Published in Nat Rev Neurosci on November 01, 2007
High-resolution analysis of parent-of-origin allelic expression in the mouse brain. Science (2010) 5.91
Base-resolution analyses of sequence and parent-of-origin dependent DNA methylation in the mouse genome. Cell (2012) 4.00
Analysis of copy number variations at 15 schizophrenia-associated loci. Br J Psychiatry (2013) 3.01
Mammalian genomic imprinting. Cold Spring Harb Perspect Biol (2011) 2.59
Cognitive dysfunction in psychiatric disorders: characteristics, causes and the quest for improved therapy. Nat Rev Drug Discov (2012) 2.44
Gene-environment interactions in schizophrenia: review of epidemiological findings and future directions. Schizophr Bull (2008) 2.09
Brain function and chromatin plasticity. Nature (2010) 1.75
Genome-wide analysis reveals a complex pattern of genomic imprinting in mice. PLoS Genet (2008) 1.63
Neurons show distinctive DNA methylation profile and higher interindividual variations compared with non-neurons. Genome Res (2011) 1.61
Dosage compensation of the sex chromosomes. Annu Rev Genet (2012) 1.59
Epigenetic principles and mechanisms underlying nervous system functions in health and disease. Prog Neurobiol (2008) 1.53
New insights into establishment and maintenance of DNA methylation imprints in mammals. Philos Trans R Soc Lond B Biol Sci (2013) 1.49
Epigenetic mediation of environmental influences in major psychotic disorders. Schizophr Bull (2009) 1.47
Distinct transcriptomes define rostral and caudal serotonin neurons. J Neurosci (2010) 1.43
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
Inheritance is where physiology meets evolution. J Physiol (2014) 1.29
Activation of paternally expressed genes and perinatal death caused by deletion of the Gtl2 gene. Development (2010) 1.28
Genomic imprinting of experience-dependent cortical plasticity by the ubiquitin ligase gene Ube3a. Proc Natl Acad Sci U S A (2010) 1.27
A mono-allelic bivalent chromatin domain controls tissue-specific imprinting at Grb10. EMBO J (2008) 1.27
Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring. Genet Epidemiol (2011) 1.26
Chromatin mechanisms in genomic imprinting. Mamm Genome (2009) 1.26
Sex dependent imprinting effects on complex traits in mice. BMC Evol Biol (2008) 1.22
Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size. Hum Mol Genet (2009) 1.21
Maternal transmission of Alzheimer's disease: prodromal metabolic phenotype and the search for genes. Hum Genomics (2010) 1.12
Memory enhancement: consolidation, reconsolidation and insulin-like growth factor 2. Trends Neurosci (2012) 1.08
Human-specific CpG "beacons" identify loci associated with human-specific traits and disease. Epigenetics (2012) 1.07
Parthenogenetic dopamine neurons from primate embryonic stem cells restore function in experimental Parkinson's disease. Brain (2008) 1.06
Transcriptional profiling of human liver identifies sex-biased genes associated with polygenic dyslipidemia and coronary artery disease. PLoS One (2011) 1.06
Evaluation of allelic expression of imprinted genes in adult human blood. PLoS One (2010) 1.05
Influence of photoperiod on hormones, behavior, and immune function. Front Neuroendocrinol (2010) 1.04
Change in maternal environment induced by cross-fostering alters genetic and epigenetic effects on complex traits in mice. Proc Biol Sci (2009) 1.04
Involvement of long noncoding RNAs in diseases affecting the central nervous system. RNA Biol (2012) 1.04
Phosphatidylinositol 3-kinase (PI3K) signaling via glycogen synthase kinase-3 (Gsk-3) regulates DNA methylation of imprinted loci. J Biol Chem (2010) 1.00
Strain-specific vulnerability to alcohol exposure in utero via hippocampal parent-of-origin expression of deiodinase-III. FASEB J (2011) 0.99
