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Michael J. Owen, PhD - Related publications

Affiliations: 
Psychological Medicine, Neuropsychiatric Genetics and Genomics Cardiff University, Cardiff, Wales, United Kingdom 
Website:
http://conference.iepa.org.au/speakers/professor-michael-j-owen/
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50 most relevant papers in past 60 days:
Year Citation  Score
2019 Bi X, Feng L, Wang S, Lin Z, Li T, Zhao B, Zhu H, Zhang H. Common genetic variants have associations with human cortical brain regions and risk of schizophrenia. Genetic Epidemiology. PMID 30941828 DOI: 10.1002/gepi.22203   
2019 Harold D, Connolly S, Riley BP, Kendler KS, McCarthy SE, McCombie WR, Richards A, Owen MJ, O'Donovan MC, Walters J, , , Donohoe G, Gill M, Corvin A, et al. Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 30801977 DOI: 10.1002/ajmg.b.32716   
2019 Sozuguzel MD, Sazci A, Yildiz M. Female gender specific association of the Reelin (RELN) gene rs7341475 variant with schizophrenia. Molecular Biology Reports. PMID 30980267 DOI: 10.1007/s11033-019-04803-w   
2019 Bejaoui Y, Witte M, Abdelhady M, Eldarouti M, Abdallah NMA, Elghzaly AA, Tawhid Z, Gaballah MA, Busch H, Munz M, Wendorff M, Ellinghaus E, Franke A, Ibrahim SM. Genome-wide association study of psoriasis in an Egyptian population. Experimental Dermatology. PMID 30921485 DOI: 10.1111/exd.13926   
2019 Liu CM, Liu YL, Hwu HG, Fann CS, Yang UC, Hsu PC, Chang CC, Chen WJ, Hwang TJ, Hsieh MH, Liu CC, Chien YL, Lin YT, Tsuang MT. Genetic associations and expression of extra-short isoforms of disrupted-in-schizophrenia 1 in a neurocognitive subgroup of schizophrenia. Journal of Human Genetics. PMID 30976040 DOI: 10.1038/s10038-019-0597-1   
2019 Isvoranu AM, Guloksuz S, Epskamp S, van Os J, Borsboom D, . Toward incorporating genetic risk scores into symptom networks of psychosis. Psychological Medicine. 1-8. PMID 30867074 DOI: 10.1017/S003329171900045X   
2019 Luo X, Chen S, Xue L, Chen JH, Shi YW, Zhao H. SNP Variation of Gene and Schizophrenia in a Chinese Population: A Hospital-Based Case-Control Study. Frontiers in Genetics. 10: 175. PMID 30891068 DOI: 10.3389/fgene.2019.00175   
2019 Nudel R, Benros ME, Krebs MD, Allesøe RL, Lemvigh CK, Bybjerg-Grauholm J, Børglum AD, Daly MJ, Nordentoft M, Mors O, Hougaard DM, Mortensen PB, Buil A, Werge T, Rasmussen S, et al. Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders. European Journal of Human Genetics : Ejhg. PMID 30976114 DOI: 10.1038/s41431-019-0402-9   
2019 Cai XY, Cheng L, Yu CX, Wu YY, Fang L, Zheng XD, Zhou FS, Sheng YJ, Zhu J, Zheng J, Wu YY, Xiao FL. GWAS Follow-up Study Discovers a Novel Genetic Signal on 10q21.2 for Atopic Dermatitis in Chinese Han Population. Frontiers in Genetics. 10: 174. PMID 30915103 DOI: 10.3389/fgene.2019.00174   
2019 Chang X, Qu H, Liu Y, Glessner J, Hou C, Wang F, Li J, Sleiman P, Hakonarson H. Microduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa. Journal of Psychiatric Research. 113: 34-38. PMID 30878790 DOI: 10.1016/j.jpsychires.2019.01.021   
2019 Thyme SB, Pieper LM, Li EH, Pandey S, Wang Y, Morris NS, Sha C, Choi JW, Herrera KJ, Soucy ER, Zimmerman S, Randlett O, Greenwood J, McCarroll SA, Schier AF. Phenotypic Landscape of Schizophrenia-Associated Genes Defines Candidates and Their Shared Functions. Cell. PMID 30929901 DOI: 10.1016/j.cell.2019.01.048   
