Novel Transcribed Sequences within the BWS/WT2 Region in 11p15.5: Tissue-Specific Expression Correlates with Cancer Type

The retinoblastoma protein and cell cycle control

1995 • 4,873 citations

Identification of the breast cancer susceptibility gene BRCA2

1995 • 3,581 citations

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1996 • 1,746 citations

Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector.

1992 • 1,651 citations

Human Retinoblastoma Susceptibility Gene: Cloning, Identification, and Sequence

1987 • 1,436 citations

A gene map of the human genome.

1996 • 986 citations

Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution.

1995 • 910 citations

Relaxation of imprinted genes in human cancer

1993 • 792 citations

A Gene Map of the Human Genome

1996 • 737 citations

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

1993 • 710 citations

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

1994 • 466 citations

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

1989 • 448 citations

Disruption of insulin–like growth factor 2 imprinting in Beckwith–Wiedemann syndrome

1993 • 427 citations

Introduction of a Normal Human Chromosome 11 into a Wilms' Tumor Cell Line Controls Its Tumorigenic Expression

1987 • 407 citations

PowerBLAST: A New Network BLAST Application for Interactive or Automated Sequence Analysis and Annotation

1997 • 356 citations

Reduction to Homozygosity of Genes on Chromosome 11 in Human Breast Neoplasia

1987 • 329 citations

Epigenetic lesions at the H19 locus in Wilms' tumour patients

1994 • 318 citations

Allelotype of pancreatic adenocarcinoma using xenograft enrichment.

1995 • 308 citations

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1989 • 306 citations

Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15.

1996 • 302 citations

Activation of an imprinted allele of the insulin-like growth factor II gene implicated in rhabdomyosarcoma.

1994 • 218 citations

Imprinting mutations in the Beckwith—Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2–H19 domain

1995 • 215 citations

Tumor Cell Growth Arrest Caused by Subchromosomal Transferable DNA Fragments from Chromosome 11

1993 • 177 citations

Report of the committee on chromosome and gene loss in human neoplasia

1991 • 158 citations

Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors

1996 • 139 citations

Preparation and screening of an arrayed human genomic library generated with the P1 cloning system.

1994 • 130 citations

Suppression of Tumorigenicity in Wilms Tumor by the p15.5-p14 Region of Chromosome 11

1991 • 124 citations

Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors

1996 • 115 citations

Parental Imprinting of Human Chromosome Region 11p15.3-pter Involved in the Beckwith-Wiedemann Syndrome and Various Human Neoplasia

1994 • 111 citations

Human chromosome 11 contains two different growth suppressor genes for embryonal rhabdomyosarcoma.

1992 • 111 citations

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

1995 • 108 citations

Congenital Pancreatoblastoma in Beckwith Wiedemann Syndrome

1988 • 98 citations

The G401 cell line, utilized for studies of chromosomal changes in Wilms' tumor, is derived from a rhabdoid tumor of the kidney.

1993 • 95 citations

Magnetic bead capture of expressed sequences encoded within large genomic segments

1993 • 90 citations

A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5

1996 • 76 citations

A 1-Mb Physical Map and PAC Contig of the Imprinted Domain in 11p15.5 That Contains TAPA1 and the BWSCR1/WT2 Region

1997 • 66 citations

Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17

1995 • 64 citations

Fishing for complements: finding genes by direct selection

1994 • 64 citations

Mono- and bi-allelic expression of insulin-like growth factor II gene in human muscle tumors

1994 • 64 citations

A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues

1996 • 59 citations

727 ISOLATION OF FOUR UNUSUAL PEDIATRIC SOLID TUMOR CELL LINES

1978 • 47 citations

Localization of a Tumor Suppressor Gene in 11p15.5 Using the G401 Wilms' Tumor Assay

1996 • 47 citations

Localization of beckwith‐wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5

1994 • 47 citations

Isolation of a diverged homeobox gene, M0X1, from the BRCA1 region on 17q21 by solution hybrid capture

1994 • 41 citations

Direct selection of expressed sequences within a 1-Mb region flanking BRCA1 on human chromosome 17q21

1995 • 19 citations