Laura J Scott


Ontology type: schema:Person     


Person Info

NAME

Laura J

SURNAME

Scott

Publications in SciGraph latest 50 shown

  • 2022-10-12 A saturated map of common genetic variants associated with human height in NATURE
  • 2022-09-07 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention in NATURE GENETICS
  • 2022-05-20 ACE2 expression in adipose tissue is associated with cardio-metabolic risk factors and cell type composition—implications for COVID-19 in INTERNATIONAL JOURNAL OF OBESITY
  • 2022-04-11 Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia in NATURE GENETICS
  • 2022-04-08 Rare coding variants in ten genes confer substantial risk for schizophrenia in NATURE
  • 2022-03-28 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci in NATURE COMMUNICATIONS
  • 2021-05-31 The trans-ancestral genomic architecture of glycemic traits in NATURE GENETICS
  • 2021-05-17 Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology in NATURE GENETICS
  • 2021-03-05 Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder in MOLECULAR PSYCHIATRY
  • 2021-01-22 Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder in MOLECULAR PSYCHIATRY
  • 2020-09-30 Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D in NATURE COMMUNICATIONS
  • 2019-11-04 Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power in NATURE
  • 2019-10-31 Associations of autozygosity with a broad range of human phenotypes in NATURE COMMUNICATIONS
  • 2019-10-28 Genomic prediction of depression risk and resilience under stress in NATURE HUMAN BEHAVIOUR
  • 2019-07-31 Exome sequencing of Finnish isolates enhances rare-variant association power in NATURE
  • 2019-07-29 New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders in NATURE HUMAN BEHAVIOUR
  • 2019-05-22 Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls in NATURE
  • 2019-05-01 Genome-wide association study identifies 30 loci associated with bipolar disorder in NATURE GENETICS
  • 2018-12-21 Trans-ethnic association study of blood pressure determinants in over 750,000 individuals in NATURE GENETICS
  • 2018-09-14 Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans in NATURE COMMUNICATIONS
  • 2017-12-19 Sequence data and association statistics from 12,940 type 2 diabetes cases and controls in SCIENTIFIC DATA
  • 2017-11-07 Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass in NATURE COMMUNICATIONS
  • 2017-07-19 Large meta-analysis of genome-wide association studies identifies five loci for lean body mass in NATURE COMMUNICATIONS
  • 2016-08-29 Next-generation genotype imputation service and methods in NATURE GENETICS
  • 2016-07-11 The genetic architecture of type 2 diabetes in NATURE
  • 2016-06-29 The genetic regulatory signature of type 2 diabetes in human skeletal muscle in NATURE COMMUNICATIONS
  • 2016-04-12 Fine-Mapping of Type 2 Diabetes Loci in THE GENETICS OF TYPE 2 DIABETES AND RELATED TRAITS
  • 2015-11-09 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-07-01 Directional dominance on stature and cognition in diverse human populations in NATURE
  • 2014-02-09 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility in NATURE GENETICS
  • 2012-12-23 Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion in NATURE GENETICS
  • 2012-09-16 What Will Diabetes Genomes Tell Us? in CURRENT DIABETES REPORTS
  • 2010-10-10 Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index in NATURE GENETICS
  • 2010-10-10 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution in NATURE GENETICS
  • 2010-06-27 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis in NATURE GENETICS
  • 2010-01-17 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge in NATURE GENETICS
  • 2010-01-17 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk in NATURE GENETICS
  • 2009-08-07 Circulating β-carotene levels and type 2 diabetes—cause or effect? in DIABETOLOGIA
  • 2009-05-10 Genome-wide association study identifies eight loci associated with blood pressure in NATURE GENETICS
  • 2008-12-07 Common variants at 30 loci contribute to polygenic dyslipidemia in NATURE GENETICS
  • 2008-12-07 Variants in MTNR1B influence fasting glucose levels in NATURE GENETICS
  • 2008-10-14 Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes in DIABETOLOGIA
  • 2008-03-30 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes in NATURE GENETICS
  • 2008-01-13 Common variants in the GDF5-UQCC region are associated with variation in human height in NATURE GENETICS
  • 2006-03 Erratum: Corrigendum: Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies in NATURE GENETICS
  • 2006-01-15 Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies in NATURE GENETICS
  • 2005-09-02 Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns in HUMAN GENETICS
  • 2004-10-27 Variation in the resistin gene is associated with obesity and insulin-related phenotypes in Finnish subjects in DIABETOLOGIA
  • 2003-04-25 Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome in NATURE
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