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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
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Mark
Constitutional and acquired genetic variants in ARID5B in pediatric B-cell precursor acute lymphoblastic leukemia
(
- Contribution to journal › Article
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Mark
TLE3 Is a Novel Fusion Partner of JAK2 in Myeloid/Lymphoid Neoplasm With Eosinophilia Responding to JAK2 Inhibition
(
- Contribution to journal › Article
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Mark
Loss of Chromosome Y in Neuroblastoma Is Associated With High-Risk Disease, 11q-Deletion, and Telomere Maintenance
(
- Contribution to journal › Article
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Mark
Precision Diagnostics in Myeloid Malignancies : Development and Validation of a National Capture-Based Gene Panel
(
- 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 cryptic EWSR1::DDIT3 fusion in myxoid liposarcoma: Potential pitfalls with FISH and cytogenetics
(
- 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
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
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Mark
Giemsa-negative chromosome bands preferentially recombine in cancer-associated translocations and gene fusions
(
- 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
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
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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
- 2021
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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
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Mark
Sister chromatid cohesion defects are associated with chromosomal copy number heterogeneity in high hyperdiploid childhood acute lymphoblastic leukemia
(
- Contribution to journal › Article
- 2020
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Mark
Deep sequencing of myxoinflammatory fibroblastic sarcoma
(
- Contribution to journal › Article
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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
- 2019
-
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
Most gene fusions in cancer are stochastic events
(
- Contribution to journal › Article
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Mark
Cancer chromosome breakpoints cluster in gene-rich genomic regions
(
- 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
Telomere length, telomerase reverse transcriptase promoter mutations, and melanoma risk
(
- Contribution to journal › Article
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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
A field guide for cancer diagnostics using cell-free DNA : From principles to practice and clinical applications
(
- Contribution to journal › Scientific review
- 2017
-
Mark
Soft tissue angiofibroma : Clinicopathologic, immunohistochemical and molecular analysis of 14 cases
(
- Contribution to journal › Article
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Mark
Pediatric T-cell acute lymphoblastic leukemia
(
- Contribution to journal › Scientific review
- 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
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
Trisomy 8 in pediatric acute myeloid leukemia : A NOPHO-AML study
(
- 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
-
Mark
Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas.
(
- Contribution to journal › Article
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Mark
Metabolic gene variants associated with chromosomal aberrations in healthy humans.
(
- Contribution to journal › Article
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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
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
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
Telomere length in circulating lymphocytes: Association with chromosomal aberrations.
(
- Contribution to journal › Letter
- 2014
-
Mark
Ploidy and clinical characteristics of childhood acute myeloid leukemia: A NOPHO-AML study
(
- Contribution to journal › Article
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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
Exomic analysis of myxoid liposarcomas, synovial sarcomas, and osteosarcomas
(
- Contribution to journal › Article
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Mark
Amplification of 2p as a genomic marker for transformation in lymphoma
(
- Contribution to journal › Article
-
Mark
Clear cell sarcoma of the kidney demonstrates an embryonic signature indicative of a primitive nephrogenic origin.
(
- Contribution to journal › Article
- 2013
-
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
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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
- 2012
-
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
-
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
-
Mark
Amplification and overexpression of the ABCC3 (MRP3) gene in primary breast cancer
(
- Contribution to journal › Article
-
Mark
Telomere length and LINE1 methylation is associated with chromosomal aberrations in peripheral blood.
2012) In Genes, Chromosomes and Cancer(
- Contribution to journal › Article
-
Mark
Disease-associated patterns of disomic chromosomes in hyperhaploid neoplasms.
(
- Contribution to journal › Article
-
Mark
A novel GTF2I/NCOA2 fusion gene emphasizes the role of NCOA2 in soft tissue angiofibroma development.
2012) In Genes, Chromosomes and Cancer(
- Contribution to journal › Letter
-
Mark
High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.
(
- Contribution to journal › Article
-
Mark
Increased gene copy number of KIT and VEGFR2 at 4q12 in primary breast cancer is related to an aggressive phenotype and impaired prognosis.
(
- Contribution to journal › Article
-
Mark
Fusion of the AHRR and NCOA2 genes through a recurrent translocation t(5;8)(p15;q13) in soft tissue angiofibroma results in upregulation of aryl hydrocarbon receptor target genes.
(
- Contribution to journal › Article
- 2011
-
Mark
Prognostic Value of SOX2 Expression in Neuroblastoma
(
- Contribution to journal › Letter
-
Mark
Fusion Gene Microarray Reveals Cancer Type-Specificity Among Fusion Genes
(
- Contribution to journal › Article
-
Mark
Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion.
(
- Contribution to journal › Article
-
Mark
High-resolution genomic screening in mantle cell lymphoma--specific changes correlate with genomic complexity, the proliferation signature and survival.
