Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Catherine Potter"'
Autor:
Catherine Potter, Jill McKay, Alexandra Groom, Dianne Ford, Lisa Coneyworth, John C Mathers, Caroline L Relton
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e76506 (2013)
This study examines the relationship between common genetic variation within DNA methyltransferase genes and inter-individual variation in DNA methylation. Eleven polymorphisms spanning DNMT1 and DNMT3B were genotyped. Global and gene specific (IGF2,
Externí odkaz:
https://doaj.org/article/45c4ef06a51b402493b1475f4a2e7a00
Autor:
Jill A McKay, Alexandra Groom, Catherine Potter, Lisa J Coneyworth, Dianne Ford, John C Mathers, Caroline L Relton
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e33290 (2012)
Inter-individual variation in patterns of DNA methylation at birth can be explained by the influence of environmental, genetic and stochastic factors. This study investigates the genetic and non-genetic determinants of variation in DNA methylation in
Externí odkaz:
https://doaj.org/article/48cbefab78034e16b204bce913ec5dae
Autor:
Catherine, Potter, Anthony Vincent, Moorman, Caroline Laura, Relton, Dianne, Ford, John Cummings, Mathers, Gordon, Strathdee, Jill Ann, McKay
Publikováno v:
Molecular nutritionfood research. 62(22)
Inadequate maternal folate intake is associated with increased childhood acute lymphoblastic leukemia (ALL) risk. Folate provides methyl groups for DNA methylation, which is dramatically disrupted in ALL. Whether or not maternal folate (and related B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d26c7941e9ab98e8c03f5741044e59af
https://pubmed.ncbi.nlm.nih.gov/30192066
https://pubmed.ncbi.nlm.nih.gov/30192066
Autor:
Robin N Beaumont, Nicole M Warrington, Alana Cavadino, Jessica Tyrrell, Michael Nodzenski, Momoko Horikoshi, Frank Geller, Ronny Myhre, Rebecca C Richmond, Lavinia Paternoster, Jonathan P Bradfield, Eskil Kreiner-Møller, Ville Huikari, Sarah Metrustry, Kathryn L Lunetta, Jodie N Painter, Jouke-Jan Hottenga, Catherine Allard, Sheila J Barton, Ana Espinosa, Julie A Marsh, Catherine Potter, Ge Zhang
Publikováno v:
Human Molecular Genetics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=r3c4b2081b22::457dde875fd9cae1005c4d85053458d8
Publikováno v:
Journal of Mixed Methods Research. 8:278-298
Increasing recognition of the role of social conditions in health has led to calls for methods that can be used to change social conditions. Popular education has demonstrated great promise as a methodology that can be used to address the underlying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c47d394c7c99bc8a617794c954dfe379
https://doi.org/10.1177/1558689813510785
https://doi.org/10.1177/1558689813510785
Publikováno v:
The Cochrane Library
University of Manchester-PURE
University of Manchester-PURE
Reason for withdrawal from publication Protocol withdrawn. Cochrane Oral Health was unable to maintain contact with the contact author. The co-authors are unable to take over this protocol.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3fe2e64d25b83a7b89fc844feaf0367
https://doi.org/10.1002/14651858.cd010688.pub2
https://doi.org/10.1002/14651858.cd010688.pub2
Autor:
James C. McConnell, Nicholas D. Embleton, Alexandra Groom, Daniel Swan, Valérie Turcot, Caroline L Relton, Catherine Potter, Mark S. Pearce
Publikováno v:
Gene. 499:99-107
There is considerable interest in defining the relationship between epigenetic variation and the risk of common complex diseases. Strategies which assist in the prioritisation of target loci that have the potential to be epigenetically regulated migh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f309d0ec0d8f203fbd1ac538a94bc969
https://doi.org/10.1016/j.gene.2012.02.001
https://doi.org/10.1016/j.gene.2012.02.001
Autor:
Alexandra Groom, Caroline L Relton, Mark S. Pearce, Nicholas D. Embleton, John C. Mathers, Valérie Turcot, George Davey Smith, Daniel Swan, Catherine Potter, Ghazaleh Fatemifar, David M. Evans, Susan M. Ring
Publikováno v:
Diabetes
Rapid postnatal growth is associated with increased risk of childhood adiposity. The aim of this study was to establish whether this pathway is mediated by altered DNA methylation and gene expression. Two distinct cohorts, one preterm (n = 121) and o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::735586783d89077a6b07d5fd4d277cb0
http://europepmc.org/articles/PMC3266428
http://europepmc.org/articles/PMC3266428
Autor:
