Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia. - Test2 - elhamkhani - TriplyDB

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.

http://www.wikidata.org/entity/Q35764622

about

The shock of the new: progress in schizophrenia genomics The Kraepelinian dichotomy - going, going... but still not gone What have we learnt about the causes of ADHD?Dopamine-prolactin pathway potentially contributes to the schizophrenia and type 2 diabetes comorbidity A genetic model for neurodevelopmental disease CNVs: harbingers of a rare variant revolution in psychiatric genetics Genetic Sources of Subcomponents of Event-Related Potential in the Dimension of Psychosis Analyzed From the B-SNIP Study CNVs in neuropsychiatric disorders The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation The emergence of human-evolutionary medical genomics Genome-wide analysis of copy number variation in type 1 diabetes Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder Schizophrenia.Increased de novo copy number variants in the offspring of older males Inheritance model introduces differential bias in CNV calls between parents and offspring Social and nonsocial cognition in bipolar disorder and schizophrenia: relative levels of impairment.Genomic structural variation in psychiatric disorders.De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.Ontogenetic de novo copy number variations (CNVs) as a source of genetic individuality: studies on two families with MZD twins for schizophrenia.Genetic architectures of psychiatric disorders: the emerging picture and its implications.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.Relative burden of large CNVs on a range of neurodevelopmental phenotypes.High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy.Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders.Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders.The 2nd Schizophrenia International Research Society Conference, 10-14 April 2010, Florence, Italy: summaries of oral sessions.Review of functional magnetic resonance imaging studies comparing bipolar disorder and schizophrenia.Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders.Hybridization and amplification rate correction for affymetrix SNP arrays.The genetics of early-onset bipolar disorder: A systematic review.Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder.RNA-Seq analysis implicates dysregulation of the immune system in schizophrenia De novo CNVs in bipolar affective disorder and schizophrenia.Neurodevelopment, GABA system dysfunction, and schizophrenia Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample.Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder

P2860

Q22241409-1299AFD0-CCD7-4EAE-B72E-A1F70A5B5AD6 Q22241683-F6C70059-2B50-427B-9AE4-FF2688C9FE27 Q22242372-E5BC2F8B-19CA-48E9-BCD1-2C06429A9AA1 Q26752342-36EB6006-A69C-4EFB-BBA9-F2BF798B4AE5 Q26860566-19A6331B-61E5-4156-AF12-A199775355F3 Q27022289-ADEDDDE5-E57A-4AAA-ACDF-BAB99BB32E27 Q27329481-FFEB1449-FF69-4826-8CE6-320BA4CDE79A Q28083143-D70FF185-82C0-4FBC-BF77-73C723C48BAB Q28685216-F44C4E14-D3E7-4B46-A3E2-D9916495C279 Q28729955-30C3205D-9225-4029-A57A-492941A0D1E1 Q28748452-E23CE31E-AFDA-42D6-80C7-70E5F7FDA92D Q28943293-7CB47192-3119-4C02-B71A-70DD93388089 Q30251961-DFD3DC95-B515-4434-900D-7C316EC1A3A7 Q30468811-690E5B7B-143C-482E-83D2-D158DC3524E5 Q30540543-CBA5B972-0D97-48D7-A50C-C7A48D2CE2EE Q30560264-424B79A8-FD7D-498E-B92A-4D2255707357 Q33354553-EAD30550-7279-48E1-ADB3-CD882B0ED958 Q33398247-FB955704-B688-4674-A1D2-AEF1D825BA5D Q33649276-C3313308-282B-4CBC-AA71-F919DCAE00DA Q33762566-D20C245B-6F54-445F-9C1E-C454889BF7B1 Q33772616-625C13A2-FBDC-41F1-AACF-6676B36977D4 Q33844724-D29DD829-6AB5-4BBD-9545-D43EE06CDEF9 Q33949729-1B8DF2B7-9F8E-4FEB-BE60-831E745EC86C Q33960019-E63D95F4-3E3A-4B83-843E-0089D32BFDA0 Q33965270-47698103-D9EF-4650-8434-A0E2A67DFD6D Q34079175-49D43057-FF4F-4B9B-85BC-0C2908C56919 Q34084054-F4A36FE2-9C7C-4F05-A5D7-1EC465BC5CD9 Q34181876-A5636444-9BCB-424F-B241-E5EF5AD43122 Q34267003-A7DC1453-C702-40AE-A8B9-172D7C5B0E0A Q34279073-B57449FE-6FC0-448D-A346-58A5538F04F9 Q34282771-BAC76EC6-35C4-4D87-BBC0-2040E4BA4936 Q34288660-09E33096-174C-4515-977C-F658C6FC4636 Q34301294-3C1B2AF3-A554-4051-87B3-484FFDE0701E Q34479877-8B338604-2D5A-464B-B6F2-5A9542539E58 Q34507224-FD5DC682-01EF-4C99-8124-B1DCD56507C6 Q34530641-7D9A1B39-B207-47AF-A377-433AE38ED679 Q34555512-E02F2C5E-9FF0-4F36-9CAE-6F5D0550587E Q34675943-7C9BBD27-4ED0-4E78-A5B7-11404C57A0D8 Q34873753-80AFE663-3E94-4701-BDB7-31BC8372F13D Q35246537-B622577D-1D42-4912-893A-4ADC7C463A58

P2860

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.

http://www.wikidata.org/entity/Q35764622

description

2010 nî lūn-bûn

@nan

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

2010年论文

@zh

2010年论文

@zh-cn

name

Rare copy number variants: a p ...... ar disorder and schizophrenia.

