Lista de obras - Wan-Yu Lin - Dominio Público Uruguay

A Fuzzy Permutation Method for False Discovery Rate Control

artículo científico publicado en 2016

A Sequence Kernel Association Test for Dichotomous Traits in Family Samples under a Generalized Linear Mixed Model

artículo científico publicado en 2015

Adaptive combination of Bayes factors as a powerful method for the joint analysis of rare and common variants

artículo científico publicado en 2017

Adaptive combination of P-values for family-based association testing with sequence data

artículo científico publicado en 2014

Associating Multivariate Quantitative Phenotypes with Genetic Variants in Family Samples with a Novel Kernel Machine Regression Method

artículo científico publicado en 2015

Association testing of clustered rare causal variants in case-control studies.

artículo científico publicado en 2014

Beyond Rare-Variant Association Testing: Pinpointing Rare Causal Variants in Case-Control Sequencing Study

artículo científico publicado en 2016

Conditioning adaptive combination of P-values method to analyze case-parent trios with or without population controls

artículo científico publicado en 2016

Discovering joint associations between disease and gene pairs with a novel similarity test.

artículo científico publicado en 2010

Evaluation of pooled association tests for rare variant identification.

artículo científico publicado en 2011

Genome-Wide Gene-Environment Interaction Analysis Using Set-Based Association Tests

article

Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.

artículo científico publicado en 2013

Haplotype-based methods for detecting uncommon causal variants with common SNPs

artículo científico publicado en 2012

Identifying single-nucleotide polymorphisms responsible for the linkage signal of rheumatoid arthritis on chromosome 6 by joint modeling of linkage and association

artículo científico publicado en 2007

Improving power of genome-wide association studies with weighted false discovery rate control and prioritized subset analysis

artículo científico publicado en 2012

Incorporating prior knowledge to facilitate discoveries in a genome-wide association study on age-related macular degeneration

artículo científico publicado en 2010

Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis

artículo científico publicado en 2014

Linkage analyses of rheumatoid arthritis and related quantitative phenotypes: the GAW15 experience

artículo científico publicado en 2007

Long-term changes in adiposity and glycemic control are associated with past adenovirus infection

artículo científico publicado en 2012

Multivariate dimensionality reduction approaches to identify gene-gene and gene-environment interactions underlying multiple complex traits

artículo científico publicado en 2014

Nuclear magnetic resonance- and mass spectrometry-based metabolomics to study maleic acid toxicity from repeated dose exposure in rats

artículo científico publicado en 2017

One- and two-locus models for mapping rheumatoid arthritis-susceptibility genes on chromosome 6.

artículo científico publicado en 2007

Performing different kinds of physical exercise differentially attenuates the genetic effects on obesity measures: Evidence from 18,424 Taiwan Biobank participants

artículo científico publicado en 2019

Polygenic approaches to detect gene-environment interactions when external information is unavailable

scientific article published on 01 November 2019

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

artículo científico publicado en 2009

Presenting the uncertainties of odds ratios using empirical-Bayes prediction intervals

artículo científico publicado en 2012

Rare variant association testing by adaptive combination of P-values

artículo científico publicado en 2014

Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples

artículo científico publicado en 2016

Reducing bias of allele frequency estimates by modeling SNP genotype data with informative missingness

artículo científico publicado en 2012

Response to Comment on: Lin et al. Long-term changes in adiposity and glycemic control are associated with past adenovirus infection. Diabetes Care 2013;36:701-707.

artículo científico publicado en 2013

Restricted Use of Erythropoiesis-Stimulating Agent is Safe and Associated with Deferred Dialysis Initiation in Stage 5 Chronic Kidney Disease

scientific article published on 08 March 2017

Robust multipoint simultaneous identical-by-descent mapping for two linked loci.

