Willem H. Ouwehand

发表

Genomic atlas of the human plasma proteome

Stephen Burgess, David Stacey, Bram P. Prins, 2018, Nature.

Tahini associated thrombocytopenia

Willem H. Ouwehand, J Arnold, Ga Smith, 1998 .

Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits

Berthold Göttgens, Nicole Soranzo, Suthesh Sivapalaratnam, 2011, PLoS genetics.

Comparison of Methods for Competitive Tests of Pathway Analysis

Marina Evangelou, Frank Dudbridge, Lorenz Wernisch, 2012, PloS one.

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

Christian Gieger, Ming-Huei Chen, Luigi Ferrucci, 2009, Nature Genetics.

Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia

William J. Astle, Warren S. Alexander, Edna C. Hardeman, 2017, The Journal of clinical investigation.

Multiple Loci Are Associated with White Blood Cell Phenotypes

Christian Gieger, Yusuke Nakamura, Kazuhiko Yamamoto, 2011, PLoS genetics.

Consequences of natural perturbations in the human plasma proteome

Stephen Burgess, David Stacey, Bram P. Prins, 2017, bioRxiv.

Complex Exon-Intron Marking by Histone Modifications Is Not Determined Solely by Nucleosome Distribution

Peter Saffrey, Ian Dunham, Cordelia Langford, 2010, PloS one.

Genome-Wide Haplotype Analysis of Cis Expression Quantitative Trait Loci in Monocytes

Andreas Ziegler, Nilesh J. Samani, Panos Deloukas, 2013, PLoS genetics.

New gene functions in megakaryopoiesis and platelet formation

Christian Gieger, Yusuke Nakamura, Ian J. Deary, 2011, Nature.

Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing

Andrew R. Webster, Topun Austin, Kathleen Stirrups, 2018, Genome Medicine.

Whole-genome sequencing of rare disease patients in a national healthcare system

William J. Astle, Willem H. Ouwehand, K. Stirrups, 2019, bioRxiv.

A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk

Martin Vingron, Matthias Heinig, Helge G. Roider, 2010, Nature.

Threonine-145/Methionine-145 variants of baculovirus produced recombinant ligand binding domain of GPIbα express HPA-2 epitopes and show equal binding of von Willebrand factor

Peter A. Smethurst, Willem H. Ouwehand, W. Ouwehand, 2000 .

Transcriptional diversity during lineage commitment of human blood progenitors

Randy J. Read, William J. Astle, Paul Flicek, 2014, Science.

Seventy-five genetic loci influencing the human red blood cell

Christian Gieger, Ian J. Deary, Uwe Völker, 2012, Nature.

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Christian Gieger, Jianxin Shi, Inês Barroso, 2013, Nature Genetics.

Whole genome sequencing of a sporadic primary immunodeficiency cohort

Antonis Pantazis, Keith W. Muir, David J. Williams, 2020, Nature.

Saturation analysis for whole-genome bisulfite sequencing data

Michael J. Ziller, Alexander Meissner, Simon Heath, 2016, Nature Biotechnology.

Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression

John C. Marioni, Ewan Birney, Daniel D. Seaton, 2020, Nature Communications.

A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies

Sylvia Richardson, Kathleen Stirrups, Wendy N. Erber, 2016, Science Translational Medicine.

Meta-Analysis of Genome-Wide Scans for Human Adult Stature Identifies Novel Loci and Associations with Measures of Skeletal Frame Size

Inês Barroso, Kourosh R. Ahmadi, Nicole Soranzo, 2009, PLoS genetics.

De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

Henning Gall, Fengyuan Hu, Kevin Rue-Albrecht, 2018, American journal of human genetics.