Karolina Perglerova

Prague, PR, Czech Republic

Last Updated: 09/26/2026

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Found 10 publications

Number of RUNX1 mutations, wild-type allele loss and additional mutations impact on prognosis in adult RUNX1-mutated AML.

Number of RUNX1 mutations, wild-type allele loss and additional mutations impact on prognosis in adult RUNX1-mutated AML.

Journal: Leukemia
Published: May 11, 2017

Molecular landscape of acute promyelocytic leukemia at diagnosis and relapse.

Molecular landscape of acute promyelocytic leukemia at diagnosis and relapse.

Journal: Haematologica
Published: March 26, 2017

Acute myeloid leukemias with ring sideroblasts show a unique molecular signature straddling secondary acute myeloid leukemia and de novo acute myeloid leukemia.

Acute myeloid leukemias with ring sideroblasts show a unique molecular signature straddling secondary acute myeloid leukemia and de novo acute myeloid leukemia.

Journal: Haematologica
Published: January 07, 2017

The new provisional WHO entity 'RUNX1 mutated AML' shows specific genetics but no prognostic influence of dysplasia.

The new provisional WHO entity 'RUNX1 mutated AML' shows specific genetics but no prognostic influence of dysplasia.

Journal: Leukemia
Published: May 24, 2016

Feasibility of BAALC gene expression for detection of minimal residual disease and risk stratification in normal karyotype acute myeloid leukaemia.

Feasibility of BAALC gene expression for detection of minimal residual disease and risk stratification in normal karyotype acute myeloid leukaemia.

Journal: British journal of haematology
Published: May 06, 2016

Changes in cytogenetics and molecular genetics in acute myeloid leukemia from childhood to adult age groups.

Changes in cytogenetics and molecular genetics in acute myeloid leukemia from childhood to adult age groups.

Journal: Cancer
Published: March 24, 2016

Subtype-specific patterns of molecular mutations in acute myeloid leukemia.

Subtype-specific patterns of molecular mutations in acute myeloid leukemia.

Journal: Leukemia
Published: January 22, 2016

Karyotype evolution and acquisition of FLT3 or RAS pathway alterations drive progression of myelodysplastic syndrome to acute myeloid leukemia.

Karyotype evolution and acquisition of FLT3 or RAS pathway alterations drive progression of myelodysplastic syndrome to acute myeloid leukemia.

Journal: Haematologica
Published: August 22, 2015

Next-generation deep-sequencing detects multiple clones of CALR mutations in patients with BCR-ABL1 negative MPN.

Next-generation deep-sequencing detects multiple clones of CALR mutations in patients with BCR-ABL1 negative MPN.

Journal: Leukemia
Published: July 30, 2015

Genetic characterization of T-PLL reveals two major biologic subgroups and JAK3 mutations as prognostic marker.

Genetic characterization of T-PLL reveals two major biologic subgroups and JAK3 mutations as prognostic marker.

Journal: Genes, chromosomes & cancer
Published: July 27, 2015
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Last Updated: 09/26/2026