Barlow DH, Ellard KK, Sauer-Zavala S, Bullis JR, Carl JR (2014) The origins of neuroticism. Perspect Psychol Sci 9:481–496. https://doi.org/10.1177/1745691614544528
Article
PubMed
Google Scholar
Bidwell LC, McGeary JE, Gray JC, Palmer RH, Knopik VS, MacKillop J (2015) NCAM1-TTC12-ANKK1-DRD2 variants and smoking motives as intermediate phenotypes for nicotine dependence. Psychopharmacology 232:1177–1186. https://doi.org/10.1007/s00213-014-3748-2
CAS
Article
PubMed
Google Scholar
Brainstorm C, Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, Lee PH, Turley P, Grenier-Boley B, Chouraki V, Kamatani Y, Berr C, Letenneur L, Hannequin D, Amouyel P, Boland A, Deleuze JF, Duron E, Vardarajan BN, Reitz C, Goate AM, Huentelman MJ, Kamboh MI, Larson EB, Rogaeva E, St George-Hyslop P, Hakonarson H, Kukull WA, Farrer LA, Barnes LL, Beach TG, Demirci FY, Head E, Hulette CM, Jicha GA, Kauwe JSK, Kaye JA, Leverenz JB, Levey AI, Lieberman AP, Pankratz VS, Poon WW, Quinn JF, Saykin AJ, Schneider LS, Smith AG, Sonnen JA, Stern RA, Van Deerlin VM, Van Eldik LJ, Harold D, Russo G, Rubinsztein DC, Bayer A, Tsolaki M, Proitsi P, Fox NC, Hampel H, Owen MJ, Mead S, Passmore P, Morgan K, Nothen MM, Rossor M, Lupton MK, Hoffmann P, Kornhuber J, Lawlor B, McQuillin A, Al-Chalabi A, Bis JC, Ruiz A, Boada M, Seshadri S, Beiser A, Rice K, van der Lee SJ, De Jager PL, Geschwind DH, Riemenschneider M, Riedel-Heller S, Rotter JI, Ransmayr G, Hyman BT, Cruchaga C, Alegret M, Winsvold B, Palta P, Farh KH, Cuenca-Leon E, Furlotte N et al (2018) Analysis of shared heritability in common disorders of the brain. Science. https://doi.org/10.1126/science.aap8757
Article
Google Scholar
Buckley PF, Miller BJ, Lehrer DS, Castle DJ (2009) Psychiatric comorbidities and schizophrenia. Schizophr Bull 35:383–402. https://doi.org/10.1093/schbul/sbn135
Article
PubMed
Google Scholar
Cai L, Wan CL, He L, de Jong S, Chou KC (2015) Gestational influenza increases the risk of psychosis in adults. Med Chem 11:676–682
CAS
Article
Google Scholar
Cai L, Huang T, Su J, Zhang X, Chen W, Zhang F, He L, Chou KC (2018) Implications of newly identified brain eQTL genes and their interactors in schizophrenia. Mol Ther Nucleic Acids 12:433–442. https://doi.org/10.1016/j.omtn.2018.05.026
CAS
Article
PubMed
PubMed Central
Google Scholar
Corfield EC, Yang Y, Martin NG, Nyholt DR (2017) A continuum of genetic liability for minor and major depression. Transl Psychiatry 7:e1131. https://doi.org/10.1038/tp.2017.99
CAS
Article
PubMed
PubMed Central
Google Scholar
Cross-Disorder Group of the Psychiatric Genomics C (2013) Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. Lancet 381:1371–1379. https://doi.org/10.1016/S0140-6736(12)62129-1
CAS
Article
Google Scholar
Cross-Disorder Group of the Psychiatric Genomics C, Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, Andreassen OA, Anjorin A, Anney R, Anttila V, Arking DE, Asherson P, Azevedo MH, Backlund L, Badner JA, Bailey AJ, Banaschewski T, Barchas JD, Barnes MR, Barrett TB, Bass N, Battaglia A, Bauer M, Bayes M, Bellivier F, Bergen SE, Berrettini W, Betancur C, Bettecken T, Biederman J, Binder EB, Black DW, Blackwood DH, Bloss CS, Boehnke M, Boomsma DI, Breen G, Breuer R, Bruggeman R, Cormican P, Buccola NG, Buitelaar JK, Bunney WE, Buxbaum JD, Byerley WF, Byrne EM, Caesar S, Cahn W, Cantor RM, Casas M, Chakravarti A, Chambert K, Choudhury K, Cichon S, Cloninger CR, Collier DA, Cook EH, Coon H, Cormand B, Corvin A, Coryell WH, Craig DW, Craig IW, Crosbie J, Cuccaro ML, Curtis D, Czamara D, Datta S, Dawson G, Day R, De Geus EJ, Degenhardt F, Djurovic S, Donohoe GJ, Doyle AE, Duan J, Dudbridge F, Duketis E, Ebstein RP, Edenberg HJ, Elia J, Ennis S, Etain B, Fanous A, Farmer AE, Ferrier IN, Flickinger M, Fombonne E, Foroud T, Frank J, Franke B et al (2013) Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 45:984–994. https://doi.org/10.1038/ng.2711
