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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
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Mark
Insertion of the CXXC domain of KMT2A into YAP1 : An unusual mechanism behind the formation of a chimeric oncogenic protein
(
- Contribution to journal › Article
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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
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Mark
Giemsa-negative chromosome bands preferentially recombine in cancer-associated translocations and gene fusions
(
- Contribution to journal › Article
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Mark
A cryptic EWSR1::DDIT3 fusion in myxoid liposarcoma: Potential pitfalls with FISH and cytogenetics
(
- Contribution to journal › Article
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Mark
Inactivation of RB1, CDKN2A and TP53 have distinct effects on genomic stability at side-by-side comparison in karyotypically normal cells
(
- Contribution to journal › Article
- 2022
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Mark
Amplification of ERBB2 (HER2) in embryonal rhabdomyosarcoma : A potential treatment target in rare cases?
(
- Contribution to journal › Article
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Mark
N-terminus DUX4-immunohistochemistry is a reliable methodology for the diagnosis of DUX4-fused B-lymphoblastic leukemia/lymphoma (N-terminus DUX4 IHC for DUX4-fused B-ALL)
(
- Contribution to journal › Article
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Mark
Merged testing for colorectal cancer syndromes and re-evaluation of genetic variants improve diagnostic yield : Results from a nationwide prospective cohort
(
- Contribution to journal › Article
- 2021
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Mark
Sister chromatid cohesion defects are associated with chromosomal copy number heterogeneity in high hyperdiploid childhood acute lymphoblastic leukemia
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- Contribution to journal › Article
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Mark
Clinical and genomic characterization of patients diagnosed with the provisional entity Acute myeloid leukemia with BCR-ABL1, a Swedish population-based study
(
- Contribution to journal › Article
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Mark
Single-cell sequencing in translational cancer research and challenges to meet clinical diagnostic needs
(
- Contribution to journal › Scientific review
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Mark
Genomic and transcriptomic characterization of desmoplastic small round cell tumors
(
- Contribution to journal › Article
- 2020
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Mark
Farewell message from the Editor-in-Chief of Genes, Chromosomes & Cancer
(
- Contribution to journal › Debate/Note/Editorial
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Mark
SFPQ-ABL1-positive B-cell precursor acute lymphoblastic leukemias
2020) In Genes, Chromosomes and Cancer(
- Contribution to journal › Letter
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Mark
Deep sequencing of myxoinflammatory fibroblastic sarcoma
(
- Contribution to journal › Article
- 2019
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Mark
Clonal evolution through genetic bottlenecks and telomere attrition : Potential threats to in vitro data reproducibility
(
- Contribution to journal › Scientific review
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Mark
Cancer chromosome breakpoints cluster in gene-rich genomic regions
(
- Contribution to journal › Article
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Mark
Most gene fusions in cancer are stochastic events
(
- Contribution to journal › Article
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Mark
Genetic profiling of a chondroblastoma-like osteosarcoma/malignant phosphaturic mesenchymal tumor of bone reveals a homozygous deletion of CDKN2A, intragenic deletion of DMD, and a targetable FN1-FGFR1 gene fusion
(
- Contribution to journal › Article
- 2018
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Mark
A field guide for cancer diagnostics using cell-free DNA : From principles to practice and clinical applications
(
- Contribution to journal › Scientific review
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Mark
Improved cytogenetic characterization and risk stratification of pediatric acute lymphoblastic leukemia using single nucleotide polymorphism array analysis : A single center experience of 296 cases
(
- Contribution to journal › Article
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Mark
Telomere length, telomerase reverse transcriptase promoter mutations, and melanoma risk
(
- Contribution to journal › Article
- 2017
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Mark
Pediatric T-cell acute lymphoblastic leukemia
(
- Contribution to journal › Scientific review
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Mark
Soft tissue angiofibroma : Clinicopathologic, immunohistochemical and molecular analysis of 14 cases
(
- Contribution to journal › Article
- 2016
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Mark
BCOR internal tandem duplication and YWHAE-NUTM2B/E fusion are mutually exclusive events in clear cell sarcoma of the kidney.
(
- Contribution to journal › Article
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Mark
Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis.
(
- Contribution to journal › Article
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Mark
Gene fusions in soft tissue tumors: Recurrent and overlapping pathogenetic themes.
(
- Contribution to journal › Scientific review
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Mark
Patterns and Frequencies of Acquired and Constitutional Uniparental Isodisomies in Pediatric and Adult B-Cell Precursor Acute Lymphoblastic Leukemia.
(
- Contribution to journal › Article
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Mark
Trisomy 8 in pediatric acute myeloid leukemia : A NOPHO-AML study
(
- Contribution to journal › Article
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Mark
Genomic profiling and directed ex vivo drug analysis of an unclassifiable myelodysplastic/myeloproliferative neoplasm progressing into acute myeloid leukemia
(
- Contribution to journal › Article
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Mark
Improved minimal residual disease detection by targeted quantitative polymerase chain reaction in Nucleophosmin 1 type a mutated acute myeloid leukemia
(
- Contribution to journal › Article
- 2015
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Mark
Impact of a paternal origin of germline BRCA1/2 mutations on the age at breast and ovarian cancer diagnosis in a Southern Swedish cohort.
(
- Contribution to journal › Article
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Mark
Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas.
(
- Contribution to journal › Article
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Mark
Cooperative genetic changes in pediatric B-cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1.
(
- Contribution to journal › Article
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Mark
Telomere length in circulating lymphocytes: Association with chromosomal aberrations.
(
- Contribution to journal › Letter
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Mark
A Population-Based Single Nucleotide Polymorphism Array Analysis of Genomic Aberrations in Younger Adult Acute Lymphoblastic Leukemia Patients
(
- Contribution to journal › Article
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Mark
Metabolic gene variants associated with chromosomal aberrations in healthy humans.
(
- Contribution to journal › Article
- 2014
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Mark
Confined trisomy 8 mosaicism of meiotic origin: A rare cause of aneuploidy in childhood cancer.
(
- Contribution to journal › Article
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Mark
Clear cell sarcoma of the kidney demonstrates an embryonic signature indicative of a primitive nephrogenic origin.
(
- Contribution to journal › Article
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Mark
Exomic analysis of myxoid liposarcomas, synovial sarcomas, and osteosarcomas
(
- Contribution to journal › Article
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Mark
Ploidy and clinical characteristics of childhood acute myeloid leukemia: A NOPHO-AML study
(
- Contribution to journal › Article
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Mark
Amplification of 2p as a genomic marker for transformation in lymphoma
(
- Contribution to journal › Article
- 2013
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Mark
Submicroscopic genomic imbalances in burkitt lymphomas/leukemias: Association with age and further evidence that 8q24/MYC translocations are not sufficient for leukemogenesis.
(
- Contribution to journal › Article
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Mark
Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor.
(
- Contribution to journal › Article
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Mark
Histological specificity of alterations and expression of KIT and KITLG in non-small cell lung carcinoma.
(
- Contribution to journal › Article
- 2012
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Mark
Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data
(
- Contribution to journal › Article
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Mark
Amplification and overexpression of the ABCC3 (MRP3) gene in primary breast cancer
(
- Contribution to journal › Article
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Mark
Copy Number Defects of G1-Cell Cycle Genes in Neuroblastoma are Frequent and Correlate with High Expression of E2F Target Genes and a Poor Prognosis
(
- Contribution to journal › Article
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Mark
Telomere length and LINE1 methylation is associated with chromosomal aberrations in peripheral blood.
2012) In Genes, Chromosomes and Cancer(
- Contribution to journal › Article