Skip to main content

Genetik und Gen-Umwelt-Interaktionen bei psychischen Erkrankungen

  • Chapter
  • First Online:
Psychiatrie, Psychosomatik, Psychotherapie

Part of the book series: Springer Reference Medizin ((SRM))

Zusammenfassung

Die genetische Forschung hat in der Psychiatrie seit über 100 Jahren eine sehr wechselhafte Geschichte. So wurde über viele Jahrzehnte des 20. Jahrhunderts in Psychologie und Psychiatrie eine heftige, teilweise verbitterte Diskussion über „Gene oder Umwelt“ („nature vs. nurture“) geführt. Sind psychische Eigenschaften und Störungen auf genetisch-konstitutionelle Faktoren oder auf Umwelteinflüsse wie z. B. psychosoziale Belastungen zurückführbar? Heute ist allgemein anerkannt, dass die Wahrheit in der Mitte liegt. Es ist unstreitig: Psychische Eigenschaften und v. a. psychische Störungen werden sowohl von genetischen Anlagen als auch von Umweltbedingungen beeinflusst, noch wenig bekannt sind die Mechanismen der Interaktion beider Ebenen. Das gesamte Feld der psychiatrischen Genetik hat sich im Rahmen der sich rapide entwickelnden technischen Möglichkeiten von der Analyse familiärer Ähnlichkeitsmuster in Familien-, Zwillings- und Adoptionsstudien auf die molekulargenetische Analyse psychischer Eigenschaften und Störungen verschoben. Der vollzogene methodische „Paradigmenwechsel“ hat das Interesse an dem klinischen Forschungsfeld der psychiatrischen Genetik massiv gesteigert. Die molekulargenetische Analyse ist mittlerweile zur wichtigsten Erkenntnisquelle der Pathophysiologie und Neurobiologie psychischer Störungen geworden. Sie stellt auch die Nosologie psychischer Krankheiten zunehmend in Frage. Die heutige klinische Nützlichkeit liegt in der Früherkennung („diagnostische und prädikative Marker“) und Entwicklung neuer, molekularer Wirkprinzipien für Therapie und Prävention. Bisher sind jedoch in der Umsetzung der genetischen Erkenntnisfortschritte in die klinische Basis noch keine durchschlagenden, nachhaltigen Erfolge erzielt worden. Dieser Ertrag ist erst langfristig zu erwarten.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Institutional subscriptions

Similar content being viewed by others

Literatur

  • Abkevich V, Camp NJ, Hensel CH et al (2003) Predisposition locus for major depression at chromosome 12q22–12q23.2. Am J Hum Genet 73:1271–1281

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Allen AJ, Griss ME, Folley BS et al (2009) Endophenotypes in schizophrenia: a selective review. Schizophr Res 109:24–37

    Article  PubMed  PubMed Central  Google Scholar 

  • Angst J (1966) Zur Ätiologie und Nosologie endogener depressiver Psychosen. Springer, Berlin/Heidelberg/New York

    Book  Google Scholar 

  • Baker M, Mackenzie IR, Pickering-Brown SM et al (2006) Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 442:916–919

    Article  CAS  PubMed  Google Scholar 

  • Barden N, Harvey M, Gagné B et al (2006) Analysis of single nucleotide polymorphisms in genes in the chromsome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder. Am J Med Genet Part B Neuropsychiatr Genet 141B:374–382

    Article  CAS  Google Scholar 

  • Baron M (1996) Further reflections on linkage results in schizophrenia. Am J Med Genet 67:430–432

    Article  CAS  PubMed  Google Scholar 

  • Beckmann H, Franzek E, Stöber G (1996) Genetic heterogeneity in catatonic schizophrenia: a family genetic study. Am J Med Genet 67:289–300

    Article  CAS  PubMed  Google Scholar 

  • Bergem AL (2002) Norwegian twin registers and norwegian twin studies – an overview. Twin Res 5:407–414

    PubMed  Google Scholar 

  • Bergem ALM, Engedal K, Kringlen E (1997) The role of heredity in late-onset Alzheimer disease and vascular dementia – a twin study. Arch Gen Psychiatry 54:264–270

    Article  CAS  PubMed  Google Scholar 

  • Bienvenu OJ, Davydow DS, Kendler KS (2011) Psychiatric ‚diseases‘ versus behavioral disorders and degree of genetic influence. Psychol Med 41:33–40

    Article  CAS  PubMed  Google Scholar 

  • Bierut LJ, Stitzel JA, Wang JC (2008) Variants in nicotinic receptors and risk for nicotine dependence. Am J Psychiatry 165:1163–1171

    Article  PubMed  PubMed Central  Google Scholar 

  • Binder EB, Nemeroff CB (2009) The CRF system, stress, depression and anxiety – insights from human genetic studies. Mol Psychiatry 144:1–15

    Article  CAS  Google Scholar 

  • Black DW, Noyes R, Goldstein RB, Blum N (1992) A family study of obsessive-compulsive disorder. Arch Gen Psychiatry 49:362–368

    Article  CAS  PubMed  Google Scholar 

  • Brena RM, Huang TH-M, Plass C (2006) Toward a human epigenome. Nat Genet 38:1359–1360

    Article  CAS  PubMed  Google Scholar 

  • Cadoret RJ, O’Gorman TW, Troughton E (1985) Alcoholism and antisocial personality: interrelationships, genetic and environmental factors. Arch Gen Psychiatry 42:161–167

    Article  CAS  PubMed  Google Scholar 

  • Cadoret RJ, Yates WR, Troughton E et al (1995) Adoption study demonstrating two genetic pathways to drug abuse. Arch Gen Psychiatry 52:42–52

    Article  CAS  PubMed  Google Scholar 

  • Cannon TD (2005) The inheritance of intermediate phenotypes for schizophrenia. Curr Opin Psychiatry 18:135–140

    Article  PubMed  Google Scholar 

  • Cannon TD, Zorrilla LE, Shtasel D et al (1994) Neuropsychological functioning in siblings discordant for schizophrenia and healthy volunteers. Arch Gen Psychiatry 51:651–661

    Article  CAS  PubMed  Google Scholar 

  • Caselli RJ, Beach TG, Yaari R, Reiman EM (2006) Alzheimer’s disease a century later. J Clin Psychiatry 67:1784–1800

    Article  CAS  PubMed  Google Scholar 

  • Caspi A, Moffitt TE (2006) Gene-environment interactions in psychiatry: joining forces with neuroscience. Nat Rev Neurosci 7:583–590

    Article  CAS  PubMed  Google Scholar 

  • Caspi A, Sugden K, Moffitt TE et al (2003) Influence of life stresss on depression: moderation by a polymorphism in the 5-HTT gene. Science 301:386–389

    Article  CAS  PubMed  Google Scholar 

  • Chen WJ, Loh EW, Hsu Y-PP, Cheng ATA (1997) Alcohol dehydrogenase und aldehyde dehydrogenase genotypes and alcoholism among Taiwanese aborigines. Biol Psychiatry 41:703–709

