Yunpeng Wang

• Nievergelt, Caroline M.; Maihofer, Adam X.; Atkinson, Elizabeth G.; Chen, Chia-Yen; Choi, Karmel W. & Coleman, Jonathan R. I. [Vis alle 235 forfattere av denne artikkelen] (2024). Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. Nature Genetics. ISSN 1061-4036. doi: 10.1038/s41588-024-01707-9.
• Reppe, Sjur; Gundersen, Sveinung; Sandve, Geir Kjetil Ferkingstad; Wang, Yunpeng; Andreassen, Ole & Medina-Gomez, Carolina [Vis alle 10 forfattere av denne artikkelen] (2024). Identification of Transcripts with Shared Roles in the Pathogenesis of Postmenopausal Osteoporosis and Cardiovascular Disease. International Journal of Molecular Sciences. ISSN 1661-6596. 25(10). doi: 10.3390/ijms25105554. Vis sammendrag

  Epidemiological evidence suggests existing comorbidity between postmenopausal osteoporosis (OP) and cardiovascular disease (CVD), but identification of possible shared genes is lacking. The skeletal global transcriptomes were analyzed in trans-iliac bone biopsies (n=84) from clinically well-characterized postmenopausal women (50 to 86 years) using microchips and RNA sequencing. Thousand transcripts highly correlated with areal bone mineral density (aBMD) were further analyzed using bioinformatics, and common genes overlapping with CVD and their biological mechanisms, pathways and functions were identified. Fifty genes (45 mRNAs, 5 miRNAs) were discovered with established roles in oxidative stress, inflammatory response, endothelial function, fibrosis, dyslipidemia and osteoblastogenesis/calcification. These pleiotropic genes with possible CVD comorbidity functions were also present in transcriptomes of microvascular endothelial cells and cardiomyocytes and differentially expressed between healthy and osteoporotic women with fragility fractures. The results were supported by a genetic pleiotropy-informed conditional False Discovery Rate approach identifying overlap in single nucleotide polymorphisms (SNPs) within several genes encoding the aBMD and CVD associated transcripts.The study provides transcriptional and genomic evidence for genes of importance for both BMD regulation and CVD risk in a large collection of postmenopausal bone biopsies. Most of the transcripts identified in the CVD risk categories have no previously recognized roles in OP pathogenesis and provide novel avenues for exploring the mechanistic basis for the biological association between CVD and OP.

• Leonardsen, Esten Høyland; Persson, Karin Ester Torun; Grødem, Edvard Olaf Sætersdal; Dinsdale, Nicola; SCHELLHORN, TILL & Roe, James Michael [Vis alle 16 forfattere av denne artikkelen] (2024). Constructing personalized characterizations of structural brain aberrations in patients with dementia using explainable artificial intelligence. npj Digital Medicine. 7(1). doi: 10.1038/s41746-024-01123-7.
• Iakunchykova, Olena; Pan, Mengyu; Amlien, Inge; Roe, James Michael; Walhovd, Kristine B & Fjell, Anders Martin [Vis alle 9 forfattere av denne artikkelen] (2024). Genetic evidence for the causal effects of C–reactive protein on self-reported habitual sleep duration. Brain, Behavior, and Immunity - Health (BBI - Health). ISSN 2666-3546. 37. doi: 10.1016/j.bbih.2024.100754.
• He, Qiang; Wang, Wenjing; Xu, Dingkang; Xiong, Yang; Tao, Chuanyuan & You, Chao [Vis alle 185 forfattere av denne artikkelen] (2024). Potential causal association between gut microbiome and posttraumatic stress disorder. Translational Psychiatry. ISSN 2158-3188. 14(1). doi: 10.1038/s41398-024-02765-7.
• Zhang, Liyuan; Yuan, Xiuxia; Li, Xue; Xiaoyun, Zhang; Hu, Shaohua & Andreassen, Ole [Vis alle 8 forfattere av denne artikkelen] (2024). Gut microbial diversity moderates polygenic risk of schizophrenia. Frontiers in Psychiatry. ISSN 1664-0640. 15. doi: 10.3389/fpsyt.2024.1275719. Fulltekst i vitenarkiv
• Iakunchykova, Olena; Leonardsen, Esten Høyland & Wang, Yunpeng (2024). Genetic evidence for causal effects of immune dysfunction in psychiatric disorders: where are we? Translational Psychiatry. ISSN 2158-3188. 14(1), s. 1–11. doi: 10.1038/s41398-024-02778-2.
• Walhovd, Kristine B; Krogsrud, Stine Kleppe; Amlien, Inge; Sørensen, Øystein; Wang, Yunpeng & Bråthen, Anne Cecilie Sjøli [Vis alle 14 forfattere av denne artikkelen] (2023). Fetal influence on the human brain through the lifespan. eLIFE. ISSN 2050-084X. 12. doi: 10.7554/eLife.86812.
• Fjell, Anders Martin; Sørensen, Øystein; Wang, Yunpeng; Amlien, Inge; Baaré, William F. C. & Bartrés-Faz, David [Vis alle 24 forfattere av denne artikkelen] (2023). No phenotypic or genotypic evidence for a link between sleep duration and brain atrophy. Nature Human Behaviour. ISSN 2397-3374. 7, s. 2008–2022. doi: 10.1038/s41562-023-01707-5. Fulltekst i vitenarkiv
• Roe, James Michael; Vidal-Piñeiro, Didac; Amlien, Inge; Pan, Mengyu; Sneve, Markus Handal & de Schotten, Michel Thiebaut [Vis alle 14 forfattere av denne artikkelen] (2023). Tracing the development and lifespan change of population-level structural asymmetry in the cerebral cortex. eLIFE. ISSN 2050-084X. 12, s. 1–32. doi: 10.7554/eLife.84685.
• Iakunchykova, Olena; Schirmer, Henrik; Vangberg, Torgil Riise; Wang, Yunpeng; Benavente, Ernest D. & van Es, René [Vis alle 12 forfattere av denne artikkelen] (2023). Machine-learning-derived heart and brain age are independently associated with cognition. European Journal of Neurology. ISSN 1351-5101. 30(9), s. 2611–2619. doi: 10.1111/ene.15902. Fulltekst i vitenarkiv
• Fjell, Anders Martin; Sørensen, Øystein; Wang, Yunpeng; Amlien, Inge; Baaré, William F C & Bartrés-Faz, David [Vis alle 21 forfattere av denne artikkelen] (2023). Is Short Sleep Bad for the Brain? Brain Structure and Cognitive Function in Short Sleepers. Journal of Neuroscience. ISSN 0270-6474. 43(28), s. 5241–5250. doi: 10.1523/JNEUROSCI.2330-22.2023. Fulltekst i vitenarkiv
• Sun, Jiangming; Borné, Yan; Edsfeldt, Andreas; Wang, Yunpeng; Pan, Mengyu & Melander, Olle [Vis alle 8 forfattere av denne artikkelen] (2023). Genetic Susceptibility to Mood Disorders and Risk of Stroke: A Polygenic Risk Score and Mendelian Randomization Study. Stroke. ISSN 0039-2499. 54(5), s. 1340–1346. doi: 10.1161/STROKEAHA.122.041026.
• Leonardsen, Esten Høyland; Vidal-Piñeiro, Didac; Roe, James Michael; Frei, Oleksandr; Shadrin, Alexey & Iakunchykova, Olena [Vis alle 14 forfattere av denne artikkelen] (2023). Genetic architecture of brain age and its casual relations with brain and mental disorders. Molecular Psychiatry. ISSN 1359-4184. doi: 10.1038/s41380-023-02087-y. Fulltekst i vitenarkiv
• Pan, Mengyu; Roe, James Michael; Nudel, Ron; Schork, Andrew J.; Iakunchykova, Olena & Fjell, Anders Martin [Vis alle 11 forfattere av denne artikkelen] (2023). Circulating S100B levels at birth and risk of six major neuropsychiatric or neurological disorders: a two-sample Mendelian Randomization Study. Translational Psychiatry. ISSN 2158-3188. 13(1). doi: 10.1038/s41398-023-02478-3.
• Cheng, Weiqiu; van der Meer, Dennis; Parker, Nadine; Hindley, Guy Frederick Lanyon; O'Connell, Kevin Sean & Wang, Yunpeng [Vis alle 20 forfattere av denne artikkelen] (2022). Shared genetic architecture between schizophrenia and subcortical brain volumes implicates early neurodevelopmental processes and brain development in childhood. Molecular Psychiatry. ISSN 1359-4184. doi: 10.1038/s41380-022-01751-z. Fulltekst i vitenarkiv
• Walhovd, Kristine B; Nyberg, Lars; Lindenberger, Ulman; Amlien, Inge; Sørensen, Øystein & Wang, Yunpeng [Vis alle 20 forfattere av denne artikkelen] (2022). Brain aging differs with cognitive ability regardless of education. Scientific Reports. ISSN 2045-2322. 12(1). doi: 10.1038/s41598-022-17727-6.
• Hu, Maolin; Zong, Xiaofen; Sweeney, John A.; Bishop, Jeffrey R; Liao, Yanhui & Giase, Gina [Vis alle 15 forfattere av denne artikkelen] (2022). Risperidone-induced changes in DNA methylation in peripheral blood from first-episode schizophrenia patients parallel changes in neuroimaging and cognitive phenotypes. Psychiatry Research. ISSN 0165-1781. 317. doi: 10.1016/j.psychres.2022.114789. Vis sammendrag

