Irving I. Gottesman, Ph.D. - Related publications

Affiliations: 
University of Virginia, Charlottesville, VA 
 University of Minnesota, Twin Cities, Minneapolis, MN 
Area:
behavioral genetics, schizophrenia
NOTE: We are testing a new system for identifying relevant work based on semantic analysis that identifies similarities between recently published papers and the current author's publications. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches.
50 most relevant papers in past 60 days:
Year Citation  Score
2020 Smeland OB, Frei O, Dale AM, Andreassen OA. The polygenic architecture of schizophrenia - rethinking pathogenesis and nosology. Nature Reviews. Neurology. 16: 366-379. PMID 32528109 DOI: 10.1038/s41582-020-0364-0   
2020 Campbell PD, Granato M. Zebrafish as a tool to study schizophrenia-associated copy number variants. Disease Models & Mechanisms. 13. PMID 32433025 DOI: 10.1242/dmm.043877   
2020 Gao M, Zeng K, Li Y, Liu YP, Xia X, Xu FL, Yao J, Wang BJ. Association between gene polymorphisms and schizophrenia among the Han population in northern China. The Journal of International Medical Research. 48: 300060520932801. PMID 32567430 DOI: 10.1177/0300060520932801   
2020 Bani-Fatemi A, Roy A, Dai N, Dada O, Adanty C, Kiruparajah L, Kolla N, Strauss J, Zai C, Graff A, Gerretsen P, De Luca V. Genome-wide association study of aggression and violence in schizophrenia. Neuroscience Letters. 135061. PMID 32445792 DOI: 10.1016/j.neulet.2020.135061   
2020 Birnbaum R, Weinberger DR. Special Article: Translational Science Update. Pharmacological Implications of Emerging Schizophrenia Genetics: Can the Bridge From 'Genomics' to 'Therapeutics' be Defined and Traversed? Journal of Clinical Psychopharmacology. PMID 32433256 DOI: 10.1097/JCP.0000000000001215   
2020 Xie X, Zu M, Zhang L, Bai T, Wei L, Huang W, Ji GJ, Qiu B, Hu P, Tian Y, Wang K. A common variant of the NOTCH4 gene modulates functional connectivity of the occipital cortex and its relationship with schizotypal traits. Bmc Psychiatry. 20: 363. PMID 32646407 DOI: 10.1186/s12888-020-02773-z   
2020 Peters T, Nüllig L, Antel J, Naaresh R, Laabs BH, Tegeler L, Amhaouach C, Libuda L, Hinney A, Hebebrand J. The Role of Genetic Variation of BMI, Body Composition, and Fat Distribution for Mental Traits and Disorders: A Look-Up and Mendelian Randomization Study. Frontiers in Genetics. 11: 373. PMID 32373164 DOI: 10.3389/fgene.2020.00373   
2020 Frajman A, Maggio N, Muler I, Haroutunian V, Katsel P, Yitzhaky A, Weiser M, Hertzberg L. Gene expression meta-analysis reveals the down-regulation of three GABA receptor subunits in the superior temporal gyrus of patients with schizophrenia. Schizophrenia Research. PMID 32376074 DOI: 10.1016/j.schres.2020.04.027   
2020 Koch E, Rosenthal B, Lundquist A, Chen CH, Kauppi K. Interactome overlap between schizophrenia and cognition. Schizophrenia Research. PMID 32546371 DOI: 10.1016/j.schres.2020.06.002   
2020 Zhou J, Ma C, Wang K, Li X, Jian X, Zhang H, Yuan J, Yin J, Chen J, Shi Y. Identification of rare and common variants in BNIP3L: a schizophrenia susceptibility gene. Human Genomics. 14: 16. PMID 32393399 DOI: 10.1186/s40246-020-00266-4   
2020 Su P, Zhang H, Wong AHC, Liu F. The DISC1 R264Q variant increases affinity for the dopamine D2 receptor and increases GSK3 activity. Molecular Brain. 13: 87. PMID 32493513 DOI: 10.1186/s13041-020-00625-1   