Relative contribution of additive, dominance, and imprinting effects to phenotypic variation in body size and growth between divergent selection lines of mice. Evolution (2008) 0.99
The secret language of destiny: stress imprinting and transgenerational origins of disease. Front Genet (2012) 0.97
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. Genes Brain Behav (2014) 0.97
Specific changes in the expression of imprinted genes in prostate cancer--implications for cancer progression and epigenetic regulation. Asian J Androl (2012) 0.95
Imprinting of the Y chromosome influences dosage compensation in roX1 roX2 Drosophila melanogaster. Genetics (2009) 0.93
Allele-specific distribution of RNA polymerase II on female X chromosomes. Hum Mol Genet (2011) 0.91
A model for transgenerational imprinting variation in complex traits. PLoS One (2010) 0.89
Mosaic analysis with double markers reveals cell-type-specific paternal growth dominance. Cell Rep (2013) 0.89
Imprinted gene expression in hybrids: perturbed mechanisms and evolutionary implications. Heredity (Edinb) (2014) 0.88
Snx14 regulates neuronal excitability, promotes synaptic transmission, and is imprinted in the brain of mice. PLoS One (2014) 0.88
A computational framework for the inheritance pattern of genomic imprinting for complex traits. Brief Bioinform (2011) 0.88
T2DM: Why Epigenetics? J Nutr Metab (2011) 0.87
Genomic imprinting effects of the X chromosome on brain morphology. J Neurosci (2013) 0.86
Role of CpG context and content in evolutionary signatures of brain DNA methylation. Epigenetics (2011) 0.86
Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami-Ogata syndrome). Eur J Hum Genet (2015) 0.86
Identification and characterization of long non-coding RNAs related to mouse embryonic brain development from available transcriptomic data. PLoS One (2013) 0.86
Spatiotemporal expression pattern of Mirg, an imprinted non-coding gene, during mouse embryogenesis. J Mol Histol (2011) 0.85
Epigenetic regulation of glial fibrillary acidic protein by DNA methylation in human malignant gliomas. Neuro Oncol (2010) 0.85
A statistical design for testing transgenerational genomic imprinting in natural human populations. PLoS One (2011) 0.85
Different yet similar: evolution of imprinting in flowering plants and mammals. F1000Prime Rep (2014) 0.85
Epigenetic and genetic variation at the IGF2/H19 imprinting control region on 11p15.5 is associated with cerebellum weight. Epigenetics (2012) 0.84
Postnatal changes in the expression pattern of the imprinted signalling protein XLαs underlie the changing phenotype of deficient mice. PLoS One (2012) 0.84
Phenotype and Stability of Neural Differentiation of Androgenetic Murine ES Cell-Derived Neural Progenitor Cells. Cell Med (2013) 0.83
Functional neuronal cells generated by human parthenogenetic stem cells. PLoS One (2012) 0.83
Epigenetic Regulation of Infant Neurobehavioral Outcomes. Med Epigenet (2014) 0.83
Human intelligence and polymorphisms in the DNA methyltransferase genes involved in epigenetic marking. PLoS One (2010) 0.83
Brain-expressed imprinted genes and adult behaviour: the example of Nesp and Grb10. Mamm Genome (2013) 0.82
A model for family-based case-control studies of genetic imprinting and epistasis. Brief Bioinform (2013) 0.82
Antagonistic roles in fetal development and adult physiology for the oppositely imprinted Grb10 and Dlk1 genes. BMC Biol (2014) 0.81
Ontogeny, conservation and functional significance of maternally inherited DNA methylation at two classes of non-imprinted genes. Development (2014) 0.81
Evolutionary approaches to autism- an overview and integration. Mcgill J Med (2011) 0.81
Quantitative and functional interrogation of parent-of-origin allelic expression biases in the brain. Elife (2015) 0.81
DNA methyltransferase candidate polymorphisms, imprinting methylation, and birth outcome. PLoS One (2013) 0.81
