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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

PLoS genetics, 2009-06, Vol.5 (6), p.e1000529-e1000529

2009

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Genetic evidence for role of integration of fast and slow neurotransmission in schizophrenia

Molecular psychiatry, 2017-06, Vol.22 (6), p.792-801

2017

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Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci

Molecular psychiatry, 2015-02, Vol.20 (2), p.207-214

2015

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Cancer risk in individuals with autism spectrum disorder

Annals of oncology, 2022-07, Vol.33 (7), p.713-719

2022

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

PLoS genetics, 2009-02, Vol.5 (2), p.e1000384-e1000384

2009

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Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension

PLoS genetics, 2010-10, Vol.6 (10), p.e1001177-e1001177

2010

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TATES: efficient multivariate genotype-phenotype analysis for genome-wide association studies

PLoS genetics, 2013-01, Vol.9 (1), p.e1003235-e1003235

2013

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Regularized machine learning in the genetic prediction of complex traits

PLoS genetics, 2014-11, Vol.10 (11), p.e1004754-e1004754

2014

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Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases

PLoS genetics, 2011-08, Vol.7 (8), p.e1002216-e1002216

2011

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The genetic interpretation of area under the ROC curve in genomic profiling

PLoS genetics, 2010-02, Vol.6 (2), p.e1000864-e1000864

2010

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Temporal dynamics of host molecular responses differentiate symptomatic and asymptomatic influenza a infection

PLoS genetics, 2011-08, Vol.7 (8), p.e1002234-e1002234

2011

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Commutation Relations, Normal Ordering, and Stirling Numbers

1, 2015

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Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci

PLoS genetics, 2011-03, Vol.7 (3), p.e1002026-e1002026

2011

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Genetic variation in an individual human exome

PLoS genetics, 2008-08, Vol.4 (8), p.e1000160-e1000160

2008

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Comparison of family history and SNPs for predicting risk of complex disease

PLoS genetics, 2012-10, Vol.8 (10), p.e1002973-e1002973

2012

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Accounting for Population Structure in Gene-by-Environment Interactions in Genome-Wide Association Studies Using Mixed Models

PLoS genetics, 2016-03, Vol.12 (3), p.e1005849-e1005849

2016

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Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium

PLoS genetics, 2011-04, Vol.7 (4), p.e1001371

2011

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Plasma kallikrein activates the epithelial sodium channel in vitro but is not essential for volume retention in nephrotic mice

Acta Physiologica, 2018-09, Vol.224 (1), p.e13060-n/a

2018

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Polygenic risk for psychiatric disorders correlates with executive function in typical development

Genes, brain and behavior, 2019-04, Vol.18 (4), p.e12480-n/a

2019

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Improved statistics for genome-wide interaction analysis

PLoS genetics, 2012-04, Vol.8 (4), p.e1002625-e1002625

2012

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Practical issues in imputation-based association mapping

PLoS genetics, 2008-12, Vol.4 (12), p.e1000279-e1000279

2008

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The key role of genomics in modern vaccine and drug design for emerging infectious diseases

PLoS genetics, 2009-10, Vol.5 (10), p.e1000612-e1000612

2009

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Age, gender, and cancer but not neurodegenerative and cardiovascular diseases strongly modulate systemic effect of the Apolipoprotein E4 allele on lifespan

PLoS genetics, 2014-01, Vol.10 (1), p.e1004141-e1004141

2014

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Epistatic module detection for case-control studies: a Bayesian model with a Gibbs sampling strategy

PLoS genetics, 2009-05, Vol.5 (5), p.e1000464-e1000464

2009

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Hierarchical generalized linear models for multiple groups of rare and common variants: jointly estimating group and individual-variant effects

PLoS genetics, 2011-12, Vol.7 (12), p.e1002382-e1002382

2011

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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

Genetic evidence for role of integration of fast and slow neurotransmission in schizophrenia

Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci

Cancer risk in individuals with autism spectrum disorder

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

Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension

TATES: efficient multivariate genotype-phenotype analysis for genome-wide association studies

Regularized machine learning in the genetic prediction of complex traits

Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases

The genetic interpretation of area under the ROC curve in genomic profiling

Temporal dynamics of host molecular responses differentiate symptomatic and asymptomatic influenza a infection

Commutation Relations, Normal Ordering, and Stirling Numbers

Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci

Genetic variation in an individual human exome

Comparison of family history and SNPs for predicting risk of complex disease

Accounting for Population Structure in Gene-by-Environment Interactions in Genome-Wide Association Studies Using Mixed Models

Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium

Plasma kallikrein activates the epithelial sodium channel in vitro but is not essential for volume retention in nephrotic mice

Polygenic risk for psychiatric disorders correlates with executive function in typical development

Improved statistics for genome-wide interaction analysis

Practical issues in imputation-based association mapping

The key role of genomics in modern vaccine and drug design for emerging infectious diseases

Age, gender, and cancer but not neurodegenerative and cardiovascular diseases strongly modulate systemic effect of the Apolipoprotein E4 allele on lifespan

Epistatic module detection for case-control studies: a Bayesian model with a Gibbs sampling strategy

Hierarchical generalized linear models for multiple groups of rare and common variants: jointly estimating group and individual-variant effects

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