Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource, 1 online resource.
- Language
-
Englisch
- Bibliographic citation
-
Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach ; volume:14 ; number:1 ; day:23 ; month:5 ; year:2023 ; pages:1-13 ; date:12.2023
Molecular autism ; 14, Heft 1 (23.5.2023), 1-13, 12.2023
- Creator
-
Donnelly, Nicholas
Cunningham, Adam
Salas, Sergio Marco
Bracher-Smith, Matthew
Chawner, Samuel
Stochl, Jan
Ford, Tamsin
Raymond, F. Lucy
Escott-Price, Valentina
Bree, Marianne B. M. van den
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13229-023-00549-2
- URN
-
urn:nbn:de:101:1-2023091608572162431346
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:59 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Donnelly, Nicholas
- Cunningham, Adam
- Salas, Sergio Marco
- Bracher-Smith, Matthew
- Chawner, Samuel
- Stochl, Jan
- Ford, Tamsin
- Raymond, F. Lucy
- Escott-Price, Valentina
- Bree, Marianne B. M. van den
- SpringerLink (Online service)
Other Objects (12)
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy
A de novo CSDE1 variant causing neurodevelopmental delay, intellectual disability, neurologic and psychiatric symptoms in a child of consanguineous parents
Autosomal dominant intellectual disability
Gender differences in psychiatric diagnoses in older people with intellectual disability: a register study
The role of glia in epilepsy, intellectual disability, and other neurodevelopmental disorders in tuberous sclerosis complex
A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative features
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations
Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy
High Incidence of Copy Number Variants in Adults with Intellectual Disability and Co-morbid Psychiatric Disorders
Genetics of autosomal recessive intellectual disability
Intellectual disability and nutrition‐related health
Psychiatric care utilization among older people with intellectual disability in comparison with the general population: a register study
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy
A de novo CSDE1 variant causing neurodevelopmental delay, intellectual disability, neurologic and psychiatric symptoms in a child of consanguineous parents
Autosomal dominant intellectual disability
Gender differences in psychiatric diagnoses in older people with intellectual disability: a register study
The role of glia in epilepsy, intellectual disability, and other neurodevelopmental disorders in tuberous sclerosis complex
A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative features
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations
Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy
High Incidence of Copy Number Variants in Adults with Intellectual Disability and Co-morbid Psychiatric Disorders
Genetics of autosomal recessive intellectual disability
Intellectual disability and nutrition‐related health
Psychiatric care utilization among older people with intellectual disability in comparison with the general population: a register study
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy
A de novo CSDE1 variant causing neurodevelopmental delay, intellectual disability, neurologic and psychiatric symptoms in a child of consanguineous parents
Autosomal dominant intellectual disability
Gender differences in psychiatric diagnoses in older people with intellectual disability: a register study
The role of glia in epilepsy, intellectual disability, and other neurodevelopmental disorders in tuberous sclerosis complex
A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative features
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations
Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy
High Incidence of Copy Number Variants in Adults with Intellectual Disability and Co-morbid Psychiatric Disorders
Genetics of autosomal recessive intellectual disability
Intellectual disability and nutrition‐related health