(Q34539696)

English

A complete genetic association scan of the 22q11 deletion region and functional evidence reveal an association between DGCR2 and schizophrenia.

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scholarly article

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25 December 2019

A complete genetic association scan of the 22q11 deletion region and functional evidence reveal an association between DGCR2 and schizophrenia (English)

1 reference

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25 December 2019

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25 December 2019

Abraham Weizman

6

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25 December 2019

7

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Benjamin Yakir

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25 December 2019

8

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Ruth Navon

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25 December 2019

author name string

Anat Levit

2

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25 December 2019

Mao-Liang Chen

3

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25 December 2019

Chia-Hsiang Chen

4

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25 December 2019

Michal Bronstein

5

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25 December 2019

Ariel Darvasi

9

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25 December 2019

publication date

17 June 2006

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25 December 2019

number of pages

11

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25 December 2019

120

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25 December 2019

2

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25 December 2019

160-170

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25 December 2019

https://scigraph.springernature.com/pub.10.1007/s00439-006-0195-0

0 references

Sensorimotor gating and schizophrenia. Human and animal model studies

1 reference

https://api.crossref.org/works/10.1007%2FS00439-006-0195-0

21 January 2018

Chronic antipsychotics treatment regulates MAOA, MAOB and COMT gene expression in rat frontal cortex

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A highly significant association between a COMT haplotype and schizophrenia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of regulatory variation in mouse genes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative technologies for allele frequency estimation of SNPs in DNA pools.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

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Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

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Allelic Variation in Human Gene Expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variation in the 22q11 locus and susceptibility to schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is the WKL1 gene associated with schizophrenia?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A survey of the 22q11 microdeletion in a large cohort of schizophrenia patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The stanley foundation brain collection and neuropathology consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Score tests for association between traits and haplotypes when linkage phase is ambiguous

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessment of the frequency of the 22q11 deletion in Afrikaner schizophrenic patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multifactor dimensionality reduction software for detecting gene-gene and gene-environment interactions.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for 22q11 deletions in a schizophrenia population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16783572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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