Cargando…

Susceptibility scoring in family-based association testing

BACKGROUND: Family-based association testing is an important part of genetic epidemiology. Tests are available to include multiple siblings, unaffected offspring, and to adjust for environmental covariates. We explore a susceptibility residual method of adjustment for covariates. RESULTS: Through si...

Descripción completa

Detalles Bibliográficos
Autores principales:	Poisson, Laila M, Rybicki, Benjamin A, Coon, Steven W, Barnholtz-Sloan, Jill S, Chase, Gary A
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2003
Materias:	Proceedings
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866485/ https://www.ncbi.nlm.nih.gov/pubmed/14975117 http://dx.doi.org/10.1186/1471-2156-4-S1-S49

Ejemplares similares

Analysis of gene × environment interactions in sibships using mixed models
por: Barnholtz-Sloan, Jill S, et al.
Publicado: (2003)

Use of susceptibility scoring in conjunction with the genotypic transmission disequilibrium test
por: Benke, Kelly S, et al.
Publicado: (2005)

Identifying stage-specific protein subnetworks for colorectal cancer
por: Erten, Sinan, et al.
Publicado: (2012)

Assessing the impact of global versus local ancestry in association studies
por: Kang, Sun Jung, et al.
Publicado: (2009)

Multifactor-dimensionality reduction versus family-based association tests in detecting susceptibility loci in discordant sib-pair studies
por: Meng, Yan, et al.
Publicado: (2005)

Genomic screening in family-based association testing
por: Murphy, Amy, et al.
Publicado: (2005)

Comparison of family-based association tests in chromosome regions selected by linkage-based confidence intervals
por: Lewinger, Juan Pablo, et al.
Publicado: (2005)

Testing rare variants for hypertension using family-based tests with different weighting schemes
por: Wang, Xuexia, et al.
Publicado: (2016)

Application of family-based tests of association for rare variants to pathways
por: Greco, Brian, et al.
Publicado: (2014)

Single-marker and multi-marker mixed models for polygenic score analysis in family-based data
por: Bohossian, Nora, et al.
Publicado: (2014)

Identifying susceptibility genes by using joint tests of association and linkage and accounting for epistasis
por: Millstein, Joshua, et al.
Publicado: (2005)

Comparing family-based rare variant association tests for dichotomous phenotypes
por: Wang, Longfei, et al.
Publicado: (2016)

Comparison of type I error for multiple test corrections in large single-nucleotide polymorphism studies using principal components versus haplotype blocking algorithms
por: Nicodemus, Kristin K, et al.
Publicado: (2005)

Genome-wide association study of rheumatoid arthritis by a score test based on wavelet transformation
por: Jiang, Renfang, et al.
Publicado: (2009)

Quantitative synteny scoring improves homology inference and partitioning of gene families
por: Ali, Raja Hashim, et al.
Publicado: (2013)

Linkage, case-control association, and family-based association tests for complex disorders
por: Suarez, Brian K, et al.
Publicado: (2007)

Power of the 2-locus TDT for testing the interaction of two susceptibility genes
por: Kotti, Salma, et al.
Publicado: (2007)

Relating drug response to epigenetic and genetic markers using a region-based kernel score test
por: Yasmeen, Summaira, et al.
Publicado: (2018)

A new family-based association test via a least-squares method
por: Yang, Song, et al.
Publicado: (2005)

Family-based association test using normal approximation to gene dropping null distribution
por: Jiang, Yuan, et al.
Publicado: (2014)

Family-based tests applied to extended pedigrees identify rare variants related to hypertension
por: Xu, Mengyuan, et al.
Publicado: (2014)

New score tests for age-at-onset linkage analysis in general pedigrees
por: Callegaro, Andrea, et al.
Publicado: (2009)

A comparative analysis of family-based and population-based association tests using whole genome sequence data
por: Zhou, Jin J, et al.
Publicado: (2014)

The evolution of the tape measure protein: units, duplications and losses
por: Belcaid, Mahdi, et al.
Publicado: (2011)

Adjustment of familial relatedness in association test for rare variants
por: Li, Cong, et al.
Publicado: (2014)

Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data
por: Huang, Jing, et al.
Publicado: (2014)

Evaluation of the power and type I error of recently proposed family-based tests of association for rare variants
por: Hainline, Allison, et al.
Publicado: (2014)

A new transmission test for affected sib-pair families
por: Xu, Hongyan, et al.
Publicado: (2007)

Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data
por: Saad, Mohamad, et al.
Publicado: (2016)

On combining family- and population-based sequencing data
por: Katsumata, Yuriko, et al.
Publicado: (2016)

Prioritization of family member sequencing for the detection of rare variants
por: Sippy, Rachel, et al.
Publicado: (2016)

Genome-wide association tests by using block information in family data
por: Tang, Rui, et al.
Publicado: (2007)

Integrative methylation score to identify epigenetic modifications associated with lipid changes resulting from fenofibrate treatment in families
por: Wang, Biqi, et al.
Publicado: (2018)

Incorporating patient and family preferences into evidence-based medicine
por: Siminoff, Laura A
Publicado: (2013)

Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set
por: Yip, Wai-Ki, et al.
Publicado: (2011)

Application of family-based association testing to assess the genotype-phenotype association involved in complex traits using single-nucleotide polymorphisms
por: Wang, Ming-Hsi, et al.
Publicado: (2005)

Re-alignment of the unmapped reads with base quality score
por: Peng, Xiaoqing, et al.
Publicado: (2015)

A new score statistic to test for association given linkage in affected sibling pair-control designs
por: Houwing-Duistermaat, Jeanine J, et al.
Publicado: (2007)

Extended T(2 )tests for longitudinal family data in whole genome sequencing studies
por: Liu, Yiwei, et al.
Publicado: (2014)

Exhaustive prediction of disease susceptibility to coding base changes in the human genome
por: Kulkarni, Vinayak, et al.
Publicado: (2008)

Cannot write session to /tmp/vufind_sessions/sess_6j1p674rnouvchsu1ul33t9eed