Published in Adv Exp Med Biol on January 01, 2012
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Autism spectrum disorders and race, ethnicity, and nativity: a population-based study. Pediatrics (2014) 0.93
Cerebellar oxidative DNA damage and altered DNA methylation in the BTBR T+tf/J mouse model of autism and similarities with human post mortem cerebellum. PLoS One (2014) 0.89
DNA methylation markers in the postnatal developing rat brain. Brain Res (2013) 0.82
Epigenetics of inflammation, maternal infection, and nutrition. J Nutr (2015) 0.81
Epigenetics and nutritional environmental signals. Integr Comp Biol (2014) 0.80
Dysregulated A to I RNA editing and non-coding RNAs in neurodegeneration. Front Genet (2013) 0.80
Perspectives on the use of stem cells for autism treatment. Stem Cells Int (2013) 0.80
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Assessing the impact of copy number variants on miRNA genes in autism by Monte Carlo simulation. PLoS One (2014) 0.79
Epigenetic effects of casein-derived opioid peptides in SH-SY5Y human neuroblastoma cells. Nutr Metab (Lond) (2015) 0.78
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Putting the 'epi' into epigenetics research in psychiatry. J Epidemiol Community Health (2013) 0.76
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Sevoflurane-induced down-regulation of hippocampal oxytocin and arginine vasopressin impairs juvenile social behavioral abilities. J Mol Neurosci (2014) 0.75
The maternal body as environment in autism science. Soc Stud Sci (2016) 0.75
Monoallelic yet combinatorial expression of variable exons of the protocadherin-alpha gene cluster in single neurons. Nat Genet (2005) 2.98
ICF, an immunodeficiency syndrome: DNA methyltransferase 3B involvement, chromosome anomalies, and gene dysregulation. Autoimmunity (2008) 1.43
DHPLC is superior to SSCP in screening p53 mutations in esophageal cancer tissues. Int J Cancer (2005) 1.40
Three novel DNMT3B mutations in Japanese patients with ICF syndrome. Am J Med Genet (2002) 1.18
Methyl CpG-binding protein 2 (a mutation of which causes Rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brains. J Neuropathol Exp Neurol (2007) 1.10
Direct interaction of post-synaptic density-95/Dlg/ZO-1 domain-containing synaptic molecule Shank3 with GluR1 alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor. J Neurochem (2006) 1.09
Analysis of renal cell carcinoma as a first step for developing mass spectrometry-based diagnostics. J Am Soc Mass Spectrom (2012) 1.04
A role for strain differences in waveforms of ultrasonic vocalizations during male-female interaction. PLoS One (2011) 1.04
Multivariate analysis of temporal descriptions of open-field behavior in wild-derived mouse strains. Behav Genet (2006) 1.04
Maternal diabetes increases the risk of caudal regression caused by retinoic acid. Diabetes (2002) 1.00
Ambient imaging mass spectrometry by electrospray ionization using solid needle as sampling probe. J Mass Spectrom (2009) 0.97
22q13 Microduplication in two patients with common clinical manifestations: a recognizable syndrome? Am J Med Genet A (2007) 0.96
Secreted protein-based reporter systems for monitoring inflammatory events: critical interference by endoplasmic reticulum stress. J Immunol Methods (2006) 0.96
Genetic mapping of social interaction behavior in B6/MSM consomic mouse strains. Behav Genet (2009) 0.95
Genetic and clinical factors associated with reticular pseudodrusen in exudative age-related macular degeneration. Graefes Arch Clin Exp Ophthalmol (2014) 0.95
Association of LOC387715 A69S genotype with visual prognosis after photodynamic therapy for polypoidal choroidal vasculopathy. Retina (2010) 0.94
Ultradian components in the locomotor activity rhythms of the genetically normal mouse, Mus musculus. J Exp Biol (2010) 0.94
Combined hypermethylation and chromosome loss associated with inactivation of SSI-1/SOCS-1/JAB gene in human hepatocellular carcinomas. Cancer Lett (2002) 0.94
Slo2 sodium-activated K+ channels bind to the PDZ domain of PSD-95. Biochem Biophys Res Commun (2003) 0.93
Association of LOC387715 A69S with vitreous hemorrhage in polypoidal choroidal vasculopathy. Am J Ophthalmol (2008) 0.93
Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients. J Hum Genet (2013) 0.92
Transthyretin accelerates vascular Abeta deposition in a mouse model of Alzheimer's disease. Brain Pathol (2008) 0.92
