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Gene amplification in neoplasia: A cytogenetic survey of 80 131 cases.
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- Genes, Chromosomes & Cancer, 2024, v. 63, n. 1, p. 1, doi. 10.1002/gcc.23214
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A cloud‐based resource for genome coordinate‐based exploration and large‐scale analysis of chromosome aberrations and gene fusions in cancer.
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- Genes, Chromosomes & Cancer, 2023, v. 62, n. 8, p. 441, doi. 10.1002/gcc.23128
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Giemsa‐negative chromosome bands preferentially recombine in cancer‐associated translocations and gene fusions.
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- Genes, Chromosomes & Cancer, 2023, v. 62, n. 2, p. 61, doi. 10.1002/gcc.23095
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Farewell message from the Editor‐in‐Chief of Genes, Chromosomes & Cancer.
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- Genes, Chromosomes & Cancer, 2020, v. 59, n. 1, p. 3, doi. 10.1002/gcc.22815
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Most gene fusions in cancer are stochastic events.
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- Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 607, doi. 10.1002/gcc.22745
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Cancer chromosome breakpoints cluster in gene‐rich genomic regions.
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- Genes, Chromosomes & Cancer, 2019, v. 58, n. 3, p. 149, doi. 10.1002/gcc.22713
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Gene fusions in soft tissue tumors: Recurrent and overlapping pathogenetic themes.
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- Genes, Chromosomes & Cancer, 2016, v. 55, n. 4, p. 291, doi. 10.1002/gcc.22335
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Disease-associated patterns of disomic chromosomes in hyperhaploid neoplasms.
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- Genes, Chromosomes & Cancer, 2012, v. 51, n. 6, p. 536, doi. 10.1002/gcc.21947
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Response to letter by the ISCN standing committee.
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- Genes, Chromosomes & Cancer, 2007, v. 46, n. 5, p. 516, doi. 10.1002/gcc.20434
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ISCN (2005) is not acceptable for describing clonal evolution in cancer.
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- Genes, Chromosomes & Cancer, 2007, v. 46, n. 3, p. 213, doi. 10.1002/gcc.20414
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Characteristic sequence motifs at the breakpoints of the hybrid genes FUS/CHOP, EWS/CHOP and FUS/ERG in myxoid liposarcoma and acute myeloid leukemia.
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- Oncogene, 1997, v. 15, n. 11, p. 1357, doi. 10.1038/sj.onc.1201281
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Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours.
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- International Journal of Cancer, 2005, v. 116, n. 3, p. 401, doi. 10.1002/ijc.21021
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Dissecting karyotypic patterns in malignant melanomas: Temporal clustering of losses and gains in melanoma karyotypic evolution.
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- International Journal of Cancer, 2004, v. 108, n. 1, p. 57, doi. 10.1002/ijc.11558
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- Article
Different patterns of chromosomal imbalances in metastasising and non-metastasising primary breast carcinomas.
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- International Journal of Cancer, 1999, v. 84, n. 4, p. 370, doi. 10.1002/(SICI)1097-0215(19990820)84:4<370::AID-IJC7>3.0.CO;2-7
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Cytogenetic findings in invasive breast carcinomas with prognostically favourable histology: A less complex karyotypic pattern?
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- International Journal of Cancer, 1998, v. 79, n. 4, p. 361, doi. 10.1002/(SICI)1097-0215(19980821)79:4<361::AID-IJC9>3.0.CO;2-T
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The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias.
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- Human Molecular Genetics, 2010, v. 19, n. 16, p. 3150
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Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies.
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- Human Molecular Genetics, 2004, v. 13, n. 14, p. 1479, doi. 10.1093/hmg/ddh164
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Frequent miRNA-convergent fusion gene events in breast cancer.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01176-1
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Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia.
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- Nature Communications, 2016, v. 7, n. 6, p. 11790, doi. 10.1038/ncomms11790
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Cytogenetic and Molecular Genetic Evolution of Chronic Myeloid Leukemia.
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- Acta Haematologica, 2002, v. 107, n. 2, p. 76, doi. 10.1159/000046636
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Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders.
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- Genes, Chromosomes & Cancer, 2005, v. 43, n. 4, p. 350, doi. 10.1002/gcc.20212
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Statistical behavior of complex cancer karyotypes.
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- Genes, Chromosomes & Cancer, 2005, v. 42, n. 4, p. 327, doi. 10.1002/gcc.20143
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Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia.
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- Genes, Chromosomes & Cancer, 2005, v. 42, n. 2, p. 144, doi. 10.1002/gcc.20133
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MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23).
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 4, p. 400, doi. 10.1002/gcc.20097
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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).
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 223, doi. 10.1002/gcc.20078
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A model for karyotypic evolution in testicular germ cell tumors.
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- Genes, Chromosomes & Cancer, 2004, v. 40, n. 3, p. 172, doi. 10.1002/gcc.20032
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Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas.
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- Genes, Chromosomes & Cancer, 2004, v. 39, n. 3, p. 195, doi. 10.1002/gcc.10314
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Introduction to special issue for Alfred G. Knudson.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 4, p. 285, doi. 10.1002/gcc.10280
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Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13).
