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Träfflista för sökning "WFRF:(Smoller JW) srt2:(2011-2014)"

Search: WFRF:(Smoller JW) > (2011-2014)

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1.	Bergen, SE, et al. (author) Genetic modifiers and subtypes in schizophrenia: investigations of age at onset, severity, sex and family history 2014 In: Schizophrenia research. - : Elsevier BV. - 1573-2509 .- 0920-9964. ; 154:1-3, s. 48-53 Journal article (peer-reviewed)
2.	Kong, J, et al. (author) Functional connectivity of the frontoparietal network predicts cognitive modulation of pain 2013 In: Pain. - : Ovid Technologies (Wolters Kluwer Health). - 1872-6623 .- 0304-3959. ; 154:3, s. 459-467 Journal article (peer-reviewed)
3.	Kong, J, et al. (author) S1 is associated with chronic low back pain: a functional and structural MRI study 2013 In: Molecular pain. - : SAGE Publications. - 1744-8069. ; 9, s. 43- Journal article (peer-reviewed)abstract A fundamental characteristic of neural circuits is the capacity for plasticity in response to experience. Neural plasticity is associated with the development of chronic pain disorders. In this study, we investigated 1) brain resting state functional connectivity (FC) differences between patients with chronic low back pain (cLBP) and matched healthy controls (HC); 2) FC differences within the cLBP patients as they experienced different levels of endogenous low back pain evoked by exercise maneuvers, and 3) morphometric differences between cLBP patients and matched HC We found the dynamic character of FC in the primary somatosensory cortex (S1) in cLBP patients, i.e., S1 FC decreased when the patients experienced low intensity LBP as compared with matched healthy controls, and FC at S1 increased when cLBP patients experienced high intensity LBP as compared with the low intensity condition. In addition, we also found increased cortical thickness in the bilateral S1 somatotopically associated with the lower back in cLBP patients as compared to healthy controls. Our results provide evidence of structural plasticity co-localized with areas exhibiting FC changes in S1 in cLBP patients.
4.	Lee, SH, et al. (author) Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs 2013 In: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 45:9, s. 984- Journal article (peer-reviewed)
5.	Manchia, M, et al. (author) Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report 2013 In: PloS one. - : Public Library of Science (PLoS). - 1932-6203. ; 8:6, s. e65636- Journal article (peer-reviewed)
6.	Middeldorp, CM, et al. (author) The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data 2011 In: Translational psychiatry. - : Springer Science and Business Media LLC. - 2158-3188. ; 1, s. e50- Journal article (peer-reviewed)
7.	Ripke, S, et al. (author) Biological insights from 108 schizophrenia-associated genetic loci 2014 In: Nature. - : Springer Science and Business Media LLC. - 1476-4687 .- 0028-0836. ; 511:7510, s. 421- Journal article (peer-reviewed)
8.	Sellgren, C, et al. (author) An inflammatory pathway linked to psychosis in bipolar disorder 2014 In: BIPOLAR DISORDERS. - 1398-5647. ; 16, s. 65-65 Conference paper (other academic/artistic)
9.	Sklar, P, et al. (author) Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 2011 In: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 43:10, s. 977-U162 Journal article (peer-reviewed)
10.	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.

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Result 1-10 of 11

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Type of publication: journal article (10); conference paper (1)

Type of content: peer-reviewed (10); other academic/artistic (1)

Author/Editor: Smoller, JW (11); Sullivan, PF (7); Ripke, S (7); Rietschel, M (6); Schulze, TG (6); Cichon, S (5); show more...; Wray, NR (5); Lee, PH (4); Landén, Mikael, 1966 (4); Landen, M (4); Craddock, N (4); Mattheisen, M (4); Levinson, DF (4); Lichtenstein, P. (4); Sklar, P (4); Steinberg, S (3); Hottenga, JJ (3); Willemsen, G (3); Andreassen, OA (3); Melle, I (3); Djurovic, S (3); Boomsma, DI (3); Breen, G (3); Corvin, A (3); Gurling, H (3); St Clair, D (3); Hultman, CM (3); Magnusson, PKE (3); OSBY, U (3); McMahon, FJ (3); Montgomery, GW (3); Muller-Myhsok, B (3); Nothen, MM (3); Martin, NG (3); Lucae, S (3); Backlund, L (3); Degenhardt, F (3); Meier, S (3); Bauer, M (3); Palotie, A (3); Shi, JX (3); Knowles, JA (3); Middeldorp, CM (3); Schalling, M (3); Stefansson, K (3); Bellivier, F. (3); Etain, B. (3); Jamain, S. (3); Frisen, L. (3); Herms, S. (3); show less...

University: Karolinska Institutet (11); University of Gothenburg (4); Umeå University (1)

Language: English (11)

Research subject (UKÄ/SCB): Medical and Health Sciences (5)

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