CAS
Article
Google Scholar
Deguchi S, Katsushima K, Hatanaka A, Shinjo K, Ohka F, Wakabayashi T, Zong H, Natsume A, Kondo Y (2017) Oncogenic effects of evolutionarily conserved noncoding RNA ECONEXIN on gliomagenesis. Oncogene 36:4629–4640. https://doi.org/10.1038/onc.2017.88
CAS
Article
PubMed
Google Scholar
Demontis D, Walters RK, Martin J, Mattheisen M, Als TD, Agerbo E, Baldursson G, Belliveau R, Bybjerg-Grauholm J, Baekvad-Hansen M, Cerrato F, Chambert K, Churchhouse C, Dumont A, Eriksson N, Gandal M, Goldstein JI, Grasby KL, Grove J, Gudmundsson OO, Hansen CS, Hauberg ME, Hollegaard MV, Howrigan DP, Huang H, Maller JB, Martin AR, Martin NG, Moran J, Pallesen J, Palmer DS, Pedersen CB, Pedersen MG, Poterba T, Poulsen JB, Ripke S, Robinson EB, Satterstrom FK, Stefansson H, Stevens C, Turley P, Walters GB, Won H, Wright MJ, Consortium AWGotPG, Early L, Genetic Epidemiology C, andMe Research T, Andreassen OA, Asherson P, Burton CL, Boomsma DI, Cormand B, Dalsgaard S, Franke B, Gelernter J, Geschwind D, Hakonarson H, Haavik J, Kranzler HR, Kuntsi J, Langley K, Lesch KP, Middeldorp C, Reif A, Rohde LA, Roussos P, Schachar R, Sklar P, Sonuga-Barke EJS, Sullivan PF, Thapar A, Tung JY, Waldman ID, Medland SE, Stefansson K, Nordentoft M, Hougaard DM, Werge T, Mors O, Mortensen PB, Daly MJ, Faraone SV, Borglum AD, Neale BM (2019) Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nat Genet 51:63–75. https://doi.org/10.1038/s41588-018-0269-7
CAS
Article
PubMed
Google Scholar
Direk N, Williams S, Smith JA, Ripke S, Air T, Amare AT, Amin N, Baune BT, Bennett DA, Blackwood DHR, Boomsma D, Breen G, Buttenschon HN, Byrne EM, Borglum AD, Castelao E, Cichon S, Clarke TK, Cornelis MC, Dannlowski U, De Jager PL, Demirkan A, Domenici E, van Duijn CM, Dunn EC, Eriksson JG, Esko T, Faul JD, Ferrucci L, Fornage M, de Geus E, Gill M, Gordon SD, Grabe HJ, van Grootheest G, Hamilton SP, Hartman CA, Heath AC, Hek K, Hofman A, Homuth G, Horn C, Jan Hottenga J, Kardia SLR, Kloiber S, Koenen K, Kutalik Z, Ladwig KH, Lahti J, Levinson DF, Lewis CM, Lewis G, Li QS, Llewellyn DJ, Lucae S, Lunetta KL, MacIntyre DJ, Madden P, Martin NG, McIntosh AM, Metspalu A, Milaneschi Y, Montgomery GW, Mors O, Mosley TH Jr, Murabito JM, Muller-Myhsok B, Nothen MM, Nyholt DR, O’Donovan MC, Penninx BW, Pergadia ML, Perlis R, Potash JB, Preisig M, Purcell SM, Quiroz JA, Raikkonen K, Rice JP, Rietschel M, Rivera M, Schulze TG, Shi J, Shyn S, Sinnamon GC, Smit JH, Smoller JW, Snieder H, Tanaka T, Tansey KE, Teumer A, Uher R, Umbricht D, Van der Auwera S, Ware EB, Weir DR, Weissman MM, Willemsen G, Yang J, Zhao W et al (2017) An analysis of two genome-wide association meta-analyses identifies a new locus for broad depression phenotype. Biol Psychiatry 82:322–329. https://doi.org/10.1016/j.biopsych.2016.11.013
CAS
Article
PubMed
Google Scholar
