Adrianos Skaros
Overview
Explore the profile of Adrianos Skaros including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
3
Citations
57
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Mihailovich M, Germain P, Shyti R, Pozzi D, Noberini R, Liu Y, et al.
J Clin Invest
. 2024 Jul;
134(14).
PMID: 39007270
Copy number variation (CNV) at 7q11.23 causes Williams-Beuren syndrome (WBS) and 7q microduplication syndrome (7Dup), neurodevelopmental disorders (NDDs) featuring intellectual disability accompanied by symmetrically opposite neurocognitive features. Although significant progress...
2.
Lopez-Tobon A, Shyti R, Villa C, Cheroni C, Fuentes-Bravo P, Trattaro S, et al.
Sci Adv
. 2023 Nov;
9(48):eadh2726.
PMID: 38019906
Copy number variations at 7q11.23 cause neurodevelopmental disorders with shared and opposite manifestations. Deletion causes Williams-Beuren syndrome featuring hypersociability, while duplication causes 7q11.23 microduplication syndrome (7Dup), frequently exhibiting autism spectrum...
3.
Zanella M, Vitriolo A, Andirko A, Martins P, Sturm S, ORourke T, et al.
Sci Adv
. 2019 Dec;
5(12):eaaw7908.
PMID: 31840056
We undertook a functional dissection of chromatin remodeler BAZ1B in neural crest (NC) stem cells (NCSCs) from a uniquely informative cohort of typical and atypical patients harboring 7q11.23 copy number...