Srdjan
Djurovic
Adjunct Professor
Visit Address:
Haukeland universitetssykehus, Laboratoriebygget
5021 Bergen
Postal Address:
Postboks 7804
5021 Bergen
E-mail:
Journal articles
- 2014. Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci. Molecular Psychiatry. doi: doi: 10.1038/mp.2013.195
- 2014. Identifying common genetic variants in blood pressure due to polygenic pleiotropy with associated phenotypes. Hypertension. 63: 819-826. doi: 10.1161/HYPERTENSIONAHA.113.02077
- 2014. Shared common variants in prostate cancer and blood lipids. International Journal of Epidemiology. 43: 1205-1214. doi: 10.1093/ije/dyu090
- 2014. An attempt to identify single nucleotide polymorphisms contributing to possible relationships between personality traits and oxytocin-related genes. Neuropsychobiology. 69: 25-30. doi: 10.1159/000356965
- 2014. Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: A report from the Cognitive Genomics consorTium (COGENT). Molecular Psychiatry. 19: 168-174. doi: 10.1038/mp.2013.166
- 2014. Biological insights from 108 schizophrenia-associated genetic loci. Nature. 511: 421-427. doi: 10.1038/nature13595
- 2014. Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry. 19: 108-114.
- 2013. BDNF val66met modulates the association between childhood trauma, cognitive and brain abnormalities in psychoses. Progress in Neuro-psychopharmacology and Biological Psychiatry. 46: 181-188. doi: 10.1016/j.pnpbp.2013.07.008
- 2013. Is Met Variant of the BDNF VAL66MET-Combined with Childhood Trauma - A Risk Factor of Brain Abnormalities in Psychoses? Biological Psychiatry. 73: 287S-287S.
- 2013. A comprehensive family-based replication study of schizophrenia genes. JAMA psychiatry. 70: 573-581. doi: 10.1001/jamapsychiatry.2013.288
- 2013. Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors. American Journal of Human Genetics. 92: 197-209. doi: 10.1016/j.ajhg.2013.01.001
- 2013. Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate. PLoS Genetics. 9. 16 pages. doi: 10.1371/journal.pgen.1003455
- 2013. ZNF804A and cortical thickness in schizophrenia and bipolar disorder. Psychiatry Research : Neuroimaging. 212: 154-157. doi: 10.1016/j.pscychresns.2013.01.007
- 2013. A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder. PLoS ONE. 8. 9 pages. doi: 10.1371/journal.pone.0081052
- 2013. Association analysis between suicidal behaviour and candidate genes of bipolar disorder and schizophrenia. Journal of Affective Disorders. doi: 10.1016/jad.2013.12.18
- 2013. Variant of TREM2 Associated with the Risk of Alzheimer's Disease. New England Journal of Medicine. 368: 107-116. doi: 10.1056/NEJMoa1211103
- 2013. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 45: 984-994. doi: 10.1038/ng.2711
- 2013. Pathway analysis of genetic markers associated with a functional MRI faces paradigm implicates polymorphisms in calcium responsive pathways. NeuroImage. 70: 143-149. doi: 10.1016/j.neuroimage.2012.12.035
- 2013. Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia. Molecular Psychiatry. 8 pages. doi: 10.1038/mp.2013.138
- 2013. No evidence for association between bipolar disorder risk gene variants and brain structural phenotypes. Journal of Affective Disorders. 151: 291-297. doi: 10.1016/j.jad.2013.06.008
- 2013. CACNA1C Risk Variant and Amygdala Activity in Bipolar Disorder, Schizophrenia and Healthy Controls. PLoS ONE. 8. 6 pages. doi: 10.1371/journal.pone.0056970
- 2012. Serotonin Transporter Gene Polymorphism, Childhood Trauma, and Cognition in Patients With Psychotic Disorders. Schizophrenia Bulletin. 38: 15-22. doi: 10.1093/schbul/sbr113
- 2012. Interaction between (BDNF) VAL66Met, childhood adverse events and impaired cognition in patients with schizophrenia spectrum and bipolar disorder. Early Intervention in Psychiatry. 6: 45-45.
