1 - 25 of 48 results for author:"Ring S.M." in Literature citations
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| Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. UK Primary Biliary Cirrhosis (PBC) Consortium Nat. Genet. 44:1137-1141(2012) · Mapped (3) |
| WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk. Zheng H.F., Tobias J.H., Duncan E., Evans D.M., Eriksson J., Paternoster L., Yerges-Armstrong L.M., Lehtimaki T., Bergstrom U., Kahonen M. et al. PLoS Genet. 8:e1002745-e1002745(2012) · Mapped (10) |
| Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus. Medina-Gomez C., Kemp J.P., Estrada K., Eriksson J., Liu J., Reppe S., Evans D.M., Heppe D.H., Vandenput L., Herrera L. et al. PLoS Genet. 8:e1002718-e1002718(2012) · Mapped (5) |
| Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development. Kinsler V.A., Abu-Amero S., Budd P., Jackson I.J., Ring S.M., Northstone K., Atherton D.J., Bulstrode N.W., Stanier P., Hennekam R.C. et al. J. Invest. Dermatol. 132:2026-2032(2012) · Mapped (21) |
| A genome-wide association meta-analysis identifies new childhood obesity loci. Early Growth Genetics Consortium Nat. Genet. 44:526-531(2012) · Mapped (3) |
| Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight. Ishida M., Monk D., Duncan A.J., Abu-Amero S., Chong J., Ring S.M., Pembrey M.E., Hindmarsh P.C., Whittaker J.C., Stanier P. et al. Am. J. Hum. Genet. 90:715-719(2012) · Mapped (1) |
| Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position. Paternoster L., Zhurov A.I., Toma A.M., Kemp J.P., St Pourcain B., Timpson N.J., McMahon G., McArdle W., Ring S.M., Smith G.D. et al. Am. J. Hum. Genet. 90:478-485(2012) · Mapped (2) |
| Postnatal growth and DNA methylation are associated with differential gene expression of the TACSTD2 gene and childhood fat mass. Groom A., Potter C., Swan D.C., Fatemifar G., Evans D.M., Ring S.M., Turcot V., Pearce M.S., Embleton N.D., Smith G.D. et al. Diabetes 61:391-400(2012) · Mapped (3) |
| New gene functions in megakaryopoiesis and platelet formation. Gieger C., Radhakrishnan A., Cvejic A., Tang W., Porcu E., Pistis G., Serbanovic-Canic J., Elling U., Goodall A.H., Labrune Y. et al. Nature 480:201-208(2011) · Mapped (22) |
| Genetic variation at CHRNA5-CHRNA3-CHRNB4 interacts with smoking status to influence body mass index. Freathy R.M., Kazeem G.R., Morris R.W., Johnson P.C., Paternoster L., Ebrahim S., Hattersley A.T., Hill A., Hingorani A.D., Holst C. et al. Int J Epidemiol 40:1617-1628(2011) · Mapped (15) |
| Association of genetic Loci with glucose levels in childhood and adolescence: a meta-analysis of over 6,000 children. Barker A., Sharp S.J., Timpson N.J., Bouatia-Naji N., Warrington N.M., Kanoni S., Beilin L.J., Brage S., Deloukas P., Evans D.M. et al. Diabetes 60:1805-1812(2011) · Mapped (18) |
| Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone. Paternoster L., Lorentzon M., Vandenput L., Karlsson M.K., Ljunggren O., Kindmark A., Mellstrom D., Kemp J.P., Jarett C.E., Holly J.M. et al. PLoS Genet. 6:e1001217-e1001217(2010) · Mapped (3) |
| Association of COMT Val(108/158)Met genotype and cigarette smoking in pregnant women. Munafo M.R., Freathy R.M., Ring S.M., St Pourcain B., Smith G.D. Nicotine Tob. Res. 13:55-63(2011) · Mapped (7) |
| PCSK6 is associated with handedness in individuals with dyslexia. Scerri T.S., Brandler W.M., Paracchini S., Morris A.P., Ring S.M., Richardson A.J., Talcott J.B., Stein J., Monaco A.P. Hum. Mol. Genet. 20:608-614(2011) · Mapped (3) |
| Prenatal and infant acetaminophen exposure, antioxidant gene polymorphisms, and childhood asthma. Shaheen S.O., Newson R.B., Ring S.M., Rose-Zerilli M.J., Holloway J.W., Henderson A.J. J. Allergy Clin. Immunol. 126:1141-8.e7(2010) · Mapped (30) |
| Maternal Nrf2 and gluthathione-S-transferase polymorphisms do not modify associations of prenatal tobacco smoke exposure with asthma and lung function in school-aged children. Henderson A.J., Newson R.B., Rose-Zerilli M., Ring S.M., Holloway J.W., Shaheen S.O. Thorax 65:897-902(2010) · Mapped (21) |
| Genetic markers of adult obesity risk are associated with greater early infancy weight gain and growth. Elks C.E., Loos R.J., Sharp S.J., Langenberg C., Ring S.M., Timpson N.J., Ness A.R., Davey Smith G., Dunger D.B., Wareham N.J. et al. PLoS Med. 7:e1000284-e1000284(2010) · Mapped (18) |
| Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Genetic Investigation of ANthropometric Traits (GIANT) Consortium Nat. Genet. 42:430-435(2010) · Mapped (7) |
| Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Wellcome Trust Case Control Consortium Nature 464:713-720(2010) · Mapped (3) |
| A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. Medland S.E., Zayats T., Glaser B., Nyholt D.R., Gordon S.D., Wright M.J., Montgomery G.W., Campbell M.J., Henders A.K., Timpson N.J. et al. Am. J. Hum. Genet. 86:519-525(2010) · Mapped (2) |
| Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. Pillas D., Hoggart C.J., Evans D.M., O'Reilly P.F., Sipila K., Lahdesmaki R., Millwood I.Y., Kaakinen M., Netuveli G., Blane D. et al. PLoS Genet. 6:e1000856-e1000856(2010) · Mapped (22) |
| Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. Australo-Anglo-American Spondyloarthritis Consortium (TASC) Nat. Genet. 42:123-127(2010) · Mapped (29) |
| Glutathione-S-transferase genes and asthma phenotypes: a Human Genome Epidemiology (HuGE) systematic review and meta-analysis including unpublished data. Minelli C., Granell R., Newson R., Rose-Zerilli M.J., Torrent M., Ring S.M., Holloway J.W., Shaheen S.O., Henderson J.A. Int J Epidemiol 39:539-562(2010) · Mapped (14) |
| Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region. UK IBD Genetics Consortium Nat. Genet. 41:1330-1334(2009) · Mapped (70) |
| A non-synonymous variant in ADH1B is strongly associated with prenatal alcohol use in a European sample of pregnant women. Zuccolo L., Fitz-Simon N., Gray R., Ring S.M., Sayal K., Smith G.D., Lewis S.J. Hum. Mol. Genet. 18:4457-4466(2009) · Mapped (10) |