2019 Stevenson A, Akena D, Stroud RE, Atwoli L, Campbell MM, Chibnik LB, Kwobah E, Kariuki SM, Martin AR, de Menil V, Newton CRJC, Sibeko G, Stein DJ, Teferra S, Zingela Z, et al. Neuropsychiatric Genetics of African Populations-Psychosis (NeuroGAP-Psychosis): a case-control study protocol and GWAS in Ethiopia, Kenya, South Africa and Uganda. Bmj Open. 9: e025469. PMID 30782936 DOI: 10.1136/bmjopen-2018-025469   
2019 Dekker AM, Diekstra FP, Pulit SL, Tazelaar GHP, van der Spek RA, van Rheenen W, van Eijk KR, Calvo A, Brunetti M, Damme PV, Robberecht W, Hardiman O, McLaughlin R, Chiò A, Sendtner M, et al. Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis. Scientific Reports. 9: 5931. PMID 30976013 DOI: 10.1038/s41598-019-42091-3   
2019 Paquette M, Bernard S, Baass A. SLC22A3 is associated with lipoprotein (a) concentration and cardiovascular disease in familial hypercholesterolemia. Clinical Biochemistry. PMID 30772277 DOI: 10.1016/j.clinbiochem.2019.02.008   
2019 Namkung H, Lee BJ, Sawa A. Causal Inference on Pathophysiological Mediators in Psychiatry. Cold Spring Harbor Symposia On Quantitative Biology. PMID 30850434 DOI: 10.1101/sqb.2018.83.037655   
2019 Garg P, Sharp AJ. Screening for rare epigenetic variations in autism and schizophrenia. Human Mutation. PMID 30900359 DOI: 10.1002/humu.23740   
2019 Huckins LM, Dobbyn A, Ruderfer DM, Hoffman G, Wang W, Pardiñas AF, Rajagopal VM, Als TD, T Nguyen H, Girdhar K, Boocock J, Roussos P, Fromer M, Kramer R, Domenici E, ... , ... , ... , et al. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature Genetics. PMID 30911161 DOI: 10.1038/s41588-019-0364-4   
2019 Bien SA, Su YR, Conti DV, Harrison TA, Qu C, Guo X, Lu Y, Albanes D, Auer PL, Banbury BL, Berndt SI, Bézieau S, Brenner H, Buchanan DD, Caan BJ, et al. Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer. Human Genetics. PMID 30820706 DOI: 10.1007/s00439-019-01989-8   
2019 Lin YP, Liu CY, Chen KY. Assessment of Genetic Differentiation and Linkage Disequilibrium in Using Genome-Wide High-Density SNP Markers. G3 (Bethesda, Md.). PMID 30858236 DOI: 10.1534/g3.118.200862   
2019 Lancaster TM, Hill MJ, Sims R, Williams J. Microglia - mediated immunity partly contributes to the genetic association between Alzheimer's disease and hippocampal volume. Brain, Behavior, and Immunity. PMID 30776473 DOI: 10.1016/j.bbi.2019.02.011   
2019 Mah W, Won H. The three-dimensional landscape of the genome in human brain tissue unveils regulatory mechanisms leading to schizophrenia risk. Schizophrenia Research. PMID 30894290 DOI: 10.1016/j.schres.2019.03.007   
2019 Veyssiere M, Perea J, Michou L, Boland A, Caloustian C, Olaso R, Deleuze JF, Cornelis F, Petit-Teixeira E, Chaudru V. A novel nonsense variant in SUPT20H gene associated with Rheumatoid Arthritis identified by Whole Exome Sequencing of multiplex families. Plos One. 14: e0213387. PMID 30845214 DOI: 10.1371/journal.pone.0213387   
2019 Hong EP, Kim BJ, Cho SS, Yang JS, Choi HJ, Kang SH, Jeon JP. Genomic Variations in Susceptibility to Intracranial Aneurysm in the Korean Population. Journal of Clinical Medicine. 8. PMID 30823506 DOI: 10.3390/jcm8020275   
2019 Raghavan NS, Vardarajan B, Mayeux R. Genomic variation in educational attainment modifies Alzheimer disease risk. Neurology. Genetics. 5: e310. PMID 30863791 DOI: 10.1212/NXG.0000000000000310   
2019 Le BD, Stein JL. Mapping causal pathways from genetics to neuropsychiatric disorders using genome-wide imaging genetics: current status and future directions. Psychiatry and Clinical Neurosciences. PMID 30864184 DOI: 10.1111/pcn.12839   
