Microarray comparative genomic hybridization analysis of 59 patients with schizophrenia (Q59697660)

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11 January 2020

title

Microarray comparative genomic hybridization analysis of 59 patients with schizophrenia (English)

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Hirotomo Saitsu

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Hiroshi Kunugi

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Norio Niikawa

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author name string

Takeshi Mizuguchi

1

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Masanari Itokawa

3

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Akira Sano

4

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Osamu Shimokawa

5

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Yukiko Yoshimura

6

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Naoki Harada

7

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Noriko Miyake

8

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Akira Nishimura

9

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Nadiya Sosonkina

11

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Naomichi Matsumoto

14

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publication date

7 August 2008

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Journal of Human Genetics

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published in

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volume

53

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issue

10

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page(s)

914-919

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https://scigraph.springernature.com/pub.10.1007/s10038-008-0327-6

11 January 2020

exact match

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BAC array CGH reveals genomic aberrations in idiopathic mental retardation.

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Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion

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The DISC locus in psychiatric illness

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Karyotype analysis of 161 unrelated schizophrenics: no increased rates of X chromosome mosaicism or inv(9), using ethnically matched and age-stratified controls.

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

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

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Suggestive linkage of schizophrenia to 5p13 in Costa Rica.

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Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia.

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Fine mapping of an isodicentric Y chromosomal breakpoint from a schizophrenic patient

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Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia

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Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia

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

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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

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

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Live and let die: regulatory mechanisms in Fas-mediated apoptosis.

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Strong association of de novo copy number mutations with autism

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

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A case of schizophrenia with a dicentric Y chromosome

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A highly significant association between a COMT haplotype and schizophrenia.

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10.1007/S10038-008-0327-6

Identifiers

DOI

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11 January 2020

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