(Q60445525)

English

Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study

scientific article published on 07 June 2018

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scholarly article

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30 March 2020

Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study (English)

1 reference

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30 March 2020

Anders Rosengren

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30 March 2020

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30 March 2020

Anders D. Børglum

17

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30 March 2020

Merete Nordentoft

18

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30 March 2020

Preben Bo Mortensen

20

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30 March 2020

Daniel Geschwind

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Daniel H Geschwind

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30 March 2020

Benjamin M. Neale

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Benjamin M Neale

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30 March 2020

Mark Joseph Daly

12

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Mark J Daly

1 reference

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30 March 2020

David M Hougaard

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David M Hougaard

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30 March 2020

Wesley K Thompson

23

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Wesley K Thompson

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30 March 2020

Carsten Bøcker Pedersen

22

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Carsten Pedersen

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30 March 2020

16

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Ole Mors

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30 March 2020

24

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Thomas Werge

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30 March 2020

Marie Bækvad-Hansen

10

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Marie Baekvad-Hansen

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30 March 2020

Jonas Bybjerg-Grauholm

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Jonas Bybjerg-Grauholm

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30 March 2020

author name string

Line Olsen

1

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30 March 2020

Thomas Sparsø

2

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30 March 2020

Shantel M Weinsheimer

3

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30 March 2020

Marcelo Bertalan Quintanilha Dos Santos

4

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30 March 2020

Wiktor Mazin

5

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30 March 2020

Xabier Calle Sanchez

7

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30 March 2020

Louise K Hoeffding

8

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30 March 2020

Henriette Schmock

9

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30 March 2020

Marianne G Pedersen

14

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30 March 2020

publication date

7 June 2018

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30 March 2020

The Lancet Psychiatry

1 reference

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30 March 2020

5

1 reference

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30 March 2020

573-580

1 reference

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30 March 2020

7

1 reference

Europe PubMed Central

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30 March 2020

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

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Autism genetics: opportunities and challenges for clinical translation

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

22q11.2 deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

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Copy-number variation in the pathogenesis of autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

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A copy number variation morbidity map of developmental delay

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Copy number variation in schizophrenia in Sweden

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of 22q11 microdeletion

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems.

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence that duplications of 22q11.2 protect against schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of case-cohort designs

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Tutorial in biostatistics: competing risks and multi-state models

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

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Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study.

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS2215-0366%2818%2930168-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Microduplication 22q11.2: a description of the clinical, developmental and behavioral characteristics during childhood.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29886042

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/29886042

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/S2215-0366(18)30168-8

1 reference

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30 March 2020

1 reference

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30 March 2020

1 reference

Europe PubMed Central

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30 March 2020

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