(Q35629165)

9 August 2017

title

Single nucleotide polymorphisms predict symptom severity of autism spectrum disorder (English)

1 reference

single-nucleotide polymorphism

9 August 2017

main subject

autism spectrum disorder

0 references

autism

0 references

1 reference

Yun Jiao

1

1 reference

9 August 2017

Rong Chen

2

1 reference

9 August 2017

Xiaoyan Ke

3

1 reference

9 August 2017

Lu Cheng

4

1 reference

9 August 2017

Kangkang Chu

5

1 reference

9 August 2017

Zuhong Lu

6

1 reference

9 August 2017

Edward H Herskovits

7

1 reference

9 August 2017

language of work or name

English

0 references

publication date

1 June 2012

1 reference

Journal of Autism and Developmental Disorders

9 August 2017

published in

1 reference

9 August 2017

volume

42

1 reference

9 August 2017

issue

6

1 reference

9 August 2017

page(s)

971-983

1 reference

Genetics of autistic disorders: review and clinical implications

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Association study between BDNF gene polymorphisms and autism by three-dimensional gel-based microarray.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Classification with high-dimensional genetic data: assigning patients and genetic features to known classes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

GABA(A) receptor downregulation in brains of subjects with autism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

The genetics of autistic disorders and its clinical relevance: a review of the literature

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Investigation of autism and GABA receptor subunit genes in multiple ethnic groups

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Tree-structured supervised learning and the genetics of hypertension

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Autism as a disorder of neural information processing: directions for research and targets for therapy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Association of tryptophan 2,3 dioxygenase gene polymorphism with autism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Association between a GABRB3 polymorphism and autism.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Toward objective classification of childhood autism: Childhood Autism Rating Scale (CARS)

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Diagnostic uses of the Vineland Adaptive Behavior Scales

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Plasma amino acid levels in children with autism and their families

12 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

Density and distribution of hippocampal neurotransmitter receptors in autism: an autoradiographic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

The International HapMap Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

Microarray-based approach for high-throughput genotyping of single-nucleotide polymorphisms with layer-by-layer dual-color fluorescence hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

Microarray-based method for genotyping of functional single nucleotide polymorphisms using dual-color fluorescence hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

Association of GABRB3 polymorphisms with autism spectrum disorders in Korean trios

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

A partition-ligation-combination-subdivision EM algorithm for haplotype inference with multiallelic markers: update of the SHEsis (http://analysis.bio-x.cn).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

Detecting high-order interactions of single nucleotide polymorphisms using genetic programming

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

Penalized logistic regression for detecting gene interactions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

Genetics of childhood disorders: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

Sequence analysis using logic regression.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Plasma excitatory amino acids in autism.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

[Developmental disorders in the fourth edition of the American classification: diagnostic and statistical manual of mental disorders (DSM IV -- optional book)]

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244507

Identifying SNPs predictive of phenotype using random forests

25 September 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10803-011-1327-5

SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21786105

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

An improved gel-based DNA microarray method for detecting single nucleotide mismatch

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21786105

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/21786105

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10803-011-1327-5

1 reference

9 August 2017

1 reference

9 August 2017

1 reference