| Year |
Citation |
Score |
| 2021 |
McErlean P, Bell CG, Hewitt RJ, Busharat Z, Ogger PP, Ghai P, Albers GJ, Calamita E, Kingston S, Molyneaux PL, Beck S, Lloyd CM, Maher TM, Byrne AJ. DNA Methylome Alterations are Associated with Airway Macrophage Differentiation and Phenotype During Lung Fibrosis. American Journal of Respiratory and Critical Care Medicine. PMID 34280322 DOI: 10.1164/rccm.202101-0004OC |
0.403 |
|
| 2019 |
Bell CG, Lowe R, Adams PD, Baccarelli AA, Beck S, Bell JT, Christensen BC, Gladyshev VN, Heijmans BT, Horvath S, Ideker T, Issa JJ, Kelsey KT, Marioni RE, Reik W, et al. DNA methylation aging clocks: challenges and recommendations. Genome Biology. 20: 249. PMID 31767039 DOI: 10.1186/S13059-019-1824-Y |
0.517 |
|
| 2019 |
Bowler EH, Smith-Vidal A, Lester A, Bell J, Wang Z, Bell CG, Wang Y, Divecha N, Skipp PJ, Ewing RM. Deep proteomic analysis of Dnmt1 mutant/hypomorphic colorectal cancer cells reveals dysregulation of epithelial-mesenchymal transition and subcellular re-localization of Beta-Catenin. Epigenetics. 1-15. PMID 31448663 DOI: 10.1080/15592294.2019.1656154 |
0.329 |
|
| 2018 |
Curtis EM, Krstic N, Cook E, D'Angelo S, Crozier SR, Moon RJ, Murray R, Garratt E, Costello P, Cleal J, Ashley B, Bishop NJ, Kennedy S, Papageorghiou AT, Schoenmakers I, ... ... Bell CG, et al. Gestational vitamin D supplementation leads to reduced perinatal RXRA DNA methylation: Results from the MAVIDOS trial. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 30321476 DOI: 10.1002/Jbmr.3603 |
0.334 |
|
| 2018 |
Thurner M, van de Bunt M, Torres JM, Mahajan A, Nylander V, Bennett AJ, Gaulton KJ, Barrett A, Burrows C, Bell CG, Lowe R, Beck S, Rakyan VK, Gloyn AL, McCarthy MI. Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci. Elife. 7. PMID 29412141 DOI: 10.7554/Elife.31977 |
0.564 |
|
| 2018 |
Bell CG, Gao F, Yuan W, Roos L, Acton RJ, Xia Y, Bell J, Ward K, Mangino M, Hysi PG, Wang J, Spector TD. Obligatory and facilitative allelic variation in the DNA methylome within common disease-associated loci. Nature Communications. 9: 8. PMID 29295990 DOI: 10.1038/S41467-017-01586-1 |
0.442 |
|
| 2018 |
Thurner M, Bunt Mvd, Torres JM, Mahajan A, Nylander V, Bennett AJ, Gaulton KJ, Barrett A, Burrows C, Bell CG, Lowe R, Beck S, Rakyan VK, Gloyn AL, McCarthy MI. Author response: Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci Elife. DOI: 10.7554/Elife.31977.047 |
0.517 |
|
| 2018 |
Curtis EM, Titcombe P, Edwards M, Barton S, Tsai P, Dennison EM, Bell J, Spector T, Valdes AM, Bell CG, Harvey NC, Cooper C. 090 DNA methylation and its relationship with musculoskeletal health in older adults from the Hertfordshire Cohort Study: findings from an epigenome-wide association study Rheumatology. 57. DOI: 10.1093/Rheumatology/Key075.314 |
0.319 |
|
| 2017 |
Bell CG. The Epigenomic Analysis of Human Obesity. Obesity (Silver Spring, Md.). 25: 1471-1481. PMID 28845613 DOI: 10.1002/Oby.21909 |
0.409 |
|
| 2017 |
Curtis EM, Murray R, Titcombe P, Cook E, Clarke-Harris R, Costello P, Garratt E, Holbrook JD, Barton S, Inskip H, Godfrey KM, Bell CG, Cooper C, Lillycrop KA, Harvey NC. Perinatal DNA methylation at CDKN2A is associated with offspring bone mass: Findings from the Southampton Women's Survey. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 28419547 DOI: 10.1002/Jbmr.3153 |
0.332 |
|
| 2017 |
Acton RJ, Bell CG. Cancer detection and tissue of origin determination with novel annotation and scoring of cell-free methylated DNA Ame Medical Journal. 2: 110-110. DOI: 10.21037/Amj.2017.08.02 |