Ville Huikari, Jessica Tyrrell, Sylvain Sebert, Rachel M. Freathy, Lavinia Paternoster, Marjo-Riitta Järvelin, H. Rob Taal, Catherine Potter, Ellen A. Nohr, Debbie A Lawlor, Alana Cavadino, Mads Melbye, Frank Geller, Susan M. Ring, Rachel Bakker, Caroline L Relton, Marie-Jo Brion, George Davey Smith, Timothy M. Frayling, Andrew T. Hattersley, Verena Sengpiel, Lynn P. Lowe, Graham Watt, Jennifer T. Christie, Bo Jacobsson, Jeffrey C. Murray, Jane W. Y. Ng, Anna-Liisa Hartikainen, Elina Hyppönen, Ronny Myhre, Bjarke Feenstra, Albert Hofman, Vincent W. V. Jaddoe, Thorkild I. A. Sørensen, Alex McConnachie, Craig E. Pennell, Per Magnus, Shah Ebrahim, William L. Lowe, Paul C. D. Johnson, Marika Kaakinen, Chris Power, Naveed Sattar
Publikováno v:
Human Molecular Genetics, 21(24), 5344-5358. Oxford University Press
Human Molecular Genetics
Human Molecular Genetics; Vol 21
Tyrrell, J, Huikari, V, Christie, J T, Cavadino, A, Bakker, R, Brion, M-J A, Geller, F, Paternoster, L, Myhre, R, Potter, C, Johnson, P C D, Ebrahim, S, Feenstra, B, Hartikainen, A-L, Hattersley, A T, Hofman, A, Kaakinen, M, Lowe, L P, Magnus, P, McConnachie, A, Melbye, M, Ng, J W Y, Nøhr, E A, Power, C, Ring, S M, Sebert, S P, Sengpiel, V, Taal, H R, Watt, G C M, Sattar, N, Relton, C L, Jacobsson, B, Frayling, T M, Sørensen, T I A, Murray, J C, Lawlor, D A, Pennell, C E, Jaddoe, V W V, Hypponen, E, Lowe, W L, Jarvelin, M-R, Davey Smith, G, Freathy, R M & Early Growth Genetics (EGG) Consortium 2012, ' Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight ', Human Molecular Genetics, vol. 21, no. 24, pp. 5344-58 . https://doi.org/10.1093/hmg/dds372
Human Molecular Genetics
Human Molecular Genetics; Vol 21
Tyrrell, J, Huikari, V, Christie, J T, Cavadino, A, Bakker, R, Brion, M-J A, Geller, F, Paternoster, L, Myhre, R, Potter, C, Johnson, P C D, Ebrahim, S, Feenstra, B, Hartikainen, A-L, Hattersley, A T, Hofman, A, Kaakinen, M, Lowe, L P, Magnus, P, McConnachie, A, Melbye, M, Ng, J W Y, Nøhr, E A, Power, C, Ring, S M, Sebert, S P, Sengpiel, V, Taal, H R, Watt, G C M, Sattar, N, Relton, C L, Jacobsson, B, Frayling, T M, Sørensen, T I A, Murray, J C, Lawlor, D A, Pennell, C E, Jaddoe, V W V, Hypponen, E, Lowe, W L, Jarvelin, M-R, Davey Smith, G, Freathy, R M & Early Growth Genetics (EGG) Consortium 2012, ' Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight ', Human Molecular Genetics, vol. 21, no. 24, pp. 5344-58 . https://doi.org/10.1093/hmg/dds372
Maternal smoking during pregnancy is associated with low birth weight. Common variation at rs1051730 is robustly associated with smoking quantity and was recently shown to influence smoking cessation during pregnancy, but its influence on birth weigh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa1d6c3e1e95f5155cf4de173cf152c6
https://hdl.handle.net/1765/60308
https://hdl.handle.net/1765/60308
Autor:
Loreto Santa-Marina, Frank Geller, Julie A. Marsh, Mike Bartels, Xavier Estivill, Christine Power, Ronny Myhre, Momoko Horikoshi, Ellen A. Nohr, Andrew T. Hattersley, Jani Heikkinen, Andrew R. Wood, Debbie A Lawlor, Alana Cavadino, Dorret I. Boomsma, Berthold Hocher, Louis J. Muglia, Wei Ang, Marie-France Hivert, Jodie N. Painter, Eina Hypponen, Marcus A. Tuke, Timothy M. Frayling, Kathryn L. Lunetta, Sheila J. Barton, Luigi Bouchard, Leda Chatzi, Shikta Das, Eskil Kreiner-Møller, Sylvain Sebert, David M. Evans, Ana Espinosa, Lavinia Paternoster, Marc Vaudel, Katherine S. Ruth, Diane J. Berry, Denise M. Scholtens, Hakon Hakonarson, William L. Lowe, Christoph Reichetzeder, Samuel E. Jones, Tim D. Spector, John W. Holloway, Rachel M. Freathy, Rebecca C Richmond, Caroline L Relton, Penelope A. Lind, Mads Melbye, Susan M. Ring, Marjo-Riitta Järvelin, Catherine Allard, Anna Murray, Craig E. Pennell, Mark I. McCarthy, Albert Hofman, Grant W. Montgomery, Joanne M. Murabito, Bjarke Feenstra, Hans Bisgaard, Hanieh Yaghootkar, M. Geoffrey Hayes, Struan F.A. Grant, Vincent W. V. Jaddoe, Michael N. Weedon, Robin N Beaumont, Jonathan P. Bradfield, Gonneke Willemsen, Ville Huikari, Jessica Tyrrell, Catherine Potter, Michael Nodzenski, Hazel Inskip, Janine F. Felix, Ge Zhang, Letizia Marullo, Sarah Metrustry, Jouke-Jan Hottenga, Manolis Kogevinas, Jeffrey C. Murray, Verena Sengpiel, Sarah E. Medland, Pål R. Njølstad, Øyvind Helgeland, Bo Jacobsson, Thorkild I. A. Sørensen, Nicole M. Warrington
Genome-wide association studies (GWAS) of birth weight have focused on fetal genetics, while relatively little is known about how maternal genetic variation influences fetal growth. We aimed to identify maternal genetic variants associated with birth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7de6db3e8ca51ea18bcc941cf889d92b
https://doi.org/10.1101/034207
https://doi.org/10.1101/034207
