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Allelic frequencies and patterns of single-nucleotide polymorphisms in candidate genes for asthma and atopy in Iceland.
Hakonarson H, Bjornsdottir US, Ostermann E, Arnason T, Adalsteinsdottir AE, Halapi E, Shkolny D, Kristjansson K, Gudnadottir SA, Frigge ML, Gislason D, Gislason T, Kong A, Gulcher J, Stefansson K. Hakonarson H, et al. Among authors: kong a. Am J Respir Crit Care Med. 2001 Dec 1;164(11):2036-44. doi: 10.1164/ajrccm.164.11.2101086. Am J Respir Crit Care Med. 2001. PMID: 11739132
Familial aggregation of Parkinson's disease in Iceland.
Sveinbjörnsdottir S, Hicks AA, Jonsson T, Pétursson H, Guğmundsson G, Frigge ML, Kong A, Gulcher JR, Stefansson K. Sveinbjörnsdottir S, et al. Among authors: kong a. N Engl J Med. 2000 Dec 14;343(24):1765-70. doi: 10.1056/NEJM200012143432404. N Engl J Med. 2000. PMID: 11114315 Free article.
The role of linkage studies for common diseases.
Gulcher JR, Kong A, Stefansson K. Gulcher JR, et al. Among authors: kong a. Curr Opin Genet Dev. 2001 Jun;11(3):264-7. doi: 10.1016/s0959-437x(00)00188-x. Curr Opin Genet Dev. 2001. PMID: 11377961 Review.
Association between the gene encoding 5-lipoxygenase-activating protein and stroke replicated in a Scottish population.
Helgadottir A, Gretarsdottir S, St Clair D, Manolescu A, Cheung J, Thorleifsson G, Pasdar A, Grant SF, Whalley LJ, Hakonarson H, Thorsteinsdottir U, Kong A, Gulcher J, Stefansson K, MacLeod MJ. Helgadottir A, et al. Among authors: kong a. Am J Hum Genet. 2005 Mar;76(3):505-9. doi: 10.1086/428066. Epub 2005 Jan 7. Am J Hum Genet. 2005. PMID: 15640973 Free PMC article.
Mapping of a familial essential tremor gene, FET1, to chromosome 3q13.
Gulcher JR, Jónsson P, Kong A, Kristjánsson K, Frigge ML, Kárason A, Einarsdóttir IE, Stefánsson H, Einarsdóttir AS, Sigurthoardóttir S, Baldursson S, Björnsdóttir S, Hrafnkelsdóttir SM, Jakobsson F, Benedickz J, Stefánsson K. Gulcher JR, et al. Among authors: kong a. Nat Genet. 1997 Sep;17(1):84-7. doi: 10.1038/ng0997-84. Nat Genet. 1997. PMID: 9288103
Genetic factors contribute to the risk of developing endometriosis.
Stefansson H, Geirsson RT, Steinthorsdottir V, Jonsson H, Manolescu A, Kong A, Ingadottir G, Gulcher J, Stefansson K. Stefansson H, et al. Among authors: kong a. Hum Reprod. 2002 Mar;17(3):555-9. doi: 10.1093/humrep/17.3.555. Hum Reprod. 2002. PMID: 11870102
A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13.
Arngrímsson R, Sigurõardóttir S, Frigge ML, Bjarnadóttir RI, Jónsson T, Stefánsson H, Baldursdóttir A, Einarsdóttir AS, Palsson B, Snorradóttir S, Lachmeijer AM, Nicolae D, Kong A, Bragason BT, Gulcher JR, Geirsson RT, Stefánsson K. Arngrímsson R, et al. Among authors: kong a. Hum Mol Genet. 1999 Sep;8(9):1799-805. doi: 10.1093/hmg/8.9.1799. Hum Mol Genet. 1999. PMID: 10441346
Parental origin of sequence variants associated with complex diseases.
Kong A, Steinthorsdottir V, Masson G, Thorleifsson G, Sulem P, Besenbacher S, Jonasdottir A, Sigurdsson A, Kristinsson KT, Jonasdottir A, Frigge ML, Gylfason A, Olason PI, Gudjonsson SA, Sverrisson S, Stacey SN, Sigurgeirsson B, Benediktsdottir KR, Sigurdsson H, Jonsson T, Benediktsson R, Olafsson JH, Johannsson OT, Hreidarsson AB, Sigurdsson G; DIAGRAM Consortium; Ferguson-Smith AC, Gudbjartsson DF, Thorsteinsdottir U, Stefansson K. Kong A, et al. Nature. 2009 Dec 17;462(7275):868-74. doi: 10.1038/nature08625. Nature. 2009. PMID: 20016592 Free PMC article.
1,665 results