Neuregulin 1 and schizophreniaSTEFANSSON, Hreinn; STEINTHORSDOTTIR, Valgerdur; THORGEIRSSON, Thorgeir E et al.Annals of medicine (Helsinki). 2004, Vol 36, Num 1, pp 62-71, issn 0785-3890, 10 p.Article

A Chromosome 10 Variant With a 12 Mb Inversion [inv(10)(q11.22q21.1)] Identical by Descent and Frequent in the Swedish PopulationENTESARIAN, Miriam; CARLSSON, Birgit; MAHMOUD REZA MANSOURI et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 3, pp 380-386, issn 1552-4825, 7 p.Article

The Adult Reading History Questionnaire (ARHQ) in Icelandic: Psychometric Properties and Factor StructureBJORNSDOTTIR, Gyda; HALLDORSSON, Jonas G; STEINBERG, Stacy et al.Journal of learning disabilities. 2014, Vol 47, Num 6, pp 532-542, issn 0022-2194, 11 p.Article

A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)FOSSDAL, Ragnheidur; JONASSON, Fridbert; KRISTJANSDOTTIR, Gudlaug T et al.Human molecular genetics (Print). 2004, Vol 13, Num 9, pp 975-981, issn 0964-6906, 7 p.Article

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar DisorderCICHON, Sven; MÜHLEISEN, Thomas W; PRIEBE, Lutz et al.American journal of human genetics. 2011, Vol 88, Num 3, pp 372-381, issn 0002-9297, 10 p.Article

No Association Between a Common Single Nucleotide Polymorphism, rs4141463, in the MACROD2 Gene and Autism Spectrum DisorderCURRAN, Sarah; BOSTON, Patrick; MUGLIA, Pierandrea et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2011, Vol 156, Num 6, pp 633-639, issn 1552-4841, 7 p.Article

Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar DisorderVASSOS, Evangelos; STEINBERG, Stacy; CZERSKI, Piotr M et al.Biological psychiatry (1969). 2012, Vol 72, Num 8, pp 645-650, issn 0006-3223, 6 p.Article

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1ANTTILA, Verneri; STEFANSSON, Hreinn; ARTTO, Ville et al.Nature genetics. 2010, Vol 42, Num 10, pp 869-873, issn 1061-4036, 5 p.Article

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionGUDBJARTSSON, Daniel F; BJORNSDOTTIR, Unnur S; WILLIAMS, Carolyn et al.Nature genetics. 2009, Vol 41, Num 3, pp 342-347, issn 1061-4036, 6 p.Article

Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination RateKONG, Augustine; THORLEIFSSON, Gudmar; JONASDOTTIR, Aslaug et al.Science (Washington, D.C.). 2008, Vol 319, Num 5868, pp 1398-1401, issn 0036-8075, 4 p.Article

Support for involvement of the AHI1 locus in schizophreniaINGASON, Andres; SIGMUNDSSON, Thordur; STEFANSSON, Kari et al.European journal of human genetics. 2007, Vol 15, Num 9, pp 988-991, issn 1018-4813, 4 p.Article

Variant of TREM2 Associated with the Risk of Alzheimer's DiseaseJONSSON, Thorlakur; STEFANSSON, Hreinn; RUJESCU, Dan et al.The New England journal of medicine. 2013, Vol 368, Num 2, pp 107-116, issn 0028-4793, 10 p.Article

Association Study of Nonsynonymous Single Nucleotide Polymorphisms in SchizophreniaCARRERA, Noa; ARROJO, Manuel; RIVERO, Olga et al.Biological psychiatry (1969). 2012, Vol 71, Num 2, pp 169-177, issn 0006-3223, 9 p.Article

Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia PatientsBUIZER-VOSKAMP, Jacobine E; MUNTJEWERFF, Jan-Willem; RISK, Genetic et al.Biological psychiatry (1969). 2011, Vol 70, Num 7, pp 655-662, issn 0006-3223, 8 p.Article

Many sequence variants affecting diversity of adult human heightGUDBJARTSSON, Daniel F; WALTERS, G. Bragi; HELGADOTTIR, Anna et al.Nature genetics. 2008, Vol 40, Num 5, pp 609-615, issn 1061-4036, 7 p.Article

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysmHELGADOTTIR, Anna; THORLEIFSSON, Gudmar; KYO, Yoshiki et al.Nature genetics. 2008, Vol 40, Num 2, pp 217-224, issn 1061-4036, 8 p.Article

Large recurrent microdeletions associated with schizophreniaSTEFANSSON, Hreinn; RUJESCU, Dan; HANSEN, Thomas et al.Nature (London). 2008, Vol 455, Num 7210, pp 232-236, issn 0028-0836, 5 p.Article

A common inversion under selection in EuropeansSTEFANSSON, Hreinn; HELGASON, Agnar; DESNICA, Natasa et al.Nature genetics. 2005, Vol 37, Num 2, pp 129-137, issn 1061-4036, 9 p.Article

A Mouse Model that Recapitulates Cardinal Features of the 15q13.3 Microdeletion Syndrome Including Schizophrenia- and Epilepsy-Related AlterationsKIM FEJGIN; NIELSEN, Jacob; LARSEN, Peter H et al.Biological psychiatry (1969). 2014, Vol 76, Num 2, pp 128-137, issn 0006-3223, 10 p.Article

Psychometric properties of the Icelandic NEO-FFI in a general population sample compared to a sample recruited for a study on the genetics of addictionBJORNSDOTTIR, Gyda; JONSSON, Fridrik H; HANSDOTTIR, Ingunn et al.Personality and individual differences. 2014, Vol 58, pp 71-75, issn 0191-8869, 5 p.Article

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's diseaseKELLER, Margaux F; SAAD, Mohamad; SCHULTE, Claudia et al.Human molecular genetics (Print). 2012, Vol 21, Num 22, pp 4996-5009, issn 0964-6906, 14 p.Article

Identification of low-frequency variants associated with gout and serum uric acid levelsSULEM, Patrick; GUDBJARTSSON, Daniel F; MAGNUSSON, Gisli et al.Nature genetics. 2011, Vol 43, Num 11, pp 1127-1130, issn 1061-4036, 4 p.Article

Variant in the sequence of the LINGO1 gene confers risk of essential tremorSTEFANSSON, Hreinn; STEINBERG, Stacy; BÖTTCHER, Yvonne et al.Nature genetics. 2009, Vol 41, Num 3, pp 277-279, issn 1061-4036, 3 p.Article

Detection of sharing by descent, long-range phasing and haplotype imputationKONG, Augustine; MASSON, Gisli; SULEM, Patrick et al.Nature genetics. 2008, Vol 40, Num 9, pp 1068-1075, issn 1061-4036, 8 p.Article

A mutation in APP protects against Alzheimer's disease and age-related cognitive declineJONSSON, Thorlakur; ATWAL, Jasvinder K; HOYTE, Kwame et al.Nature (London). 2012, Vol 488, Num 7409, pp 96-99, issn 0028-0836, 4 p.Article