High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy.
about
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concernsUnraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern.Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?The human clinical phenotypes of altered CHRNA7 copy numberThe utility of chromosomal microarray analysis in developmental and behavioral pediatrics.The immature dentate gyrus represents a shared phenotype of mouse models of epilepsy and psychiatric diseaseReciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia.The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart diseasePathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disordersMolecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature.Dosage-sensitivity of imprinted genes expressed in the brain: 15q11-q13 and neuropsychiatric illness.Modelling the genetic contribution to mental illness: a timely end for the psychiatric rodent?New discoveries in schizophrenia genetics reveal neurobiological pathways: A review of recent findings.Novel promoters and coding first exons in DLG2 linked to developmental disorders and intellectual disability.The impact of genetics on future drug discovery in schizophrenia.Genetic and epigenetic mechanisms of epilepsy: a review.Reduced Slc1a1 expression is associated with neuroinflammation and impaired sensorimotor gating and cognitive performance in mice: Implications for schizophrenia.Characterization of a Novel Mutation in SLC1A1 Associated with Schizophrenia.A Novel Relationship for Schizophrenia, Bipolar, and Major Depressive Disorder. Part 8: a Hint from Chromosome 8 High Density Association Screen.15q11.2 Duplication Encompassing Only the UBE3A Gene Is Associated with Developmental Delay and Neuropsychiatric Phenotypes.The complex behavioral phenotype of 15q13.3 microdeletion syndrome.Case report: Neuronal migration disorder associated with chromosome 15q13.3 duplication in a boy with autism and seizures.Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes.Case history and genome-wide scans for copy number variants in a family with patient having 15q11.1-q11.2 duplication and 22q11.2 deletion, and schizophrenia.3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patientsClinical and genetic study of a family with a paternally inherited 15q11-q13 duplication
P2860
Q24603800-E915BD4C-0E0F-49E5-AF1E-3E889AC4E0A4Q26859057-8C475F75-0080-4C4F-A0EE-C9E784F84414Q30241067-E044ADC2-380F-413F-B9F5-E43955BCBA1FQ33792567-3C2B85C5-88A7-4AB2-91C5-18DF8BF033F0Q34249436-61FEE44F-7448-4255-ABAC-D74078883B3DQ36144791-44C07992-5CFB-4563-8758-A8A6897EEC52Q37052357-7FC39D99-07B1-4453-B826-849A998DD116Q37119969-21A457B7-4822-4063-8128-DA7F15FB4771Q37337299-294E3F04-008B-4D93-A71D-8918CD309229Q37432642-F5872865-8DE5-48CC-81EC-C4B84A9A7719Q37470598-9AD37F5F-7457-44A2-9957-48A227281102Q37593048-7D5C07E8-5AED-4B05-BD17-23150BA80C0DQ38093545-6276157E-4B35-47E1-9903-1A0A97232F26Q38108660-FF3926C1-F0F6-4E0F-8FAB-5896B21FAA73Q38214995-ED967EA1-2BC8-4FD4-ADB6-3757E76CBA7CQ38614141-C0598C10-B581-4FBD-878E-6DAEF61A35DCQ38671614-E00324DC-87B1-4F48-B21B-543FA619C285Q38682213-DC900040-95AA-4593-9696-1DD958946776Q41057615-DE27226B-47A0-4D7C-A71F-8523E3AAD399Q41495551-D30993B3-22AE-41BB-9A1B-3B463CC89132Q42154902-5E415288-A958-4016-8C9A-30560741355DQ48040604-FC261B7B-132C-489B-BAC7-6980FC134DC0Q48224906-2BED09AA-70B6-4664-9D88-96C2D6357F5CQ48266603-B4E1836F-FE6F-4ABF-951D-A288ABD452C0Q48842137-CBACCC12-54C7-4C98-84AD-A3C8D30E390EQ52562177-179DA961-81F1-4E50-BD8F-5F6912AD383EQ52958635-5BEFB4E1-E472-444D-8574-426BEE93FA96Q57720152-A14BE238-17E5-49A0-8F96-AF88C57CF0DAQ57737823-A03CB1C1-B3A4-49A7-804D-5321354433CD
P2860
High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy.
description
2011 nî lūn-bûn
@nan
2011 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
High frequency of known copy n ...... ed schizophrenia and epilepsy.
@ast
High frequency of known copy n ...... ed schizophrenia and epilepsy.
@en
High frequency of known copy n ...... ed schizophrenia and epilepsy.
@nl
type
label
High frequency of known copy n ...... ed schizophrenia and epilepsy.
@ast
High frequency of known copy n ...... ed schizophrenia and epilepsy.
@en
High frequency of known copy n ...... ed schizophrenia and epilepsy.
@nl
prefLabel
High frequency of known copy n ...... ed schizophrenia and epilepsy.
@ast
High frequency of known copy n ...... ed schizophrenia and epilepsy.
@en
High frequency of known copy n ...... ed schizophrenia and epilepsy.
@nl
P2093
P2860
P356
P1433
P1476
High frequency of known copy n ...... ed schizophrenia and epilepsy.
@en
P2093
April L Hall
Arthur L Beaudet
Larissa R Stewart
Sung-Hae L Kang
P2860
P2888
P356
10.1186/1471-2350-12-154
P50
P577
2011-11-25T00:00:00Z
P5875
P6179
1011617544