0.356 |
|
| 2016 |
Roos L, Sandling JK, Bell CG, Glass D, Mangino M, Spector TD, Deloukas P, Bataille V, Bell JT. Higher Naevus Count Exhibits A Distinct DNA Methylation Signature in Healthy Human Skin: Implications for Melanoma. The Journal of Investigative Dermatology. PMID 27993549 DOI: 10.1016/J.Jid.2016.11.029 |
0.363 |
|
| 2016 |
Bell CG. Insights in human epigenomic dynamics through comparative primate analysis. Genomics. PMID 27702613 DOI: 10.1016/J.Ygeno.2016.09.003 |
0.356 |
|
| 2016 |
Bell CG, Xia Y, Yuan W, Gao F, Ward K, Roos L, Mangino M, Hysi PG, Bell J, Wang J, Spector TD. Novel regional age-associated DNA methylation changes within human common disease-associated loci. Genome Biology. 17: 193. PMID 27663977 DOI: 10.1186/S13059-016-1051-8 |
0.403 |
|
| 2015 |
Willemsen G, Ward KJ, Bell CG, Christensen K, Bowden J, Dalgård C, Harris JR, Kaprio J, Lyle R, Magnusson PK, Mather KA, Ordoňana JR, Perez-Riquelme F, Pedersen NL, Pietiläinen KH, et al. The Concordance and Heritability of Type 2 Diabetes in 34,166 Twin Pairs From International Twin Registers: The Discordant Twin (DISCOTWIN) Consortium. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 18: 762-71. PMID 26678054 DOI: 10.1017/Thg.2015.83 |
0.337 |
|
| 2015 |
Pipinikas CP, Dibra H, Karpathakis A, Feber A, Novelli M, Oukrif D, Fusai G, Valente R, Caplin M, Meyer T, Teschendorff A, Bell C, Morris TJ, Salomoni P, Luong TV, et al. Epigenetic dysregulation and poorer prognosis in DAXX-deficient pancreatic neuroendocrine tumours. Endocrine-Related Cancer. 22: L13-8. PMID 25900181 DOI: 10.1530/Erc-15-0108 |
0.458 |
|
| 2014 |
Yuan W, Xia Y, Bell CG, Yet I, Ferreira T, Ward KJ, Gao F, Loomis AK, Hyde CL, Wu H, Lu H, Liu Y, Small KS, Viñuela A, Morris AP, et al. An integrated epigenomic analysis for type 2 diabetes susceptibility loci in monozygotic twins. Nature Communications. 5: 5719. PMID 25502755 DOI: 10.1038/Ncomms6719 |
0.422 |
|
| 2014 |
Roos L, Spector TD, Bell CG. Using epigenomic studies in monozygotic twins to improve our understanding of cancer. Epigenomics. 6: 299-309. PMID 25111484 DOI: 10.2217/Epi.14.13 |
0.321 |
|
| 2014 |
Wilson GA, Butcher LM, Foster HR, Feber A, Roos C, Walter L, Woszczek G, Beck S, Bell CG. Human-specific epigenetic variation in the immunological Leukotriene B4 Receptor (LTB4R/BLT1) implicated in common inflammatory diseases. Genome Medicine. 6: 19. PMID 24598577 DOI: 10.1186/Gm536 |
0.535 |
|
| 2014 |
Bell CG, Wilson GA, Beck S. Human-specific CpG 'beacons' identify human-specific prefrontal cortex H3K4me3 chromatin peaks. Epigenomics. 6: 21-31. PMID 24579944 DOI: 10.2217/Epi.13.74 |
0.527 |
|
| 2012 |
Bell CG, Wilson GA, Butcher LM, Roos C, Walter L, Beck S. Human-specific CpG "beacons" identify loci associated with human-specific traits and disease. Epigenetics : Official Journal of the Dna Methylation Society. 7: 1188-99. PMID 22968434 DOI: 10.4161/Epi.22127 |
0.579 |
|
| 2011 |
Bell CG. Integration of genomic and epigenomic DNA methylation data in common complex diseases by haplotype-specific methylation analysis. Personalized Medicine. 8: 243-251. PMID 29783524 DOI: 10.2217/Pme.11.14 |
0.445 |
|
| 2011 |
Rakyan VK, Beyan H, Down TA, Hawa MI, Maslau S, Aden D, Daunay A, Busato F, Mein CA, Manfras B, Dias KR, Bell CG, Tost J, Boehm BO, Beck S, et al. Identification of type 1 diabetes-associated DNA methylation variable positions that precede disease diagnosis. Plos Genetics. 7: e1002300. PMID 21980303 DOI: 10.1371/Journal.Pgen.1002300 |
