(Q33920498)

30 July 2017

1 reference

title

Chromosomal abnormalities and schizophrenia (English)

1 reference

30 July 2017

0 references

A S Bassett

1

1 reference

PubMed ID

10813803

30 July 2017

E W Chow

series ordinal

2

1 reference

PubMed ID

10813803

30 July 2017

R Weksberg

series ordinal

3

1 reference

30 July 2017

1 January 2000

1 reference

American Journal of Medical Genetics Part A

30 July 2017

1 reference

30 July 2017

97

1 reference

30 July 2017

1

1 reference

30 July 2017

45-51

1 reference

22q11 deletion syndrome: a genetic subtype of schizophrenia

30 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Phenotype of adults with the 22q11 deletion syndrome: A review

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Linkage of familial schizophrenia to chromosome 13q32

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Forebrain induction, retinoic acid, and vulnerability to schizophrenia: insights from molecular and genetic analysis in developing mice

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

'Pfropfschizophrenie' revisited. Schizophrenia in people with mild learning disability

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Support for a chromosome 18p locus conferring susceptibility to functional psychoses in families with schizophrenia, by association and linkage analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

The annual incidence of DiGeorge/velocardiofacial syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

22q11 deletion syndrome in adults with schizophrenia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Three independent lines of evidence suggest retinoids as causal to schizophrenia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

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.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Cytogenetic abnormalities on chromosome 18 associated with bipolar affective disorder or schizophrenia.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Prevalence of 22q11 microdeletion

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Evidence of chromosomal fragile sites in schizophrenic patients.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Chromosomal aberrations and bipolar affective disorder

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Childhood antecedents of schizophrenia and affective illness: social adjustment at ages 7 and 11

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

A contribution to the differential diagnosis of the "group of schizophrenias": structural abnormality of chromosome 4

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Schizophrenia: genetic tools for unraveling the nature of a complex disorder

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Behavioural phenotypes in dysmorphic syndromes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Schizophrenia and mental retardation in an adult male with a de novo interstitial deletion 9(q32q34.1)

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Chromosomal aberrations and schizophrenia. Autosomes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

‘Pfropfschizophrenie’ revisited

5 July 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%28200021%2997%3A1%3C45%3A%3AAID-AJMG6%3E3.0.CO%3B2-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%28200021%2997%3A1%3C45%3A%3AAID-AJMG6%3E3.0.CO%3B2-9

Transition from adolescence to early adulthood: adaptation and psychiatric status of women with 47,XXX.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%28200021%2997%3A1%3C45%3A%3AAID-AJMG6%3E3.0.CO%3B2-9

Identification of Sequence Variants and Analysis of the Role of the Catechol-O-Methyl-Transferase Gene in Schizophrenia Susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%28200021%2997%3A1%3C45%3A%3AAID-AJMG6%3E3.0.CO%3B2-9

Genetic basis of schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%28200021%2997%3A1%3C45%3A%3AAID-AJMG6%3E3.0.CO%3B2-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%28200021%2997%3A1%3C45%3A%3AAID-AJMG6%3E3.0.CO%3B2-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%28200021%2997%3A1%3C45%3A%3AAID-AJMG6%3E3.0.CO%3B2-9

Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%28200021%2997%3A1%3C45%3A%3AAID-AJMG6%3E3.0.CO%3B2-9

Systematic chromosome examination of two families with schizophrenia and two families with manic depressive illness.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188305

Cytogenetic studies of familial schizophrenics

29 October 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%28200021%2997%3A1%3C45%3A%3AAID-AJMG6%3E3.0.CO%3B2-9

Chromosomal translocation t(2;18)(q21;q23) in a schizophrenic individual and his daughter

21 January 2018

1 reference

12 December 2020

Chromosomal fragile site 1q21 in schizophrenic patients

1 reference

12 December 2020

Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3.

1 reference

12 December 2020

Velocardiofacial manifestations and microdeletions in schizophrenic inpatients

1 reference

12 December 2020

Schizophrenia and sex chromosome anomalies

1 reference

12 December 2020

Late‐Onset psychosis in the velo‐cardio‐facial syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

The association between triple X and psychosis

1 reference

12 December 2020

Pericentric region of chromosome 9 is a possible candidate region for linkage study of schizophrenia

1 reference

12 December 2020

Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus

1 reference

12 December 2020

A balanced 2:18 translocation and familial schizophrenia: falling short of an association

1 reference

12 December 2020

High resolution cytogenetic study in schizophrenia

1 reference

12 December 2020

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

1 reference

12 December 2020

Chromosome 22 workshop report

1 reference

12 December 2020

10.1002/(SICI)1096-8628(200021)97:1<45::AID-AJMG6>3.0.CO;2-9

Identifiers

DOI

1 reference

30 July 2017

1 reference

30 July 2017

1 reference

PubMed ID

10813803