Willem H. Ouwehand
Molecular Biology · 2003–2022
A researcher in the Science corpus: 28 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 351 citations into it
- Plant Science — 23 citations into it
- Statistics and Probability — 16 citations into it
Whom Willem H. Ouwehand trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- Terence P. Speed (in Molecular Biology)
- Radford M. Neal (in Statistics and Probability)
Papers from Willem H. Ouwehand's perspective
Ordered by how strongly the researchers Willem H. Ouwehand trusts endorse each paper. Same corpus, a different order for every researcher.
- Velvet: algorithms for de novo short read assembly using de Bruijn graphs.
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- Mapping short DNA sequencing reads and calling variants using mapping quality scores. (Genome Research)
- Biological sequence analysis
- Pattern Recognition and Machine Learning
- ABySS: a parallel assembler for short read sequence data. (Genome Research)
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- The Ensembl Variant Effect Predictor
- A global reference for human genetic variation
Their papers
- Genomewide Association Analysis of Coronary Artery Disease (2007) — 2,121 citations
- The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data (2013) — 826 citations
- Dindel: accurate indel calls from short-read data. (2011) — 455 citations
- Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells (2016) — 619 citations
- Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants (2009) — 1,094 citations
- The Human Phenotype Ontology in 2017 (2016) — 742 citations
- DNA methylation and body-mass index: a genome-wide analysis. (2014) — 729 citations
- Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity (2014) — 1,546 citations
- Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis (2018) — 511 citations
- eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data (2016) — 120 citations
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression (2021) — 1,862 citations
- Altered TMPRSS2 usage by SARS-CoV-2 Omicron impacts infectivity and fusogenicity (2022) — 904 citations
- Rare coding variants in 10 genes confer substantial risk for schizophrenia (2022) — 659 citations
- The Polygenic and Monogenic Basis of Blood Traits and Diseases (2020) — 602 citations
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) — 744 citations
- Genomic atlas of the human plasma proteome (2018) — 1,884 citations
- Genetic evidence of assortative mating in humans (2017) — 288 citations
- Allelic Landscape of Human Blood Cell Trait Variation and Links (2016)
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014)
- Identification of seven loci affecting mean telomere length and their association with disease (2013) — 909 citations