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

29 November 2017

title

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

1 reference

genome-wide association study

29 November 2017

0 references

1 reference

based on heuristic

inferred from title

genetic predisposition to disease

1 reference

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

19 November 2024

R M Cantor

1 reference

29 November 2017

A. T-H Lu

1 reference

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

English

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publication date

14 December 2010

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full work available at URL

29 November 2017

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

1 reference

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

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

19 November 2024

1 reference

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

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

19 November 2024

1 reference

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

19 November 2024

1 reference

29 November 2017

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29 November 2017

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29 November 2017

page(s)

215-222

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Finding the missing heritability of complex diseases

29 November 2017

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

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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 [...]

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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.

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

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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

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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.

21 January 2018

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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