(Q57822917)

English

Blindly Using Wald's Test Can Miss Rare Disease-Causal Variants in Case-Control Association Studies

article published in 2012

In more languages

edit

Statements

instance of

scholarly article

0 references

title

Blindly Using Wald's Test Can Miss Rare Disease-Causal Variants in Case-Control Association Studies (English)

0 references

1 reference

Chao Xing

4

0 references

author name string

Guan Xing

series ordinal

1

0 references

Chang-Yun Lin

series ordinal

2

0 references

Stephen P. Wooding

series ordinal

3

0 references

language of work or name

English

0 references

publication date

18 January 2012

0 references

published in

Annals of Human Genetics

0 references

volume

76

0 references

issue

2

0 references

page(s)

168-177

0 references

cites work

Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

The $\chi^2$ Test of Goodness of Fit

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

Polymorphisms associated with cholesterol and risk of cardiovascular events

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

Small-Sample Comparisons of Exact Levels for Chi-Squared Goodness-of-Fit Statistics

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

An evaluation of statistical approaches to rare variant analysis in genetic association studies

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

Testing for an unusual distribution of rare variants

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

X. On the criterion that a given system of deviations from the probable in the case of a correlated system of variables is such that it can be reasonably supposed to have arisen from random sampling

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

Mutations in BRIP1 confer high risk of ovarian cancer

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

From genotypes to genes: doubling the sample size

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

Identification of low-frequency variants associated with gout and serum uric acid levels

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

The Dallas Heart Study: a population-based probability sample for the multidisciplinary study of ethnic differences in cardiovascular health.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

Rare-variant association testing for sequencing data with the sequence kernel association test

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

Adjusting for covariates in logistic regression models

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2011.00700.X

retrieved

21 January 2018

Identifiers

DOI

10.1111/J.1469-1809.2011.00700.X

0 references

PubMed publication ID

22256951

0 references

(Q57822917)

Blindly Using Wald's Test Can Miss Rare Disease-Causal Variants in Case-Control Association Studies

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)