- 2012. Interaction Between (bdnf) Va166met, Childhood Adverse Events and Impaired Cognition in Patients with Schizophrenia Spectrum and Bipolar Disorder. Biological Psychiatry. 71: 160S-160S.
- 2012. Interactions between BDNF Val66Met gene polymorphism, childhood adverse events and brain volume changes in schizophrenia and bipolar disorder. Early Intervention in Psychiatry. 6: 30-30.
- 2012. Genome-wide association study identifies genetic loci associated with body mass index and high density lipoprotein-cholesterol levels during psychopharmacological treatment - a cross-sectional naturalistic study. Psychiatry Research. 197: 327-336. doi: 10.1016/j.psychres.2011.12.036
- 2012. Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans. Proceedings of the National Academy of Science of the United States of America. 109: 3985-3990. doi: 10.1073/pnas.1105829109
- 2012. Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach. Translational psychiatry. doi: 10.1038/tp.2012.67
- 2012. Association between a genetic variant in the serotonin transporter gene (SLC6A4) and suicidal behavior in patients with schizophrenia. Behavioral and Brain Functions. 8. 8 pages. doi: 10.1186/1744-9081-8-24
- 2012. Linkage-disequilibrium-based binning affects the interpretation of GWASs. American Journal of Human Genetics. 90: 727-733. doi: 10.1016/j.ajhg.2012.02.025
- 2012. Up-Regulation of NOTCH4 Gene Expression in Bipolar Disorder. American Journal of Psychiatry. 169: 1292-1300. doi: 10.1176/appi.ajp.2012.11091431
- 2012. Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders. PLoS ONE. 7. 14 pages. doi: 10.1371/journal.pone.0031687
- 2012. DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. PLoS ONE. 7. 12 pages. doi: 10.1371/journal.pone.0035424
- 2012. Lack of association between the regulator of G-protein signaling 4 (RGS4) rs951436 polymorphism and schizophrenia. Psychiatric Genetics. 22: 263-264. doi: 10.1097/YPG.0b013e32834f3558
- 2012. Effect of DISC1 SNPs on Brain Structure in Healthy Controls and Patients With a History of Psychosis. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 159B: 722-730. doi: 10.1002/ajmg.b.32076
- 2012. Genome-wide study identifies PTPRO and WDR72 and FOXQ1-SUMO1P1 interaction associated with neurocognitive function. Journal of Psychiatric Research. 46: 271-278. doi: 10.1016/j.jpsychires.2011.11.001
- 2012. Connection between Genetic and Clinical Data in Bipolar Disorder. PLoS ONE. 7. 9 pages. doi: 10.1371/journal.pone.0044623
- 2012. Associations Between Variants Near a Monoaminergic Pathways Gene (PHOX2B) and Amygdala Reactivity: A Genome-Wide Functional Imaging Study. Twin Research and Human Genetics. 15: 273-285. doi: 10.1017/thg.2012.5
- 2012. Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics. 44: 552-561. doi: 10.1038/ng.2250
- 2012. Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder. Biological Psychiatry. 72: 645-650. doi: 10.1016/j.biopsych.2012.02.040
- 2012. TCF4 sequence variants and mRNA levels are associated with neurodevelopmental characteristics in psychotic disorders. Translational psychiatry. 2. doi: 10.1038/tp.2012.39
- 2011. SEROTONIN TRANSPORTER GENE POLYMORPHISMS, CHILDHOOD TRAUMA AND COGNITION IN PATIENTS WITH PSYCHOTIC DISORDERS. Schizophrenia Bulletin. 37: 80-80.