2020 Yang Y, Zhang L, Guo D, Zhang L, Yu H, Liu Q, Su X, Shao M, Song M, Zhang Y, Ding M, Lu Y, Liu B, Li W, Yue W, et al. Association of With Schizophrenia: Findings From Two Independent Samples of Han Chinese Population. Frontiers in Psychiatry. 11: 446. PMID 32581860 DOI: 10.3389/fpsyt.2020.00446   
2020 Chaumette B, Sengupta SM, Lepage M, Malla A, Iyer SN, Kebir O, , Dion PA, Rouleau GA, Krebs MO, Shah JL, Joober R. A polymorphism in the glutamate metabotropic receptor 7 is associated with cognitive deficits in the early phases of psychosis. Schizophrenia Research. PMID 32624350 DOI: 10.1016/j.schres.2020.06.019   
2020 Tao R, Li C, Jaffe AE, Shin JH, Deep-Soboslay A, Yamin R, Weinberger DR, Hyde TM, Kleinman JE. Cannabinoid receptor CNR1 expression and DNA methylation in human prefrontal cortex, hippocampus and caudate in brain development and schizophrenia. Translational Psychiatry. 10: 158. PMID 32433545 DOI: 10.1038/s41398-020-0832-8   
2020 Hederih J, Nuninga JO, van Eijk K, van Dellen E, Smit DJA, Oranje B, Luykx JJ. Genetic underpinnings of schizophrenia-related electroencephalographical intermediate phenotypes: A systematic review and meta-analysis. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 110001. PMID 32525059 DOI: 10.1016/j.pnpbp.2020.110001   
2020 Su Y, Yang L, Li Z, Wang W, Xing M, Fang J, Cheng Y, Lin G, Cui D. The interaction of ASAH1 and NGF gene involving in neurotrophin signaling pathway contributes to schizophrenia susceptibility and psychopathology. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 110015. PMID 32569620 DOI: 10.1016/j.pnpbp.2020.110015   
2020 Nguyen TH, Dobbyn A, Brown RC, Riley BP, Buxbaum JD, Pinto D, Purcell SM, Sullivan PF, He X, Stahl EA. mTADA is a framework for identifying risk genes from de novo mutations in multiple traits. Nature Communications. 11: 2929. PMID 32522981 DOI: 10.1038/s41467-020-16487-z   
2020 Yoshida K, Müller DJ. Pharmacogenetics of Antipsychotic Drug Treatment: Update and Clinical Implications. Molecular Neuropsychiatry. 5: 1-26. PMID 32399466 DOI: 10.1159/000492332   
2020 Liu X, Nudel R, Thompson WK, Appadurai V, Schork AJ, Buil A, Rasmussen S, Allesøe RL, Werge T, Mors O, Børglum AD, Hougaard DM, Mortensen PB, Nordentoft M, Benros ME. Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - findings from a Danish population-based study. Brain, Behavior, and Immunity. PMID 32534018 DOI: 10.1016/j.bbi.2020.06.014   
2020 Accogli A, Eric Jarvis G, Schiavetto A, Lai L, Amirali EL, Jimenez Cruz DA, Rivière JB, Trakadis Y. Psychiatric features and variable neurodevelopment outcome in four females with IQSEC2 spectrum disorder. Journal of Genetics. 99. PMID 32529990   
2020 Bulik C, Kennedy M, Wade T. ANGI - Anorexia Nervosa Genetics Initiative. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 1-2. PMID 32482201 DOI: 10.1017/thg.2020.24   
2020 Finucane BM, Myers SM, Martin CL, Ledbetter DH. Long overdue: including adults with brain disorders in precision health initiatives. Current Opinion in Genetics & Development. 65: 47-52. PMID 32544666 DOI: 10.1016/j.gde.2020.05.001   
2020 Martinez AP, Wickham S, Rowse G, Milne E, Bentall RP. Robust association between autistic traits and psychotic-like experiences in the adult general population: epidemiological study from the 2007 Adult Psychiatric Morbidity Survey and replication with the 2014 APMS. Psychological Medicine. 1-7. PMID 32441234 DOI: 10.1017/S0033291720001373   
