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Search Results to Warren Cheung

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Cheung, Warren

One or more keywords matched the following items that are connected to Cheung, Warren

Item Type	Name
Concept	Cardiovascular Diseases
Concept	Disease
Concept	Disease Models, Animal
Concept	Immune System Diseases
Concept	Metabolic Diseases
Concept	Genetic Predisposition to Disease
Concept	Rare Diseases
Concept	Polycomb Repressive Complex 2
Concept	Non-alcoholic Fatty Liver Disease
Academic Article	Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Academic Article	Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.
Academic Article	Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements.
Academic Article	H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis.
Academic Article	Compensating for literature annotation bias when predicting novel drug-disease relationships through Medical Subject Heading Over-representation Profile (MeSHOP) similarity.
Academic Article	Inferring novel gene-disease associations using Medical Subject Heading Over-representation Profiles.
Academic Article	Single-cell analysis of human adipose tissue identifies depot and disease specific cell types.
Academic Article	Asthma-associated polymorphisms in 17q12-21 locus modulate methylation and gene expression of GSDMA in na?ve CD4+ T cells.
Academic Article	Immune cell residency in the nasal mucosa may partially explain respiratory disease severity across the age range.
Academic Article	Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes.
Academic Article	Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort.
Academic Article	Adverse Maternal Environments Perturb Hepatic DNA Methylome and Transcriptome Prior to the Adult-Onset Non-Alcoholic Fatty Liver Disease in Mouse Offspring.
Academic Article	Pangenome graphs improve the analysis of structural variants in rare genetic diseases.
Academic Article	Complex trait associations in rare diseases and impacts on Mendelian variant interpretation.

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