How to make DNA methylome wide association studies more powerful

Por Lin, Xinyi, Barton, Sheila, Holbrook, Joanna D
Publicado no Epigenomics (2016)

Coadaptation in mother and infant regulated by a paternally expressed imprinted gene.

Por Curley, James P., Barton, Sheila, Surani, Azim, Keverne, Eric B.
Publicado em 2004

MicroRNA expression profiling of single whole embryonic stem cells

Por Tang, Fuchou, Hajkova, Petra, Barton, Sheila C., Lao, Kaiqin, Surani, M. Azim
Publicado em 2006

Leukotriene B(4) receptor locus gene characterisation and association studies in asthma

Por Tulah, Asif S, Beghé, Bianca, Barton, Sheila J, Holloway, John W, Sayers, Ian
Publicado em 2012

Comparison of manual and semi-automated analysis tools for quantifying left ventricular volumes and mass in Children

Por Bryant, Jennifer A, Godfrey, Keith M, Hanson, Mark A, Barton, Sheila, Peebles, Charles R
Publicado em 2011

Cardiovascular magnetic resonance: interstudy reproducibility of measurements of left ventricular function in children

Por Bryant, Jennifer A, Godfrey, Keith M, Hanson, Mark A, Barton, Sheila, Peebles, Charles R
Publicado em 2011

The Polycomb-Group Gene Ezh2 Is Required for Early Mouse Development

Por O'Carroll, Dónal, Erhardt, Sylvia, Pagani, Michaela, Barton, Sheila C., Surani, M. Azim, Jenuwein, Thomas
Publicado em 2001

Influence of sex chromosome constitution on the genomic imprinting of germ cells

Por Durcova-Hills, Gabriela, Hajkova, Petra, Sullivan, Stephen, Barton, Sheila, Surani, M. Azim, McLaren, Anne
Publicado em 2006

Specification of germ cell fate in mice.

Por Saitou, Mitinori, Payer, Bernhard, Lange, Ulrike C, Erhardt, Sylvia, Barton, Sheila C, Surani, M Azim
Publicado em 2003

Correction of unexpected distributions of P values from analysis of whole genome arrays by rectifying violation of statistical assumptions

Por Barton, Sheila J, Crozier, Sarah R, Lillycrop, Karen A, Godfrey, Keith M, Inskip, Hazel M
Publicado em 2013

Topical intranasal corticosteroids in 4-11 year old children with persistent bilateral otitis media with effusion in primary care: double blind randomised placebo controlled trial

Por Williamson, Ian, Benge, Sarah, Barton, Sheila, Petrou, Stavros, Letley, Louise, Fasey, Nicky, Haggard, Mark, Little, Paul
Publicado em 2009

Normal Germ Line Establishment in Mice Carrying a Deletion of the Ifitm/Fragilis Gene Family Cluster

Por Lange, Ulrike C., Adams, David J., Lee, Caroline, Barton, Sheila, Schneider, Robert, Bradley, Allan, Surani, M. Azim
Publicado em 2008

Cdkn1c (p57(Kip2)) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7

Por Andrews, Stuart C, Wood, Michelle D, Tunster, Simon J, Barton, Sheila C, Surani, M Azim, John, Rosalind M
Publicado em 2007

DNA methylation at birth within the promoter of ANRIL predicts markers of cardiovascular risk at 9 years

Por Murray, Robert, Bryant, Jennifer, Titcombe, Phil, Barton, Sheila J., Inskip, Hazel, Harvey, Nicholas C., Cooper, Cyrus, Lillycrop, Karen, Hanson, Mark, Godfrey, Keith M.
Publicado no Clin Epigenetics (2016)

Maternal microRNAs are essential for mouse zygotic development

Por Tang, Fuchou, Kaneda, Masahiro, O’Carroll, Dónal, Hajkova, Petra, Barton, Sheila C., Sun, Y. Andrew, Lee, Caroline, Tarakhovsky, Alexander, Lao, Kaiqin, Surani, M. Azim
Publicado em 2007

Identification of Lipocalin and Apolipoprotein A1 as Biomarkers of Chronic Obstructive Pulmonary Disease

Por Nicholas, Benjamin L., Skipp, Paul, Barton, Sheila, Singh, Dave, Bagmane, Dinesh, Mould, Richard, Angco, Gilbert, Ward, Jon, Guha-Niyogi, Binita, Wilson, Susan, Howarth, Peter, Davies, Donna E., Rennard, Stephen, O'Connor, C. David, Djukanović, Ratko
Publicado em 2010

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)

Response to Antenatal Cholecalciferol Supplementation Is Associated With Common Vitamin D–Related Genetic Variants

Por Moon, Rebecca J., Harvey, Nicholas C., Cooper, Cyrus, D’Angelo, Stefania, Curtis, Elizabeth M., Crozier, Sarah R., Barton, Sheila J., Robinson, Sian M., Godfrey, Keith M., Graham, Nikki J., Holloway, John W., Bishop, Nicholas J., Kennedy, Stephen, Papageorghiou, Aris T., Schoenmakers, Inez, Fraser, Robert, Gandhi, Saurabh V., Prentice, Ann, Inskip, Hazel M., Javaid, M. Kassim
Publicado no J Clin Endocrinol Metab (2017)

Association between perinatal methylation of the neuronal differentiation regulator HES1 and later childhood neurocognitive function and behaviour

Por Lillycrop, Karen A, Costello, Paula M, Teh, Ai Ling, Murray, Robert J, Clarke-Harris, Rebecca, Barton, Sheila J, Garratt, Emma S, Ngo, Sherry, Sheppard, Allan M, Wong, Johnny, Dogra, Shaillay, Burdge, Graham C, Cooper, Cyrus, Inskip, Hazel M, Gale, Catharine R, Gluckman, Peter D, Harvey, Nicholas C, Chong, Yap-Seng, Yap, Fabian, Meaney, Michael J, Rifkin-Graboi, Anne, Holbrook, Joanna D, Godfrey, Keith M
Publicado no Int J Epidemiol (2015)

Identification of PCDH1 as a Novel Susceptibility Gene for Bronchial Hyperresponsiveness

Por Koppelman, Gerard H., Meyers, Deborah A., Howard, Timothy D., Zheng, S. Lilly, Hawkins, Greg A., Ampleford, Elizabeth J., Xu, Jianfeng, Koning, Henk, Bruinenberg, Marcel, Nolte, Ilja M., van Diemen, Cleo C., Boezen, H. Marike, Timens, Wim, Whittaker, Paul A., Stine, O. Colin, Barton, Sheila J., Holloway, John W., Holgate, Stephen T., Graves, Penelope E., Martinez, Fernando D., van Oosterhout, Antoon J., Bleecker, Eugene R., Postma, Dirkje S.
Publicado em 2009