  Background Second generation antipsychotics such as risperidone are first-line pharmacotherapy treatment choices for schizophrenia. However, our ability to reliably predict and monitor treatment reaction is impeded by the lack of relevant biomarkers. As a biomarker for the susceptibility of schizophrenia and clozapine treatment response, DNA methylation (DNAm) has been studied, but the impact of antipsychotics on DNAm has not been explored in drug-naïve patients. Objective The aim of the present study was to examine changes of DNAm after short-term antipsychotic therapy in first-episode drug-naïve schizophrenia (FES) to identify the beneficial and adverse effect of risperidone on DNAm and their relation to treatment outcome. Methods Thirty-eight never treated schizophrenia patients and 38 demographically matched individuals (healthy controls) were assessed at baseline and at 8-week follow-up with symptom ratings, and cognitive and functional imaging procedures, at which time a blood draw for DNAm studies was performed. During the 8-week period, patients received treatment with risperidone monotherapy. An independent data set was used as replication. Results We identified brain related pathways enriched in 4,888 FES-associated CpG sites relative to controls. Risperidone administration in patients altered DNAm in 5,979 CpG sites relative to baseline. Significant group differences in DNAm at follow-up were seen in FES patients at 6,760 CpG sites versus healthy controls. Through comparison of effect size, we found 87.54% out of the risperidone-associated changes in DNAm showed possible beneficial effect, while only 12.46% showed potential adverse effect. There were 580 DNAm sites in which changes shifted methylation levels to be indistinguishable from controls after risperidone treatment. The DNAm changes of some sites that normalized after treatment were correlated with treatment-related changes in symptom severity, spontaneous neurophysiological activity, and cognition. We replicated our results in an independent data set. Conclusion The normalizing effect of risperidone monotherapy on gene DNAm, and its correlation with clinically relevant phenotypes, indicates that risperidone therapy is associated with DNAm changes that are related to changes in brain physiology, cognition and symptom severity.

• Krantz, Mette Falkenberg; Ellersgaard, Ditte; Andersen, Klaus Kaae; Hemager, Nicoline; Christiani, Camilla & Spang, Katrine Søborg [Vis alle 23 forfattere av denne artikkelen] (2022). Accumulation of Disadvantages Across Multiple Domains Amongst Subgroups of Children of Parents with Schizophrenia or Bipolar Disorder: Clustering Data from the Danish High Risk and Resilience Study VIA 7. Schizophrenia Bulletin Open. ISSN 2632-7899. 3(1). doi: 10.1093/schizbullopen/sgac010. Vis sammendrag

  Objective Children with familial high-risk of schizophrenia (FHR-SZ) or bipolar disorder (FHR-BP) are frequently affected in a range of domains known to be precursors of severe mental illness. No previous studies have gathered known precursors to examine whether they distribute evenly across familial high risk (FHR) children or if they cluster among a smaller group. Since such examination holds the potential to identify high and low risk of severe mental illness groups, we aimed to cluster FHR and control children affected to various degrees. Method In The Danish High Risk and Resilience Study VIA 7, a clinical cohort study, 514 7-year-old children with FHR-SZ or FHR-BP and matched controls were assessed in domains of motor function, neurocognition, emotional control, behavior, social cognition, self-perception, language, psychotic experiences, and psychopathology, and grouped using cluster analysis. Associations between clusters and parents' level of education, functioning, caregiver status, child's level of stimulation and support in the home, and polygenic risk scores were examined. Results A total of four groups including one of broadly affected children were identified. The broadly affected group was represented 4–5-fold (18.1%) amongst FHR-SZ children and 2–3-fold (10.2%) amongst FHR-BP children, compared to controls (4.1%) (P

• Allesøe, Rosa Lundbye; Nudel, Ron; Thompson, Wesley K.; Wang, Yunpeng; Nordentoft, Merete & Børglum, Anders D [Vis alle 10 forfattere av denne artikkelen] (2022). Deep learning-based integration of genetics with registry data for stratification of schizophrenia and depression. Science Advances. ISSN 2375-2548. 8(26). doi: 10.1126/sciadv.abi7293. Vis sammendrag

  Currently, psychiatric diagnoses are, in contrast to most other medical fields, based on subjective symptoms and observable signs and call for new and improved diagnostics to provide the most optimal care. On the basis of a deep learning approach, we performed unsupervised patient stratification of 19,636 patients with depression [major depressive disorder (MDD)] and/or schizophrenia (SCZ) and 22,467 population controls from the iPSYCH2012 case cohort. We integrated data of disorder severity, history of mental disorders and disease comorbidities, genetics, and medical birth data. From this, we stratified the individuals in six and seven unique clusters for MDD and SCZ, respectively. When censoring data until diagnosis, we could predict MDD clusters with areas under the curve (AUCs) of 0.54 to 0.80 and SCZ clusters with AUCs of 0.71 to 0.86. Overall cases and controls could be predicted with an AUC of 0.81, illustrating the utility of data-driven subgrouping in psychiatry.