Ducci F, Kaakinen M, Pouta A, Hartikainen AL, Veijola J, Isohanni M, Charoen P, Coin L, Hoggart C, Ekelund J, Peltonen L, Freimer N, Elliott P, Schumann G, Jarvelin MR (2011) TTC12-ANKK1-DRD2 and CHRNA5-CHRNA3-CHRNB4 influence different pathways leading to smoking behavior from adolescence to mid-adulthood. Biol Psychiatry 69:650–660. https://doi.org/10.1016/j.biopsych.2010.09.055
CAS
Article
PubMed
Google Scholar
Fagerberg L, Hallstrom BM, Oksvold P, Kampf C, Djureinovic D, Odeberg J, Habuka M, Tahmasebpoor S, Danielsson A, Edlund K, Asplund A, Sjostedt E, Lundberg E, Szigyarto CA, Skogs M, Takanen JO, Berling H, Tegel H, Mulder J, Nilsson P, Schwenk JM, Lindskog C, Danielsson F, Mardinoglu A, Sivertsson A, von Feilitzen K, Forsberg M, Zwahlen M, Olsson I, Navani S, Huss M, Nielsen J, Ponten F, Uhlen M (2014) Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. Mol Cell Proteomics 13:397–406. https://doi.org/10.1074/mcp.M113.035600
CAS
Article
PubMed
Google Scholar
Flavell SW, Cowan CW, Kim TK, Greer PL, Lin Y, Paradis S, Griffith EC, Hu LS, Chen C, Greenberg ME (2006) Activity-dependent regulation of MEF2 transcription factors suppresses excitatory synapse number. Science 311:1008–1012. https://doi.org/10.1126/science.1122511
CAS
Article
PubMed
Google Scholar
Gelernter J, Yu Y, Weiss R, Brady K, Panhuysen C, Yang BZ, Kranzler HR, Farrer L (2006) Haplotype spanning TTC12 and ANKK1, flanked by the DRD2 and NCAM1 loci, is strongly associated to nicotine dependence in two distinct American populations. Hum Mol Genet 15:3498–3507. https://doi.org/10.1093/hmg/ddl426
CAS
Article
PubMed
Google Scholar
Gore FM, Bloem PJ, Patton GC, Ferguson J, Joseph V, Coffey C, Sawyer SM, Mathers CD (2011) Global burden of disease in young people aged 10–24 years: a systematic analysis. Lancet 377:2093–2102. https://doi.org/10.1016/S0140-6736(11)60512-6
Article
PubMed
Google Scholar
Harrington AJ, Raissi A, Rajkovich K, Berto S, Kumar J, Molinaro G, Raduazzo J, Guo Y, Loerwald K, Konopka G, Huber KM, Cowan CW (2016) MEF2C regulates cortical inhibitory and excitatory synapses and behaviors relevant to neurodevelopmental disorders. Elife. https://doi.org/10.7554/eLife.20059
Article
PubMed
PubMed Central
Google Scholar
Hettema JM, Neale MC, Myers JM, Prescott CA, Kendler KS (2006) A population-based twin study of the relationship between neuroticism and internalizing disorders. Am J Psychiatry 163:857–864. https://doi.org/10.1176/ajp.2006.163.5.857
Article
PubMed
Google Scholar
Hill WD, Weiss A, Liewald DC, Davies G, Porteous DJ, Hayward C, McIntosh AM, Gale CR, Deary IJ (2019) Genetic contributions to two special factors of neuroticism are associated with affluence, higher intelligence, better health, and longer life. Mol Psychiatry. https://doi.org/10.1038/s41380-019-0387-3
Article
PubMed
Google Scholar
Huang T, Liu CL, Li LL, Cai MH, Chen WZ, Xu YF, O’Reilly PF, Cai L, He L (2016) A new method for identifying causal genes of schizophrenia and anti-tuberculosis drug-induced hepatotoxicity. Sci Rep 6:32571. https://doi.org/10.1038/srep32571
CAS
Article
PubMed
PubMed Central
Google Scholar
Hyde CL, Nagle MW, Tian C, Chen X, Paciga SA, Wendland JR, Tung JY, Hinds DA, Perlis RH, Winslow AR (2016) Identification of 15 genetic loci associated with risk of major depression in individuals of European descent. Nat Genet 48:1031–1036. https://doi.org/10.1038/ng.3623
CAS
Article
PubMed
PubMed Central
Google Scholar
