(Q59697660)

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11 January 2020

title

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

1 reference

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11 January 2020

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2

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11 January 2020

Hirotomo Saitsu

10

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11 January 2020

Hiroshi Kunugi

13

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11 January 2020

12

Norio Niikawa

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11 January 2020

author name string

Takeshi Mizuguchi

1

1 reference

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11 January 2020

Masanari Itokawa

3

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11 January 2020

Akira Sano

4

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11 January 2020

Osamu Shimokawa

5

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11 January 2020

Yukiko Yoshimura

6

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11 January 2020

Naoki Harada

7

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11 January 2020

Noriko Miyake

8

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11 January 2020

Akira Nishimura

9

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11 January 2020

Nadiya Sosonkina

11

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11 January 2020

Naomichi Matsumoto

14

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11 January 2020

publication date

7 August 2008

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Journal of Human Genetics

11 January 2020

published in

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11 January 2020

volume

53

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11 January 2020

issue

10

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11 January 2020

page(s)

914-919

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Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

11 January 2020

cites work

1 reference

12 December 2020

BAC array CGH reveals genomic aberrations in idiopathic mental retardation.

1 reference

12 December 2020

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

1 reference

12 December 2020

Peripheral myelin protein 22 is expressed in human central nervous system

1 reference

12 December 2020

Chromosomal abnormalities and schizophrenia

1 reference

12 December 2020

Cytogenetic findings in 250 schizophrenics: evidence confirming an excess of the X chromosome aneuploidies and pericentric inversion of chromosome 9

1 reference

12 December 2020

Brief report: association of sex chromosome anomalies with childhood-onset psychotic disorders

1 reference

12 December 2020

The hyperpolarization-activated HCN1 channel is important for motor learning and neuronal integration by cerebellar Purkinje cells

1 reference

12 December 2020

Clinical and molecular cytogenetic observations in three cases of "trisomy 12p syndrome".

1 reference

12 December 2020

Cytogenetic and molecular analysis in trisomy 12p.

1 reference

12 December 2020

Hereditary recurrent focal neuropathies: clinical and molecular features

1 reference

12 December 2020

De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy

1 reference

12 December 2020

Detection of large-scale variation in the human genome

1 reference

12 December 2020

The DISC locus in psychiatric illness

1 reference

12 December 2020

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

1 reference

12 December 2020

Sex chromosome aneuploidy and aging

1 reference

12 December 2020

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

1 reference

12 December 2020

Pathophysiology of HCN channels

1 reference

12 December 2020

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

1 reference

12 December 2020

Suggestive linkage of schizophrenia to 5p13 in Costa Rica.

1 reference

12 December 2020

Molecular mechanisms of schizophrenia

1 reference

12 December 2020

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

1 reference

12 December 2020

Recent advances in the genetics of schizophrenia

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12 December 2020

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

1 reference

12 December 2020

Genetic basis of schizophrenia

1 reference

12 December 2020

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

1 reference

12 December 2020

The molecular genetics of schizophrenia: new findings promise new insights

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

The impact of array genomic hybridization on mental retardation research: a review of current technologies and their clinical utility.

1 reference

12 December 2020

Schizophrenia and velo-cardio-facial syndrome.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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12 December 2020

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

1 reference

12 December 2020

Strong association of de novo copy number mutations with autism

1 reference

12 December 2020

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

1 reference

12 December 2020

A case of schizophrenia with a dicentric Y chromosome

1 reference

12 December 2020

A highly significant association between a COMT haplotype and schizophrenia.

1 reference

12 December 2020

10.1007/S10038-008-0327-6

Identifiers

DOI

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11 January 2020

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