0.579 |
|
| 2011 |
Bell CG. Accessing and selecting genetic markers from available resources. Methods in Molecular Biology (Clifton, N.J.). 760: 1-17. PMID 21779987 DOI: 10.1007/978-1-61779-176-5_1 |
0.313 |
|
| 2010 |
Bell CG, Finer S, Lindgren CM, Wilson GA, Rakyan VK, Teschendorff AE, Akan P, Stupka E, Down TA, Prokopenko I, Morison IM, Mill J, Pidsley R, Deloukas P, et al. Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus. Plos One. 5: e14040. PMID 21124985 DOI: 10.1371/Journal.Pone.0014040 |
0.597 |
|
| 2010 |
Bell CG, Beck S. The epigenomic interface between genome and environment in common complex diseases. Briefings in Functional Genomics. 9: 477-85. PMID 21062751 DOI: 10.1093/Bfgp/Elq026 |
0.569 |
|
| 2010 |
Bell CG, Teschendorff AE, Rakyan VK, Maxwell AP, Beck S, Savage DA. Genome-wide DNA methylation analysis for diabetic nephropathy in type 1 diabetes mellitus. Bmc Medical Genomics. 3: 33. PMID 20687937 DOI: 10.1186/1755-8794-3-33 |
0.496 |
|
| 2010 |
Teschendorff AE, Menon U, Gentry-Maharaj A, Ramus SJ, Weisenberger DJ, Shen H, Campan M, Noushmehr H, Bell CG, Maxwell AP, Savage DA, Mueller-Holzner E, Marth C, Kocjan G, Gayther SA, et al. Age-dependent DNA methylation of genes that are suppressed in stem cells is a hallmark of cancer. Genome Research. 20: 440-6. PMID 20219944 DOI: 10.1101/Gr.103606.109 |
0.524 |
|
| 2010 |
Bell CG, Finer S, Lindgren CM, Wilson GA, Rakyan VK, Teschendorff AE, Akan P, Stupka E, Down TA, Prokopenko I, Morison IM, Mill J, Pidsley R, Deloukas P, Frayling TM, et al. LD relationship for FTO Association SNPs and rs7202116. Plos One. DOI: 10.1371/Journal.Pone.0014040.T004 |
0.453 |
|
| 2009 |
Bell CG, Beck S. Advances in the identification and analysis of allele-specific expression. Genome Medicine. 1: 56. PMID 19490587 DOI: 10.1186/Gm56 |
0.555 |
|
| 2007 |
Bell CG, Meyre D, Petretto E, Levy-Marchal C, Hercberg S, Charles MA, Boyle C, Weill J, Tauber M, Mein CA, Aitman TJ, Froguel P, Walley AJ. 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. European Journal of Human Genetics : Ejhg. 15: 320-7. PMID 17164796 DOI: 10.1038/Sj.Ejhg.5201754 |
0.502 |
|
| 2005 |
Bell CG, Meyre D, Samson C, Boyle C, Lecoeur C, Tauber M, Jouret B, Jaquet D, Levy-Marchal C, Charles MA, Weill J, Gibson F, Mein CA, Froguel P, Walley AJ. Association of melanin-concentrating hormone receptor 1 5' polymorphism with early-onset extreme obesity. Diabetes. 54: 3049-55. PMID 16186414 DOI: 10.2337/Diabetes.54.10.3049 |
0.456 |
|
| 2005 |
Guérardel A, Barat-Houari M, Vasseur F, Dina C, Vatin V, Clément K, Eberlé D, Vasseur-Delannoy V, Bell CG, Galan P, Hercberg S, Helbecque N, Potoczna N, Horber FF, Boutin P, et al. Analysis of sequence variability in the CART gene in relation to obesity in a Caucasian population. Bmc Genetics. 6: 19. PMID 15823203 DOI: 10.1186/1471-2156-6-19 |
0.435 |
|
| 2005 |
Bell CG, Walley AJ, Froguel P. The genetics of human obesity. Nature Reviews. Genetics. 6: 221-34. PMID 15703762 DOI: 10.1038/Nrg1556 |
0.455 |
|
| 2004 |
Bell CG, Benzinou M, Siddiq A, Lecoeur C, Dina C, Lemainque A, Clément K, Basdevant A, Guy-Grand B, Mein CA, Meyre D, Froguel P. Genome-wide linkage analysis for severe obesity in french caucasians finds significant susceptibility locus on chromosome 19q. Diabetes. 53: 1857-65. PMID 15220211 DOI: 10.2337/Diabetes.53.7.1857 |
0.435 |
|
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