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

University of Virginia, Charlottesville, VA 
 University of Minnesota, Twin Cities, Minneapolis, MN 
behavioral genetics, schizophrenia
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50 most relevant papers in past 60 days:
Year Citation  Score
2020 Xu FL, Yao J, Wu X, Xia X, Xing JX, Xuan JF, Liu YP, Wang BJ. Association Analysis Between SNPs in the Promoter Region of and Schizophrenia in the Northern Chinese Han Population. Neuropsychiatric Disease and Treatment. 16: 985-992. PMID 32346293 DOI: 10.2147/NDT.S250282   
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 Wu Y, Li X, Liu J, Luo XJ, Yao YG. SZDB2.0: an updated comprehensive resource for schizophrenia research. Human Genetics. PMID 32385526 DOI: 10.1007/s00439-020-02171-1   
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 Zeng K, Li Y, Gao M, Liu YP, Xu FL, Xia X, Yao J, Wang BJ. Association of ADH7 Gene Polymorphism with Schizophrenia in the Han Population of Northern China: a Case-Control Study. Journal of Molecular Neuroscience : Mn. PMID 32388801 DOI: 10.1007/s12031-020-01578-9   
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 Mealer RG, Williams SE, Daly MJ, Scolnick EM, Cummings RD, Smoller JW. Glycobiology and schizophrenia: a biological hypothesis emerging from genomic research. Molecular Psychiatry. PMID 32377000 DOI: 10.1038/s41380-020-0753-1   
2020 Halvorsen M, Huh R, Oskolkov N, Wen J, Netotea S, Giusti-Rodriguez P, Karlsson R, Bryois J, Nystedt B, Ameur A, Kähler AK, Ancalade N, Farrell M, Crowley JJ, Li Y, et al. Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. Nature Communications. 11: 1842. PMID 32296054 DOI: 10.1038/s41467-020-15707-w   
2020 Liu L, Wu J, Qing L, Li J, Yang H, Ji A, Yan M, Hu L, Nie S. DNA Methylation Analysis of the NR3C1 Gene in Patients with Schizophrenia. Journal of Molecular Neuroscience : Mn. PMID 32281042 DOI: 10.1007/s12031-020-01525-8   
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 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 Hook PW, McCallion AS. Leveraging mouse chromatin data for heritability enrichment informs common disease architecture and reveals cortical layer contributions to schizophrenia. Genome Research. 30: 528-539. PMID 32303558 DOI: 10.1101/gr.256578.119   
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 Hall LS, Pain O, O'Brien HE, Anney R, Walters JTR, Owen MJ, O'Donovan MC, Bray NJ. Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders. Molecular Psychiatry. PMID 32366953 DOI: 10.1038/s41380-020-0743-3   
2020 Li XN, Zheng JL, Wei XH, Wang BJ, Yao J. No association between the Ser9Gly polymorphism of the dopamine receptor D3 gene and schizophrenia: a meta-analysis of family-based association studies. Bmc Medical Genetics. 21: 85. PMID 32316934 DOI: 10.1186/s12881-020-01018-w   
2020 Zhou J, Ma C, Wang K, Li X, Zhang H, Chen J, Li Z, Shi Y. Rare and common variants analysis of the EMB gene in patients with schizophrenia. Bmc Psychiatry. 20: 135. PMID 32213169 DOI: 10.1186/s12888-020-02513-3   
2020 Chang JP, Huang KH, Lin CH, Lane HY. Genetic Effects and on Visual Learning of Patients with Schizophrenia. Neuropsychiatric Disease and Treatment. 16: 771-780. PMID 32256073 DOI: 10.2147/NDT.S235675   
2020 Imamura A, Morimoto Y, Ono S, Kurotaki N, Kanegae S, Yamamoto N, Kinoshita H, Tsujita T, Okazaki Y, Ozawa H. Genetic and environmental factors of schizophrenia and autism spectrum disorder: insights from twin studies. Journal of Neural Transmission (Vienna, Austria : 1996). PMID 32285255 DOI: 10.1007/s00702-020-02188-w   