Ikeda M, Takahashi A, Kamatani Y, Okahisa Y, Kunugi H, Mori N, Sasaki T, Ohmori T, Okamoto Y, Kawasaki H, Shimodera S, Kato T, Yoneda H, Yoshimura R, Iyo M, Matsuda K, Akiyama M, Ashikawa K, Kashiwase K, Tokunaga K, Kondo K, Saito T, Shimasaki A, Kawase K, Kitajima T, Matsuo K, Itokawa M, Someya T, Inada T, Hashimoto R, Inoue T, Akiyama K, Tanii H, Arai H, Kanba S, Ozaki N, Kusumi I, Yoshikawa T, Kubo M, Iwata N (2018) A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder. Mol Psychiatry 23:639–647. https://doi.org/10.1038/mp.2016.259
CAS
Article
PubMed
Google Scholar
Insel TR, Wang PS (2010) Rethinking mental illness. JAMA 303:1970–1971. https://doi.org/10.1001/jama.2010.555
CAS
Article
PubMed
Google Scholar
International Schizophrenia C, Purcell SM, Wray NR, Stone JL, Visscher PM, O’Donovan MC, Sullivan PF, Sklar P (2009) Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460:748–752. https://doi.org/10.1038/nature08185
CAS
Article
Google Scholar
Jin DY, Spencer F, Jeang KT (1998) Human T cell leukemia virus type 1 oncoprotein Tax targets the human mitotic checkpoint protein MAD1. Cell 93:81–91
CAS
Article
Google Scholar
Kappel DB, Schuch JB, Rovaris DL, da Silva BS, Cupertino RB, Winkler C, Teche SP, Vitola ES, Karam RG, Rohde LA, Bau CHD, Grevet EH, Mota NR (2017) Further replication of the synergistic interaction between LPHN3 and the NTAD gene cluster on ADHD and its clinical course throughout adulthood. Prog Neuropsychopharmacol Biol Psychiatry 79:120–127. https://doi.org/10.1016/j.pnpbp.2017.06.011
CAS
Article
PubMed
Google Scholar
Karch CM, Goate AM (2015) Alzheimer’s disease risk genes and mechanisms of disease pathogenesis. Biol Psychiatry 77:43–51. https://doi.org/10.1016/j.biopsych.2014.05.006
CAS
Article
PubMed
Google Scholar
Kessler RC, Chiu WT, Demler O, Merikangas KR, Walters EE (2005) Prevalence, severity, and comorbidity of 12-month DSM-IV disorders in the National Comorbidity Survey Replication. Arch Gen Psychiatry 62:617–627. https://doi.org/10.1001/archpsyc.62.6.617
Article
PubMed
PubMed Central
Google Scholar
Kotov R, Gamez W, Schmidt F, Watson D (2010) Linking “big” personality traits to anxiety, depressive, and substance use disorders: a meta-analysis. Psychol Bull 136:768–821. https://doi.org/10.1037/a0020327
Article
PubMed
Google Scholar
Kuleshov MV, Jones MR, Rouillard AD, Fernandez NF, Duan Q, Wang Z, Koplev S, Jenkins SL, Jagodnik KM, Lachmann A, McDermott MG, Monteiro CD, Gundersen GW, Ma’ayan A (2016) Enrichr: a comprehensive gene set enrichment analysis web server 2016 update. Nucleic Acids Res 44:W90–W97. https://doi.org/10.1093/nar/gkw377
CAS
Article
PubMed
PubMed Central
Google Scholar
Lai MC, Lombardo MV, Baron-Cohen S (2014) Autism. Lancet 383:896–910. https://doi.org/10.1016/S0140-6736(13)61539-1
Article
PubMed
Google Scholar
Lambert L, Bienvenu T, Allou L, Valduga M, Echenne B, Diebold B, Mignot C, Heron D, Roth V, Saunier A, Moustaine A, Jonveaux P, Philippe C (2012) MEF2C mutations are a rare cause of Rett or severe Rett-like encephalopathies. Clin Genet 82:499–501. https://doi.org/10.1111/j.1399-0004.2012.01861.x
CAS
Article
PubMed
Google Scholar
Lawlor DA, Harbord RM, Sterne JA, Timpson N, Davey Smith G (2008) Mendelian randomization: using genes as instruments for making causal inferences in epidemiology. Stat Med 27:1133–1163. https://doi.org/10.1002/sim.3034
Article
PubMed
Google Scholar
Lee FS, Heimer H, Giedd JN, Lein ES, Sestan N, Weinberger DR, Casey BJ (2014) Mental health. Adolescent mental health—opportunity and obligation. Science 346:547–549. https://doi.org/10.1126/science.1260497