2019 Li J, Teng W, Yu Y, Hou X, Shan Z. Linkage Analysis of the Chromosome 5q31-33 Region Identifies JAKMIP2 as a Risk Factor for Graves' Disease in the Chinese Han Population. Medical Science Monitor : International Medical Journal of Experimental and Clinical Research. 25: 1439-1451. PMID 30796769 DOI: 10.12659/MSM.911489   
2019 Bin Wei Y, McCarthy M, Ren H, Carrillo-Roa T, Shekhtman T, DeModena A, Liu JJ, Leckband SG, Mors O, Rietschel M, Henigsberg N, Cattaneo A, Binder EB, Aitchison KJ, Kelsoe JR. A functional variant in the serotonin receptor 7 gene (HTR7), rs7905446, is associated with good response to SSRIs in bipolar and unipolar depression. Molecular Psychiatry. PMID 30874608 DOI: 10.1038/s41380-019-0397-1   
2019 Lu HF, Hung KS, Chu HW, Wong HS, Kim J, Choi BY, Kim MK, Tai YT, Ikegawa S, Cho EC, Chang WC. A meta-analysis of genome-wide association studies identifies three loci associated with stiffness index of the calcaneus. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 30779856 DOI: 10.1002/jbmr.3703   
2019 Wu Z, Wang Y, Dai Z, Qiu Y, Xu L, Zhu Z. Genetic Variants of ABO and SOX6 are Associated with Adolescent Idiopathic Scoliosis in Chinese Han Population. Spine. PMID 30994600 DOI: 10.1097/BRS.0000000000003062   
2019 Wang C, Deng S, Sun L, Li L, Hu YQ. A nonparametric test for association with multiple loci in the retrospective case-control study. Statistical Methods in Medical Research. 962280219842892. PMID 30987531 DOI: 10.1177/0962280219842892   
2019 Wei CJ, Cui P, Li H, Lang WJ, Liu GY, Ma XF. Shared genes between Alzheimer's disease and ischemic stroke. Cns Neuroscience & Therapeutics. PMID 30859738 DOI: 10.1111/cns.13117   
2019 Safarova MS, Satterfield BA, Fan X, Austin EE, Ye Z, Bastarache L, Zheng N, Ritchie MD, Borthwick KM, Williams MS, Larson EB, Scrol A, Jarvik GP, Crosslin DR, Leppig K, et al. A phenome-wide association study to discover pleiotropic effects of , , and . Npj Genomic Medicine. 4: 3. PMID 30774981 DOI: 10.1038/s41525-019-0078-7   
2019 Mufford M, Cheung J, Jahanshad N, van der Merwe C, Ding L, Groenewold N, Koen N, Chimusa ER, Dalvie S, Ramesar R, , Knowles JA, Lochner C, Hibar DP, Paschou P, et al. Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry. Translational Psychiatry. 9: 120. PMID 30902966 DOI: 10.1038/s41398-019-0452-3   
2019 Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Bellenguez C, Frizatti A, Chouraki V, Martin ER, Sleegers K, ... , ... , ... , ... , et al. Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. 51: 414-430. PMID 30820047 DOI: 10.1038/s41588-019-0358-2   
2019 Irgam K, Reddy BM, Annamaneni S, Rayabarapu P. The genetic susceptibility profile of the South Indian women with polycystic ovary syndrome and the universality of the lack of association of type 2 diabetes genes. Gene. 701: 113-120. PMID 30910557 DOI: 10.1016/j.gene.2019.03.042   
2019 Bhattacharyya C, Majumder PP, Pandit B. An exome wide association study of pulmonary tuberculosis patients and their asymptomatic household contacts. Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases. PMID 30898644 DOI: 10.1016/j.meegid.2019.03.006   
2019 Hellwege JN, Stallings S, Torstenson ES, Carroll R, Borthwick KM, Brilliant MH, Crosslin D, Gordon A, Hripcsak G, Jarvik GP, Linneman JG, Devi P, Peissig PL, Sleiman PAM, Hakonarson H, et al. Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network. Scientific Reports. 9: 6077. PMID 30988330 DOI: 10.1038/s41598-019-42427-z   
