Molecular cytometry of cancer.

[1]  C. Cohen.  Image cytometric analysis in pathology. , 1996, Human pathology.

[2]  F. Waldman,et al.  Fluorescence in situ hybridization for detecting erbB-2 amplification in breast tumor fine needle aspiration biopsies. , 1996, Acta cytologica.

[3]  S. Hilsenbeck,et al.  Genetic aberrations detected by comparative genomic hybridization predict outcome in node-negative breast cancer. , 1995, The American journal of pathology.

[4]  F. Waldman,et al.  Autofluorescence correction for fluorescence in situ hybridization. , 1995, Cytometry.

[5]  D. Pinkel,et al.  Karyotypic heterogeneity and its relation to labeling index in interphase breast tumor cells. , 1995, Cytometry.

[6]  Joe W. Gray,et al.  Interactive algorithms for rapid enumeration of hybridization signals in individual whole-cell nuclei inside intact-tissue specimens , 1995, Electronic Imaging.

[7]  S. Devries,et al.  Identification of gains and losses of DNA sequences in primary bladder cancer by comparative genomic hybridization , 1995, Genes, chromosomes & cancer.

[8]  S. Devries,et al.  Analysis of changes in DNA sequence copy number by comparative genomic hybridization in archival paraffin-embedded tumor samples. , 1994, The American journal of pathology.

[9]  A. Nagler,et al.  Detection of minimal residual disease state in chronic myelogenous leukemia patients using fluorescence in situ hybridization. , 1994, Cancer genetics and cytogenetics.

[10]  E. Bergstralh,et al.  Aneuploidy and aneusomy of chromosome 7 detected by fluorescence in situ hybridization are markers of poor prognosis in prostate cancer. , 1994, Cancer research.

[11]  J Piper,et al.  Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors , 1994, Genes, chromosomes & cancer.

[12]  A D Carothers,et al.  Counting, measuring, and mapping in FISH-labelled cells: sample size considerations and implications for automation. , 1994, Cytometry.

[13]  M R Speicher,et al.  Chromosomal gains and losses in uveal melanomas detected by comparative genomic hybridization. , 1994, Cancer research.

[14]  E. Speel,et al.  Combined immunocytochemistry and fluorescence in situ hybridization for simultaneous tricolor detection of cell cycle, genomic, and phenotypic parameters of tumor cells. , 1994, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[15]  R. Chaganti,et al.  Genetic changes in epithelial solid neoplasia. , 1994, Cancer research.

[16]  J. Katzmann,et al.  Comparison of fluorescence in situ hybridization with flow cytometry and static image analysis in ploidy analysis of paraffin-embedded prostate adenocarcinoma. , 1994, Human pathology.

[17]  G. Hortobagyi,et al.  Quantitative analysis of chromosome in situ hybridization signal in paraffin-embedded tissue sections. , 1994, Cytometry.

[18]  S. Wolman.  Fluorescence in situ hybridization: a new tool for the pathologist. , 1994, Human pathology.

[19]  Amir Waks,et al.  Multidisciplinary approach for detecting subcellular objects in low level light fluorescence microscopy , 1994, Electronic Imaging.

[20]  J. Piper,et al.  Automatic fluorescence metaphase finder speeds translocation scoring in FISH painted chromosomes. , 1994, Cytometry.

[21]  S. Knuutila,et al.  Detection of minimal residual disease using fluorescence DNA in situ hybridization: a follow-up study in leukemia and lymphoma patients. , 1994, Leukemia.

[22]  P. Carroll,et al.  Physical deletion of the p53 gene in bladder cancer. Detection by fluorescence in situ hybridization. , 1994, The American journal of pathology.

[23]  J W Gray,et al.  Thick-section fluorescence in situ hybridization on formalin-fixed, paraffin-embedded archival tissue provides a histogenetic profile. , 1994, The American journal of pathology.

[24]  P. Troncoso,et al.  Trisomy 7: A potential cytogenetic marker of human prostate cancer progression , 1994, Genes, chromosomes & cancer.

[25]  W. Hong,et al.  Increased polysomies of chromosomes 7 and 17 during head and neck multistage tumorigenesis. , 1993, Cancer research.

[26]  R. Cajulis,et al.  Detection of numerical chromosomal abnormalities in malignant cells in fine needle aspirates by fluorescence in situ hybridization of interphase cell nuclei with chromosome-specific probes. , 1993, Acta cytologica.

[27]  D. Schlessinger,et al.  Chromosomal bar codes produced by multicolor fluorescence in situ hybridization with multiple YAC clones and whole chromosome painting probes. , 1993, Human molecular genetics.

[28]  J. Stone,et al.  FISH: a useful technique in the verification of clonality of random chromosome abnormalities. , 1993, Cancer genetics and cytogenetics.

[29]  F. Ramaekers,et al.  Detection of Genetic Aberrations in Bladder Cancer Using in Situ Hybridization a , 1993, Annals of the New York Academy of Sciences.

[30]  L L Wheeless,et al.  The Clinical Utility of DNA Cytometry , 1993, Annals of the New York Academy of Sciences.

[31]  J. Anastasi.  Fluorescence in Situ Hybridization in Leukemia , 1993 .

