Clinical phenotype of ASD-associated DYRK1A haploinsufficiency-Reference-Cited by-同舟云学术

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Clinical phenotype of ASD-associated DYRK1A haploinsufficiency

Published:2017-10-05 Issue:1 Volume:8 Page:
ISSN:2040-2392
Container-title:Molecular Autism
language:en
Short-container-title:Molecular Autism

Author:

Earl Rachel K.,Turner Tychele N.,Mefford Heather C.,Hudac Caitlin M.,Gerdts Jennifer,Eichler Evan E.,Bernier Raphael A.

Funder

National Institute of Mental Health

Publisher

Springer Science and Business Media LLC

Subject

Psychiatry and Mental health,Developmental Biology,Developmental Neuroscience,Molecular Biology

Link

http://link.springer.com/content/pdf/10.1186/s13229-017-0173-5.pdf

Reference54 articles.

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2. Lord C, Petkova E, Hus V, Gan W, Lu F, Martin DM, et al. A multisite study of the clinical diagnosis of different autism spectrum disorders. Arch Gen Psychiatry. 2012;69(3):306–13. doi: 10.1001/archgenpsychiatry.2011.148 . Epub 2011/11/09. PubMed PMID: 22065253; PubMed Central PMCID: PMCPMC3626112

3. Higdon R, Earl RK, Stanberry L, Hudac CM, Montague E, Stewart E, et al. The promise of multi-omics and clinical data integration to identify and target personalized healthcare approaches in autism spectrum disorders. Omics : a journal of integrative biology. 2015;19(4):197–208. doi: 10.1089/omi.2015.0020 . Epub 2015/04/02. PubMed PMID: 25831060; PubMed Central PMCID: PMCPMC4389910

4. Jeste SS, Geschwind DH. Disentangling the heterogeneity of autism spectrum disorder through genetic findings. Nat Rev Neurol. 2014;10(2):74–81. doi: 10.1038/nrneurol.2013.278 . Epub 2014/01/29. PubMed PMID: 24468882; PubMed Central PMCID: PMCPMC4125617

5. O'Roak BJ, Deriziotis P, Lee C, Vives L, Schwartz JJ, Girirajan S, et al. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nat Genet. 2011;43(6):585–9. doi: 10.1038/ng.835 . Epub 2011/05/17. PubMed PMID: 21572417; PubMed Central PMCID: PMCPMC3115696

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3. Visual and auditory attention in individuals with DYRK1A and SCN2A disruptive variants;Autism Research;2024-07-30

4. Shared and divergent mental health characteristics of ADNP-, CHD8- and DYRK1A-related neurodevelopmental conditions;Journal of Neurodevelopmental Disorders;2024-04-15

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