Common DNA methylation alterations in multiple brain regions in autism
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Title
Common DNA methylation alterations in multiple brain regions in autism
Authors
Keywords
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Journal
MOLECULAR PSYCHIATRY
Volume 19, Issue 8, Pages 862-871
Publisher
Springer Nature
Online
2013-09-03
DOI
10.1038/mp.2013.114
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Note: Only part of the references are listed.- A cell epigenotype specific model for the correction of brain cellular heterogeneity bias and its application to age, brain region and major depression
- (2013) Jerry Guintivano et al. Epigenetics
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- (2013) Angelo Labate et al. EPILEPSY RESEARCH
- Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis
- (2013) Yun Liu et al. NATURE BIOTECHNOLOGY
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- (2013) Jacob Gratten et al. NATURE GENETICS
- A common mode of recognition for methylated CpG
- (2013) Yiwei Liu et al. TRENDS IN BIOCHEMICAL SCIENCES
- Complex epigenetic regulation of Engrailed-2 (EN-2) homeobox gene in the autism cerebellum
- (2013) S J James et al. Translational Psychiatry
- PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome
- (2012) Sarah E. Heron et al. AMERICAN JOURNAL OF HUMAN GENETICS
- DNA methylome signature in rheumatoid arthritis
- (2012) Kazuhisa Nakano et al. ANNALS OF THE RHEUMATIC DISEASES
- Proteins involved in establishment and maintenance of imprinted methylation marks
- (2012) R. Strogantsev et al. Briefings in Functional Genomics
- Pathogenic SYNGAP1 Mutations Impair Cognitive Development by Disrupting Maturation of Dendritic Spine Synapses
- (2012) James P. Clement et al. CELL
- Exploring genome-wide DNA methylation profiles altered in hepatocellular carcinoma using Infinium HumanMethylation 450 BeadChips
- (2012) Jing Shen et al. Epigenetics
- DNA methylation shows genome-wide association ofNFIX,RAPGEF2andMSRB3with gestational age at birth
- (2012) Hwajin Lee et al. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY
- Bump hunting to identify differentially methylated regions in epigenetic epidemiology studies
- (2012) Andrew E Jaffe et al. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY
- Global Cerebral and Regional Multimodal Neuroimaging Markers of the Neurobiology of Autism
- (2012) Khader M. Hasan et al. JOURNAL OF CHILD NEUROLOGY
- Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions
- (2012) Shinji Ono et al. JOURNAL OF HUMAN GENETICS
- Genetic architectures of psychiatric disorders: the emerging picture and its implications
- (2012) Patrick F. Sullivan et al. NATURE REVIEWS GENETICS
- PRRT2 mutation causes benign familial infantile convulsions
- (2012) B. de Vries et al. NEUROLOGY
- PRRT2 mutations cause hemiplegic migraine
- (2012) F. Riant et al. NEUROLOGY
- Genome-Wide DNA Methylation Scan in Major Depressive Disorder
- (2012) Sarven Sabunciyan et al. PLoS One
- Brain Transcriptional and Epigenetic Associations with Autism
- (2012) Matthew R. Ginsberg et al. PLoS One
- Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions
- (2012) Hsien-Yang Lee et al. Cell Reports
- Base-Pair Resolution DNA Methylation Sequencing Reveals Profoundly Divergent Epigenetic Landscapes in Acute Myeloid Leukemia
- (2012) Altuna Akalin et al. PLoS Genetics
- Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood
- (2012) Matthew N Davies et al. GENOME BIOLOGY
- Epigenetic Signatures of Autism
- (2011) Hennady P. Shulha ARCHIVES OF GENERAL PSYCHIATRY
- Contactin 4 as an autism susceptibility locus
- (2011) Catherine E. Cottrell et al. Autism Research
- The Autism Candidate Gene Neurobeachin Encodes a Scaffolding Protein Implicated in Membrane Trafficking and Signaling
- (2011) K. Volders et al. CURRENT MOLECULAR MEDICINE
- Validation of a DNA methylation microarray for 450,000 CpG sites in the human genome
- (2011) Juan Sandoval et al. Epigenetics