    Article  CAS  PubMed  Google Scholar 

  • Chowdari KV, Mirnics K, Semwal P et al (2002) Association and linkage analyses of RGS4 polymorphisms in schizophrenia. Hum Mol Genet 11:1373–1380

    Article  CAS  PubMed  Google Scholar 

  • Chumakov I, Blumenfeld M, Guerassimenko O et al (2002) Genetic and phyiological data implicating the new human gene G72 and the gene for D-Amino acid oxidase in schizophrenia. Proc Natl Acad Sci U S A 99:13675–13680

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Cloninger CR (1987) Neurogenetic adaptive mechanism in alcoholism. Science 236:412–420

    Article  Google Scholar 

  • Cloninger CR, Bohmann M, Sigvardsson S (1981) Inheritance of alcohol abuse: cross-fostering analysis of adopted men. Arch Gen Psychiatry 38:861–868

    Article  CAS  PubMed  Google Scholar 

  • Collins FS (2001) Contemplating the end of the beginning. Genome Res 11:641–643

    Article  CAS  PubMed  Google Scholar 

  • CONVERGE consortium (2015) Sparse whole-genome sequencing identifies two loci for major depressive disorder. Nature 523:588–591

    Article  PubMed Central  CAS  Google Scholar 

  • Corder EH, Saunders AM, Strittmatter WJ et al (1993) Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer’s disease in late onset families. Science 261:921–923

    Article  CAS  PubMed  Google Scholar 

  • Cross-Disorder Group of the Psychiatric Genomics Consortium (2013) Genetic relationship between five psychiatric diasorders estimated from genome-wide SNPs. Nat Genet 45:984–994

    Article  PubMed Central  CAS  Google Scholar 

  • Cruts M, Gijselninck I, van der Zee J et al (2006) Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 442:920–924

    Article  CAS  PubMed  Google Scholar 

  • David SP, Hamidovic A, Chen GK et al (2012) Genome-wide meta-analyses of smoking behaviors in African Americans. Transl Psychiatry 2:e119

    Google Scholar 

  • Davies GE, Soundy TJ (2009) The genetics of smoking and nicotine addiction. S D Med Spec No: 43–49

    Google Scholar 

  • De Jager PL, Srivastava G, Lunnon K et al (2014) Alzheimer’s disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci. Nat Neurosci 17:1156–1163

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Distel M, Rebollo-Mesa I, Willemsen G (2009) Familial resemblance of borderline personality disorder features: genetic or cultural transmission? PLoS ONE 4(e5334):1–8

    Google Scholar 

  • Drago A, Giegling I, Schäfer M et al (2013) AKAP13, CACNA1, GRIK4 and GRIA1 genetic variations may be associated with haloperidol efficacy during acute treatment. Eur Neuropsychopharmacol 23:887–894

    Article  CAS  PubMed  Google Scholar 

  • Drago A, Giegling I, Schäfer M et al (2014) Genome-wide association study supports the role of the immunological system and of the neurodevelopmental processes in response to haloperidol treatment. Pharmacogenet Genomics 24:314–319

    Article  CAS  PubMed  Google Scholar 

  • Edvardsen J, Torgersen S, Røysamb E et al (2008) Heritability of bipolar spectrum disorders. Unity or heterogeneity? J Affect Disord 106:229–240

    Article  PubMed  Google Scholar 

  • Elliott JC, Carey KB, Bonafide KE (2012) Does family history of alcohol problems influence college and university drinking or substance use? A meta-analytical review. Addiction 107:1774–1785

    Article  PubMed  Google Scholar 

  • ENCODE Project Consortium (2012) An integrated encyclopedia of DNA elements in the human genome. Nature 489:57–74

    Article  CAS  Google Scholar 

  • Esterberg ML, Trotman HD, Holtzman C et al (2010) The impact of a family history of psychosis on age-at-onset and positive and negative symptoms of schizophrenia: a meta-analysis. Schizophr Res 120:121–130

    Article  PubMed  Google Scholar 

  • Euler S, Sollberger D, Bader K et al (2015) Persönlichkeitsstörungen und Sucht: Systematische Literaturübersicht zu Epidemiologie, Verlauf und Behandlung. Fortschr Neurol Psychiatr 83:544–554

    Google Scholar 

  • Fabbri C, Serretti A (2015) Pharmacogenetics of major depressive disorder: top genes and pathways toward clinical applications. Curr Psychiatry Rep 17(7):50 (doi: 10.1007/s11920-015-0594-9)

    Google Scholar 

  • Fanous AH, van den Oord EJ, Riley BP et al (2005) Relationship between a high-risk haplotype in the DTNBP1 (dysbindin) gene and clinical features of schizophrenia. Am J Psychiatry 162:1824–1832

    Article  PubMed  Google Scholar 

  • Faraone SV, Seidman LJ, Kremen WS et al (1995) Neuropsychological functioning among the nonpsychotic relatives of schizophrenic patients: a diagnostic efficiency analysis. J Abnorm Psychol 104:286–304

    Article  CAS  PubMed  Google Scholar 

  • Farmer AE, McGuffin P, Gottesman II (1987) Twin concordance for DSM-III schizophrenia: scrutinising the validity of the definition. Arch Gen Psychiatry 44:634–641

    Article  CAS  PubMed  Google Scholar 

  • Farmer A, Elkin A, McGuffin P (2007) The genetics of bipolar affective disorder. Curr Opin Psychiatry 20:8–12

    Article  PubMed  Google Scholar 

  • Fazzari MJ, Greally JM (2004) Epigenomics: beyond CpG islands. Nat Rev Genet 5:446–455

    Article  CAS  PubMed  Google Scholar 

  • Ferreira MA, O’Donovan MC, Meng YA et al (2008) Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. Nat Genet 40:1056–1058

    Google Scholar 

  • Foroud T, Edenberg HJ, Goate A et al (2000) Alcoholism susceptibility loci: confirmation studies in a replicate sample and further mapping. Alcohol Clin Exp Res 24:933–945

    Article  CAS  PubMed  Google Scholar 

  • Frank J, Cichon S, Treutlein J et al (2012) Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster. Addict Biol 17:171–180

    Google Scholar 

  • Franke P, Maier W, Hardt J et al (1994) Attentional abilities and measures of schizotypy: their variation and covariation in schizophrenic patients, their siblings, and normal control subjects. Psychiatry Res 54:259–272

    Article  CAS  PubMed  Google Scholar 

  • Franzek E, Beckmann H (1996) Die genetische Heterogenität der Schizophrenie. Ergebnisse einer systematischen Zwillingsstudie. Nervenarzt 67:583–594

    CAS  PubMed  Google Scholar 

  • Friedman D, Cornblatt BA, Vaughan H, Erlenmeyer-Kimling L (1988) Auditory event-related potentials in children at risk for schizophrenia: the complete initial sample. Psychiatry Res 26:203–221

    Article  CAS  PubMed  Google Scholar 

  • Fromer M, Pocklington AJ, Kavanagh DH et al (2014) De novo mutations in schizophrenia implicate synaptic networks. Nature 506:179–184

