Microdeletions of 3q29 confer high risk for schizophrenia. - Wikidata - awgldk - TriplyDB

Microdeletions of 3q29 confer high risk for schizophrenia.

Microdeletions of 3q29 confer high risk for schizophrenia.

http://www.wikidata.org/entity/Q34050937

about

Human genetics and genomics a decade after the release of the draft sequence of the human genome CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 The PHR proteins: intracellular signaling hubs in neuronal development and axon degeneration Genetics and genomics of psychiatric disease Abnormal kalirin signaling in neuropsychiatric disorders.Differential expression of PDZ domain-containing proteins in human diseases - challenging topics and novel issues The impact of NMDA receptor hypofunction on GABAergic neurons in the pathophysiology of schizophrenia Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications Mosaic copy number variation in schizophrenia Microarray Analysis of Copy Number Variants on the Human Y Chromosome Reveals Novel and Frequent Duplications Overrepresented in Specific Haplogroups Multiplex ligation-dependant probe amplification study of children with idiopathic mental retardation in South India Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.Copy Number Variation detection from 1000 Genomes Project exon capture sequencing data.Robust regression analysis of copy number variation data based on a univariate score.Neurogenetic analysis of childhood disintegrative disorder.Consensus paper of the WFSBP Task Force on Biological Markers: Criteria for biomarkers and endophenotypes of schizophrenia part II: Cognition, neuroimaging and genetics.De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study.DNA methylation as a putative mechanism for reduced dendritic spine density in the superior temporal gyrus of subjects with schizophrenia.Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.Potential Value of Genomic Copy Number Variations in Schizophrenia.Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia.The genetic variability and commonality of neurodevelopmental disease.Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy.Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?Neurogenetics: advancing the "next-generation" of brain research.RNA-Seq analysis implicates dysregulation of the immune system in schizophrenia PAK1 protein expression in the auditory cortex of schizophrenia subjects.Copy number variants in German patients with schizophrenia Population-specific haplotype association of the postsynaptic density gene DLG4 with schizophrenia, in family-based association studies.Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation Homozygous deficiency of ubiquitin-ligase ring-finger protein RNF168 mimics the radiosensitivity syndrome of ataxia-telangiectasia.Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defects.Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: risk and transmission in extended pedigrees.Dendritic spine alterations in schizophrenia.Further evidence for a male-selective genetic association of synapse-associated protein 97 (SAP97) gene with schizophrenia Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia.

