CNVs: harbingers of a rare variant revolution in psychiatric genetics - Wikidata - awgldk - TriplyDB

CNVs: harbingers of a rare variant revolution in psychiatric genetics

CNVs: harbingers of a rare variant revolution in psychiatric genetics

http://www.wikidata.org/entity/Q27022289

about

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 forestSV: structural variant discovery through statistical learning Dishing out mini-brains: Current progress and future prospects in brain organoid research Analysis of conditional heterozygous STXBP1 mutations in human neurons Different Facets of Copy Number Changes: Permanent, Transient, and Adaptive The PsychENCODE project Moving from capstones toward cornerstones: successes and challenges in applying systems biology to identify mechanisms of autism spectrum disorders Genetics and genomics of psychiatric disease Characterizing autism spectrum disorders by key biochemical pathways.Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders Therapeutic approaches for shankopathies Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice Spine pruning drives antipsychotic-sensitive locomotion via circuit control of striatal dopamine.Reversal of phenotypes in MECP2 duplication mice using genetic rescue or antisense oligonucleotides.Investigating the effects of copy number variants on reading and language performance.Genetic aspects of autism spectrum disorders: insights from animal models Genetic Counseling for Autism Spectrum Disorder in an Evolving Theoretical Landscape The Psychiatric Genomics Consortium Posttraumatic Stress Disorder Workgroup: Posttraumatic Stress Disorder Enters the Age of Large-Scale Genomic Collaboration CNVs in neuropsychiatric disorders Complex and multi-allelic copy number variation in human disease Genetic and genomic analyses as a basis for new diagnostic nosologies Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms A copy number variation map of the human genome The clustering of functionally related genes contributes to CNV-mediated disease Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia Pleiotropy in complex traits: challenges and strategies The Genetics of Stress-Related Disorders: PTSD, Depression, and Anxiety Disorders The newly identified migration inhibitory protein regulates the radial migration in the developing neocortex Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders.The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies CNVs conferring risk of autism or schizophrenia affect cognition in controls Schizophrenia.Investigation of SHANK3 in schizophrenia.Identification of Distinct Psychosis Biotypes Using Brain-Based Biomarkers Molecular substrates of schizophrenia: homeostatic signaling to connectivity Microendophenotypes of psychiatric disorders: phenotypes of psychiatric disorders at the level of molecular dynamics, synapses, neurons, and neural circuits Using whole-exome sequencing to identify inherited causes of autism.Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies

P2860

Q24597718-C554E1DA-3587-4A78-BAB2-D3749526204E Q24603800-21AC9321-47D6-42C7-AB9F-B7C19CB5B5D6 Q24612419-BA98AE07-72DB-49B1-9DAB-7139B3E9C999 Q26252573-7E22608A-F41D-4C3B-95C8-8DA0D6486920 Q26269829-A67D0FE0-AEEF-4C40-AA8A-A35B2261C9B0 Q26769649-1A25A723-35BD-4CA3-83A5-74FAECE0790B Q26775498-EE30DC2C-0688-4D7D-A02D-A9FDFCE4700A Q26779153-F0A5E879-7AED-422E-80C6-765A95A57228 Q26781213-219E9432-5584-4B3A-A5BA-EE7438F40101 Q26781645-72324B09-30E7-4699-9D8B-08D4C81E8566 Q26783154-4B6D9EB0-DE7A-4CF7-BF78-7AE16B517F0F Q27024976-457884E5-EF97-4F2B-BE83-83D7BDE948BE Q27305223-6C5017A9-9EE1-48B8-990A-6B17CA392EE3 Q27312463-5B20BEA7-55D3-4648-9BC8-70F8225087A6 Q27314897-90377AC2-E3F6-45B7-9A8C-0C874D82165D Q27320217-0210B65E-ACD7-457C-92F6-212FCD985E25 Q27687011-EC9B6445-4AA0-430F-A6E2-8CFE972ADF9B Q28076465-75B05AC1-9392-479B-B527-504D318263ED Q28081561-DDF45E5C-98A6-44ED-8FCC-98657F98FD7D Q28083143-EB98E639-3D54-4400-BE8A-6770E1ED1E2C Q28083824-A07AEAC3-6DF1-469D-B626-930EEF09F25B Q28083879-70E0870B-A55B-4F2E-8058-AB6C25A3F6DA Q28087577-49A0C483-0134-4ED9-9AAB-8D254FCD25B1 Q28256361-744D8D99-0D6E-4BA0-8E3B-1B774AEA81AB Q28260701-4326B30A-33A6-4057-AA1F-5364F6AA42AC Q28262977-82F0EAA2-6F3B-4D71-B8D1-192707A79CEA Q28390545-EFD23480-06F1-47C9-AD9F-69F3E1618BCD Q28396166-61D31823-B13E-4150-A275-228487FAF640 Q28513285-A7294424-25EF-4816-905D-7604E3407F5B Q28655713-2273A1C1-1E41-45B4-B31A-67F8DD1E6744 Q28685216-5E38B574-1929-4246-9968-F57E72AF50FE Q28943394-C792B381-7DCD-444C-8E77-6E42712D8FA6 Q29308426-58E5FFCA-0B48-4673-80AF-E99B2CD83804 Q30251961-8356AAC0-B0BE-4537-9879-CECCE1539FAF Q30313279-4724CA59-16D7-4D55-B5EB-BD8127ABB16C Q30363008-1ABF5CE7-4902-4869-B788-DEEB59469FF4 Q30383611-76F36B1F-DAD6-4571-B0DB-E815F1D975A2 Q30409099-B4A1D971-28C6-4FED-9C77-F1FE32657CA8 Q30418126-D3D6B20A-DD4C-448A-B08B-45906CA120B3 Q30425482-6A576F38-40E2-452B-8AC5-EB933A3A63A3

