Gabriella Doddato
Overview
Explore the profile of Gabriella Doddato including associated specialties, affiliations and a list of published articles.
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21
Citations
337
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Recent Articles
11.
Privitera F, Calonaci A, Doddato G, Papa F, Baldassarri M, Pinto A, et al.
Genes (Basel)
. 2021 Sep;
12(9).
PMID: 34573300
Retinoblastoma (RB) is an ocular tumor of the pediatric age caused by biallelic inactivation of the gene (13q14). About 10% of cases are due to gross-sized molecular deletions. The deletions...
12.
Doddato G, Valentino F, Giliberti A, Papa F, Tita R, Bruno L, et al.
Front Oncol
. 2021 Sep;
11:740860.
PMID: 34485163
[This corrects the article DOI: 10.3389/fonc.2021.649435.].
13.
Valentino F, Bruno L, Doddato G, Giliberti A, Tita R, Resciniti S, et al.
Brain Sci
. 2021 Aug;
11(7).
PMID: 34356170
Intellectual disability (ID) and autism spectrum disorder (ASD) belong to neurodevelopmental disorders and occur in ~1% of the general population. Due to disease heterogeneity, identifying the etiology of ID and...
14.
Baldassarri M, Fava F, Fallerini C, Daga S, Benetti E, Zguro K, et al.
J Pers Med
. 2021 Jul;
11(6).
PMID: 34203982
The clinical presentation of COVID-19 is extremely heterogeneous, ranging from asymptomatic to severely ill patients. Thus, host genetic factors may be involved in determining disease presentation and progression. Given that...
15.
Doddato G, Valentino F, Giliberti A, Papa F, Tita R, Bruno L, et al.
Front Oncol
. 2021 May;
11:649435.
PMID: 34026625
Hereditary Breast and Ovarian Cancer (HBOC) syndrome is a condition in which the risk of breast and ovarian cancer is higher than in the general population. The prevalent pathogenesis is...
16.
Baldassarri M, Picchiotti N, Fava F, Fallerini C, Benetti E, Daga S, et al.
EBioMedicine
. 2021 Mar;
65:103246.
PMID: 33647767
Background: While SARS-CoV-2 similarly infects men and women, COVID-19 outcome is less favorable in men. Variability in COVID-19 severity may be explained by differences in the host genome. Methods: We...
17.
Lopergolo D, Bocci S, Pinto A, Valentino F, Doddato G, Ginanneschi F, et al.
Neurol Sci
. 2021 Jan;
42(6):2509-2513.
PMID: 33459893
The Charcot-Marie-Tooth (CMT) disease is the most common inherited peripheral neuropathy with great clinical and genetic heterogeneity. Mutations in DNM2 have been associated with CMT dominant intermediate B (CMTDIB). However,...
18.
Daga S, Fallerini C, Baldassarri M, Fava F, Valentino F, Doddato G, et al.
Eur J Hum Genet
. 2021 Jan;
29(5):745-759.
PMID: 33456056
Within the GEN-COVID Multicenter Study, biospecimens from more than 1000 SARS-CoV-2 positive individuals have thus far been collected in the GEN-COVID Biobank (GCB). Sample types include whole blood, plasma, serum,...
19.
Curro A, Doddato G, Bruttini M, Zollino M, Marangi G, Zappella M, et al.
Eur J Med Genet
. 2020 Nov;
64(1):104102.
PMID: 33220470
Genetic conditions comprise a wide spectrum of different phenotypes, rapidly expanding due to new diagnostic methodologies. Patients' facial features and clinical history represent the key elements leading clinicians to the...
20.
Palmieri M, Di Sarno L, Tommasi A, Curro A, Doddato G, Baldassarri M, et al.
J Vasc Surg Venous Lymphat Disord
. 2020 Aug;
9(3):740-744.
PMID: 32858245
Objective: Germline mutations of either the endothelial cell-specific tyrosine kinase receptor TIE2 or the glomulin (GLMN) gene are responsible for rare inherited venous malformations. Both genes affect the hepatocyte growth...