• Jefsen, Oskar Hougaard; Nudel, Ron; Wang, Yunpeng; Bybjerg-Grauholm, Jonas; Hemager, Nicoline & Christiani, Camilla A J [Vis alle 17 forfattere av denne artikkelen] (2022). Genetic assortative mating for schizophrenia and bipolar disorder. European psychiatry. ISSN 0924-9338. 65(1). doi: 10.1192/j.eurpsy.2022.2304.
• Hemager, Nicoline; Christiani, Camilla Jerlang; Thorup, Anne Amalie Elgaard; Spang, Katrine Søborg; Ellersgaard, Ditte & Burton, Birgitte Klee [Vis alle 14 forfattere av denne artikkelen] (2022). Neurocognitive heterogeneity in 7-year-old children at familial high risk of schizophrenia or bipolar disorder: The Danish high risk and resilience study - VIA 7. Journal of Affective Disorders. ISSN 0165-0327. 302, s. 214–223. doi: 10.1016/j.jad.2022.01.096.
• Leonardsen, Esten Høyland; Peng, Han; Kaufmann, Tobias; Agartz, Ingrid; Andreassen, Ole & Celius, Elisabeth Gulowsen [Vis alle 19 forfattere av denne artikkelen] (2022). Deep neural networks learn general and clinically relevant representations of the ageing brain. NeuroImage. ISSN 1053-8119. 256. doi: 10.1016/j.neuroimage.2022.119210. Fulltekst i vitenarkiv Vis sammendrag

  The discrepancy between chronological age and the apparent age of the brain based on neuroimaging data — the brain age delta — has emerged as a reliable marker of brain health. With an increasing wealth of data, approaches to tackle heterogeneity in data acquisition are vital. To this end, we compiled raw structural magnetic resonance images into one of the largest and most diverse datasets assembled (n=53542), and trained convolutional neural networks (CNNs) to predict age. We achieved state-of-the-art performance on unseen data from unknown scanners (n=2553), and showed that higher brain age delta is associated with diabetes, alcohol intake and smoking. Using transfer learning, the intermediate representations learned by our model complemented and partly outperformed brain age delta in predicting common brain disorders. Our work shows we can achieve generalizable and biologically plausible brain age predictions using CNNs trained on heterogeneous datasets, and transfer them to clinical use cases.

• Amare, Azmeraw T.; Schubert, Klaus Oliver; Hou, Liping; Clark, Scott R.; Papiol, Sergi & Cearns, Micah [Vis alle 309 forfattere av denne artikkelen] (2021). Association of polygenic score for major depression with response to lithium in patients with bipolar disorder. Molecular Psychiatry. ISSN 1359-4184. 26(6), s. 2457–2470. doi: 10.1038/s41380-020-0689-5.
• Blokland, Gabriella A. M.; Grove, Jakob; Chen, Chia-Yen; Cotsapas, Chris; Tobet, Stuart & Handa, Robert [Vis alle 50 forfattere av denne artikkelen] (2021). Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Biological Psychiatry. ISSN 0006-3223. 91, s. 102–117. doi: 10.1016/j.biopsych.2021.02.972. Fulltekst i vitenarkiv Vis sammendrag

  Background Sex differences in incidence and/or presentation of schizophrenia (SCZ), major depressive disorder (MDD), and bipolar disorder (BIP) are pervasive. Previous evidence for shared genetic risk and sex differences in brain abnormalities across disorders suggest possible shared sex-dependent genetic risk. Methods We conducted the largest to date genome-wide genotype-by-sex (G×S) interaction of risk for these disorders using 85,735 cases (33,403 SCZ, 19,924 BIP, and 32,408 MDD) and 109,946 controls from the PGC (Psychiatric Genomics Consortium) and iPSYCH. Results Across disorders, genome-wide significant single nucleotide polymorphism–by-sex interaction was detected for a locus encompassing NKAIN2 (rs117780815, p = 3.2 × 10−8), which interacts with sodium/potassium-transporting ATPase (adenosine triphosphatase) enzymes, implicating neuronal excitability. Three additional loci showed evidence (p < 1 × 10−6) for cross-disorder G×S interaction (rs7302529, p = 1.6 × 10−7; rs73033497, p = 8.8 × 10−7; rs7914279, p = 6.4 × 10−7), implicating various functions. Gene-based analyses identified G×S interaction across disorders (p = 8.97 × 10−7) with transcriptional inhibitor SLTM. Most significant in SCZ was a MOCOS gene locus (rs11665282, p = 1.5 × 10−7), implicating vascular endothelial cells. Secondary analysis of the PGC-SCZ dataset detected an interaction (rs13265509, p = 1.1 × 10−7) in a locus containing IDO2, a kynurenine pathway enzyme with immunoregulatory functions implicated in SCZ, BIP, and MDD. Pathway enrichment analysis detected significant G×S interaction of genes regulating vascular endothelial growth factor receptor signaling in MDD (false discovery rate-corrected p < .05). Conclusions In the largest genome-wide G×S analysis of mood and psychotic disorders to date, there was substantial genetic overlap between the sexes. However, significant sex-dependent effects were enriched for genes related to neuronal development and immune and vascular functions across and within SCZ, BIP, and MDD at the variant, gene, and pathway levels.

• Maihofer, Adam X.; Choi, Karmel W.; Coleman, Jonathan R.I.; Daskalakis, Nikolaos P.; Denckla, Christy A. & Ketema, Elizabeth [Vis alle 181 forfattere av denne artikkelen] (2021). Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information. Biological Psychiatry. ISSN 0006-3223. s. 1–11. doi: 10.1016/j.biopsych.2021.09.020. Fulltekst i vitenarkiv
• Li, Xue; Fan, Xiaoduo; Yuan, Xiuxia; Pang, Lijuan; Hu, Shaohua & Wang, Yunpeng [Vis alle 8 forfattere av denne artikkelen] (2021). The Role of Butyric Acid in Treatment Response in Drug-Naïve First Episode Schizophrenia. Frontiers in Psychiatry. ISSN 1664-0640. 12. doi: 10.3389/fpsyt.2021.724664.
• Uddin, Md Jamal; Ekstrøm, Claus Thorn; Hemager, Nicoline; Christiani, Camilla A J; Gregersen, Maja & Ellersgaard, Ditte Vestbjerg [Vis alle 23 forfattere av denne artikkelen] (2021). Is the Association Between Parents’ Mental Illness and Child Psychopathology Mediated via Home Environment and Caregiver’s Psychosocial Functioning? A Mediation Analysis of the Danish High Risk and Resilience Study—VIA7, a Population-Based Cohort Study. Schizophrenia Bulletin Open. ISSN 2632-7899. 2(1). doi: 10.1093/schizbullopen/sgab024.
• Andlauer, Till F.M.; Guzman-Parra, José; Streit, Fabian; Strohmaier, Jana; González, Maria José & Flores, Susana Gil [Vis alle 50 forfattere av denne artikkelen] (2021). Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. Molecular Psychiatry. ISSN 1359-4184. 26, s. 1286–1298. doi: 10.1038/s41380-019-0558-2. Fulltekst i vitenarkiv
• Wang, Yunpeng; Grydeland, Håkon; Roe, James Michael; Pan, Mengyu; Magnussen, Fredrik & Amlien, Inge [Vis alle 17 forfattere av denne artikkelen] (2021). Associations of circulating C-reactive proteins, APOE ε4, and brain markers for Alzheimer’s disease in healthy samples across the lifespan. Brain, Behavior, and Immunity. ISSN 0889-1591. 100. doi: 10.1016/j.bbi.2021.12.008. Fulltekst i vitenarkiv
• Vidal-Piñeiro, Didac; Wang, Yunpeng; Krogsrud, Stine Kleppe; Amlien, Inge; Baaré, William FC & Bartres-Faz, David [Vis alle 31 forfattere av denne artikkelen] (2021). Individual variations in ‘brain age’ relate to early-life factors more than to longitudinal brain change. eLIFE. ISSN 2050-084X. 10. doi: 10.7554/eLife.69995. Fulltekst i vitenarkiv
• Fjell, Anders Martin; Grydeland, Håkon; Wang, Yunpeng; Amlien, Inge; Bartrés-Faz, David & Brandmaier, Andreas M. [Vis alle 24 forfattere av denne artikkelen] (2021). The genetic organization of longitudinal subcortical volumetric change is stable throughout the lifespan running title: Genetics of subcortical lifespan change. eLIFE. ISSN 2050-084X. 10, s. 1–22. doi: 10.7554/eLife.66466. Fulltekst i vitenarkiv Vis sammendrag

  Development and aging of the cerebral cortex show similar topographic organization and are governed by the same genes. It is unclear whether the same is true for subcortical regions, which follow fundamentally different ontogenetic and phylogenetic principles. We tested the hypothesis that genetically governed neurodevelopmental processes can be traced throughout life by assessing to which degree brain regions that develop together continue to change together through life. Analyzing over 6000 longitudinal MRIs of the brain, we used graph theory to identify five clusters of coordinated development, indexed as patterns of correlated volumetric change in brain structures. The clusters tended to follow placement along the cranial axis in embryonic brain development, suggesting continuity from prenatal stages, and correlated with cognition. Across independent longitudinal datasets, we demonstrated that developmental clusters were conserved through life. Twin-based genetic correlations revealed distinct sets of genes governing change in each cluster. Single-nucleotide polymorphisms-based analyses of 38,127 cross-sectional MRIs showed a similar pattern of genetic volume–volume correlations. In conclusion, coordination of subcortical change adheres to fundamental principles of lifespan continuity and genetic organization.

