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From genome-wide associations to candidate causal variants by statistical fine-mapping

Nature reviews. Genetics, 2018-08, Vol.19 (8), p.491

2018

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Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups

American journal of human genetics, 2020-05, Vol.106 (5), p.707-716

2020

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A rare variant analysis framework using public genotype summary counts to prioritize disease-predisposition genes

Nature communications, 2022-05, Vol.13 (1), p.2592-2592, Article 2592

2022

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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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A review of kernel methods for genetic association studies

Genetic epidemiology, 2019-03, Vol.43 (2), p.122-136

2019

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Genomic Similarity and Kernel Methods I: Advancements by Building on Mathematical and Statistical Foundations

Human heredity, 2010-01, Vol.70 (2), p.109-131

Schaid, Daniel J.

2010

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Sex Differences in Older Adults' Immune Responses to Seasonal Influenza Vaccination

Frontiers in immunology, 2019-02, Vol.10, p.180-180

2019

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2dFDR: a new approach to confounder adjustment substantially increases detection power in omics association studies

Genome Biology, 2021-07, Vol.22 (1), p.208-208, Article 208

2021

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Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary Statistics

Genetics (Austin), 2016-11, Vol.204 (3), p.933-958

2016

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Genomic Similarity and Kernel Methods II: Methods for Genomic Information

Human heredity, 2010-01, Vol.70 (2), p.132-140

Schaid, Daniel J.

2010

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Score Tests for Association between Traits and Haplotypes when Linkage Phase Is Ambiguous

American journal of human genetics, 2002-02, Vol.70 (2), p.425-434

2002

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A large population-based association study between HLA and KIR genotypes and measles vaccine antibody responses

PloS one, 2017-02, Vol.12 (2), p.e0171261-e0171261

2017

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Citalopram and escitalopram plasma drug and metabolite concentrations: genome‐wide associations

British journal of clinical pharmacology, 2014-08, Vol.78 (2), p.373-383

2014

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Genome analysis and pleiotropy assessment using causal networks with loss of function mutation and metabolomics

BMC genomics, 2019-05, Vol.20 (1), p.395-395, Article 395

2019

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Genome-Wide Associations and Functional Genomic Studies of Musculoskeletal Adverse Events in Women Receiving Aromatase Inhibitors

Journal of clinical oncology, 2010-11, Vol.28 (31), p.4674-4682

2010

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From classical mendelian randomization to causal networks for systematic integration of multi-omics

Frontiers in genetics, 2022-09, Vol.13, p.990486

2022

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Current perspectives in assessing humoral immunity after measles vaccination

Expert review of vaccines, 2019-01, Vol.18 (1), p.75-87

2019

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Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders

Nature communications, 2022-06, Vol.13 (1), p.3428-3428, Article 3428

2022

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Comprehensively Evaluating cis-Regulatory Variation in the Human Prostate Transcriptome by Using Gene-Level Allele-Specific Expression

American journal of human genetics, 2015-06, Vol.96 (6), p.869-882

2015

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A multi-locus genetic risk score for abdominal aortic aneurysm

Atherosclerosis, 2016-03, Vol.246, p.274-279

2016

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An expanded variant list and assembly annotation identifies multiple novel coding and noncoding genes for prostate cancer risk using a normal prostate tissue eQTL data set

PloS one, 2019-04, Vol.14 (4), p.e0214588-e0214588

2019

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Polymorphisms in STING Affect Human Innate Immune Responses to Poxviruses

Frontiers in immunology, 2020-10, Vol.11, p.567348-567348

2020

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A microRNA Transcriptome-wide Association Study of Prostate Cancer Risk

Frontiers in genetics, 2022-03, Vol.13, p.836841-836841

2022

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Aromatase Inhibitor-Associated Bone Fractures: A Case-Cohort GWAS and Functional Genomics

Molecular endocrinology (Baltimore, Md.), 2014-10, Vol.28 (10), p.1740-1751

2014

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Genetic Predictors of Chemotherapy-Induced Peripheral Neuropathy from Paclitaxel, Carboplatin and Oxaliplatin: NCCTG/Alliance N08C1, N08CA and N08CB Study

Cancers, 2021-03, Vol.13 (5), p.1084

2021

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From genome-wide associations to candidate causal variants by statistical fine-mapping

Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups

A rare variant analysis framework using public genotype summary counts to prioritize disease-predisposition genes

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

A review of kernel methods for genetic association studies

Genomic Similarity and Kernel Methods I: Advancements by Building on Mathematical and Statistical Foundations

Sex Differences in Older Adults' Immune Responses to Seasonal Influenza Vaccination

2dFDR: a new approach to confounder adjustment substantially increases detection power in omics association studies

Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary Statistics

Genomic Similarity and Kernel Methods II: Methods for Genomic Information

Score Tests for Association between Traits and Haplotypes when Linkage Phase Is Ambiguous

A large population-based association study between HLA and KIR genotypes and measles vaccine antibody responses

Citalopram and escitalopram plasma drug and metabolite concentrations: genome‐wide associations

Genome analysis and pleiotropy assessment using causal networks with loss of function mutation and metabolomics

Genome-Wide Associations and Functional Genomic Studies of Musculoskeletal Adverse Events in Women Receiving Aromatase Inhibitors

From classical mendelian randomization to causal networks for systematic integration of multi-omics

Current perspectives in assessing humoral immunity after measles vaccination

Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders

Comprehensively Evaluating cis-Regulatory Variation in the Human Prostate Transcriptome by Using Gene-Level Allele-Specific Expression

A multi-locus genetic risk score for abdominal aortic aneurysm

An expanded variant list and assembly annotation identifies multiple novel coding and noncoding genes for prostate cancer risk using a normal prostate tissue eQTL data set

Polymorphisms in STING Affect Human Innate Immune Responses to Poxviruses

A microRNA Transcriptome-wide Association Study of Prostate Cancer Risk

Aromatase Inhibitor-Associated Bone Fractures: A Case-Cohort GWAS and Functional Genomics

Genetic Predictors of Chemotherapy-Induced Peripheral Neuropathy from Paclitaxel, Carboplatin and Oxaliplatin: NCCTG/Alliance N08C1, N08CA and N08CB Study

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