2020 Crespi BJ. Evolutionary and genetic insights for clinical psychology. Clinical Psychology Review. 78: 101857. PMID 32371239 DOI: 10.1016/j.cpr.2020.101857   
2020 Wu Y, Cao H, Baranova A, Huang H, Li S, Cai L, Rao S, Dai M, Xie M, Dou Y, Hao Q, Zhu L, Zhang X, Yao Y, Xu M, et al. Multi-trait analysis for genome-wide association study of five psychiatric disorders. Translational Psychiatry. 10: 209. PMID 32606422 DOI: 10.1038/s41398-020-00902-6   
2020 Kibinge NK, Relton CL, Gaunt TR, Richardson TG. Characterizing the Causal Pathway for Genetic Variants Associated with Neurological Phenotypes Using Human Brain-Derived Proteome Data. American Journal of Human Genetics. PMID 32413284 DOI: 10.1016/j.ajhg.2020.04.007   
2020 Yang XP, Yan C, Yuan Z, Zhou J, Miao JX, He R, Zhu G. Association study of SNCA gene polymorphisms with schizophrenia in a Chinese North Han population. European Review For Medical and Pharmacological Sciences. 24: 4979-4987. PMID 32432761 DOI: 10.26355/eurrev_202005_21189   
2020 Zhang C, Xiao X, Li T, Li M. Translational genomics and beyond in bipolar disorder. Molecular Psychiatry. PMID 32424235 DOI: 10.1038/s41380-020-0782-9   
2020 Torrico B, Antón-Galindo E, Fernàndez-Castillo N, Rojo-Francàs E, Ghorbani S, Pineda-Cirera L, Hervás A, Rueda I, Moreno E, Fullerton JM, Casadó V, Buitelaar JK, Rommelse N, Franke B, Reif A, et al. Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses. Journal of Clinical Medicine. 9. PMID 32545830 DOI: 10.3390/jcm9061851   
2020 Accogli A, Severino M, Riva A, Madia F, Balagura G, Iacomino M, Carlini B, Baldassari S, Giacomini T, Croci C, Pisciotta L, Messana T, Boni A, Russo A, Bilo L, et al. Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations. Seizure. 80: 145-152. PMID 32570172 DOI: 10.1016/j.seizure.2020.05.023   
2020 Brown SJ, Elias MS, Bradley M. Genetics in Atopic Dermatitis: Historical Perspective and Future Prospects. Acta Dermato-Venereologica. PMID 32412647 DOI: 10.2340/00015555-3513   
2020 Zhou H, Sealock JM, Sanchez-Roige S, Clarke TK, Levey DF, Cheng Z, Li B, Polimanti R, Kember RL, Smith RV, Thygesen JH, Morgan MY, Atkinson SR, Thursz MR, Nyegaard M, et al. Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. Nature Neuroscience. PMID 32451486 DOI: 10.1038/s41593-020-0643-5   
2020 Zhang M, Liu N, Chen H, Zhang N. Oxytocin receptor gene, childhood maltreatment and borderline personality disorder features among male inmates in China. Bmc Psychiatry. 20: 332. PMID 32580785 DOI: 10.1186/s12888-020-02710-0   
2020 Fedorenko OY, Paderina DZ, Loonen AJM, Pozhidaev IV, Boiko AS, Kornetova EG, Bokhan NA, Wilffert B, Ivanova SA. Association of ANKK1 polymorphism with antipsychotic-induced hyperprolactinemia. Human Psychopharmacology. e2737. PMID 32383805 DOI: 10.1002/hup.2737   
2020 Yurko R, G'Sell M, Roeder K, Devlin B. A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk. Proceedings of the National Academy of Sciences of the United States of America. PMID 32522875 DOI: 10.1073/pnas.1918862117   
2020 Srivastava A. Diagnosis of haemophilia and other inherited bleeding disorders - Is a new paradigm needed? Haemophilia : the Official Journal of the World Federation of Hemophilia. PMID 32537805 DOI: 10.1111/hae.14042   
2020 Lewis CM, Vassos E. Polygenic risk scores: from research tools to clinical instruments. Genome Medicine. 12: 44. PMID 32423490 DOI: 10.1186/s13073-020-00742-5   
