- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource, 1 online resource.
- Language
-
Englisch
- Bibliographic citation
-
Phenotypic effects of genetic variants associated with autism ; volume:29 ; number:7 ; day:26 ; month:6 ; year:2023 ; pages:1671-1680 ; date:7.2023
Nature medicine ; 29, Heft 7 (26.6.2023), 1671-1680, 7.2023
- Creator
-
Rolland, Thomas
Cliquet, Freddy
Anney, Richard
Moreau, Clara
Traut, Nicolas
Mathieu, Alexandre
Huguet, Guillaume
Duan, Jinjie
Warrier, Varun
Portalier, Swan
Dry, Louise
Leblond, Claire S.
Douard, Elise
Amsellem, Frédérique
Malesys, Simon
Maruani, Anna
Toro, Roberto
Børglum, Anders
Grove, Jakob
Baron-Cohen, Simon
Packer, Alan
Chung, Wendy K.
Jacquemont, Sébastien
Delorme, Richard
Bourgeron, Thomas
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41591-023-02408-2
- URN
-
urn:nbn:de:101:1-2023102413015149416394
- 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
- Rolland, Thomas
- Cliquet, Freddy
- Anney, Richard
- Moreau, Clara
- Traut, Nicolas
- Mathieu, Alexandre
- Huguet, Guillaume
- Duan, Jinjie
- Warrier, Varun
- Portalier, Swan
- Dry, Louise
- Leblond, Claire S.
- Douard, Elise
- Amsellem, Frédérique
- Malesys, Simon
- Maruani, Anna
- Toro, Roberto
- Børglum, Anders
- Grove, Jakob
- Baron-Cohen, Simon
- Packer, Alan
- Chung, Wendy K.
- Jacquemont, Sébastien
- Delorme, Richard
- Bourgeron, Thomas
- SpringerLink (Online service)
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Association between rare, genetic variants linked to autism and ultrasonography fetal anomalies in children with autism spectrum disorder
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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
Dystrophin genetic variants and autism
Genetic correlates of phenotypic heterogeneity in autism
The Autism Simplex Collection : an international, expertly phenotyped autism sample for genetic and phenotypic analyses
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder
Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1
Phenotypic overlap between atopic dermatitis and autism
Genetic variants associated mRNA stability in lung
Association between rare, genetic variants linked to autism and ultrasonography fetal anomalies in children with autism spectrum disorder
Both rare and common genetic variants contribute to autism in the Faroe Islands
Common genetic variants, acting additively, are a major source of risk for autism
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
Dystrophin genetic variants and autism
Genetic correlates of phenotypic heterogeneity in autism
The Autism Simplex Collection : an international, expertly phenotyped autism sample for genetic and phenotypic analyses
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder
Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1
Phenotypic overlap between atopic dermatitis and autism
Genetic variants associated mRNA stability in lung
Association between rare, genetic variants linked to autism and ultrasonography fetal anomalies in children with autism spectrum disorder
Both rare and common genetic variants contribute to autism in the Faroe Islands
Common genetic variants, acting additively, are a major source of risk for autism
The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8