- 2011. Common Sequence Variants in the Major Histocompatibility Complex Region Associate with Cerebral Ventricular Size in Schizophrenia. Biological Psychiatry. 70: 696-698. doi: 10.1016/j.biopsych.2011.02.034
- 2011. Intron 12 in NTRK3 is associated with bipolar disorder. Psychiatry Research. 185: 358-362. doi: 10.1016/j.psychres.2010.05.011
- 2011. Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia. Archives of General Psychiatry. 68: 781-790. doi: 10.1001/archgenpsychiatry.2011.81
- 2011. Lack of association between two dopamine D2 receptor gene polymorphisms and schizophrenia. Psychiatric Genetics. 21: 214-215. doi: 10.1097/YPG.0b013e328341e020
- 2011. GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia. Molecular Psychiatry. 16: 1117-1129. doi: 10.1038/mp.2010.96
- 2011. Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder. American Journal of Human Genetics. 88: 372-381. doi: 10.1016/j.ajhg.2011.01.017
- 2011. Syndecan-4 is essential for development of concentric myocardial hypertrophy via stretch-induced activation of the calcineurin-NFAT pathway. PLoS ONE. 6. Published 2011-11-05. doi: 10.1371/journal.pone.0028302
- 2011. At-Risk Variant in TCF7L2 for Type II Diabetes Increases Risk of Schizophrenia. Biological Psychiatry. 70: 59-63. doi: 10.1016/j.biopsych.2011.01.031
- 2011. Kynurenine 3-monooxygenase (KMO) polymorphisms in schizophrenia: An association study. Schizophrenia Research. 127: 270-272. doi: 10.1016/j.schres.2010.10.002
- 2011. The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia. Biological Psychiatry. 70: 35-42. doi: 10.1016/j.biopsych.2011.01.030
- 2011. Copy number variations of chromosome 16p13.1 region associated with schizophrenia. Molecular Psychiatry. 16: 17-25. doi: 10.1038/mp.2009.101
- 2011. Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness. American Journal of Psychiatry. 168: 408-417. doi: 10.1176/appi.ajp.2010.09111660
- 2011. Combinations of SNPs Related to Signal Transduction in Bipolar Disorder. PLoS ONE. 6. 11 pages. doi: 10.1371/journal.pone.0023812
- 2011. Candidate Gene Analysis of the Human Natural Killer-1 Carbohydrate Pathway and Perineuronal Nets in Schizophrenia: B3GAT2 Is Associated with Disease Risk and Cortical Surface Area. Biological Psychiatry. 69: 90-96. doi: 10.1016/j.biopsych.2010.07.035
- 2011. Copy number variations in affective disorders and meta-analysis. Psychiatric Genetics. 21: 319-322. doi: 10.1097/YPG.0b013e3283463deb
- 2011. Meta-Analysis of Heterogeneous Data Sources for Genome-Scale Identification of Risk Genes in Complex Phenotypes. Genetic Epidemiology. 35: 318-332. doi: 10.1002/gepi.20580
- 2011. Genome-wide association study identifies five new schizophrenia loci. Nature Genetics. 43: 969-976. doi: 10.1038/ng.940
- 2011. Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Nature Genetics. 43: 977-983. doi: 10.1038/ng.943
- 2011. Expanding the range of ZNF804A variants conferring risk of psychosis. Molecular Psychiatry. 16: 59-66. doi: 10.1038/mp.2009.149
- 2011. Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Human Molecular Genetics. 20: 4076-4081. doi: 10.1093/hmg/ddr325
- 2011. Association Analysis of ANK3 Gene Variants in Nordic Bipolar Disorder and Schizophrenia Case-Control Samples. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 156B: 969-974. doi: 10.1002/ajmg.b.31244
- 2011. Dual association of a TRKA polymorphism with schizophrenia. Psychiatric Genetics. 21: 125-131. doi: 10.1097/YPG.0b013e3283437194
- 2010. Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. Journal of Psychiatric Research. 44: 748-753. doi: 10.1016/j.jpsychires.2010.02.002
