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Pulmonary Pharmacology & Therapeutics|June 5, 2025
A novel macrolide, EP395, with reduced antibacterial activity and an enhancing effect on respiratory epithelial barrierThorarinn Gudjonsson, Jon Petur Joelsson, Ari Jon Arason, et al.
Genome Biology|July 5, 2014
Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorderRuqi Tang, Hyun Ji Noh, Dongqing Wang, et al.
Molecular Oncology|June 10, 2026
MITF maintains genome stability in nonmelanocyte lineagesDrifa H Gudmundsdottir, Adrián López García de Lomana, Thejus B Venkatesh, et al.
Respiratory Research|June 26, 2019
Azithromycin induces epidermal differentiation and multivesicular bodies in airway epitheliaAri Jon Arason, Jon Petur Joelsson, Bryndis Valdimarsdottir, et al.
Annals of the Rheumatic Diseases|September 19, 2009
A STAT4 risk allele is associated with ischaemic cerebrovascular events and anti-phospholipid antibodies in systemic lupus erythematosusElisabet Svenungsson, Johanna Gustafsson, Dag Leonard, et al.
Human Molecular Genetics|December 8, 2007
Comprehensive evaluation of the genetic variants of interferon regulatory factor 5 (IRF5) reveals a novel 5 bp length polymorphism as strong risk factor for systemic lupus erythematosusSnaevar Sigurdsson, Harald H H Göring, Gudlaug Kristjansdottir, et al.
Plos Genetics|February 12, 2014
Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24Caryline Agler, Dahlia M Nielsen, Ganokon Urkasemsin, et al.
American Journal of Human Genetics|January 20, 2005
Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosusSnaevar Sigurdsson, Gunnel Nordmark, Harald H H Göring, et al.
Nature Genetics|August 8, 2017
Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritabilityErna V Ivarsdottir, Valgerdur Steinthorsdottir, Maryam S Daneshpour, et al.
Human Molecular Genetics|August 2, 2014
Rare mutations associating with serum creatinine and chronic kidney diseaseGardar Sveinbjornsson, Evgenia Mikaelsdottir, Runolfur Palsson, et al.
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