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 (Q60445525)

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scientific article published on 07 June 2018

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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)

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Anders Rosengren

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Anders D. Børglum

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Merete Nordentoft

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Preben Bo Mortensen

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30 March 2020

Daniel Geschwind

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30 March 2020

Benjamin M. Neale

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30 March 2020

Mark Joseph Daly

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Mark J Daly

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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

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30 March 2020

Carsten Bøcker Pedersen

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Carsten Pedersen

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30 March 2020

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Ole Mors

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30 March 2020

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Thomas Werge

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30 March 2020

Marie Bækvad-Hansen

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30 March 2020

Jonas Bybjerg-Grauholm

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30 March 2020

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Line Olsen

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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

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30 March 2020

Xabier Calle Sanchez

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30 March 2020

Louise K Hoeffding

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30 March 2020

Henriette Schmock

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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

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30 March 2020

5

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30 March 2020

573-580

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30 March 2020

7

1 reference

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30 March 2020

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

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Autism genetics: opportunities and challenges for clinical translation

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7 January 2021

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22q11.2 deletion syndrome

1 reference

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7 January 2021

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

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

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

1 reference

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

1 reference

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

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

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Evidence that duplications of 22q11.2 protect against schizophrenia

1 reference

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

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Analysis of case-cohort designs

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

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7 January 2021

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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

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7 January 2021

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

1 reference

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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

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

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Identifiers

10.1016/S2215-0366(18)30168-8

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1 reference

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30 March 2020

1 reference

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30 March 2020

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