(Q35834878)

10 August 2017

An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males (English)

1 reference

Margaret A. Pericak-Vance

10 August 2017

autism spectrum disorder

0 references

autism

0 references

author

15

object named as

Margaret A Pericak-Vance

0 references

Jonathan L Haines

14

object named as

Jonathan L Haines

1 reference

10 August 2017

13

Hakon Hakonarson

1 reference

10 August 2017

3

Kai Wang

1 reference

10 August 2017

7

Michael L Cuccaro

1 reference

10 August 2017

Ren-Hua Chung

1

1 reference

10 August 2017

Deqiong Ma

2

1 reference

10 August 2017

Dale J Hedges

4

1 reference

10 August 2017

James M Jaworski

5

1 reference

10 August 2017

John R Gilbert

6

1 reference

10 August 2017

Harry H Wright

8

1 reference

10 August 2017

Ruth K Abramson

9

1 reference

10 August 2017

Ioanna Konidari

10

1 reference

10 August 2017

Patrice L Whitehead

11

1 reference

10 August 2017

Gerard D Schellenberg

12

1 reference

10 August 2017

Eden R Martin

16

1 reference

10 August 2017

4 November 2011

1 reference

10 August 2017

1 reference

10 August 2017

2

1 reference

10 August 2017

1

1 reference

10 August 2017

18

1 reference

A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Accuracy of CNV Detection from GWAS Data

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

CAPL: a novel association test using case-control and family data and accounting for population stratification

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

A genome-wide scan for common alleles affecting risk for autism

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Autism Genetic Database (AGD): a comprehensive database including autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Common genetic variants on 5p14.1 associate with autism spectrum disorders

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Mutations in the calcium-related gene IL1RAPL1 are associated with autism

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Familial deletion within NLGN4 associated with autism and Tourette syndrome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

TBL1-TBLR1 and beta-catenin recruit each other to Wnt target-gene promoter for transcription activation and oncogenesis

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

PLINK: a tool set for whole-genome association and population-based linkage analyses

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Population structure and eigenanalysis

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

X-APL: an improved family-based test of association in the presence of linkage for the X chromosome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

The ups and downs of Wnt signaling in prevalent neurological disorders

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

11 July 2018

The prevalence of autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Prevalence of autism in a US metropolitan area

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

A genomewide screen for autism susceptibility loci

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Genomic control for association studies

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Direct regulation of the Xenopus engrailed-2 promoter by the Wnt signaling pathway, and a molecular screen for Wnt-responsive genes, confirm a role for Wnt signaling during neural patterning in Xenopus.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Xp deletions associated with autism in three females

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Association study with two markers of a human homeogene in infantile autism

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Prevalence of parent-reported diagnosis of autism spectrum disorder among children in the US, 2007.

11 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-18

Genomic screen and follow-up analysis for autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-18

The APL test: extension to general nuclear families and haplotypes and examination of its robustness

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-18

A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-18

Evidence supporting WNT2 as an autism susceptibility gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-18

Brief report: non-random X chromosome inactivation in females with autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-18

Association of autistic spectrum disorders with dystrophinopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-18

Population-specific GSTM1 copy number variation

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Neuropsychiatric disorders in males with duchenne muscular dystrophy: frequency rate of attention-deficit hyperactivity disorder (ADHD), autism spectrum disorder, and obsessive--compulsive disorder

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autism

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

Developmental expression of Wnt signaling factors in mouse brain

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305893

A patient with Duchenne muscular dystrophy and autism demonstrates a hemizygous deletion affecting Dystrophin

24 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22050706

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Evolutionary features of the 4-Mb Xq21.3 XY homology region revealed by a map at 60-kb resolution

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22050706

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The Xp contiguous deletion syndrome and autism

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22050706

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/2040-2392-2-18

1 reference

Dimensions Publication ID

10 August 2017

0 references

1 reference

10 August 2017

PubMed publication ID

22050706

1 reference