(Q52552534)

3 May 2018

title

Chromosome aberrations in a schizophrenia population (English)

1 reference

https://api.crossref.org/works/10.1016/S0920-9964(02)00504-2

3 April 2024

main subject

schizophrenia

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chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14623367

3 April 2024

schizophrenic psychology

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14623367

3 April 2024

Osman Demirhan

1 reference

3 May 2018

Deniz Taştemir

series ordinal

1 reference

3 May 2018

language of work or name

English

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publication date

1 December 2003

1 reference

3 May 2018

full work available at URL

https://api.elsevier.com/content/article/PII:S0920996402005042?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0920-9964(02)00504-2

https://api.elsevier.com/content/article/PII:S0920996402005042?httpAccept=text/plain

3 April 2024

1 reference

https://api.crossref.org/works/10.1016/S0920-9964(02)00504-2

3 April 2024

published in

Schizophrenia Research

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3 May 2018

volume

1 reference

3 May 2018

issue

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3 May 2018

page(s)

1-7

1 reference

3 May 2018

Screening for 22q11 deletions in a schizophrenia population.

cites work

1 reference

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7 January 2021

Chromosome aberrations in patients with paranoid psychosis

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7 January 2021

Genetics of schizophrenia and the new millennium: progress and pitfalls

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https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

Chromosomal aberrations and schizophrenia. Autosomes

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https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

22q11 deletion syndrome: a genetic subtype of schizophrenia

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https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

Partial trisomy chromosome 5 cosegregating with schizophrenia

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https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

Chromosomal abnormalities and schizophrenia

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7 January 2021

Identification of an interstitial deletion in an adult female with schizophrenia, mental retardation, and dysmorphic features: further support for a putative schizophrenia-susceptibility locus at 5q21-23.1.

1 reference

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7 January 2021

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

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7 January 2021

Forty four probands with an additional "marker" chromosome.

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7 January 2021

Differential rates of psychiatric disorders in adults with Down's syndrome compared with other mentally handicapped adults

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https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

Cytogenetic studies of males with schizophrenia. Screening for the fragile X chromosome and other chromosomal abnormalities

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https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

Schizophrenia and sex chromosome anomalies

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7 January 2021

‘Pfropfschizophrenie’ revisited

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7 January 2021

Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22

1 reference

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7 January 2021

Genome scan of European-American schizophrenia pedigrees: Results of the NIMH genetics initiative and millennium consortium

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7 January 2021

Brief report: translocation involving chromosomes 1 and 7 in a boy with childhood-onset schizophrenia

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7 January 2021

Velocardiofacial manifestations and microdeletions in schizophrenic inpatients

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7 January 2021

Chromosomal localization of three human D5 dopamine receptor genes

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7 January 2021

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

1 reference

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7 January 2021

A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci

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7 January 2021

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

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7 January 2021

Constitutive heterochromatin of chromosome 1 and Duffy blood group alleles in schizophrenia

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https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

Association of schizophrenia and partial trisomy of chromosome 5p. A case report

1 reference

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7 January 2021

Linkage results on 11Q21-22 in Eastern Quebec pedigrees densely affected by schizophrenia

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

A case of small cerebral cyst and pericentric inversion of chromosome 9 that developed schizophrenia-like psychosis

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7 January 2021

Chromosome 22qII deletions. An under-recognised cause of idiopathic learning disability.

1 reference

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7 January 2021

Clinical and neurobiological correlates of cytogenetic abnormalities in childhood-onset schizophrenia

1 reference

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7 January 2021

Chromosome 22 workshop report

1 reference

https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

Chromosome 18 translocation (18;21) (p11.1;p11.1) associated with psychosis in one family

1 reference

https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

Association within a family of a balanced autosomal translocation with major mental illness

1 reference

https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

Differential diagnosis and treatment of depressive features in Down's syndrome: a case illustration.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

Major depression in Down's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

Population studies of inv(9) chromosomes in 4,300 japanese: Incidence, sex difference and clinical significance

1 reference

https://api.crossref.org/works/10.1016%2FS0920-9964%2802%2900504-2

7 January 2021

Pericentric inversions of chromosome 9 in Taiwanese fetuses

1 reference

https://api.crossref.org/works/10.1016/S0920-9964(02)00504-2

Genome scan of schizophrenia

3 April 2024

1 reference

https://api.crossref.org/works/10.1016/S0920-9964(02)00504-2

Family and genetic studies on the relationship of schizophrenia to affective disorders

3 April 2024

1 reference

https://api.crossref.org/works/10.1016/S0920-9964(02)00504-2

Pericentric inversion of chromosome 9: prevalence in 300 Down syndrome families and molecular studies of nondisjunction

3 April 2024

1 reference

https://api.crossref.org/works/10.1016/S0920-9964(02)00504-2

3 April 2024

Identifiers

1 reference

3 May 2018

1 reference

3 May 2018