- 2010. A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample. Journal of Affective Disorders. 126: 312-316. doi: 10.1016/j.jad.2010.04.007
- 2010. Osteoprotegerin levels in patients with severe mental disorders. Journal of Psychiatry & Neuroscience. 35: 304-310. doi: 10.1503/jpn.090088
- 2010. A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia. Human Molecular Genetics. 19: 1379-1386. doi: 10.1093/hmg/ddq009
- 2010. Association Study of PDE48 gene variants in Scandinavian schizophrenia and bipolar disorder multicenter case-control samples. American Journal of Medical Genetics. 153B: 86-96. doi: 10.1002/ajmg.b.30958
- 2010. Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples. Molecular Psychiatry. 15: 463-472. doi: 10.1038/mp.2008.110
- 2010. Sex-dependent association of common variants of microcephaly genes with brain structure. Proceedings of the National Academy of Science of the United States of America. 107: 384-388. doi: 10.1073/pnas.0908454107
- 2010. The Tryptophan Hydroxylase 1 (TPH1) Gene, Schizophrenia Susceptibility, and Suicidal Behavior: A Multi-Centre Case-Control Study and Meta-Analysis. American Journal of Medical Genetics. 153B: 387-396. doi: 10.1002/ajmg.b.30991
- 2010. SRD5A2 is associated with increased cortisol metabolism in schizophrenia spectrum disorders. Progress in Neuro-psychopharmacology and Biological Psychiatry. 34: 1500-1506. doi: 10.1016/j.pnpbp.2010.08.013
- 2010. Association Analysis of PALB2 and BRCA2 in Bipolar Disorder and Schizophrenia in a Scandinavian Case–Control Sample. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 153B: 1276-1280. doi: 10.1002/ajmg.b.31098
- 2010. Association Between Methylenetetrahydrofolate Reductase (MTHFR) C677T Polymorphism and Age of Onset in Schizophrenia. American Journal of Medical Genetics. 153B: 610-618. doi: 10.1002/ajmg.b.31030
- 2010. Catechol O-methyltransferase variants and cognitive performance in schizophrenia and bipolar disorder versus controls. Schizophrenia Research. 122: 31-37. doi: 10.1016/j.schres.2010.05.007
- 2009. Tyrosine hydroxylase Val81Met polymorphism: lack of association with schizophrenia. Psychiatric Genetics. 19: 273-274. doi: 10.1097/YPG.0b013e32832a4fcd
- 2009. A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE). Schizophrenia Research. 107: 242-248. doi: 10.1016/j.schres.2008.10.010
- 2009. Association of MCTP2 gene variants with schizophrenia in three independent samples of Scandinavian origin (SCOPE). Psychiatry Research. 168: 256-258. doi: 10.1016/j.psychres.2008.08.007
- 2009. Copy number variations of chromosome 16p13.1 region associated with schizophrenia. Molecular Psychiatry. 1-9.
- 2009. A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations. Proceedings of the National Academy of Science of the United States of America. 106: 15483-15488. doi: 10.1073/pnas.0901866106
- 2009. DTNBP1, NRG1, DAOA, DAO and GRM3 Polymorphisms and Schizophrenia: An Association Study. Neuropsychobiology. 59: 142-150. doi: 10.1159/000218076
- 2009. Evidence for a possible association of neurotrophin receptor (NTRK-3) gene polymorphisms with hippocampal function and schizophrenia. Neurobiology of Disease. 34: 518-524. doi: 10.1016/j.nbd.2009.03.011
- 2009. Disruption of the neurexin 1 gene is associated with schizophrenia. Human Molecular Genetics. 18: 988-996. doi: 10.1093/hmg/ddn351
- 2009. ASSOCIATION BETWEEN THE TRYPTOPHAN HYDROXYLASE 1 (TPH1) GENE, SCHIZOPHRENIA SUSCEPTIBILITY, AND SUICIDAL BEHAVIOR. Schizophrenia Bulletin. 35: 121-121.