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Fyer AJ, Mannuzza S, Chapman TF et al (1995) Specificity in familial aggregation of phobic disorders. Arch Gen Psychiatry 52:564–573

    Article  CAS  PubMed  Google Scholar 

  • Garriock H, Kraft JB, Shyn SI et al (2010) A genomewide association study of citalopram response in major depressive disorders. Biol Psychiatry 67:133–138

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Gatz M, Fratiglioni L, Johansson B et al (2005) Complete ascertainment of dementia in the swedish twin registry: the HARMONY study. Neurobiol Aging 26:439–447

    Article  PubMed  Google Scholar 

  • Gatz M, Reynolds CA, Fratiglioni L et al (2006) Role of genes and environments for explaining Alzheimer disease. Arch Gen Psychiatry 63:168–174

    Article  PubMed  Google Scholar 

  • Gelernter J, Kranzler HR (2009) Genetics of alcohol dependence. Hum Genet 126:91–99

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • GENDEP Investigators, MARS Investigators, STAR*D Investigators (2013) Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies. Am J Psychiatry 170:207–217

    Article  Google Scholar 

  • Genetics of Personality Consortium, de Moor MH, van den Berg SM et al (2015) Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorder. JAMA Psychiat 72:642–650

    Google Scholar 

  • Geschwind DH, Flint J (2015) Genetics and genomics of psychiatric disease. Science 349:1489–1494

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Giegling I, Balzarro B, Porcelli S et al (2013) Influence of ANKK1 and DRD2 polymorphisms in response to haloperidol. Eur Arch Psychiatry Clin Neurosci 263:65–74

    Article  PubMed  Google Scholar 

  • Giegling I, Hosak L, Mössner R, Serretti A, Bellivier F, Claes S, Collier DA (2017) Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics. World J Biol Psychiatry 23:1–14. doi: 10.1080/15622975.2016.1268715

    Google Scholar 

  • Gilligan SB, Reich T, Cloninger CR (1987) Etiologic heterogeneity in alcoholism. Genet Epidemiol 4:395–414

    Article  CAS  PubMed  Google Scholar 

  • Girard SL, Gauthier J, Noreau A et al (2011) Increased exonic de novo mutation rate in individuals with schizophrenia. Nat Genet 43:860–863

    Article  CAS  PubMed  Google Scholar 

  • Glahn DC, Knowles EE, McKay DR et al (2014) Arguments for the sake of endophenotypes: examining common misconceptions about the use of endophenotypes in psychiatric genetics. Am J Med Genet B Neuropsychiatr Genet 165B:122–130

    Article  PubMed  CAS  Google Scholar 

  • Goldman D, Oroszi G, Ducci F (2005) The genetics of addictions: uncovering the genes. Nat Rev Genet 6:521–532

    Article  CAS  PubMed  Google Scholar 

  • Goldstein BL, Klein DN (2014) A review of selected candidate endophenotypes for depression. Clin Psychol Rev 34:417–427

    Article  PubMed  PubMed Central  Google Scholar 

  • Goldstein RB, Wickramaratne PJ, Horwarth E, Weissman MM (1997) Familial aggregation and phenomenology of „early“-onset (at or before age 20 years) panic disorders. Arch Gen Psychiatry 54:271–278

    Article  CAS  PubMed  Google Scholar 

  • Gottesman II, Bertelsen A (1989) Confirming unexpressed genotypes for schizophrenia. Arch Gen Psychiatry 46:867–872

    Article  CAS  PubMed  Google Scholar 

  • Gottesman II, Gould TD (2003) The endophenotype concept in psychiatry: etymology and strategic intentions. Am J Psychiatry 160:636–645

    Article  PubMed  Google Scholar 

  • Grayton HM, Fernandes C, Rujescu D, Collier DA (2012) Copy number variations in neurodevelopmental disorders. Prog Neurobiol 99:81–91

    Article  CAS  PubMed  Google Scholar 

  • Green MF, Nuechterlein KH, Breitmeier B (1997) Backward masking performance in unaffected siblings of schizophrenic patients. Arch Gen Psychiatry 54:465–472

    Article  CAS  PubMed  Google Scholar 

  • Green EK, Grozeva D, Jones I et al (2009) The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia. Mol Psychiatry 15:1016–1022

    Google Scholar 

  • Greenwood TA, Light GA, Swerdlow NR et al (2016) Gating deficit heritability and correlation with increased clinical severity in schizophrenia patients with positive family history. Am J Psychiatry 173:385–391

    Google Scholar 

  • Hansell NK, Agrawal A, Whitfield JB et al (2010) Linkage analysis of alcohol dependence symptoms in the community. Alcohol Clin Exp Res 34:158–163

    Article  PubMed  Google Scholar 

  • Harold D, Abraham R, Hollingworth P et al (2009) Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer’s disease. Nat Genet 41:1088–1093

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Harrison PJ, Owen MJ (2003) Genes for schizophrenia? Recent findings and their pathophysiological implications. Lancet 361:417–419

    Article  CAS  PubMed  Google Scholar 

  • Hasler G, Drevets WC, Manji HK, Charney DS (2004) Discovering endophenotypes for major depression. Neuropsychopharmacol 29:1765–1781

    Article  CAS  Google Scholar 

  • Hasler G, Drevets WC, Gould TD et al (2006) Toward constructing an endophenotype strategy for bipolar disorders. Biol Psychiatry 60:93–105

    Article  PubMed  Google Scholar 

  • Heath AC, Meyer J, Eaves LJ, Martin NG (1991a) The inheritance of alcohol consumption patterns in a general population twin sample: I. Multidimensional scaling of quantity/frequency data. J Stud Alcohol 52:345–351

    Article  CAS  PubMed  Google Scholar 

  • Heath AC, Meyer J, Jardine R, Martin NG (1991b) The inheritance of alcohol consumption patterns in a general population twin sample: II. Determinants of consumption frequency and quantity consumed. J Stud Alcohol 52:425–433

    Article  CAS  PubMed  Google Scholar 

  • Hettema JM, Neale MC, Myers JM et al (2006) A population-based twin study of the relationship between neuroticism and internalizing disorders. Am J Psychiatry 163:857–864

    Article  PubMed  Google Scholar 

  • Heun R, Kölsch H, Jessen F (2006) Risk factors and early signs of Alzheimer’s disease in a family study sample. Risk of AD. Eur Arch Psychiatry Clin Neurosci 256:28–36

    Article  PubMed  Google Scholar 

  • Hicks BM, Krueger RF, Iacano WG et al (2004) Family transmission and heritability of externalizing disorders: a twin-family study. Arch Gen Psychiatry 61:922–928

    Article  PubMed  Google Scholar 

  • Higuchi S, Muramatsu T, Shigemori K et al (1992) The relationship between low Km aldehyde dehydrogenase phenotype and drinking behavior in Japanese. J Stud Alcohol 53:170–175

    Article  CAS  PubMed  Google Scholar 

  • Higuchi S, Matsushita S, Kashima H (2006) New findings on the genetic influences on alcohol use and dependence. Curr Opin Psychiatry 19:253–265

