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Reconstruction of the full transmission dynamics of COVID-19 in Wuhan

Nature (London), 2020-08, Vol.584 (7821), p.420-424

2020

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Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test

American journal of human genetics, 2011-07, Vol.89 (1), p.82-93

2011

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ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies

American journal of human genetics, 2019-03, Vol.104 (3), p.410-421

2019

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Rare-Variant Association Analysis: Study Designs and Statistical Tests

American journal of human genetics, 2014-07, Vol.95 (1), p.5-23

2014

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Group testing via hypergraph factorization applied to COVID-19

Nature communications, 2022-04, Vol.13 (1), p.1837-1837, Article 1837

2022

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Accurate and efficient estimation of local heritability using summary statistics and the linkage disequilibrium matrix

Nature communications, 2023-12, Vol.14 (1), p.7954-7954, Article 7954

2023

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Operating characteristics of the rank‐based inverse normal transformation for quantitative trait analysis in genome‐wide association studies

Biometrics, 2020-12, Vol.76 (4), p.1262-1272

2020

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Sequence Kernel Association Tests for the Combined Effect of Rare and Common Variants

American journal of human genetics, 2013-06, Vol.92 (6), p.841-853

2013

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Nongenic cancer-risk SNPs affect oncogenes, tumour-suppressor genes, and immune function

British journal of cancer, 2020-02, Vol.122 (4), p.569-577

2020

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General Framework for Meta-analysis of Rare Variants in Sequencing Association Studies

American journal of human genetics, 2013-07, Vol.93 (1), p.42-53

2013

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Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies

American journal of human genetics, 2012-08, Vol.91 (2), p.224-237

2012

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Association between Smoking History and Tumor Mutation Burden in Advanced Non-Small Cell Lung Cancer

Cancer research (Chicago, Ill.), 2021-05, Vol.81 (9), p.2566-2573

2021

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Estimation and testing for the effect of a genetic pathway on a disease outcome using logistic kernel machine regression via logistic mixed models

BMC bioinformatics, 2008-06, Vol.9 (1), p.292-292, Article 292

2008

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Detecting epistasis with the marginal epistasis test in genetic mapping studies of quantitative traits

PLoS genetics, 2017-07, Vol.13 (7), p.e1006869-e1006869

2017

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Aberrant lipid metabolism disrupts calcium homeostasis causing liver endoplasmic reticulum stress in obesity

Nature (London), 2011-05, Vol.473 (7348), p.528-531

2011

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The effect of correlation in false discovery rate estimation

Biometrika, 2011-03, Vol.98 (1), p.199-214

2011

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Powerful gene set analysis in GWAS with the Generalized Berk-Jones statistic

PLoS genetics, 2019-03, Vol.15 (3), p.e1007530

2019

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Improved Ancestry Estimation for both Genotyping and Sequencing Data using Projection Procrustes Analysis and Genotype Imputation

American journal of human genetics, 2015-06, Vol.96 (6), p.926-937

2015

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Control for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed Models

American journal of human genetics, 2016-04, Vol.98 (4), p.653-666

2016

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Powerful SNP-Set Analysis for Case-Control Genome-wide Association Studies

American journal of human genetics, 2010-06, Vol.86 (6), p.929-942

2010

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Smoking History as a Potential Predictor of Immune Checkpoint Inhibitor Efficacy in Metastatic Non-Small Cell Lung Cancer

JNCI : Journal of the National Cancer Institute, 2021-11, Vol.113 (12), p.1761-1769

2021

Volltextzugriff (PDF)

RAFFI: Accurate and fast familial relationship inference in large scale biobank studies using RaPID

PLoS genetics, 2021-01, Vol.17 (1), p.e1009315-e1009315

2021

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Quality of Life and Satisfaction with Outcome among Prostate-Cancer Survivors

The New England journal of medicine, 2008-03, Vol.358 (12), p.1250-1261

2008

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Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb

PLoS genetics, 2019-06, Vol.15 (6), p.e1008202-e1008202

2019

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Fast and robust adjustment of cell mixtures in epigenome-wide association studies with SmartSVA

BMC genomics, 2017-05, Vol.18 (1), p.413-413, Article 413

2017

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Reconstruction of the full transmission dynamics of COVID-19 in Wuhan

Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test

ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies

Rare-Variant Association Analysis: Study Designs and Statistical Tests

Group testing via hypergraph factorization applied to COVID-19

Accurate and efficient estimation of local heritability using summary statistics and the linkage disequilibrium matrix

Operating characteristics of the rank‐based inverse normal transformation for quantitative trait analysis in genome‐wide association studies

Sequence Kernel Association Tests for the Combined Effect of Rare and Common Variants

Nongenic cancer-risk SNPs affect oncogenes, tumour-suppressor genes, and immune function

General Framework for Meta-analysis of Rare Variants in Sequencing Association Studies

Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies

Association between Smoking History and Tumor Mutation Burden in Advanced Non-Small Cell Lung Cancer

Estimation and testing for the effect of a genetic pathway on a disease outcome using logistic kernel machine regression via logistic mixed models

Detecting epistasis with the marginal epistasis test in genetic mapping studies of quantitative traits

Aberrant lipid metabolism disrupts calcium homeostasis causing liver endoplasmic reticulum stress in obesity

The effect of correlation in false discovery rate estimation

Powerful gene set analysis in GWAS with the Generalized Berk-Jones statistic

Improved Ancestry Estimation for both Genotyping and Sequencing Data using Projection Procrustes Analysis and Genotype Imputation

Control for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed Models

Powerful SNP-Set Analysis for Case-Control Genome-wide Association Studies

Smoking History as a Potential Predictor of Immune Checkpoint Inhibitor Efficacy in Metastatic Non-Small Cell Lung Cancer

RAFFI: Accurate and fast familial relationship inference in large scale biobank studies using RaPID

Quality of Life and Satisfaction with Outcome among Prostate-Cancer Survivors

Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb

Fast and robust adjustment of cell mixtures in epigenome-wide association studies with SmartSVA

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