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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1982 1
1983 4
1988 2
2001 1
2005 1
2006 1
2010 2
2011 2
2013 1
2014 1
2016 1
2024 0

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16 results

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Page 1
Aspartylglucosaminuria in the United States.
Hreidarsson S, Thomas GH, Valle DL, Stevenson RE, Taylor H, McCarty J, Coker SB, Green WR. Hreidarsson S, et al. Clin Genet. 1983 Jun;23(6):427-35. doi: 10.1111/j.1399-0004.1983.tb01977.x. Clin Genet. 1983. PMID: 6883788
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
Isles AR, Ingason A, Lowther C, Walters J, Gawlick M, Stöber G, Rees E, Martin J, Little RB, Potter H, Georgieva L, Pizzo L, Ozaki N, Aleksic B, Kushima I, Ikeda M, Iwata N, Levinson DF, Gejman PV, Shi J, Sanders AR, Duan J, Willis J, Sisodiya S, Costain G, Werge TM, Degenhardt F, Giegling I, Rujescu D, Hreidarsson SJ, Saemundsen E, Ahn JW, Ogilvie C, Girirajan SD, Stefansson H, Stefansson K, O'Donovan MC, Owen MJ, Bassett A, Kirov G. Isles AR, et al. Among authors: hreidarsson sj. PLoS Genet. 2016 May 6;12(5):e1005993. doi: 10.1371/journal.pgen.1005993. eCollection 2016 May. PLoS Genet. 2016. PMID: 27153221 Free PMC article.
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: hreidarsson s. Nature. 2014 Jan 16;505(7483):361-6. doi: 10.1038/nature12818. Epub 2013 Dec 18. Nature. 2014. PMID: 24352232
Ceruloplasmin, superoxide dismutase and copper in autistic patients.
Tórsdóttir G, Hreidarsson S, Kristinsson J, Snaedal J, Jóhannesson T. Tórsdóttir G, et al. Among authors: hreidarsson s. Basic Clin Pharmacol Toxicol. 2005 Feb;96(2):146-8. doi: 10.1111/j.1742-7843.2005.pto960210.x. Basic Clin Pharmacol Toxicol. 2005. PMID: 15679479 Free article. No abstract available.
Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness.
Ingason A, Kirov G, Giegling I, Hansen T, Isles AR, Jakobsen KD, Kristinsson KT, le Roux L, Gustafsson O, Craddock N, Möller HJ, McQuillin A, Muglia P, Cichon S, Rietschel M, Ophoff RA, Djurovic S, Andreassen OA, Pietiläinen OP, Peltonen L, Dempster E, Collier DA, St Clair D, Rasmussen HB, Glenthøj BY, Kiemeney LA, Franke B, Tosato S, Bonetto C, Saemundsen E, Hreidarsson SJ; GROUP Investigators; Nöthen MM, Gurling H, O'Donovan MC, Owen MJ, Sigurdsson E, Petursson H, Stefansson H, Rujescu D, Stefansson K, Werge T. Ingason A, et al. Among authors: hreidarsson sj. Am J Psychiatry. 2011 Apr;168(4):408-17. doi: 10.1176/appi.ajp.2010.09111660. Epub 2011 Feb 15. Am J Psychiatry. 2011. PMID: 21324950 Free PMC article.
Age of walking in the cognitively impaired.
Hreidarsson SJ, Shapiro BK, Capute AJ. Hreidarsson SJ, et al. Clin Pediatr (Phila). 1983 Apr;22(4):248-50. doi: 10.1177/000992288302200402. Clin Pediatr (Phila). 1983. PMID: 6825371
No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.
Curran S, Bolton P, Rozsnyai K, Chiocchetti A, Klauck SM, Duketis E, Poustka F, Schlitt S, Freitag CM, Lee I, Muglia P; ITAN; Poot M, Staal W, de Jonge MV, Ophoff RA, Lewis C, Skuse D, Mandy W, Vassos E, Fossdal R, Magnusson P, Hreidarsson S, Saemundsen E, Stefansson H, Stefansson K, Collier D. Curran S, et al. Among authors: hreidarsson s. Am J Med Genet B Neuropsychiatr Genet. 2011 Sep;156B(6):633-9. doi: 10.1002/ajmg.b.31201. Epub 2011 Jun 8. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21656903
16 results