    Article  PubMed  Google Scholar 

  • Hill SY, Shen S, Zezza N et al (2004) A genome wide search for alcoholism susceptibility genes. Am J Med Genet B Neuropsychiatr Genet 128B:102–113

    Article  PubMed  PubMed Central  Google Scholar 

  • Hill SY, Weeks DE, Jones BL et al (2012) ASTN1 and alcohol dependence: family-based association analysis in multiplex alcohol dependence families. Am J Med Genet B Neuropsychiatr Genet 159B:445–455

    Article  PubMed  CAS  Google Scholar 

  • Holmans P, Craddock N (1997) Efficient strategies for genome scanning using maximum-likelihood affected-sib-pair analysis. Am J Hum Genet 60:657–666

    CAS  PubMed  PubMed Central  Google Scholar 

  • Holzman PS, Kringlen E, Matthysse S et al (1988) A single dominant gene can account for eye tracking dysfunctions and schizophrenia in offspring of discordant twins. Arch Gen Psychiatry 45:641–647

    Article  CAS  PubMed  Google Scholar 

  • Hung RJ, McKay JD, Gaborieau V et al (2008) A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. Nature 452:633–637

    Article  CAS  PubMed  Google Scholar 

  • Hyland P, Shevlin M, Elklit A et al (2016) Social, familial and psychological risk factors for mood and anxiety disorders in childhood and early adulthood: a birth cohort study using the Danish Registry System. Soc Psychiatry Psychiatr Epidemiol

    Google Scholar 

  • Ingason A, Giegling I, Hartmann AM et al (2015) Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia. Transl Psychiatry 5:e656

    Google Scholar 

  • International Genomics of Alzheimer’s Disease Consortium (IGAP) (2015) Convergent genetic and expression data implicate immunity in Alzheimer’s disease. Alzheimers Dement 11:658–671

    Article  Google Scholar 

  • International Human Genome Sequencing Consortium (2001) Initial sequencing and analysis of the human genome. Nature 409:860–921

    Article  Google Scholar 

  • International Schizophrenia Consortium (2008) Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455:237–241

    Article  CAS  Google Scholar 

  • International Schizophrenia Consortium, Purcell SM, Wray NR et al (2009) Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460:748–752

    PubMed Central  Google Scholar 

  • Iqbal K, Liu F, Gong CX (2016) Tau and neurodegenerative disease: the story so far. Nat Rev Neurol 12:15–27

    Article  CAS  PubMed  Google Scholar 

  • Ising M, Lucae S, Binder EB et al (2009) A genomewide association study points to multiple loci that predict antidepressant drug treatment outcome in depression. Arch Gen Psychiatry 66:966–975

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Jacobs RH, Orr JL, Gowins JR et al (2015) Biomarkers of intergenerational risk for depression: a review of mechanisms in longitudinal high-risk (LHR) studies. J Affect Disord 175:494–506

    Article  PubMed  PubMed Central  Google Scholar 

  • Jeronimus BF, Ormel J, Aleman A et al (2013) Negative and positive life events are associated with small but lasting change in neuroticism. Psychol Med 43:2403–2415

    Article  CAS  PubMed  Google Scholar 

  • Jones L, Holmans PA, Hamshere ML et al (2010) Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer’s disease. PLoS One 5(11):e13950

    Google Scholar 

  • Jonsson T, Stefansson H, Steinberg S et al (2013) Variant of TREM2 associated with the risk of Alzheimer’s disease. N Engl J Med 368:107–116

    Article  CAS  PubMed  Google Scholar 

  • Kaprio J, Viken R, Koskenvuo M et al (1992) Consistency and change in patterns of social drinking: a 6-year follow-up of the Finnish twin cohort. Alcohol Clin Exp Res 16:234–240

    Article  CAS  PubMed  Google Scholar 

  • Keefe RSE, Silverman JM, Mohs RC et al (1997) Eye tracking, attention, and schizotypal symptoms in nonpsychotic relatives of patients with schizophrenia. Arch Gen Psychiatry 54:169–176

    Article  CAS  PubMed  Google Scholar 

  • Kelsoe JR, Ginns EI, Egeland JA et al (1989) Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish. Nature 342:238–243

    Article  CAS  PubMed  Google Scholar 

  • Kendler KS, Diehl SR (1993) The genetics of schizophrenia: a current, genetic-epidemiologic perspective. Schizophr Bull 19:261–285

    Article  CAS  PubMed  Google Scholar 

  • Kendler KS, Kessler RC, Neale MC et al (1993) The prediction of major depression in women: toward an integrated etiologic model. Am J Psychiatry 150:1139–1148

    Article  CAS  PubMed  Google Scholar 

  • Kendler KS, McGuire M, Gruenberg AM, Walsh D (1995a) Schizotypal symptoms and signs in the Roscommon Family Study. Their factor structure and familial relationship with psychotic and affective disorders. Arch Gen Psychiatry 52:296–303

    Article  CAS  PubMed  Google Scholar 

  • Kendler KS, Walters EE, Neale MC et al (1995b) The structure of the genetic and environmental risk factors for six major psychiatric disorders in women. Arch Gen Psychiatry 52:374–383

    Article  CAS  PubMed  Google Scholar 

  • Kendler KS, Karkowski-Shuman L, Walsh D (1996) Age at onset in schizophrenia and risk of illness in relatives. Br J Psychiatry 169:213–218

    Article  CAS  PubMed  Google Scholar 

  • Kendler KS, Prescott CA, Myers J, Neale MC (2003a) The structure of genetic and environmental risk factors for common psychiatric and substance use disorders in men and women. Arch Gen Psychiatry 60:929–937

    Article  PubMed  Google Scholar 

  • Kendler KS, Jacobson KC, Prescott CA, Neale M (2003b) Specificity of genetic and environmental risk factors for use and abuse/dependence of cannabis, cocaine, hallucinogens, sedatives, stimulants, and opiates in male twins. Am J Psychiatry 160:687–695

    Article  PubMed  Google Scholar 

  • Kendler KS, Myers J, Potter J, Opalesky J (2009) A web-based study of personality, psychopathology and substance use in twin, other relative and relationship pairs. Twin Res Hum Genet 12:137–141

    Article  PubMed  Google Scholar 

  • Keshavan MS, Tandon R, Boutros NN, Nasrallah HA (2008) Schizophrenia, „just the facts“: what we know in 2008 Part 3: Neurobiology. Schizophr Res 6:89–107

    Article  Google Scholar 

  • Kety SS (1983) Mental illness in the biological and adoptive relatives of schizophrenic adoptees, findings relevant to genetic and environmental factors in etiology. Am J Psychiatry 140:720–727

    Article  CAS  PubMed  Google Scholar 

  • Kinney DK, Holzman PS, Jacobsen B et al (1997) Thought disorder in schizophrenic and control adoptees and their relatives. Arch Gen Psychiatry 54:475–479

    Article  CAS  PubMed  Google Scholar 

  • Kirov G, Grozeva D, Norton N et al (2009) Support for the involvement of large copy number variants in the pathogenesis of schizophrenia. Hum Mol Genet 18:1497–1503

