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Gestational Vitamin D Supplementation Leads to Reduced Perinatal RXRA DNA Methylation: Results From the MAVIDOS Trial.

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, Fraser R, Gandhi SV, Prentice A, Javaid MK, Inskip HM, Godfrey KM, Bell CG, Lillycrop KA, Cooper C, Harvey NC; MAVIDOS Trial Group.

J Bone Miner Res. 2019 Feb;34(2):231-240. doi: 10.1002/jbmr.3603. Epub 2019 Jan 18.


Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci.

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.

Elife. 2018 Feb 7;7. pii: e31977. doi: 10.7554/eLife.31977.


Obligatory and facilitative allelic variation in the DNA methylome within common disease-associated loci.

Bell CG, Gao F, Yuan W, Roos L, Acton RJ, Xia Y, Bell J, Ward K, Mangino M, Hysi PG, Wang J, Spector TD.

Nat Commun. 2018 Jan 2;9(1):8. doi: 10.1038/s41467-017-01586-1.


DNA methylation of amino acid transporter genes in the human placenta.

Simner C, Novakovic B, Lillycrop KA, Bell CG, Harvey NC, Cooper C, Saffery R, Lewis RM, Cleal JK.

Placenta. 2017 Dec;60:64-73. doi: 10.1016/j.placenta.2017.10.010. Epub 2017 Oct 31.


Microelectrode generator-collector systems for electrolytic titration: theoretical and practical considerations.

Bell CG, Seelanan P, O'Hare D.

Analyst. 2017 Oct 23;142(21):4048-4057. doi: 10.1039/c7an01450c.


The Epigenomic Analysis of Human Obesity.

Bell CG.

Obesity (Silver Spring). 2017 Sep;25(9):1471-1481. doi: 10.1002/oby.21909. Review.


Perinatal DNA Methylation at CDKN2A Is Associated With Offspring Bone Mass: Findings From the Southampton Women's Survey.

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.

J Bone Miner Res. 2017 Oct;32(10):2030-2040. doi: 10.1002/jbmr.3153. Epub 2017 May 22.


Higher Nevus Count Exhibits a Distinct DNA Methylation Signature in Healthy Human Skin: Implications for Melanoma.

Roos L, Sandling JK, Bell CG, Glass D, Mangino M, Spector TD, Deloukas P, Bataille V, Bell JT.

J Invest Dermatol. 2017 Apr;137(4):910-920. doi: 10.1016/j.jid.2016.11.029. Epub 2016 Dec 18.


Insights in human epigenomic dynamics through comparative primate analysis.

Bell CG.

Genomics. 2016 Oct;108(3-4):115-125. doi: 10.1016/j.ygeno.2016.09.003. Epub 2016 Oct 1. Review.


Novel regional age-associated DNA methylation changes within human common disease-associated loci.

Bell CG, Xia Y, Yuan W, Gao F, Ward K, Roos L, Mangino M, Hysi PG, Bell J, Wang J, Spector TD.

Genome Biol. 2016 Sep 23;17(1):193.


Contribution of Heritability and Epigenetic Factors to Skeletal Muscle Mass Variation in United Kingdom Twins.

Livshits G, Gao F, Malkin I, Needhamsen M, Xia Y, Yuan W, Bell CG, Ward K, Liu Y, Wang J, Bell JT, Spector TD.

J Clin Endocrinol Metab. 2016 Jun;101(6):2450-9. doi: 10.1210/jc.2016-1219. Epub 2016 May 4.


The stress regulator FKBP51 drives chronic pain by modulating spinal glucocorticoid signaling.

Maiarù M, Tochiki KK, Cox MB, Annan LV, Bell CG, Feng X, Hausch F, Géranton SM.

Sci Transl Med. 2016 Feb 10;8(325):325ra19. doi: 10.1126/scitranslmed.aab3376.


Integrative DNA methylome analysis of pan-cancer biomarkers in cancer discordant monozygotic twin-pairs.

Roos L, van Dongen J, Bell CG, Burri A, Deloukas P, Boomsma DI, Spector TD, Bell JT.