Long noncoding RNAs in imprinting and X chromosome inactivation. Biomolecules (2014) 0.81
Genomic imprinting of Grb10: coadaptation or conflict? PLoS Biol (2014) 0.80
dsPIG: a tool to predict imprinted genes from the deep sequencing of whole transcriptomes. BMC Bioinformatics (2012) 0.80
Dietary betaine supplementation to gestational sows enhances hippocampal IGF2 expression in newborn piglets with modified DNA methylation of the differentially methylated regions. Eur J Nutr (2014) 0.80
Recommendations for Accurate Resolution of Gene and Isoform Allele-Specific Expression in RNA-Seq Data. PLoS One (2015) 0.80
Stemming epigenetics in marine stramenopiles. Curr Genomics (2011) 0.80
Advanced paternal age effects in neurodevelopmental disorders-review of potential underlying mechanisms. Transl Psychiatry (2017) 0.80
Expression and imprinting analysis of AK044800, a transcript from the Dlk1-Dio3 imprinted gene cluster during mouse embryogenesis. Mol Cells (2013) 0.79
Characters, functions and clinical perspectives of long non-coding RNAs. Mol Genet Genomics (2016) 0.79
Expression at the imprinted dlk1-gtl2 locus is regulated by proneural genes in the developing telencephalon. PLoS One (2012) 0.79
New Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain. Annu Rev Neurosci (2016) 0.78
Neocortical development as an evolutionary platform for intragenomic conflict. Front Neuroanat (2013) 0.78
Chromatin modifiers, cognitive disorders, and imprinted genes. Dev Cell (2010) 0.78
Human Parthenogenetic Embryonic Stem Cell-Derived Neural Stem Cells Express HLA-G and Show Unique Resistance to NK Cell-Mediated Killing. Mol Med (2015) 0.78
Schizophrenia and birthplace of paternal and maternal grandfather in the Jerusalem perinatal cohort prospective study. Schizophr Res (2009) 0.77
Upregulation of imprinted genes in mice: an insight into the intensity of gene expression and the evolution of genomic imprinting. Epigenetics (2010) 0.77
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. PLoS Genet (2016) 0.77
A conceptual contribution to battles in the brain. Biol Philos (2010) 0.77
Genomic Imprinting: A New Epigenetic Perspective of Sleep Regulation. PLoS Genet (2016) 0.77
Rapid birth-and-death evolution of imprinted snoRNAs in the Prader-Willi syndrome locus: implications for neural development in Euarchontoglires. PLoS One (2014) 0.77
Known unknowns for allele-specific expression and genomic imprinting effects. F1000Prime Rep (2014) 0.76
Parent-of-Origin DNA Methylation Dynamics during Mouse Development. Cell Rep (2016) 0.76
Third trimester phthalate exposure is associated with DNA methylation of growth-related genes in human placenta. Sci Rep (2016) 0.76
The imprinted gene LRRTM1 mediates schizotypy and handedness in a nonclinical population. J Hum Genet (2014) 0.76
A Comprehensive Guide to the MAGE Family of Ubiquitin Ligases. J Mol Biol (2017) 0.75
Of rodents and humans: A comparative review of the neurobehavioral effects of early life SSRI exposure in preclinical and clinical research. Int J Dev Neurosci (2016) 0.75
Mitochondrial Gene Expression Profiles Are Associated with Maternal Psychosocial Stress in Pregnancy and Infant Temperament. PLoS One (2015) 0.75
Analysis of Genome-Wide Monoallelic Expression Patterns in Three Major Cell Types of Mouse Visual Cortex Using Laser Capture Microdissection. PLoS One (2016) 0.75
No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci. PLoS One (2015) 0.75
Heritability of fear of humans in urban and rural populations of a bird species. Sci Rep (2016) 0.75
Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the DPYD enigma. Transl Neurosci (2015) 0.75
LEVERAGING LOCAL IDENTITY-BY-DESCENT INCREASES THE POWER OF CASE/CONTROL GWAS WITH RELATED INDIVIDUALS. Ann Appl Stat (2014) 0.75
Hypomethylation of serum blood clot DNA, but not plasma EDTA-blood cell pellet DNA, from vitamin B12-deficient subjects. PLoS One (2013) 0.75