Dilinoleoyl-phosphatidylethanolamine from Hericium erinaceum protects against ER stress-dependent Neuro2a cell death via protein kinase C pathway. J Nutr Biochem (2005) 0.92
Angiographic lesion size associated with LOC387715 A69S genotype in subfoveal polypoidal choroidal vasculopathy. Retina (2009) 0.91
A transcriptional repressor MeCP2 causing Rett syndrome is expressed in embryonic non-neuronal cells and controls their growth. Brain Res Dev Brain Res (2005) 0.90
The protocadherins, PCDHB1 and PCDH7, are regulated by MeCP2 in neuronal cells and brain tissues: implication for pathogenesis of Rett syndrome. BMC Neurosci (2011) 0.90
QTL analysis of measures of mouse home-cage activity using B6/MSM consomic strains. Mamm Genome (2010) 0.90
Genetic diversity underlying capsaicin intake in the Mishima battery of mouse strains. Brain Res Bull (2002) 0.90
Comparison of Genomic and Epigenomic Expression in Monozygotic Twins Discordant for Rett Syndrome. PLoS One (2013) 0.89
Characteristics of probe electrospray generated from a solid needle. J Phys Chem B (2008) 0.89
Methylation status of the p15 and p16 genes in paediatric myelodysplastic syndrome and juvenile myelomonocytic leukaemia. Br J Haematol (2005) 0.88
Oligodendrocyte transcription factor 1 (Olig1) is a Smad cofactor involved in cell motility induced by transforming growth factor-β. J Biol Chem (2013) 0.87
Molecular characterization of the Pb recombination hotspot in the mouse major histocompatibility complex class II region. Genomics (2002) 0.87
SDOP-DB: a comparative standardized-protocol database for mouse phenotypic analyses. Bioinformatics (2010) 0.86
Adult onset X-linked chronic granulomatous disease in a woman patient caused by a de novo mutation in paternal-origin CYBB gene and skewed inactivation of normal maternal X chromosome. Intern Med (2008) 0.86
Length variation of CAG/CAA triplet repeats in 50 genes among 16 inbred mouse strains. Gene (2005) 0.85
B6-MSM consomic mouse strains reveal multiple loci for genetic variation in sucrose octaacetate aversion. Behav Genet (2011) 0.85
Familial 14-Mb deletion at 21q11.2-q21.3 and variable phenotypic expression. J Hum Genet (2002) 0.85
Aqueous humor cytokine levels in patients with polypoidal choroidal vasculopathy and neovascular age-related macular degeneration. Ophthalmic Res (2014) 0.85
Epigenetic understanding of gene-environment interactions in psychiatric disorders: a new concept of clinical genetics. Clin Epigenetics (2012) 0.84
Behavioral characterization of escalated aggression induced by GABA(B) receptor activation in the dorsal raphe nucleus. Psychopharmacology (Berl) (2012) 0.83
Role of complement factor H I62V and age-related maculopathy susceptibility 2 A69S variants in the clinical expression of polypoidal choroidal vasculopathy. Ophthalmology (2011) 0.83
QTL analyses of spontaneous activity by using mouse strains from Mishima battery. Mamm Genome (2002) 0.83
Sequence-specific microscopic visualization of DNA methylation status at satellite repeats in individual cell nuclei and chromosomes. Nucleic Acids Res (2013) 0.82
Mutational analysis of the WASP gene in 2 Korean families with Wiskott-Aldrich syndrome. Int J Hematol (2003) 0.82
Application of probe electrospray to direct ambient analysis of biological samples. Rapid Commun Mass Spectrom (2008) 0.82
Mosaic genealogy of the Mus musculus genome revealed by 21 nuclear genes from its three subspecies. Genes Genet Syst (2008) 0.81
An Xp22.12 microduplication including RPS6KA3 identified in a family with variably affected intellectual and behavioral disabilities. J Hum Genet (2013) 0.81
Analysis of histone modification around the CpG island region of the p15 gene in acute myeloblastic leukemia. Leuk Res (2006) 0.81
Multigenic factors associated with a hydrocephalus-like phenotype found in inter-subspecific consomic mouse strains. Mamm Genome (2008) 0.81
QTL analyses of temporal and intensity components of home-cage activity in KJR and C57BL/6J strains. BMC Genet (2009) 0.81
Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation. Hum Genet (2011) 0.80
[Analysis of 14 individuals who requested predictive genetic testing for hereditary neuromuscular diseases]. Rinsho Shinkeigaku (2002) 0.80