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Klein DN, Shankman SA, Lewinsohn PM et al (2004) Family study of chronic depression in a community sample of young adults. Am J Psychiatry 161:646–653

    Article  PubMed  Google Scholar 

  • Lambert JC, Amouyel P (2010) Deciphering genetic susceptibility to frontotemporal lobar dementia. Nat Genet 42:189–190

    Article  CAS  PubMed  Google Scholar 

  • Lambert JC, Heath S, Even G, European Alzheimer’s Disease Initiative Investigators et al (2009) Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer’s disease. Nat Genet 41:1094–1099

    Article  CAS  PubMed  Google Scholar 

  • Lambert JC, Ibrahim-Verbaas CA, Harold D et al (2013) Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer’s disease. Nat Genet 45:1452–1458

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lau JY, Eley TC (2010) The genetics of mood disorders. Annu Rev Clin Psychol 27:313–337

    Article  Google Scholar 

  • Lauer CJ, Schreiber W, Holsboer F, Krieg JC (1995) In quest of identifying vulnerability markers for psychiatric disorders by all-night polysomnography. Arch Gen Psychiatry 52:145–153

    Article  CAS  PubMed  Google Scholar 

  • Laursen TM, Labouriau R, Licht RW et al (2005) Family history of psychiatric Illness as a risk factor for schizoaffective disorder. Arch Gen Psychiatry 62:841–848

    Article  PubMed  Google Scholar 

  • Lerer B (2002) Pharmacogenetics of psychotropic drugs. Cambridge University Press, Cambridge

    Book  Google Scholar 

  • Lewis CM, Levinson DF, Wise LH et al (2003) Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: schizophrenia. Am J Hum Genet 73:34–48

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Li D, Sulovari A, Cheng C et al (2014) Association of gamma-aminobutyric acid A receptor α2 gene (GABRA2) with alcohol use disorder. Neuropsychopharmacology 39:907–918

    Article  CAS  PubMed  Google Scholar 

  • Liang HC, Russell C, Mitra V et al (2015) Glycosylation of human plasma clusterin yields a novel candidate biomarker of Alzheimer’s Disease. J Proteome Res 14:5063–5076

    Article  CAS  PubMed  Google Scholar 

  • Lichtenstein P, Yip BH, Björk C et al (2009) Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study. Lancet 373:234–239

    Article  CAS  PubMed  Google Scholar 

  • Lieb R, Wittchen HU, Hofler M et al (2000) Parental psychopathology, parenting styles, and the risk of social phobia in offspring: a prospective-longitudinal community study. Arch Gen Psychiatry 57:859–866

    Article  CAS  PubMed  Google Scholar 

  • Lill CM, Rengmark A, Pihlstrøm L et al (2015) The role of TREM2 R47H as a risk factor for Alzheimer’s disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson’s disease. Alzheimers Dement 11:1407–1416

    Article  PubMed  PubMed Central  Google Scholar 

  • Lionel AC, Tammimies K, Vaags AK et al (2014) Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. Hum Mol Genet 23:2752–2768

    Article  CAS  PubMed  Google Scholar 

  • Liu JZ, Tozzi F, Waterworth DM et al (2010) Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nat Genet 42:436–440

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Long JC, Knowler WC, Hanson RL et al (1998) Evidence for genetic linkage to alcohol dependence on chromosomes 4 and 11 from an autosome-wide scan in an American Indian population. Am J Med Genet 81:216–221

    Article  CAS  PubMed  Google Scholar 

  • Lubke GH, Laurin C, Amin N et al (2014) Genome-wide analyses of borderline personality features. Mol Psychiatry 19:923–929

    Article  CAS  PubMed  Google Scholar 

  • Lynskey MT, Agrawal A, Henders A et al (2012) An Australian twin study of cannabis and other illicit drug use and misuse, and other psychopathology. Twin Res Hum Genet 15:631–641

    Article  PubMed  PubMed Central  Google Scholar 

  • Maier W, Zobel A (2008) Contribution of allelic variations to the phenotype of response to antidepressants and antipsychotics. A Review. Eur Arch Psychiatry Clin Neurosci 258(Supp 1):12–20

    Article  PubMed  Google Scholar 

  • Maier W, Lichtermann D, Minges J et al (1993a) Continuity and discontinuity of affective disorders and schizophrenia. Arch Gen Psychiatry 50:871–883

    Article  CAS  PubMed  Google Scholar 

  • Maier W, Lichtermann D, Minges J et al (1993b) A controlled family study in panic disorder. J Psychiatr Res 27(Suppl 1):79–87

    Article  PubMed  Google Scholar 

  • Maier W, Lichtermann D, Minges J, Heun R (1994) Personality disorders among the relatives of schizophrenia patients. Schizophr Bull 20:481–493

    Article  CAS  PubMed  Google Scholar 

  • Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium, Ripke S, Wray NR et al (2013) A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry 18:497–511

    Article  CAS  Google Scholar 

  • Mandelli L, Serretti A (2013) Gene environment interaction studies in depression and suicidal behavior: an update. Neurosci Biobehav Rev 37:2375–2397

    Article  PubMed  Google Scholar 

  • Mannuzza S, Scneier FR, Chapman TF et al (1995) Generalized social phobia: reliability and validity. Arch Gen Psychiatry 52:230–237

    Article  CAS  PubMed  Google Scholar 

  • Maron E, Hettema JM, Shlik J (2010) Advances in molecular genetics of panic disorder. Mol Psychiatry 15:1–21

    Article  CAS  Google Scholar 

  • Maze I, Shen L, Zhang B et al (2014) Analytical tools and current challenges in the modern era of neuroepigenomics. Nat Neurosci 17:1476–1490

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • McCutcheon VV, Grant JD, Heath AC et al (2012) Environmental influences predominate in remission from alcohol use disorder in young adult twins. Psychol Med 42:2421–2431

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • McGue M, Gottesman II (1991) The genetic epidemiology of schizophrenia and the design of linkage studies. Eur Arch Psychiatry Clin Neurosci 240:174–181

    Article  CAS  PubMed  Google Scholar 

  • McGue M, Pickens RW, Sviskis DS (1992) Sex and age effects on the inheritance of alcohol problems: a twin study. J Abnorm Psychol 101:3–17

    Article  CAS  PubMed  Google Scholar 

  • McGuffin P, Farmer AE, Gottesmann II et al (1984) Twin concordance for operationally defined schizophrenia. Confirmation of familiality and heritability. Arch Gen Psychiatry 41:541–545

    Article  CAS  PubMed  Google Scholar 

  • McGuffin P, Rijsdijk F, Andrew M et al (2003) The heritability of bipolar affective disorder and the genetic relationship to unipolar depression. Arch Gen Psychiatry 60:497–502

    Article  PubMed  Google Scholar 

  • McGuffin P, Knight J, Breen G et al (2005) Whole genome linkage scan of recurrent depressive disorder from the depression network study. Hum Mol Genet 14:3337–3345

    Article  CAS  PubMed  Google Scholar 

  • McQueen MB, Devlin B, Faraone SV et al (2005) Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q. Am J Hum Genet 77:582–595

