Vitamin D Status Is Not Associated with Outcomes of Experimentally-Induced Muscle Weakness and Pain in Young, Healthy Volunteers

por Ring, Susan M., Dannecker, Erin A., Peterson, Catherine A.
Publicado em 2010

Assessment of rates of recanting and hair testing as a biological measure of drug use in a general population sample of young people

por Taylor, Michelle, Sullivan, John, Ring, Susan M., Macleod, John, Hickman, Matthew
Publicado no Addiction (2016)

Genome-wide association study identifies SNPs in the MHC class II loci that are associated with self-reported history of whooping cough

por McMahon, George, Ring, Susan M., Davey-Smith, George, Timpson, Nicholas J.
Publicado no Hum Mol Genet (2015)

Association of COMT Val(108/158)Met Genotype and Cigarette Smoking in Pregnant Women

por Munafò, Marcus R., Freathy, Rachel M., Ring, Susan M., St Pourcain, Beate, Davey Smith, George
Publicado em 2011

Umbilical cord PUFA are determined by maternal and child fatty acid desaturase (FADS) genetic variants in the Avon Longitudinal Study of Parents and Children (ALSPAC)

por Lattka, Eva, Koletzko, Berthold, Zeilinger, Sonja, Hibbeln, Joseph R., Klopp, Norman, Ring, Susan M., Steer, Colin D.
Publicado em 2012

A non-synonymous variant in ADH1B is strongly associated with prenatal alcohol use in a European sample of pregnant women

por Zuccolo, Luisa, Fitz-Simon, Nicola, Gray, Ron, Ring, Susan M., Sayal, Kapil, Smith, George Davey, Lewis, Sarah J.
Publicado em 2009

Coronary artery disease, genetic risk and the metabolome in young individuals

por Battram, Thomas, Hoskins, Luke, Hughes, David A., Kettunen, Johannes, Ring, Susan M., Smith, George Davey, Timpson, Nicholas J.
Publicado no Wellcome Open Res (2019)

Prenatal alcohol exposure and childhood atopic disease: A Mendelian randomization approach()

por Shaheen, Seif O., Rutterford, Clare, Zuccolo, Luisa, Ring, Susan M., Davey Smith, George, Holloway, John W., Henderson, A. John
Publicado em 2014

Genome-wide association study identifies common and low-frequency variants at the AMH gene locus that strongly predict serum AMH levels in males

por Perry, John R.B., McMahon, George, Day, Felix R., Ring, Susan M, Nelson, Scott M., Lawlor, Debbie A.
Publicado no Hum Mol Genet (2016)

Prenatal and infant acetaminophen exposure, antioxidant gene polymorphisms and childhood asthma

por Shaheen, Seif O, Newson, Roger B, Ring, Susan M, Rose-Zerilli, Matthew J, Holloway, John W, Henderson, A John
Publicado no J Allergy Clin Immunol (2010)

Maternal selenium status in pregnancy, offspring glutathione peroxidase 4 genotype, and childhood asthma

por Shaheen, Seif O., Rutterford, Clare M., Lewis, Sarah J., Ring, Susan M., Holloway, John W., Golding, Jean, Henderson, A. John
Publicado no J Allergy Clin Immunol (2015)

Developmental Changes Within the Genetic Architecture of Social Communication Behavior: A Multivariate Study of Genetic Variance in Unrelated Individuals

por St Pourcain, Beate, Eaves, Lindon J., Ring, Susan M., Fisher, Simon E., Medland, Sarah, Evans, David M., Davey Smith, George
Publicado no Biol Psychiatry (2018)

Refining associations between <it>TAS2R38 </it>diplotypes and the 6-<it>n</it>-propylthiouracil (PROP) taste test: findings from the Avon Longitudinal Study of Parents and Children

por Bartoshuk Linda M, Ring Susan M, Day Ian NM, Heron Jon, Timpson Nicholas J, Horwood Jeremy, Emmett Pauline, Davey-Smith George
Publicado em 2007-07-01

Refining associations between TAS2R38 diplotypes and the 6-n-propylthiouracil (PROP) taste test: findings from the Avon Longitudinal Study of Parents and Children

por Timpson, Nicholas J, Heron, Jon, Day, Ian NM, Ring, Susan M, Bartoshuk, Linda M, Horwood, Jeremy, Emmett, Pauline, Davey-Smith, George
Publicado em 2007

Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment

por Powers, Natalie R., Eicher, John D., Butter, Falk, Kong, Yong, Miller, Laura L., Ring, Susan M., Mann, Matthias, Gruen, Jeffrey R.
Publicado em 2013

Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment

por Powers, Natalie R., Eicher, John D., Butter, Falk, Kong, Yong, Miller, Laura L., Ring, Susan M., Mann, Matthias, Gruen, Jeffrey R.
Publicado em 2014

Maternal thyroid function and child educational attainment: prospective cohort study

por Nelson, Scott M, Haig, Caroline, McConnachie, Alex, Sattar, Naveed, Ring, Susan M, Smith, George D, Lawlor, Debbie A, Lindsay, Robert S
Publicado no BMJ (2018)

Maternal and offspring fasting glucose and type 2 diabetes-associated genetic variants and cognitive function at age 8: a Mendelian randomization study in the Avon Longitudinal Stu...

por Bonilla, Carolina, Lawlor, Debbie A, Ben–Shlomo, Yoav, Ness, Andrew R, Gunnell, David, Ring, Susan M, Smith, George Davey, Lewis, Sarah J
Publicado em 2012

A common genetic variant in the 15q24 nicotinic acetylcholine receptor gene cluster (CHRNA5–CHRNA3–CHRNB4) is associated with a reduced ability of women to quit smoking in pregnanc...

por Freathy, Rachel M., Ring, Susan M., Shields, Beverley, Galobardes, Bruna, Knight, Beatrice, Weedon, Michael N., Smith, George Davey, Frayling, Timothy M., Hattersley, Andrew T.
Publicado em 2009

Associations of Prenatal Nicotine Exposure and the Dopamine Related Genes ANKK1 and DRD2 to Verbal Language

por Eicher, John D., Powers, Natalie R., Cho, Kelly, Miller, Laura L., Mueller, Kathryn L., Ring, Susan M., Tomblin, J. Bruce, Gruen, Jeffrey R.
Publicado em 2013