Monoallelic Expression of HumanPEG1/MESTIs Paralleled by Parent-Specific Methylation in Fetuses

Molecular Cloning: A Laboratory Manual

2001 • 133,517 citations

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.

1989 • 3,707 citations

Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer

1992 • 1,413 citations

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

1991 • 904 citations

Uniparental disomy as a mechanism for human genetic disease.

1988 • 477 citations

A paternal–specific methylation imprint marks the alleles of the mouse H19 gene

1995 • 410 citations

Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation

1995 • 299 citations

Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization

1995 • 274 citations

The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans

1993 • 238 citations

Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth.

1996 • 223 citations

Promoter-specific imprinting of the human insulin-like growth factor-II gene

1994 • 222 citations

Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?

1989 • 210 citations

Autosomal and X-chromosome imprinting

1990 • 176 citations

Overlapping patterns of IGF2 and H19 expression during human development: biallelic IGF2 expression correlates with a lack of H19 expression

1994 • 139 citations

Promoter-specific IGF2 imprinting status and its plasticity during human liver development

1995 • 117 citations

Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COL1A2 locus.

1992 • 109 citations

Establishment of functional imprinting of the H19 gene in human developing placentae

1995 • 109 citations

Parental imprinting of the Mas protooncogene in mouse

1994 • 104 citations

Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea.

1994 • 99 citations

Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.

1994 • 89 citations

Genetic imprinting map.

1990 • 84 citations

Human insulin-like growth factor type I and type II receptors are not imprinted

1993 • 78 citations

Maternal-Specific Methylation of the HumanIGF2RGene Is Not Accompanied by Allele-Specific Transcription

1996 • 70 citations

Genomic Imprinting and Chromosomal Localization of the HumanMESTGene

1996 • 50 citations

A Novel Mesoderm‐Specific cDNA Isolated from a Mouse Embryonal Carcinoma Cell Line

1993 • 47 citations

TheMASProto-Oncogene Is Not Imprinted in Humans

1996 • 16 citations

Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2

1993 • 10 citations