Clin Epigenetics. 2016 Jan 20;8:7. doi: 10.1186/s13148-016-0172-y. eCollection 2016.


The Concordance and Heritability of Type 2 Diabetes in 34,166 Twin Pairs From International Twin Registers: The Discordant Twin (DISCOTWIN) Consortium.

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, Sachdev PS, Boomsma DI, Spector T.

Twin Res Hum Genet. 2015 Dec;18(6):762-71. doi: 10.1017/thg.2015.83.


An integrated epigenomic analysis for type 2 diabetes susceptibility loci in monozygotic twins.

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, Berdasco M, Esteller M, Brosnan MJ, Deloukas P, McCarthy MI, John SL, Bell JT, Wang J, Spector TD.

Nat Commun. 2014 Dec 12;5:5719. doi: 10.1038/ncomms6719.


Using epigenomic studies in monozygotic twins to improve our understanding of cancer.

Roos L, Spector TD, Bell CG.

Epigenomics. 2014 Jun;6(3):299-309. doi: 10.2217/epi.14.13. Review.


Human-specific epigenetic variation in the immunological Leukotriene B4 Receptor (LTB4R/BLT1) implicated in common inflammatory diseases.

Wilson GA, Butcher LM, Foster HR, Feber A, Roos C, Walter L, Woszczek G, Beck S, Bell CG.

Genome Med. 2014 Mar 5;6(3):19. doi: 10.1186/gm536. eCollection 2014.


Human-specific CpG 'beacons' identify human-specific prefrontal cortex H3K4me3 chromatin peaks.

Bell CG, Wilson GA, Beck S.

Epigenomics. 2014 Feb;6(1):21-31. doi: 10.2217/epi.13.74.


A review of mathematical models for the formation of vascular networks.

Scianna M, Bell CG, Preziosi L.

J Theor Biol. 2013 Sep 21;333:174-209. doi: 10.1016/j.jtbi.2013.04.037. Epub 2013 May 16. Review.


The long-time chronoamperometric current at an inlaid microband (or laminar) electrode.

Bell CG.

Sensors (Basel). 2013 Jan 4;13(1):626-47. doi: 10.3390/s130100626.


Human-specific CpG "beacons" identify loci associated with human-specific traits and disease.

Bell CG, Wilson GA, Butcher LM, Roos C, Walter L, Beck S.

Epigenetics. 2012 Oct;7(10):1188-99. doi: 10.4161/epi.22127. Epub 2012 Sep 11.


Identification of type 1 diabetes-associated DNA methylation variable positions that precede disease diagnosis.

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, Leslie RD.

PLoS Genet. 2011 Sep;7(9):e1002300. doi: 10.1371/journal.pgen.1002300. Epub 2011 Sep 29.


Accessing and selecting genetic markers from available resources.

Bell CG.

Methods Mol Biol. 2011;760:1-17. doi: 10.1007/978-1-61779-176-5_1.


Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus.

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; International Type 2 Diabetes 1q Consortium, Deloukas P, Frayling TM, Hattersley AT, McCarthy MI, Beck S, Hitman GA.

PLoS One. 2010 Nov 18;5(11):e14040. doi: 10.1371/journal.pone.0014040.


The epigenomic interface between genome and environment in common complex diseases.

Bell CG, Beck S.

Brief Funct Genomics. 2010 Dec;9(5-6):477-85. doi: 10.1093/bfgp/elq026. Epub 2010 Nov 8. Review.


A theoretical analysis of the surface tension profiles of strongly interacting polymer-surfactant systems.

Bell CG, Breward CJ, Howell PD, Penfold J, Thomas RK.

J Colloid Interface Sci. 2010 Oct 15;350(2):486-93. doi: 10.1016/j.jcis.2010.07.020. Epub 2010 Jul 16.


Genome-wide DNA methylation analysis for diabetic nephropathy in type 1 diabetes mellitus.

Bell CG, Teschendorff AE, Rakyan VK, Maxwell AP, Beck S, Savage DA.