CAS
Article
PubMed
PubMed Central
Google Scholar
Li H, Radford JC, Ragusa MJ, Shea KL, McKercher SR, Zaremba JD, Soussou W, Nie Z, Kang YJ, Nakanishi N, Okamoto S, Roberts AJ, Schwarz JJ, Lipton SA (2008) Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivo. Proc Natl Acad Sci USA 105:9397–9402. https://doi.org/10.1073/pnas.0802876105
Article
PubMed
Google Scholar
Liu G, Mattick JS, Taft RJ (2013) A meta-analysis of the genomic and transcriptomic composition of complex life. Cell Cycle 12:2061–2072. https://doi.org/10.4161/cc.25134
CAS
Article
PubMed
PubMed Central
Google Scholar
Lonnqvist JE, Verkasalo M, Haukka J, Nyman K, Tiihonen J, Laaksonen I, Leskinen J, Lonnqvist J, Henriksson M (2009) Premorbid personality factors in schizophrenia and bipolar disorder: results from a large cohort study of male conscripts. J Abnorm Psychol 118:418–423. https://doi.org/10.1037/a0015127
Article
PubMed
Google Scholar
Macare C, Bates TC, Heath AC, Martin NG, Ettinger U (2012) Substantial genetic overlap between schizotypy and neuroticism: a twin study. Behav Genet 42:732–742. https://doi.org/10.1007/s10519-012-9558-6
Article
PubMed
Google Scholar
Macare C, Ducci F, Zhang Y, Ruggeri B, Jia T, Kaakinen M, Kalsi G, Charoen P, Casoni F, Peters J, Bromberg U, Hill M, Buxton J, Blakemore A, Veijola J, Buchel C, Banaschewski T, Bokde ALW, Conrod P, Flor H, Frouin V, Gallinat J, Garavan H, Gowland PA, Heinz A, Ittermann B, Lathrop M, Martinot JL, Paus T, Desrivieres S, Munafo M, Jarvelin MR, Schumann G, Consortium I (2018) A neurobiological pathway to smoking in adolescence: TTC12-ANKK1-DRD2 variants and reward response. Eur Neuropsychopharmacol 28:1103–1114. https://doi.org/10.1016/j.euroneuro.2018.07.101
CAS
Article
PubMed
PubMed Central
Google Scholar
Michielsen M, Comijs HC, Semeijn EJ, Beekman AT, Deeg DJ, Kooij JJ (2014) Attention deficit hyperactivity disorder and personality characteristics in older adults in the general Dutch population. Am J Geriatr Psychiatry 22:1623–1632. https://doi.org/10.1016/j.jagp.2014.02.005
Article
PubMed
Google Scholar
Mitchell AC, Javidfar B, Pothula V, Ibi D, Shen EY, Peter CJ, Bicks LK, Fehr T, Jiang Y, Brennand KJ, Neve RL, Gonzalez-Maeso J, Akbarian S (2018) MEF2C transcription factor is associated with the genetic and epigenetic risk architecture of schizophrenia and improves cognition in mice. Mol Psychiatry 23:123–132. https://doi.org/10.1038/mp.2016.254
CAS
Article
PubMed
Google Scholar
Mohammadi A, Amooeian VG, Rashidi E (2018) Dysfunction in brain-derived neurotrophic factor signaling pathway and susceptibility to schizophrenia, Parkinson’s and Alzheimer’s diseases. Curr Gene Ther 18:45–63. https://doi.org/10.2174/1566523218666180302163029
CAS
Article
PubMed
Google Scholar
Mota NR, Araujo-Jnr EV, Paixao-Cortes VR, Bortolini MC, Bau CH (2012) Linking dopamine neurotransmission and neurogenesis: the evolutionary history of the NTAD (NCAM1-TTC12-ANKK1-DRD2) gene cluster. Genet Mol Biol 35:912–918
CAS
Article
Google Scholar
Mota NR, Rovaris DL, Kappel DB, Picon FA, Vitola ES, Salgado CA, Karam RG, Rohde LA, Grevet EH, Bau CH (2015) NCAM1-TTC12-ANKK1-DRD2 gene cluster and the clinical and genetic heterogeneity of adults with ADHD. Am J Med Genet B Neuropsychiatr Genet 168:433–444. https://doi.org/10.1002/ajmg.b.32317
CAS
Article
PubMed
Google Scholar