2019 Zhang K, Han M, Liu Y, Lin X, Liu X, Zhu H, He Y, Zhang Q, Liu J. Whole-genome resequencing from bulked-segregant analysis reveals gene set based association analyses for the Vibrio anguillarum resistance of turbot (Scophthalmus maximus). Fish & Shellfish Immunology. PMID 30807856 DOI: 10.1016/j.fsi.2019.02.041   
2019 Xin J, Du M, Gu D, Ge Y, Li S, Chu H, Meng Y, Shen H, Zhang Z, Wang M. Combinations of Single Nucleotide Polymorphisms Identified in Genome-wide Association Studies Determine Risk for Colorectal Cancer. International Journal of Cancer. PMID 30859566 DOI: 10.1002/ijc.32267   
2019 Ferreira LE, Secolin R, Lopes-Cendes I, Cabral NL, de França PHC. Association and interaction of genetic variants with occurrence of ischemic stroke among Brazilian patients. Gene. PMID 30738964 DOI: 10.1016/j.gene.2019.01.041   
2019 Cavalli M, Baltzer N, Umer HM, Grau J, Lemnian I, Pan G, Wallerman O, Spalinskas R, Sahlén P, Grosse I, Komorowski J, Wadelius C. Allele specific chromatin signals, 3D interactions, and motif predictions for immune and B cell related diseases. Scientific Reports. 9: 2695. PMID 30804403 DOI: 10.1038/s41598-019-39633-0   
2019 Vadgama N, Pittman A, Simpson M, Nirmalananthan N, Murray R, Yoshikawa T, De Rijk P, Rees E, Kirov G, Hughes D, Fitzgerald T, Kristiansen M, Pearce K, Cerveira E, Zhu Q, et al. De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes. European Journal of Human Genetics : Ejhg. PMID 30886340 DOI: 10.1038/s41431-019-0376-7   
2019 Geng X, Irvin MR, Hidalgo B, Aslibekyan S, Srinivasasainagendra V, An P, Frazier-Wood AC, Tiwari HK, Dave T, Ryan K, Ordovas JM, Straka RJ, Feitosa MF, Hopkins PN, Borecki I, et al. An Exome-Wide Sequencing Study of the GOLDN Cohort Reveals Novel Associations of Coding Variants and Fasting Plasma Lipids. Frontiers in Genetics. 10: 158. PMID 30863429 DOI: 10.3389/fgene.2019.00158   
2019 Yang W, Liu H, Duan B, Xu X, Carmody D, Luo S, Walsh KM, Abbruzzese JL, Zhang X, Chen X, Wei Q. Three novel genetic variants in NRF2 signaling pathway genes are associated with pancreatic cancer risk. Cancer Science. PMID 30972876 DOI: 10.1111/cas.14017   
2019 Richardson TG, Harrison S, Hemani G, Davey Smith G. An atlas of polygenic risk score associations to highlight putative causal relationships across the human phenome. Elife. 8. PMID 30835202 DOI: 10.7554/eLife.43657   
2019 Castellanos-Rubio A, Ghosh S. Disease-Associated SNPs in Inflammation-Related lncRNAs. Frontiers in Immunology. 10: 420. PMID 30906297 DOI: 10.3389/fimmu.2019.00420   
2019 Padula MC, Leccese P, Pellizzieri E, Padula AA, Gilio M, Carbone T, Lascaro N, Tramontano G, Martelli G, D'Angelo S. Distribution of rs17482078 and rs27044 ERAP1 polymorphisms in a group of Italian Behçet's syndrome patients: a preliminary case-control study. Internal and Emergency Medicine. PMID 30820838 DOI: 10.1007/s11739-019-02056-w   
2019 Pirim D, Radwan ZH, Wang X, Niemsiri V, Hokanson JE, Hamman RF, Feingold E, Bunker CH, Demirci FY, Kamboh MI. Apolipoprotein E-C1-C4-C2 gene cluster region and inter-individual variation in plasma lipoprotein levels: a comprehensive genetic association study in two ethnic groups. Plos One. 14: e0214060. PMID 30913229 DOI: 10.1371/journal.pone.0214060   
2019 Wang Q, Chen R, Cheng F, Wei Q, Ji Y, Yang H, Zhong X, Tao R, Wen Z, Sutcliffe JS, Liu C, Cook EH, Cox NJ, Li B. A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data. Nature Neuroscience. PMID 30988527 DOI: 10.1038/s41593-019-0382-7   
2019 Majumder P, Ghosh S, Dey SK. Matrix metalloproteinase gene polymorphisms in chronic periodontitis: a case-control study in the Indian population. Journal of Genetics. 98. PMID 30945680