(Q36817275)

English

Schizophrenia Spectrum Disorders in a Danish 22q11.2 Deletion Syndrome Cohort Compared to the Total Danish Population--A Nationwide Register Study

scientific article published on 5 January 2016

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scholarly article

1 reference

Europe PubMed Central

16 August 2017

Schizophrenia Spectrum Disorders in a Danish 22q11.2 Deletion Syndrome Cohort Compared to the Total Danish Population--A Nationwide Register Study (English)

1 reference

Europe PubMed Central

16 August 2017

1 reference

based on heuristic

inferred from title

6

object named as

Thomas Werge

1 reference

Europe PubMed Central

16 August 2017

Carsten Bøcker Pedersen

object named as

Carsten B Pedersen

4

0 references

Preben Bo Mortensen

5

object named as

Preben B Mortensen

1 reference

Europe PubMed Central

16 August 2017

author name string

Anders Vangkilde

1

1 reference

Europe PubMed Central

16 August 2017

Line Olsen

2

1 reference

Europe PubMed Central

16 August 2017

Louise K Hoeffding

3

1 reference

Europe PubMed Central

16 August 2017

Betina Trabjerg

7

1 reference

Europe PubMed Central

16 August 2017

language of work or name

0 references

publication date

5 January 2016

1 reference

Europe PubMed Central

16 August 2017

Schizophrenia Bulletin

1 reference

Europe PubMed Central

16 August 2017

42

1 reference

Europe PubMed Central

16 August 2017

3

1 reference

Europe PubMed Central

16 August 2017

824-831

1 reference

Europe PubMed Central

16 August 2017

CNVs in neuropsychiatric disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Copy number variation in schizophrenia in Sweden

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

A comprehensive assessment of parental age and psychiatric disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

The penetrance of copy number variations for schizophrenia and developmental delay.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Existing data sources for clinical epidemiology: Danish registries for studies of medical genetic diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Genotype-phenotype correlation in 22q11.2 deletion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

CNVs: harbingers of a rare variant revolution in psychiatric genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Meta-analysis of paternal age and schizophrenia risk in male versus female offspring

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

No evidence of time trends in the urban-rural differences in schizophrenia risk among five million people born in Denmark from 1910 to 1986.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Evidence of a dose-response relationship between urbanicity during upbringing and schizophrenia risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Velo-cardio-facial syndrome: a distinctive behavioral phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

A population study of chromosome 22q11 deletions in infancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Electronic data processing in the Danish cytogenetic central register and EDP problems of registers in general.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

29 September 2017

Skin cancer as a marker of sun exposure: a case of serious immortality bias

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

27 June 2018

Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

27 June 2018

A comprehensive nationwide study of the incidence rate and lifetime risk for treated mental disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

The validity of the schizophrenia diagnosis in the Danish Psychiatric Central Research Register is good

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

Full spectrum of psychiatric disorders related to foreign migration: a Danish population-based cohort study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

The Danish Psychiatric Central Research Register.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

The Danish Civil Registration System.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

Full spectrum of psychiatric outcomes among offspring with parental history of mental disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

Penetrance for copy number variants associated with schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

Severe mental disorders in offspring with 2 psychiatrically ill parents.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

Genetic counseling for the 22q11.2 deletion.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

Elaboration on immigration and risk for schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

The Danish Civil Registration System. A cohort of eight million persons.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

Clinical features of 78 adults with 22q11 Deletion Syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

Paternal and maternal age as risk factors for psychosis: findings from Denmark, Sweden and Australia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4838106

5 September 2018

The landscape of copy number variations in Finnish families with autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBV195

21 January 2018

Covariance Analysis of Censored Survival Data Using Log-Linear Analysis Techniques

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBV195

21 January 2018

Paternal Age at Birth of First Child and Risk of Schizophrenia

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBV195

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/26738530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atypical copy number abnormalities in 22q11.2 region: report of three cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/26738530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/SCHBUL/SBV195

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

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