• Walhovd, Kristine Beate; Fjell, Anders Martin; Wang, Yunpeng; Amlien, Inge; Mowinckel, Athanasia Monika & Lindenberger, Ulman [Vis alle 29 forfattere av denne artikkelen] (2021). Education and income show heterogeneous relationships to lifespan brain and cognitive differences across European and US cohorts. Cerebral Cortex. ISSN 1047-3211. 32(4), s. 839–854. doi: 10.1093/cercor/bhab248. Fulltekst i vitenarkiv
• Yuan, Xiuxia; Wang, Yunpeng; Li, Xue; Jiang, Jiajun; Kang, Yulin & Pang, Lijuan [Vis alle 13 forfattere av denne artikkelen] (2021). Gut microbial biomarkers for the treatment response in first-episode, drug-naïve schizophrenia: a 24-week follow-up study. Translational Psychiatry. ISSN 2158-3188. 11, s. 1–9. doi: 10.1038/s41398-021-01531-3. Fulltekst i vitenarkiv Vis sammendrag

  Preclinical studies have shown that the gut microbiota can play a role in schizophrenia (SCH) pathogenesis via the gut-brain axis. However, its role in the antipsychotic treatment response is unclear. Here, we present a 24-week follow-up study to identify gut microbial biomarkers for SCH diagnosis and treatment response, using a sample of 107 first-episode, drug-naïve SCH patients, and 107 healthy controls (HCs). We collected biological samples at baseline (all participants) and follow-up time points after risperidone treatment (SCH patients). Treatment response was assessed using the Positive and Negative Symptoms Scale total (PANSS-T) score. False discovery rate was used to correct for multiple testing. We found that SCH patients showed lower α-diversity (the Shannon and Simpson’s indices) compared to HCs at baseline (p = 1.21 × 10−9, 1.23 × 10−8, respectively). We also found a significant difference in β-diversity between SCH patients and HCs (p = 0.001). At baseline, using microbes that showed different abundance between patients and controls as predictors, a prediction model can distinguish patients from HCs with an area under the curve (AUC) of 0.867. In SCH patients, after 24 weeks of risperidone treatment, we observed an increase of α-diversity toward the basal level of HCs. At the genus level, we observed decreased abundance of Lachnoclostridium (p = 0.019) and increased abundance Romboutsia (p = 0.067). Moreover, the treatment response in SCH patients was significantly associated with the basal levels of Lachnoclostridium and Romboutsia (p = 0.005 and 0.006, respectively). Our results suggest that SCH patients may present characteristic microbiota, and certain microbiota biomarkers may predict treatment response in this patient population.

• Sun, Jiangming; Wang, Yunpeng; Folkersen, Lasse; Borne, Yan; Amlien, Inge & Buil, Alfonso [Vis alle 13 forfattere av denne artikkelen] (2021). Translating polygenic risk scores for clinical use by estimating the confidence bounds of risk prediction. Nature Communications. ISSN 2041-1723. doi: 10.1038/s41467-021-25014-7. Fulltekst i vitenarkiv Vis sammendrag

  A promise of genomics in precision medicine is to provide individualized genetic risk pre- dictions. Polygenic risk scores (PRS), computed by aggregating effects from many genomic variants, have been developed as a useful tool in complex disease research. However, the application of PRS as a tool for predicting an individual’s disease susceptibility in a clinical setting is challenging because PRS typically provide a relative measure of risk evaluated at the level of a group of people but not at individual level. Here, we introduce a machine-learning technique, Mondrian Cross-Conformal Prediction (MCCP), to estimate the confidence bounds of PRS-to-disease-risk prediction. MCCP can report disease status conditional probability value for each individual and give a prediction at a desired error level. Moreover, with a user-defined prediction error rate, MCCP can estimate the proportion of sample (coverage) with a correct prediction.

• Krogsrud, Stine Kleppe; Mowinckel, Athanasia Monika; Sederevicius, Donatas; Vidal-Piñeiro, Didac; Amlien, Inge Kasbohm & Wang, Yunpeng [Vis alle 9 forfattere av denne artikkelen] (2021). Relationships between apparent cortical thickness and working memory across the lifespan - Effects of genetics and socioeconomic status. Developmental Cognitive Neuroscience. ISSN 1878-9293. 51, s. 1–11. doi: 10.1016/j.dcn.2021.100997.
• Cheng, Weiqiu; Frei, Oleksandr; van der Meer, Dennis; Wang, Yunpeng; O`Connell, Kevin & Chu, Yunhan [Vis alle 20 forfattere av denne artikkelen] (2021). Genetic Association Between Schizophrenia and Cortical Brain Surface Area and Thickness. JAMA psychiatry. ISSN 2168-6238. 78(9), s. 1020–1030. doi: 10.1001/jamapsychiatry.2021.1435. Fulltekst i vitenarkiv
• Grydeland, Håkon; Sederevicius, Donatas; Wang, Yunpeng; Bartres-Faz, David; Bertram, Lars & Dobricic, Valerija [Vis alle 16 forfattere av denne artikkelen] (2021). Self-Reported Sleep Relates to Microstructural Hippocampal Decline in β-Amyloid Positive Adults Beyond Genetic Risk. Sleep. ISSN 0161-8105. 44(11). doi: 10.1093/sleep/zsab110. Fulltekst i vitenarkiv Vis sammendrag

  Background To test the hypothesis that worse self-reported sleep relates to memory decay and reduced hippocampal integrity as indexed by increased intra-hippocampal water diffusion, and that the relations are stronger in the presence of β-amyloid (Aβ) accumulation, a marker of Alzheimer’s disease (AD) pathology. Methods Two-hundred and forty-three cognitively healthy participants, aged 19-81 years, completed the Pittsburgh Sleep Quality Index, and 2 diffusion tensor imaging sessions, on average 3 years apart, allowing measures of decline in hippocampal microstructural integrity as indexed by increased mean diffusivity. We measured memory decay using delayed recall from the California Verbal Learning Test. 18F-Flutemetamol positron emission tomography, in 108 participants above 44 years of age, yielded 23 Aβ positive. Genotyping enabled controlling for APOE ε4 status, and polygenic scores for sleep efficiency and AD. Results Worse global sleep quality and sleep efficiency related to more rapid reduction in hippocampal microstructural integrity over time. Focusing on sleep efficiency, the relation was stronger in presence of Aβ accumulation. Sleep efficiency related to memory decay indirectly via hippocampal integrity decline. The results were not explained by genetic risk for sleep efficiency and AD. Conclusions Poor self-reported sleep efficiency related to decline in hippocampal integrity, especially in the presence of Aβ accumulation. Poor sleep and hippocampal microstructural decline may partly explain memory decline in older adults with Aβ pathology. The relationships were not explained by genetic risk. Poor self-reported sleep efficiency might constitute a risk factor for AD, although the causal mechanisms driving the of observed associations remain unknown.