Muench C, Schwandt M, Jung J, Cortes CR, Momenan R, Lohoff FW (2018) The major depressive disorder GWAS-supported variant rs10514299 in TMEM161B-MEF2C predicts putamen activation during reward processing in alcohol dependence. Transl Psychiatry 8:131. https://doi.org/10.1038/s41398-018-0184-9
CAS
Article
PubMed
PubMed Central
Google Scholar
Nagel M, Jansen PR, Stringer S, Watanabe K, de Leeuw CA, Bryois J, Savage JE, Hammerschlag AR, Skene NG, Munoz-Manchado AB, andMe Research T, White T, Tiemeier H, Linnarsson S, Hjerling-Leffler J, Polderman TJC, Sullivan PF, van der Sluis S, Posthuma D (2018) Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. Nat Genet 50:920–927. https://doi.org/10.1038/s41588-018-0151-7
CAS
Article
PubMed
Google Scholar
Nelson EC, Lynskey MT, Heath AC, Wray N, Agrawal A, Shand FL, Henders AK, Wallace L, Todorov AA, Schrage AJ, Saccone NL, Madden PA, Degenhardt L, Martin NG, Montgomery GW (2013) ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure. JAMA Psychiatry 70:325–333. https://doi.org/10.1001/jamapsychiatry.2013.282
CAS
Article
PubMed
PubMed Central
Google Scholar
Newman DL, Moffitt TE, Caspi A, Silva PA (1998) Comorbid mental disorders: implications for treatment and sample selection. J Abnorm Psychol 107:305–311
CAS
Article
Google Scholar
Nikitin A, Egorov S, Daraselia N, Mazo I (2003) Pathway studio–the analysis and navigation of molecular networks. Bioinformatics 19:2155–2157
CAS
Article
Google Scholar
Numakawa T, Adachi N, Richards M, Chiba S, Kunugi H (2013) Brain-derived neurotrophic factor and glucocorticoids: reciprocal influence on the central nervous system. Neuroscience 239:157–172. https://doi.org/10.1016/j.neuroscience.2012.09.073
CAS
Article
PubMed
Google Scholar
Okamoto S, Krainc D, Sherman K, Lipton SA (2000) Antiapoptotic role of the p38 mitogen-activated protein kinase-myocyte enhancer factor 2 transcription factor pathway during neuronal differentiation. Proc Natl Acad Sci USA 97:7561–7566. https://doi.org/10.1073/pnas.130502697
CAS
Article
PubMed
Google Scholar
Okbay A, Beauchamp JP, Fontana MA, Lee JJ, Pers TH, Rietveld CA, Turley P, Chen GB, Emilsson V, Meddens SF, Oskarsson S, Pickrell JK, Thom K, Timshel P, de Vlaming R, Abdellaoui A, Ahluwalia TS, Bacelis J, Baumbach C, Bjornsdottir G, Brandsma JH, Pina Concas M, Derringer J, Furlotte NA, Galesloot TE, Girotto G, Gupta R, Hall LM, Harris SE, Hofer E, Horikoshi M, Huffman JE, Kaasik K, Kalafati IP, Karlsson R, Kong A, Lahti J, van der Lee SJ, deLeeuw C, Lind PA, Lindgren KO, Liu T, Mangino M, Marten J, Mihailov E, Miller MB, van der Most PJ, Oldmeadow C, Payton A, Pervjakova N, Peyrot WJ, Qian Y, Raitakari O, Rueedi R, Salvi E, Schmidt B, Schraut KE, Shi J, Smith AV, Poot RA, St Pourcain B, Teumer A, Thorleifsson G, Verweij N, Vuckovic D, Wellmann J, Westra HJ, Yang J, Zhao W, Zhu Z, Alizadeh BZ, Amin N, Bakshi A, Baumeister SE, Biino G, Bonnelykke K, Boyle PA, Campbell H, Cappuccio FP, Davies G, De Neve JE, Deloukas P, Demuth I, Ding J, Eibich P, Eisele L, Eklund N, Evans DM, Faul JD, Feitosa MF, Forstner AJ, Gandin I, Gunnarsson B, Halldorsson BV, Harris TB, Heath AC, Hocking LJ, Holliday EG, Homuth G, Horan MA et al (2016) Genome-wide association study identifies 74 loci associated with educational attainment. Nature 533:539–542. https://doi.org/10.1038/nature17671
CAS
Article
PubMed
PubMed Central
Google Scholar
