The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders. - Wikidata - awgldk - TriplyDB

The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.

The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.

http://www.wikidata.org/entity/Q30468033

about

MicroRNAs: Key Regulators in the Central Nervous System and Their Implication in Neurological Diseases Hippocampal-Prefrontal Interactions in Cognition, Behavior and Psychiatric Disease Characterizing autism spectrum disorders by key biochemical pathways.Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndrome Synaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophrenia.Dendritic spine pathology in schizophrenia The Danish 22q11 research initiative The effect of hypocalcemia in early childhood on autism-related social and communication skills in patients with 22q11 deletion syndrome Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.Chronic overload of SEPT4, a parkin substrate that aggregates in Parkinson's disease, causes behavioral alterations but not neurodegeneration in mice Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders Evidence for altered hippocampal function in a mouse model of the human 22q11.2 microdeletion.Mediator and human disease Convergent microRNA actions coordinate neocortical development.Default mode network connectivity and reciprocal social behavior in 22q11.2 deletion syndrome.Avoiding mouse traps in schizophrenia genetics: lessons and promises from current and emerging mouse models.Animal models of psychiatric disorders that reflect human copy number variation.22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis.MicroRNAs as the cause of schizophrenia in 22q11.2 deletion carriers, and possible implications for idiopathic disease: a mini-review.Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome 22q11.2 deletion syndrome: attitudes towards disclosing the risk of psychiatric illness.Association of IL-12p70 and IL-6:IL-10 ratio with autism-related behaviors in 22q11.2 deletion syndrome: a preliminary report Evidence that COMT genotype and proline interact on negative-symptom outcomes in schizophrenia and bipolar disorder.Genotype-Dependent Effects of COMT Inhibition on Cognitive Function in a Highly Specific, Novel Mouse Model of Altered COMT Activity.Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion.The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.System-based proteomic and metabonomic analysis of the Df(16)A+/- mouse identifies potential miR-185 targets and molecular pathway alterations MicroRNA dysregulation in neuropsychiatric disorders and cognitive dysfunction Losing your inhibition: linking cortical GABAergic interneurons to schizophrenia.Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature.Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications.Using hiPSCs to model neuropsychiatric copy number variations (CNVs) has potential to reveal underlying disease mechanisms.MicroRNA-independent functions of DGCR8 are essential for neocortical development and TBR1 expression.Performance on a computerized neurocognitive battery in 22q11.2 deletion syndrome: A comparison between US and Israeli cohorts.Decreased protein S-palmitoylation in dorsolateral prefrontal cortex in schizophrenia.PRODH rs450046 and proline x COMT Val¹⁵⁸ Met interaction effects on intelligence and startle in adults with 22q11 deletion syndrome.Polymorphism within a Neuronal Activity-Dependent Enhancer of NgR1 Is Associated with Corpus Callosum Morphology in Humans.Altered Brain Structure-Function Relationships Underlie Executive Dysfunction in 22q11.2 Deletion Syndrome.The schizophrenia/bipolar disorder candidate gene GNB1L is regulated in human temporal cortex by a cis-acting element located within the 3'-region.

P2860

Q26744819-A7CD087A-149A-4069-BFE8-586A29D60DBA Q26767711-CBF6ADF3-565A-4768-B9C0-517548E91820 Q26781645-E8C56094-BA26-4D21-A5F4-7F3F000C07A8 Q26824150-481B851C-B143-4E54-804E-672E93C5CC05 Q26829347-85A562B6-D463-4227-B5C7-41459D7D51AA Q26991935-32409DEB-7E91-47FB-9917-8C52729B25D6 Q28658990-E54652D7-FAB9-47E0-A227-0D21517EEE78 Q29399323-C81BAE32-9C7A-4AEA-8856-69AF4837E07E Q30241067-5750AC66-8572-450F-936C-DD88CA422A09 Q30450371-B2C16F68-F943-4E20-B1C4-049E4B04CB05 Q30458768-D9AFE418-B20D-40DE-A589-6765F3F9FE88 Q30531730-E3448C5C-EACE-46A9-8B1F-87324426F18F Q33909044-2D36776A-6A22-4FA0-B2F2-7C0B0432F026 Q33953643-4A4EFBA5-3144-4A5E-8454-050B241327C6 Q34152385-B71C4A5E-D920-4F37-A7B1-B6FA9CD7A2AD Q34206314-BF2FAEAF-7F21-42AC-ACD3-D61A77955F6A Q34294530-D8684005-0E66-45BE-A539-8B21219D225A Q34393037-846D8193-D06C-4FE1-AEBA-A75ED140D114 Q34394249-56B7A4DB-EE23-4788-B77E-A279184DE2FD Q34491810-85038733-3F77-4D45-9701-85B23F1B7917 Q35599290-4E4996C9-38E9-44AF-A809-F9AB2454A19D Q36431058-456BF44E-048D-4D23-89B0-567C9B46A4E8 Q36892242-C542DFFE-606F-43A3-BCC3-C6F9F0BBEE5A Q37307172-0C596C74-491C-4D00-A600-7AC6E70602BA Q37402659-D2D2563B-2368-4A4E-B950-A4E5EA787811 Q37412947-472253C0-FE76-446C-874B-3F96550BBC57 Q37419966-030426B3-A63B-49EC-88E9-CA9E12EE9606 Q37660911-FCB52ED3-AF52-4FFA-88E2-09FF41427867 Q37992401-2B652604-F6B2-4783-8DA1-DF5BD0934070 Q38064198-32108662-6400-4249-AF96-7D822A19D2E0 Q38084601-8FE794CD-3748-4A1E-A645-D3275EA397CC Q38616673-3C2237E7-C468-4E0E-8EB8-2F16113F7A5A Q38637625-41CD3634-0B38-4228-99B0-0E2FCE17A1A6 Q38715102-0F5F4AEA-C651-4270-B667-8AF8761B4834 Q39750431-FE787BE0-6EC9-47CE-A985-B2F043F2C509 Q39997649-418A9E82-A6D3-4131-A721-E4DCB7937FFD Q40841854-91EC09CF-6D97-4BE5-B2F7-0863B370FFB7 Q41289413-F4B86150-953F-4B23-BFFE-7F9042ECDF94 Q41290471-74A8DF08-4299-449B-B88C-7E53A2AFDB81 Q41458270-1D1B2B3B-76A6-4315-8648-D9C1E935A278

