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Author Details
Full Name
Christopher G Bell
Affiliation
William Harvey Research Institute, Queen Mary University of London
ORCID
Career Start Year
2004
Papers
44
H Index
24
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37683633
Integration of genetic fine-mapping and multi-omics data reveals candidate effector genes for hypertension.
Am J Hum Genet
2023
37579157
CRISPR/dCas9 DNA methylation editing is heritable during human hematopoiesis and shapes immune progeny.
Proc Natl Acad Sci U S A
2023
33402692
Somatostatin receptor 2 expression in nasopharyngeal cancer is induced by Epstein Barr virus infection: impact on prognosis, imaging and therapy.
Nat Commun
2021
33976121
The genomic loci of specific human tRNA genes exhibit ageing-related DNA hypermethylation.
Nat Commun
2021
34280322
DNA Methylome Alterations Are Associated with Airway Macrophage Differentiation and Phenotype during Lung Fibrosis.
Am J Respir Crit Care Med
2021
31448663
Deep proteomic analysis of Dnmt1 mutant/hypomorphic colorectal cancer cells reveals dysregulation of epithelial-mesenchymal transition and subcellular re-localization of Beta-Catenin.
Epigenetics
2020
30321476
Gestational Vitamin D Supplementation Leads to Reduced Perinatal RXRA DNA Methylation: Results From the MAVIDOS Trial.
J Bone Miner Res
2019
31767039
DNA methylation aging clocks: challenges and recommendations.
Genome Biol
2019
29295990
Obligatory and facilitative allelic variation in the DNA methylome within common disease-associated loci.
Nat Commun
2018
29412141
Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci.
Elife
2018
27993549
Higher Nevus Count Exhibits a Distinct DNA Methylation Signature in Healthy Human Skin: Implications for Melanoma.
J Invest Dermatol
2017
28419547
Perinatal DNA Methylation at CDKN2A Is Associated With Offspring Bone Mass: Findings From the Southampton Women's Survey.
J Bone Miner Res
2017
29208242
DNA methylation of amino acid transporter genes in the human placenta.
Placenta
2017
28980672
Microelectrode generator-collector systems for electrolytic titration: theoretical and practical considerations.
Analyst
2017
28845613
The Epigenomic Analysis of Human Obesity.
Obesity (Silver Spring)
2017
26865567
The stress regulator FKBP51 drives chronic pain by modulating spinal glucocorticoid signaling.
Sci Transl Med
2016
27702613
Insights in human epigenomic dynamics through comparative primate analysis.
Genomics
2016
27663977
Novel regional age-associated DNA methylation changes within human common disease-associated loci.
Genome Biol
2016
27144936
Contribution of Heritability and Epigenetic Factors to Skeletal Muscle Mass Variation in United Kingdom Twins.
J Clin Endocrinol Metab
2016
26798410
Integrative DNA methylome analysis of pan-cancer biomarkers in cancer discordant monozygotic twin-pairs.
Clin Epigenetics
2016
25900181
Epigenetic dysregulation and poorer prognosis in DAXX-deficient pancreatic neuroendocrine tumours.
Endocr Relat Cancer
2015
26678054
The Concordance and Heritability of Type 2 Diabetes in 34,166 Twin Pairs From International Twin Registers: The Discordant Twin (DISCOTWIN) Consortium.
Twin Res Hum Genet
2015
24598577
Human-specific epigenetic variation in the immunological Leukotriene B4 Receptor (LTB4R/BLT1) implicated in common inflammatory diseases.
Genome Med
2014
25502755
An integrated epigenomic analysis for type 2 diabetes susceptibility loci in monozygotic twins.
Nat Commun
2014
25111484
Using epigenomic studies in monozygotic twins to improve our understanding of cancer.
Epigenomics
2014
24579944
Human-specific CpG 'beacons' identify human-specific prefrontal cortex H3K4me3 chromatin peaks.
Epigenomics
2014
22968434
Human-specific CpG "beacons" identify loci associated with human-specific traits and disease.
Epigenetics
2012
21980303
Identification of type 1 diabetes-associated DNA methylation variable positions that precede disease diagnosis.
PLoS Genet
2011
29783524
Integration of genomic and epigenomic DNA methylation data in common complex diseases by haplotype-specific methylation analysis.
Per Med
2011
21779987
Accessing and selecting genetic markers from available resources.
Methods Mol Biol
2011
20219944
Age-dependent DNA methylation of genes that are suppressed in stem cells is a hallmark of cancer.
Genome Res
2010
21124985
Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus.
PLoS One
2010
21062751
The epigenomic interface between genome and environment in common complex diseases.
Brief Funct Genomics
2010
20687937
Genome-wide DNA methylation analysis for diabetic nephropathy in type 1 diabetes mellitus.
BMC Med Genomics
2010
19291541
Molecular confirmation of pathological specimen integrity in Australasia.
Pathology
2009
19490587
Advances in the identification and analysis of allele-specific expression.
Genome Med
2009
18038321
First molecular confirmation of an Australian case of type III hereditary angioedema.
Pathology
2008
17164796
No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases.
Eur J Hum Genet
2007
17259292
Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophy.
J Med Genet
2007
16648851
Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease.
Nat Genet
2006
15703762
The genetics of human obesity.
Nat Rev Genet
2005
16186414
Association of melanin-concentrating hormone receptor 1 5' polymorphism with early-onset extreme obesity.
Diabetes
2005
15823203
Analysis of sequence variability in the CART gene in relation to obesity in a Caucasian population.
BMC Genet
2005
15220211
Genome-wide linkage analysis for severe obesity in french caucasians finds significant susceptibility locus on chromosome 19q.
Diabetes
2004
1 - 44 of 44
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