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Journals and Conferences
Common sequence variants at the haptoglobin gene (HP) have been associated with blood lipid levels. Through whole-genome sequencing of 8,453 Icelanders, we discovered a splice donor founder mutation… (More)
OBJECTIVE Single-nucleotide polymorphisms predisposing to coronary artery disease (CAD) have been shown to predict cardiovascular risk in healthy individuals when combined into a genetic risk score… (More)
BACKGROUND AND AIMS Shorter stature is an established risk factor for coronary artery disease (CAD), but less is known about its association with extent of the disease. METHODS We assessed the… (More)
Sick building syndrome (SBS), blood eosinophils, formaldehyde, and VOC-emissions from newly painted indoor surfaces.
BACKGROUND Dilated cardiomyopathy (DCM) is an important cause of heart failure. Variants in >50 genes have been reported to cause DCM, but causative variants have been found in less than half of… (More)
We describe a 77 year old man with a prior history of recurrent airway infections, who presented with a history of cough, dyspnea and increased mucous production that had lasted several months. On… (More)
Asthma and bronchial hyperresponsiveness in relation to occupational exposures in a younger mid-Swedish population. In: Advances in the prevention of occupational respiratory diseases.
Pulmonary alveolar proteinosis (PAP) is a rare lung disease of unknown origin, where an amorphous lipoprotein material accumulates in the alveoli of the lungs. We describe a young male with a four… (More)