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- 2024
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Mark
Gene amplification in neoplasia : A cytogenetic survey of 80 131 cases
(
- Contribution to journal › Article
- 2023
-
Mark
A cloud-based resource for genome coordinate-based exploration and large-scale analysis of chromosome aberrations and gene fusions in cancer
(
- Contribution to journal › Article
-
Mark
Giemsa-negative chromosome bands preferentially recombine in cancer-associated translocations and gene fusions
(
- Contribution to journal › Article
- 2022
-
Mark
Transcriptomics paving the way for improved diagnostics and precision medicine of acute leukemia
(
- Contribution to journal › Article
- 2021
-
Mark
HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions
(
- Contribution to journal › Debate/Note/Editorial
- 2020
-
Mark
Farewell message from the Editor-in-Chief of Genes, Chromosomes & Cancer
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Analysis of fusion transcripts indicates widespread deregulation of snoRNAs and their host genes in breast cancer
(
- Contribution to journal › Article
- 2019
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Mark
Cancer chromosome breakpoints cluster in gene-rich genomic regions
(
- Contribution to journal › Article
-
Mark
Most gene fusions in cancer are stochastic events
(
- Contribution to journal › Article
- 2017
-
Mark
Frequent miRNA-convergent fusion gene events in breast cancer
(
- Contribution to journal › Article
- 2016
-
Mark
Gene fusions in soft tissue tumors: Recurrent and overlapping pathogenetic themes.
(
- Contribution to journal › Scientific review
-
Mark
Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia
(
- Contribution to journal › Article
- 2015
-
Mark
The emerging complexity of gene fusions in cancer.
(
- Contribution to journal › Scientific review
-
Mark
Preface to the Fourth Edition
2015)(
- Chapter in Book/Report/Conference proceeding › Foreword/Postscript
-
Mark
How it all began : Cancer cytogenetics before sequencing
2015) p.1-10(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Cytogenetic nomenclature
2015) p.19-25(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Nonrandom chromosome abnormalities in cancer : An overview
2015) p.26-41(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Tumors of the skin
2015) p.555-565(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
A short history of chromosome rearrangements and gene fusions in cancer
2015) p.3-11(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2012
-
Mark
Whole-exome sequencing of pediatric acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Disease-associated patterns of disomic chromosomes in hyperhaploid neoplasms.
(
- Contribution to journal › Article
- 2010
-
Mark
The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias
(
- Contribution to journal › Article
-
Mark
Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis.
(
- Contribution to journal › Article
- 2009
-
Mark
Cancer Chromosomes: From Meaningless Noise to Proof of Principle.
(
- Contribution to journal › Published meeting abstract
- 2008
-
Mark
Molecular screening for new fusion genes in cancer
(
- Contribution to journal › Debate/Note/Editorial
- 2007
-
Mark
Response to letter by the ISCN standing committee
(
- Contribution to journal › Letter
-
Mark
The impact of translocations and gene fusions on cancer causation.
(
- Contribution to journal › Scientific review
- 2006
-
Mark
A gene fusion network in human neoplasia.
(
- Contribution to journal › Article
-
Mark
A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42
(
- Contribution to journal › Article
- 2005
-
Mark
Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Statistical behavior of complex cancer karyotypes.
(
- Contribution to journal › Scientific review
-
Mark
Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders.
(
- Contribution to journal › Article
-
Mark
Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours.
(
- Contribution to journal › Article
-
Mark
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
(
- Contribution to journal › Article
-
Mark
Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations.
(
- Contribution to journal › Article
-
Mark
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations
(
- Contribution to journal › Article
- 2004
-
Mark
High frequencies of chromosomal aberrations in multiple myeloma and monoclonal gammopathy of undetermined significance in direct chromosome preparation.
(
- Contribution to journal › Article
-
Mark
Identification of a commonly amplified 4.3 Mb region with overexpression of the C8FW gene, encoding a phosphoprotein regulated by mitogenic pathways, but not of the MYC gene in MYC-containing double minutes in myeloid malignancies.
