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A Novel Adaptive Method for the Analysis of Next-Generation Sequencing Data to Detect Complex Trait Associations with Rare Variants Due to Gene Main Effects and Interactions ⬇️

artículo científico publicado el 14 de octubre de 2010

A Unified Method for Detecting Secondary Trait Associations with Rare Variants: Application to Sequence Data ⬇️

artículo científico publicado el 15 de noviembre de 2012

A flexible likelihood framework for detecting associations with secondary phenotypes in genetic studies using selected samples: application to sequence data ⬇️

artículo científico publicado el 14 de diciembre de 2011

A unified framework for detecting rare variant quantitative trait associations in pedigree and unrelated individuals via sequence data ⬇️

artículo científico publicado el 28 de abril de 2012

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

artículo científico publicado en 2019

Causal relationship and shared genetic loci between psoriasis and type 2 diabetes through trans-disease meta-analysis

artículo científico publicado en 2020

Estimating Genetic Effects and Quantifying Missing Heritability Explained by Identified Rare-Variant Associations ⬇️

artículo científico publicado el 27 de septiembre de 2012

Exome chip meta-analysis fine maps causal variants and elucidates the genetic architecture of rare coding variants in smoking and alcohol use

artículo científico publicado en 2018

Exome-wide association study of plasma lipids in >300,000 individuals

artículo científico publicado en 2017

Genetic variants in CETP increase risk of intracerebral hemorrhage

artículo científico publicado en 2016

Meta-analysis of gene-level tests for rare variant association

artículo científico publicado en 2013

Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

artículo científico publicado en 2019

Model-based assessment of replicability for genome-wide association meta-analysis

artículo científico publicado en 2021

PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

article

Proper conditional analysis in the presence of missing data: Application to large scale meta-analysis of tobacco use phenotypes

artículo científico publicado en 2018

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2017

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

article

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2019

Rare and low-frequency coding variants alter human adult height

artículo científico publicado en 2017

Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease

scientific journal article

Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

article

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

artículo científico publicado en 2018

Replication Strategies for Rare Variant Complex Trait Association Studies via Next-Generation Sequencing ⬇️

artículo científico publicado el 10 de diciembre de 2010

SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations ⬇️

artículo científico publicado el 3 de mayo de 2012

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