Fluorescence in situ hybridization evaluation of chromosome deletion patterns in prostate cancer.

A Cell Cycle Regulator Potentially Involved in Genesis of Many Tumor Types

1994 • 2,821 citations

High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid Clones

1990 • 1,357 citations

The FHIT Gene, Spanning the Chromosome 3p14.2 Fragile Site and Renal Carcinoma–Associated t(3;8) Breakpoint, Is Abnormal in Digestive Tract Cancers

1996 • 1,008 citations

An STS-Based Map of the Human Genome

1995 • 782 citations

The FHIT Gene at 3p14.2 Is Abnormal in Lung Cancer

1996 • 547 citations

Genetic changes in primary and recurrent prostate cancer by comparative genomic hybridization.

1995 • 490 citations

In situ hybridization as a tool to study numerical chromosome aberrations in solid bladder tumors

1988 • 462 citations

Allelic loss of chromosomes 16q and 10q in human prostate cancer.

1990 • 456 citations

A first-generation physical map of the human genome

1993 • 446 citations

Homozygous deletion and frequent allelic loss of chromosome 8p22 loci in human prostate cancer.

1993 • 364 citations

Allelic loss on chromosome 8p12-21 in microdissected prostatic intraepithelial neoplasia.

1995 • 289 citations

Deletion mapping of chromosomes 8, 10, and 16 in human prostatic carcinoma

1991 • 286 citations

Loss of heterozygosity for loci on the long arm of chromosome 6 in human malignant melanoma.

1991 • 233 citations

Chromosome analysis of 97 primary breast carcinomas: Identification of eight karyotypic subgroups

1995 • 203 citations

Comparative genomic hybridization, allelic imbalance, and fluorescence in situ hybridization on chromosome 8 in prostate cancer

1994 • 195 citations

Loss of chromosome arm 8p loci in prostate cancer: Mapping by quantitative allelic imbalance

1994 • 187 citations

Molecular genetic analysis of chromosome 22 in 81 cases of meningioma.

1990 • 173 citations

Frequency and pattern of karyotypic abnormalities in human prostate cancer.

1990 • 172 citations

Evidence for three tumor suppressor gene loci on chromosome 8p in human prostate cancer.

1995 • 171 citations

Allelic loss in locally metastatic, multisampled prostate cancer.

1994 • 170 citations

Cytogenetic analysis of 57 primary prostatic adenocarcinomas

1992 • 169 citations

Codeletion of p15 and p16 in primary malignant mesothelioma.

1995 • 165 citations

Recurrent deletions of specific chromosomal sites in 1p, 3p, 6q, and 9p in human malignant mesothelioma.

1993 • 163 citations

Potential markers of prostate cancer aggressiveness detected by fluorescence in situ hybridization in needle biopsies.

1994 • 146 citations

Aneuploidy and aneusomy of chromosome 7 detected by fluorescence in situ hybridization are markers of poor prognosis in prostate cancer.

1994 • 138 citations

Loss of heterozygosity of chromosome 8 microsatellite loci implicates a candidate tumor suppressor gene between the loci D8S87 and D8S133 in human prostate cancer.

1994 • 135 citations

Frequent allelic losses on chromosomes 2q, 18q, and 22q in advanced non-small cell lung carcinoma.

1994 • 133 citations

Mapping of chromosomal gains and losses in prostate cancer by comparative genomic hybridization

1995 • 129 citations

Chromosomal abnormalities and related events in prostate cancer

1992 • 120 citations

Fluorescence in situ hybridization analysis of 8p allelic loss and chromosome 8 instability in human prostate cancer.

1994 • 118 citations

The MTS1 gene is frequently mutated in primary human esophageal tumors.

1994 • 112 citations

A genetic model of melanoma tumorigenesis based on allelic losses

1995 • 99 citations

Recurring loss involving chromosomes 1, 3, and 22 in malignant mesothelioma: Possible sites of tumor suppressor genes

1989 • 99 citations

Homozygous deletion on chromosome 9p and loss of heterozygosity on 9q, 6p, and 6q in primary human small cell lung cancer

1994 • 97 citations

Sensitive detection of chromosome copy number aberrations in prostate cancer by fluorescence in situ hybridization.

1994 • 89 citations

Metaphase and interphase cytogenetics with Alu-PCR-amplified yeast artificial chromosome clones containing the BCR gene and the protooncogenes c-raf-1, c-fms, and c-erbB-2.

1992 • 80 citations

Extensive genetic alterations in prostate cancer revealed by dual PCR and FISH analysis

1993 • 79 citations

Proximal 6q, a region showing allele loss in primary breast cancer

1995 • 78 citations

Cytogenetic aberrations in osteosarcomas

1994 • 76 citations

Deletion mapping of chromosome 8p in prostate cancer by fluorescence in situ hybridization.

1994 • 72 citations

Trisomy 12 in pediatric granulosa-stromal cell tumors. Demonstration by a modified method of fluorescence in situ hybridization on paraffin-embedded material.

1992 • 70 citations

Common region of deletion on the long arm of chromosome 6 in non‐Hodgkin's lymphoma and acute lymphoblastic leukaemia

1994 • 67 citations

Defining the extent and nature of cytogenetic events in prostatic adenocarcinoma: Paraffin FISH vs. metaphase analysis

1993 • 56 citations

Chromosome 1 abnormalities in cervical carcinoma

1988 • 56 citations

Analysis of prostatic tumor cultures using fluorescence in-situ hybridization (FISH)

1992 • 55 citations

Analysis of the NF2 tumor‐suppressor gene and of chromosome 22 deletions in gliomas

1995 • 51 citations

Structural chromosome 1 aberrations in transitional cell carcinoma of the bladder: interphase cytogenetics combining a centromeric, telomeric, and library DNA probe.

1992 • 50 citations

Novel fluorescence in situ hybridization approaches in solid tumors. Characterization of frozen specimens, touch preparations, and cytological preparations.

1995 • 50 citations

Tissue culture loss of aneuploid cells from carcinomas of the prostate

1993 • 48 citations

Aneusomy of chromosomes 7 and 17 detected by fish in prostate cancer and the effects of selection in vitro

1994 • 46 citations

Evaluation of 20 archival prostate tumor specimens by fluorescence in situ hybridization (FISH)

1994 • 45 citations