• Shen, Xueyi; Howard, David M.; Adams, Mark J.; Hill, W. David; Clarke, Toni-Kim & McIntosh, Andrew M. [Vis alle 202 forfattere av denne artikkelen] (2020). A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank. Nature Communications. ISSN 2041-1723. 11(1). doi: 10.1038/s41467-020-16022-0.
• Coleman, Jonathan R. I.; Peyrot, Wouter J.; Purves, Kirstin L.; Davis, Katrina A. S.; Rayner, Christopher & Choi, Shing Wan [Vis alle 215 forfattere av denne artikkelen] (2020). Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. Molecular Psychiatry. ISSN 1359-4184. 25(7), s. 1430–1446. doi: 10.1038/s41380-019-0546-6.
• Tao, Qi; Miao, Yun; Li, Huihui; Yuan, Xiuxia; Huang, Xufeng & Wang, Yunpeng [Vis alle 10 forfattere av denne artikkelen] (2020). Insulin Resistance and Oxidative Stress: In Relation to Cognitive Function and Psychopathology in Drug-Naïve, First-Episode Drug-Free Schizophrenia. Frontiers in Psychiatry. ISSN 1664-0640. doi: 10.3389/fpsyt.2020.537280. Fulltekst i vitenarkiv
• Hofer, Edith; Roshchupkin, Gennady V.; Adams, Hieab H H; Knol, Maria J.; Lin, Honghuang & Li, Shuo [Vis alle 51 forfattere av denne artikkelen] (2020). Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. Nature Communications. ISSN 2041-1723. 11. doi: 10.1038/s41467-020-18367-y. Fulltekst i vitenarkiv
• Grasby, Katrina L.; Jahanshad, Neda; Painter, Jodie N; Colodro-Conde, Lucía; Bralten, Janita & Hibar, DP [Vis alle 50 forfattere av denne artikkelen] (2020). The genetic architecture of the human cerebral cortex. Science. ISSN 0036-8075. 367(6484). doi: 10.1126/science.aay6690. Fulltekst i vitenarkiv Vis sammendrag

  INTRODUCTION The cerebral cortex underlies our complex cognitive capabilities. Variations in human cortical surface area and thickness are associated with neurological, psychological, and behavioral traits and can be measured in vivo by magnetic resonance imaging (MRI). Studies in model organisms have identified genes that influence cortical structure, but little is known about common genetic variants that affect human cortical structure. RATIONALE To identify genetic variants associated with human cortical structure at both global and regional levels, we conducted a genome-wide association meta-analysis of brain MRI data from 51,665 individuals across 60 cohorts. We analyzed the surface area and average thickness of the whole cortex and 34 cortical regions with known functional specializations. RESULTS We identified 306 nominally genome-wide significant loci (P < 5 × 10−8) associated with cortical structure in a discovery sample of 33,992 participants of European ancestry. Of the 299 loci for which replication data were available, 241 loci influencing surface area and 14 influencing thickness remained significant after replication, with 199 loci passing multiple testing correction (P < 8.3 × 10−10; 187 influencing surface area and 12 influencing thickness). Common genetic variants explained 34% (SE = 3%) of the variation in total surface area and 26% (SE = 2%) in average thickness; surface area and thickness showed a negative genetic correlation (rG = −0.32, SE = 0.05, P = 6.5 × 10−12), which suggests that genetic influences have opposing effects on surface area and thickness. Bioinformatic analyses showed that total surface area is influenced by genetic variants that alter gene regulatory activity in neural progenitor cells during fetal development. By contrast, average thickness is influenced by active regulatory elements in adult brain samples, which may reflect processes that occur after mid-fetal development, such as myelination, branching, or pruning. When considered together, these results support the radial unit hypothesis that different developmental mechanisms promote surface area expansion and increases in thickness. To identify specific genetic influences on individual cortical regions, we controlled for global measures (total surface area or average thickness) in the regional analyses. After multiple testing correction, we identified 175 loci that influence regional surface area and 10 that influence regional thickness. Loci that affect regional surface area cluster near genes involved in the Wnt signaling pathway, which is known to influence areal identity. We observed significant positive genetic correlations and evidence of bidirectional causation of total surface area with both general cognitive functioning and educational attainment. We found additional positive genetic correlations between total surface area and Parkinson’s disease but did not find evidence of causation. Negative genetic correlations were evident between total surface area and insomnia, attention deficit hyperactivity disorder, depressive symptoms, major depressive disorder, and neuroticism. CONCLUSION This large-scale collaborative work enhances our understanding of the genetic architecture of the human cerebral cortex and its regional patterning. The highly polygenic architecture of the cortex suggests that distinct genes are involved in the development of specific cortical areas. Moreover, we find evidence that brain structure is a key phenotype along the causal pathway that leads from genetic variation to differences in general cognitive function.

• Coleman, Jonathan R.I.; Gaspar, Helena A; Bryois, Julien; Byrne, Enda M; Forstner, Andreas J & Holmans, Peter A [Vis alle 51 forfattere av denne artikkelen] (2020). The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls. Biological Psychiatry. ISSN 0006-3223. doi: 10.1016/j.biopsych.2019.10.015. Vis sammendrag

  Background: Mood disorders (including major depressive disorder and bipolar disorder) affect 10% to 20% of the population. They range from brief, mild episodes to severe, incapacitating conditions that markedly impact lives. Multiple approaches have shown considerable sharing of risk factors across mood disorders despite their diagnostic distinction. Methods: To clarify the shared molecular genetic basis of major depressive disorder and bipolar disorder and to highlight disorder-specific associations, we meta-analyzed data from the latest Psychiatric Genomics Consortium genome-wide association studies of major depression (including data from 23andMe) and bipolar disorder, and an additional major depressive disorder cohort from UK Biobank (total: 185,285 cases, 439,741 controls; nonoverlapping N = 609,424). Results: Seventy-three loci reached genome-wide significance in the meta-analysis, including 15 that are novel for mood disorders. More loci from the Psychiatric Genomics Consortium analysis of major depression than from that for bipolar disorder reached genome-wide significance. Genetic correlations revealed that type 2 bipolar disorder correlates strongly with recurrent and single-episode major depressive disorder. Systems biology analyses highlight both similarities and differences between the mood disorders, particularly in the mouse brain cell types implicated by the expression patterns of associated genes. The mood disorders also differ in their genetic correlation with educational attainment-the relationship is positive in bipolar disorder but negative in major depressive disorder. Conclusions: The mood disorders share several genetic associations, and genetic studies of major depressive disorder and bipolar disorder can be combined effectively to enable the discovery of variants not identified by studying either disorder alone. However, we demonstrate several differences between these disorders. Analyzing subtypes of major depressive disorder and bipolar disorder provides evidence for a genetic mood disorders spectrum.

