Family-based genome-wide association studies (Q37389487)

20 August 2017

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title

Family-based genome-wide association studies (English)

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genome-wide association study

20 August 2017

main subject

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author

Peter M. Visscher

series ordinal

2

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20 August 2017

Beben Benyamin

1

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author name string

Allan F McRae

series ordinal

3

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20 August 2017

publication date

1 February 2009

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20 August 2017

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20 August 2017

volume

10

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20 August 2017

issue

2

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20 August 2017

page(s)

181-190

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Genome-wide association studies for common diseases and complex traits

20 August 2017

cites work

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Genomic imprinting effects on brain development and function

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Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

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Strong association of de novo copy number mutations with autism

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21 January 2018

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Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data

21 January 2018

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Maximum-likelihood estimation of haplotype frequencies in nuclear families

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study

21 January 2018

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Genome-wide association with bone mass and geometry in the Framingham Heart Study

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Genomic control for association studies

21 January 2018

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The power of genomic control

21 January 2018

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Association testing with Mendel.

21 January 2018

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

21 January 2018

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Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

21 January 2018

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Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4

21 January 2018

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Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci

21 January 2018

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Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

21 January 2018

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A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

21 January 2018

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Systematic association mapping identifies NELL1 as a novel IBD disease gene

21 January 2018

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Risk alleles for multiple sclerosis identified by a genomewide study

21 January 2018

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A common genetic variant is associated with adult and childhood obesity

21 January 2018

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A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

21 January 2018

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A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study

21 January 2018

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Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

21 January 2018

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A 100K genome-wide association scan for diabetes and related traits in the Framingham Heart Study: replication and integration with other genome-wide datasets

21 January 2018

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Demonstrating stratification in a European American population

21 January 2018

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Residual linkage: why do linkage peaks not disappear after an association study?

21 January 2018

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Power of QTL detection using association tests with family controls

21 January 2018

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

21 January 2018

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

21 January 2018

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10.2217/14622416.10.2.181

21 January 2018

Identifiers

DOI

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20 August 2017

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