Identification and characterization of a novel member of the EXT gene family, EXTL2.

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1987 • 2,333 citations

The multistep nature of cancer

1993 • 1,872 citations

[27] Local alignment statistics

1996 • 729 citations

Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse

1993 • 664 citations

The natural history of hereditary multiple exostoses.

1994 • 593 citations

Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)

1995 • 421 citations

A YAC contig map of the human genome.

1995 • 333 citations

The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes

1996 • 331 citations

Mapping the Gene for Hereditary Cutaneous Malignant Melanoma–Dysplastic Nevus to Chromosome Lp

1989 • 320 citations

Hereditary multiple exostoses.

1991 • 305 citations

Maximum Discrimination Hidden Markov Models of Sequence Consensus

1995 • 248 citations

A gene for hereditary multiple exostoses maps to chromosome 19p

1994 • 211 citations

Positional cloning of a gene involved in hereditary multiple exostoses

1996 • 200 citations

Genetic heterogeneity in families with hereditary multiple exostoses.

1993 • 197 citations

Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8.

1995 • 194 citations

HEREDITARY MULTIPLE EXOSTOSIS.

1964 • 164 citations

Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11

1994 • 162 citations

Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family.

1997 • 147 citations

Evidence for two tumour suppressor loci on chromosomal bands 1p35–36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification

1995 • 143 citations

Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11.

1995 • 138 citations

Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies.

1997 • 128 citations

Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas.

1994 • 122 citations

Biologic and clinical significance of cytogenetic and molecular cytogenetic abnormalities in benign and malignant cartilaginous lesions

1993 • 116 citations

A hypervariable repeated sequence on human chromosome 1p36

1987 • 114 citations

Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer.

1995 • 107 citations

Chromosomal rearrangements in chondromatous tumors

1990 • 97 citations

Genetic and Physical Mapping.

1993 • 74 citations

Development of a panel of monochromosomal somatic cell hybrids for rapid gene mapping

1995 • 73 citations

Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses

1994 • 72 citations

Cytogenetic characterization of tenosynovial giant cell tumors (nodular tenosynovitis).

1994 • 66 citations

Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors.

1994 • 66 citations

The prognostic significance of nuclear DNA content in malignant epithelial tumors of the ovary

1990 • 63 citations

Chromosome changes in metastatic human melanoma

1988 • 58 citations

Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11.

1995 • 58 citations

Chromosome 1 abnormalities in cervical carcinoma

1988 • 56 citations

The human vigilin gene: identification, chromosomal localization and expression pattern

1994 • 38 citations

Cytogenetic studies of four human lung adenocarcinoma cell lines

1987 • 33 citations

Cytogenetic analysis of short term cultured squamous cell carcinomas of the lung

1995 • 31 citations

Hereditary multiple exostoses: Confirmation of linkage to chromosomes 8 and 11

1996 • 24 citations

Regional mapping of a liver α-subunit gene of phosphorylase kinase (PHKA) to the distal region of human chromosome Xp

1992 • 19 citations