• Walhovd, Kristine B; Fjell, Anders Martin; Sørensen, Øystein; Mowinckel, Athanasia Monika; Reinbold, Céline Sonja & Idland, Ane-Victoria [Vis alle 12 forfattere av denne artikkelen] (2020). Genetic risk for Alzheimer disease predicts hippocampal volume through the human lifespan. Neurology: Genetics. ISSN 2376-7839. 6(5). doi: 10.1212/NXG.0000000000000506. Fulltekst i vitenarkiv
• Wang, Yunpeng; Nudel, Ron; Benros, Michael Eriksen; Skogstrand, Kristin; Fishilevich, Simon & Lancet, Doron [Vis alle 14 forfattere av denne artikkelen] (2020). Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. PLoS Genetics. ISSN 1553-7390. doi: 10.1371/journal.pgen.1009163. Fulltekst i vitenarkiv
• Còrdova Palomera, Aldo; van der Meer, Dennis; Kaufmann, Tobias; Bettella, Francesco; Wang, Yunpeng & Alnæs, Dag [Vis alle 40 forfattere av denne artikkelen] (2020). Genetic control of variability in subcortical and intracranial volumes. Molecular Psychiatry. ISSN 1359-4184. s. 1–8. doi: 10.1038/s41380-020-0664-1. Fulltekst i vitenarkiv
• Smeland, Olav Bjerkehagen; Shadrin, Alexey A.; Bahrami, Shahram; Broce, Iris J.; Tesli, Martin Steen & Frei, Oleksandr [Vis alle 22 forfattere av denne artikkelen] (2020). Genome-wide Association Analysis of Parkinson’s Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci. Biological Psychiatry. ISSN 0006-3223. 89(3), s. 227–235. doi: 10.1016/j.biopsych.2020.01.026. Fulltekst i vitenarkiv Vis sammendrag

  BACKGROUND:Parkinson’s disease (PD) and schizophrenia (SCZ) are heritable brain disorders that involvedysregulation of the dopaminergic system. Epidemiological studies have reported potential comorbidity between thedisorders, and movement disturbances are common in patients with SCZ before treatment with antipsychotic drugs.Despite this, little is known about shared genetic etiology between the disorders.METHODS:We analyzed recent large genome-wide association studies on patients with SCZ (N= 77,096) and PD(N= 417,508) using a conditional/conjunctional false discovery rate (FDR) approach to evaluate overlap incommon genetic variants and improve statistical power for genetic discovery. Using a variety of biologicalresources, we functionally characterized the identified genomic loci.RESULTS:We observed genetic enrichment in PD conditional onassociations with SCZ and vice versa, indicatingpolygenic overlap. We then leveraged this cross-trait enrichment using conditional FDR analysis and identified 9 novel PDrisk loci and 1 novel SCZ locus at conditional FDR,.01. Furthermore, we identified 9 genomic loci jointly associated withPD and SCZ at conjunctional FDR,.05. There was an even distribution of antagonistic and agonistic effect directionsamong the shared loci, in line with the insignificant genetic correlation between the disorders. Of 67 genes mapped to theshared loci, 65 are expressed in the human brain and show cell type–specific expression profiles.CONCLUSIONS:Altogether, the study increases understanding of the genetic architectures underlying SCZ and PD,indicating that common molecular genetic mechanisms may contribute to overlapping pathophysiological and clinicalfeatures between the disorders.

• Fjell, Anders Martin; Sederevicius, Donatas; Sneve, Markus Handal; de Lange, Ann-Marie Glasø; Bråthen, Anne Cecilie Sjøli & Idland, Ane-Victoria [Vis alle 16 forfattere av denne artikkelen] (2020). Self-reported sleep problems are related to amyloid deposition in cortical regions with high HOMER1 gene expression. Cerebral Cortex. ISSN 1047-3211. 30(4), s. 2144–2156. doi: 10.1093/cercor/bhz228. Fulltekst i vitenarkiv
• Choi, Karmel W.; Chen, Chia-Yen; Stein, Murray B.; Klimentidis, Yann C.; Wang, Min-Jung & Koenen, Karestan C. [Vis alle 203 forfattere av denne artikkelen] (2019). Assessment of bidirectional relationships between physical activity and depression among adults a 2-sample Mendelian randomization study. JAMA psychiatry. ISSN 2168-6238. 76(4), s. 399–408. doi: 10.1001/jamapsychiatry.2018.4175.
• Bauer, Anna E.; Liu, Xiaoqin; Byrne, Enda M.; Sullivan, Patrick F.; Wray, Naomi R. & Agerbo, Esben [Vis alle 21 forfattere av denne artikkelen] (2019). Genetic risk scores for major psychiatric disorders and the risk of postpartum psychiatric disorders. Translational Psychiatry. ISSN 2158-3188. 9:288, s. 1–12. doi: 10.1038/s41398-019-0629-9.
• Nudel, Ron; Wang, Yunpeng; Appadurai, Vivek; Schork, Andrew J.; Buil, Alfonso & Agerbo, Esben [Vis alle 16 forfattere av denne artikkelen] (2019). A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population. Translational Psychiatry. ISSN 2158-3188. 9, s. 1–10. doi: 10.1038/s41398-019-0622-3.
• Lee, Phil H.; Antilla, Verneri; Won, Hyejung; Feng, Yen-Chen A.; Rosenthal, Jacob & Zhu, Zhaozhong [Vis alle 66 forfattere av denne artikkelen] (2019). Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Cell. ISSN 0092-8674. 179(7), s. 1469–1482. doi: 10.1016/j.cell.2019.11.020. Fulltekst i vitenarkiv
• Nievergelt, Caroline M.; Maihofer, Adam X.; Klengel, Torsten; Atkinson, Elizabeth G.; Chen, Chia-Yen & Choi, Karmel W. [Vis alle 179 forfattere av denne artikkelen] (2019). International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Nature Communications. ISSN 2041-1723. 10:4558, s. 1–16. doi: 10.1038/s41467-019-12576-w. Fulltekst i vitenarkiv
• Gasse, Christiane; Wimberley, Theresa; Wang, Yunpeng; Mors, Ole; Børglum, Anders & Als, Thomas Damm [Vis alle 10 forfattere av denne artikkelen] (2019). Schizophrenia polygenic risk scores, urbanicity and treatment-resistant schizophrenia. Schizophrenia Research. ISSN 0920-9964. 212, s. 79–85. doi: 10.1016/j.schres.2019.08.008.
• Stahl, Eli A.; Breen, Gerome; Forstner, Andreas J.; McQuillin, Andrew; Ripke, Stephan & Trubetskoy, Vassily [Vis alle 277 forfattere av denne artikkelen] (2019). Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics. ISSN 1061-4036. 51(5), s. 793–803. doi: 10.1038/s41588-019-0397-8. Fulltekst i vitenarkiv
• Frei, Oleksandr; Holland, Dominic; Smeland, Olav Bjerkehagen; Shadrin, Alexey A.; Fan, Chun Chieh & Mæland, Steffen [Vis alle 12 forfattere av denne artikkelen] (2019). Bivariate causal mixture model quantifies polygenic overlap between complex traits beyond genetic correlation. Nature Communications. ISSN 2041-1723. 10(1). doi: 10.1038/s41467-019-10310-0. Fulltekst i vitenarkiv
• Wang, Yunpeng; Karstoft, Karen-Inge; Nievergelt, Caroline M.; Maihofer, Adam X.; Stein, Murray B. & Ursano, Robert J. [Vis alle 13 forfattere av denne artikkelen] (2019). Post-traumatic stress following military deployment: Genetic associations and cross-disorder genetic correlations. Journal of Affective Disorders. ISSN 0165-0327. 252, s. 350–357. doi: 10.1016/j.jad.2019.04.070.
• Drange, Ole Kristian; Smeland, Olav Bjerkehagen; Shadrin, Alexey A.; Finseth, Per Ivar; Witoelar, Aree & Frei, Oleksandr [Vis alle 52 forfattere av denne artikkelen] (2019). Genetic Overlap Between Alzheimer’s Disease and Bipolar Disorder Implicates the MARK2 and VAC14 Genes. Frontiers in Neuroscience. ISSN 1662-4548. 13. doi: 10.3389/fnins.2019.00220. Fulltekst i vitenarkiv Vis sammendrag