- 2009. Common variants conferring risk of schizophrenia. Nature. 460: 744-747. doi: 10.1038/nature08186
- 2009. The Tryptophan hydroxylase 1 (TPH1) gene, schizophrenia susceptibility, and suicidal behavior: A multi-centre case-control study and meta-analysis. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. doi: 10.1002/ajmg.b.30991
- 2009. No association between DGKH and bipolar disorder in a Scandinavian case-control sample. Psychiatric Genetics. 19: 269-272. doi: 10.1097/YPG.0b013e32832d302f
- 2009. Association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age of onset in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
- 2009. DYSBINDIN AND D-AMINO-ACID-OXIDASE GENE POLYMORPHISMS ASSOCIATED WITH POSITIVE AND NEGATIVE SYMPTOMS IN SCHIZOPHRENIA. Schizophrenia Bulletin. 35: 105-105.
- 2009. Dysbindin and D-Amino-Acid-Oxidase Gene Polymorphisms Associated with Positive and Negative Symptoms in Schizophrenia. Neuropsychobiology. 60: 31-36. doi: 10.1159/000235799
- 2009. Three-cohort targeted gene screening reveals a non-synonymous TRKA polymorphism associated with schizophrenia. Journal of Psychiatric Research. 43: 1195-1199. doi: 10.1016/j.jpsychires.2009.04.006
- 2008. A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE). Schizophrenia Research.
- 2008. Two methylenetetrahydrofolate reductase gene (MTHFR) polymorphisms, schizophrenia and bipolar disorder: An association study. American Journal of Medical Genetics. 147B: 976-982. doi: 10.1002/ajmg.b.30671
- 2008. Association Analysis of Schizophrenia on 18 Genes Involved in Neuronal Migration: MDGA1 as a New Susceptibility Gene. American Journal of Medical Genetics. 147B: 1089-1100. doi: 10.1002/ajmg.b.30726
- 2008. Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples. Molecular Psychiatry.
- 2008. Interaction between health behaviour, mental distress and the polymorphism of the serotonin transporter gene among adolescents in Oslo, Norway. European psychiatry. 23: S174-S174.
- 2008. The estrogen hypothesis of schizophrenia implicates glucose metabolism: association study in three independent samples. BMC Medical Genetics. 9: 39. doi: 10.1186/1471-2350-9-39
- 2008. Disruption of the neurexin 1 gene is associated with schizophrenia. Human Molecular Genetics.
- 2008. Association between a disrupted-in-schizophrenia 1 (DISC1) single nucleotide polymorphism and schizophrenia in a combined Scandinavian case-control sample. Schizophrenia Research. 106: 237-241. doi: 10.1016/j.schres.2008.08.024
- 2008. Large recurrent microdeletions associated with schizophrenia. Nature. 455: 232-U61. doi: 10.1038/nature07229
- 2008. A novel myogenic cell line with phenotypic properties of muscle progenitors. Journal of Molecular Medicine. 86: 105-115. doi: 10.1007/s00109-007-0268-0
- 2007. The effect of red wine on plasma leptin levels and vasoactive factors from adipose tissue: A randomized crossover trial. Alcohol and Alcoholism. 42: 525-528. doi: 10.1093/alcalc/agm056
- 2007. Brain expressed microRNAs implicated in schizophrenia etiology. PLoS ONE. 12,2: e873.
- 2007. Brief Research Communication Two methylenetetrahydrofolate reductase gene (MTHFR) polymorphisms, schizophrenia and bipolar disorder: An association study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
- 2005. Activity of peroxisomal enzymes, and levels of polyamines in LPA-transgenic mice on two different diets. Lipids in Health and Disease. 4. 12 pages.
- 2004. Comparison of nonviral transfection and adeno-associated viral transduction on cardiomyocytes. Molecular Biotechnology. 28: 21-31.
- 2004. Variations in transfection efficiency of VEGF(165) and VEGF(121)-cDNA - Its effects on proliferation and migration of human endothelial cells. Molecular Biotechnology. 26: 7-16.
- 2004. Human apoB contributes to increased serum total apo(a) level in LPA transgenic mice. Lipids in Health and Disease. 11: 8.
- 2003. Effect of cholesterol feeding on apo(a), CYP7A1 and LXR alpha expression in LPA transgenic mice. Atherosclerosis Supplements. 4: 296-296.
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