about
microRNA expression in the prefrontal cortex of individuals with schizophrenia and schizoaffective disorderFunctional consequences of PRODH missense mutationsCOMT genetic variation confers risk for psychotic and affective disorders: a case control studyEarly interventions in risk groups for schizophrenia: what are we waiting for?Practical guidelines for managing adults with 22q11.2 deletion syndromePhosphoinositides: tiny lipids with giant impact on cell regulationCognitive remediation for adolescents with 22q11 deletion syndrome (22q11DS): a preliminary study examining effectiveness, feasibility, and fidelity of a hybrid strategy, remote and computer-based intervention.Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion SyndromeEffect of C-Terminal S-Palmitoylation on D2 Dopamine Receptor Trafficking and StabilityTbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndromeEvidence that the gene encoding ZDHHC8 contributes to the risk of schizophreniaCross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depressionUsing mice to model Obsessive Compulsive Disorder: From genes to circuits.The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice.22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.Behavioral and neurobiological changes in C57BL/6 mouse exposed to cuprizone: effects of antipsychotics.Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal studyAnalysis of TBX1 variation in patients with psychotic and affective disorders.Advances in white matter imaging: a review of in vivo magnetic resonance methodologies and their applicability to the study of development and aging.Schizophrenia and 22q11.2 deletion syndrome.Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease.Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophreniaVelo-Cardio-Facial Syndrome.No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients.The development of cognitive control in children with chromosome 22q11.2 deletion syndromeProdromal symptoms in adolescents with 22q11.2 deletion syndrome and schizotypal personality disorder.Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: a 3-year follow-up study.Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome.A comprehensive network and pathway analysis of candidate genes in major depressive disorder.Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis.Genotype-phenotype correlation in 22q11.2 deletion syndrome.Subtyping schizophrenia: implications for genetic research.Identifying patterns of anxiety and depression in children with chromosome 22q11.2 deletion syndrome: comorbidity predicts behavioral difficulties and impaired functional communications.How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome.Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome.
P2860
Q21184126-BBEAB6AC-E10B-405E-97D3-F7C6754202CBQ24338650-6CE59D41-6993-409F-806F-F0A2E702B64DQ24816526-1A8EE6A6-728E-44DE-83FE-95AF2619837BQ26747545-A2278670-D601-4129-850C-7D281A733949Q27002798-1CBEE77B-55A2-4B19-86F8-C7F1DA0F02FFQ27012953-26F4425B-04F7-4485-A9F7-D1CA6E6C24AEQ27303880-7DA5A612-8F88-4DB4-9B5C-1F650CDC7955Q28081645-942DF67F-D90B-4A0A-BE21-262A2D90D536Q28550695-5D9B9E00-0B0D-4920-877F-CA07216FB1B1Q28587462-266BFACE-85F4-480E-83FD-2BFAD4D53DA6Q28591536-6BB4F5E7-541A-46A3-B345-EEC8978B8C20Q28943274-0D25336B-1FC2-4B7F-A994-9E8EEF8D9C8BQ30357295-656432C5-0CA5-4E19-8AF1-11DDEB08F5DEQ30468033-A53035AA-82B0-4656-B22B-E420573963D4Q30476572-AF291735-D3B2-48A9-AF3D-BF1A7CFEEB9AQ30478713-49755B24-5BD8-42A5-967D-6F19F1F30F24Q30480908-5F4D088E-0330-4828-A5C4-3DE12D1F2BADQ30482602-EE6F9B0E-A209-4964-BADC-82FBBB51F97DQ30499844-94B9A7AA-612F-4262-A102-5A70A165D644Q30545900-BE0AD948-A2DB-4078-AE0D-7755735092ADQ31051830-4E8A26EF-F426-4E92-AB7E-595D74F679A6Q31155236-8832B909-94B5-4E8D-8D28-610639252D3AQ33590242-CE5E3081-9BE2-4A69-9137-6772C9228AFDQ33608652-74097BF2-A9B4-44D7-B3B2-155531992831Q33612908-2F5F5B52-7B8C-41D1-A25D-EB1BC6290FD5Q33707657-2254A1A9-779C-4DD0-9923-EC106E540870Q33730345-C935676A-FD48-4595-854D-466D9017222CQ33878153-E511BA24-9718-4200-AA9C-9FA2072F4B4AQ34054916-6BF0A3E1-F6F3-422D-87BB-B92BEC5A7533Q34131454-2CB93A6B-54C3-4F5F-8E3D-6E046E4D4A0EQ34333537-6787D5A9-C178-4FAE-9C1B-14B23B261F87Q34344833-140FA4A3-AA2B-4E6A-88F9-082BE26550F2Q34393037-833087B8-A31C-4789-917F-2FBF48860038Q34514307-66594E7B-CEF1-49EF-83C4-FD32EBCA2597Q34542103-13B48504-5D80-4750-8DE9-C1BDDA4BC38FQ34624127-6EED96F5-9DAE-493C-93D2-68032A02A9CAQ34669660-B7DDCF3C-C1D5-438F-A5CE-3F154AA2A547Q35081406-2830020C-C35F-4572-A3EF-BB5FEA788255Q35115389-4FD610FC-65FB-4A1D-9835-FEFD2DBA8FDDQ35124119-6632F694-B14F-4E80-A01C-3D7151DC41A7
P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
The schizophrenia phenotype in 22q11 deletion syndrome
@ast
The schizophrenia phenotype in 22q11 deletion syndrome
@en
The schizophrenia phenotype in 22q11 deletion syndrome
@nl
type
label
The schizophrenia phenotype in 22q11 deletion syndrome
@ast
The schizophrenia phenotype in 22q11 deletion syndrome
@en
The schizophrenia phenotype in 22q11 deletion syndrome
@nl
prefLabel
The schizophrenia phenotype in 22q11 deletion syndrome
@ast
The schizophrenia phenotype in 22q11 deletion syndrome
@en
The schizophrenia phenotype in 22q11 deletion syndrome
@nl
P2093
P2860
P1476
The schizophrenia phenotype in 22q11 deletion syndrome
@en
P2093
Anne S Bassett
Eva W C Chow
Janice Husted
Mirona Gheorghiu
Rosanna Weksberg
P2860
P304
P356
10.1176/APPI.AJP.160.9.1580
P407
P577
2003-09-01T00:00:00Z