P2860

Q21245451-5802F3D3-03D0-41C3-BA07-98DCA5B7BCB4 Q24603800-18914B07-17D8-4B65-98FE-9BD003CB7073 Q26752306-F24F8D54-8F3D-4A0B-B83A-81B98D3C879A Q26781213-A648DFCF-4A2B-4CB5-807E-FD249D67FF43 Q26824648-7CC5A1CD-1C30-49F8-8E40-483ACB797E8E Q27015135-38A30DE1-A8B9-4324-8CD5-15B807046315 Q28081110-ED3C5477-0C0C-4830-A200-16066FBAA808 Q28304430-78FE4105-997E-4391-9DFB-F4D237BDC9F2 Q28387422-229AD21D-694F-48AA-9FC8-084464BA93CC Q28608266-B6F8B969-3F0D-4D66-96DF-F50273B45A85 Q30009572-C9CE6312-F447-4FE8-AB38-4AD140794E65 Q30241067-C72DEFB3-D84F-41CC-8D00-A2E08A081B31 Q30577661-BCA00C7C-4F66-43ED-945E-E5490F4F4812 Q30754963-347B7E49-068A-4AEB-BB93-223C574647F9 Q30843918-9CDBD905-70F0-43D8-9E9C-B39C2B4F2F34 Q31108616-3317BA9B-8211-48C0-B243-9CCDDB27926C Q33398247-DEC5F778-C3E3-4C89-9C2D-2CC34738A5AF Q33573331-2BD25EFB-2777-420F-9B03-0109D976ECC5 Q33707704-D0182F51-9C6E-43A9-8285-BBC5F03197EC Q33740241-FF35A303-BD8D-497D-ABEB-44941337A213 Q33772616-8283A3A2-18E6-46AB-A4DA-4970FD658EDE Q33819207-40F03FB1-3C0E-402B-B271-B2750B2E50D9 Q33960019-23AA80B5-70C7-4FE6-B22A-57A80ACD88A9 Q33965270-10633A9E-6711-4EAA-B49E-8BA9C335CBDD Q33991709-CB701A96-7879-4484-85F6-3D6E11708DD9 Q34084054-7D4902C0-7F59-4E28-93FC-AB6EDD5CCD89 Q34249436-9E2A106D-6C92-4799-A39E-CB0EE3BE4E86 Q34315505-78B8E52B-4ED7-43E2-951E-2A11EE3896A4 Q34530641-DD174834-7256-4F61-A934-9EFE7D45AD92 Q34683597-97490991-0A45-4D1A-BD00-D4A1887DBCCD Q34811896-4FB634EB-B59B-406A-95DB-DD4E7E47E00E Q34922527-705A5B88-797D-4CF0-9BCB-0EBA3EB2453B Q35187746-3901430F-2025-4DCC-BF3E-097B5FC1E3AA Q35227435-B6B7DF99-A9AA-471B-B271-1A54F634F1FE Q35533264-296FBA51-0A11-46A2-8BEC-B8E657F39107 Q35573434-DB807BAF-88A2-4589-98B7-CBACE782E2AD Q35680429-836D70C2-B3F7-4D03-91D4-DE856018C7AD Q35744819-F5C46D10-EA96-425B-A161-35D2B7332DD2 Q35764564-0C823AAB-2AF0-4960-BD88-37A3866072A0 Q35861470-B36A9CBC-87DE-4330-9C57-3BA8CCED247D

P2860

Microdeletions of 3q29 confer high risk for schizophrenia.

http://www.wikidata.org/entity/Q34050937

description

2010 nî lūn-bûn

@nan

2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Microdeletions of 3q29 confer high risk for schizophrenia.

@ast

Microdeletions of 3q29 confer high risk for schizophrenia.

@en

Microdeletions of 3q29 confer high risk for schizophrenia.

@nl

type

label

Microdeletions of 3q29 confer high risk for schizophrenia.

@ast

Microdeletions of 3q29 confer high risk for schizophrenia.

@en

Microdeletions of 3q29 confer high risk for schizophrenia.

@nl

prefLabel

Microdeletions of 3q29 confer high risk for schizophrenia.

@ast

Microdeletions of 3q29 confer high risk for schizophrenia.

@en

Microdeletions of 3q29 confer high risk for schizophrenia.

@nl

P1433

Q34050937-7DEE0ACF-E60C-4708-81F6-B6F90B0EF90E

P1476

Q34050937-D8230476-C625-4F9E-BB1E-67B276C1BDE7

P2093

Q34050937-08BECA6D-9B58-48AF-A36B-87C94FCB1E12

Q34050937-2EBF56C2-3102-4782-8650-4A8888E90BD4

Q34050937-87344AFE-6852-43D3-82DD-FC98D6D4BE92

Q34050937-A0F39F4A-AB77-4085-97E3-DE05153590B0

Q34050937-A1ECC46A-1227-45C4-8C5E-EB39B2D564AB

Q34050937-A6043D93-CAE6-46FA-86D4-E93B126F5F24

Q34050937-BC30E1DA-A0B5-4BE8-8629-D5392AB7BF46

Q34050937-DB0B4C55-6EC1-4B16-8CC6-B772F052F5A8

Q34050937-E8DBD251-2DAC-4D34-ABCF-E02AF0BBE201

Q34050937-EBBAA563-BD15-4060-9FC4-FE28FCA7F91F

P2860

Q34050937-0C95E04E-CB0D-4884-A056-BDBBFBE03CB9

Q34050937-11AD79C1-BEA9-4224-80A6-A525544EC52B

Q34050937-18B474BB-76B2-4337-9D4E-7DFE0DF42ED6

Q34050937-2F3DF8C0-DDBA-4437-90C3-23160621FBC4

Q34050937-30E1CD33-9D91-4081-9F60-889BF9621594

Q34050937-364A5E58-148B-4FA2-B588-83A2B895621E

Q34050937-3BC67605-1971-4EB4-862F-E274D09632FF

Q34050937-4A1569CE-B4BE-48B2-B902-78EDAE270A24

Q34050937-4BAF484E-8706-491E-AFA2-3B9CEB0D4F7D

Q34050937-4F53936B-C9D7-4432-9B0D-7723FDF34A7D

P304

Q34050937-0B4A7AF0-4E5E-493E-946A-1FCE3E217C8E

P31

Q34050937-B536F65F-2F4C-4F08-9706-58C07CAE671F

P356

Q34050937-BA613989-8C69-4957-A47D-CA0FF38B38D7

P407

Q34050937-E3A56FBB-D85D-416D-9AEE-C55C15A8B1A8

P433

Q34050937-A6F617F9-EE70-4626-AE5C-1E0CE710E3C2

P478

Q34050937-5378D7FE-1B05-4745-8BFC-59A03667E4C9

P50

Q34050937-16923212-FA58-4747-A0BE-AE4500CE2E80

Q34050937-85CFE236-16BA-41AC-AEB2-CB28C6756D6E

Q34050937-A617F33F-53DD-432C-814E-7950E99BE966

P577

Q34050937-E582E42A-501E-46A9-8EE9-A396003922C4

P5875

Q34050937-CC648A05-8A98-4AB6-8A0B-4C9458266697

P698

Q34050937-FE69492D-5E5F-41F4-8787-99B8E2EB8502

P921

Q34050937-330B318F-C943-428E-BB97-8E2FA93F5DFD

P932

Q34050937-C7A94721-41F2-469E-BE7F-779B0D052519

P356

J.AJHG.2010.07.013

P1433

American Journal of Human Genetics

P1476

Microdeletions of 3q29 confer high risk for schizophrenia.

@en

P2093

Adele A Mitchell

http://www.w3.org/2001/XMLSchema#string

Ann E Pulver

http://www.w3.org/2001/XMLSchema#string

Anne F Dodd

http://www.w3.org/2001/XMLSchema#string

David J Cutler

http://www.w3.org/2001/XMLSchema#string

David Valle

http://www.w3.org/2001/XMLSchema#string

Jennifer Gladys Mulle

http://www.w3.org/2001/XMLSchema#string

M Katharine Rudd

http://www.w3.org/2001/XMLSchema#string

Nara L Sobreira

http://www.w3.org/2001/XMLSchema#string

Paula S Wolyniec

http://www.w3.org/2001/XMLSchema#string

Stephen T Warren

http://www.w3.org/2001/XMLSchema#string

P2860

Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia

Rare chromosomal deletions and duplications increase risk of schizophrenia

3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome.

Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios

Medicine. The future of psychiatric research: genomes and neural circuits

Common variants conferring risk of schizophrenia

The role of SAP97 in synaptic glutamate receptor dynamics

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry

Microduplications of 16p11.2 are associated with schizophrenia

P304

229-236

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1016/J.AJHG.2010.07.013

http://www.w3.org/2001/XMLSchema#string

P407

P433

2

http://www.w3.org/2001/XMLSchema#string

P478

87

http://www.w3.org/2001/XMLSchema#string

P50

P577

2010-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

45536038

http://www.w3.org/2001/XMLSchema#string

P698

20691406

http://www.w3.org/2001/XMLSchema#string

P921

P932

2917706

http://www.w3.org/2001/XMLSchema#string