Leveraging Prior Information to Detect Causal Variants via Multi-Variant Regression
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Leveraging Prior Information to Detect Causal Variants via Multi-Variant Regression
Authors
Keywords
-
Journal
PLoS Computational Biology
Volume 9, Issue 6, Pages e1003093
Publisher
Public Library of Science (PLoS)
Online
2013-06-07
DOI
10.1371/journal.pcbi.1003093
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Prioritizing Genetic Variants for Causality on the Basis of Preferential Linkage Disequilibrium
- (2012) Qianqian Zhu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A Permutation Procedure to Correct for Confounders in Case-Control Studies, Including Tests of Rare Variation
- (2012) Michael P. Epstein et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Incorporating prior information into association studies
- (2012) G. Darnell et al. BIOINFORMATICS
- Commentary: Genome-wide significance thresholds via Bayes factors
- (2012) Jon Wakefield INTERNATIONAL JOURNAL OF EPIDEMIOLOGY
- Reconsidering Association Testing Methods Using Single-Variant Test Statistics as Alternatives to Pooling Tests for Sequence Data with Rare Variants
- (2012) Daniel D. Kinnamon et al. PLoS One
- A Genome-wide Comparison of the Functional Properties of Rare and Common Genetic Variants in Humans
- (2011) Qianqian Zhu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
- (2011) Michael C. Wu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Inosine Triphosphate Protects Against Ribavirin-Induced Adenosine Triphosphate Loss by Adenylosuccinate Synthase Function
- (2011) Yuki Hitomi et al. GASTROENTEROLOGY
- Adaptive tests for association analysis of rare variants
- (2011) Wei Pan et al. GENETIC EPIDEMIOLOGY
- Incorporating model uncertainty in detecting rare variants: the Bayesian risk index
- (2011) Melanie A. Quintana et al. GENETIC EPIDEMIOLOGY
- An Optimal Weighted Aggregated Association Test for Identification of Rare Variants Involved in Common Diseases
- (2011) Jae Hoon Sul et al. GENETICS
- Bayesian shrinkage analysis of QTLs under shape-adaptive shrinkage priors and accurate re-estimation of genetic effects
- (2011) C M Mutshinda et al. HEREDITY
- A rare variant in MYH6 is associated with high risk of sick sinus syndrome
- (2011) Hilma Holm et al. NATURE GENETICS
- Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data
- (2011) Gregory M. Cooper et al. NATURE REVIEWS GENETICS
- A Knowledge-Based Weighting Framework to Boost the Power of Genome-Wide Association Studies
- (2011) Miao-Xin Li et al. PLoS One
- A New Testing Strategy to Identify Rare Variants with Either Risk or Protective Effect on Disease
- (2011) Iuliana Ionita-Laza et al. PLoS Genetics
- Testing for an Unusual Distribution of Rare Variants
- (2011) Benjamin M. Neale et al. PLoS Genetics
- Computational and statistical approaches to analyzing variants identified by exome sequencing
- (2011) Nathan O Stitziel et al. GENOME BIOLOGY
- To Identify Associations with Rare Variants, Just WHaIT: Weighted Haplotype and Imputation-Based Tests
- (2010) Yun Li et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Pooled Association Tests for Rare Variants in Exon-Resequencing Studies
- (2010) Alkes L. Price et al. AMERICAN JOURNAL OF HUMAN GENETICS
- ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C
- (2010) Jacques Fellay et al. NATURE
- Single-nucleotide evolutionary constraint scores highlight disease-causing mutations
- (2010) Gregory M Cooper et al. NATURE METHODS
- Comprehensive Approach to Analyzing Rare Genetic Variants
- (2010) Thomas J. Hoffmann et al. PLoS One
- Rare Variants Create Synthetic Genome-Wide Associations
- (2010) Samuel P. Dickson et al. PLOS BIOLOGY
- Bayesian Semiparametric Multiple Shrinkage
- (2009) Richard F. MacLehose et al. BIOMETRICS
- Finding the missing heritability of complex diseases
- (2009) Teri A. Manolio et al. NATURE
- 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
- (2009) Ingo Helbig et al. NATURE GENETICS
- Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes
- (2009) S. Nejentsev et al. SCIENCE
- A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic
- (2009) Bo Eskerod Madsen et al. PLoS Genetics
- Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data
- (2008) Bingshan Li et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Bayesian LASSO for Quantitative Trait Loci Mapping
- (2008) Nengjun Yi et al. GENETICS
- Prioritized Subset Analysis: Improving Power in Genome-wide Association Studies
- (2007) Chun Li et al. HUMAN HEREDITY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now