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Meaney MJ (2001) Maternal care, gene expression, and the transmission of individual differences in stress reactivity across generations. Annu Rev Neurosci 24:1161–1192

    Article  CAS  PubMed  Google Scholar 

  • Mendlewicz J, Papadimitriou GN, Wilmotte J (1993) Family study of panic disorder: comparison with generalized anxiety disorder, major depression and normal subjects. Psychiatr Genet 3:73–78

    Article  Google Scholar 

  • Merikangas KR, Low NC (2005) Genetic epidemiology of anxiety disorders. In: Handbook of Experimental Pharmacology. Springer, Berlin/Heidelberg, S 163–179

    Google Scholar 

  • Merikangas KR, Stolar M, Stevens DE et al (1998) Familial transmission of substance use disorders. Arch Gen Psychiatry 55:973–979

    Article  CAS  PubMed  Google Scholar 

  • Merikangas KR, Cui L, Heaton L et al (2014) Independence of familial transmission of mania and depression: results of the NIMH family study of affective spectrum disorders. Mol Psychiatry 19:214–219

    Article  CAS  PubMed  Google Scholar 

  • Meyer-Lindenberg A (2009) Neural connectivity as an intermediate phenotype: brain networks under genetic control. Hum Brain Mapp 30:1938–1946

    Article  PubMed  Google Scholar 

  • Meyer-Lindenberg A, Tost H (2014) Neuroimaging and plasticity in schizophrenia. Restor Neurol Neurosci 32(1):119–127

    PubMed  Google Scholar 

  • Montoliu-Gaya L, Villegas S (2015) Protein structures in Alzheimer’s disease: the basis for rationale therapeutic design. Arch Biochem Biophys 588:1–14

    Article  CAS  PubMed  Google Scholar 

  • Mortensen PB, Pedersen CB, Hougaard DM et al (2010) A Danish National Birth Cohort study of maternal HSV-2 antibodies as a risk factor for schizophrenia in their offspring. Schizophr Res 122:257–263

    Google Scholar 

  • Munafò MR, Freimer NB, Ng W et al (2009) 5-HTTLPR genotype and anxiety-related personality traits: a meta-analysis and new data. Am J Med Genet B Neuropsychiatr Genet 150B:271–281

    Article  PubMed  PubMed Central  Google Scholar 

  • Nazarian R, Starcevic M, Spencer MJ, Dell’Angelica EC (2006) Reinvestigation of the dysbindin subunit of BLOC-1 (biogenesis of lysosome-related organelles complex-1) as dystrobrevin-binding protein. Biochem J 395:587–589

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ng MY, Levinson DF, Faraone SV et al (2009) Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Mol Psychiatry 14:774–785

    Article  CAS  PubMed  Google Scholar 

  • Noyes R, Clarkson C, Crowe RR et al (1987) A family study of generalized anxiety disorder. Am J Psychiatry 144:1019–1024

    Article  PubMed  Google Scholar 

  • Nurnberger JI, Blehar MC, Kaufmann CA et al (1994) Diagnostic interview for genetic studies. Arch Gen Psychiatry 51:849–859

    Article  PubMed  Google Scholar 

  • O’Donovan MC, Craddock N, Norton N et al (2008) Molecular genetics of schizophrenia collaboration. Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat Genet 40:1053–1055

    Article  PubMed  CAS  Google Scholar 

  • Ormel J, Jeronimus BF, Kotov R et al (2013) Neuroticism and common mental disorders: meaning and utility of a complex relationship. Clin Psychol Rev 33:686–697

    Article  PubMed  PubMed Central  Google Scholar 

  • Otowa T, Yoshida E, Sugaya N et al (2009) Genome-wide association study of panic disorder in the Japanese population. J Hum Genet 54:122–126

    Article  CAS  PubMed  Google Scholar 

  • Otowa T, Hek K, Lee M et al (2016) Meta-analysis of genome-wide association studies of anxiety disorders. Mol Psychiatry 21:1391–1399

    Google Scholar 

  • Park S, Holzman PS, Goldman-Rakic S (1995) Spatial working memory deficits in the relatives of schizophrenic patients. Arch Gen Psychiatry 52:821–828

    Article  CAS  PubMed  Google Scholar 

  • Park BL, Kim JW, Cheong HS et al (2013) Extended genetic effects of ADH cluster genes on the risk ofalcohol dependence: from GWAS to replication. Hum Genet 132:657–668

    Article  CAS  PubMed  Google Scholar 

  • Pauls DL, Alsobrook JP 2nd, Goodman W et al (1995) A family study of obsessive-compulsive disorder. Am J Psychiatry 152:76–84

    Article  CAS  PubMed  Google Scholar 

  • Peng W, Wang HY, Miyahara Y et al (2008) Tumor-associated galectin-3 modulates the function of tumor-reactive T cells. Cancer Res 68:7228–7236

    Google Scholar 

  • Peralta V, Goldberg X, Ribeiro M et al (2015) Familiality of psychotic disorders: a polynosologic study in multiplex families. Schizophr Bull 42:975–983

    Google Scholar 

  • Perris C (1966) A study of bipolar (manic-depressive) and unipolar recurrent depressive psychoses, introduction. Acta Psychiatr Scand 194(Suppl):9–14

    Article  CAS  Google Scholar 

  • Polderman TJ, Benyamin B, de Leeuw CA et al (2015) Meta-analysis of the heritability of human traits based on fifty years of twin studies. Nat Genet 47:702–709

    Google Scholar 

  • Prescott CA, Sullivan PF, Kuo PH et al (2006) Genomewide linkage study in the Irish affected sib pair study of alcohol dependence: evidence for a susceptibility region for symptoms of alcohol dependence on chromosome 4. Mol Psychiatry 11:603–611

    Article  CAS  PubMed  Google Scholar 

  • Propping P (1989) Psychiatrische Genetik. Befunde und Konzepte. Springer, Berlin/Heidelberg/New York/Tokio

    Book  Google Scholar 

  • Purcell SM, Moran JL, Fromer M (2014) A polygenic burden of rare disruptive mutations in schizophrenia. Nature 506:185–190

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Puzzo D, Gulisano W, Arancio O, Palmeri A (2015) The keystone of Alzheimer pathogenesis might be sought in Aβ physiology. Neuroscience 307:26–36

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Reich T, Edenberg HJ, Goate A et al (1998) Genome-wide search for genes affecting the risk for alcohol dependence. Am J Med Genet 81:207–215

    Article  CAS  PubMed  Google Scholar 

  • Richmond-Rakerd LS, Slutske WS, Deutsch AR et al (2015) Progression in substance use initiation: a multilevel discordant monozygotic twin design. J Abnorm Psychol 124:596–605

    Article  PubMed  PubMed Central  Google Scholar 

  • Rietschel M, Treutlein J (2013) The genetics of alcohol dependence. Ann N Y Acad Sci 1282:39–70

    Article  CAS  PubMed  Google Scholar 

  • Risch N (1990) Linkage strategies for genetically complex traits. I. Multilocus models. Am J Hum Genet 46:222–228