P2860

The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.

http://www.wikidata.org/entity/Q30468033

description

2010 nî lūn-bûn

@nan

2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հոտեմբերին 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

The 22q11.2 microdeletion: fif ...... xity of psychiatric disorders.

@ast

The 22q11.2 microdeletion: fif ...... xity of psychiatric disorders.

@en

type

label

The 22q11.2 microdeletion: fif ...... xity of psychiatric disorders.

@ast

The 22q11.2 microdeletion: fif ...... xity of psychiatric disorders.

@en

prefLabel

The 22q11.2 microdeletion: fif ...... xity of psychiatric disorders.

@ast

The 22q11.2 microdeletion: fif ...... xity of psychiatric disorders.

@en

P1433

Q30468033-9C9B906D-66C4-443D-9EBC-357E6B2ABB73

P1476

Q30468033-2227F52B-4682-456D-A6DA-29BFDD895407

P2093

Q30468033-107012B0-55FD-47AB-AF06-DAFE64E3331C

Q30468033-15D98DBE-BE0C-413F-87E6-A6F9982E6622

Q30468033-61B5177E-C12F-4FDC-8E41-852E820E0666

Q30468033-68A17C74-B7B2-476A-AF83-360949D3E28A

Q30468033-694BF884-4927-48EE-9AAC-E0304CDAD6B7

Q30468033-8973CC3A-E82B-46D8-9F70-FB4071152618

Q30468033-A6133F9E-F422-4B73-B940-28BFB43D9914

Q30468033-AF4F46B2-1C5A-409F-8337-179A79D10791

Q30468033-B4450676-DDB6-449A-B3EB-6760ACDC3D42

Q30468033-BD1C7F62-D240-464B-99DC-2273EDBC8E09

P2860

Q30468033-00ADB3FD-EFE6-42EC-B0CB-D04FD81F9857

Q30468033-03F5872B-1335-4B96-A74A-50CFB195FD34

Q30468033-044570BA-1A27-4B8B-AFA8-B3D30317598F

Q30468033-0727B948-4ED4-4C45-8701-6BC20867CB48

Q30468033-07622575-C2F4-4B0D-8BA8-1D6117ADB162

Q30468033-09D73E60-CE43-40E5-9FFA-C8236E62E494

Q30468033-0A20A0AE-9D45-45E7-8462-546E64AA7F10

Q30468033-0B53A7F5-A847-490E-B940-FA0F43D8AC68

Q30468033-0D1D9679-492D-40CE-AA50-1EB7D0D983EA

Q30468033-0E53D8D5-9E3C-429C-9150-B9B82904A14A

P304

Q30468033-3089586E-0239-47A7-A9B8-8541BD530B36

P31

Q30468033-36273FC3-5BA2-40FE-AEBC-48BBBE402C99

P356

Q30468033-B4A57201-38D5-482D-8908-8BBD74A9C164

P433

Q30468033-2DBE4A8F-0628-4F2A-A09A-5CCD95363A0C

P478

Q30468033-B12C57F4-341B-47F1-8C35-D324C5FE8991

P577

Q30468033-B50FF9D0-C2FD-4CAA-A421-9C34227512F8

P5875

Q30468033-A5DFCAEE-D258-44D4-B9D6-BFA98D702812

P698

Q30468033-4F13C8F5-ECFB-47AB-9854-86084F0655E1

P932

Q30468033-57F6D81F-E45A-4A86-9C6A-42305D700EB2

P356

J.IJDEVNEU.2010.09.007

P1433

International Journal of Developmental Neuroscience

P1476

The 22q11.2 microdeletion: fif ...... xity of psychiatric disorders.

@en

P2093

Bin Xu

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

Florence Chaverneff

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

Gregg W Crabtree

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

Joseph A Gogos

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

Jun Mukai

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

Karine Fenelon

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

Kimberly L Stark

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

Liam J Drew

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

Maria Karayiorgou

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

Pei-Ken Hsu

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

P2860

microRNA expression in the prefrontal cortex of individuals with schizophrenia and schizoaffective disorder

The dopamine hypothesis of schizophrenia: version III--the final common pathway

Large-scale recording of neuronal ensembles

Rare chromosomal deletions and duplications increase risk of schizophrenia

Role of TBX1 in human del22q11.2 syndrome

Functional consequences of PRODH missense mutations

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

Genetic variation in the 22q11 locus and susceptibility to schizophrenia

High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.

P304

259-281

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

P31

scholarly article

P356

10.1016/J.IJDEVNEU.2010.09.007

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

P433

3

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

P478

29

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

P577

2010-10-08T00:00:00Z

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

P5875

47335791

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

P698

20920576

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

P932

3074020

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