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Page 1
Genetic variants associated with syncope implicate neural and autonomic processes.
Aegisdottir HM, Thorolfsdottir RB, Sveinbjornsson G, Stefansson OA, Gunnarsson B, Tragante V, Thorleifsson G, Stefansdottir L, Thorgeirsson TE, Ferkingstad E, Sulem P, Norddahl G, Rutsdottir G, Banasik K, Christensen AH, Mikkelsen C, Pedersen OB, Brunak S, Bruun MT, Erikstrup C, Jacobsen RL, Nielsen KR, Sørensen E, Frigge ML, Hjorleifsson KE, Ivarsdottir EV, Helgadottir A, Gretarsdottir S, Steinthorsdottir V, Oddsson A, Eggertsson HP, Halldorsson GH, Jones DA, Anderson JL, Knowlton KU, Nadauld LD; DBDS Genomic Consortium; Haraldsson M, Thorgeirsson G, Bundgaard H, Arnar DO, Thorsteinsdottir U, Gudbjartsson DF, Ostrowski SR, Holm H, Stefansson K. Aegisdottir HM, et al. Among authors: halldorsson gh. Eur Heart J. 2023 Mar 21;44(12):1070-1080. doi: 10.1093/eurheartj/ehad016. Eur Heart J. 2023. PMID: 36747475
Reliability of vessel diameter measurements with a retinal oximeter.
Blondal R, Sturludottir MK, Hardarson SH, Halldorsson GH, Stefánsson E. Blondal R, et al. Among authors: halldorsson gh. Graefes Arch Clin Exp Ophthalmol. 2011 Sep;249(9):1311-7. doi: 10.1007/s00417-011-1680-2. Epub 2011 Apr 16. Graefes Arch Clin Exp Ophthalmol. 2011. PMID: 21499769 Clinical Trial.
Retinal oximetry with a scanning laser ophthalmoscope.
Kristjansdottir JV, Hardarson SH, Halldorsson GH, Karlsson RA, Eliasdottir TS, Stefánsson E. Kristjansdottir JV, et al. Among authors: halldorsson gh. Invest Ophthalmol Vis Sci. 2014 Apr 15;55(5):3120-6. doi: 10.1167/iovs.13-13255. Invest Ophthalmol Vis Sci. 2014. PMID: 24736055
Automatic retinal oximetry.
Hardarson SH, Harris A, Karlsson RA, Halldorsson GH, Kagemann L, Rechtman E, Zoega GM, Eysteinsson T, Benediktsson JA, Thorsteinsson A, Jensen PK, Beach J, Stefánsson E. Hardarson SH, et al. Among authors: halldorsson gh. Invest Ophthalmol Vis Sci. 2006 Nov;47(11):5011-6. doi: 10.1167/iovs.06-0039. Invest Ophthalmol Vis Sci. 2006. PMID: 17065521
Automatic registration of retina images based on genetic techniques.
Troglio G, Benediktsson JA, Serpico SB, Moser G, Karlsson RA, Halldorsson GH, Stefansson E. Troglio G, et al. Among authors: halldorsson gh. Annu Int Conf IEEE Eng Med Biol Soc. 2008;2008:5419-24. doi: 10.1109/IEMBS.2008.4650440. Annu Int Conf IEEE Eng Med Biol Soc. 2008. PMID: 19163943
Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis.
Steinthorsdottir V, Thorleifsson G, Aradottir K, Feenstra B, Sigurdsson A, Stefansdottir L, Kristinsdottir AM, Zink F, Halldorsson GH, Munk Nielsen N, Geller F, Melbye M, Gudbjartsson DF, Geirsson RT, Thorsteinsdottir U, Stefansson K. Steinthorsdottir V, et al. Among authors: halldorsson gh. Nat Commun. 2016 Jul 25;7:12350. doi: 10.1038/ncomms12350. Nat Commun. 2016. PMID: 27453397 Free PMC article.
Adiposity-Dependent Regulatory Effects on Multi-tissue Transcriptomes.
Glastonbury CA, Viñuela A, Buil A, Halldorsson GH, Thorleifsson G, Helgason H, Thorsteinsdottir U, Stefansson K, Dermitzakis ET, Spector TD, Small KS. Glastonbury CA, et al. Among authors: halldorsson gh. Am J Hum Genet. 2016 Sep 1;99(3):567-579. doi: 10.1016/j.ajhg.2016.07.001. Am J Hum Genet. 2016. PMID: 27588447 Free PMC article.
A genome-wide association study yields five novel thyroid cancer risk loci.
Gudmundsson J, Thorleifsson G, Sigurdsson JK, Stefansdottir L, Jonasson JG, Gudjonsson SA, Gudbjartsson DF, Masson G, Johannsdottir H, Halldorsson GH, Stacey SN, Helgason H, Sulem P, Senter L, He H, Liyanarachchi S, Ringel MD, Aguillo E, Panadero A, Prats E, Garcia-Castaño A, De Juan A, Rivera F, Xu L, Kiemeney LA, Eyjolfsson GI, Sigurdardottir O, Olafsson I, Kristvinsson H, Netea-Maier RT, Jonsson T, Mayordomo JI, Plantinga TS, Hjartarson H, Hrafnkelsson J, Sturgis EM, Thorsteinsdottir U, Rafnar T, de la Chapelle A, Stefansson K. Gudmundsson J, et al. Among authors: halldorsson gh. Nat Commun. 2017 Feb 14;8:14517. doi: 10.1038/ncomms14517. Nat Commun. 2017. PMID: 28195142 Free PMC article.
Diversity in non-repetitive human sequences not found in the reference genome.
Kehr B, Helgadottir A, Melsted P, Jonsson H, Helgason H, Jonasdottir A, Jonasdottir A, Sigurdsson A, Gylfason A, Halldorsson GH, Kristmundsdottir S, Thorgeirsson G, Olafsson I, Holm H, Thorsteinsdottir U, Sulem P, Helgason A, Gudbjartsson DF, Halldorsson BV, Stefansson K. Kehr B, et al. Among authors: halldorsson bv, halldorsson gh. Nat Genet. 2017 Apr;49(4):588-593. doi: 10.1038/ng.3801. Epub 2017 Feb 27. Nat Genet. 2017. PMID: 28250455
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.
Styrkarsdottir U, Helgason H, Sigurdsson A, Norddahl GL, Agustsdottir AB, Reynard LN, Villalvilla A, Halldorsson GH, Jonasdottir A, Magnusdottir A, Oddson A, Sulem G, Zink F, Sveinbjornsson G, Helgason A, Johannsdottir HS, Helgadottir A, Stefansson H, Gretarsdottir S, Rafnar T, Almdahl IS, Brækhus A, Fladby T, Selbæk G, Hosseinpanah F, Azizi F, Koh JM, Tang NLS, Daneshpour MS, Mayordomo JI, Welt C, Braund PS, Samani NJ, Kiemeney LA, Lohmander LS, Christiansen C, Andreassen OA; arcOGEN consortium; Magnusson O, Masson G, Kong A, Jonsdottir I, Gudbjartsson D, Sulem P, Jonsson H, Loughlin J, Ingvarsson T, Thorsteinsdottir U, Stefansson K. Styrkarsdottir U, et al. Among authors: halldorsson gh. Nat Genet. 2017 May;49(5):801-805. doi: 10.1038/ng.3816. Epub 2017 Mar 20. Nat Genet. 2017. PMID: 28319091
79 results