- Comparative methylome analysis of benign and malignant peripheral nerve sheath tumors
- (2011) A. Feber et al. GENOME RESEARCH
- High density DNA methylation array with single CpG site resolution
- (2011) Marina Bibikova et al. GENOMICS
- Zinc Finger Protein ZFP57 Requires Its Co-factor to Recruit DNA Methyltransferases and Maintains DNA Methylation Imprint in Embryonic Stem Cells via Its Transcriptional Repression Domain
- (2011) Xiaopan Zuo et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis
- (2011) D A Rossignol et al. MOLECULAR PSYCHIATRY
- Transcriptomic analysis of autistic brain reveals convergent molecular pathology
- (2011) Irina Voineagu et al. NATURE
- Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia
- (2011) Wan-Jin Chen et al. NATURE GENETICS
- The NADH-ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism
- (2010) T. Marui et al. ACTA PSYCHIATRICA SCANDINAVICA
- Troubles du langage chez les enfants porteurs d’anomalies morphologiques de l’hippocampe
- (2010) G. Agostini et al. ARCHIVES DE PEDIATRIE
- Comparison of Beta-value and M-value methods for quantifying methylation levels by microarray analysis
- (2010) Pan Du et al. BMC BIOINFORMATICS
- Hypermethylation of CpG Islands and Shores around Specific MicroRNAs and Mirtrons Is Associated with the Phenotype and Presence of Bladder Cancer
- (2010) Ewa Dudziec et al. CLINICAL CANCER RESEARCH
- SFARI Gene: an evolving database for the autism research community
- (2010) S. Banerjee-Basu et al. Disease Models & Mechanisms
- Global methylation profiling of lymphoblastoid cell lines reveals epigenetic contributions to autism spectrum disorders and a novel autism candidate gene, RORA, whose protein product is reduced in autistic brain
- (2010) AnhThu Nguyen et al. FASEB JOURNAL
- A Complementary Role for the Tetraspanins CD37 and Tssc6 in Cellular Immunity
- (2010) K. H. Gartlan et al. JOURNAL OF IMMUNOLOGY
- Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation
- (2010) Simone Berkel et al. NATURE GENETICS
- ENCODE whole-genome data in the UCSC genome browser (2011 update)
- (2010) Brian J. Raney et al. NUCLEIC ACIDS RESEARCH
- Parent-Of-Origin Effects in Autism Identified through Genome-Wide Linkage Analysis of 16,000 SNPs
- (2010) Delphine Fradin et al. PLoS One
- Copy number variation has little impact on bead-array-based measures of DNA methylation
- (2009) E. Andrés Houseman et al. BIOINFORMATICS
- Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
- (2009) Simon G Gregory et al. BMC Medicine
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- (2009) Joseph T. Glessner et al. NATURE
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- The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores
- (2009) Rafael A Irizarry et al. NATURE GENETICS
- Gene expression profiles in the common marmoset brain determined using a newly developed common marmoset-specific DNA microarray
- (2009) Toshifumi Fukuoka et al. NEUROSCIENCE RESEARCH
- Epigenomic Profiling Reveals DNA-Methylation Changes Associated with Major Psychosis
- (2008) Jonathan Mill et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- (2008) Dan E. Arking et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mechanisms of imprinting of the Prader-Willi/Angelman region
- (2008) Bernhard Horsthemke et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Novel de novo SHANK3 mutation in autistic patients
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- MECP2promoter methylation and X chromosome inactivation in autism
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- A Maternal-Zygotic Effect Gene, Zfp57, Maintains Both Maternal and Paternal Imprints
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- Disruption of contactin 4 in three subjects with autism spectrum disorder
- (2008) J Roohi et al. JOURNAL OF MEDICAL GENETICS
- The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13
- (2008) Amber Hogart et al. NEUROBIOLOGY OF DISEASE
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