Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1476-5578

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome ; day:29 ; month:6 ; year:2022 ; pages:1-10
Molecular psychiatry ; (29.6.2022), 1-10

Creator: Alver, Maris
Mancini, Valentina
Läll, Kristi
Schneider, Maude
Romano, Luciana
Mägi, Reedik
Dermitzakis, Emmanouil T.
Eliez, Stephan
Reymond, Alexandre

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41380-022-01674-9

URN: urn:nbn:de:101:1-2022082021042984673959

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:37 AM CEST

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Alver, Maris
Mancini, Valentina
Läll, Kristi
Schneider, Maude
Romano, Luciana
Mägi, Reedik
Dermitzakis, Emmanouil T.
Eliez, Stephan
Reymond, Alexandre
SpringerLink (Online service)

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Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome

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Other Objects (12)

Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome

Complement Activation in 22q11.2 Deletion Syndrome

Genotype-phenotype correlation in 22q11.2 deletion syndrome

A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Developmental trajectories of executive functions in 22q11.2 deletion syndrome

Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR

Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome

Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome

A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review

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Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome

Complement Activation in 22q11.2 Deletion Syndrome

Genotype-phenotype correlation in 22q11.2 deletion syndrome

A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Developmental trajectories of executive functions in 22q11.2 deletion syndrome

Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR

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Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome

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Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome

Complement Activation in 22q11.2 Deletion Syndrome

Genotype-phenotype correlation in 22q11.2 deletion syndrome

A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

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A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review

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