Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2040-2392
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder ; volume:12 ; number:1 ; day:6 ; month:10 ; year:2021 ; pages:1-12 ; date:12.2021
Molecular autism ; 12, Heft 1 (6.10.2021), 1-12, 12.2021
- Creator
-
Mahjani, Behrang
De Rubeis, Silvia
Gustavsson Mahjani, Christina
Mulhern, Maureen
Xu, Xinyi
Klei, Lambertus
Satterstrom, F. Kyle
Fu, Jack
Talkowski, Michael E.
Reichenberg, Abraham
Sandin, Sven
Hultman, Christina M.
Grice, Dorothy E.
Roeder, Kathryn
Devlin, Bernie
Buxbaum, Joseph D.
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13229-021-00465-3
- URN
-
urn:nbn:de:101:1-2021122320291325883452
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:34 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Mahjani, Behrang
- De Rubeis, Silvia
- Gustavsson Mahjani, Christina
- Mulhern, Maureen
- Xu, Xinyi
- Klei, Lambertus
- Satterstrom, F. Kyle
- Fu, Jack
- Talkowski, Michael E.
- Reichenberg, Abraham
- Sandin, Sven
- Hultman, Christina M.
- Grice, Dorothy E.
- Roeder, Kathryn
- Devlin, Bernie
- Buxbaum, Joseph D.
- SpringerLink (Online service)
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Phenotypic effects of genetic variants associated with autism
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Neuronal Systems Potentially Involved in Autism Spectrum Disorder
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Phenotypic and ancestry-related assortative mating in autism
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Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder
THBD sequence variants potentially related to recurrent pregnancy loss
Estimated prevalence of potentially damaging variants in the leptin gene
Phenotypic effects of genetic variants associated with autism
Dystrophin genetic variants and autism
Genetic correlates of phenotypic heterogeneity in autism
Phenotypic overlap between atopic dermatitis and autism
Neuronal Systems Potentially Involved in Autism Spectrum Disorder
The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8
Phenotypic and ancestry-related assortative mating in autism
Statistical significance and its critics: practicing damaging science, or damaging scientific practice?
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder