Finding Suitable Phenotypes for Genetic Studies of Schizophrenia: Heritability and Segregation Analysis
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Richard J. Sinke | René S. Kahn | Chantal Kemner | Roel A. Ophoff | Behrooz Z. Alizadeh | R. Ophoff | R. Kahn | R. Sinke | C. Kemner | B. Alizadeh | M. Sitskoorn | Margriet M. Sitskoorn | J. Selten | Jean-Paul Selten | Maartje F. Aukes | M. Aukes
[1] N. Craddock,et al. Single major locus models for bipolar disorder are implausible. , 1997, American journal of medical genetics.
[2] L. Almasy,et al. Multipoint quantitative-trait linkage analysis in general pedigrees. , 1998, American journal of human genetics.
[3] B Müller-Myhsok,et al. Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia. , 1999, American journal of medical genetics.
[4] E. Kraepelin. Psychiatrie : ein Lehrbuch für Studi[e]rende und Aerzte , 1976 .
[5] A. Tuulio-Henriksson,et al. Heritability of cognitive functions in families with bipolar disorder , 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[6] P. Venables,et al. INPUT DYSFUNCTION IN SCHIZOPHRENIA. , 1964, Progress in experimental personality research.
[7] T. Bouchard,et al. Genetic and environmental influences on human psychological differences. , 2003, Journal of neurobiology.
[8] Wiepke Cahn,et al. Brain volumes in relatives of patients with schizophrenia: a meta-analysis. , 2007, Archives of general psychiatry.
[9] G. Box. An analysis of transformations (with discussion) , 1964 .
[10] A. Fanous,et al. Genetic heterogeneity, modifier genes, and quantitative phenotypes in psychiatric illness: searching for a framework , 2006, Molecular Psychiatry.
[11] B. Maher,et al. Progress in experimental personality research , 1964 .
[12] L Kruglyak,et al. Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[13] A. Mcghie,et al. Disorders of attention and perception in early schizophrenia. , 1961, The British journal of medical psychology.
[14] Denis C. Shields,et al. Segregation analysis of complex phenotypes: an application to schizophrenia and auditory P300 latency. , 1994 .
[15] D. Carmelli,et al. Evidence for genetic mediation of executive control: a study of aging male twins. , 2002, The journals of gerontology. Series B, Psychological sciences and social sciences.
[16] Michael F. Green,et al. Development of a computerized assessment for visual masking , 2002, International journal of methods in psychiatric research.
[17] Leena Peltonen,et al. Genetic linkage and association between chromosome 1q and working memory function in schizophrenia , 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[18] L. Hong,et al. Evidence of Missense Mutations on the Neuregulin 1 Gene Affecting Function of Prepulse Inhibition , 2008, Biological Psychiatry.
[19] S. R. Ross,et al. Positive and Negative Symptoms of Schizotypy and the Five-Factor Model: A Domain and Facet Level Analysis , 2002, Journal of personality assessment.
[20] D. Sheehan,et al. The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. , 1998, The Journal of clinical psychiatry.
[21] Tyrone D. Cannon,et al. The inheritance of neuropsychological dysfunction in twins discordant for schizophrenia. , 2000, American journal of human genetics.
[22] R. Elston,et al. The finite polygenic mixed model: An alternative formulation for the mixed model of inheritance , 1994, Theoretical and Applied Genetics.
[23] G. Carey,et al. Codistribution of a sensory gating deficit and schizophrenia in multi-affected families , 1991, Psychiatry Research.
[24] D E Weeks,et al. Polygenic disease: methods for mapping complex disease traits. , 1995, Trends in genetics : TIG.
[25] M. Egan,et al. Prefrontal neurons and the genetics of schizophrenia , 2001, Biological Psychiatry.
[26] H. Akaike. A new look at the statistical model identification , 1974 .
[27] Tyrone D. Cannon,et al. Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q. , 2004, Human molecular genetics.
[28] M. Boehnke,et al. Commingling and segregation analyses: Comparison of results from a simulation study of a quantitative trait , 1990, Genetic epidemiology.
[29] M. Baron,et al. Genetics of schizophrenia and the new millennium: progress and pitfalls. , 2001, American journal of human genetics.
[30] I. Gottesman,et al. Twin studies of schizophrenia: from bow-and-arrow concordances to star wars Mx and functional genomics. , 2000, American journal of medical genetics.
[31] Robert C. Elston,et al. Evidence for a Major Gene Influence on Tumor Necrosis Factor-α Expression in Tuberculosis: Path and Segregation Analysis , 2005, Human Heredity.
[32] S. Faraone,et al. The genetics of schizophrenia , 1999, Current psychiatry reports.
[33] Nick Craddock,et al. The genetic deconstruction of psychosis. , 2007, Schizophrenia bulletin.
[34] R. Bagby,et al. Relationship between the five-factor model of personality and unipolar, bipolar and schizophrenic patients , 1997, Psychiatry Research.
[35] Jordan B. Peterson,et al. Sources of openness/intellect: cognitive and neuropsychological correlates of the fifth factor of personality. , 2005, Journal of personality.
[36] S Matthysse,et al. The genetic transmission of schizophrenia: application of Mendelian latent structure analysis to eye tracking dysfunctions in schizophrenia and affective disorder. , 1986, Journal of psychiatric research.
[37] F. Rijsdijk,et al. Reaction time, inhibition, working memory and ‘delay aversion’ performance: genetic influences and their interpretation , 2006, Psychological Medicine.
