(Q52675847)

5 May 2018

title

Intragenic CNVs for epigenetic regulatory genes in intellectual disability: Survey identifies pathogenic and benign single exon changes. (English)

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5 May 2018

disability affecting intellectual abilities

main subject

intellectual disability

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based on heuristic

inferred from title

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10

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5 May 2018

Farah R. Zahir

object named as

Farah R Zahir

1

0 references

Sonia Mayo

object named as

Sonia Mayo

3

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Carolyn J. Brown

4

object named as

Carolyn J Brown

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5 May 2018

9

Jacques L Michaud

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5 May 2018

author name string

Tracy Tucker

2

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5 May 2018

Emilia L Lim

5

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5 May 2018

Jonathan Taylor

6

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5 May 2018

Marco A Marra

7

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5 May 2018

Fadi F Hamdan

8

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5 May 2018

language of work or name

English

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publication date

1 November 2016

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5 May 2018

American Journal of Medical Genetics

published in

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5 May 2018

volume

170

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5 May 2018

issue

11

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5 May 2018

page(s)

2916-2926

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5 May 2018

Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disability

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs

21 January 2018

1 reference

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Diagnostic genome profiling in mental retardation

21 January 2018

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Identification and characterization of three new components of the mSin3A corepressor complex

21 January 2018

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Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization

21 January 2018

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The histone demethylase Kdm3a is essential to progression through differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Identification of the GGPS1 genes encoding geranylgeranyl diphosphate synthases from mouse and human

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Jumonji represses alpha-cardiac myosin heavy chain expression via inhibiting MEF2 activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

JUMONJI, a critical factor for cardiac development, functions as a transcriptional repressor

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Unwinding chromatin for development and growth: a few genes at a time.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Jarid2 is a PRC2 component in embryonic stem cells required for multi-lineage differentiation and recruitment of PRC1 and RNA Polymerase II to developmental regulators.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Jmjd1a and Jmjd2c histone H3 Lys 9 demethylases regulate self-renewal in embryonic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Organogenesis of the liver, thymus and spleen is affected in jumonji mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Positive association of schizophrenia to JARID2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Immune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Genetics of Early Onset Cognitive Impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

I-TASSER: a unified platform for automated protein structure and function prediction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Expression and association data strongly support JARID2 involvement in nonsyndromic cleft lip with or without cleft palate

21 January 2018

1 reference

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Roles of jumonji and jumonji family genes in chromatin regulation and development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

IFITM/Mil/Fragilis Family Proteins IFITM1 and IFITM3 Play Distinct Roles in Mouse Primordial Germ Cell Homing and Repulsion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Role of Jhdm2a in regulating metabolic gene expression and obesity resistance

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

The ENCODE Project at UC Santa Cruz

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Disruption of the epigenetic code: an emerging mechanism in mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

ATP-dependent chromatin-remodeling complexes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Allelic variation and differential expression of the mSIN3A histone deacetylase complex gene Arid4b promote mammary tumor growth and metastasis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

JHDM2A, a JmjC-containing H3K9 demethylase, facilitates transcription activation by androgen receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

PBAF chromatin-remodeling complex requires a novel specificity subunit, BAF200, to regulate expression of selective interferon-responsive genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Quantitative real-time polymerase chain reaction for the verification of genomic imbalances detected by microarray-based comparative genomic hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

Epigenetic impacts on neurodevelopment: pathophysiological mechanisms and genetic modes of action

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

ARID2: a new tumor suppressor gene in hepatocellular carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37669

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.37669

1 reference

5 May 2018

1 reference

5 May 2018