Susan M Ring

Ontology type: schema:Person     

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Susan M



Publications in SciGraph latest 50 shown

  • 2018-12 Better governance, better access: practising responsible data sharing in the METADAC governance infrastructure in HUMAN GENOMICS
  • 2018-05 Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability in NATURE GENETICS
  • 2018-02 ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties in MOLECULAR PSYCHIATRY
  • 2017-12 Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development in MOLECULAR AUTISM
  • 2017-12 Epigenome-wide association study of asthma and wheeze in childhood and adolescence in CLINICAL EPIGENETICS
  • 2017-08 Age at menarche and lung function: a Mendelian randomization study in EUROPEAN JOURNAL OF EPIDEMIOLOGY
  • 2017-06 Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk in NATURE GENETICS
  • 2016-12 Systematic identification of genetic influences on methylation across the human life course in GENOME BIOLOGY
  • 2016-12 Genome-wide analysis identifies 12 loci influencing human reproductive behavior in NATURE GENETICS
  • 2016-10 Genome-wide associations for birth weight and correlations with adult disease in NATURE
  • 2016-08 Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine in NATURE GENETICS
  • 2016-08 Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence in HUMAN GENETICS
  • 2016-05 Genome-wide association study identifies 74 loci associated with educational attainment in NATURE
  • 2015-06 Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence in HUMAN GENETICS
  • 2014-12 Establishing a large prospective clinical cohort in people with head and neck cancer as a biomedical resource: head and neck 5000 in BMC CANCER
  • 2014-12 Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence in MOLECULAR AUTISM
  • 2014-12 A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans in NATURE COMMUNICATIONS
  • 2014-10 Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche in NATURE
  • 2014-07 Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ in HUMAN GENETICS
  • 2013-12 Common variation contributes to the genetic architecture of social communication traits in MOLECULAR AUTISM
  • 2013-08 A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci in NATURE GENETICS
  • 2013-08 Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization in NATURE GENETICS
  • 2013-08 Genome-wide meta-analysis identifies new susceptibility loci for migraine in NATURE GENETICS
  • 2013-06 Identification of heart rate‚Äďassociated loci and their effects on cardiac conduction and rhythm disorders in NATURE GENETICS
  • 2013-01 New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism in NATURE GENETICS
  • 2012-12 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 Study of Parents and Children in BMC MEDICAL GENETICS
  • 2012-08 Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2012-05 Common variants at 12q15 and 12q24 are associated with infant head circumference in NATURE GENETICS
  • 2012-05 A genome-wide association meta-analysis identifies new childhood obesity loci in NATURE GENETICS
  • 2011-12 New gene functions in megakaryopoiesis and platelet formation in NATURE
  • 2011-11 Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function in NATURE GENETICS
  • 2009-12 Observational study on variability between biobanks in the estimation of DNA concentration in BMC RESEARCH NOTES
  • 2009-12 Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region in NATURE GENETICS
  • 2008-06 Common variants near MC4R are associated with fat mass, weight and risk of obesity in NATURE GENETICS
  • 2008-05 Association analysis of the IGF1 gene with childhood growth, IGF-1 concentrations and type 1 diabetes in DIABETOLOGIA
  • 2007-12 Refining associations between TAS2R38 diplotypes and the 6-n-propylthiouracil (PROP) taste test: findings from the Avon Longitudinal Study of Parents and Children in BMC GENETICS
  • 2005-12 Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans in BMC GENETICS
  • 2000-09 A new human genetic resource: a DNA bank established as part of the Avon Longitudinal Study of Pregnancy and Childhood (ALSPAC) in EUROPEAN JOURNAL OF HUMAN GENETICS
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