Common DNA methylation alterations in multiple brain regions in autism. (Q34287640)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23999529%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

title

Common DNA methylation alterations in multiple brain regions in autism (English)

1 reference

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8 March 2020

0 references

0 references

2

1 reference

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8 March 2020

Andrew P. Feinberg

6

1 reference

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8 March 2020

Christine Ladd-Acosta

1

object named as

C Ladd-Acosta

1 reference

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8 March 2020

author name string

E Briem

3

1 reference

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8 March 2020

M D Fallin

4

1 reference

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8 March 2020

W E Kaufmann

5

1 reference

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8 March 2020

language of work or name

English

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publication date

3 September 2013

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8 March 2020

1 reference

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8 March 2020

volume

19

1 reference

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8 March 2020

issue

8

1 reference

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8 March 2020

page(s)

862-871

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23999529%20AND%20SRC:MED&resulttype=core&format=json

A cell epigenotype specific model for the correction of brain cellular heterogeneity bias and its application to age, brain region and major depression

8 March 2020

cites work

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Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis

6 July 2018

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Exploring genome-wide DNA methylation profiles altered in hepatocellular carcinoma using Infinium HumanMethylation 450 BeadChips

6 July 2018

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Pathogenic SYNGAP1 mutations impair cognitive development by disrupting maturation of dendritic spine synapses

6 July 2018

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CpG island shore methylation regulates caveolin-1 expression in breast cancer

6 July 2018

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Brain transcriptional and epigenetic associations with autism

6 July 2018

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Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.

6 July 2018

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Genetic architectures of psychiatric disorders: the emerging picture and its implications

6 July 2018

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Proteins involved in establishment and maintenance of imprinted methylation marks.

6 July 2018

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Base-pair resolution DNA methylation sequencing reveals profoundly divergent epigenetic landscapes in acute myeloid leukemia

6 July 2018

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DNA methylome signature in rheumatoid arthritis

6 July 2018

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Bump hunting to identify differentially methylated regions in epigenetic epidemiology studies.

6 July 2018

1 reference

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PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome

6 July 2018

1 reference

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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

6 July 2018

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Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia

6 July 2018

1 reference

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Epigenetic signatures of autism: trimethylated H3K4 landscapes in prefrontal neurons

6 July 2018

1 reference

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Transcriptomic analysis of autistic brain reveals convergent molecular pathology

6 July 2018

1 reference

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Validation of a DNA methylation microarray for 450,000 CpG sites in the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4184909

The autism candidate gene Neurobeachin encodes a scaffolding protein implicated in membrane trafficking and signaling

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4184909

Comparative methylome analysis of benign and malignant peripheral nerve sheath tumors.

6 July 2018

1 reference

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Contactin 4 as an autism susceptibility locus

6 July 2018

1 reference

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Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis

6 July 2018

1 reference

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Comparison of Beta-value and M-value methods for quantifying methylation levels by microarray analysis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4184909

ENCODE whole-genome data in the UCSC genome browser (2011 update)

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4184909

The NADH‐ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism

6 July 2018

1 reference

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Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs

6 July 2018

1 reference

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A complementary role for the tetraspanins CD37 and Tssc6 in cellular immunity

6 July 2018

1 reference

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Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

6 July 2018

1 reference

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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

6 July 2018

1 reference

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Differential methylation of tissue- and cancer-specific CpG island shores distinguishes human induced pluripotent stem cells, embryonic stem cells and fibroblasts

6 July 2018

1 reference

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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

6 July 2018

1 reference

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The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores

6 July 2018

1 reference

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A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints

6 July 2018

1 reference

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The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

6 July 2018

1 reference

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Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.

6 July 2018

1 reference

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Disruption of contactin 4 in three subjects with autism spectrum disorder

6 July 2018

1 reference

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Tetraspanins-structural and signalling scaffolds that regulate platelet function

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4184909

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4184909

Contribution of SHANK3 mutations to autism spectrum disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4184909

Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4184909

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4184909

Epigenetics of autism spectrum disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4184909

Combinatorial microRNA target predictions

6 July 2018

1 reference

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Heritable and nonheritable risk factors for autism spectrum disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4184909

Micro RNAs are complementary to 3' UTR sequence motifs that mediate negative post-transcriptional regulation

6 July 2018

1 reference

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

6 July 2018

1 reference

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Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

6 July 2018

1 reference

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CACNA1H mutations in autism spectrum disorders.

6 July 2018

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SFARI Gene: an evolving database for the autism research community

21 January 2018

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Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease

21 January 2018

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Mechanisms of imprinting of the Prader-Willi/Angelman region.

21 January 2018

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A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A

21 January 2018

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Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

21 January 2018

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Complex epigenetic regulation of engrailed-2 (EN-2) homeobox gene in the autism cerebellum

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2013.114

MECP2 promoter methylation and X chromosome inactivation in autism

21 January 2018

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High density DNA methylation array with single CpG site resolution

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2013.114

MethPrimer: designing primers for methylation PCRs

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2013.114

DNA methylation shows genome-wide association of NFIX, RAPGEF2 and MSRB3 with gestational age at birth

21 January 2018

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Copy number variation has little impact on bead-array-based measures of DNA methylation.

21 January 2018

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Epigenomic profiling reveals DNA-methylation changes associated with major psychosis

21 January 2018

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Genome-wide DNA methylation scan in major depressive disorder

21 January 2018

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Gene expression profiles in the common marmoset brain determined using a newly developed common marmoset-specific DNA microarray

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2013.114

Global cerebral and regional multimodal neuroimaging markers of the neurobiology of autism: development and cognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.114

Language disorders in children with morphologic abnormalities of the hippocampus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.114

Hippocampus in autism: a Golgi analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.114

Novel de novo SHANK3 mutation in autistic patients

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2013.114

Autistic disorder in 2 children with mitochondrial disorders

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2013.114

Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood

21 January 2018

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Dramatic increase in autism prevalence parallels explosion of research into its biology and causes

21 January 2018

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Amygdala and hippocampus enlargement during adolescence in autism

28 October 2018

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Hypermethylation of CpG islands and shores around specific microRNAs and mirtrons is associated with the phenotype and presence of bladder cancer

28 October 2018

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12 December 2020

Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions

1 reference

12 December 2020

PRRT2 mutations cause hemiplegic migraine

1 reference

12 December 2020

PRRT2 mutation causes benign familial infantile convulsions

1 reference

12 December 2020

Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP

1 reference

12 December 2020

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12 December 2020

Functional variants ofTSPAN8are associated with bipolar disorder and schizophrenia

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12 December 2020

Identifiers

DOI

10.1038/MP.2013.114

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23999529%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23999529%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

PubMed publication ID

23999529

1 reference