Mit1/Lb9andCopg2, new members of mouse imprinted genes closely linked toPeg1/Mest

Disruption of imprinting caused by deletion of the H19 gene region in mice

1995 • 765 citations

Imprinted expression of the Igf2r gene depends on an intronic CpG island

1997 • 578 citations

The Sins of the Fathers and Mothers

1999 • 489 citations

Imprinting and the Initiation of Gene Silencing in the Germ Line

1998 • 359 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

Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein

1996 • 252 citations

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

1994 • 243 citations

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

1999 • 229 citations

Human PEG1/MEST, an Imprinted Gene on Chromosome 7

1997 • 158 citations

Identification of the Meg1 / Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver–Russell syndrome gene

1998 • 155 citations

Maternal uniparental disomy 7 in Silver-Russell syndrome.

1997 • 153 citations

The Human Homolog of a Mouse-Imprinted Gene, Peg3, Maps to a Zinc Finger Gene-Rich Region of Human Chromosome 19q13.4

1997 • 108 citations

Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse

1997 • 98 citations

Screening for imprinted genes by allelic message display: Identification of a paternally expressed gene Impact on mouse chromosome 18

1997 • 93 citations

Cloning of humanneuronatin gene and its localization to chromosome-20q11.2–12: the deduced protein is a novel ‘proteolipid’

1996 • 81 citations

2-COP, a Novel Imprinted Gene on Chromosome 7q32, Defines a New Imprinting Cluster in the Human Genome

1999 • 80 citations

Zim1, a Maternally Expressed Mouse Kruppel-Type Zinc-Finger Gene Located in Proximal Chromosome 7

1999 • 60 citations

Paternally inherited deletion of CSH1 in a patient with Silver-Russell syndrome.

1998 • 40 citations

Strain-Dependent Developmental Relaxation of Imprinting of an Endogenous Mouse Gene, Kvlqt1

1998 • 37 citations

Assignment of Growth Factor Receptor-Bound Protein 10 (GRB10) to Human Chromosome 7p11.2–p12

1997 • 33 citations

Genomic Imprinting

1997 • 12 citations