2020 Jiang X, Alfredsson L. Modifiable environmental exposure and risk of rheumatoid arthritis-current evidence from genetic studies. Arthritis Research & Therapy. 22: 154. PMID 32571398 DOI: 10.1186/s13075-020-02253-5   
2020 Brown EE, Sturm AC, Cuchel M, Braun LT, Duell PB, Underberg JA, Jacobson TA, Hegele RA. Genetic testing in dyslipidemia: A scientific statement from the National Lipid Association. Journal of Clinical Lipidology. PMID 32507592 DOI: 10.1016/j.jacl.2020.04.011   
2020 Mighell TL, Thacker S, Fombonne E, Eng C, O'Roak BJ. An Integrated Deep-Mutational-Scanning Approach Provides Clinical Insights on PTEN Genotype-Phenotype Relationships. American Journal of Human Genetics. PMID 32442409 DOI: 10.1016/j.ajhg.2020.04.014   
2020 Rafi SK, Butler MG. The 15q11.2 BP1-BP2 Microdeletion () Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Phenotypes. International Journal of Molecular Sciences. 21. PMID 32384786 DOI: 10.3390/ijms21093296   
2020 Liu H, Sun Y, Zhang X, Li S, Hu D, Xiao L, Chen Y, He L, Wang DW. Integrated Analysis of Summary Statistics to Identify Pleiotropic Genes and Pathways for the Comorbidity of Schizophrenia and Cardiometabolic Disease. Frontiers in Psychiatry. 11: 256. PMID 32425817 DOI: 10.3389/fpsyt.2020.00256   
2020 Ghafouri-Fard S, Noroozi R, Vafaee R, Branicki W, Poṡpiech E, Pyrc K, Łabaj PP, Omrani MD, Taheri M, Sanak M. Effects of host genetic variations on response to, susceptibility and severity of respiratory infections. Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie. 128: 110296. PMID 32480226 DOI: 10.1016/j.biopha.2020.110296   
2020 Lin H, Wang F, Rosato AJ, Farrer LA, Henderson DC, Zhang H. Prefrontal cortex eQTLs/mQTLs enriched in genetic variants associated with alcohol use disorder and other diseases. Epigenomics. PMID 32496132 DOI: 10.2217/epi-2019-0270   
2020 Fears SC, Service SK, Kremeyer B, Araya C, Araya X, Bejarano J, Ramirez M, Castrillón G, Gomez-Franco J, Lopez MC, Montoya G, Montoya P, Aldana I, Teshiba TM, Al-Sharif NB, et al. Genome-wide mapping of brain phenotypes in extended pedigrees with strong genetic loading for bipolar disorder. Molecular Psychiatry. PMID 32606377 DOI: 10.1038/s41380-020-0805-6   
2020 Ning Z, Pawitan Y, Shen X. High-definition likelihood inference of genetic correlations across human complex traits. Nature Genetics. PMID 32601477 DOI: 10.1038/s41588-020-0653-y   
2020 Campuzano O, Sarquella-Brugada G, Arbelo E, Cesar S, Jordà P, Pérez-Serra A, Toro R, Brugada J, Brugada R. Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic Interpretation. Journal of Clinical Medicine. 9. PMID 32549272 DOI: 10.3390/jcm9061866   
2020 Park S, Daily JW, Song MY, Kwon HK. Gene-gene and gene-lifestyle interactions of AKAP11, KCNMA1, PUM1, SPTBN1, and EPDR1 on osteoporosis risk in middle-aged adults. Nutrition (Burbank, Los Angeles County, Calif.). 79: 110859. PMID 32619791 DOI: 10.1016/j.nut.2020.110859   
2020 Hughes DA, Bacigalupe R, Wang J, Rühlemann MC, Tito RY, Falony G, Joossens M, Vieira-Silva S, Henckaerts L, Rymenans L, Verspecht C, Ring S, Franke A, Wade KH, Timpson NJ, et al. Genome-wide associations of human gut microbiome variation and implications for causal inference analyses. Nature Microbiology. PMID 32572223 DOI: 10.1038/s41564-020-0743-8   
2020 McAuley ABT, Hughes DC, Tsaprouni LG, Varley I, Suraci B, Roos TR, Herbert AJ, Kelly AL. Genetic association research in football: a systematic review. European Journal of Sport Science. 1-52. PMID 32466725 DOI: 10.1080/17461391.2020.1776401