(Q30578631)

15 September 2017

A variational Bayes discrete mixture test for rare variant association (English)

1 reference

15 September 2017

20

Charles Kooperberg

1 reference

15 September 2017

7

James G Wilson

1 reference

15 September 2017

17

Deborah A Nickerson

1 reference

15 September 2017

2

James Y Dai

1 reference

15 September 2017

9

Leslie A Lange

1 reference

15 September 2017

Christopher J O'Donnell

15

object named as

Christopher J O'Donnell

1 reference

15 September 2017

14

Rebecca D Jackson

1 reference

15 September 2017

Benjamin A Logsdon

1

1 reference

15 September 2017

Paul L Auer

3

1 reference

15 September 2017

Jill M Johnsen

4

1 reference

15 September 2017

Santhi K Ganesh

5

1 reference

15 September 2017

Nicholas L Smith

6

1 reference

15 September 2017

Russell P Tracy

8

1 reference

15 September 2017

Shuo Jiao

10

1 reference

15 September 2017

Stephen S Rich

11

1 reference

15 September 2017

Guillaume Lettre

12

1 reference

15 September 2017

Christopher S Carlson

13

1 reference

15 September 2017

Mark M Wurfel

16

1 reference

15 September 2017

Hua Tang

18

1 reference

15 September 2017

Alexander P Reiner

19

1 reference

15 September 2017

NHLBI GO Exome Sequencing Project

21

1 reference

15 September 2017

1 January 2014

1 reference

15 September 2017

1 reference

15 September 2017

38

1 reference

15 September 2017

1

1 reference

15 September 2017

21-30

1 reference

Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project

15 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Incorporating prior biologic information for high-dimensional rare variant association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

A unified mixed-effects model for rare-variant association in sequencing studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Optimal tests for rare variant effects in sequencing association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

In vivo analysis of the role of O-glycosylations of von Willebrand factor.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Evolution and functional impact of rare coding variation from deep sequencing of human exomes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

von Willebrand factor: at the crossroads of bleeding and thrombosis.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Five years of GWAS discovery

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Estimation of quantitative trait locus effects with epistasis by variational Bayes algorithms

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Incorporating model uncertainty in detecting rare variants: the Bayesian risk index

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Comparison of statistical tests for disease association with rare variants

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Genetic determinants of von Willebrand factor levels and activity in relation to the risk of cardiovascular disease: a review

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Bayesian analysis of rare variants in genetic association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Comprehensive approach to analyzing rare genetic variants

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Hierarchical modeling for estimating relative risks of rare genetic variants: properties of the pseudo-likelihood method

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Missing heritability and strategies for finding the underlying causes of complex disease

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Pooled association tests for rare variants in exon-resequencing studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

A data-adaptive sum test for disease association with multiple common or rare variants

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Genetic heterogeneity in human disease

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

A method and server for predicting damaging missense mutations

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

A variational Bayes algorithm for fast and accurate multiple locus genome-wide association analysis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Finding the missing heritability of complex diseases

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

An evaluation of statistical approaches to rare variant analysis in genetic association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

A groupwise association test for rare mutations using a weighted sum statistic

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Genetic variation in an individual human exome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

PLINK: a tool set for whole-genome association and population-based linkage analyses

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

A variational Bayesian mixture modelling framework for cluster analysis of gene-expression data

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

von Willebrand factor and factor VIII as risk factors for arterial and venous thrombosis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

The allelic architecture of human disease genes: common disease-common variant... or not?

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Prediction of deleterious human alleles

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030763

Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study

14 July 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21772

GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21772

A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21772

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21772

Characterisation of mutations and molecular studies of type 2 von Willebrand disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24482836

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24482836

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/GEPI.21772

1 reference

15 September 2017

1 reference

15 September 2017

PubMed publication ID

24482836

1 reference