| scholarly article | Q13442814 |
| P50 | author | Cisca Wijmenga | Q20196322 |
| P2093 | author name string | R A Ophoff | |
| R J Sinke | |||
| R S Kahn | |||
| A F Bardoel | |||
| S C Bakker | |||
| B J Jungerius | |||
| M L C Hoogendoorn | |||
| R Van't Slot | |||
| P2860 | cites work | cDNA cloning of a third human C2-domain-containing class II phosphoinositide 3-kinase, PI3K-C2gamma, and chromosomal assignment of this gene (PIK3C2G) to 12p12 | Q22008624 |
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| Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies | Q29614926 | ||
| Schizophrenia: genes and environment | Q33842577 | ||
| Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22. | Q33906350 | ||
| Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia | Q33941953 | ||
| Genomewide linkage scan for bipolar-disorder susceptibility loci among Ashkenazi Jewish families | Q33998507 | ||
| Oligodendrocyte dysfunction in schizophrenia and bipolar disorder | Q34246905 | ||
| Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia | Q34426266 | ||
| Cloning and characterization of a novel class II phosphoinositide 3-kinase containing C2 domain | Q34461363 | ||
| The PIP5K2A and RGS4 genes are differentially associated with deficit and non-deficit schizophrenia | Q34616234 | ||
| Gene expression profiling with DNA microarrays: advancing our understanding of psychiatric disorders. | Q35014684 | ||
| White matter changes in schizophrenia: evidence for myelin-related dysfunction | Q35125866 | ||
| The use of microarrays to characterize neuropsychiatric disorders: postmortem studies of substance abuse and schizophrenia | Q35207357 | ||
| Screening of PIP5K2A promoter region for mutations in bipolar disorder and schizophrenia | Q38322318 | ||
| Brain morphology and schizophrenia. A magnetic resonance imaging study of limbic, prefrontal cortex, and caudate structures | Q41102237 | ||
| Evidence that the inositol phospholipids are necessary for exocytosis. Loss of inositol phospholipids and inhibition of secretion in permeabilized cells caused by a bacterial phospholipase C and removal of ATP. | Q41882249 | ||
| A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder | Q42675472 | ||
| Polymorphism screening of PIK4CA: possible candidate gene for chromosome 22q11-linked psychiatric disorders. | Q44259408 | ||
| Altered thalamic membrane phospholipids in schizophrenia: a postmortem study | Q44953140 | ||
| Control of neurite outgrowth and growth cone motility by phosphatidylinositol-3-kinase | Q46931834 | ||
| Genome-wide scan in Portuguese Island families identifies 5q31-5q35 as a susceptibility locus for schizophrenia and psychosis | Q47292298 | ||
| Loss and altered spatial distribution of oligodendrocytes in the superior frontal gyrus in schizophrenia | Q47820010 | ||
| The role of oligodendrocyte pathology in schizophrenia | Q48267380 | ||
| Structural evaluation of the prefrontal cortex in schizophrenia | Q48413878 | ||
| Electron microscopy of oligodendroglia in severe mental illness. | Q48772850 | ||
| Prosaposin deficiency -- a rarely diagnosed, rapidly progressing, neonatal neurovisceral lipid storage disease. Report of a further patient | Q48862963 | ||
| Structural abnormalities in frontal, temporal, and limbic regions and interconnecting white matter tracts in schizophrenic patients with prominent negative symptoms | Q49078641 | ||
| Analytical implications of epidemiological concepts of interaction. | Q51173023 | ||
| Oligodendroglial density in the prefrontal cortex in schizophrenia and mood disorders: a study from the Stanley Neuropathology Consortium. | Q51943076 | ||
| Pedigree disequilibrium tests for multilocus haplotypes. | Q52010978 | ||
| The Comprehensive Assessment of Symptoms and History (CASH). An instrument for assessing diagnosis and psychopathology. | Q52042140 | ||
| Convergent Evidence for 2′,3′-Cyclic Nucleotide 3′-Phosphodiesterase as a Possible Susceptibility Gene for Schizophrenia | Q57279160 | ||
| A controlled study of brain structure in monozygotic twins concordant and discordant for schizophrenia | Q57403363 | ||
| Demonstrating stratification in a European American population | Q57418313 | ||
| Association between polymorphism of the SNAP29 gene promoter region and schizophrenia | Q57437355 | ||
| Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q | Q58070633 | ||
| Structural Brain Abnormalities in Patients With Schizophrenia and Their Healthy Siblings | Q60610031 | ||
| An international two–stage genome–wide search for schizophrenia susceptibility genes | Q71794031 | ||
| Volumetric measure of the frontal and temporal lobe regions in schizophrenia: relationship to negative symptoms | Q73782419 | ||
| Polymorphism in SNAP29 gene promoter region associated with schizophrenia | Q73794712 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | schizophrenia | Q41112 |
| P304 | page(s) | 1060-8 | |
| P577 | publication date | 2008-11-01 | |
| P1433 | published in | Molecular Psychiatry | Q6895973 |
| P1476 | title | An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia | |
| P478 | volume | 13 |
| Q37620241 | A Case-Control Study of the Association between Polymorphisms in the Fibrinogen Alpha Chain Gene and Schizophrenia. |
| Q36966486 | A catalog of hemizygous variation in 127 22q11 deletion patients |
| Q33458936 | A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review |
| Q34326175 | A gene co-expression network in whole blood of schizophrenia patients is independent of antipsychotic-use and enriched for brain-expressed genes |
