[HTML][HTML] De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell�…

S Chen, J Wang, E Cicek, K Roeder, H Yu, B Devlin�- Molecular autism, 2020 - Springer
Background Whole-exome sequencing studies have been useful for identifying genes that,
when mutated, affect risk for autism spectrum disorder (ASD). Nonetheless, the association�…

De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types

S Chen, J Wang, E Cicek, K Roeder…�- Molecular�…, 2020 - pubmed.ncbi.nlm.nih.gov
Background Whole-exome sequencing studies have been useful for identifying genes that,
when mutated, affect risk for autism spectrum disorder (ASD). Nonetheless, the association�…

[HTML][HTML] De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell�…

S Chen, J Wang, E Cicek…�- Molecular�…, 2020 - molecularautism.biomedcentral.com
Whole-exome sequencing studies have been useful for identifying genes that, when
mutated, affect risk for autism spectrum disorder (ASD). Nonetheless, the association signal�…

[PDF][PDF] De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types

S Chen, J Wang, E Cicek, K Roeder, H Yu, B Devlin - 2020 - yulab.org
Background: Whole-exome sequencing studies have been useful for identifying genes that,
when mutated, affect risk for autism spectrum disorder (ASD). Nonetheless, the association�…

De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types.

S Chen, J Wang, E Cicek, K Roeder, H Yu…�- Molecular�…, 2020 - search.ebscohost.com
Background: Whole-exome sequencing studies have been useful for identifying genes that,
when mutated, affect risk for autism spectrum disorder (ASD). Nonetheless, the association�…

De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types.

S Chen, J Wang, E Cicek, K Roeder, H Yu…�- Molecular�…, 2020 - europepmc.org
Background Whole-exome sequencing studies have been useful for identifying genes that,
when mutated, affect risk for autism spectrum disorder (ASD). Nonetheless, the association�…

[HTML][HTML] De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell�…

S Chen, J Wang, E Cicek, K Roeder, H Yu…�- Molecular�…, 2020 - ncbi.nlm.nih.gov
Background Whole-exome sequencing studies have been useful for identifying genes that,
when mutated, affect risk for autism spectrum disorder (ASD). Nonetheless, the association�…

[PDF][PDF] De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types

S Chen, J Wang, E Cicek, K Roeder, H Yu, B Devlin - 2020 - repository.bilkent.edu.tr
Background: Whole-exome sequencing studies have been useful for identifying genes that,
when mutated, affect risk for autism spectrum disorder (ASD). Nonetheless, the association�…

De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types

S Chen, J Wang, E Cicek, K Roeder, H Yu…�- Molecular�…, 2020 - search.proquest.com
Background Whole-exome sequencing studies have been useful for identifying genes that,
when mutated, affect risk for autism spectrum disorder (ASD). Nonetheless, the association�…

De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types

S Chen, J Wang, E Cicek, K Roeder, H Yu, B Devlin�- Molecular Autism, 2020 - cir.nii.ac.jp
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Whole-exome sequencing studies have been useful for identifying genes that, when�…