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Multi-resolution localization of causal variants across the genome

Nature communications, 2020-02, Vol.11 (1), p.1093-1093, Article 1093

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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Controlling the Rate of GWAS False Discoveries

Genetics (Austin), 2017-01, Vol.205 (1), p.61-75

2017

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Publisher Correction: Multi-resolution localization of causal variants across the genome

Nature communications, 2020-04, Vol.11 (1), p.1799-1799, Article 1799

2020

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Exploratory Gene Ontology Analysis with Interactive Visualization

Scientific reports, 2019-05, Vol.9 (1), p.7793-7793, Article 7793

2019

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GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studies

Nature communications, 2022-11, Vol.13 (1), p.7209-16, Article 7209

2022

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Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

Nature genetics, 2009-01, Vol.41 (1), p.35-46

2009

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Genetic regulation of gene expression and splicing during a 10-year period of human aging

Genome Biology, 2019-11, Vol.20 (1), p.230-230, Article 230

2019

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Exposure to NO2, CO, and PM2.5 is linked to regional DNA methylation differences in asthma

Clinical epigenetics, 2018-01, Vol.10 (1), p.2-2, Article 2

2018

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Increased activation product of complement 4 protein in plasma of individuals with schizophrenia

Translational psychiatry, 2021-09, Vol.11 (1), p.486-8, Article 486

2021

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The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology

Nature genetics, 2004-10, Vol.36 (10), p.1045-1051

2004

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Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

American journal of human genetics, 2008-10, Vol.83 (4), p.504-510

2008

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Network Component Analysis: Reconstruction of Regulatory Signals in Biological Systems

Proceedings of the National Academy of Sciences - PNAS, 2003-12, Vol.100 (26), p.15522-15527

2003

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Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder

Proceedings of the National Academy of Sciences - PNAS, 2016-02, Vol.113 (6), p.E754-E761

2016

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Robust discrimination between self and non-self neurites requires thousands of Dscam1 isoforms

Nature (London), 2009-10, Vol.461 (7264), p.644-648

2009

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Bayesian sparse hidden components analysis for transcription regulation networks

Bioinformatics, 2006-03, Vol.22 (6), p.739-746

2006

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Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients

Biological psychiatry (1969), 2011-10, Vol.70 (7), p.655-662

2011

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Reconstructing DNA copy number by joint segmentation of multiple sequences

BMC bioinformatics, 2012-08, Vol.13 (1), p.205-205, Article 205

2012

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Distribution and dynamics of Lamp1-containing endocytic organelles in fibroblasts deficient in BLOC-3

Journal of cell science, 2005-11, Vol.118 (22), p.5243-5255

2005

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A molecular screening approach to identify and characterize inhibitors of glioblastoma stem cells

Molecular cancer therapeutics, 2011-10, Vol.10 (10), p.1818-1828

2011

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MULTILAYER KNOCKOFF FILTER: CONTROLLED VARIABLE SELECTION AT MULTIPLE RESOLUTIONS

The annals of applied statistics, 2019-03, Vol.13 (1), p.1-33

2019

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Multi-resolution localization of causal variants across the genome

Organoid Modeling of the Tumor Immune Microenvironment

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

Progenitor identification and SARS-CoV-2 infection in human distal lung organoids

Controlling the Rate of GWAS False Discoveries

Publisher Correction: Multi-resolution localization of causal variants across the genome

Exploratory Gene Ontology Analysis with Interactive Visualization

GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studies

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

Genetic regulation of gene expression and splicing during a 10-year period of human aging

Exposure to NO2, CO, and PM2.5 is linked to regional DNA methylation differences in asthma

Increased activation product of complement 4 protein in plasma of individuals with schizophrenia

The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

Network Component Analysis: Reconstruction of Regulatory Signals in Biological Systems

Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder

Robust discrimination between self and non-self neurites requires thousands of Dscam1 isoforms

Genome-wide mapping of brain phenotypes in extended pedigrees with strong genetic loading for bipolar disorder

Bayesian sparse hidden components analysis for transcription regulation networks

Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients

Reconstructing DNA copy number by joint segmentation of multiple sequences

Distribution and dynamics of Lamp1-containing endocytic organelles in fibroblasts deficient in BLOC-3

A molecular screening approach to identify and characterize inhibitors of glioblastoma stem cells

MULTILAYER KNOCKOFF FILTER: CONTROLLED VARIABLE SELECTION AT MULTIPLE RESOLUTIONS

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

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