The Long-Time Chronoamperometric Current at an Inlaid Microband (or Laminar) Electrode

Por Bell, Christopher G.
Publicado em 2013

Advances in the identification and analysis of allele-specific expression

Por Bell, Christopher G, Beck, Stephan
Publicado em 2009

The epigenomic interface between genome and environment in common complex diseases

Por Bell, Christopher G., Beck, Stephan
Publicado em 2010

Human-specific CpG “beacons” identify loci associated with human-specific traits and disease

Por Bell, Christopher G., Wilson, Gareth A., Butcher, Lee M., Roos, Christian, Walter, Lutz, Beck, Stephan
Publicado em 2012

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

Por Bell, Christopher G, Teschendorff, Andrew E, Rakyan, Vardhman K, Maxwell, Alexander P, Beck, Stephan, Savage, David A
Publicado em 2010

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

Por Roos, Leonie, van Dongen, Jenny, Bell, Christopher G., Burri, Andrea, Deloukas, Panos, Boomsma, Dorret I., Spector, Tim D., Bell, Jordana T.
Publicado no Clin Epigenetics (2016)

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

Por Maiarù, Maria, Tochiki, Keri K., Cox, Marc B., Annan, Leonette V., Bell, Christopher G., Feng, Xixi, Hausch, Felix, Géranton, Sandrine M.
Publicado no Sci Transl Med (2016)

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

Por Roos, Leonie, Sandling, Johanna K., Bell, Christopher G., Glass, Daniel, Mangino, Massimo, Spector, Tim D., Deloukas, Panos, Bataille, Veronique, Bell, Jordana T.
Publicado no J Invest Dermatol (2017)

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

Por Wilson, Gareth A, Butcher, Lee M, Foster, Holly R, Feber, Andrew, Roos, Christian, Walter, Lutz, Woszczek, Grzegorz, Beck, Stephan, Bell, Christopher G
Publicado em 2014

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

Por Bell, Christopher G., Xia, Yudong, Yuan, Wei, Gao, Fei, Ward, Kirsten, Roos, Leonie, Mangino, Massimo, Hysi, Pirro G., Bell, Jordana, Wang, Jun, Spector, Timothy D.
Publicado no Genome Biol (2016)

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

Por Livshits, Gregory, Gao, Fei, Malkin, Ida, Needhamsen, Maria, Xia, Yudong, Yuan, Wei, Bell, Christopher G., Ward, Kirsten, Liu, Yuan, Wang, Jun, Bell, Jordana T., Spector, Tim D.
Publicado no J Clin Endocrinol Metab (2016)

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

Por Bell, Christopher G., Gao, Fei, Yuan, Wei, Roos, Leonie, Acton, Richard J., Xia, Yudong, Bell, Jordana, Ward, Kirsten, Mangino, Massimo, Hysi, Pirro G., Wang, Jun, Spector, Timothy D.
Publicado no Nat Commun (2018)

Analysis of sequence variability in the <it>CART </it>gene in relation to obesity in a Caucasian population

Por Hercberg Serge, Galan Pilar, Bell Christopher G, Vasseur-Delannoy Valérie, Eberlé Delphine, Clément Karine, Vatin Vincent, Dina Christian, Vasseur Francis, Barat-Houari Mouna, Guérardel Audrey, Helbecque Nicole, Potoczna Natascha, Horber Fritz F, Boutin Philippe, Froguel Philippe
Publicado em 2005-04-01

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

Por Guérardel, Audrey, Barat-Houari, Mouna, Vasseur, Francis, Dina, Christian, Vatin, Vincent, Clément, Karine, Eberlé, Delphine, Vasseur-Delannoy, Valérie, Bell, Christopher G, Galan, Pilar, Hercberg, Serge, Helbecque, Nicole, Potoczna, Natascha, Horber, Fritz F, Boutin, Philippe, Froguel, Philippe
Publicado em 2005

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

Por Curtis, Elizabeth M, Murray, Robert, Titcombe, Philip, Cook, Eloïse, Clarke‐Harris, Rebecca, Costello, Paula, Garratt, Emma, Holbrook, Joanna D, Barton, Sheila, Inskip, Hazel, Godfrey, Keith M, Bell, Christopher G, Cooper, Cyrus, Lillycrop, Karen A, Harvey, Nicholas C
Publicado no J Bone Miner Res (2017)

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

Por Taylor, Peter J, Maroulis, Sarah, Mullan, Glenda L, Pedersen, Robyn L, Baumli, Aurora, Elakis, George, Piras, Sara, Walsh, Corrina, Prósper‐Gutiérrez, Benito, De La Puente‐Alonso, Fernando, Bell, Christopher G, Mowat, David R, Johnston, Heather M, Buckley, Michael F
Publicado em 2007

Identification of Type 1 Diabetes–Associated DNA Methylation Variable Positions That Precede Disease Diagnosis

Por Rakyan, Vardhman K., Beyan, Huriya, Down, Thomas A., Hawa, Mohammed I., Maslau, Siarhei, Aden, Deeqo, Daunay, Antoine, Busato, Florence, Mein, Charles A., Manfras, Burkhard, Dias, Kerith-Rae M., Bell, Christopher G., Tost, Jörg, Boehm, Bernhard O., Beck, Stephan, Leslie, R. David
Publicado em 2011

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

Por Thurner, Matthias, van de Bunt, Martijn, Torres, Jason M, Mahajan, Anubha, Nylander, Vibe, Bennett, Amanda J, Gaulton, Kyle J, Barrett, Amy, Burrows, Carla, Bell, Christopher G, Lowe, Robert, Beck, Stephan, Rakyan, Vardhman K, Gloyn, Anna L, McCarthy, Mark I
Publicado no eLife (2018)

Integrated Genetic and Epigenetic Analysis Identifies Haplotype-Specific Methylation in the FTO Type 2 Diabetes and Obesity Susceptibility Locus

Por Bell, Christopher G., Finer, Sarah, Lindgren, Cecilia M., Wilson, Gareth A., Rakyan, Vardhman K., Teschendorff, Andrew E., Akan, Pelin, Stupka, Elia, Down, Thomas A., Prokopenko, Inga, Morison, Ian M., Mill, Jonathan, Pidsley, Ruth, Deloukas, Panos, Frayling, Timothy M., Hattersley, Andrew T., McCarthy, Mark I., Beck, Stephan, Hitman, Graham A.
Publicado em 2010

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

Por Teschendorff, Andrew E., Menon, Usha, Gentry-Maharaj, Aleksandra, Ramus, Susan J., Weisenberger, Daniel J., Shen, Hui, Campan, Mihaela, Noushmehr, Houtan, Bell, Christopher G., Maxwell, A. Peter, Savage, David A., Mueller-Holzner, Elisabeth, Marth, Christian, Kocjan, Gabrijela, Gayther, Simon A., Jones, Allison, Beck, Stephan, Wagner, Wolfgang, Laird, Peter W., Jacobs, Ian J., Widschwendter, Martin
Publicado em 2010