(
- Contribution to journal › Article
-
Mark
Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients.
(
- Contribution to journal › Article
-
Mark
Dissecting karyotypic patterns in malignant melanomas: Temporal clustering of losses and gains in melanoma karyotypic evolution.
(
- Contribution to journal › Article
-
Mark
A model for karyotypic evolution in testicular germ cell tumors.
(
- Contribution to journal › Article
-
Mark
Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas.
(
- Contribution to journal › Article
-
Mark
Tumor karyotype predicts clinical outcome in colorectal cancer patients
(
- Contribution to journal › Article
-
Mark
MDS/AML-associated cytogenetic abnormalities in multiple myeloma and monoclonal gammopathy of undetermined significance: Evidence for frequent de novo occurrence and multipotent stem cell involvement of del(20q).
(
- Contribution to journal › Article
-
Mark
The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.
(
- Contribution to journal › Article
-
Mark
MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23).
(
- Contribution to journal › Article
-
Mark
Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia
(
- Contribution to journal › Scientific review
-
Mark
Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.
(
- Contribution to journal › Article
-
Mark
Wilms tumors develop through two distinct karyotypic pathways.
(
- Contribution to journal › Article
-
Mark
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.
(
- Contribution to journal › Article
-
Mark
Statistical dissection of cytogenetic patterns in lung cancer reveals multiple modes of karyotypic evolution independent of histological classification.
(
- Contribution to journal › Article
-
Mark
Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer
(
- Contribution to journal › Article
- 2003
-
Mark
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Genomic characterization of MOZ/CBP and CBP/MOZ chimeras in acute myeloid leukemia suggests the involvement of a damage-repair mechanism in the origin of the t(8;16)(p11;p13).
(
- Contribution to journal › Article
-
Mark
A pooled analysis of karyotypic patterns, breakpoints and imbalances in 783 cytogenetically abnormal multiple myelomas reveals frequently involved chromosome segments as well as significant age- and sex-related differences.
(
- Contribution to journal › Article
-
Mark
Cytogenetic and morphologic subgroups of myelodysplastic syndromes in relation to occupational and hobby exposures.
(
- Contribution to journal › Article
-
Mark
Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13).
(
- Contribution to journal › Article
-
Mark
Clinical and genetic studies of ETV6/ABL1-positive chronic myeloid leukaemia in blast crisis treated with imatinib mesylate.
(
- Contribution to journal › Article
-
Mark
Power law distribution of chromosome aberrations in cancer.
(
- Contribution to journal › Article
-
Mark
Cytogenetic and Molecular Genetic Evolution of Philadelphia-Chromosome-Positive Chronic Myeloid Leukaemia
2003) p.44-61(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Ovarian Carcinoma Develops through Multiple Modes of Chromosomal Evolution.
(
- Contribution to journal › Article
-
Mark
A Novel Gene, MSI2, Encoding a Putative RNA-binding Protein Is Recurrently Rearranged at Disease Progression of Chronic Myeloid Leukemia and Forms a Fusion Gene with HOXA9 as a Result of the Cryptic t(7;17)(p15;q23).
(
- Contribution to journal › Article
- 2002
-
Mark
Cytogenetic and molecular genetic evolution of chronic myeloid leukemia.
(
- Contribution to journal › Scientific review
-
Mark
RT-PCR analysis of acute myeloid leukemia with t(8;16)(p11;p13): Identification of a novel MOZ/CBP transcript and absence of CBP/MOZ expression.
(
- Contribution to journal › Letter
-
Mark
Expression of NUP98/TOP1, but not of TOP1/NUP98, in a treatment-related myelodysplastic syndrome with t(10;20;11)(q24;q11;p15).
(
- Contribution to journal › Article
-
Mark
Unique balanced chromosome abnormalities in treatment-related myelodysplastic syndromes and acute myeloid leukemia: Report from an international workshop
(
- Contribution to journal › Article
-
Mark
Acute myeloid leukemia with inv(16)(p13q22): Involvement of cervical lymph nodes and tonsils is common and may be a negative prognostic sign.