Oliver PL, Chodroff RA, Gosal A, Edwards B, Cheung AF, Gomez-Rodriguez J, Elliot G, Garrett LJ, Lickiss T, Szele F, Green ED, Molnar Z, Ponting CP (2015) Disruption of Visc-2, a brain-expressed conserved long noncoding RNA, does not elicit an overt anatomical or behavioral phenotype. Cereb Cortex 25:3572–3585. https://doi.org/10.1093/cercor/bhu196
Article
PubMed
Google Scholar
Park SH, Guastella AJ, Lynskey M, Agrawal A, Constantino JN, Medland SE, Song YJC, Martin NG, Colodro-Conde L (2017) Neuroticism and the overlap between autistic and ADHD traits: findings from a population sample of young adult australian twins. Twin Res Hum Genet 20:319–329. https://doi.org/10.1017/thg.2017.38
Article
PubMed
Google Scholar
Peschansky VJ, Wahlestedt C (2014) Non-coding RNAs as direct and indirect modulators of epigenetic regulation. Epigenetics 9:3–12. https://doi.org/10.4161/epi.27473
CAS
Article
PubMed
Google Scholar
Quilty LC, Meusel LA, Bagby RM (2008) Neuroticism as a mediator of treatment response to SSRIs in major depressive disorder. J Affect Disord 111:67–73. https://doi.org/10.1016/j.jad.2008.02.006
CAS
Article
PubMed
Google Scholar
Riccelli R, Indovina I, Staab JP, Nigro S, Augimeri A, Lacquaniti F, Passamonti L (2017) Neuroticism modulates brain visuo-vestibular and anxiety systems during a virtual rollercoaster task. Hum Brain Mapp 38:715–726. https://doi.org/10.1002/hbm.23411
Article
PubMed
Google Scholar
Ruderfer DM, Fanous AH, Ripke S, McQuillin A, Amdur RL, Schizophrenia Working Group of the Psychiatric Genomics C, Bipolar Disorder Working Group of the Psychiatric Genomics C, Cross-Disorder Working Group of the Psychiatric Genomics C, Gejman PV, O’Donovan MC, Andreassen OA, Djurovic S, Hultman CM, Kelsoe JR, Jamain S, Landen M, Leboyer M, Nimgaonkar V, Nurnberger J, Smoller JW, Craddock N, Corvin A, Sullivan PF, Holmans P, Sklar P, Kendler KS (2014) Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia. Mol Psychiatry 19:1017–1024. https://doi.org/10.1038/mp.2013.138
CAS
Article
PubMed
Google Scholar
Sao T, Yoshino Y, Yamazaki K, Ozaki Y, Mori Y, Ochi S, Yoshida T, Mori T, Iga JI, Ueno SI (2018) MEF2C mRNA expression and cognitive function in Japanese patients with Alzheimer’s disease. Psychiatry Clin Neurosci 72:160–167. https://doi.org/10.1111/pcn.12618
CAS
Article
PubMed
Google Scholar
Shalizi A, Gaudilliere B, Yuan Z, Stegmuller J, Shirogane T, Ge Q, Tan Y, Schulman B, Harper JW, Bonni A (2006) A calcium-regulated MEF2 sumoylation switch controls postsynaptic differentiation. Science 311:1012–1017. https://doi.org/10.1126/science.1122513
CAS
Article
PubMed
Google Scholar
Shannon P, Markiel A, Ozier O, Baliga NS, Wang JT, Ramage D, Amin N, Schwikowski B, Ideker T (2003) Cytoscape: a software environment for integrated models of biomolecular interaction networks. Genome Res 13:2498–2504. https://doi.org/10.1101/gr.1239303
CAS
Article
PubMed
PubMed Central
Google Scholar
Smith EM, Reynolds S, Orchard F, Whalley HC, Chan SW (2018) Cognitive biases predict symptoms of depression, anxiety and wellbeing above and beyond neuroticism in adolescence. J Affect Disord 241:446–453. https://doi.org/10.1016/j.jad.2018.08.051
Article
PubMed
Google Scholar
Speed D, Hemani G, Speed MS, Major Depressive Disorder Working Group of the Psychiatric Genomics C, Borglum AD, Ostergaard SD (2019) Investigating the causal relationship between neuroticism and depression via Mendelian randomization. Acta Psychiatr Scand 139:395–397. https://doi.org/10.1111/acps.13009
CAS
Article
PubMed