    CAS  PubMed  PubMed Central  Google Scholar 

  • Risch N, Herrell R, Lehner T et al (2009) Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis. JAMA 301:2462–2471

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Rommelse NN, Van der Stigchel S, Sergeant JA (2008) A review on eye movement studies in childhood and adolescent psychiatry. Brain Cogn 68:391–414

    Article  PubMed  Google Scholar 

  • Rosenberg DR, Sweeney JA, Squires-Wheeler E et al (1997) Eye-tracking dysfunction in offspring from the New York high-risk project: diagnostic specificity and the role of attention. Psychiatry Res 66:121–130

    Article  CAS  PubMed  Google Scholar 

  • Ross CA, Margolis RL, Reading SAJ et al (2006) Neurobiology of Schizophrenia. Neuron 52:139–153

    Article  CAS  PubMed  Google Scholar 

  • Rüdin E (1916) Zur Vererbung und Neuentstehung der Dementia praecox. In: Studien über Vererbung und Entstehung geistiger Störungen. Handbuch der Erbkrankheiten, Bd 2, Die Schizophrenie. Springer, Berlin

    Google Scholar 

  • Rujescu D, Bender A, Keck M et al (2006) A pharmacological model for psychosis based on N-methyl-D-aspartate receptor hypofunction: molecular, cellular, functional and behavioral abnormalities. Biol Psychiatry 59:721–729

    Article  CAS  PubMed  Google Scholar 

  • Rujescu D, Ingason A, Cichon S et al (2009) Disruption of the neurexin 1 gene is associated with schizophrenia. Hum Mol Genet 18:988–996

    Article  CAS  PubMed  Google Scholar 

  • Saccone SF, Hinrichs AL, Saccone NL et al (2007) Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs. Hum Mol Genet 16:36–49

    Article  CAS  PubMed  Google Scholar 

  • Salvatore JE, Gottesman II, Dick DM (2015) Endophenotypes for alcohol use disorder: an update on the field. Curr Addict Rep 2:76–90

    Article  PubMed  PubMed Central  Google Scholar 

  • Saunders AM, Schmader K, Breitner JC et al (1993) Apolipoprotein E epsilon 4 allele distributions in late-onset Alzheimer’s disease and in other amyloid-forming diseases. Lancet 342:710–711

    Article  CAS  PubMed  Google Scholar 

  • Schizophrenia Working Group of the Psychiatric Genomics Consortium (2014) Biological insights from 108 schizophrenia-associated genetic loci. Nature 511:421–427

    Article  PubMed Central  CAS  Google Scholar 

  • Schlaepfer IR, Hoft NR, Ehringer MA (2008) The genetic components of alcohol and nicotine co-addiction: from genes to behavior. Curr Drug Abuse Rev 1:124–134

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Schulze G, Hedeker D, Zandi P et al (2006) What is familial about familial bipolar disorder? Arch Gen Psychiatry 63:1368–1376

    Article  PubMed  Google Scholar 

  • Serretti A, Kato M, De Ronchi D, Kinoshita T (2007) Meta-analysis of serotonin transporter gene promoter polymorphism (5-HTTLPR) association with selective serotonin reuptake inhibitor efficacy in depressed patients. Mol Psychiatry 12:247–257

    Article  CAS  PubMed  Google Scholar 

  • Shi J, Levinson DF, Duan J et al (2009) Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature 460:753–757

    CAS  PubMed  PubMed Central  Google Scholar 

  • Shih RA, Belmonte PL, Zandi PP (2004) A review of the evidence from family, twin and adoption studies for a genetic contribution to adult psychiatric disorders. Int Rev Psychiatry 16:260–283

    Article  PubMed  Google Scholar 

  • Shimada-Sugimoto M, Otowa T, Hettema JM (2015) Genetics of anxiety disorders: genetic epidemiological and molecular studies in humans. Psychiatry Clin Neurosci 69:388–401

    Article  CAS  PubMed  Google Scholar 

  • Shprintzen RJ (2008) Velo-cardio-facial syndrome: 30 years of study Dev Disabil Res Rev 14:3–10

    Article  PubMed  PubMed Central  Google Scholar 

  • Silberg J, Rutter M, Neale M, Eaves L (2001) Genetic moderation of environmental risk for depression and anxiety in adolescent girls. Br J Psychiatry 179:116–121

    Article  CAS  PubMed  Google Scholar 

  • Sklar P, Smoller JW, Fan J et al (2008) Whole-genome association study of bipolar disorder. Mol Psychiatry 13:558–569

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sleegers K, Lambert JC, Bertram L et al (2009) The pursuit of susceptibility genes for Alzheimer’s disease: progress and prospects. Trends Genet 2:84–93

    Google Scholar 

  • Slutske WS, True WR, Scherrer JF et al (1999) The heritability of alcoholism symptoms: „indicators of genetic and environmental influence in alcohol-dependent individuals“ revisited. Alcohol Clin Exp Res 23:759–769

    Google Scholar 

  • Stefansson H, Sarginson J, Kong A et al (2003) Association of neuregulin 1 with schizophrenia confirmed in a Scottish population. Am J Hum Genet 72:83–87

    Article  CAS  PubMed  Google Scholar 

  • Stefansson H, Rujescu D, Cichon S et al (2008) Large recurrent microdeletions associated with schizophrenia. Nature 455:232–236

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Stefansson H, Ophoff RA, Steinberg S, Genetic Risk and Outcome in Psychosis (GROUP) et al (2009) Common variants conferring risk of schizophrenia. Nature 460:744–747

    CAS  PubMed  PubMed Central  Google Scholar 

  • Stein MB, Chartier MJ, Hazen AL et al (1998) A direct-interview family study of generalized social phobia. Am J Psychiatry 155:90–97

    Article  CAS  PubMed  Google Scholar 

  • Steinberg S, Stefansson H, Jonsson T et al (2015) Loss-of-function variants in ABCA7 confer risk of Alzheimer’s disease. Nat Genet 47:445–447

    Article  CAS  PubMed  Google Scholar 

  • Straub RE, Jiang Y, MacLean CJ et al (2002) Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia. Am J Hum Genet 71:337–348

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Strittmatter WJ, Saunders AM, Schmechel D et al (1993) Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease. Proc Natl Acad Sci U S A 90:1977–1981

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sullivan PF, Kendler KS (1999) The gentic epidemiology of smoking. Nicotine Tob Res 1(Suppl 2):51–57

    Article  Google Scholar 

  • Sullivan PF, Neale MC, Kendler KS (2000) Genetic epidemiology of major depression: review and meta-analysis. Am J Psychiatry 157:1552–1562

    Article  CAS  PubMed  Google Scholar 

  • Sullivan PF, Kendler KS, Neale MC (2003) Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies. Arch Gen Psychiatry 60:1187–1192

    Article  PubMed  Google Scholar 

  • Sullivan PF, de Geus EJ, Willemsen G et al (2009) Genome-wide association for major depressive disorder: a possible role for the presynaptic protein Piccolo. Mol Psychiatry 14:359–375