(
- Contribution to journal › Article
-
Mark
Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.
(
- Contribution to journal › Article
-
Mark
Cytogenetic features of multiple myeloma: impact of gender, age, disease phase, culture time, and cytokine stimulation
(
- Contribution to journal › Article
-
Mark
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group
(
- Contribution to journal › Article
-
Mark
Dissecting karyotypic patterns in colorectal tumors: two distinct but overlapping pathways in the adenoma-carcinoma transition.
(
- Contribution to journal › Article
-
Mark
Multivariate analysis of chromosomal imbalances in breast cancer delineates cytogenetic pathways and reveals complex relationships among imbalances.
(
- Contribution to journal › Article
-
Mark
Pooled analysis of clinical and cytogenetic features in treatment-related and de novo adult acute myeloid leukemia and myelodysplastic syndromes based on a consecutive series of 761 patients analyzed 1976-1993 and on 5098 unselected cases reported in the literature 1974-2001.
(
- Contribution to journal › Article
-
Mark
Prognostic implications of BCL6 rearrangement in uniformly treated patients with diffuse large B-cell lymphoma--a Nordic Lymphoma Group study.
(
- Contribution to journal › Article
-
Mark
Coping with complexity. multivariate analysis of tumor karyotypes.
(
- Contribution to journal › Article
-
Mark
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group.
(
- Contribution to journal › Article
- 2001
-
Mark
Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH
(
- Contribution to journal › Article
-
Mark
Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)
(
- Contribution to journal › Article
-
Mark
Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution
(
- Contribution to journal › Article
-
Mark
Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL
(
- Contribution to journal › Article
-
Mark
Isodicentric 7p, idic(7)(q11.2), in acute myeloid
(
- Contribution to journal › Article
-
Mark
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors
(
- Contribution to journal › Article
-
Mark
The prognostic impact of karyotypic subgroups in myelodysplastic syndromes is strongly modified by sex
(
- Contribution to journal › Article
-
Mark
Paired multiplex reverse-transcriptase polymerase chain reaction (PMRT-PCR) analysis as a rapid and accurate diagnostic tool for the detection of MLL fusion genes in hematologic malignancies
(
- Contribution to journal › Article
-
Mark
Are occupational, hobby, or lifestyle exposures associated with Philadelphia chromosome positive chronic myeloid leukaemia?
(
- Contribution to journal › Article
-
Mark
Identification of cytogenetic subgroups and karyotypic pathways in transitional cell carcinoma
(
- Contribution to journal › Article
-
Mark
The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology
(
- Contribution to journal › Article
- 2000
-
Mark
RT-PCR analysis of the MOZ-CBP and CBP-MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13)
(
- Contribution to journal › Article
-
Mark
Granulocytic sarcomas in body cavities in childhood acute myeloid leukemias with 11q23/MLL rearrangements
(
- Contribution to journal › Article
-
Mark
Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias
(
- Contribution to journal › Article
-
Mark
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
(
- Contribution to journal › Article
-
Mark
Survival time in a population-based consecutive series of adult acute myeloid leukemia--the prognostic impact of karyotype during the time period 1976-1993
(
- Contribution to journal › Article
-
Mark
Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p
(
- Contribution to journal › Article
- 1999
-
Mark
A single-center population-based consecutive series of 1500 cytogenetically investigated adult hematological malignancies: karyotypic features in relation to morphology, age and gender
(
- Contribution to journal › Article
-
Mark
Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations
(
- Contribution to journal › Article
-
Mark
Cytogenetic polyclonality in hematologic malignancies
(
- Contribution to journal › Article
-
Mark
Prognostic implications of cytogenetic aberrations in diffuse large B-cell lymphomas
(
- Contribution to journal › Article
-
Mark
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells
(
- Contribution to journal › Article
- 1998
-
Mark
Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization
(
- Contribution to journal › Article
-
Mark
Frequent rearrangements of chromosomes 1, 7, and 8 in primary liver cancer
(
- Contribution to journal › Article