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340 results

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Page 1
Identification of genetic overlap and novel risk loci for attention-deficit/hyperactivity disorder and bipolar disorder.
O'Connell KS, Shadrin A, Bahrami S, Smeland OB, Bettella F, Frei O, Krull F, Askeland RB, Walters GB, Davíðsdóttir K, Haraldsdóttir GS, Guðmundsson ÓÓ, Stefánsson H, Fan CC, Steen NE, Reichborn-Kjennerud T, Dale AM, Stefánsson K, Djurovic S, Andreassen OA. O'Connell KS, et al. Among authors: stefansson h, stefansson k. Mol Psychiatry. 2021 Aug;26(8):4055-4065. doi: 10.1038/s41380-019-0613-z. Epub 2019 Dec 2. Mol Psychiatry. 2021. PMID: 31792363
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: stefansson h, stefansson k. Hum Mol Genet. 1999 Sep;8(9):1799-805. doi: 10.1093/hmg/8.9.1799. Hum Mol Genet. 1999. PMID: 10441346
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: stefansson k. Hum Reprod. 2002 Mar;17(3):555-9. doi: 10.1093/humrep/17.3.555. Hum Reprod. 2002. PMID: 11870102
A susceptibility gene for late-onset idiopathic Parkinson's disease.
Hicks AA, Pétursson H, Jónsson T, Stefánsson H, Jóhannsdóttir HS, Sainz J, Frigge ML, Kong A, Gulcher JR, Stefánsson K, Sveinbjörnsdóttir S. Hicks AA, et al. Among authors: stefansson h, stefansson k. Ann Neurol. 2002 Nov;52(5):549-55. doi: 10.1002/ana.10324. Ann Neurol. 2002. PMID: 12402251
Association of neuregulin 1 with schizophrenia confirmed in a Scottish population.
Stefansson H, Sarginson J, Kong A, Yates P, Steinthorsdottir V, Gudfinnsson E, Gunnarsdottir S, Walker N, Petursson H, Crombie C, Ingason A, Gulcher JR, Stefansson K, St Clair D. Stefansson H, et al. Among authors: stefansson k. Am J Hum Genet. 2003 Jan;72(1):83-7. doi: 10.1086/345442. Epub 2002 Dec 11. Am J Hum Genet. 2003. PMID: 12478479 Free PMC article.
Neuregulin 1 in schizophrenia: out of Iceland.
Stefánsson H, Thorgeirsson TE, Gulcher JR, Stefánsson K. Stefánsson H, et al. Among authors: stefansson k. Mol Psychiatry. 2003 Jul;8(7):639-40. doi: 10.1038/sj.mp.4001384. Mol Psychiatry. 2003. PMID: 12874596 No abstract available.
Neuregulin 1 and schizophrenia.
Stefansson H, Steinthorsdottir V, Thorgeirsson TE, Gulcher JR, Stefansson K. Stefansson H, et al. Among authors: stefansson k. Ann Med. 2004;36(1):62-71. doi: 10.1080/07853890310017585. Ann Med. 2004. PMID: 15000348 Free article. Review.
Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype.
Li T, Stefansson H, Gudfinnsson E, Cai G, Liu X, Murray RM, Steinthorsdottir V, Januel D, Gudnadottir VG, Petursson H, Ingason A, Gulcher JR, Stefansson K, Collier DA. Li T, et al. Among authors: stefansson h, stefansson k. Mol Psychiatry. 2004 Jul;9(7):698-704. doi: 10.1038/sj.mp.4001485. Mol Psychiatry. 2004. PMID: 15007393
Multiple novel transcription initiation sites for NRG1.
Steinthorsdottir V, Stefansson H, Ghosh S, Birgisdottir B, Bjornsdottir S, Fasquel AC, Olafsson O, Stefansson K, Gulcher JR. Steinthorsdottir V, et al. Among authors: stefansson h, stefansson k. Gene. 2004 Nov 10;342(1):97-105. doi: 10.1016/j.gene.2004.07.029. Gene. 2004. PMID: 15527969
340 results