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The human transcriptome across tissues and individuals

Science (American Association for the Advancement of Science), 2015-05, Vol.348 (6235), p.660-665

2015

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ToxPi Graphical User Interface 2.0: Dynamic exploration, visualization, and sharing of integrated data models

BMC bioinformatics, 2018-03, Vol.19 (1), p.80-80, Article 80

2018

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Assessment of beating parameters in human induced pluripotent stem cells enables quantitative in vitro screening for cardiotoxicity

Toxicology and applied pharmacology, 2013-12, Vol.273 (3), p.500-507

2013

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Risk Characterization of Environmental Samples Using In Vitro Bioactivity and Polycyclic Aromatic Hydrocarbon Concentrations Data

Toxicological sciences, 2021-01, Vol.179 (1), p.108-120

2021

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Control of false discoveries in grouped hypothesis testing for eQTL data

BMC bioinformatics, 2024-04, Vol.25 (1), p.147-147, Article 147

2024

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Population-based toxicity screening in human induced pluripotent stem cell-derived cardiomyocytes

Toxicology and applied pharmacology, 2019-10, Vol.381, p.114711-114711, Article 114711

2019

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A powerful and flexible approach to the analysis of RNA sequence count data

Bioinformatics, 2011-10, Vol.27 (19), p.2672-2678

2011

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Standardizing benchmark dose calculations to improve science-based decisions in human health assessments

Environmental health perspectives, 2014-05, Vol.122 (5), p.499-505

2014

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Functional Architectures of Local and Distal Regulation of Gene Expression in Multiple Human Tissues

American journal of human genetics, 2017-04, Vol.100 (4), p.605-616

2017

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HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues

BMC bioinformatics, 2018-03, Vol.19 (1), p.95-95, Article 95

2018

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Grouping of complex substances using analytical chemistry data: A framework for quantitative evaluation and visualization

PloS one, 2019-10, Vol.14 (10), p.e0223517

2019

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seeQTL: a searchable database for human eQTLs

Bioinformatics, 2012-02, Vol.28 (3), p.451-452

2012

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CONVERGENCE AND PREDICTION OF PRINCIPAL COMPONENT SCORES IN HIGH-DIMENSIONAL SETTINGS

The Annals of statistics, 2010-12, Vol.38 (6), p.3605-3629

2010

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Sex differences in the human peripheral blood transcriptome

BMC genomics, 2014-01, Vol.15 (1), p.33-33

2014

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Classification of estrogenic compounds by coupling high content analysis and machine learning algorithms

PLoS computational biology, 2020-09, Vol.16 (9), p.e1008191

2020

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In vitro screening for population variability in toxicity of pesticide-containing mixtures

Environment international, 2015-12, Vol.85, p.147-155

2015

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A resource for integrated genomic analysis of the human liver

Scientific reports, 2022-09, Vol.12 (1), p.15151-12, Article 15151

2022

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Metabolomic Evaluation of Neutrophilic Airway Inflammation in Cystic Fibrosis

Chest, 2015-08, Vol.148 (2), p.507-515

2015

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Heading down the wrong pathway: on the influence of correlation within gene sets

BMC genomics, 2010-10, Vol.11 (1), p.574-574, Article 574

2010

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A Pipeline for High-Throughput Concentration Response Modeling of Gene Expression for Toxicogenomics

Frontiers in genetics, 2017-11, Vol.8, p.168-168

2017

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Characterizing PFAS hazards and risks: a human population-based in vitro cardiotoxicity assessment strategy

Human genomics, 2024-09, Vol.18 (1), p.1-23, Article 92

2024

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Homologous Recombination and Translesion DNA Synthesis Play Critical Roles on Tolerating DNA Damage Caused by Trace Levels of Hexavalent Chromium

PloS one, 2016-12, Vol.11 (12), p.e0167503

2016

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Genetic Modifiers of Lung Disease in Cystic Fibrosis

The New England journal of medicine, 2005-10, Vol.353 (14), p.1443-1453

2005

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Integrated study of copy number states and genotype calls using high-density SNP arrays

Nucleic acids research, 2009-09, Vol.37 (16), p.5365-5377

2009

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The human transcriptome across tissues and individuals

ToxPi Graphical User Interface 2.0: Dynamic exploration, visualization, and sharing of integrated data models

Molecular subtypes in head and neck cancer exhibit distinct patterns of chromosomal gain and loss of canonical cancer genes

Assessment of beating parameters in human induced pluripotent stem cells enables quantitative in vitro screening for cardiotoxicity

Risk Characterization of Environmental Samples Using In Vitro Bioactivity and Polycyclic Aromatic Hydrocarbon Concentrations Data

Control of false discoveries in grouped hypothesis testing for eQTL data

Population-based toxicity screening in human induced pluripotent stem cell-derived cardiomyocytes

A powerful and flexible approach to the analysis of RNA sequence count data

Standardizing benchmark dose calculations to improve science-based decisions in human health assessments

Functional Architectures of Local and Distal Regulation of Gene Expression in Multiple Human Tissues

HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues

Grouping of complex substances using analytical chemistry data: A framework for quantitative evaluation and visualization

seeQTL: a searchable database for human eQTLs

CONVERGENCE AND PREDICTION OF PRINCIPAL COMPONENT SCORES IN HIGH-DIMENSIONAL SETTINGS

Sex differences in the human peripheral blood transcriptome

Classification of estrogenic compounds by coupling high content analysis and machine learning algorithms

In vitro screening for population variability in toxicity of pesticide-containing mixtures

A resource for integrated genomic analysis of the human liver

Metabolomic Evaluation of Neutrophilic Airway Inflammation in Cystic Fibrosis

Heading down the wrong pathway: on the influence of correlation within gene sets

A Pipeline for High-Throughput Concentration Response Modeling of Gene Expression for Toxicogenomics

Characterizing PFAS hazards and risks: a human population-based in vitro cardiotoxicity assessment strategy

Homologous Recombination and Translesion DNA Synthesis Play Critical Roles on Tolerating DNA Damage Caused by Trace Levels of Hexavalent Chromium

Genetic Modifiers of Lung Disease in Cystic Fibrosis

Integrated study of copy number states and genotype calls using high-density SNP arrays

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