List of works by Asmundur Oddsson

A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease

scientific article published on September 2015

A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome

scientific article published on 24 March 2022

A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease

scientific article published in Nature Communications

A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis

scientific article published on 14 January 2019

A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin

scientific article published on 17 May 2018

Characterizing mutagenic effects of recombination through a sequence-level genetic map

scientific article published on 01 January 2019

Epigenetic and genetic components of height regulation

scientific article

Expression and subcellular distribution of novel glomerulus-associated proteins dendrin, ehd3, sh2d4a, plekhh2, and 2310066E14Rik

scientific journal article

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

scientific article published on 17 March 2020

Genome-wide association meta-analysis yields 20 loci associated with gallstone disease

scientific article published in Nature Communications

Glcci1 deficiency leads to proteinuria

scientific article published on 23 September 2011

Glomerulus proteome analysis with two-dimensional gel electrophoresis and mass spectrometry

scientific article published on 01 December 2007

Identification of sequence variants influencing immunoglobulin levels.

scientific article published on 19 June 2017

Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits

scientific article published in 2021

Loss-of-function variants in ATM confer risk of gastric cancer

scientific article

Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits

scientific article

Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis

scientific article published on 23 April 2020

Sequence variant at 4q25 near PITX2 associates with appendicitis

scientific article

Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density

scientific article published on 20 March 2019

Survival in patients with familial and sporadic myeloproliferative neoplasms

scientific article published on June 2015

The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis

scientific article published in 2021

The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

scientific article published on 30 January 2014

The nature of nurture: Effects of parental genotypes

scientific article

Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits

scientific article published in Nature Communications

Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis

scientific article published on 20 March 2017

Zebrafish: a model system for the study of vertebrate renal development, function, and pathophysiology.

scientific article published on July 2011

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