| Response to letter to the editor from Schulze et al.—“Is there a phenotypic difference between probands in case‐control versus family‐based association studies?” |
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| Allelic variants interaction of dopamine receptor D4 polymorphism correlate with personality traits in young Korean female population |
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| A “line item” approach to the identification of genes involved in polygenic behavioral disorders: The Adrenergic α<sub>2A</sub><i>(ADRA2A)</i> gene |
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| Continuing the search for dyslexia genes on 6p |
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| Transcriptional activities of cholecystokinin promoter haplotypes and their relevance to panic disorder susceptibility |
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| Suicide and serotonin: Study of variation at seven serotonin receptor genes in suicide completers |
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| Allelic variation in serotonin transporter function associated with the intensity dependence of the auditory evoked potential |
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| Modest evidence for linkage and possible confirmation of association between NOTCH4 and schizophrenia in a large veterans affairs cooperative study sample |
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European Americans; African Americans; racially mixed or other races |
| Family‐based and case‐control association studies of catechol‐<i>O</i>‐methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism |
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| Is there a phenotypic difference between probands in case‐control versus family‐based association studies? |
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| Variation in the coding sequence and flanking splice junctions of the estrogen receptor alpha (<i>ERα</i>) gene does not play an important role in genetic susceptibility to bipolar disorder or bipolar |
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| Gender‐specific molecular heterosis and association studies: Dopamine D2 receptor gene and smoking |
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| Distribution of haplotypes derived from three common variants of the <i>NR4A2</i> gene in Japanese patients with schizophrenia |
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Japanese |
| Linkage mapping of beta 2 EEG waves via non‐parametric regression |
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| Association analysis of the HOPA<sup>12bp</sup> polymorphism in schizophrenia and manic depressive illness |
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| An investigation of the <i>5‐HT<sub>2C</sub></i> receptor gene as a migraine candidate gene |
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| Association study between dopamine D<sub>3</sub> receptor gene variant and personality traits |
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Swedish population |
| Dopamine Beta‐Hydroxylase (DBH) gene and schizophrenia phenotypic variability: A genetic association study |
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| Association of a <i>MAOA</i> gene variant with generalized anxiety disorder, but not with panic disorder or major depression |
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| Role of elastin polymorphisms in panic disorder |
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| Association of an exonic <i>LDHA</i> polymorphism with altered respiratory response in probands at high risk for panic disorder |
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| Absence of MeCP2 mutations in patients from the South Carolina autism project |
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| Functional variation in promoter region of monoamine oxidase A and subtypes of alcoholism: Haplotype analysis |
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| Human nuclear transcription factor gene <i>CREM</i>: Genomic organization, mutation screening, and association analysis in panic disorder |
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German, Italian, Spanish |
| Association of GABA<sub>A</sub> receptors and alcohol dependence and the effects of genetic imprinting |
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| Genetic refinement and physical mapping of a 2.3 Mb probable disease region associated with a bipolar affective disorder susceptibility locus on chromosome 4q35 |
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| Heritability of attention problems in children: I. cross‐sectional results from a study of twins, age 3–12 years |
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| Relationship between functional dopamine D2 and D3 receptors gene polymorphisms and neuroleptic malignant syndrome |
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| Association of the 3′ UTR transcription factor LBP‐1c/CP2/LSF polymorphism with late‐onset Alzheimer's disease |
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| Testing the test—why pursue a better test for Huntington disease? |
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| Tridimensional personality questionnaire trait of harm avoidance (anxiety proneness) is linked to a locus on chromosome 8p21 |
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| Possible parent‐of‐origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder |
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| Association of EEG coherence and an exonic <i>GABA<sub>B</sub>R1</i> gene polymorphism |
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| Defining the autism minimum candidate gene region on chromosome 7 |
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| Association analysis of monoamine oxidase A and attention deficit hyperactivity disorder |
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| Polymorphisms of dopamine receptors and tardive dyskinesia among Chinese patients with schizophrenia |
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| Genetic linkage and association between chromosome 1q and working memory function in schizophrenia |
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Finnish; 'population of Finland' |
| Generalized Cognitive Impairment in Male Adolescents With Schizotypal Personality Disorder |
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| Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q‐rich‐associated protein) and schizophrenia |
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| Association between the dopamine receptor D4 (DRD4) gene and obsessive‐compulsive disorder |
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ethnically‐matched controls |
| Early‐onset schizophrenia and dopamine‐related gene polymorphism |
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| Association study between the fibronectin gene and schizophrenia |
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| CAG repeat polymorphisms in KCNN3 (HSKCa3) and PPP2R2B show no association or linkage to schizophrenia |
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"Xhosa population"; "African populations" |
| The real problem in association studies |
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| D2 dopamine receptor gene in psychiatric and neurologic disorders and its phenotypes |
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| Positive association of the AMPA receptor subunit GluR4 gene (<i>GRIA4</i>) haplotype with schizophrenia: Linkage disequilibrium mapping using SNPs evenly distributed across the gene region |
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| Polymorphism screening of PIK4CA: Possible candidate gene for chromosome 22q11‐linked psychiatric disorders |
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| Lack of association between serotonin 5‐HT1B receptor gene polymorphism and suicidal behavior |
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German |
| No association between non‐violent suicidal behavior and the serotonin transporter promoter polymorphism |
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West European Caucasians; same ethnic origin |
| Fine mapping of an isodicentric Y chromosomal breakpoint from a schizophrenic patient |
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| Obsessive‐compulsive symptom dimensions in affected sibling pairs diagnosed with Gilles de la Tourette syndrome |
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| Selectivity of verbal memory deficit in schizophrenic patients and their relatives |
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| Familial aggregation of psychotic symptoms in a replication set of 69 bipolar disorder pedigrees |
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| Genetic variation in apolipoprotein D affects the risk of Alzheimer disease in African‐Americans |
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