  Background: Alzheimer’s disease (AD) and bipolar disorder (BIP) are complex traits influenced by numerous common genetic variants, most of which remain to be detected. Clinical and epidemiological evidence suggest that AD and BIP are related. However, it is not established if this relation is of genetic origin. Here, we applied statistical methods based on the conditional false discovery rate (FDR) framework to detect genetic overlap between AD and BIP and utilized this overlap to increase the power to identify common genetic variants associated with either or both traits. Methods: We obtained genome wide association studies data from the International Genomics of Alzheimer’s Project part 1 (17,008 AD cases and 37,154 controls) and the Psychiatric Genetic Consortium Bipolar Disorder Working Group (20,352 BIP cases and 31,358 controls). We used conditional QQ-plots to assess overlap in common genetic variants between AD and BIP. We exploited the genetic overlap to re-rank test-statistics for AD and BIP and improve detection of genetic variants using the conditional FDR framework. Results: Conditional QQ-plots demonstrated a polygenic overlap between AD and BIP. Using conditional FDR, we identified one novel genomic locus associated with AD, and nine novel loci associated with BIP. Further, we identified two novel loci jointly associated with AD and BIP implicating the MARK2 gene (lead SNP rs10792421, conjunctional FDR = 0.030, same direction of effect) and the VAC14 gene (lead SNP rs11649476, conjunctional FDR = 0.022, opposite direction of effect). Conclusion: We found polygenic overlap between AD and BIP and identified novel loci for each trait and two jointly associated loci. Further studies should examine if the shared loci implicating the MARK2 and VAC14 genes could explain parts of the shared and distinct features of AD and BIP.

