Sequence-based Structural Features between Kvlqt1 and Tapa1 on Mouse Chromosome 7F4/F5 Corresponding to the Beckwith-Wiedemann Syndrome Region on Human 11p15.5 : long-stretches of Unusually Well Conserved Intronic Sequences of Kvlqt1 between Mouse and Human

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1997 • 71,835 citations

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

1995 • 910 citations

Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2

1998 • 641 citations

The Sins of the Fathers and Mothers

1999 • 489 citations

Gametic Imprinting in Mammals

1995 • 444 citations

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith–Wiedemann syndrome

1999 • 405 citations

Loss of imprinting of a paternally expressed transcript, with antisense orientation to K _V LQT1, occurs frequently in Beckwith–Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

1999 • 360 citations

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements

1997 • 354 citations

Genomic imprinting of p57KIP2, a cyclin–dependent kinase inhibitor, in mouse

1995 • 288 citations

Capture of retrotransposon DNA at the sites of chromosomal double-strand breaks

1996 • 252 citations

Multiple Mechanisms Regulate Imprinting of the Mouse Distal Chromosome 7 Gene Cluster

1998 • 245 citations

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

1997 • 237 citations

Retrotransposon reverse-transcriptase-mediated repair of chromosomal breaks

1996 • 235 citations

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

1999 • 229 citations

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

1993 • 177 citations

The IPL Gene on Chromosome 11p15.5 is Imprinted in Humans and Mice and is Similar to TDAG51, Implicated in Fas Expression and Apoptosis

1997 • 164 citations

Low Frequency of p57KIP2 Mutation in Beckwith-Wiedemann Syndrome

1997 • 141 citations

Coding Mutations in p57 Are Present in Some Cases of Beckwith-Wiedemann Syndrome but Are Rare or Absent in Wilms Tumors

1997 • 140 citations

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

1996 • 139 citations

Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression

2000 • 138 citations

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

1994 • 111 citations

Syntenic Organization of the Mouse Distal Chromosome 7 Imprinting Cluster and the Beckwith-Wiedemann Syndrome Region in Chromosome 11p15.5

1998 • 109 citations

Beckwith-wiedemann syndrome, tumourigenesis and imprinting

1992 • 105 citations

IMPT1, an imprinted gene similar to polyspecific transporter and multi- drug resistance genes

1998 • 101 citations

Imprinting of mouse Kvlqt1 is developmentally regulated

1998 • 98 citations

New p57 KIP2 mutations in Beckwith-Wiedemann syndrome

1997 • 96 citations

A 2.5-Mb Transcript Map of a Tumor-Suppressing Subchromosomal Transferable Fragment from 11p15.5, and Isolation and Sequence Analysis of Three Novel Genes

1997 • 89 citations

Comparative Genomic Sequencing Identifies Novel Tissue-Specific Enhancers and Sequence Elements for Methylation-Sensitive Factors Implicated in Igf2/H19 Imprinting

2000 • 80 citations

Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting

1999 • 71 citations

A novel method for making nested deletions and its application for sequencing of a 300 kb region of human APP locus

1997 • 70 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

Transcriptional map of 170-kb region at chromosome 11p15.5: Identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples

1998 • 57 citations

A model system to study genomic imprinting of human genes

1998 • 56 citations

Beck-Wiedemann syndrome and Wilms' tumour

1997 • 52 citations

Genomic organization and chromosomal localization of the TAPA-1 gene.

1991 • 52 citations

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

1996 • 47 citations

Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5.

1998 • 44 citations

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

1997 • 25 citations

A Human p57KIP2 Transgene Is Not Activated by Passage Through the Maternal Mouse Germline

1999 • 23 citations

A Novel Gene, ITM, Located between p57KIP2 and IPL, Is Imprinted in Mice

1998 • 16 citations

Sequence-ready 1-Mb YAC, BAC and Cosmid Contigs Covering the Distal Imprinted Region of Mouse Chromosome 7

1999 • 10 citations