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Prognostic heterogeneity and clonal dynamics within distinct subgroups of myelodysplastic syndrome and acute myeloid leukemia with TP53 disruptions

EJHaem, 2023-11, Vol.4 (4), p.1059-1070

2023

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Rare gene fusion rearrangement SPTNB1-PDGFRB in an atypical myeloproliferative neoplasm

Molecular cytogenetics, 2018-10, Vol.11 (1), p.56-56, Article 56

2018

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Natural history of clonal haematopoiesis seen in real-world haematology settings

British journal of haematology, 2024-05, Vol.204 (5), p.1844-1855

2024

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The evolving clinical testing landscape of genomic aberrations in solid tumors and hematological malignancies – Insights from evidence-based reviews for B-ALL and breast, brain, and renal cell neoplasia

Cancer genetics, 2020-06, Vol.244, p.60-61

2020

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Clinico-genomic profiling and clonal dynamic modeling of TP53-aberrant myelodysplastic syndrome and acute myeloid leukemia

Leukemia & lymphoma, 2021-12, Vol.62 (14), p.3348-3360

2021

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Cytogenetic Abnormalities in a Series of 1029 Patients With Primary Myelodysplastic Syndromes : A Report From the US With a Focus on Some Undefined Single Chromosomal Abnormalities

Cancer, 2008-12, Vol.113 (12), p.3331-3340

2008

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Systemic mastocytosis with associated clonal hematological non‐mast cell lineage disease: Clinical significance and comparison of chomosomal abnormalities in SM and AHNMD components

American journal of hematology, 2013-03, Vol.88 (3), p.219-224

2013

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Mammary Analogue Secretory Carcinoma of the Thyroid Mimicking Locally Advanced Papillary Thyroid Carcinoma: A Rare Case Report

International journal of surgical pathology, 2018-08, Vol.26 (5), p.459-463

2018

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Elderly do benefit from induction chemotherapy: High dose mitoxantrone‐based (“5 + 1”) induction chemotherapy regimen in newly diagnosed acute myeloid leukemia

American journal of hematology, 2019-02, Vol.94 (2), p.209-215

2019

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Chronic basophilic leukemia: a rare form of chronic myeloproliferative neoplasm

Human pathology, 2009-08, Vol.40 (8), p.1194-1199

2009

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Assessing copy number aberrations and copy-neutral loss-of-heterozygosity across the genome as best practice: An evidence-based review from the Cancer Genomics Consortium (CGC) working group for chronic lymphocytic leukemia

Cancer genetics, 2018-12, Vol.228-229, p.236-250

2018

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Novel FGFR3 rearrangement t(4;22)(p16;q11.2) in a patient with chronic lymphocytic leukemia/small lymphocytic lymphoma

Annals of hematology, 2013-10, Vol.92 (10), p.1433-1435

2013

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CGC Working Group Recommendations for CLL: Utility of Molecular Technologies Such as Microarrays and NGS for Routine Diagnostic Use

Cancer genetics, 2017-08, Vol.214, p.37-38

2017

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Improved detection rate of cytogenetic abnormalities in chronic lymphocytic leukemia and other mature B-cell neoplasms with use of CpG-oligonucleotide DSP30 and interleukin 2 stimulation

American journal of clinical pathology, 2013-05, Vol.139 (5), p.662-669

2013

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Eosinophilia with FIP1L1-PDGFRA fusion in a patient with chronic myelomonocytic leukemia

Journal of clinical oncology, 2008-04, Vol.26 (12), p.2040-2041

2008

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Mosaic tetraploidy and transient GFI1 mutation in a patient with severe chronic neutropenia

Pediatric blood & cancer, 2008-03, Vol.50 (3), p.630-632

2008

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Validation of DNA probes for preimplantation genetic diagnosis (PGD) by fluorescence in situ hybridization (FISH) R1

Prenatal diagnosis, 2006-11, Vol.26 (11), p.1042-1050

2006

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18 - CGC Working Group Recommendations for CLL: Utility of Molecular Technologies Such as Microarrays and NGS for Routine Diagnostic Use

Cancer genetics, 2017-08, Vol.214-215, p.37-38

2017

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Clinical picture: Multicolour karyotyping

The Lancet (British edition), 2001-04, Vol.357 (9264), p.1240-1240

2001

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Cytogenetic abnormalities in a series of 1029 patients with primary myelodysplastic syndromes