[32]  D Rutovitz,et al.  Comparative genomic hybridization: a rapid new method for detecting and mapping DNA amplification in tumors. , 1993, Seminars in cancer biology.

[33]  D. Pinkel,et al.  Molecular cytogenetics: diagnosis and prognostic assessment. , 1992, Current opinion in biotechnology.

[34]  R. Cajulis,et al.  Detection of numerical chromosomal abnormalities in malignant cells on body fluids by fluorescence in situ hybridization of interphase cell nuclei with chromosome‐specific probes , 1992, Diagnostic cytopathology.

[35]  D. Pinkel,et al.  Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors , 2022 .

[36]  Z Chen,et al.  Application of fluorescence in situ hybridization in hematological disorders. , 1992, Cancer genetics and cytogenetics.

[37]  F. Mitelman,et al.  Cytogenetic analysis in the diagnosis of acute leukemia , 1992, Cancer.

[38]  D J Schaid,et al.  Fluorescence in situ hybridization: a sensitive method for trisomy 8 detection in bone marrow specimens. , 1992, Blood.

[39]  D. Pinkel,et al.  Deletion of chromosome 17p loci in breast cancer cells detected by fluorescence in situ hybridization. , 1992, Cancer research.

[40]  D. Ruiter,et al.  In situ detection of supernumerary aberrations of chromosome-specific repetitive DNA targets in interphase nuclei in human melanoma cell lines and tissue sections. , 1992, The Journal of investigative dermatology.

[41]  B H Mayall,et al.  Centromeric copy number of chromosome 7 is strongly correlated with tumor grade and labeling index in human bladder cancer. , 1991, Cancer research.

[42]  M. L. Le Beau,et al.  Direct correlation of cytogenetic findings with cell morphology using in situ hybridization: an analysis of suspicious cells in bone marrow specimens of two patients completing therapy for acute lymphoblastic leukemia. , 1991, Blood.

[43]  F. Ramaekers,et al.  Detection of numerical chromosome aberrations using in situ hybridization in paraffin sections of routinely processed bladder cancers. , 1991, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

[44]  A. Sandberg.  Chromosome abnormalities in human cancer and leukemia. , 1991, Mutation research.

[45]  J. Rowley.  Molecular cytogenetics: Rosetta stone for understanding cancer--twenty-ninth G. H. A. Clowes memorial award lecture. , 1990, Cancer research.

[46]  Y. Nakamura,et al.  Genetic alterations during colorectal-tumor development. , 1988, The New England journal of medicine.

[47]  F. Waldman,et al.  Molecular Cytogenetics of Solid Tumor Progression , 1996 .

[48]  M R Speicher,et al.  Quantitative analysis of comparative genomic hybridization. , 1995, Cytometry.

[49]  P. Lichter,et al.  Image analysis in comparative genomic hybridization. , 1995, Cytometry.

[50]  D Rutovitz,et al.  Computer image analysis of comparative genomic hybridization. , 1995, Cytometry.

[51]  T. Raap.  Editorial: Cytometry for CGH , 1995 .

[52]  J. M. García-Sagredo,et al.  Hardware and software requirements for quantitative analysis of comparative genomic hybridization. , 1995, Cytometry.

[53]  D. Visscher,et al.  Chromosomal aneuploidy in proliferative breast disease. , 1994, Human pathology.

[54]  P. Sanseau,et al.  Two simple procedures for releasing chromatin from routinely fixed cells for fluorescence in situ hybridization. , 1994, Cytogenetics and cell genetics.

[55]  H. Döhner,et al.  Fluorescence in situ hybridization in leukemias: 'the FISH are spawning!'. , 1994, Leukemia.

[56]  F. Patrone,et al.  Trisomy 8 detection in Ph+ CML patients using conventional cytogenetic and interphase fluorescence in situ hybridization techniques. , 1994, Cancer genetics and cytogenetics.

[57]  J. Stone,et al.  Identification of complex t(15;17) in APL by FISH. , 1994, Cancer genetics and cytogenetics.

[58]  A. Jauch,et al.  Copyright ©) American Society for Investigative Pathology Comparative Genomic Hybridization of Human Malignant Gliomas Reveals Multiple Amplification Sites and Nonrandom Chromosomal Gains and Losses , 2022 .

[59]  T Takahashi,et al.  Prognostic significance of p53 mutations and 3p deletions in primary resected non-small cell lung cancer. , 1993, Cancer research.

[60]  J. Gray,et al.  Molecular cytogenetics: solid tumors and leukemia. , 1993, Blood cells.

[61]  W. Hittelman,et al.  Interphase cytogenetics in paraffin sections of lung tumors by non-isotopic in situ hybridization. Mapping genotype/phenotype heterogeneity. , 1993, The American journal of pathology.

[62]  H. Kantarjian,et al.  Detection of residual proliferating leukemic cells by fluorescence in situ hybridization in CML patients in complete remission after interferon treatment. , 1993, Leukemia.

[63]  F. Ramaekers,et al.  Chromosome detection by in situ hybridization in cancer cell populations which were flow cytometrically sorted after immunolabeling. , 1992, Cytometry.

[64]  J Vrolijk,et al.  Fluorescence ratio measurements of double-labeled probes for multiple in situ hybridization by digital imaging microscopy. , 1992, Cytometry.