Works by Ring, Susan M.
Results: 56
Vitamin D Status Is Not Associated with Outcomes of Experimentally-Induced Muscle Weakness and Pain in Young, Healthy Volunteers.
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- Journal of Nutrition & Metabolism, 2010, p. 1, doi. 10.1155/2010/674240
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- Article
Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis.
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- 2019
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- journal article
A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts.
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- Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-018-0190-2
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- Article
Better governance, better access: practising responsible data sharing in the METADAC governance infrastructure.
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- Human Genomics, 2018, v. 12, n. 1, p. N.PAG, doi. 10.1186/s40246-018-0154-6
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- Article
Programming of Adiposity in Childhood and Adolescence: Associations With Birth Weight and Cord Blood Adipokines.
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- 2016
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- journal article
Ghrelin receptor gene polymorphisms and body size in children and adults.
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- 2008
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- journal article
ACTN3 genotype, athletic status, and life course physical capability: meta-analysis of the published literature and findings from nine studies.
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- Human Mutation, 2011, v. 32, n. 9, p. 1008, doi. 10.1002/humu.21526
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- Article
Adult height variants affect birth length and growth rate in children.
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- Human Molecular Genetics, 2011, v. 20, n. 20, p. 4069, doi. 10.1093/hmg/ddr309
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- Article
PCSK6 is associated with handedness in individuals with dyslexia.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 608, doi. 10.1093/hmg/ddq475
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- Article
A non-synonymous variant in ADH1B is strongly associated with prenatal alcohol use in a European sample of pregnant women.
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- Human Molecular Genetics, 2009, v. 18, n. 22, p. 4457, doi. 10.1093/hmg/ddp388
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- Article
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 pregnancy.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2922, doi. 10.1093/hmg/ddp216
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- Article
Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development.
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- Molecular Autism, 2017, v. 8, p. 1, doi. 10.1186/s13229-017-0131-2
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- Article
Association of COMT Val(108/158)Met genotype and cigarette smoking in pregnant women.
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- 2011
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- journal article
Association of COMT Val108/158Met Genotype and Cigarette Smoking in Pregnant Women.
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- Nicotine & Tobacco Research, 2011, v. 13, n. 2, p. 55, doi. 10.1093/ntr/ntq209
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- Article
Does Bone Resorption Stimulate Periosteal Expansion? A Cross-Sectional Analysis of β-C-telopeptides of Type I Collagen (CTX), Genetic Markers of the RANKL Pathway, and Periosteal Circumference as Measured by pQCT.
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- Journal of Bone & Mineral Research, 2014, v. 29, n. 4, p. 1015, doi. 10.1002/jbmr.2093
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- Article
Type 2 Diabetes Risk Alleles Are Associated With Reduced Size at Birth.
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- Diabetes, 2009, v. 58, n. 6, p. 1428, doi. 10.2337/db08-1739
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- Article
Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus.
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- 2004
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- journal article
Analysis of the vitamin D receptor gene sequence variants in type 1 diabetes.
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- 2004
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- journal article
Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.
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- Nature Communications, 2015, v. 6, n. 5, p. 7171, doi. 10.1038/ncomms8171
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- Article
Common variation near ROBO2 is associated with expressive vocabulary in infancy.
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- Nature Communications, 2014, v. 5, n. 9, p. 4831, doi. 10.1038/ncomms5831
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- Article
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.
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- Nature Communications, 2014, v. 5, n. 9, p. 4871, doi. 10.1038/ncomms5871
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- Article
Assessment of rates of recanting and hair testing as a biological measure of drug use in a general population sample of young people.
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- Addiction, 2017, v. 112, n. 3, p. 477, doi. 10.1111/add.13645
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- Article
Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development.
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- Journal of Investigative Dermatology, 2012, v. 132, n. 8, p. 2026, doi. 10.1038/jid.2012.95
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- Article
Phenotypic Dissection of Bone Mineral Density Reveals Skeletal Site Specificity and Facilitates the Identification of Novel Loci in the Genetic Regulation of Bone Mass Attainment.
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- PLoS Genetics, 2014, v. 10, n. 6, p. 1, doi. 10.1371/journal.pgen.1004423
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- Article
Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill.
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- PLoS Genetics, 2013, v. 9, n. 9, p. 1, doi. 10.1371/journal.pgen.1003751
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- Article
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.
