Allele-specific replication timing of imprinted gene regions

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

1991 • 1,773 citations

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

1990 • 1,357 citations

Parental imprinting of the mouse H19 gene

1991 • 1,192 citations

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

1991 • 904 citations

Relaxation of imprinted genes in human cancer

1993 • 792 citations

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

1993 • 710 citations

Replication Timing of Genes and Middle Repetitive Sequences

1984 • 561 citations

Detection of sickle cell beta S-globin allele by hybridization with synthetic oligonucleotides.

1983 • 536 citations

A deletion of the human beta-globin locus activation region causes a major alteration in chromatin structure and replication across the entire beta-globin locus.

1990 • 477 citations

DIFFERENTIAL IMPRINTING AND EXPRESSION OF MATERNAL AND PATERNAL GENOMES

1988 • 451 citations

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism

1993 • 411 citations

Monoallelic expression of the human H19 gene

1992 • 409 citations

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

1992 • 305 citations

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

1992 • 265 citations

Physical linkage of two mammalian imprinted genes, H19 and insulin–like growth factor 2

1992 • 261 citations

Role of replication time in the control of tissue-specific gene expression.

1987 • 249 citations

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

1992 • 243 citations

Gamma delta beta-thalassemia due to a de novo mutation deleting the 5' beta-globin gene activation-region hypersensitive sites.

1989 • 240 citations

Isolation of the human insulin-like growth factor genes: insulin-like growth factor II and insulin genes are contiguous.

1985 • 212 citations

A DNA methylation imprint, determined by the sex of the parent, distinguishes the angelman and Prader-Willi syndromes

1992 • 212 citations

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

1992 • 203 citations

Parental imprinting of the human H19 gene

1992 • 176 citations

HAIRPIN-TAIL: A CASE OF POST-REDUCTIONAL GENE ACTION IN THE MOUSE EGG?

1974 • 163 citations

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11–13) by YAC cloning and FISH analysis

1992 • 160 citations

Three mutant insulins in man

1983 • 158 citations

Evolution of Insulin-Like Growth Factor II: Characterization of the Mouse IGF-II Gene and Identification of Two Pseudo-Exons

1990 • 131 citations

Genetic analysis of genomic imprinting: An Imprintor-1 gene controls inactivation of the paternal copy of the mouse Tme locus

1992 • 102 citations

A molecular genetic linkage map of mouse chromosome 7

1990 • 91 citations

Genomic imprinting and embryonal tumours

1989 • 88 citations

Analysis of DNA replication during S-phase by means of dynamic chromosome banding at high resolution

1990 • 85 citations

Parental origin of chromosomes involved in the translocation t(9;22)

1992 • 83 citations

Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse.

1993 • 80 citations

Fluorescence and Giemsa banding studies of the allocyclic X chromosome in embryonic and adult mouse cells

1973 • 57 citations

Mouse Chromosome 7

1992 • 53 citations

Seminars in developmental biology

1995 • 52 citations

Correlation between X-chromosome inactivation and cell differentiation in female preimplantation mouse embryos

1985 • 49 citations

Replication asynchrony between homologs 15q11.2: Cytogenetic evidence for genomic imprinting

1991 • 41 citations

Report of the committee on the genetic constitution of chromosome 11

1991 • 35 citations

Polymorphic variants in human chromosome 15

1981 • 10 citations