Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site

Genomic imprinting: parental influence on the genome

2001 • 2,253 citations

AU-rich elements: characterization and importance in mRNA degradation

1995 • 1,936 citations

Interspersed repeats and other mementos of transposable elements in mammalian genomes

1999 • 959 citations

Genome Organization, Function, and Imprinting in Prader-Willi and Angelman Syndromes

2001 • 628 citations

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

2000 • 573 citations

Sequence patterns indicate an enzymatic involvement in integration of mammalian retroposons

1997 • 546 citations

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons

1997 • 495 citations

Insulators and Boundaries: Versatile Regulatory Elements in the Eukaryotic Genome

2001 • 386 citations

Estimation of divergence times from multiprotein sequences for a few mammalian species and several distantly related organisms

2001 • 333 citations

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome

2000 • 320 citations

Molecular Phylogeny and Divergence Time Estimates for Major Rodent Groups: Evidence from Multiple Genes

2001 • 279 citations

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

1997 • 247 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

A Novel Imprinted Gene, Encoding a RING Zinc-Finger Protein, and Overlapping Antisense Transcript in the Prader-Willi Syndrome Critical Region

1999 • 225 citations

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

1992 • 212 citations

An imprinted, mammalian bicistronic transcript encodes two independent proteins

1999 • 189 citations

The Human Magel2 Gene and Its Mouse Homologue Are Paternally Expressed and Mapped to the Prader-Willi Region

1999 • 183 citations

Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution

1996 • 154 citations

A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome

2001 • 152 citations

Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype

2000 • 149 citations

Small Evolutionarily Conserved RNA, Resembling C/D Box Small Nucleolar RNA, Is Transcribed from PWCR1, a Novel Imprinted Gene in the Prader-Willi Deletion Region, Which Is Highly Expressed in Brain

2000 • 128 citations

A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and Angelman syndromes

1999 • 121 citations

Imprinting of a RING Zinc-Finger Encoding Gene in the Mouse Chromosome Region Homologous to the Prader-Willi Syndrome Genetic Region

1999 • 110 citations

An Imprinted Mouse Transcript Homologous to the Human Imprinted in Prader-Willi Syndrome (IPW) Gene

1997 • 105 citations

The Ancient Source of a Distinct Gene Family Encoding Proteins Featuring RING and C3H Zinc-Finger Motifs with Abundant Expression in Developing Brain and Nervous System

2000 • 105 citations

Segmental Duplications: What's Missing, Misassigned, and Misassembled—and Should We Care?: Figure 1.

2001 • 102 citations

A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15

2001 • 73 citations

A novel ATPase on mouse chromosome 7 is a candidate gene for increased body fat

2000 • 65 citations

Structure of the Highly Conserved HERC2 Gene and of Multiple Partially Duplicated Paralogs in Human

2000 • 58 citations

Identification of a Testis-Specific Gene (C15orf2) in the Prader–Willi Syndrome Region on Chromosome 15

2000 • 50 citations

Concerted regulation and molecular evolution of the duplicated SNRPB'/B and SNRPN loci

1999 • 43 citations

Structure and function correlations at the imprinted mouse Snrpn locus

1998 • 40 citations

In vivo analysis of Frat1 deficiency suggests compensatory activity of Frat3

1999 • 40 citations

The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region.

1997 • 38 citations

Characterization of TH1 and CTSZ, two non-imprinted genes downstream of GNAS1 in chromosome 20q13

2000 • 24 citations

Imprints of disease at GNAS1

2001 • 24 citations

Sequence of a cDNA Encoding Mouse F₁F₀-ATP Synthase g Subunit

1999 • 5 citations