artículo científico publicado en 2007

Sex-specific autosomal genetic effects across 26 human complex traits

artículo científico publicado en 2020

Short-Term Effects of Very-Low-Phosphate and Low-Phosphate Diets on Fibroblast Growth Factor 23 in Hemodialysis Patients: A Randomized Crossover Trial

artículo científico publicado en 2019

Similarity-based multimarker association tests for continuous traits.

artículo científico publicado en 2012

Taiwan's Response to Influenza: A Seroepidemiological Evaluation of Policies and Implications for Pandemic Preparedness

artículo científico publicado en 2022

The impact of petrochemical industrialisation on life expectancy and per capita income in Taiwan: an 11-year longitudinal study.

artículo científico publicado en 2014

Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4

article

Lista de obras de Wan-Yu Lin

A Fuzzy Permutation Method for False Discovery Rate Control

A Sequence Kernel Association Test for Dichotomous Traits in Family Samples under a Generalized Linear Mixed Model

Adaptive combination of Bayes factors as a powerful method for the joint analysis of rare and common variants

Adaptive combination of P-values for family-based association testing with sequence data

Associating Multivariate Quantitative Phenotypes with Genetic Variants in Family Samples with a Novel Kernel Machine Regression Method

Association testing of clustered rare causal variants in case-control studies.

Beyond Rare-Variant Association Testing: Pinpointing Rare Causal Variants in Case-Control Sequencing Study

Conditioning adaptive combination of P-values method to analyze case-parent trios with or without population controls

Discovering joint associations between disease and gene pairs with a novel similarity test.

Evaluation of pooled association tests for rare variant identification.

Genome-Wide Gene-Environment Interaction Analysis Using Set-Based Association Tests

Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.

Haplotype-based methods for detecting uncommon causal variants with common SNPs

Identifying single-nucleotide polymorphisms responsible for the linkage signal of rheumatoid arthritis on chromosome 6 by joint modeling of linkage and association

Improving power of genome-wide association studies with weighted false discovery rate control and prioritized subset analysis

Incorporating prior knowledge to facilitate discoveries in a genome-wide association study on age-related macular degeneration

Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis

Linkage analyses of rheumatoid arthritis and related quantitative phenotypes: the GAW15 experience

Long-term changes in adiposity and glycemic control are associated with past adenovirus infection

Multivariate dimensionality reduction approaches to identify gene-gene and gene-environment interactions underlying multiple complex traits

Nuclear magnetic resonance- and mass spectrometry-based metabolomics to study maleic acid toxicity from repeated dose exposure in rats

One- and two-locus models for mapping rheumatoid arthritis-susceptibility genes on chromosome 6.

Performing different kinds of physical exercise differentially attenuates the genetic effects on obesity measures: Evidence from 18,424 Taiwan Biobank participants

Polygenic approaches to detect gene-environment interactions when external information is unavailable

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

Presenting the uncertainties of odds ratios using empirical-Bayes prediction intervals

Rare variant association testing by adaptive combination of P-values

Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples

Reducing bias of allele frequency estimates by modeling SNP genotype data with informative missingness

Response to Comment on: Lin et al. Long-term changes in adiposity and glycemic control are associated with past adenovirus infection. Diabetes Care 2013;36:701-707.

Restricted Use of Erythropoiesis-Stimulating Agent is Safe and Associated with Deferred Dialysis Initiation in Stage 5 Chronic Kidney Disease

Robust multipoint simultaneous identical-by-descent mapping for two linked loci.

Sex-specific autosomal genetic effects across 26 human complex traits

Short-Term Effects of Very-Low-Phosphate and Low-Phosphate Diets on Fibroblast Growth Factor 23 in Hemodialysis Patients: A Randomized Crossover Trial

Similarity-based multimarker association tests for continuous traits.

Taiwan's Response to Influenza: A Seroepidemiological Evaluation of Policies and Implications for Pandemic Preparedness

The impact of petrochemical industrialisation on life expectancy and per capita income in Taiwan: an 11-year longitudinal study.

Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4