Lorraine Southam


Ontology type: schema:Person     


Person Info

NAME

Lorraine

SURNAME

Southam

Publications in SciGraph latest 50 shown

  • 2019-02 Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data in NATURE GENETICS
  • 2018-12 Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits in NATURE COMMUNICATIONS
  • 2018-12 Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits in NATURE COMMUNICATIONS
  • 2018-12 Combination therapy as a potential risk factor for the development of type 2 diabetes in patients with schizophrenia: the GOMAP study in BMC PSYCHIATRY
  • 2018-11-02 Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps in NATURE GENETICS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-04 Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis in NATURE GENETICS
  • 2018-01 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2017-12 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-06-23 Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations in NATURE COMMUNICATIONS
  • 2017-05-26 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits in NATURE COMMUNICATIONS
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2016-11-23 A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape in NATURE COMMUNICATIONS
  • 2016-11 Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps in NATURE GENETICS
  • 2016-10 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension in NATURE GENETICS
  • 2015-12 Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel in NATURE COMMUNICATIONS
  • 2015-12 TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport in NATURE COMMUNICATIONS
  • 2015-12 Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility in NATURE COMMUNICATIONS
  • 2015-12 Whole-genome sequence-based analysis of thyroid function in NATURE COMMUNICATIONS
  • 2015-07-01 Directional dominance on stature and cognition in diverse human populations in NATURE
  • 2014-12 Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants in NATURE COMMUNICATIONS
  • 2014-12 A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans in NATURE COMMUNICATIONS
  • 2014-10 A genome-wide association study of anorexia nervosa in MOLECULAR PSYCHIATRY
  • 2014-10 Using ancestry-informative markers to identify fine structure across 15 populations of European origin in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-12 A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates in NATURE COMMUNICATIONS
  • 2011-05 The effect of genome-wide association scan quality control on imputation outcome for common variants in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-12 Association of a functional microsatellite within intron 1 of the BMP5 gene with susceptibility to osteoarthritis in BMC MEDICAL GENETICS
  • 2009-09 Is the thrifty genotype hypothesis supported by evidence based on confirmed type 2 diabetes- and obesity-susceptibility variants? in DIABETOLOGIA
  • 2005-08 Genetic evidence for a family-based Scandinavian settlement of Shetland and Orkney during the Viking periods in HEREDITY
  • 2004-09 Genetics of osteoarthritis in ARTHRITIS RESEARCH & THERAPY
  • 2002-09 Finer linkage mapping of a primary hip osteoarthritis susceptibility locus on chromosome 6 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2001-10 A radiation hybrid transcript map of the mouse genome in NATURE GENETICS
  • 2000-01 Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1996-12 Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3) in NATURE
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