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 Jacobs A, Hagin M, Shugol M, Shomron N, Pillar N, Fañanás L, Serretti A, Vieta E, Popovic D. The black sheep of the family- whole-exome sequencing in family of lithium response discordant bipolar monozygotic twins. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 34: 19-27. PMID 32305265 DOI: 10.1016/j.euroneuro.2020.03.009   
2020 Courtois E, Schmid M, Wajsbrot O, Barau C, Le Corvoisier P, Aouizerate B, Bellivier F, Belzeaux R, Dubertret C, Kahn JP, Leboyer M, Olie E, Passerieux C, Polosan M, Etain B, ... , et al. Contribution of common and rare damaging variants in familial forms of bipolar disorder and phenotypic outcome. Translational Psychiatry. 10: 124. PMID 32345981 DOI: 10.1038/s41398-020-0783-0   
2020 Maes MS, Lu JY, Tiwari AK, Freeman N, de Luca V, Müller DJ, Voineskos AN, Potkin SG, Lieberman JA, Meltzer HY, Remington G, Kennedy JL, Zai CC. Schizophrenia-associated gene dysbindin-1 and tardive dyskinesia. Drug Development Research. PMID 32394511 DOI: 10.1002/ddr.21681   
2020 Baker M, Hong SI, Kang S, Choi DS. Rodent models for psychiatric disorders: problems and promises. Laboratory Animal Research. 36: 9. PMID 32322555 DOI: 10.1186/s42826-020-00039-z   
2020 Sanchez-Roige S, Palmer AA. Emerging phenotyping strategies will advance our understanding of psychiatric genetics. Nature Neuroscience. 23: 475-480. PMID 32231337 DOI: 10.1038/s41593-020-0609-7   
2020 Zhao W, Zhang Q, Chen X, Li Y, Li X, Du B, Deng X, Ji F, Wang C, Xiang YT, Dong Q, Chen C, Li J. The VNTR of the gene is associated with brain activations during a memory span task and their training-induced plasticity. Psychological Medicine. 1-6. PMID 32308175 DOI: 10.1017/S0033291720000720   
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 Komatsu H, Takeuchi H, Kikuchi Y, Ono C, Yu Z, Iizuka K, Takano Y, Kakuto Y, Funakoshi S, Ono T, Ito J, Kunii Y, Hino M, Nagaoka A, Iwasaki Y, et al. Ethnicity-Dependent Effects of Schizophrenia Risk Variants of the OLIG2 Gene on OLIG2 Transcription and White Matter Integrity. Schizophrenia Bulletin. PMID 32285113 DOI: 10.1093/schbul/sbaa049   
2020 Rodrigue AL, Alexander-Bloch AF, Knowles EEM, Mathias SR, Mollon J, Koenis MMG, Perrone-Bizzozero NI, Almasy L, Turner JA, Calhoun VD, Glahn DC. Genetic Contributions to Multivariate Data-Driven Brain Networks Constructed via Source-Based Morphometry. Cerebral Cortex (New York, N.Y. : 1991). PMID 32318716 DOI: 10.1093/cercor/bhaa082   
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 Gao JY, Ma P, Li Y, Yan CX, Zhang Q, Yang XX, Shi Q, Zhang B, Wen XP. Association between a Polymorphism and Susceptibility to Schizophrenia. Biomed Research International. 2020: 1216303. PMID 32280673 DOI: 10.1155/2020/1216303   
2020 Zhang J, Xie S, Gonzales S, Liu J, Wang X. A fast and powerful eQTL weighted method to detect genes associated with complex trait using GWAS summary data. Genetic Epidemiology. PMID 32350919 DOI: 10.1002/gepi.22297   
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 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 Sjaarda CP, Kaiser B, McNaughton AJ, Hudson ML, Harris-Lowe L, Lou K, Guerin A, Ayub M, Liu X. duplication on chromosome 19 observed in nuclear family displaying neurodevelopmental disorders. Cold Spring Harbor Molecular Case Studies. PMID 32321736 DOI: 10.1101/mcs.a004721   
2020 Boks MP, He Y, Schubart CD, van Gastel W, Elkrief L, Huguet G, van Eijk K, Vinkers CH, Kahn RS, Paus T, Conrod P, Hol EM, de Witte LD. Cannabinoids and psychotic symptoms: A potential role for a genetic variant in the P2X purinoceptor 7 (P2RX7) gene. Brain, Behavior, and Immunity. PMID 32330591 DOI: 10.1016/j.bbi.2020.04.051   
