in breast cancer tissues considering germline BRCA1/2 mutation statusIzabela Laczmanska, Rafal Matkowski, Stanislaw Supplitt, et al.Genes, Chromosomes & Cancer|November 2, 2020
Broad phenotypic spectrum of germ line 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemiaAgata Pastorczak, Anna Hogendorf, Zuzanna Urbanska, et al.Environmental and Molecular Mutagenesis|October 8, 2004
Markers of individual susceptibility and DNA repair rate in workers exposed to xenobiotics in a tire plantPavel Vodicka, Rajiv Kumar, Rudolf Stetina, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|May 25, 2017
Cell-free fetal DNA testing in prenatal diagnosis: Recommendations of the Polish Gynecological Society and the Polish Human Genetics SocietyPiotr Sieroszewski, Mirosław Wielgos, Stanislaw Radowicki, et al.European Journal of Human Genetics : EJHG|May 1, 2018
Comprehensive genomic analysis of patients with disorders of cerebral cortical developmentWojciech Wiszniewski, Pawel Gawlinski, Tomasz Gambin, et al.Pageof 3