Gabriella Doddato
Overview
Explore the profile of Gabriella Doddato 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
21
Citations
337
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.
Nunziata A, Antropoli A, Bianco L, Del Fabbro S, Arrigo A, Doddato G, et al.
Ophthalmic Genet
. 2025 Feb;
:1-4.
PMID: 39967245
Background: Pathogenic variants in the gene are linked to a spectrum of ciliopathies, which can present with ophthalmic symptoms. In this study, we describe the multimodal imaging findings of a...
2.
Doddato G, Fabbiani A, Fallerini C, Bruttini M, Hadjistilianou T, Landi M, et al.
Front Genet
. 2023 Feb;
14:1143795.
PMID: 36761000
[This corrects the article DOI: 10.3389/fgene.2021.761264.].
3.
Bruno L, Doddato G, Baldassarri M, Lo Rizzo C, Resciniti S, Bruttini M, et al.
Am J Med Genet A
. 2022 Oct;
191(1):284-288.
PMID: 36210549
No abstract available.
4.
Privitera F, Trusso M, Valentino F, Doddato G, Fallerini C, Brunelli G, et al.
Braz J Psychiatry
. 2022 Jul;
45(1):11-19.
PMID: 35881528
Objective: Bipolar disorder is a heritable chronic mental disorder that causes psychosocial impairment through depressive/manic episodes. Familial transmission of bipolar disorder does not follow simple Mendelian patterns of inheritance. The...
5.
Loberti L, Bruno L, Granata S, Doddato G, Resciniti S, Fava F, et al.
Hum Mol Genet
. 2022 Jul;
31(24):4131-4142.
PMID: 35861666
KBG syndrome (KBGS) is characterized by distinctive facial gestalt, short stature and variable clinical findings. With ageing, some features become more recognizable, allowing a differential diagnosis. We aimed to better...
6.
Doddato G, Fabbiani A, Scandurra V, Canitano R, Mencarelli M, Renieri A, et al.
Genes (Basel)
. 2022 Apr;
13(4).
PMID: 35456494
Genetic defects in the SHANK2 gene, encoding for synaptic scaffolding protein, are associated with a variety of neurodevelopmental conditions, including autism spectrum disorders and mild to moderate intellectual disability. Until...
7.
Bruno L, Doddato G, Valentino F, Baldassarri M, Tita R, Fallerini C, et al.
Int J Mol Sci
. 2021 Dec;
22(24).
PMID: 34948243
Intellectual disability (ID) is characterized by impairments in the cognitive processes and in the tasks of daily life. It encompasses a clinically and genetically heterogeneous group of neurodevelopmental disorders often...
8.
Doddato G, Fabbiani A, Fallerini C, Bruttini M, Hadjistilianou T, Landi M, et al.
Front Genet
. 2021 Dec;
12:761264.
PMID: 34925453
Spondyloocular syndrome (SOS) is a skeletal disorder caused by pathogenic variants in gene encoding a xylotransferase involved in the biosynthesis of proteoglycans. This condition, with autosomal recessive inheritance, has a...
9.
Bruno L, Fava F, Baldassarri M, Salvati V, Scandurra V, Canitano R, et al.
J Autism Dev Disord
. 2021 Oct;
52(10):4605-4607.
PMID: 34709531
No abstract available.
10.
Palmieri M, Curro A, Tommasi A, Di Sarno L, Doddato G, Baldassarri M, et al.
JVS Vasc Sci
. 2021 Oct;
1:176-180.
PMID: 34617046
Objective: Somatic mosaicism of gene is currently recognized as the only established molecular basis of arteriovenous malformations (AVM). However, given the limitations of the current technologies, somatic mutations are detected...