Genomic imprinting and the social brain.

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And baby makes three: genomic imprinting in plant embryos. PLoS Genet (2013) 0.77

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The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus. Nature (1991) 3.48

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat Genet (1998) 3.38

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Nat Genet (1997) 3.32

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature (1997) 3.27

Regulation of maternal behavior and offspring growth by paternally expressed Peg3. Science (1999) 3.07

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Hum Mol Genet (2004) 2.89

What good is genomic imprinting: the function of parent-specific gene expression. Nat Rev Genet (2003) 2.82

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The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain. Nat Genet (1997) 2.77

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Parental antagonism, relatedness asymmetries, and genomic imprinting. Proc Biol Sci (1997) 2.58

A role for the Ras signalling pathway in synaptic transmission and long-term memory. Nature (1997) 2.16

The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding. Nat Genet (2004) 2.13

Role of paternal and maternal genomes in mouse development. Nature (1984) 2.12

Resourceful imprinting. Nature (2004) 2.10

Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein. Nat Genet (1996) 2.06

Kin recognition and the 'armpit effect': evidence of self-referent phenotype matching. Proc Biol Sci (2000) 2.04

Regulation of supply and demand for maternal nutrients in mammals by imprinted genes. J Physiol (2003) 2.01

Sex chromosome genes directly affect brain sexual differentiation. Nat Neurosci (2002) 1.95

Sexually dimorphic gene expression in mouse brain precedes gonadal differentiation. Brain Res Mol Brain Res (2003) 1.93

Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain. Nat Genet (1997) 1.92

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Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome. Hum Mol Genet (2000) 1.76

Coadaptation in mother and infant regulated by a paternally expressed imprinted gene. Proc Biol Sci (2004) 1.72

Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice. Nat Genet (2005) 1.70

Paternal kin discrimination in wild baboons. Proc Biol Sci (1999) 1.69

Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization. Nat Genet (1995) 1.67

Peg3/Pw1 is an imprinted gene involved in the TNF-NFkappaB signal transduction pathway. Nat Genet (1998) 1.61

Angelman's syndrome in infancy. Dev Med Child Neurol (1990) 1.61

Paternal relatedness and age proximity regulate social relationships among adult female rhesus macaques. Proc Natl Acad Sci U S A (2001) 1.61

Pw1/Peg3 is a potential cell death mediator and cooperates with Siah1a in p53-mediated apoptosis. Proc Natl Acad Sci U S A (2000) 1.60

Imprinted gene expression in the brain. Neurosci Biobehav Rev (2005) 1.59

Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism. Pediatr Res (2000) 1.53

Identification of a cluster of X-linked imprinted genes in mice. Nat Genet (2005) 1.50

Wild female baboons bias their social behaviour towards paternal half-sisters. Proc Biol Sci (2003) 1.44

Genomic imprinting, sex-biased dispersal, and social behavior. Ann N Y Acad Sci (2000) 1.41

Imprinted gene in postnatal growth role. Nature (1998) 1.35

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Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome. Biol Psychiatry (2003) 1.27

Imprinted Nesp55 influences behavioral reactivity to novel environments. Mol Cell Biol (2005) 1.25

Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy. Lancet (2002) 1.24

Imprinted genes, cognition and behaviour. Trends Cogn Sci (2000) 1.19

Novelty seeking behavior in the rat is dependent upon the integrity of the noradrenergic system. Brain Res Cogn Brain Res (1995) 1.18

Kinship and genomic imprinting. Results Probl Cell Differ (1999) 1.17

The evolution of X-linked genomic imprinting. Genetics (2001) 1.13

Prader-Willi syndrome and the evolution of human childhood. Am J Hum Biol (2003) 1.13

Neural control of tongue movement with respect to respiration and swallowing. Crit Rev Oral Biol Med (2001) 1.13

Genomic imprinting of the X chromosome: a novel mechanism for the evolution of sexual dimorphism. J Lab Clin Med (1999) 1.05

Distinctive patterns of memory function in subgroups of females with Turner syndrome: evidence for imprinted loci on the X-chromosome affecting neurodevelopment. Neuropsychologia (2000) 1.03

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Sex specific X chromosome expression caused by genomic imprinting. J Theor Biol (1999) 1.02

The nose knows who's who: chemosensory individuality and mate recognition in mice. Horm Behav (2004) 1.01

Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome. Clin Genet (1991) 1.00

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Urinary odour preferences in mice. Nature (2001) 0.99

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Imprinted genes and mother-offspring interactions. Early Hum Dev (2004) 0.95

Genomic imprinting, maternal care, and brain evolution. Horm Behav (2001) 0.95

Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome. J Med Genet (2003) 0.93

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Effects of environmental events on smiling and laughing behavior in Angelman syndrome. Am J Ment Retard (2002) 0.92

Imprinted genes and mental dysfunction. Ann Med (2001) 0.89

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Just how happy is the happy puppet? An emotion signaling and kinship theory perspective on the behavioral phenotype of children with Angelman syndrome. Med Hypotheses (2004) 0.80

A possible role for imprinted genes in inbreeding avoidance and dispersal from the natal area in mice. Proc Biol Sci (2002) 0.80

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The archaeogenetics of Europe. Curr Biol (2010) 2.71

Genomic imprinting effects on brain development and function. Nat Rev Neurosci (2007) 2.42

