Genome-wide association studies of quantitative traits with related individuals: little (power) lost but much to be gained (Q57242463)

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

A common variant of HMGA2 is associated with adult and childhood height in the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Searching for genetic determinants in the new millennium

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Efficient study designs for test of genetic association using sibship data and unrelated cases and controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

The value of relatives with phenotypes but missing genotypes in association studies for quantitative traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Sex differences in heritability of BMI: a comparative study of results from twin studies in eight countries.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Mapping genetic loci that determine leukocyte telomere length in a large sample of unselected female sibling pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Variance components analyses of multiple asthma traits in a large sample of Australian families ascertained through a twin proband.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

GenomEUtwin: A Strategy to Identify Genetic Influences on Health and Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

A general test of association for quantitative traits in nuclear families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

PBAT: tools for family-based association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Case-control association testing with related individuals: a more powerful quasi-likelihood score test

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Family-based association tests for genomewide association scans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990

inferred from DOI database lookup

7 January 2021

based on heuristic

The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases I. DNA pooling

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201990