(Q33745742)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20064257%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

Genetic copy number variants in sib pairs both affected with schizophrenia (English)

1 reference

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16 January 2020

0 references

1

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16 January 2020

Chih-min Liu

2

1 reference

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16 January 2020

Hai-Gwo Hwu

5

1 reference

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16 January 2020

author name string

Chun-Chiang Wen

3

1 reference

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16 January 2020

Shun-Min Chang

4

1 reference

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16 January 2020

publication date

11 January 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20064257%20AND%20SRC:MED&resulttype=core&format=json

Journal of Biomedical Science

16 January 2020

published in

1 reference

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16 January 2020

volume

17

1 reference

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16 January 2020

page(s)

2

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https://scigraph.springernature.com/pub.10.1186/1423-0127-17-2

16 January 2020

exact match

0 references

cites work

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Large recurrent microdeletions associated with schizophrenia

21 June 2018

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Amplicons on chromosome 3 contain oncogenes induced by recurrent exposure to 12-O-tetradecanoylphorbol-13-acetate and sodium n-butyrate and Epstein-Barr virus reactivation in a nasopharyngeal carcinoma cell line.

21 June 2018

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Strong association of de novo copy number mutations with sporadic schizophrenia

21 June 2018

1 reference

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 June 2018

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Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

21 June 2018

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Strong association of de novo copy number mutations with autism

21 June 2018

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Global variation in copy number in the human genome

21 June 2018

1 reference

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Identification of DNA copy-number aberrations by array-comparative genomic hybridization in patients with schizophrenia

21 June 2018

1 reference

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Determination of cytochrome P450 2D6 (CYP2D6) gene copy number by real-time quantitative PCR.

21 June 2018

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Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH.

21 June 2018

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Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis

21 June 2018

1 reference

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Detection of large-scale variation in the human genome

21 June 2018

1 reference

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Large-scale copy number polymorphism in the human genome

21 June 2018

1 reference

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Nurr1-RXR heterodimers mediate RXR ligand-induced signaling in neuronal cells.

21 June 2018

1 reference

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12p-amplicon structure analysis in testicular germ cell tumors of adolescents and adults by array CGH.

21 June 2018

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Molecular genetic studies of schizophrenia: challenges and insights

21 June 2018

1 reference

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

21 June 2018

1 reference

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Genomic structure and localisation within a linkage hotspot of Disrupted In Schizophrenia 1, a gene disrupted by a translocation segregating with schizophrenia.

21 June 2018

1 reference

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Disruption of two novel genes by a translocation co-segregating with schizophrenia

21 June 2018

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Twin studies in schizophrenia with special emphasis on concordance figures

21 June 2018

1 reference

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21 June 2018

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Three independent lines of evidence suggest retinoids as causal to schizophrenia

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Gene copy number variations in Asian patients with congenital bilateral absence of the vas deferens

21 June 2018

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DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling.

30 October 2018

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Performance on the Wisconsin Card Sorting Test among adolescents in Taiwan: norms, factorial structure, and relation to schizotypy.

30 October 2018

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30 October 2018

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Congenital anomalies in relatives of schizophrenic probands may indicate a retinoid pathology.

30 October 2018

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30 October 2018

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Evidence for a susceptibility locus for schizophrenia on chromosome 6pter-p22

30 October 2018

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12 December 2020

Peutz-Jeghers syndrome diagnosed in a schizophrenic patient with a large deletion in the STK11 gene

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12 December 2020

Gene copy number variation in schizophrenia

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12 December 2020

Deficits in sustained attention in schizophrenia and affective disorders: stable versus state-dependent markers

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12 December 2020

Identifiers

DOI

10.1186/1423-0127-17-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20064257%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

16 January 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20064257%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference