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Molecular networks as sensors and drivers of common human diseases

Nature (London), 2009-09, Vol.461 (7261), p.218-223

Schadt, Eric E

2009

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variancePartition: interpreting drivers of variation in complex gene expression studies

BMC bioinformatics, 2016-11, Vol.17 (1), p.483-483, Article 483

2016

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Bayesian test for colocalisation between pairs of genetic association studies using summary statistics

PLoS genetics, 2014-05, Vol.10 (5), p.e1004383-e1004383

2014

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Deciphering bacterial epigenomes using modern sequencing technologies

Nature reviews. Genetics, 2019-03, Vol.20 (3), p.157-172

2019

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The changing privacy landscape in the era of big data

Molecular systems biology, 2012, Vol.8 (1), p.612-n/a

Schadt, Eric E

2012

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Multiscale Analysis of Independent Alzheimer’s Cohorts Finds Disruption of Molecular, Genetic, and Clinical Networks by Human Herpesvirus

Neuron (Cambridge, Mass.), 2018-07, Vol.99 (1), p.64-82.e7

2018

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A Next Generation Multiscale View of Inborn Errors of Metabolism

Cell metabolism, 2016-01, Vol.23 (1), p.13-26

2016

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Computational solutions to large-scale data management and analysis

Nature reviews. Genetics, 2010-09, Vol.11 (9), p.647-657

2010

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Systems biology of asthma and allergic diseases: A multiscale approach

Journal of allergy and clinical immunology, 2015-01, Vol.135 (1), p.31-42

2015

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Bayesian method to predict individual SNP genotypes from gene expression data

Nature genetics, 2012-05, Vol.44 (5), p.603-608

2012

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Detecting and phasing minor single-nucleotide variants from long-read sequencing data

Nature communications, 2021-05, Vol.12 (1), p.3032-13, Article 3032

2021

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The Asthma Mobile Health Study, a large-scale clinical observational study using ResearchKit

Nature biotechnology, 2017-04, Vol.35 (4), p.354-362

2017

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Anti-correlated feature selection prevents false discovery of subpopulations in scRNAseq

Nature communications, 2024-01, Vol.15 (1), p.699-699, Article 699

2024

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Characterization of the human ESC transcriptome by hybrid sequencing

Proceedings of the National Academy of Sciences - PNAS, 2013-12, Vol.110 (50), p.E4821-E4830

2013

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Assembly and diploid architecture of an individual human genome via single-molecule technologies

Nature methods, 2015-08, Vol.12 (8), p.780-786

2015

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Analysis of Transcriptional Variability in a Large Human iPSC Library Reveals Genetic and Non-genetic Determinants of Heterogeneity

Cell stem cell, 2017-04, Vol.20 (4), p.518-532.e9

2017

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Functional interpretation of genetic variants using deep learning predicts impact on chromatin accessibility and histone modification

Nucleic acids research, 2019-11, Vol.47 (20), p.10597-10611

2019

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Integrative analysis of DNA methylation and gene expression data identifies EPAS1 as a key regulator of COPD

PLoS genetics, 2015-01, Vol.11 (1), p.e1004898-e1004898

2015

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iPSC-Derived Dopamine Neurons Reveal Differences between Monozygotic Twins Discordant for Parkinson’s Disease

Cell reports (Cambridge), 2014-11, Vol.9 (4), p.1173-1182

2014

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Integrating Pathway Analysis and Genetics of Gene Expression for Genome-wide Association Studies

American journal of human genetics, 2010-04, Vol.86 (4), p.581-591

2010

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Mapping and characterizing N6-methyladenine in eukaryotic genomes using single-molecule real-time sequencing

Genome research, 2018-07, Vol.28 (7), p.1067-1078

2018

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The Origin of the Haitian Cholera Outbreak Strain

The New England journal of medicine, 2011-01, Vol.364 (1), p.33-42

2011

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Discovering genetic interactions bridging pathways in genome-wide association studies

Nature communications, 2019-09, Vol.10 (1), p.4274-18, Article 4274

2019

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Integrating large-scale functional genomic data to dissect the complexity of yeast regulatory networks

Nature genetics, 2008-07, Vol.40 (7), p.854-861

2008

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Molecular networks as sensors and drivers of common human diseases

variancePartition: interpreting drivers of variation in complex gene expression studies

Bayesian test for colocalisation between pairs of genetic association studies using summary statistics

Deciphering bacterial epigenomes using modern sequencing technologies

Integrated Systems Approach Identifies Genetic Nodes and Networks in Late-Onset Alzheimer’s Disease

The changing privacy landscape in the era of big data

Multiscale Analysis of Independent Alzheimer’s Cohorts Finds Disruption of Molecular, Genetic, and Clinical Networks by Human Herpesvirus

A Next Generation Multiscale View of Inborn Errors of Metabolism

Computational solutions to large-scale data management and analysis

Systems biology of asthma and allergic diseases: A multiscale approach

Bayesian method to predict individual SNP genotypes from gene expression data

Detecting and phasing minor single-nucleotide variants from long-read sequencing data

The Asthma Mobile Health Study, a large-scale clinical observational study using ResearchKit

Anti-correlated feature selection prevents false discovery of subpopulations in scRNAseq

Characterization of the human ESC transcriptome by hybrid sequencing

Assembly and diploid architecture of an individual human genome via single-molecule technologies

Analysis of Transcriptional Variability in a Large Human iPSC Library Reveals Genetic and Non-genetic Determinants of Heterogeneity

Functional interpretation of genetic variants using deep learning predicts impact on chromatin accessibility and histone modification

Integrative analysis of DNA methylation and gene expression data identifies EPAS1 as a key regulator of COPD

iPSC-Derived Dopamine Neurons Reveal Differences between Monozygotic Twins Discordant for Parkinson’s Disease

Integrating Pathway Analysis and Genetics of Gene Expression for Genome-wide Association Studies

Mapping and characterizing N6-methyladenine in eukaryotic genomes using single-molecule real-time sequencing

The Origin of the Haitian Cholera Outbreak Strain

Discovering genetic interactions bridging pathways in genome-wide association studies

Integrating large-scale functional genomic data to dissect the complexity of yeast regulatory networks

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