about
Correlation of an epigenetic mitotic clock with cancer riskCompound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.Neutrophil-mediated IL-6 receptor trans-signaling and the risk of chronic obstructive pulmonary disease and asthma.Maps of open chromatin guide the functional follow-up of genome-wide association signals: application to hematological traits.Assessment of patient-derived tumour xenografts (PDXs) as a discovery tool for cancer epigenomics.eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data.A donor-specific epigenetic classifier for acute graft-versus-host disease severity in hematopoietic stem cell transplantationA GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding siteSeventy-five genetic loci influencing the human red blood cellMaps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci.PhenoScanner: a database of human genotype-phenotype associations.Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.Increased DNA methylation variability in type 1 diabetes across three immune effector cell types.Genome-wide analysis of differential transcriptional and epigenetic variability across human immune cell types.UroMark-a urinary biomarker assay for the detection of bladder cancer.The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome.Assessment of RainDrop BS-seq as a method for large-scale, targeted bisulfite sequencing.Functional interpretation of non-coding sequence variation: concepts and challenges.Advances in epigenome-wide association studies for common diseases.Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.Epigenetic and Transcriptional Variability Shape Phenotypic Plasticity.Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference.Risk thresholds for alcohol consumption: combined analysis of individual-participant data for 599 912 current drinkers in 83 prospective studies.Tensorial blind source separation for improved analysis of multi-omic data.Increased DNA methylation variability in rheumatoid arthritis-discordant monozygotic twinsSelfish mutations dysregulating RAS-MAPK signaling are pervasive in aged human testesGenomic atlas of the human plasma proteomeCell and tissue type independent age-associated DNA methylation changes are not rare but commonGenetic effects on promoter usage are highly context-specific and contribute to complex traitsInterleukin-6 Receptor Signaling and Abdominal Aortic Aneurysm Growth RatesEpigenome-Wide Association Study of Incident Type 2 Diabetes in a British Population: EPIC-Norfolk StudyDeciphering the genomic, epigenomic, and transcriptomic landscapes of pre-invasive lung cancer lesionsProGeM: a framework for the prioritization of candidate causal genes at molecular quantitative trait lociAn Unbiased Lipid Phenotyping Approach To Study the Genetic Determinants of Lipids and Their Association with Coronary Heart Disease Risk Factors
P50
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P50
description
researcher
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wetenschapper
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հետազոտող
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name
Dirk S Paul
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Dirk S Paul
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Dirk S Paul
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Dirk S Paul
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Dirk S Paul
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type
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Dirk S Paul
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Dirk S Paul
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Dirk S Paul
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Dirk S Paul
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Dirk S Paul
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Dirk Paul
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Dirk S Paul
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Dirk S Paul
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Dirk S Paul
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Dirk S Paul
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Dirk S Paul
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P106
P21
P2798
P31
P496
0000-0002-8230-0116