Allowing for sex differences increases power in a GWAS of multiplex Autism families (Q44055564)

29 November 2017

Allowing for sex differences increases power in a GWAS of multiplex Autism families (English)

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genome-wide association study

29 November 2017

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2

R M Cantor

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29 November 2017

A T-H Lu

1

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PubMed ID

21151189

29 November 2017

language of work or name

English

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publication date

14 December 2010

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29 November 2017

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29 November 2017

17

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29 November 2017

215-222

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29 November 2017

2

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https://scigraph.springernature.com/pub.10.1038/mp.2010.127

29 November 2017

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A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

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

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Advances in autism genetics: on the threshold of a new neurobiology

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A genome-wide linkage and association scan reveals novel loci for autism

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

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Replication of autism linkage: fine-mapping peak at 17q21.

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Evidence for sex-specific risk alleles in autism spectrum disorder

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High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene

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

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A Heteroskedasticity-Consistent Covariance Matrix Estimator and a Direct Test for Heteroskedasticity

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Properties of case/pseudocontrol analysis for genetic association studies: Effects of recombination, ascertainment, and multiple affected offspring

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Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

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Estimation of significance thresholds for genomewide association scans

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Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyocytes

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Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia

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Estimation and testing of gene-environment interactions in family-based association studies

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Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

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Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

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Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

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A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.

21 January 2018

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Molecular mechanisms of autism: a possible role for Ca2+ signaling

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Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.

21 January 2018

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Association of common variants in the Joubert syndrome gene (AHI1) with autism

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High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility

21 January 2018

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Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

21 January 2018

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Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder

21 January 2018

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A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

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Identifying autism loci and genes by tracing recent shared ancestry

21 January 2018

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Prioritizing GWAS results: A review of statistical methods and recommendations for their application

21 January 2018

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

Exploiting gene-environment interaction to detect genetic associations

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.127

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/MP.2010.127

1 reference

29 November 2017

1 reference

PubMed ID

21151189