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- Genes, Chromosomes & Cancer, 2003, v. 36, n. 1, p. 107, doi. 10.1002/gcc.10139
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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).
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- Genes, Chromosomes & Cancer, 2003, v. 36, n. 1, p. 90, doi. 10.1002/gcc.10137
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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.
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- Genes, Chromosomes & Cancer, 2002, v. 35, n. 4, p. 372, doi. 10.1002/gcc.10131
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Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.
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- Genes, Chromosomes & Cancer, 2002, v. 35, n. 2, p. 127, doi. 10.1002/gcc.10099
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Expression of NUP98/TOP1, but not of TOP1/NUP98, in a treatment-related myelodysplastic syndrome with t(10;20;11)(q24;q11;p15).
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 249, doi. 10.1002/gcc.10066
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Unique balanced chromosome abnormalities in treatment-related myelodysplastic syndromes and acute myeloid leukemia: Report from an International Workshop.
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- Genes, Chromosomes & Cancer, 2002, v. 33, n. 4, p. 413, doi. 10.1002/gcc.10045
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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.
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- Genes, Chromosomes & Cancer, 2001, v. 32, n. 4, p. 302, doi. 10.1002/gcc.1195
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Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 2, p. 156, doi. 10.1002/gcc.1129
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Isodicentric 7p, idic(7)(q11.2), in acute myeloid leukemia associated with older age and favorable response to induction chemotherapy: A new clinical entity?
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- Genes, Chromosomes & Cancer, 2001, v. 30, n. 3, p. 261, doi. 10.1002/1098-2264(2000)9999:9999<::AID-GCC1087>3.0.CO;2-A
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Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH.
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- Genes, Chromosomes & Cancer, 2001, v. 30, n. 2, p. 161, doi. 10.1002/1098-2264(2000)9999:9999<::AID-GCC1077>3.0.CO;2-B
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Karyotypic characterization of urinary bladder transitional cell carcinomas.
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- Genes, Chromosomes & Cancer, 2000, v. 29, n. 3, p. 256, doi. 10.1002/1098-2264(2000)9999:9999<::AID-GCC1034>3.0.CO;2-O
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- Article
RT-PCR analysis of the MOZ-CBP and CBP-MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13).
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- Genes, Chromosomes & Cancer, 2000, v. 28, n. 4, p. 415, doi. 10.1002/1098-2264(200008)28:4<415::AID-GCC7>3.0.CO;2-I
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Granulocytic sarcomas in body cavities in childhood acute myeloid leukemias with 11q23/ MLL rearrangements.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 136, doi. 10.1002/(SICI)1098-2264(200002)27:2<136::AID-GCC4>3.0.CO;2-9
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Cytogenetic analysis of 363 consecutively ascertained diffuse large B-cell lymphomas.
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- Genes, Chromosomes & Cancer, 1999, v. 25, n. 2, p. 123, doi. 10.1002/(SICI)1098-2264(199906)25:2<123::AID-GCC8>3.0.CO;2-4
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Cytogenetic polyclonality in hematologic malignancies.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 222, doi. 10.1002/(SICI)1098-2264(199903)24:3<222::AID-GCC7>3.0.CO;2-A
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Cytogenetic analysis of pancreatic carcinomas: Intratumor heterogeneity and nonrandom pattern of chromosome aberrations.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 81, doi. 10.1002/(SICI)1098-2264(199810)23:2<81::AID-GCC1>3.0.CO;2-0
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Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 3, p. 203, doi. 10.1002/(SICI)1098-2264(199811)23:3<203::AID-GCC1>3.0.CO;2-5
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Frequent rearrangements of chromosomes 1, 7, and 8 in primary liver cancer.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 26, doi. 10.1002/(SICI)1098-2264(199809)23:1<26::AID-GCC5>3.0.CO;2-8
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FISH characterization of head and neck carcinomas reveals that amplification of band 11q13 is associated with deletion of distal 11q.
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- Genes, Chromosomes & Cancer, 1998, v. 22, n. 4, p. 312, doi. 10.1002/(SICI)1098-2264(199808)22:4<312::AID-GCC7>3.0.CO;2-Y
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Cytogenetic comparison of primary tumors and lymph node metastases in breast cancer patients.
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- Genes, Chromosomes & Cancer, 1998, v. 22, n. 2, p. 122, doi. 10.1002/(SICI)1098-2264(199806)22:2<122::AID-GCC6>3.0.CO;2-Z
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Cytogenetic analysis of 46 pleomorphic soft tissue sarcomas and correlation with morphologic and clinical features: A report of the CHAMP study group.
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- Genes, Chromosomes & Cancer, 1998, v. 22, n. 1, p. 16, doi. 10.1002/(SICI)1098-2264(199805)22:1<16::AID-GCC3>3.0.CO;2-A
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Cytogenetic and fluorescence in situ hybridization analyses of chromosome 19 aberrations in pancreatic carcinomas: Frequent loss of 19p13.3 and gain of 19q13.1-13.2.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 8, doi. 10.1002/(SICI)1098-2264(199801)21:1<8::AID-GCC3>3.0.CO;2-5
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