2020 Chen J, Cao H, Kaufmann T, Westlye LT, Tost H, Meyer-Lindenberg A, Schwarz E. Identification of Reproducible BCL11A Alterations in Schizophrenia Through Individual-Level Prediction of Coexpression. Schizophrenia Bulletin. PMID 32232389 DOI: 10.1093/schbul/sbaa047   
2020 Li R, Chen Y, Ritchie MD, Moore JH. Electronic health records and polygenic risk scores for predicting disease risk. Nature Reviews. Genetics. PMID 32235907 DOI: 10.1038/s41576-020-0224-1   
2020 Mazzarotto F, Olivotto I, Boschi B, Girolami F, Poggesi C, Barton PJR, Walsh R. Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing? Journal of the American Heart Association. 9: e015473. PMID 32306808 DOI: 10.1161/JAHA.119.015473   
2020 Barr PB, Salvatore JE, Wetherill L, Anokhin A, Chan G, Edenberg HJ, Kuperman S, Meyers J, Nurnberger J, Porjesz B, Schuckit M, Dick DM. A Family-Based Genome Wide Association Study of Externalizing Behaviors. Behavior Genetics. PMID 32239439 DOI: 10.1007/s10519-020-09999-3   
2020 Winder TL, Tan CA, Klemm S, White H, Westbrook JM, Wang JZ, Entezam A, Truty R, Nussbaum RL, McNally EM, Aradhya S. Clinical utility of multigene analysis in over 25,000 patients with neuromuscular disorders. Neurology. Genetics. 6: e412. PMID 32337338 DOI: 10.1212/NXG.0000000000000412   
2020 Chang HA, Fang WH, Liu YP, Tzeng NS, Shyu JF, Wan FJ, Huang SY, Chang TC, Chang CC. Sex-specific pathways among tri-allelic serotonin transporter polymorphism, trait neuroticism and generalized anxiety disorder. Journal of Psychiatry & Neuroscience : Jpn. 45: 190092. PMID 32293839 DOI: 10.1503/jpn.190092   
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 Bralten J, Widomska J, Witte W, Yu D, Mathews CA, Scharf JM, Buitelaar J, Crosbie J, Schachar R, Arnold P, Lemire M, Burton CL, Franke B, Poelmans G. Shared genetic etiology between obsessive-compulsive disorder, obsessive-compulsive symptoms in the population, and insulin signaling. Translational Psychiatry. 10: 121. PMID 32341337 DOI: 10.1038/s41398-020-0793-y   
2020 Calabrò M, Mandelli L, Crisafulli C, Nicola MD, Colombo R, Janiri L, Lee SJ, Jun TY, Wang SM, Masand PS, Patkar AA, Han C, Pae CU, Serretti A. Gene Variants Have a Cross-diagnostic Influence on Psychosis and Treatment Improvement in Mood Disorders. Clinical Psychopharmacology and Neuroscience : the Official Scientific Journal of the Korean College of Neuropsychopharmacology. 18: 231-240. PMID 32329304 DOI: 10.9758/cpn.2020.18.2.231   
2020 Cunha MFM, Sevignani G, Pavanelli GM, Carvalho M, Barreto FC. Rare inherited kidney diseases: an evolving field in Nephrology. Jornal Brasileiro De Nefrologia : 'Orgao Oficial De Sociedades Brasileira E Latino-Americana De Nefrologia. PMID 32227072 DOI: 10.1590/2175-8239-JBN-2018-0217   
2020 DeBoever C, Tanigawa Y, Aguirre M, McInnes G, Lavertu A, Rivas MA. Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases. American Journal of Human Genetics. PMID 32275883 DOI: 10.1016/j.ajhg.2020.03.007   
2020 Kawai VK, Shi M, Feng Q, Chung CP, Liu G, Cox NJ, Jarvik GP, Lee MTM, Hebbring SJ, Harley JB, Kaufman KM, Namjou B, Larson E, Gordon AS, Roden DM, ... , et al. Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis - a phenome-wide association study and inverse-variance weighted meta-analysis. Arthritis & Rheumatology (Hoboken, N.J.). PMID 32307929 DOI: 10.1002/art.41291   
2020 Mostafa T, Taymour M. Gene Polymorphisms Affecting Erectile Dysfunction. Sexual Medicine Reviews. PMID 32169432 DOI: 10.1016/j.sxmr.2020.02.001   
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 Sturchio A, Marsili L, Mahajan A, Grimberg B, Kauffman MA, Espay AJ. How Have Advances in Genetic Technology Modified Movement Disorders Nosology? European Journal of Neurology. PMID 32356310 DOI: 10.1111/ene.14294