(Q34136181)

31 July 2017

title

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals (English)

1 reference

Margaret A. Pericak-Vance

31 July 2017

0 references

10

object named as

Margaret A Pericak-Vance

0 references

Holly N Cukier

object named as

Holly N Cukier

1

0 references

Raquel Rabionet

object named as

Raquel Rabionet

2

0 references

author name string

Ioanna Konidari

3

1 reference

31 July 2017

Melissa Y Rayner-Evans

4

1 reference

31 July 2017

Mary L Baltos

5

1 reference

31 July 2017

Harry H Wright

6

1 reference

31 July 2017

Ruth K Abramson

7

1 reference

31 July 2017

Eden R Martin

8

1 reference

31 July 2017

Michael L Cuccaro

9

1 reference

31 July 2017

John R Gilbert

11

1 reference

31 July 2017

publication date

18 November 2009

1 reference

31 July 2017

1 reference

31 July 2017

volume

11

1 reference

31 July 2017

issue

3

1 reference

31 July 2017

page(s)

291-303

1 reference

https://scigraph.springernature.com/pub.10.1007/s10048-009-0228-7

31 July 2017

exact match

0 references

cites work

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5 July 2018

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5 July 2018

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5 July 2018

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Phosphorylation of methyl-CpG binding protein 2 (MeCP2) regulates the intracellular localization during neuronal cell differentiation

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Mutation analysis of methyl-CpG binding protein family genes in autistic patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Risk factors for autism: perinatal factors, parental psychiatric history, and socioeconomic status

5 July 2018

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5 July 2018

1 reference

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A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome

5 July 2018

1 reference

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5 July 2018

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Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

5 July 2018

1 reference

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Identification of MeCP2 mutations in a series of females with autistic disorder

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Mice lacking methyl-CpG binding protein 1 have deficits in adult neurogenesis and hippocampal function

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

SNP and haplotype variation in the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Comparative study of methyl-CpG-binding domain proteins

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Rett syndrome and MeCP2: linking epigenetics and neuronal function

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Epidemiological trends in rates of autism.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

MeCP2 and other methyl-CpG binding proteins

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Excess of twins among affected sibling pairs with autism: implications for the etiology of autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

The thymine glycosylase MBD4 can bind to the product of deamination at methylated CpG sites

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Autism as a strongly genetic disorder: evidence from a British twin study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Concordance for the syndrome of autism in 40 pairs of afflicted twins

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients.

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-009-0228-7

Sequence variants within exon 1 of MECP2 occur in females with mental retardation.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-009-0228-7

Obstetric and parental psychiatric variables as potential predictors of autism severity.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Autism in African American families: clinical-phenotypic findings.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

The impact of MECP2 mutations in the expression patterns of Rett syndrome patients.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941261

Another patient with MECP2 mutation without classic Rett syndrome phenotype

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19921286

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10048-009-0228-7

1 reference

31 July 2017

1 reference

31 July 2017

1 reference