Association of morphine-induced antinociception with variations in the 5' flanking and 3' untranslated regions of the mu opioid receptor gene in 10 inbred mouse strains. Pharmacogenet Genomics (2008) 0.80
Test standardization in behavioural neuroscience: a response to Stanford. J Psychopharmacol (2007) 0.80
Identification of QTLs for differential capsaicin sensitivity between mouse strains KJR and C57BL/6. Pain (2003) 0.79
Female hyper IgM syndrome type 1 with a chromosomal translocation disrupting CD40LG. Biochim Biophys Acta (2005) 0.79
Molecular evolution of cadherin-related neuronal receptor/protocadherin(alpha) (CNR/Pcdh(alpha)) gene cluster in Mus musculus subspecies. Mol Biol Evol (2005) 0.79
Genetic variants in the SKIV2L gene in exudative age-related macular degeneration in the Japanese population. Ophthalmic Genet (2014) 0.78
Functional disomy for Xq22-q23 in a girl with complex rearrangements of chromosomes 3 and X. Am J Med Genet A (2003) 0.78
Granulocyte-macrophage colony-stimulating factor induces de novo methylation of the p15 CpG island in hematopoietic cells. Cytokine (2005) 0.78
Resistance of T-cell acute lymphoblastic leukemia to tumor necrosis factor--related apoptosis-inducing ligand-mediated apoptosis. Exp Hematol (2010) 0.78
6p subtelomere deletion with congenital glaucoma, severe mental retardation, and growth impairment. Pediatr Int (2013) 0.78
Modeling Rett Syndrome Using Human Induced Pluripotent Stem Cells. CNS Neurol Disord Drug Targets (2016) 0.77
The incidence of hypoplasia of the corpus callosum in patients with dup (X)(q28) involving MECP2 is associated with the location of distal breakpoints. Am J Med Genet A (2012) 0.77
Augmentation of polysialic acid by valproic acid in early postnatal mouse hippocampus and primary cultured hippocampal neurons. J Biosci Bioeng (2008) 0.77
GENETIC FACTORS ASSOCIATED WITH CHOROIDAL VASCULAR HYPERPERMEABILITY AND SUBFOVEAL CHOROIDAL THICKNESS IN POLYPOIDAL CHOROIDAL VASCULOPATHY. Retina (2016) 0.77
Identification of both copy number variation-type and constant-type core elements in a large segmental duplication region of the mouse genome. BMC Genomics (2013) 0.76
A female patient with incomplete hemophagocytic lymphohistiocytosis caused by a heterozygous XIAP mutation associated with non-random X-chromosome inactivation skewed towards the wild-type XIAP allele. J Clin Immunol (2015) 0.76
Copy number variations due to large genomic deletion in X-linked chronic granulomatous disease. PLoS One (2012) 0.76
Putative PPAR Target Genes Express Highly in Skeletal Muscle of Insulin-Resistant MetS Model SHR/NDmc-cp Rats. J Nutr Sci Vitaminol (Tokyo) (2015) 0.76
Enhanced prepulse inhibition and low sensitivity to a dopamine agonist in HESR1 knockout mice. J Neurosci Res (2013) 0.76
Role of epigenetics in Rett syndrome. Epigenomics (2013) 0.76
Myelination of a fetus with Pelizaeus-Merzbacher disease: immunopathological study. Ann Neurol (2003) 0.75
JAK2V617F mutation-positive childhood essential thrombocythemia associated with cerebral venous sinus thrombosis. J Pediatr Hematol Oncol (2009) 0.75
Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome. Nat Commun (2016) 0.75
Differential X Chromosome Inactivation Patterns during the Propagation of Human Induced Pluripotent Stem Cells. Keio J Med (2017) 0.75
Novel etiological and therapeutic strategies for neurodiseases: epigenetic understanding of gene-environment interactions. J Pharmacol Sci (2010) 0.75
Rapid detection of drugs in biofluids using atmospheric pressure chemi/chemical ionization mass spectrometry. Rapid Commun Mass Spectrom (2009) 0.75
One third of Japanese patients with multiple osteochondromas may have mutations in genes other than EXT1 or EXT2. Genet Test (2008) 0.75
[Epigenetics]. Nihon Rinsho (2010) 0.75
Epigenomics comes of age with expanding roles in biological understanding and clinical application. J Hum Genet (2013) 0.75
[Introductory remarks]. No To Hattatsu (2015) 0.75
[Molecular mechanism in Rett syndrome]. Nihon Yakurigaku Zasshi (2015) 0.75
Pre-B-cell acute lymphoblastic leukemia in a boy with hereditary multiple exostoses caused by EXT1 deletion. Pediatr Hematol Oncol (2014) 0.75
[The epigenome in neurological disorders: a new marker for understanding neuronal dysfunction]. Brain Nerve (2014) 0.75
[Relationship between Oprm1 polymorphism and morphine sensitivity in inbred-strain mice derived from wild mice]. Nihon Shinkei Seishin Yakurigaku Zasshi (2011) 0.75