Isochromosome 13 in a patient with childhood-onset schizophrenia, ADHD, and motor tic disorder

about

Human iPSC Glial Mouse Chimeras Reveal Glial Contributions to Schizophrenia.

P2860

Q38665790-8101BFD7-A6E7-4B15-84FF-E032EF02C5D3

P2860

Isochromosome 13 in a patient with childhood-onset schizophrenia, ADHD, and motor tic disorder

Item

http://www.wikidata.org/entity/Q35742294

description

2012 nî lūn-bûn

@nan

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

2012年论文

@zh

2012年论文

@zh-cn

name

Isochromosome 13 in a patient ...... , ADHD, and motor tic disorder

@ast

Isochromosome 13 in a patient ...... , ADHD, and motor tic disorder

@en

type

Item

label

Isochromosome 13 in a patient ...... , ADHD, and motor tic disorder

@ast

Isochromosome 13 in a patient ...... , ADHD, and motor tic disorder

@en

prefLabel

Isochromosome 13 in a patient ...... , ADHD, and motor tic disorder

@ast

Isochromosome 13 in a patient ...... , ADHD, and motor tic disorder

@en

P1476

Isochromosome 13 in a patient ...... , ADHD, and motor tic disorder

@en

P2093

Billie J Carstens

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

Karen Swisshelm

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

Kirsten Floyd

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

Marianne Z Wamboldt

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

Randall G Ross

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

Sharon L Graw

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

Sherry Leonard

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

P2860

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotyping

Rare chromosomal deletions and duplications increase risk of schizophrenia

The chimeric gene CHRFAM7A, a partial duplication of the CHRNA7 gene, is a dominant negative regulator of α7*nAChR function

The Epsin 4 gene on chromosome 5q, which encodes the clathrin-associated protein enthoprotin, is involved in the genetic susceptibility to schizophrenia

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

Common variants conferring risk of schizophrenia

Microduplications of 16p11.2 are associated with schizophrenia

P2888

1755-8166-5-2

P304

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

P31

scholarly article

P356

10.1186/1755-8166-5-2

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

P433

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

P478

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

P577

2012-01-03T00:00:00Z

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

P5875

51980387

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

P6179

1023457476

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

P698

22214315

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

P921

schizophrenia

P932

3274485

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

Isochromosome 13 in a patient with childhood-onset schizophrenia, ADHD, and motor tic disorder

about

P2860

P2860

Isochromosome 13 in a patient with childhood-onset schizophrenia, ADHD, and motor tic disorder

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P5875

P6179

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P5875

P6179

P698

P921

P932