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- PLoS Genetics, 2012, v. 8, n. 7, p. 1, doi. 10.1371/journal.pgen.1002718
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- Article
Genetic Markers of Adult Obesity Risk Are Associated with Greater Early Infancy Weight Gain and Growth.
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- PLoS Medicine, 2010, v. 7, n. 5, p. 1, doi. 10.1371/journal.pmed.1000284
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- Article
The epigenetic clock and physical development during childhood and adolescence: longitudinal analysis from a UK birth cohort.
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- 2017
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- journal article
Maternal pre-pregnancy BMI and gestational weight gain, offspring DNA methylation and later offspring adiposity: findings from the Avon Longitudinal Study of Parents and Children.
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- 2015
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- journal article
Data Resource Profile: Accessible Resource for Integrated Epigenomic Studies (ARIES).
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- 2015
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- journal article
Lymphoblastoid cell lines reveal associations of adult DNA methylation with childhood and current adversity that are distinct from whole blood associations.
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- 2015
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- journal article
Genetic variation at CHRNA5-CHRNA3-CHRNB4 interacts with smoking status to influence body mass index.
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- 2011
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- journal article
Genome-wide association study of height-adjusted BMI in childhood identifies functional variant in ADCY3.
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- Obesity (19307381), 2014, v. 22, n. 10, p. 2252, doi. 10.1002/oby.20840
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- Article
The Effects of Regular Tanning Bed Use and Increased Vitamin D Status on Serum Markers of Bone Turnover in Healthy Adult Women.
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- Clinical Medicine: Women's Health, 2009, n. 2, p. 1, doi. 10.4137/CMWH.S2031
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- Article
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
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- Nature Genetics, 2013, v. 45, n. 8, p. 907, doi. 10.1038/ng.2686
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- Article
Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans.
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- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2927, doi. 10.1093/hmg/ddy206
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- Article
Collapsed methylation quantitative trait loci analysis for low frequency and rare variants.
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- Human Molecular Genetics, 2016, v. 25, n. 19, p. 4339, doi. 10.1093/hmg/ddw283
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- Article
Genome-wide association study identifies common and low-frequency variants at the AMH gene locus that strongly predict serum AMH levels in males.
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- Human Molecular Genetics, 2016, v. 25, n. 2, p. 382, doi. 10.1093/hmg/ddv465
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- Article
Prenatal and early life influences on epigenetic age in children: a study of mother--offspring pairs from two cohort studies.
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- Human Molecular Genetics, 2016, v. 25, n. 1, p. 191, doi. 10.1093/hmg/ddv456
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- Article
Genome-wide association study identifies SNPs in the MHC class II loci that are associated with self-reported history of whooping cough.
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- Human Molecular Genetics, 2015, v. 24, n. 20, p. 5930, doi. 10.1093/hmg/ddv293
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- Article
Longitudinal analysis of DNA methylation associated with birth weight and gestational age.
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- Human Molecular Genetics, 2015, v. 24, n. 13, p. 3752, doi. 10.1093/hmg/ddv119
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- Article
Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC).
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- Human Molecular Genetics, 2015, v. 24, n. 8, p. 2201, doi. 10.1093/hmg/ddu739
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- Article
Systematic identification of genetic influences on methylation across the human life course.
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- Genome Biology, 2016, v. 17, p. 1, doi. 10.1186/s13059-016-0926-z
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- Article
TRPA1 gene polymorphisms and childhood asthma.
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- Pediatric Allergy & Immunology, 2017, v. 28, n. 2, p. 191, doi. 10.1111/pai.12673
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- Article
Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence.
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- Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-18
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- Article
Refining associations between TAS2R38 diplotypes and the 6-n-propylthiouracil (PROP) taste test: findings from the Avon Longitudinal Study of Parents and Children.
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- BMC Genetics, 2007, v. 8, p. 1, doi. 10.1186/1471-2156-8-51
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- Article
Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans.
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- BMC Genetics, 2005, v. 6, p. 1, doi. 10.1186/1471-2156-6-22
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- Article
Personality, Behavior and Environmental Features Associated with <i>OXTR</i> Genetic Variants in British Mothers.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0090465
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- Article
Associations of Prenatal Nicotine Exposure and the Dopamine Related Genes <i>ANKK1</i> and <i>DRD2</i> to Verbal Language
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- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0063762
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- Article
Vitamin B-12 Status during Pregnancy and Child's IQ at Age 8: A Mendelian Randomization Study in the Avon Longitudinal Study of Parents and Children.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051084
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- Article