| Q36440064 | A lesson not learned: allele misassignment |
| Q24643934 | An association analysis of murine anxiety genes in humans implicates novel candidate genes for anxiety disorders |
| Q34823932 | Association between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypes |
| Q33616258 | Association of GRM3 polymorphism with white matter integrity in schizophrenia |
| Q35081418 | Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome |
| Q48332128 | Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome. |
| Q36498862 | Atlas-based white matter analysis in individuals with velo-cardio-facial syndrome (22q11.2 deletion syndrome) and unaffected siblings |
| Q36955877 | Biomarker investigations related to pathophysiological pathways in schizophrenia and psychosis. |
| Q58798394 | Cell Type and Species-specific Patterns in Neuronal and Non-neuronal Methylomes of Human and Chimpanzee Cortices |
| Q28308288 | Chromosome 8p as a potential hub for developmental neuropsychiatric disorders: implications for schizophrenia, autism and cancer |
| Q35115389 | Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome |
| Q39017298 | Common developmental genome deprogramming in schizophrenia - Role of Integrative Nuclear FGFR1 Signaling (INFS). |
| Q37089619 | Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome |
| Q38885442 | Defective phosphoinositide metabolism in autism |
| Q28588322 | Dixdc1 is a critical regulator of DISC1 and embryonic cortical development |
| Q36794532 | Expression of the G72/G30 gene in transgenic mice induces behavioral changes |
| Q48716339 | FGFR2 is associated with bipolar disorder: a large-scale case-control study of three psychiatric disorders in the Chinese Han population |
| Q33634654 | Family-based association study of Neuregulin 1 with psychotic bipolar disorder |
| Q37476441 | Fibroblast growth factors in schizophrenia |
| Q41501850 | Genetic deletion of fibroblast growth factor 14 recapitulates phenotypic alterations underlying cognitive impairment associated with schizophrenia. |
| Q33905809 | Genetic variations of PIP4K2A confer vulnerability to poor antipsychotic response in severely ill schizophrenia patients |
| Q37196005 | Genome-wide association analysis with gray matter volume as a quantitative phenotype in first-episode treatment-naïve patients with schizophrenia |
| Q34514307 | Genotype-phenotype correlation in 22q11.2 deletion syndrome |
| Q50304662 | Identification and molecular characterization of two novel chromosomal deletions associated with autism |
| Q102379137 | Identifying neurodevelopmental anomalies of white matter microstructure associated with high risk for psychosis in 22q11.2DS |
| Q49874112 | Impairment of social behaviors in Arhgef10 knockout mice |
| Q64890460 | In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects? |
| Q52774602 | Involvement of ARHGEF10, GEF for RhoA, in Rab6/Rab8-mediating membrane traffic. |
| Q41918413 | Isolated chromosome 8p23.2‑pter deletion: Novel evidence for developmental delay, intellectual disability, microcephaly and neurobehavioral disorders |
| Q37564007 | Linking white and grey matter in schizophrenia: oligodendrocyte and neuron pathology in the prefrontal cortex |
| Q38100883 | Mammalian phosphatidylinositol 4-kinases as modulators of membrane trafficking and lipid signaling networks. |
| Q34642754 | MicroRNA-382 expression is elevated in the olfactory neuroepithelium of schizophrenia patients |
| Q39567009 | Modulation of the FGF14:FGF14 homodimer interaction through short peptide fragments. |
| Q27691100 | Molecular mechanisms in 22q11 deletion syndrome |
| Q104503393 | Multimodal imaging improves brain age prediction and reveals distinct abnormalities in patients with psychiatric and neurological disorders |
| Q36162707 | Network-assisted Causal Gene Detection in Genome-wide Association Studies: An Improved Module Search Algorithm |
| Q47261020 | Networks of myelin covariance. |
| Q34726454 | Personalized medicine in psychiatry: problems and promises |
| Q38051210 | Phosphatidylinositol 4-kinases and PI4P metabolism in the nervous system: roles in psychiatric and neurological diseases. |
| Q90049726 | Phosphoinositides: Regulators of Nervous System Function in Health and Disease |
| Q33819207 | Potential Value of Genomic Copy Number Variations in Schizophrenia |
| Q31155236 | Schizophrenia and 22q11.2 deletion syndrome |
| Q37559492 | Searching genetic risk factors for schizophrenia and bipolar disorder: learn from the past and back to the future |
| Q34660041 | Serotonin Transporter Promoter Region (5-HTTLPR) Polymorphism Is Not Associated With Paroxetine-Induced Ejaculation Delay in Dutch Men With Lifelong Premature Ejaculation |
| Q89999211 | Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant-Mediated Risk for Neuropsychiatric Disorders |
| Q39155841 | The mood stabilizer valproate activates human FGF1 gene promoter through inhibiting HDAC and GSK-3 activities |
| Q28756691 | The role of positive selection in determining the molecular cause of species differences in disease |
| Q34913157 | Transcriptome alterations of mitochondrial and coagulation function in schizophrenia by cortical sequencing analysis |
| Q47442451 | Ulk4 deficiency leads to hypomyelination in mice |
| Q50323081 | Vibrator and PI4KIIIα govern neuroblast polarity by anchoring non-muscle myosin II. |
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