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Colocalization of GWAS and eQTL Signals Detects Target Genes

American journal of human genetics, 2016-12, Vol.99 (6), p.1245-1260

2016

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Population structure in genetic studies: Confounding factors and mixed models

PLoS genetics, 2018-12, Vol.14 (12), p.e1007309-e1007309

2018

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Accurate estimation of cell composition in bulk expression through robust integration of single-cell information

Nature communications, 2020-04, Vol.11 (1), p.1971-1971, Article 1971

2020

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Variance component model to account for sample structure in genome-wide association studies

Nature genetics, 2010-04, Vol.42 (4), p.348-354

2010

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Rare variants regulate expression of nearby individual genes in multiple tissues

PLoS genetics, 2021-06, Vol.17 (6), p.e1009596-e1009596

2021

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NRF2/ARE pathway negatively regulates BACE1 expression and ameliorates cognitive deficits in mouse Alzheimer’s models

Proceedings of the National Academy of Sciences - PNAS, 2019-06, Vol.116 (25), p.12516-12523

2019

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Rare variants in the endocytic pathway are associated with Alzheimer's disease, its related phenotypes, and functional consequences

PLoS genetics, 2021-09, Vol.17 (9), p.e1009772

2021

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CoPheScan: phenome-wide association studies accounting for linkage disequilibrium

Nature communications, 2024-07, Vol.15 (1), p.5862-13, Article 5862

2024

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Effectively identifying eQTLs from multiple tissues by combining mixed model and meta-analytic approaches

PLoS genetics, 2013-06, Vol.9 (6), p.e1003491-e1003491

2013

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Mixed models can correct for population structure for genomic regions under selection

Nature reviews. Genetics, 2013-04, Vol.14 (4), p.300-300

2013

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ForestQC: Quality control on genetic variants from next-generation sequencing data using random forest

PLoS computational biology, 2019-12, Vol.15 (12), p.e1007556-e1007556

2019

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Extracellular vesicles from adipose tissue‐derived stem cells alleviate osteoporosis through osteoprotegerin and miR‐21‐5p

Journal of extracellular vesicles, 2021-10, Vol.10 (12), p.e12152-n/a

2021

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Leveraging allelic imbalance to refine fine-mapping for eQTL studies

PLoS genetics, 2019-12, Vol.15 (12), p.e1008481-e1008481

2019

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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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Accurate diagnosis of atopic dermatitis by combining transcriptome and microbiota data with supervised machine learning

Scientific reports, 2022-01, Vol.12 (1), p.290-290, Article 290

2022

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Building an optimal predictive model for imputing tissue-specific gene expression by combining genotype and whole-blood transcriptome data

HGG advances, 2023-10, Vol.4 (4), p.100223-100223, Article 100223

2023

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Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

Genome medicine, 2022-09, Vol.14 (1), p.104-23, Article 104

2022

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Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees

American journal of human genetics, 2016-10, Vol.99 (4), p.846-859

2016

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Publisher Correction: Accurate estimation of cell composition in bulk expression through robust integration of single-cell information

Nature communications, 2020-06, Vol.11 (1), p.2891-2891, Article 2891

2020

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A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease

PloS one, 2014-10, Vol.9 (10), p.e110292-e110292

2014

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Accurate and Fast Multiple-Testing Correction in eQTL Studies

American journal of human genetics, 2015-06, Vol.96 (6), p.857-868

2015

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Engineered small extracellular vesicles displaying ACE2 variants on the surface protect against SARS‐CoV‐2 infection

Journal of extracellular vesicles, 2022-01, Vol.11 (1), p.e12179-n/a

2022

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The Minnesota Center for Twin and Family Research Genome-Wide Association Study

Twin research and human genetics, 2012-12, Vol.15 (6), p.767-774

2012

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Polygenic risk scores of endo-phenotypes identify the effect of genetic background in congenital heart disease

HGG advances, 2022-07, Vol.3 (3), p.100112, Article 100112

2022

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Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

Genome medicine, 2022-11, Vol.14 (1), p.128-128, Article 128

2022

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Colocalization of GWAS and eQTL Signals Detects Target Genes

Population structure in genetic studies: Confounding factors and mixed models

Accurate estimation of cell composition in bulk expression through robust integration of single-cell information

Variance component model to account for sample structure in genome-wide association studies

Rare variants regulate expression of nearby individual genes in multiple tissues

NRF2/ARE pathway negatively regulates BACE1 expression and ameliorates cognitive deficits in mouse Alzheimer’s models

Rare variants in the endocytic pathway are associated with Alzheimer's disease, its related phenotypes, and functional consequences

CoPheScan: phenome-wide association studies accounting for linkage disequilibrium

Effectively identifying eQTLs from multiple tissues by combining mixed model and meta-analytic approaches

Mixed models can correct for population structure for genomic regions under selection

ForestQC: Quality control on genetic variants from next-generation sequencing data using random forest

Extracellular vesicles from adipose tissue‐derived stem cells alleviate osteoporosis through osteoprotegerin and miR‐21‐5p

Leveraging allelic imbalance to refine fine-mapping for eQTL studies

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

Accurate diagnosis of atopic dermatitis by combining transcriptome and microbiota data with supervised machine learning

Building an optimal predictive model for imputing tissue-specific gene expression by combining genotype and whole-blood transcriptome data

Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees

Publisher Correction: Accurate estimation of cell composition in bulk expression through robust integration of single-cell information

A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease

Accurate and Fast Multiple-Testing Correction in eQTL Studies

Engineered small extracellular vesicles displaying ACE2 variants on the surface protect against SARS‐CoV‐2 infection

The Minnesota Center for Twin and Family Research Genome-Wide Association Study

Polygenic risk scores of endo-phenotypes identify the effect of genetic background in congenital heart disease

Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

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