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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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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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Deciphering bacterial epigenomes using modern sequencing technologies

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

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 window into third-generation sequencing

Human molecular genetics, 2010-10, Vol.19 (R2), p.R227-R240

2010

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CD47-blocking antibodies restore phagocytosis and prevent atherosclerosis

Nature (London), 2016-08, Vol.536 (7614), p.86-90

2016

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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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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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Computational solutions to large-scale data management and analysis

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

2010

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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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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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Geroscience: linking aging to chronic disease

Cell, 2014-11, Vol.159 (4), p.709-713

2014

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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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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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Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility

Nature genetics, 2018-11, Vol.50 (11), p.1584-1592

2018

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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

Volltextzugriff (PDF)

Stitching together multiple data dimensions reveals interacting metabolomic and transcriptomic networks that modulate cell regulation

PLoS biology, 2012-04, Vol.10 (4), p.e1001301-e1001301

2012

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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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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

2019

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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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Metagenomic binning and association of plasmids with bacterial host genomes using DNA methylation

Nature biotechnology, 2018-01, Vol.36 (1), p.61-69

2018

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

Molecular networks as sensors and drivers of common human diseases

variancePartition: interpreting drivers of variation in complex gene expression studies

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 window into third-generation sequencing

CD47-blocking antibodies restore phagocytosis and prevent atherosclerosis

A Next Generation Multiscale View of Inborn Errors of Metabolism

Systems biology of asthma and allergic diseases: A multiscale approach

Computational solutions to large-scale data management and analysis

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

Bayesian method to predict individual SNP genotypes from gene expression data

Geroscience: linking aging to chronic disease

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

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

Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility

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

Stitching together multiple data dimensions reveals interacting metabolomic and transcriptomic networks that modulate cell regulation

Characterization of the human ESC transcriptome by hybrid sequencing

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

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

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

Metagenomic binning and association of plasmids with bacterial host genomes using DNA methylation

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