Katarzyna Skonieczka

Constitutional mutations of the CHEK2 gene are a risk factor for MDS, but not for de novo AML

Hanna Janiszewska, Aneta Bąk, Katarzyna Skonieczka et al. · Leukemia Research · 2018 · 30 citations

Chek2 Gene, Constitutional Mutations, Somatic Variant +8

The application of conventional cytogenetics, FISH, and RT-PCR to detect genetic changes in 70 children with ALL

Krystyna Soszyńska, Barbara Mucha, Robert Dębski et al. · Annals of Hematology · 2008 · 17 citations

Genetic Analysis, Genetic Testing, Developmental Biology +11

Usefulness of classic cytogenetic testing compared to fluorescence in situ hybridization in genetic diagnosis of 58 patients with myelodysplastic syndromes

Katarzyna Skonieczka, Ewa Duszeńko, Elżbieta Wyrowińska et al. · Polskie Archiwum Medycyny Wewnętrznej · 2009 · 12 citations

Advantages and Limitations of SNP Array in the Molecular Characterization of Pediatric T-Cell Acute Lymphoblastic Leukemia

Monika Lejman, Monika Włodarczyk, Borys Styka et al. · Frontiers in Oncology · 2020 · 12 citations · Full text

Concomitance of monosomal karyotype with at least 5 chromosomal abnormalities is associated with dismal treatment outcome of AML patients with complex karyotype – retrospective analysis of Polish Adult Leukemia Group (PALG)

Agnieszka Wierzbowska, Ewa Wawrzyniak, Monika Siemieniuk‐Ryś et al. · Leukemia & lymphoma/Leukemia and lymphoma · 2016 · 11 citations