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

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scientific article published on December 14, 2010

Language	Label	Description	Also known as
English	Allowing for sex differences increases power in a GWAS of multiplex Autism families	scientific article published on December 14, 2010

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scholarly article

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Europe PubMed Central

PubMed publication ID

29 November 2017

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

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Europe PubMed Central

PubMed publication ID

29 November 2017

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genome-wide association study

1 reference

based on heuristic

inferred from title

genetic predisposition to disease

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21151189

19 November 2024

2

object named as

R M Cantor

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Europe PubMed Central

PubMed publication ID

29 November 2017

author name string

A. T-H Lu

1

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21151189

19 November 2024

language of work or name

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publication date

14 December 2010

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Europe PubMed Central

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29 November 2017

full work available at URL

https://www.nature.com/articles/mp2010127.pdf

online access status

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21151189

19 November 2024

https://www.nature.com/articles/mp2010127.pdf

1 reference

10.1038/MP.2010.127

https://api.crossref.org/works/10.1038/MP.2010.127

19 November 2024

https://www.nature.com/articles/mp2010127

1 reference

10.1038/MP.2010.127

https://api.crossref.org/works/10.1038/MP.2010.127

19 November 2024

Molecular Psychiatry

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

17

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Europe PubMed Central

PubMed publication ID

29 November 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

215-222

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Finding the missing heritability of complex diseases

1 reference

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

21 January 2018

The family based association test method: strategies for studying general genotype--phenotype associations.

1 reference

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

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Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects.

1 reference

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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

1 reference

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

1 reference

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

1 reference

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

1 reference

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

1 reference

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Molecular genetics of autism

1 reference

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A genomewide screen of 345 families for autism-susceptibility loci

1 reference

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High density SNP association study of a major autism linkage region on chromosome 17.

1 reference

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

1 reference

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The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

1 reference

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

21 January 2018

Evidence for sex-specific risk alleles in autism spectrum disorder

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Estimation of significance thresholds for genomewide association scans

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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21 January 2018

The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading [...]

1 reference

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21 January 2018

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

1 reference

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

1 reference

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21 January 2018

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.

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21 January 2018

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.

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Identifying autism loci and genes by tracing recent shared ancestry

1 reference

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

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

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7 January 2021

based on heuristic

inferred from DOI database lookup

Exploiting gene-environment interaction to detect genetic associations

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/MP.2010.127

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

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