BMC Med Genomics. 2010 Aug 5;3:33. doi: 10.1186/1755-8794-3-33.


Age-dependent DNA methylation of genes that are suppressed in stem cells is a hallmark of cancer.

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, Jones A, Beck S, Wagner W, Laird PW, Jacobs IJ, Widschwendter M.

Genome Res. 2010 Apr;20(4):440-6. doi: 10.1101/gr.103606.109. Epub 2010 Mar 10.


Advances in the identification and analysis of allele-specific expression.

Bell CG, Beck S.

Genome Med. 2009 May 29;1(5):56. doi: 10.1186/gm56.


Molecular confirmation of pathological specimen integrity in Australasia.

Bell CG, Wood DR, Cheong SJ, Kwan E, Sinosich M, Delprado W, Baumgart KW.

Pathology. 2009;41(3):280-3. doi: 10.1080/00313020902756311.


In vitro cyclic testing of the Exeter stem after cement within cement revision.

Wilson LJ, Bell CG, Weinrauch P, Crawford R.

J Arthroplasty. 2009 Aug;24(5):789-94. doi: 10.1016/j.arth.2008.02.014. Epub 2008 Jun 4.


Reducing metal debris generation during total knee arthroplasty.

Sydney SE, Pickering SA, Bell CG, Crawford R.

Orthopedics. 2007 Dec;30(12):999-1000.


First molecular confirmation of an Australian case of type III hereditary angioedema.

Bell CG, Kwan E, Nolan RC, Baumgart KW.

Pathology. 2008 Jan;40(1):82-3. No abstract available.


In vitro analysis of exeter stem torsional stability.

Bell CG, Weinrauch P, Pearcy M, Crawford R.

J Arthroplasty. 2007 Oct;22(7):1024-30.


Macroscopic modeling of the surface tension of polymer-surfactant systems.

Bell CG, Breward CJ, Howell PD, Penfold J, Thomas RK.

Langmuir. 2007 May 22;23(11):6042-52. Epub 2007 Apr 28.


Thermomechanical investigation of the cortical bone analogue in third-generation Sawbones femurs.

Bell CG, Weinrauch P, Crawford R, Pearcy M.

Proc Inst Mech Eng H. 2007 Feb;221(2):213-7.


Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophy.

Taylor PJ, Maroulis S, Mullan GL, Pedersen RL, Baumli A, Elakis G, Piras S, Walsh C, Prósper-Gutiérrez B, De La Puente-Alonso F, Bell CG, Mowat DR, Johnston HM, Buckley MF.

J Med Genet. 2007 Jun;44(6):368-72. Epub 2007 Jan 26.


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.

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.

Eur J Hum Genet. 2007 Mar;15(3):320-7. Epub 2006 Dec 13.


Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease.

Roscioli T, Cliffe ST, Bloch DB, Bell CG, Mullan G, Taylor PJ, Sarris M, Wang J, Donald JA, Kirk EP, Ziegler JB, Salzer U, McDonald GB, Wong M, Lindeman R, Buckley MF.

Nat Genet. 2006 Jun;38(6):620-2. Epub 2006 Apr 30.


Association of melanin-concentrating hormone receptor 1 5' polymorphism with early-onset extreme obesity.

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.

Diabetes. 2005 Oct;54(10):3049-55.


Analysis of sequence variability in the CART gene in relation to obesity in a Caucasian population.

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, Froguel P.

BMC Genet. 2005 Apr 11;6:19.


The genetics of human obesity.

Bell CG, Walley AJ, Froguel P.

Nat Rev Genet. 2005 Mar;6(3):221-34. Review.


Genome-wide linkage analysis for severe obesity in french caucasians finds significant susceptibility locus on chromosome 19q.

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.

Diabetes. 2004 Jul;53(7):1857-65.


Role of autoantibody (7S/19S) in the physiological immune response.

Bell CG.

Biochem Soc Trans. 1998 Feb;26(1):S55. No abstract available.


Immunoregulatory role of natural autoantibody in health & disease.

Bell CG.

Biochem Soc Trans. 1998 Feb;26(1):S53. No abstract available.


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