[38] Junghee Lee,et al. Working memory impairments in schizophrenia: a meta-analysis. , 2005, Journal of abnormal psychology.
[39] P. McGuffin,et al. Simulation of Mendelism revisited: the recessive gene for attending medical school. , 1990, American journal of human genetics.
[40] C. Robert Cloninger,et al. Evidence for the multigenic inheritance of schizophrenia. , 2001, American journal of medical genetics.
[41] N. Boutros,et al. Genetic and environmental influences on sensory gating of mid-latency auditory evoked responses: A twin study , 2007, Schizophrenia Research.
[42] René S. Kahn,et al. Cognitive deficits in relatives of patients with schizophrenia: a meta-analysis , 2004, Schizophrenia Research.
[43] Tyrone D. Cannon,et al. Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia. , 2002, American journal of medical genetics.
[44] B. Clementz,et al. Smooth pursuit ocular motor dysfunction in schizophrenia: evidence for a major gene. , 1992, The American journal of psychiatry.
[45] H. Coon,et al. Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families. , 1999, American journal of medical genetics.
[46] A. Aleman,et al. Associations between Delusion Proneness and Personality Structure in Non-Clinical Participants: Comparison between Young and Elderly Samples , 2006, Psychopathology.
[47] J. Henry,et al. A meta-analytic review of verbal fluency deficits in schizophrenia relative to other neurocognitive deficits , 2005, Cognitive neuropsychiatry.
[48] I. Gottesman,et al. The endophenotype concept in psychiatry: etymology and strategic intentions. , 2003, The American journal of psychiatry.
[49] David Wechsler,et al. Wechsler Memory scale. , 2005 .
[50] Andrew C Heath,et al. Genetic influences on prepulse inhibition of startle reflex in humans , 2003, Neuroscience Letters.
[51] N. Risch,et al. The continuous performance test, identical pairs version (CPT-IP): I. new findings about sustained attention in normal families , 1988, Psychiatry Research.
[52] H. Coon,et al. Use of a neurophysiological trait in linkage analysis of schizophrenia , 1993, Biological Psychiatry.
[53] R. Freedman,et al. Heritability of inhibitory gating of the P50 auditory-evoked potential in monozygotic and dizygotic twins. , 1996, Neuropsychobiology.
[54] John Blangero,et al. Neurocognitive endophenotypes in a multiplex multigenerational family study of schizophrenia. , 2007, The American journal of psychiatry.
[55] C. Robert Cloninger,et al. Linkage disequilibrium for schizophrenia at the chromosome 15q13-14 locus of the alpha7-nicotinic acetylcholine receptor subunit gene (CHRNA7). , 2001, American journal of medical genetics.
[56] Michael F. Green,et al. Initial heritability analyses of endophenotypic measures for schizophrenia: the consortium on the genetics of schizophrenia. , 2007, Archives of general psychiatry.
[57] J Blangero,et al. Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentials. , 1999, American journal of human genetics.
[58] B Müller-Myhsok,et al. Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease. , 1996, American journal of medical genetics.
[59] T. Hergueta,et al. The mini international neuropsychiatric interview , 1998, European Psychiatry.
[60] T. Goldberg,et al. Letter and category fluency in schizophrenic patients: a meta-analysis , 2003, Schizophrenia Research.
[61] B. Breitmeyer,et al. Forward and backward visual masking in schizophrenia: influence of age , 2003, Psychological Medicine.
[62] Michael F. Green,et al. Multi-site studies of acoustic startle and prepulse inhibition in humans: Initial experience and methodological considerations based on studies by the Consortium on the Genetics of Schizophrenia , 2007, Schizophrenia Research.
[63] Marcia A. Bockbrader,et al. Personality traits in schizophrenia and related personality disorders , 2005, Psychiatry Research.
[64] C. Duijn,et al. Cerebrovascular risk factors do not contribute to genetic variance of cognitive function The ERF study , 2007, Neurobiology of Aging.
[65] R. Kahn,et al. Modulating sensorimotor gating in healthy volunteers: the effects of desipramine and haloperidol , 2004, Psychiatry Research.
[66] Steven Matthysse,et al. Linkage of eye movement dysfunction to chromosome 6p in schizophrenia: Additional evidence , 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[67] N C Andreasen,et al. The Comprehensive Assessment of Symptoms and History (CASH). An instrument for assessing diagnosis and psychopathology. , 1992, Archives of general psychiatry.
[68] Robin M. Murray,et al. Heritability and Reliability of P300, P50 and Duration Mismatch Negativity , 2006, Behavior genetics.
[69] G. Bonney,et al. On the statistical determination of major gene mechanisms in continuous human traits: regressive models. , 1984, American journal of medical genetics.
[70] J. M. Digman. PERSONALITY STRUCTURE: EMERGENCE OF THE FIVE-FACTOR MODEL , 1990 .
[71] I. Waldman. Statistical Approaches to Complex Phenotypes: Evaluating Neuropsychological Endophenotypes for Attention-Deficit/Hyperactivity Disorder , 2005, Biological Psychiatry.
[72] D L Braff,et al. Sensorimotor gating and schizophrenia. Human and animal model studies. , 1990, Archives of general psychiatry.
[73] N. Swerdlow,et al. Effects of Background and Prepulse Characteristics on Prepulse Inhibition and Facilitation: Implications for Neuropsychiatric Research , 2006, Biological Psychiatry.
[74] M. Owen,et al. An update on the genetics of schizophrenia , 2006, Current opinion in psychiatry.