Analysis of copy number variations at 15 schizophrenia-associated loci. Br J Psychiatry (2013) 3.01
The archaeogenetics of Europe. Curr Biol (2010) 2.71
A systematic review of randomized trials comparing revascularization rate and graft patency of off-pump and conventional coronary surgery. J Thorac Cardiovasc Surg (2006) 2.39
Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness. Am J Psychiatry (2011) 1.94
Natural variation in the microcystin synthetase operon mcyABC and impact on microcystin production in Microcystis strains. J Bacteriol (2003) 1.81
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
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
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
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
Genomic imprinting and the social brain. Philos Trans R Soc Lond B Biol Sci (2006) 1.08
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
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
The 39,XO mouse as a model for the neurobiology of Turner syndrome and sex-biased neuropsychiatric disorders. Behav Brain Res (2007) 0.93
Provider perceptions of pharmacy management: lessons from the military health system. Med Care (2004) 0.92
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
What are imprinted genes doing in the brain? Epigenetics (2007) 0.90
The Role of the Y Chromosome in Brain Function. Open Neuroendocrinol J (2009) 0.90
Detection of Vibrio cholerae by real-time nucleic acid sequence-based amplification. Appl Environ Microbiol (2007) 0.90
Biological mechanisms associated with increased perseveration and hyperactivity in a genetic mouse model of neurodevelopmental disorder. Psychoneuroendocrinology (2012) 0.90
The influence of sex-linked genetic mechanisms on attention and impulsivity. Biol Psychol (2011) 0.88
Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome. Eur J Neurosci (2009) 0.87
Behavioural and cognitive profiles of mouse models for Prader-Willi syndrome. Brain Res Bull (2011) 0.84
The role of imprinted genes in mediating susceptibility to neuropsychiatric disorders. Horm Behav (2010) 0.84
What are imprinted genes doing in the brain? Adv Exp Med Biol (2008) 0.84
Altered serotonergic function may partially account for behavioral endophenotypes in steroid sulfatase-deficient mice. Neuropsychopharmacology (2011) 0.84
Dosage-sensitivity of imprinted genes expressed in the brain: 15q11-q13 and neuropsychiatric illness. Biochem Soc Trans (2013) 0.84
Impairments in impulse control in mice transgenic for the human FTDP-17 tauV337M mutation are exacerbated by age. Hum Mol Genet (2007) 0.83
Brain-expressed imprinted genes and adult behaviour: the example of Nesp and Grb10. Mamm Genome (2013) 0.82
Dissociable effects of Sry and sex chromosome complement on activity, feeding and anxiety-related behaviours in mice. PLoS One (2013) 0.80
Neuronal nitric oxide synthase, nNOS, regulates renal hemodynamics in the postnatal developing piglet. Pediatr Res (2011) 0.78
Measuring risk-taking in mice: balancing the risk between seeking reward and danger. Eur J Neurosci (2013) 0.77
Enhanced appetitive learning and reversal learning in a mouse model for Prader-Willi syndrome. Behav Neurosci (2012) 0.76
PSTAC survey in 2006 was instrumental in obtaining permanent (category I) CPT codes for MTM services performed by pharmacists. J Manag Care Pharm (2008) 0.75
The influence of hypothermia on the management of traumatic cardiac arrest. J R Army Med Corps (2015) 0.75
Modelling the genetic contribution to mental illness: a timely end for the psychiatric rodent? Eur J Neurosci (2014) 0.75
Automated profile review for transdermal fentanyl to verify opioid tolerance in the military health system. Mil Med (2013) 0.75
An overview of measuring impulsive behavior in mice. Curr Protoc Mouse Biol (2014) 0.75