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Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer.
Nat Genet. 2008 Jun;40(6):703-6. doi: 10.1038/ng.131. Epub 2008 Apr 27.
Nat Genet. 2008.
PMID: 18438407
Clinical Trial.
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits.
Stacey SN, Gudbjartsson DF, Sulem P, Bergthorsson JT, Kumar R, Thorleifsson G, Sigurdsson A, Jakobsdottir M, Sigurgeirsson B, Benediktsdottir KR, Thorisdottir K, Ragnarsson R, Scherer D, Rudnai P, Gurzau E, Koppova K, Höiom V, Botella-Estrada R, Soriano V, Juberías P, Grasa M, Carapeto FJ, Tabuenca P, Gilaberte Y, Gudmundsson J, Thorlacius S, Helgason A, Thorlacius T, Jonasdottir A, Blondal T, Gudjonsson SA, Jonsson GF, Saemundsdottir J, Kristjansson K, Bjornsdottir G, Sveinsdottir SG, Mouy M, Geller F, Nagore E, Mayordomo JI, Hansson J, Rafnar T, Kong A, Olafsson JH, Thorsteinsdottir U, Stefansson K.
Stacey SN, et al. Among authors: jonsson gf.
Nat Genet. 2008 Nov;40(11):1313-8. doi: 10.1038/ng.234. Epub 2008 Oct 12.
Nat Genet. 2008.
PMID: 18849993
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Evaluating differences in linkage disequilibrium between populations.
Hrafnkelsson B, Helgason A, Jonsson GF, Gudbjartsson DF, Jonsson T, Thorvaldsson S, Stefansson H, Steinthorsdottir V, Vidarsdottir N, Middleton D, Petersen HS, Martinez C, Snaedal J, Jonsson PV, Bjornsson S, Gulcher JR, Stefansson K.
Hrafnkelsson B, et al. Among authors: jonsson gf.
Ann Hum Genet. 2010 May;74(3):233-47. doi: 10.1111/j.1469-1809.2010.00571.x.
Ann Hum Genet. 2010.
PMID: 20529015
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CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Stefansson H, Meyer-Lindenberg A, Steinberg S, Magnusdottir B, Morgen K, Arnarsdottir S, Bjornsdottir G, Walters GB, Jonsdottir GA, Doyle OM, Tost H, Grimm O, Kristjansdottir S, Snorrason H, Davidsdottir SR, Gudmundsson LJ, Jonsson GF, Stefansdottir B, Helgadottir I, Haraldsson M, Jonsdottir B, Thygesen JH, Schwarz AJ, Didriksen M, Stensbøl TB, Brammer M, Kapur S, Halldorsson JG, Hreidarsson S, Saemundsen E, Sigurdsson E, Stefansson K.
Stefansson H, et al. Among authors: jonsson gf.
Nature. 2014 Jan 16;505(7483):361-6. doi: 10.1038/nature12818. Epub 2013 Dec 18.
Nature. 2014.
PMID: 24352232
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CDKN2A mutations and melanoma risk in the Icelandic population.
Goldstein AM, Stacey SN, Olafsson JH, Jonsson GF, Helgason A, Sulem P, Sigurgeirsson B, Benediktsdottir KR, Thorisdottir K, Ragnarsson R, Kjartansson J, Kostic J, Masson G, Kristjansson K, Gulcher JR, Kong A, Thorsteinsdottir U, Rafnar T, Tucker MA, Stefansson K.
Goldstein AM, et al. Among authors: jonsson gf.
J Med Genet. 2008 May;45(5):284-9. doi: 10.1136/jmg.2007.055376. Epub 2008 Jan 4.
J Med Genet. 2008.
PMID: 18178632
Free PMC article.
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Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder.
Gudmundsson OO, Walters GB, Ingason A, Johansson S, Zayats T, Athanasiu L, Sonderby IE, Gustafsson O, Nawaz MS, Jonsson GF, Jonsson L, Knappskog PM, Ingvarsdottir E, Davidsdottir K, Djurovic S, Knudsen GPS, Askeland RB, Haraldsdottir GS, Baldursson G, Magnusson P, Sigurdsson E, Gudbjartsson DF, Stefansson H, Andreassen OA, Haavik J, Reichborn-Kjennerud T, Stefansson K.
Gudmundsson OO, et al. Among authors: jonsson gf.
Transl Psychiatry. 2019 Oct 17;9(1):258. doi: 10.1038/s41398-019-0599-y.
Transl Psychiatry. 2019.
PMID: 31624239
Free PMC article.
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Large scale replication study of the association between HLA class II/BTNL2 variants and osteoarthritis of the knee in European-descent populations.
Valdes AM, Styrkarsdottir U, Doherty M, Morris DL, Mangino M, Tamm A, Doherty SA, Kisand K, Kerna I, Tamm A, Wheeler M, Maciewicz RA, Zhang W, Muir KR, Dennison EM, Hart DJ, Metrustry S, Jonsdottir I, Jonsson GF, Jonsson H, Ingvarsson T, Cooper C, Vyse TJ, Spector TD, Stefansson K, Arden NK.
Valdes AM, et al. Among authors: jonsson gf.
PLoS One. 2011;6(8):e23371. doi: 10.1371/journal.pone.0023371. Epub 2011 Aug 10.
PLoS One. 2011.
PMID: 21853121
Free PMC article.
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