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Citing Papers
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A unified mixed-model method for association mapping that accounts for multiple levels of relatedness
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A Genomic and Functional Inventory of Deubiquitinating Enzymes
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Five Years of GWAS Discovery
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Knockdown of DISC1 by In Utero Gene Transfer Disturbs Postnatal Dopaminergic Maturation in the Frontal Cortex and Leads to Adult Behavioral Deficits
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Human Dysbindin (DTNBP1) Gene Expression inNormal Brain and in Schizophrenic Prefrontal Cortex and Midbrain
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Cleft lip and palate: understanding genetic and environmental influences
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Cleft lip and palate
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Right hemisphere language functions and schizophrenia: the forgotten hemisphere?
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"Schizotaxia": Clinical Implications and New Directions for Research
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Deletion mapping of stature determinants on the long arm of the Y chromosome
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Transmission/disequilibrium tests for quantitative traits
2000
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Haplotyping and estimation of haplotype frequencies for closely linked biallelic multilocus genetic phenotypes including nuclear family information
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Increased Serum Levels of Inflammatory Markers in Chronic Institutionalized Patients with Schizophrenia
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Genetic variation in AKT1 is linked to dopamine-associated prefrontal cortical structure and function in humans
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The molecular genetics of schizophrenia: new findings promise new insights
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Genetic analysis of the gene coding for DARPP-32 (PPP1R1B) in Japanese patients with schizophrenia or bipolar disorder
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Theory of mind impairment: a distinct trait‐marker for schizophrenia spectrum disorders and bipolar disorder?
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Dysbindin-1 is reduced in intrinsic, glutamatergic terminals of the hippocampal formation in schizophrenia
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Mechanisms of fatty acid-induced inhibition of glucose uptake.
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Immune signalling in neural development, synaptic plasticity and disease
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The Endophenotype Concept in Psychiatry: Etymology and Strategic Intentions
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Effects of perinatal mental disorders on the fetus and child
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Genome-wide association studies for common diseases and complex traits
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Polymorphisms in the 3′-untranslated region of human and monkey dopamine transporter genes affect reporter gene expression
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Epistatic and Functional Interactions of Catechol-O-Methyltransferase (COMT) and AKT1 on Neuregulin1-ErbB Signaling in Cell Models
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Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder
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The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia
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If it goes up, must it come down? Chronic stress and the hypothalamic-pituitary-adrenocortical axis in humans.
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Modeling Madness in Mice: One Piece at a Time
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Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)
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Neuregulin 1 and schizophrenia
2004
Interaction Between Serotonin Transporter Gene Variation and RearingCondition in Alcohol Preference and Consumption in Female Primates
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Toward Reformulating the Diagnosis of Schizophrenia
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Association between AKT1 gene and Parkinson's disease: A protective haplotype
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The Future of Association Studies: Gene-Based Analysis and Replication
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Is the P300 wave an endophenotype for schizophrenia? A meta-analysis and a family study
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Social performance is more closely associated with theory of mind and autobiographical memory than with psychopathological symptoms in clinically stable patients with schizophrenia-spectrum disorders
2010
Slc15a4, AP-3, and Hermansky-Pudlak syndrome proteins are required for Toll-like receptor signaling in plasmacytoid dendritic cells
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Lithium-related genetics of bipolar disorder
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A high-performance computing toolset for relatedness and principal component analysis of SNP data
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Sexual dichotomy of an interaction between early adversity and the serotonin transporter gene promoter variant in rhesus macaques
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The Common Neural Basis of Autobiographical Memory, Prospection, Navigation, Theory of Mind, and the Default Mode: A Quantitative Meta-analysis
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Cortical inhibitory neurons and schizophrenia
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Possible association of β‐arrestin 2 gene with methamphetamine use disorder, but not schizophrenia
2006
Functional Coherence of the Human Y Chromosome
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The Human Genome Project and Its Impact on Psychiatry
2002
Schizophrenia: a common disease caused by multiple rare alleles
2007
Physical illness in patients with severe mental disorders. I. Prevalence, impact of medications and disparities in health care
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Cortical Activations During Auditory Verbal Hallucinations in Schizophrenia: A Coordinate-Based Meta-Analysis
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Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIα gene (PIP5K2A) with schizophrenia
2006
Akt/GSK3 Signaling in the Action of Psychotropic Drugs
2008
GSK-3: tricks of the trade for a multi-tasking kinase
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Effect of COMT Val 108/158 Met genotype on frontal lobe function and risk for schizophrenia
2001 Standout
Robust relationship inference in genome-wide association studies
2010 Standout
Dysbindin-1 is reduced in intrinsic, glutamatergic terminals of the hippocampal formation in schizophrenia
2004
High‐throughput single‐nucleotide polymorphism analysis of the IL1RN locus in patients with ankylosing spondylitis by matrix‐assisted laser desorption ionization‐time‐of‐flight mass spectrometry
2003
LINKAGE ANALYSIS IN PSYCHIATRIC DISORDERS : The Emerging Picture
2002
Molecular Genetics of Attention-Deficit/Hyperactivity Disorder
2005 Standout
Works of M. Trixler being referenced
Minor physical anomalies in affective disorders. A review of the literature
2008
Support for Association of Schizophrenia with Genetic Variation in the 6p22.3 Gene, Dysbindin, in Sib-Pair Families with Linkage and in an Additional Sample of Triad Families
2003
Minor physical anomalies in schizophrenia and bipolar affective disorder
2001
Theory of mind deficit in people with schizophrenia during remission
2002
Further Evidence for Association of Variants in the AKT1 Gene with Schizophrenia in a Sample of European Sib-Pair Families
2005
DNA sequence variants in the metabotropic glutamate receptor 3 and risk to schizophrenia: an association study
2008
Use of Antipsychotics in the Management of Schizophrenia during Pregnancy
2005
DAT1 gene polymorphism in alcoholism: a family-based association study
1999
Support for a Chromosome 18p Locus Conferring Susceptibility to Functional Psychoses in Families with Schizophrenia, by Association and Linkage Analysis
1998
Schizophrenics Show a Failure in the Decoding of Violations of Conversational Implicatures
2002
Transmission/Disequilibrium Tests Using Multiple Tightly Linked Markers
2000
A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6
2000
Association of tumor necrosis factor alpha gene -G308A polymorphism with schizophrenia
2003
Support for Allelic Association of a Polymorphic Site in the Promoter Region of the Serotonin Transporter Gene With Risk for Alcohol Dependence
2000
18P — A susceptibility locus for affective and schizophrenic disorder?
1996
Further evidence for a susceptibility locus on chromosome 10p14–p11 in 72 families with schizophrenia by nonparametric linkage analysis
1998
Risks associated with childbearing in schizophrenia.
1996
Yq deletion with short stature, abnormal male development, and schizoid character disorder.
1983
Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysis.
1998
Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysis
1998