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Climate change and evolving human diversity in Europe during the last glacial. Philos Trans R Soc Lond B Biol Sci (2004) 1.79

Chronology of the Grotte du Renne (France) and implications for the context of ornaments and human remains within the Châtelperronian. Proc Natl Acad Sci U S A (2010) 1.79

Imprinted gene expression in the brain. Neurosci Biobehav Rev (2005) 1.59

Pathological changes in dopaminergic nerve cells of the substantia nigra and olfactory bulb in mice transgenic for truncated human alpha-synuclein(1-120): implications for Lewy body disorders. J Neurosci (2006) 1.57

Distinct physiological and behavioural functions for parental alleles of imprinted Grb10. Nature (2011) 1.52

Mitochondrial DNA signals of late glacial recolonization of Europe from near eastern refugia. Am J Hum Genet (2012) 1.49

Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour. Hum Mol Genet (2009) 1.39

Common genetic effects on variation in impulsivity and activity in mice. J Neurosci (2004) 1.29

Volcanic ash layers illuminate the resilience of Neanderthals and early modern humans to natural hazards. Proc Natl Acad Sci U S A (2012) 1.25

Imprinted Nesp55 influences behavioral reactivity to novel environments. Mol Cell Biol (2005) 1.25

It is not all hormones: alternative explanations for sexual differentiation of the brain. Brain Res (2006) 1.17

Low concentrations of bile salts induce stress responses and reduce motility in Bacillus cereus ATCC 14579 [corrected]. J Bacteriol (2007) 1.10

X-linked imprinting: effects on brain and behaviour. Bioessays (2006) 1.08

P-Rex2 regulates Purkinje cell dendrite morphology and motor coordination. Proc Natl Acad Sci U S A (2008) 1.07

Converging pharmacological and genetic evidence indicates a role for steroid sulfatase in attention. Biol Psychiatry (2009) 1.07

X-monosomy effects on visuospatial attention in mice: a candidate gene and implications for Turner syndrome and attention deficit hyperactivity disorder. Biol Psychiatry (2006) 1.04

Imprinted genes and neuroendocrine function. Front Neuroendocrinol (2007) 1.04

Measuring impulsivity in mice using a novel operant delayed reinforcement task: effects of behavioural manipulations and d-amphetamine. Psychopharmacology (Berl) (2003) 0.99

Effects on fear reactivity in XO mice are due to haploinsufficiency of a non-PAR X gene: implications for emotional function in Turner's syndrome. Hum Mol Genet (2004) 0.98

Expression patterns of the novel imprinted genes Nap1l5 and Peg13 and their non-imprinted host genes in the adult mouse brain. Gene Expr Patterns (2004) 0.97

Increased tau phosphorylation on mitogen-activated protein kinase consensus sites and cognitive decline in transgenic models for Alzheimer's disease and FTDP-17: evidence for distinct molecular processes underlying tau abnormalities. Mol Cell Biol (2005) 0.94

The 39,XO mouse as a model for the neurobiology of Turner syndrome and sex-biased neuropsychiatric disorders. Behav Brain Res (2007) 0.93

Somatostatin receptor 2 knockout/lacZ knockin mice show impaired motor coordination and reveal sites of somatostatin action within the striatum. Eur J Neurosci (2003) 0.92

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Steroid sulfatase-deficient mice exhibit endophenotypes relevant to attention deficit hyperactivity disorder. Psychoneuroendocrinology (2011) 0.92

Cross-species approaches to pathological gambling: a review targeting sex differences, adolescent vulnerability and ecological validity of research tools. Neurosci Biobehav Rev (2013) 0.90

A comparison of multiple 5-HT receptors in two tasks measuring impulsivity. J Psychopharmacol (2005) 0.90

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The Role of the Y Chromosome in Brain Function. Open Neuroendocrinol J (2009) 0.90

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The influence of sex-linked genetic mechanisms on attention and impulsivity. Biol Psychol (2011) 0.88

Psychopathy trait scores in adolescents with childhood ADHD: the contribution of genotypes affecting MAOA, 5HTT and COMT activity. Psychiatr Genet (2009) 0.88

Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome. Eur J Neurosci (2009) 0.87

Placental programming of anxiety in adulthood revealed by Igf2-null models. Nat Commun (2013) 0.85

The role of imprinted genes in mediating susceptibility to neuropsychiatric disorders. Horm Behav (2010) 0.84

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Altered serotonergic function may partially account for behavioral endophenotypes in steroid sulfatase-deficient mice. Neuropsychopharmacology (2011) 0.84

An mTph2 SNP gives rise to alterations in extracellular 5-HT levels, but not in performance on a delayed-reinforcement task. Eur J Neurosci (2005) 0.83

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Impairments in impulse control in mice transgenic for the human FTDP-17 tauV337M mutation are exacerbated by age. Hum Mol Genet (2007) 0.83

A novel translational assay of response inhibition and impulsivity: effects of prefrontal cortex lesions, drugs used in ADHD, and serotonin 2C receptor antagonism. Neuropsychopharmacology (2013) 0.80

Dissociable effects of Sry and sex chromosome complement on activity, feeding and anxiety-related behaviours in mice. PLoS One (2013) 0.80

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Enhanced appetitive learning and reversal learning in a mouse model for Prader-Willi syndrome. Behav Neurosci (2012) 0.76

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Automated profile review for transdermal fentanyl to verify opioid tolerance in the military health system. Mil Med (2013) 0.75