(
- Contribution to journal › Article
-
Mark
Alternative lengthening of telomeres-An enhanced chromosomal instability in aggressive non-MYCN amplified and telomere elongated neuroblastomas.
(
- Contribution to journal › Article
- 2010
-
Mark
Polymorphisms in the Transforming Growth Factor Beta 1 Pathway in Relation to Colorectal Cancer Progression
(
- Contribution to journal › Article
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Mark
Genomic alterations in histopathologically normal breast tissue from BRCA1 mutation carriers may be caused by BRCA1 haploinsufficiency.
(
- Contribution to journal › Article
- 2009
-
Mark
t(19;22)(q13;q12) Translocation Leading to the Novel Fusion Gene EWSRI-ZNF444 in Soft Tissue Myoepithelial Carcinoma
(
- Contribution to journal › Article
-
Mark
Cytogenetic Analysis of 101 Giant Cell Tumors of Bone: Nonrandom Patterns of Telomeric Associations and Other Structural Aberrations
(
- Contribution to journal › Article
-
Mark
Characterization of a Hotspot Region on Chromosome 12 for Amplification in Ring Chromosomes in Atypical Lipomatous Tumors
(
- Contribution to journal › Article
-
Mark
High hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
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Mark
Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: Rare T-cell receptor gene rearrangements are associated with poor outcome.
(
- Contribution to journal › Article
-
Mark
No Genomic Aberrations in Langerhans Cell Histiocytosis as Assessed by Diverse Molecular Technologies
(
- Contribution to journal › Article
- 2008
-
Mark
Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-Cell precursor acute lymphoblastic leukemias: A nordic series of 24 cases and review of the literature
(
- Contribution to journal › Scientific review
-
Mark
Gene expression analysis of BCR/ABL1-dependent transcriptional response reveals enrichment for genes involved in negative feedback regulation.
(
- Contribution to journal › Article
-
Mark
Molecular identification of COL6A3-CSF1 fusion transcripts in tenosynovial giant cell tumors
(
- Contribution to journal › Article
-
Mark
Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia-A comparative study of four differently designed, high resolution microarray platforms.
(
- Contribution to journal › Article
-
Mark
Detection of a t(1;22)(q23;q 12) translocation leading to an EWSR1-PBX1 fusion gene in a myoepithelioma
(
- Contribution to journal › Article
-
Mark
A PCR/restriction digestion assay for the detection of the transcript variants 1 and 2 of POU5F1.
(
- Contribution to journal › Article
-
Mark
High-resolution molecular cytogenetic analysis of Wilms tumors highlights diagnostic difficulties among small round cell kidney tumors.
(
- Contribution to journal › Article
-
Mark
Identification of a novel and myeloid specific role of the leukemia-associated fusion protein DEK-NUP214 leading to increased protein synthesis.
(
- Contribution to journal › Article
-
Mark
Promoter analysis of epigenetically controlled genes in bladder cancer.
(
- Contribution to journal › Article
-
Mark
FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns.
(
- Contribution to journal › Article
- 2007
-
Mark
High-resolution genomic profiles of breast cancer cell lines assessed by tiling BAC array comparative genomic hybridization.
(
- Contribution to journal › Article
-
Mark
Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature
(
- Contribution to journal › Scientific review
-
Mark
Proposals for standardized Protocols for cytogenetic analyses of acute leukemias, chronic lymphocytic leukemia, chronic myeloid leukemia, chronic myeloproliferative disorders, and myelodysplastic syndromes
(
- Contribution to journal › Article
-
Mark
Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera
(
- Contribution to journal › Article
-
Mark
Response to letter by the ISCN standing committee
(
- Contribution to journal › Letter
-
Mark
Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype
(
- Contribution to journal › Article
-
Mark
Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome.
(
- Contribution to journal › Article
- 2006
-
Mark
Translocation-excision-deletion-amplification mechanism leading to nonsyntenic coamplification of MYC and ATBF1
(
- Contribution to journal › Article
-
Mark
Confirmation of the high frequency of the TMPRSS2/ERG fusion gene in prostate cancer.
(
- Contribution to journal › Letter
- 2005
-
Mark
Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma
(
- Contribution to journal › Article
-
Mark
Intratumor versus intertumor heterogeneity in gene expression profiles of soft-tissue sarcomas.
(
- Contribution to journal › Article
-
Mark
Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders.
(
- Contribution to journal › Article
-
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
Clear cell hidradenoma of the skin - a third tumor type with a t(11;19)-associated TORC1-MAML2 gene fusion
(
- Contribution to journal › Article
-
Mark
Telomere-mediated mitotic disturbances in immortalized ovarian epithelial cells reproduce chromosomal losses and breakpoints from ovarian carcinoma
(
- Contribution to journal › Article