• Jansen, Iris E.; Savage, Jeanne E.; Watanabe, Kyoko; Bryois, Julien; Williams, Dylan M. & Steinberg, Stacy [Vis alle 53 forfattere av denne artikkelen] (2019). Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk. Nature Genetics. ISSN 1061-4036. 51(3), s. 404–413. doi: 10.1038/s41588-018-0311-9. Fulltekst i vitenarkiv
• de Jong, Simone; Diniz, Mateus Jose Abdalla; Saloma, Andiara; Gadelha, Ary; Santoro, Marcos L. & Ota, Vanessa K. [Vis alle 22 forfattere av denne artikkelen] (2018). Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. Communications Biology. ISSN 2399-3642. 1(163). doi: 10.1038/s42003-018-0155-y. Fulltekst i vitenarkiv
• Witoelar, Aree; Rongve, Arvid; Almdahl, Ina Selseth; Ulstein, Ingun; Engvig, Andreas & White, Linda Rosemary [Vis alle 33 forfattere av denne artikkelen] (2018). Meta-analysis of Alzheimer’s disease on 9,751 samples from Norway and IGAP study identifies four risk loci. Scientific Reports. ISSN 2045-2322. 8. doi: 10.1038/s41598-018-36429-6. Fulltekst i vitenarkiv
• Wray, Naomi R.; Ripke, Stephan; Mattheisen, Manuel; Trzaskowski, MacIej; Byrne, Enda M. & Abdellaoui, Abdel [Vis alle 216 forfattere av denne artikkelen] (2018). Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics. ISSN 1061-4036. 50(5), s. 668–681. doi: 10.1038/s41588-018-0090-3.
• Psychiatric Genomics Consorti, Bipolar Sczhizophrenia; Ruderfer, Douglas M.; Ripke, Stephan; McQuillin, Andrew; Boocock, James & Stahl, Eli A. [Vis alle 52 forfattere av denne artikkelen] (2018). Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes. Cell. ISSN 0092-8674. 173(7), s. 1705–1715. doi: 10.1016/j.cell.2018.05.046.
• Bettella, Francesco; Brown, AA; Smeland, Olav Bjerkehagen; Wang, Yunpeng; Witoelar, Aree & Buil Demur, AA [Vis alle 11 forfattere av denne artikkelen] (2018). Cross-tissue eQTL enrichment of associations in schizophrenia. PLOS ONE. ISSN 1932-6203. 13(9). doi: 10.1371/journal.pone.0202812. Fulltekst i vitenarkiv
• Erlangsen, Annette; Appadurai, Vivek; Wang, Yunpeng; Turecki, Gustavo; Mors, Ole & Werge, Thomas [Vis alle 17 forfattere av denne artikkelen] (2018). Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study. Molecular Psychiatry. ISSN 1359-4184. s. 1–12. doi: 10.1038/s41380-018-0218-y.
• Zhang, Qian; Liang, Zhe; Cui, Xuean; Ji, Changmian; Li, Yun & Zhang, Pingxian [Vis alle 16 forfattere av denne artikkelen] (2018). N6-methyladenine DNA methylation in Japonica and Indica rice genomes and its association with gene expression, plant development, and stress responses. Molecular Plant. ISSN 1674-2052. 11(12), s. 1492–1508. doi: 10.1016/j.molp.2018.11.005.
• Chen, Chao; Meng, Qingtuan; Xia, Yan; Ding, Chaodong; Wang, Le & Dai, Rujia [Vis alle 27 forfattere av denne artikkelen] (2018). The transcription factor POU3F2 regulates a gene coexpression network in brain tissue from patients with psychiatric disorders. Science Translational Medicine. ISSN 1946-6234. 10:eaat8178(472), s. 1–11. doi: 10.1126/scitranslmed.aat8178.
• Bonham, Luke W.; Karch, Celeste M.; Fan, Chun C.; Tan, Chin; Geier, Ethan G. & Wang, Yunpeng [Vis alle 25 forfattere av denne artikkelen] (2018). CXCR4 involvement in neurodegenerative diseases. Translational Psychiatry. ISSN 2158-3188. 8:73, s. 1–10. doi: 10.1038/s41398-017-0049-7. Fulltekst i vitenarkiv
• Sønderby, Ida Elken; Gustafsson, Omar; Doan, Nhat Trung; Hibar, Derrek; Martin-Brevet, Sandra & Espeseth, Thomas [Vis alle 15 forfattere av denne artikkelen] (2018). Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia. Molecular Psychiatry. ISSN 1359-4184. s. 1–16. doi: 10.1038/s41380-019-0358-8. Fulltekst i vitenarkiv
• Srinivasan, Saurabh; Bettella, Francesco; Frei, Oleksandr; Hill, W. David; Wang, Yunpeng & Witoelar, Aree [Vis alle 17 forfattere av denne artikkelen] (2018). Enrichment of genetic markers of recent human evolution in educational and cognitive traits. Scientific Reports. ISSN 2045-2322. 8:12585, s. 1–9. doi: 10.1038/s41598-018-30387-9. Fulltekst i vitenarkiv
• Maier, Robert M.; Zhu, Zhihong; Lee, Sang Hong; Trzaskowski, Maciej; Ruderfer, Douglas M. & Stahl, Eli A. [Vis alle 17 forfattere av denne artikkelen] (2018). Improving genetic prediction by leveraging genetic correlations among human diseases and traits. Nature Communications. ISSN 2041-1723. 9:989, s. 1–17. doi: 10.1038/s41467-017-02769-6.
• Còrdova Palomera, Aldo; Kaufmann, Tobias; Bettella, Francesco; Wang, Yunpeng; Doan, Nhat Trung & van der Meer, Dennis [Vis alle 12 forfattere av denne artikkelen] (2018). Effects of autozygosity and schizophrenia polygenic risk on cognitive and brain developmental trajectories. European Journal of Human Genetics. ISSN 1018-4813. 26(7), s. 1049–1059. doi: 10.1038/s41431-018-0134-2.
• Li, Wen; Fan, Chun Chieh; Mäki-Marttunen, Tuomo; Thompson, Wesley Kurt; Schork, Andrew J. & Bettella, Francesco [Vis alle 10 forfattere av denne artikkelen] (2018). A molecule-based genetic association approach implicates a range of voltage-gated calcium channels associated with schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. ISSN 1552-4841. 177(4), s. 454–467. doi: 10.1002/ajmg.b.32634.
• Broce, Iris J.; Karch, Celeste M.; Wen, Natalie; Fan, Chun C.; Wang, Yunpeng & Hong Tan, Chin [Vis alle 29 forfattere av denne artikkelen] (2018). Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies. PLoS Medicine. ISSN 1549-1277. 15:e1002487(1), s. 1–20. doi: 10.1371/journal.pmed.1002487. Fulltekst i vitenarkiv
• Zuber, Verena; Jönsson, Erik Gunnar; Frei, Oleksandr; Witoelar, Aree; Thompson, Wesley Kurt & Schork, Andrew J. [Vis alle 18 forfattere av denne artikkelen] (2018). Identification of shared genetic variants between schizophrenia and lung cancer. Scientific Reports. ISSN 2045-2322. 674(8), s. 1–8. doi: 10.1038/s41598-017-16481-4. Fulltekst i vitenarkiv
• Alnæs, Dag; Kaufmann, Tobias; Doan, Nhat Trung; Còrdova Palomera, Aldo; Wang, Yunpeng & Bettella, Francesco [Vis alle 9 forfattere av denne artikkelen] (2018). Association of Heritable Cognitive Ability and Psychopathology With White Matter Properties in Children and Adolescents. JAMA psychiatry. ISSN 2168-6238. 75(3), s. 287–295. doi: 10.1001/jamapsychiatry.2017.4277.
• Seibert, Tyler M.; Fan, Chun Chieh; Wang, Yunpeng; Zuber, Verena; Karunamuni, Roshan & Parsons, J. Kellogg [Vis alle 62 forfattere av denne artikkelen] (2018). Polygenic hazard score to guide screening for aggressive prostate cancer: development and validation in large scale cohorts. The BMJ. ISSN 1756-1833. 360:j5757, s. 1–7. doi: 10.1136/bmj.j5757. Fulltekst i vitenarkiv
• Zablocki, Rong W.; Levine, Richard A.; Schork, Andrew J.; Xu, Shujing; Wang, Yunpeng & Fan, Chun C. [Vis alle 7 forfattere av denne artikkelen] (2017). Semiparametric covariate-modulated local false discovery rate for genome-wide association studies. Annals of Applied Statistics. ISSN 1932-6157. 11(4), s. 2252–2269. doi: 10.1214/17-AOAS1077.
• Rietschel, Liz; Streit, Fabian; Zhu, Gu; McAloney, Kerrie; Frank, Josef & Couvy-Duchesne, Baptiste [Vis alle 26 forfattere av denne artikkelen] (2017). Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes. Scientific Reports. ISSN 2045-2322. 7:15351, s. 1–15. doi: 10.1038/s41598-017-11852-3.
• Shadrin, Alexey A.; Smeland, Olav Bjerkehagen; Zayats, Tetyana; Schork, Andrew J; Frei, Oleksandr & Bettella, Francesco [Vis alle 19 forfattere av denne artikkelen] (2017). Novel loci associated with attention-deficit/hyperactivity disorder are revealed by leveraging polygenic overlap with educational attainment. Journal of the American Academy of Child and Adolescent Psychiatry. ISSN 0890-8567. 57(2), s. 86–95. doi: 10.1016/j.jaac.2017.11.013. Fulltekst i vitenarkiv
• Joshi, Peter K.; Pirastu, Nicola; Kentistou, Katherine A.; Fischer, Krista; Hofer, Edith & Schraut, Katharina E. [Vis alle 113 forfattere av denne artikkelen] (2017). Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Nature Communications. ISSN 2041-1723. 8:910(1), s. 1–13. doi: 10.1038/s41467-017-00934-5.
• Winsvold, Bendik K S; Bettella, Francesco; Witoelar, Aree; Anttila, Verneri; Gormley, Padhraig & Kurth, Tobias [Vis alle 18 forfattere av denne artikkelen] (2017). Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants. PLOS ONE. ISSN 1932-6203. s. 1–15. doi: 10.1371/journal.pone.0185663. Fulltekst i vitenarkiv
• Lo, Min-Tzu; Wang, Yunpeng; Kauppi, Karolina; Sanyal, Nilotpal; Fan, Chun-Chieh & Smeland, Olav Bjerkehagen [Vis alle 13 forfattere av denne artikkelen] (2017). Modeling prior information of common genetic variants improves gene discovery for neuroticism. Human Molecular Genetics. ISSN 0964-6906. 26(22), s. 4530–4539. doi: 10.1093/hmg/ddx340.
• Chen, Chi-Hua; Wang, Yunpeng; Lo, Min-Tzu; Schork, Andrew; Fan, Chun-Chieh & Holland, Dominic [Vis alle 15 forfattere av denne artikkelen] (2017). Leveraging genome characteristics to improve gene discovery for putamen subcortical brain structure. Scientific Reports. ISSN 2045-2322. 7:15736, s. 1–9. doi: 10.1038/s41598-017-15705-x.
• Smeland, Olav Bjerkehagen; Wang, Yunpeng; Frei, Oleksandr; Li, Wen; Hibar, Derrek P & Franke, Barbara [Vis alle 13 forfattere av denne artikkelen] (2017). Genetic overlap between schizophrenia and volumes of hippocampus, putamen, and intracranial volume indicates shared molecular genetic mechanisms. Schizophrenia Bulletin. ISSN 0586-7614. 44(4), s. 854–864. doi: 10.1093/schbul/sbx148.
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• Ferrari, Raffaele; Wang, Yunpeng; Vandrovcova, Jana; Guelfi, Sebastian; Witoelar, Aree & Karch, Celeste M. [Vis alle 22 forfattere av denne artikkelen] (2017). Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases. Journal of Neurology, Neurosurgery and Psychiatry. ISSN 0022-3050. 88(2), s. 152–164. doi: 10.1136/jnnp-2016-314411.
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• Devor, Anna; Andreassen, Ole Andreas; Wang, Yunpeng; Mäki-Marttunen, Tuomo; Smeland, Olav Bjerkehagen & Fan, Chun Chieh [Vis alle 18 forfattere av denne artikkelen] (2017). Genetic evidence for role of integration of fast and slow neurotransmission in schizophrenia. Molecular Psychiatry. ISSN 1359-4184. 22(6), s. 792–801. doi: 10.1038/mp.2017.33. Fulltekst i vitenarkiv

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• Iakunchykova, Olena; Benros, Michael E. & Wang, Yunpeng (2024). Author reply – Letter to the Editor “elevated C-reactive protein and IL-6 signalling are not the only determinants of sleep quality and duration”. Brain, Behavior, and Immunity - Health (BBI - Health). ISSN 2666-3546. doi: 10.1016/j.bbih.2024.100785.
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• Wang, Yunpeng (2021). How does your immune system impact your brain health?
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• Smeland, Olav Bjerkehagen; Frei, Oleksandr; Wang, Yunpeng; Fan, Chun Chieh; Alexey, Shadrin & Li, Wen [Vis alle 13 forfattere av denne artikkelen] (2017). Increased discovery of risk loci for bipolar disorder by leveraging prior probabilities of true associations using the covariate modulated mixture model (CM3).
• Smeland, Olav Bjerkehagen; Frei, Oleksandr; Wang, Yunpeng; Dale, Anders & Andreassen, Ole Andreas (2017). Combined Analysis of Large Genetic Samples. New Statistical Approaches Improve Gene Discovery.

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