Google Scholar
Su L, Shen T, Huang G, Long J, Fan J, Ling W, Jiang J (2016) Genetic association of GWAS-supported MAD1L1 gene polymorphism rs12666575 with schizophrenia susceptibility in a Chinese population. Neurosci Lett 610:98–103. https://doi.org/10.1016/j.neulet.2015.10.061
CAS
Article
PubMed
Google Scholar
Tay Y, Rinn J, Pandolfi PP (2014) The multilayered complexity of ceRNA crosstalk and competition. Nature 505:344–352. https://doi.org/10.1038/nature12986
CAS
Article
PubMed
PubMed Central
Google Scholar
Topol A, Zhu S, Hartley BJ, English J, Hauberg ME, Tran N, Rittenhouse CA, Simone A, Ruderfer DM, Johnson J, Readhead B, Hadas Y, Gochman PA, Wang YC, Shah H, Cagney G, Rapoport J, Gage FH, Dudley JT, Sklar P, Mattheisen M, Cotter D, Fang G, Brennand KJ (2016) Dysregulation of miRNA-9 in a subset of schizophrenia patient-derived neural progenitor cells. Cell Rep 15:1024–1036. https://doi.org/10.1016/j.celrep.2016.03.090
CAS
Article
PubMed
PubMed Central
Google Scholar
Trost S, Diekhof EK, Mohr H, Vieker H, Kramer B, Wolf C, Keil M, Dechent P, Binder EB, Gruber O (2016) Investigating the impact of a genome-wide supported bipolar risk variant of MAD1L1 on the human reward system. Neuropsychopharmacology 41:2679–2687. https://doi.org/10.1038/npp.2016.70
CAS
Article
PubMed
PubMed Central
Google Scholar
Tu S, Akhtar MW, Escorihuela RM, Amador-Arjona A, Swarup V, Parker J, Zaremba JD, Holland T, Bansal N, Holohan DR, Lopez K, Ryan SD, Chan SF, Yan L, Zhang X, Huang X, Sultan A, McKercher SR, Ambasudhan R, Xu H, Wang Y, Geschwind DH, Roberts AJ, Terskikh AV, Rissman RA, Masliah E, Lipton SA, Nakanishi N (2017) NitroSynapsin therapy for a mouse MEF2C haploinsufficiency model of human autism. Nat Commun 8:1488. https://doi.org/10.1038/s41467-017-01563-8
CAS
Article
PubMed
PubMed Central
Google Scholar
van Loo HM, Romeijn JW (2015) Psychiatric comorbidity: fact or artifact? Theor Med Bioeth 36:41–60. https://doi.org/10.1007/s11017-015-9321-0
Article
PubMed
PubMed Central
Google Scholar
Wang M, Zhao Y, Zhang B (2015) Efficient test and visualization of multi-set intersections. Sci Rep 5:16923. https://doi.org/10.1038/srep16923
CAS
Article
PubMed
PubMed Central
Google Scholar
Wolfe D, Dudek S, Ritchie MD, Pendergrass SA (2013) Visualizing genomic information across chromosomes with PhenoGram. BioData Min 6:18. https://doi.org/10.1186/1756-0381-6-18
CAS
Article
PubMed
PubMed Central
Google Scholar
Yang BZ, Kranzler HR, Zhao H, Gruen JR, Luo X, Gelernter J (2007) Association of haplotypic variants in DRD2, ANKK1, TTC12 and NCAM1 to alcohol dependence in independent case control and family samples. Hum Mol Genet 16:2844–2853. https://doi.org/10.1093/hmg/ddm240
CAS
Article
PubMed
Google Scholar
Zhao L, Chang H, Zhou DS, Cai J, Fan W, Tang W, Tang W, Li X, Liu W, Liu F, He Y, Bai Y, Sun Y, Dai J, Li L, Xiao X, Zhang C, Li M (2018) Replicated associations of FADS1, MAD1L1, and a rare variant at 10q26.13 with bipolar disorder in Chinese population. Transl Psychiatry 8:270. https://doi.org/10.1038/s41398-018-0337-x
CAS
Article
PubMed
PubMed Central
Google Scholar
Zweier M, Gregor A, Zweier C, Engels H, Sticht H, Wohlleber E, Bijlsma EK, Holder SE, Zenker M, Rossier E, Grasshoff U, Johnson DS, Robertson L, Firth HV, Ekici AB, Reis A, Rauch A (2010) Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression. Hum Mutat 31:722–733. https://doi.org/10.1002/humu.21253
CAS
Article
PubMed
Google Scholar