@ast

Rare copy number variants: a p ...... ar disorder and schizophrenia.

@en

type

label

Rare copy number variants: a p ...... ar disorder and schizophrenia.

@ast

Rare copy number variants: a p ...... ar disorder and schizophrenia.

@en

prefLabel

Rare copy number variants: a p ...... ar disorder and schizophrenia.

@ast

Rare copy number variants: a p ...... ar disorder and schizophrenia.

@en

P1433

Q35764622-EBD432B3-D07E-4373-AC87-7BECDD09D1CB

P1476

Q35764622-0A9098BC-520C-4466-B052-56F2FFAF1F08

P2093

Q35764622-2FCE6A0E-9BF5-4BD6-8DEA-B81D134F70EF

Q35764622-38800716-311B-40B8-96C1-113B83CB6915

Q35764622-44FE4B9E-8306-4354-A653-F168F4BDFF5D

Q35764622-8F2E1D5D-FA5E-47B2-B162-02BF4B6A6317

Q35764622-B165564D-517F-45C6-9D83-E1B35E586D38

Q35764622-B18B7A18-57E5-437E-A6BB-C4986ABBFF49

Q35764622-BE73D5DD-76B1-4965-A89C-E16543287ED8

Q35764622-C5745F3C-6AA9-4130-9F9D-B8E3F1548C93

Q35764622-CFBE5940-7FEB-40FB-9308-98BD3B399E20

Q35764622-DECA10BC-EDD1-4582-AB0C-A3ACBC135CEE

P2860

Q35764622-026DDB25-5578-4C7E-B62B-49C84E9BBB41

Q35764622-030FB24F-77D4-4B44-B8BC-638DCA485A01

Q35764622-0D57886B-41C5-4E1E-AC7A-876D6F75AF06

Q35764622-0E7BD396-1E0B-43D9-85E8-E607954FB0FA

Q35764622-21D2C776-B8AC-4023-B44E-F28C3997FBA3

Q35764622-2307C9E9-B4D0-4C75-B734-3D91061C7FA7

Q35764622-29121A0C-B390-492F-AC64-531F55C2DAC3

Q35764622-3A1FD52F-F3A1-4E32-9160-21ED4EB45B3B

Q35764622-3AAEA53D-CDEE-428E-8C02-4E4D2BF108A3

Q35764622-3D51E1DD-60A4-493A-BB96-A1C4C3C5D52F

P304

Q35764622-A3F63DD7-AAD9-4CCC-A58C-2ECD9C0C8080

P31

Q35764622-72667D3F-F489-4A4B-8333-2DD342492A0C

P356

Q35764622-176F8707-4124-4419-B9B8-426ABE3FB54B

P407

Q35764622-D65D2A95-103A-4D25-AA35-2E6F125822EA

P433

Q35764622-F9722C80-5277-443A-8D6F-661BF223C0E1

P478

Q35764622-E9B8668E-7F24-411B-9460-755BA590413B

P50

Q35764622-037C69AB-DEC0-4273-8122-EFD7DF40BC1F

Q35764622-7EB49957-CBB4-45B9-A052-F861C63BF00E

Q35764622-D0C7F0A3-6673-496B-9C0B-C4BE9D920F03

Q35764622-D9B5A10B-4602-46E6-B7D9-248258271DCE

Q35764622-E599451C-6155-468C-A45D-441616311B02

Q35764622-F0D3DBD8-AD14-48BD-821C-715677A50177

P577

Q35764622-ED090B9E-0E23-4655-A14B-12A716302A36

P698

Q35764622-4B1406DF-C8F5-4C80-9953-AC01F4071ABF

P921

Q35764622-379B9C4F-6385-4CDD-A141-71D2E14AC0F1

Q35764622-B09E428A-FB4E-47EB-8E60-E0356DD4FA9F

P932

Q35764622-C4D45901-42EC-4C60-87B7-B4141B27FE38

P356

ARCHGENPSYCHIATRY.2010.25

P1433

JAMA Psychiatry

P1476

Rare copy number variants: a p ...... ar disorder and schizophrenia.

@en

P2093

Allan H Young

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

Anne E Farmer

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

David M St Clair

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

Elaine K Green

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

Ian R Jones

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

Lisa Jones

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

Michael J Owen

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

Nick Craddock

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

Nicol Ferrier

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

Peter McGuffin

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

P2860

The complete genome of an individual by massively parallel DNA sequencing

Rare chromosomal deletions and duplications increase risk of schizophrenia

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Disruption of the neurexin 1 gene is associated with schizophrenia

Large recurrent microdeletions associated with schizophrenia

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

Global variation in copy number in the human genome

PLINK: a tool set for whole-genome association and population-based linkage analyses

P304

318-327

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

P31

scholarly article

P356

10.1001/ARCHGENPSYCHIATRY.2010.25

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

P407

P433

4

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

P478

67

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

P50

Michael C O'Donovan

Detelina Grozeva

Wellcome Trust Case Control Consortium

P577

2010-04-01T00:00:00Z

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

P698

20368508

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

P921

bipolar disorder

P932

4476027

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