Imprinted gene expression in the brain

Epigenetic programming by maternal behavior

2004 • 5,974 citations

Genomic imprinting: parental influence on the genome

2001 • 2,253 citations

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

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

Mutation of the Angelman Ubiquitin Ligase in Mice Causes Increased Cytoplasmic p53 and Deficits of Contextual Learning and Long-Term Potentiation

1998 • 820 citations

Differential activity of maternally and paternally derived chromosome regions in mice

1985 • 708 citations

Role of paternal and maternal genomes in mouse development

1984 • 704 citations

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function

1997 • 670 citations

Essential role of brain-derived neurotrophic factor in adult hippocampal function

2004 • 653 citations

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

1998 • 571 citations

Birth of parthenogenetic mice that can develop to adulthood

2004 • 507 citations

Regulation of Maternal Behavior and Offspring Growth by Paternally Expressed Peg3

1999 • 504 citations

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

1997 • 495 citations

Genomic imprinting and the strange case of the insulin-like growth factor II receptor

1991 • 494 citations

What good is genomic imprinting: the function of parent-specific gene expression

2003 • 487 citations

A role for the Ras signalling pathway in synaptic transmission and long-term memory

1997 • 474 citations

Prader-Willi syndrome.

1997 • 469 citations

Regulation of supply and demand for maternal nutrients in mammals by imprinted genes

2003 • 369 citations

Sex chromosomes and brain gender

2004 • 366 citations

Genomic Imprinting: Implications for Human Disease

1999 • 363 citations

Regulation of neocortical interneuron development and the implications for neurodevelopmental disorders

2004 • 330 citations

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

2000 • 320 citations

Regulation of supply and demand for maternal nutrients in mammals by imprinted genes

2003 • 302 citations

Cerebral Morphologic Distinctions Between Williams and Down Syndromes

1993 • 296 citations

Prader-Willi and Angelman syndromes: Sister imprinted disorders

2000 • 291 citations

Imprinting, the X-Chromosome, and the Male Brain: Explaining Sex Differences in the Liability to Autism

2000 • 291 citations

Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a

2003 • 260 citations

IV. Neuroanatomy of Williams Syndrome: A High-Resolution MRI Study

2000 • 250 citations

Anomalous Brain Morphology on Magnetic Resonance Images in Williams Syndrome and Down Syndrome

1990 • 242 citations

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

1996 • 223 citations

Genomic imprinting and the differential roles of parental genomes in brain development

1996 • 210 citations

Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS–M

1996 • 195 citations

Zac1 (Lot1), a Potential Tumor Suppressor Gene, and the Gene for ɛ-Sarcoglycan Are Maternally Imprinted Genes: Identification by a Subtractive Screen of Novel Uniparental Fibroblast Lines

2000 • 180 citations

Allelic expression of IGF2 in marsupials and birds

2000 • 177 citations

Necdin, A Postmitotic Neuron-specific Growth Suppressor, Interacts with Viral Transforming Proteins and Cellular Transcription Factor E2F1

1998 • 163 citations

Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark

2003 • 144 citations

Hippocampus-dependent learning and memory is impaired in mice lacking the Ras-guanine-nucleotide releasing factor 1 (Ras-GRF1)

2001 • 140 citations

Primate brain evolution : genetic and functional considerations

1996 • 137 citations

Imprinted genes, cognition and behaviour

2000 • 118 citations

Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior.

1995 • 116 citations

Localization of 5-HT2A Receptor in rat cerebral cortex and olfactory system revealed by immunohistochemistry using two antibodies raised in rabbit and chicken

1998 • 115 citations

Puppet‐like syndrome of Angelman

1991 • 110 citations

Distinctive patterns of memory function in subgroups of females with Turner syndrome: evidence for imprinted loci on the X-chromosome affecting neurodevelopment

2000 • 102 citations

Genetic and Functional Analysis of neuronatin in Mice with Maternal or Paternal Duplication of Distal Chr 2

1997 • 98 citations

Imprinted silencing of Slc22a2 and Slc22a3 does not need transcriptional overlap between Igf2r and Air

2003 • 89 citations

Williams Syndrome

2002 • 88 citations

Segment-Specific Expression of the neuronatin Gene during Early Hindbrain Development

1995 • 85 citations

Neuronatin mRNA: alternatively spliced forms of a novel brain-specific mammalian developmental gene

1995 • 80 citations

Discovery of a Novel, Paternally Expressed Ubiquitin-specific Processing Protease Gene through Comparative Analysis of an Imprinted Region of Mouse Chromosome 7 and Human Chromosome 19q13.4

2000 • 79 citations

Prader–Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain

2003 • 78 citations

The Mouse Murr1 Gene Is Imprinted in the Adult Brain, Presumably Due to Transcriptional Interference by the Antisense-Oriented U2af1-rs1 Gene

2003 • 76 citations

Ras-GRF, the activator of Ras, is expressed preferentially in mature neurons of the central nervous system

1997 • 74 citations

Peg3/Pw1 Is Involved in p53-mediated Cell Death Pathway in Brain Ischemia/Hypoxia

2002 • 71 citations

Cerebellar abnormalities in infants and toddlers with Williams syndrome

2002 • 68 citations

Genomic Imprinting and Endosperm Development in Flowering Plants

2003 • 66 citations

Imprinted genes and mental dysfunction

2001 • 65 citations

Genomic imprinting in the brain

1997 • 65 citations

The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene

2004 • 64 citations

Angelman and Prader‐Willi syndrome: A magnetic resonance imaging study of differences in cerebral structure

1993 • 63 citations

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

1999 • 60 citations

Imprinted Genes and the Coordination of Fetal and Postnatal Growth in Mammals

2001 • 59 citations

MR of the pituitary in patients with Prader-Willi syndrome: Size determination and imaging findings

1996 • 57 citations

Cerebellar abnormalities in infants and toddlers with Williams syndrome

2002 • 55 citations

The potential role of gene duplications in the evolution of imprinting mechanisms

2003 • 47 citations

Expression patterns of the novel imprinted genes Nap1l5 and Peg13 and their non-imprinted host genes in the adult mouse brain

2004 • 41 citations

Identification and characterisation of imprinted genes in the mouse

2004 • 36 citations

Localization of neuroendocrine secretory protein 55 messenger RNA in the rat brain

1999 • 36 citations

Paternal Imprinting of Mouse Serotonin Receptor 2A GeneHtr2in Embryonic Eye: A Conserved Imprinting Regulation on theRB/RbLocus

1998 • 36 citations

Proton magnetic resonance spectroscopy of the brain in patients with Prader-Willi syndrome

1998 • 33 citations

Angelman (?happy puppet?) syndrome ?seven new cases documented by cerebral computed tomography: review of the literature

1988 • 31 citations

Abnormal cortical development shown by 3D MRI in Prader–Willi syndrome

2002 • 28 citations

Identification and properties of imprinted genes and their control elements

2004 • 20 citations

Mental retardation, ataxia, seizures, dysmorphia, and hydrocephaly in two sibs. Angelman syndrome or new syndrome.

1993 • 2 citations

Regional cerebral blood flow in Angelman syndrome

1993 • 2 citations