P2860

CNVs: harbingers of a rare variant revolution in psychiatric genetics

http://www.wikidata.org/entity/Q27022289

description

2012 nî lūn-bûn

@nan

2012 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի մարտին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

CNVs: harbingers of a rare variant revolution in psychiatric genetics

@ast

CNVs: harbingers of a rare variant revolution in psychiatric genetics

@en

CNVs: harbingers of a rare variant revolution in psychiatric genetics

@nl

type

label

CNVs: harbingers of a rare variant revolution in psychiatric genetics

@ast

CNVs: harbingers of a rare variant revolution in psychiatric genetics

@en

CNVs: harbingers of a rare variant revolution in psychiatric genetics

@nl

prefLabel

CNVs: harbingers of a rare variant revolution in psychiatric genetics

@ast

CNVs: harbingers of a rare variant revolution in psychiatric genetics

@en

CNVs: harbingers of a rare variant revolution in psychiatric genetics

@nl

P1433

Q27022289-6B820980-A650-44CB-A0B0-F2FA0D8C4A41

P1476

Q27022289-DDED86BD-611B-4749-B848-14A02ABCC885

P2093

Q27022289-6B5D18C6-5B6F-4305-AC34-8F132E68621F

P2860

Q27022289-02ADDD3E-D052-4506-BE86-83C7929C2072

Q27022289-09514C7B-4BF6-4EF1-A663-47C7A8ED91A5

Q27022289-0B24F608-742C-42C9-9775-C41CD64FD72A

Q27022289-0C8572C2-7776-47E5-967F-7A4B6631A21A

Q27022289-0CCC08FD-2C27-4644-B605-15ADDC975A8F

Q27022289-0FFB853C-DAB7-4C9E-A1B0-89A2AF1D23FB

Q27022289-10FD2CEE-E905-406A-B678-0177CBED101C

Q27022289-136F04FD-3B62-4F47-A75E-7961BE5E77D5

Q27022289-16D456BD-5BD7-4AB8-A630-9DA5E0FFC1F5

Q27022289-1C65A9A1-A87C-404C-BB61-463FB9C1A0BC

P304

Q27022289-441EEBFE-6F93-4921-9A03-ED1580DB6EA0

P31

Q27022289-176D1234-520E-4AE6-BD26-F6EFE77BEE2E

P3181

Q27022289-661F1A86-C506-4BEE-8F70-4E20FBC15130

P356

Q27022289-2F8A019A-38AB-4F1D-B017-1621A8DCBD07

P407

Q27022289-E05DC74F-211F-40A8-82B0-3B70877CC25A

P433

Q27022289-FC0BF3B6-18D8-4DAA-A545-B25CEFF95464

P478

Q27022289-6BEB4426-3C6F-4412-B040-D60F20838B2C

P50

Q27022289-28DFF20B-F5E6-41FD-9D05-8D9FBAFB9C00

P577

Q27022289-CFFE690C-4027-49B9-B7E0-AD7227D4F2AF

P5875

Q27022289-7FCF4739-D8CE-47FE-B91E-00ADF4C47FB6

P698

Q27022289-52D0F3DC-6A61-4CFA-82F3-E4B0D5EF8967

P932

Q27022289-4AFC2981-C74C-4DAB-A0FD-13ED59DB9FE6

P3181

P356

J.CELL.2012.02.039

P1433

P1476

CNVs: harbingers of a rare variant revolution in psychiatric genetics

@en

P2093

Dheeraj Malhotra

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

P2860

The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway

Mechanisms of change in gene copy number

Variation in genome-wide mutation rates within and between human families

Autism and autism spectrum disorders: diagnostic issues for the coming decade

Genetics of austim: complex aetiology for a heterogeneous disorder

Retrotransposons Revisited: The Restraint and Rehabilitation of Parasites

Psychosocial Disability in the Course of Bipolar I and II Disorders

Rare chromosomal deletions and duplications increase risk of schizophrenia

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability

P304

1223-41

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

P31

scholarly article

P3181

1526076

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

P356

10.1016/J.CELL.2012.02.039

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

P407

P433

6

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

P478

148

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

P50

P577

2012-03-16T00:00:00Z

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

P5875

221712665

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

P698

22424231

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

P932

3351385

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