Department of Public Health and Primary Care, University of Cambridge
17 papers found
ProGeM: a framework for the prioritization of candidate causal genes at molecular quantitative trait loci
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference
Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome
Neutrophil-mediated IL-6 receptor trans-signaling and the risk of chronic obstructive pulmonary disease and asthma
UroMark—a urinary biomarker assay for the detection of bladder cancer
Correlation of an epigenetic mitotic clock with cancer risk
PhenoScanner: a database of human genotype-phenotype associations.
Quantitative comparison of DNA methylation assays for biomarker development and clinical applications
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery
eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data
Assessment of patient-derived tumour xenografts (PDXs) as a discovery tool for cancer epigenomics
Advances in epigenome-wide association studies for common diseases
Assessment of RainDrop BS-seq as a method for large-scale, targeted bisulfite sequencing.
Seventy-five genetic loci influencing the human red blood cell
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.
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