W. Cheung

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Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells

Matthew T. Maurano, Warren A. Cheung, Klaudia Walter, 2016, Cell.

Risk of re-identification of epigenetic methylation data: a more nuanced response is needed

Warren A. Cheung, T. Pastinen, S. Dyke, 2015, Clinical Epigenetics.

Edinburgh Explorer Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

Beth Wilmot, Joel Eriksson, Jie Huang, 2022 .

Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation

Warren A. Cheung, T. Spector, J. Bell, 2015, Genome Biology.

Epigenome data release: a participant-centered approach to privacy protection

Warren A. Cheung, R. Siebert, P. Flicek, 2015, Genome Biology.

Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature

Warren A. Cheung, M. Lathrop, T. Pastinen, 2022, Clinical epigenetics.

H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis

Warren A. Cheung, Dylan M. Marchione, B. Garcia, 2019, Nature Communications.

Whole-genome sequencing and deep imputation identifies non-coding variants near Engrailed-1 with large effects on bone mineral density and fracture

Matthew A. Hibbs, Stephen R. Williams, Warren A. Cheung, 2015 .

Single-cell analysis of human adipose tissue identifies depot- and disease-specific cell types

Warren A. Cheung, G. Bourque, M. Gibson, 2019, Nature Metabolism.

H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis

Warren A. Cheung, Dylan M. Marchione, B. Garcia, 2019, Nature Communications.

Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

Warren A. Cheung, K. Downes, Avik Datta, 2017, Genome Biology.

Resolving the unsolved: Comprehensive assessment of tandem repeats at scale

Zev N. Kronenberg, M. Eberle, W. Rowell, 2023, bioRxiv.

Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin‐Bound Cobalamin and Mutations in ZNF143, Which Codes for a Transcriptional Activator

Warren A. Cheung, E. Shoubridge, A. Gingras, 2016, Human mutation.

Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities

Warren A. Cheung, T. Shaikh, T. Pastinen, 2017, Human molecular genetics.

Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

Warren A. Cheung, K. Downes, Avik Datta, 2017, Genome Biology.

Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort

Warren A. Cheung, W. Rowell, Byunggil Yoo, 2023, Nature communications.

FHL2 (four and a half LIM domains 2)

W. Cheung, M. Lin, 2011 .

Increased DNA methylation variability in type 1 diabetes across three immune effector cell types

Paul Flicek, Nicole Soranzo, Simon Heath, 2016, Nature Communications.

Immune cell residency in the nasal mucosa may partially explain respiratory disease severity across the age range

Warren A. Cheung, T. Pastinen, E. Grundberg, 2021, Scientific Reports.

Adverse Maternal Environments Perturb Hepatic DNA Methylome and Transcriptome Prior to the Adult-Onset Non-Alcoholic Fatty Liver Disease in Mouse Offspring

T. Pastinen, R. Lane, W. Cheung, 2023, Nutrients.

High-resolution analyses of human sperm dynamic methylome reveal thousands of novel age-related epigenetic alterations

Warren A. Cheung, T. Pastinen, T. Kwan, 2020, Clinical epigenetics.

Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements

Warren A. Cheung, M. McCarthy, P. Deloukas, 2019, Nature Communications.

Single-cell analysis of human adipose tissue identifies depot- and disease-specific cell types

Warren A. Cheung, G. Bourque, M. Gibson, 2019, Nature Metabolism.

Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes

Orion J. Buske, Nigel J. Price, Warren A. Cheung, 2021, medRxiv.

Whole-genome sequencing identifies non-coding variants near EN 1 with large effects on bone mineral density

Beth, Matthew A. Hibbs, Stephen R. Williams, 2014 .

GSDMA drives the most replicated association with asthma in naïve CD4+ T cells

Warren A. Cheung, T. Pastinen, C. Laprise, 2019, bioRxiv.

Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

Warren A. Cheung, K. Downes, Avik Datta, 2017, Genome Biology.

Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

Warren A. Cheung, K. Downes, Avik Datta, 2017, Genome Biology.

Extravillous trophoblast cell lineage development is associated with active remodeling of the chromatin landscape

E. Grundberg, T. Arima, W. Cheung, 2023, Nature communications.

Active remodeling of the chromatin landscape directs extravillous trophoblast cell lineage development

Hiroaki, E. Grundberg, T. Arima, 2022, medRxiv.

High-resolution epigenome analysis in nasal samples derived from children with respiratory viral infections reveals striking changes upon SARS-CoV-2 infection

T. Pastinen, E. Grundberg, R. Selvarangan, 2021, medRxiv.

Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements

P. Deloukas, M. Lathrop, T. Pastinen, 2019, Nature Communications.

Epigenome data release: a participant-centered approach to privacy protection

G. Bourque, M. Hirst, T. Pastinen, 2015, Genome Biology.

Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells

Warren A. Cheung, C. A. Albers, E. Dermitzakis, 2018 .

Asthma-associated polymorphisms in 17q12-21 locus modulate methylation and gene expression of GSDMA in naïve CD4+ T cells.

Warren A. Cheung, T. Pastinen, C. Laprise, 2020, Journal of genetics and genomics = Yi chuan xue bao.