Cancer, 2008-12, Vol.113 (12), p.3331-3340

2008

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Cytogenetic abnormalities in a series of 1,029 patients with primary myelodysplastic syndromes: a report from the US with a focus on some undefined single chromosomal abnormalities

Cancer, 2008-12, Vol.113 (12), p.3331-3340

2008

Volltextzugriff (PDF)

Eosinophilia With FIP1L1-PDGFΡA Fusion in a Patient With Chronic Myelomonocytic Leukemia

Journal of clinical oncology, 2008, Vol.26 (12), p.2040-2041

2008

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Interphase FISH in plasma cell dyscrasia: increase in abnormality detection with plasma cell enrichment

Cancer genetics and cytogenetics, 2009-03, Vol.189 (2), p.112-117

2009

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Mosaic Tetraploidy and Transient Mutations in the GFI1 Gene in a Patient with Severe Chronic Neutropenia

Blood, 2006-11, Vol.108 (11), p.1281-1281

2006

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Validation of DNA probes for preimplantation genetic diagnosis (PGD) by fluorescencein situ hybridization (FISH) R1

Prenatal diagnosis, 2006-11, Vol.26 (11), p.1042-1050

2006

Volltextzugriff (PDF)

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Prognostic heterogeneity and clonal dynamics within distinct subgroups of myelodysplastic syndrome and acute myeloid leukemia with TP53 disruptions

Rare gene fusion rearrangement SPTNB1-PDGFRB in an atypical myeloproliferative neoplasm

Natural history of clonal haematopoiesis seen in real-world haematology settings

The evolving clinical testing landscape of genomic aberrations in solid tumors and hematological malignancies – Insights from evidence-based reviews for B-ALL and breast, brain, and renal cell neoplasia

Clinico-genomic profiling and clonal dynamic modeling of TP53-aberrant myelodysplastic syndrome and acute myeloid leukemia

Cytogenetic Abnormalities in a Series of 1029 Patients With Primary Myelodysplastic Syndromes : A Report From the US With a Focus on Some Undefined Single Chromosomal Abnormalities

Systemic mastocytosis with associated clonal hematological non‐mast cell lineage disease: Clinical significance and comparison of chomosomal abnormalities in SM and AHNMD components

Mammary Analogue Secretory Carcinoma of the Thyroid Mimicking Locally Advanced Papillary Thyroid Carcinoma: A Rare Case Report

Elderly do benefit from induction chemotherapy: High dose mitoxantrone‐based (“5 + 1”) induction chemotherapy regimen in newly diagnosed acute myeloid leukemia

Chronic basophilic leukemia: a rare form of chronic myeloproliferative neoplasm

Assessing copy number aberrations and copy-neutral loss-of-heterozygosity across the genome as best practice: An evidence-based review from the Cancer Genomics Consortium (CGC) working group for chronic lymphocytic leukemia

Novel FGFR3 rearrangement t(4;22)(p16;q11.2) in a patient with chronic lymphocytic leukemia/small lymphocytic lymphoma

CGC Working Group Recommendations for CLL: Utility of Molecular Technologies Such as Microarrays and NGS for Routine Diagnostic Use

Improved detection rate of cytogenetic abnormalities in chronic lymphocytic leukemia and other mature B-cell neoplasms with use of CpG-oligonucleotide DSP30 and interleukin 2 stimulation

Eosinophilia with FIP1L1-PDGFRA fusion in a patient with chronic myelomonocytic leukemia

Mosaic tetraploidy and transient GFI1 mutation in a patient with severe chronic neutropenia

Validation of DNA probes for preimplantation genetic diagnosis (PGD) by fluorescence in situ hybridization (FISH) R1

18 - CGC Working Group Recommendations for CLL: Utility of Molecular Technologies Such as Microarrays and NGS for Routine Diagnostic Use

Clinical picture: Multicolour karyotyping

Cytogenetic abnormalities in a series of 1029 patients with primary myelodysplastic syndromes

Cytogenetic abnormalities in a series of 1,029 patients with primary myelodysplastic syndromes: a report from the US with a focus on some undefined single chromosomal abnormalities

Eosinophilia With FIP1L1-PDGFΡA Fusion in a Patient With Chronic Myelomonocytic Leukemia

Interphase FISH in plasma cell dyscrasia: increase in abnormality detection with plasma cell enrichment

Mosaic Tetraploidy and Transient Mutations in the GFI1 Gene in a Patient with Severe Chronic Neutropenia

Validation of DNA probes for preimplantation genetic diagnosis (PGD) by fluorescencein situ hybridization (FISH) R1

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