SNP set association analysis for familial data (Q30564362)

17 August 2017

SNP set association analysis for familial data (English)

1 reference

17 August 2017

5

Sharon L R Kardia

1 reference

17 August 2017

3

Lawrence F Bielak

1 reference

17 August 2017

6

Patricia A Peyser

1 reference

17 August 2017

7

Xihong Lin

1 reference

17 August 2017

Elizabeth D Schifano

1

1 reference

PMCID

3683469

17 August 2017

Michael P Epstein

series ordinal

2

1 reference

PMCID

3683469

17 August 2017

Min A Jhun

series ordinal

4

1 reference

17 August 2017

11 September 2012

1 reference

17 August 2017

1 reference

17 August 2017

36

1 reference

17 August 2017

8

1 reference

17 August 2017

797-810

1 reference

Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Kernel machine SNP-set analysis for censored survival outcomes in genome-wide association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

A versatile gene-based test for genome-wide association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Powerful SNP-set analysis for case-control genome-wide association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Finding the missing heritability of complex diseases

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Association tests using kernel-based measures of multi-locus genotype similarity between individuals

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Genome-wide association scans for secondary traits using case-control samples

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Asymptotic tests of association with multiple SNPs in linkage disequilibrium

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Power comparisons between similarity-based multilocus association methods, logistic regression, and score tests for haplotypes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Estimation and testing for the effect of a genetic pathway on a disease outcome using logistic kernel machine regression via logistic mixed models

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Reproducing kernel hilbert spaces regression methods for genomic assisted prediction of quantitative traits

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

A powerful and flexible multilocus association test for quantitative traits

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Semiparametric regression of multidimensional genetic pathway data: least-squares kernel machines and linear mixed models

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Generalized genomic distance-based regression methodology for multilocus association analysis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Principal components analysis corrects for stratification in genome-wide association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

A haplotype map of the human genome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Human non-synonymous SNPs: server and survey

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Score tests for association between traits and haplotypes when linkage phase is ambiguous

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

A general test of association for quantitative traits in nuclear families

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Multipoint quantitative-trait linkage analysis in general pedigrees

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Robust variance-components approach for assessing genetic linkage in pedigrees

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3683469

Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP).

20 June 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21676

The burden of adult hypertension in the United States 1999 to 2000: a rising tide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21676

A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21676

Powerful multi-marker association tests: unifying genomic distance-based regression and logistic regression

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21676

Some results on Tchebycheffian spline functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21676

On multiple-testing correction in genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21676

A new multimarker test for family-based association studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21676

Hypothesis testing in semiparametric additive mixed models

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21676

Familial aggregation of hypertension treatment and control in the Genetic Epidemiology Network of Arteriopathy (GENOA) study

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22968922

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Ascertainment issues in variance components models

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22968922

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A Generalized Representer Theorem

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21676

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/GEPI.21676

1 reference

17 August 2017

1 reference

17 August 2017

1 reference

PMCID

3683469