Domain organization of allele–specific replication within the GABRB3 gene cluster requires a biparental 15q11–13 contribution

Parental imprinting of the mouse insulin-like growth factor II gene

1991 • 1,773 citations

Completion of mouse embryogenesis requires both the maternal and paternal genomes

1984 • 1,529 citations

Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

1984 • 1,402 citations

Parental imprinting of the mouse H19 gene

1991 • 1,192 citations

Allelic inactivation regulates olfactory receptor gene expression

1994 • 1,056 citations

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

1991 • 904 citations

Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome

1989 • 887 citations

Relaxation of imprinted genes in human cancer

1993 • 792 citations

Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

1989 • 575 citations

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

1994 • 430 citations

Monoallelic expression of the human H19 gene

1992 • 409 citations

Analysis and sorting of living cells according to deoxyribonucleic acid content.

1977 • 389 citations

Allele-specific replication timing of imprinted gene regions

1993 • 385 citations

Uniparental paternal disomy in Angelman's syndrome

1991 • 332 citations

Delineation of DNA replication time zones by fluorescence in situ hybridization.

1992 • 305 citations

THE CONTROLLING ELEMENT IN SEX CHROMOSOME BEHAVIOR IN SCIARA

1960 • 299 citations

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith–Wiedemann syndrome

1993 • 290 citations

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region

1992 • 265 citations

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region

1992 • 243 citations

Identification of a novel paternally expressed gene in the Prader - Willi syndrome region

1994 • 243 citations

Imprinting and X chromosome counting mechanisms determine Xist expression in early mouse development

1994 • 229 citations

Allele specificity of DNA replication timing in the Angelman/Prader–Willi syndrome imprinted chromosomal region

1994 • 195 citations

A candidate mouse model for Prader–Willi syndrome which shows an absence of Snrpn expression

1992 • 176 citations

Maternal imprinting of human SNRPN, a gene deleted in Prader–Willi syndrome

1994 • 163 citations

Igf2r and Igf2 gene expression in androgenetic, gynogenetic, and parthenogenetic preimplantation mouse embryos: absence of regulation by genomic imprinting.

1994 • 144 citations

Early signaling defects in human T cells anergized by T cell presentation of autoantigen.

1992 • 143 citations

Angelman syndrome due to paternal uniparental disomy of chromosome 15: A milder phenotype?

1994 • 122 citations

Nondisjunction of chromosome 15: origin and recombination.

1993 • 109 citations

Maternal but not paternal transmission of 15q11–13–linked nondeletion Angelman syndrome leads to phenotypic expression

1992 • 100 citations

Imprinting: a gamete's point of view

1994 • 95 citations

Analysis of replication timing properties of human X-chromosomal loci by fluorescence in situ hybridization.

1994 • 82 citations

Oppositely imprinted genes H19 and insulin-like growth factor 2 are coexpressed in human androgenetic trophoblast.

1993 • 79 citations

Transvection: Allelic cross talk

1988 • 66 citations

High-resolution mapping of the gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients.

1993 • 56 citations

DNA replication analysis of FMR1, XIST, and factor 8C loci by FISH shows nontranscribed X-linked genes replicate late.

1994 • 55 citations

Transvection and long‐distance gene regulation

1990 • 43 citations

Escape from genomic imprinting at the mouse T-associated maternal effect (Tme) locus.

1991 • 22 citations

Does transcription by RNA polymerase play a direct role in the initiation of replication?

1994 • 19 citations

Use of DiO-C5-3 to improve Hoechst 33342 uptake, resolution of DNA content, and survival of CHO cells

1988 • 18 citations