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1.	Marshall, CR, et al. (author) Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects 2017 In: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 49:1, s. 27-35 Journal article (peer-reviewed)
2.	Sebat, J, et al. (author) Large-scale copy number polymorphism in the human genome 2004 In: Science (New York, N.Y.). - : American Association for the Advancement of Science (AAAS). - 1095-9203 .- 0036-8075. ; 305:5683, s. 525-528 Journal article (peer-reviewed)abstract The extent to which large duplications and deletions contribute to human genetic variation and diversity is unknown. Here, we show that large-scale copy number polymorphisms (CNPs) (about 100 kilobases and greater) contribute substantially to genomic variation between normal humans. Representational oligonucleotide microarray analysis of 20 individuals revealed a total of 221 copy number differences representing 76 unique CNPs. On average, individuals differed by 11 CNPs, and the average length of a CNP interval was 465 kilobases. We observed copy number variation of 70 different genes within CNP intervals, including genes involved in neurological function, regulation of cell growth, regulation of metabolism, and several genes known to be associated with disease.
3.	Smoller, JW, et al. (author) Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 2013 In: Lancet. - 1474-547X. ; 381:9875, s. 1371-9 Journal article (peer-reviewed)abstract Findings from family and twin studies suggest that genetic contributions to psychiatric disorders do not in all cases map to present diagnostic categories. We aimed to identify specific variants underlying genetic effects shared between the five disorders in the Psychiatric Genomics Consortium: autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia.
4.	Aberg, K, et al. (author) Genomewide association study of movement-related adverse antipsychotic effects 2010 In: Biological psychiatry. - : Elsevier BV. - 1873-2402 .- 0006-3223. ; 67:3, s. 279-282 Journal article (peer-reviewed)
5.	Bergen, SE, et al. (author) THE GENETIC ARCHITECTURE OF SCHIZOPHRENIA: HOW DO CNVS AND POLYGENIC SCORES CONTRIBUTE TO DISEASE RISK? 2014 In: SCHIZOPHRENIA RESEARCH. - 0920-9964. ; 153, s. S62-S62 Conference paper (other academic/artistic)
6.	Grochowski, CM, et al. (author) Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes 2018 In: Human mutation. - : Hindawi Limited. - 1098-1004 .- 1059-7794. ; 39:7, s. 939-946 Journal article (peer-reviewed)
7.	Guha, S, et al. (author) Implication of a rare deletion at distal 16p11.2 in schizophrenia 2013 In: JAMA psychiatry. - : American Medical Association (AMA). - 2168-6238 .- 2168-622X. ; 70:3, s. 253-260 Journal article (peer-reviewed)
8.	Mulle, JG, et al. (author) Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia 2014 In: Biological psychiatry. - : Elsevier BV. - 1873-2402 .- 0006-3223. ; 75:5, s. 371-377 Journal article (peer-reviewed)
9.	Bergen, SE, et al. (author) CNVS AND POLYGENIC SCORES INTERACT TO CONTRIBUTE TO SCHIZOPHRENIA RISK 2015 In: SCHIZOPHRENIA BULLETIN. - 0586-7614. ; 41, s. S198-S198 Conference paper (other academic/artistic)
10.	Bergen, SE, et al. (author) Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia 2019 In: The American journal of psychiatry. - : American Psychiatric Association Publishing. - 1535-7228 .- 0002-953X. ; 176:1, s. 29-35 Journal article (peer-reviewed)
11.	Guha, S, et al. (author) A Rare Deletion At Distal 16p11.2 Is Implicated In Schizophrenia 2012 In: BIOLOGICAL PSYCHIATRY. - 0006-3223. ; 71:8, s. 120S-121S Conference paper (other academic/artistic)
12.	Kellett, J, et al. (author) Fixing the Achilles heel of electronic medical records: Vital information must be defined, concise, accurate and easily accessible 2023 In: European journal of internal medicine. - 1879-0828. ; 117, s. 146-147 Journal article (other academic/artistic)
13.	Kellett, J, et al. (author) Fixing the Achilles heel of electronic medical records: Vital information must be defined, concise, accurate and easily accessible 2023 In: European journal of internal medicine. - 1879-0828. ; 117, s. 146-147 Journal article (other academic/artistic)
14.	Maury, EA, et al. (author) Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions 2023 In: Cell genomics. - 2666-979X. ; 3:8, s. 100356- Journal article (peer-reviewed)

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Result 1-14 of 14

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Type of publication: journal article (11); conference paper (3)

Type of content: peer-reviewed (9); other academic/artistic (5)

Author/Editor: Sebat, J (12); Bergen, SE (6); Sullivan, PF (5); O'Donovan, MC (5); Ikeda, M. (4); Kendler, K (4); show more...; Kirov, G (4); Hultman, CM (4); Levinson, DF (4); Malhotra, D (4); Neale, B (4); Sklar, P (4); Owen, MJ (4); Rietschel, M (3); Smoller, JW (3); Purcell, S (3); Gejman, PV (3); Cormican, P. (3); O'Donovan, M (2); Palsson, R (2); Corvin, A (2); Riley, B (2); Craddock, N (2); Rujescu, D (2); Sullivan, P (2); Webb, BT (2); Fanous, AH (2); Cichon, S (2); Nothen, MM (2); Magnusson, PK (2); Degenhardt, F (2); Schulze, TG (2); Ripke, S (2); Walsh, D (2); Shi, JX (2); Daly, MJ (2); Strohmaier, J (2); Kendler, KS (2); Gill, M. (2); Ruderfer, DM (2); Guha, S. (2); McCarroll, SA (2); Howrigan, D (2); Purcell, SM (2); Genovese, G (2); Moran, JL (2); Malhotra, AK (2); Duan, J. (2); Nestadt, G. (2); Lencz, T. (2); show less...

University: Karolinska Institutet (14); University of Gothenburg (1); Umeå University (1)

Language: English (14)

Research subject (UKÄ/SCB): Medical and Health Sciences (2)

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