    Article  CAS  PubMed  Google Scholar 

  • Tambs K, Czajkowsky N, Roysamb E et al (2009) Structure of genetic and environmental risk factors for dimensional representations of DSM-IV anxiety disorders. Br J Psychiatry 195:301–307

    Article  PubMed  PubMed Central  Google Scholar 

  • Tandon R, Keshavan MS, Nasrallah HA (2008) Schizophrenia, „just the facts“ what we know in 2008. 2. Epidemiology and etiology. Schizophr Res 102:1–18

    Article  PubMed  Google Scholar 

  • Tandon R, Nasrallah HA, Keshavan MS (2009) Schizophrenia, „just the facts“ 4. Clinical features and conceptualization. Schizophr Res 110:1–23

    Article  PubMed  Google Scholar 

  • Thompson PM, Andreassen OA, Arias-Vasquez A et al (2015) ENIGMA and the individual: predicting factors that affect the brain in 35 countries worldwide. Neuroimage. doi:10.1016/j.neuroimage.2015.11.057. [Epub vor Druck]

  • Thorgeirsson TE, Geller F, Sulem P et al (2008) A variant associated with nicotine dependence, lung cancer and peripheral arterial disease. Nature 452:638–642

    Google Scholar 

  • Thorgeirsson TE, Gudbjartsson DF, Surakka I et al (2010) Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nat Genet 42:448–453

    Google Scholar 

  • Tienari P, Wynne LC, Sorri A et al (2004) Genotype-environment interaction in schizophrenia-spectrum disorder. Long-term follow-up study of Finnish adoptees. Br J Psychiatry 184:216–222

    Article  PubMed  Google Scholar 

  • Tobacco and Genetics Consortium (2010) Genome-wide meta-analyses identify multiple loci associated with smoking behavior. Nat Genet 42:441–447

    Article  CAS  Google Scholar 

  • Treutlein J, Cichon S, Ridinger M, et al (2009) Genome-wide association study of alcohol dependence. Arch Gen Psychiatry 66:773–784

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Tsuang DW, Skol AD, Faraone SV et al (2001) Examination of genetic linkage of chromosome 15 to schizophrenia in a large Veterans Affairs Cooperative Study sample. Am J Med Genet 105:662–668

    Article  CAS  PubMed  Google Scholar 

  • Uher U, Nader P, Mandy YM et al (2010) Genome-wide pharmacogenetics of antidepressant response in the GENDEP Project. Am J Psychiatry 167:555–564

    Article  PubMed  Google Scholar 

  • Van den Oord EJ, Kuo PH, Hartmann AM et al (2008) Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism. Arch Gen Psychiatry 65:1062–1071

    Article  PubMed  Google Scholar 

  • Van Os J, Marcelis M, Sham P et al (1997) Psychopathological syndromes and familial morbid risk of psychosis. Br J Psychiatry 170:241–246

    Article  PubMed  Google Scholar 

  • Venter JC, Adams MD, Myers EW et al (2001) The sequence of the human genome. Science 291:1304–1351

    Google Scholar 

  • Verhagen M, van der Meij A, van Deurzen PA et al (2010) Meta-analysis of the BDNF Val66Met polymorphism in major depressive disorder: effects of gender and ethnicity. Mol Psychiatry 15:260–271

    Article  CAS  PubMed  Google Scholar 

  • Viken RJ, Kaprio J, Koskenvuo M et al (1999) Longitudinal analyses of the determinants of drinking and of drinking to intoxication in adoslescent twins. Behav Genet 29:455–461

    Article  CAS  PubMed  Google Scholar 

  • Vink JM, Boomsma DI (2011) Interplay between heritability of smoking and environmental conditions? A comparison of two birth cohorts. BMC Public Health 11:316

    Article  PubMed  PubMed Central  Google Scholar 

  • Vogel F (1959) Moderne Probleme der Humangenetik. Ergeb Inn Med Kinderheilkd 12:52–125

    Google Scholar 

  • Wang KS, Liu X, Zhang Q et al (2011) A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence. J Psychiatr Res 45:1419–1425

    Google Scholar 

  • Wang Q, Lu Q, Zhao H (2015) A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing. Front Genet 6:149

    PubMed  PubMed Central  Google Scholar 

  • Wellcome Trust Case Control Consortium, WTCCC (2007) Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447:661–678

    Article  CAS  Google Scholar 

  • Wilde A, Chan HN, Rahman B et al (2014) A meta-analysis of the risk of major affective disorder in relatives of individuals affected by major depressive disorder or bipolar disorder. J Affect Disord 158:37–47

    Google Scholar 

  • Winokur G, Clayton P (1966) Family history studies. I. Two types of affective disorders separated according to genetic and clinical factors. Recent Adv Biol Psychiatry 9:35–50

    CAS  PubMed  Google Scholar 

  • Winterer G, Mittelstrass K, Giegling I et al (2010) Risk gene variants for nicotine dependence in the CHRNA5-CHRNA3-CHRNB4 cluster are associated with cognitive performance. Am J Med Genet B Neuropsychiatr Genet 153B:1448–1458

    Article  PubMed  Google Scholar 

  • Xu B, Roos JL, Dexheimer P, Boone B et al (2011) Exome sequencing supports a de novo mutational paradigm for schizophrenia. Nat Genet 43:864–868

    Google Scholar 

  • Xu B, Ionita-Laza I, Roos JL et al (2012) De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia. Nat Genet 44:1365–1369

    Google Scholar 

  • Zahn TP, Nurnberger JI, Berrettini WH (1989) Electrodermal activity in young adults at genetic risk for affective disorder. Arch Gen Psychiatry 46:1120–1124

    Article  CAS  PubMed  Google Scholar 

  • Zammit S, Owen MJ (2006) Stressful life events, 5-HTT genotype and risk of depression. Br J Psychiatry 188:199–201

    Article  PubMed  Google Scholar 

  • Zobel A, Maier W (2004) Endophänotypen — ein neues Konzept zur biologischen Charakterisierung psychischer Störungen. Nervenarzt 75:205–214

    Article  CAS  PubMed  Google Scholar 

  • Zuo L, Gelernter J, Zhang CK et al (2012) Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q. Neuropsychopharmacology 37:557–566

    Google Scholar 

  • Zuo L, Tan Y, Zhang X et al (2015) A new genomewide association meta-analysis of alcohol dependence. Alcohol Clin Exp Res 39:1388–1395

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Wolfgang Maier .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2017 Springer-Verlag GmbH Deutschland

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Maier, W., Giegling, I., Rujescu, D. (2017). Genetik und Gen-Umwelt-Interaktionen bei psychischen Erkrankungen. In: Möller, HJ., Laux, G., Kapfhammer, HP. (eds) Psychiatrie, Psychosomatik, Psychotherapie. Springer Reference Medizin. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-49295-6_5

Download citation

  • DOI: https://doi.org/10.1007/978-3-662-49295-6_5

  • Published:

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-662-49293-2

  • Online ISBN: 978-3-662-49295-6

  • eBook Packages: Medicine (German Language)

Publish with us

Policies and ethics