Asmundur Oddsson


Ontology type: schema:Person     


Person Info

NAME

Asmundur

SURNAME

Oddsson

Publications in SciGraph latest 50 shown

  • 2019-02 Genetics of common complex kidney stone disease: insights from genome-wide association studies in UROLITHIASIS
  • 2019-02 A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis in NATURE GENETICS
  • 2018-12 A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease in NATURE COMMUNICATIONS
  • 2018-12 Genome-wide association meta-analysis yields 20 loci associated with gallstone disease in NATURE COMMUNICATIONS
  • 2018-12 A rare missense variant in NR1H4 associates with lower cholesterol levels in COMMUNICATIONS BIOLOGY
  • 2018-12 Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis in NATURE GENETICS
  • 2018-12 Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits in NATURE COMMUNICATIONS
  • 2018-12 A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin in COMMUNICATIONS BIOLOGY
  • 2017-12 Sequence variant at 4q25 near PITX2 associates with appendicitis in SCIENTIFIC REPORTS
  • 2017-12 Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters in BMC MEDICAL GENETICS
  • 2017-12 COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA in BMC MEDICAL GENETICS
  • 2017-08 Identification of sequence variants influencing immunoglobulin levels in NATURE GENETICS
  • 2017-02-22 Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation in NATURE COMMUNICATIONS
  • 2016-11-16 Epigenetic and genetic components of height regulation in NATURE COMMUNICATIONS
  • 2016-06 Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease in NATURE GENETICS
  • 2016-02-03 Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase in NATURE COMMUNICATIONS
  • 2015-12 Common and rare variants associated with kidney stones and biochemical traits in NATURE COMMUNICATIONS
  • 2015-08 Loss-of-function variants in ATM confer risk of gastric cancer in NATURE GENETICS
  • 2014-06 The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms in LEUKEMIA
  • 2013-05 Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits in NATURE
  • 2007-12 Glomerulus proteome analysis with two-dimensional gel electrophoresis and mass spectrometry in CELLULAR AND MOLECULAR LIFE SCIENCES
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