Giulia Maneri
Overview
Explore the profile of Giulia Maneri including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
7
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0
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Recent Articles
1.
Beyond the BRCA1/2 genes in ovarian cancer: the role of germline pathogenic variants in the ATM gene
Guadagnolo D, Minucci A, Chiavassa A, Gentile G, Salvatori F, Khaleghi Hashemian N, et al.
Mol Biol Rep
. 2025 Feb;
52(1):261.
PMID: 39984762
Background: Ovarian Cancer (OC) prevention and early-stage detection represents a challenge due to the lack of effective surveillance. The identification of high-risk women is crucial as it provides access to...
2.
Ricciardi Tenore C, Tulli E, Calo C, Bertozzi R, Evangelista J, Maneri G, et al.
Genes (Basel)
. 2024 Oct;
15(10).
PMID: 39457422
Glucose 6 phosphate dehydrogenase ( is a rate-limiting enzyme of the pentose phosphate pathway. The loss of activity in red blood cells increases the risk of acute haemolytic anaemia under...
3.
Maneri G, Nero C, Giaco L, Scambia G, Minucci A
JNCI Cancer Spectr
. 2024 Oct;
8(5).
PMID: 39363506
The majority of tumor comprehensive genomic profiling (CGP) currently does not include a matched normal control. The use of a tumor-only CGP approach needs the development of a strategy to...
4.
De Paolis E, Tilocca B, Inchingolo R, Lombardi C, Perrucci A, Maneri G, et al.
Mol Biol Rep
. 2024 Jul;
51(1):849.
PMID: 39052151
Background: CFTR-related disorder (CFTR-RD) is a clinical entity associated to complex diagnostic paths and newly upgraded standard of care. In CFTR-RD, CFTR genotyping represents a diagnostic surrogate marker. In case...
5.
Concolino P, De Paolis E, Rinelli M, Maneri G, Brisighelli F, Trozzi R, et al.
Ann Lab Med
. 2024 Jun;
44(6):617-620.
PMID: 38826062
No abstract available.
6.
Reversion to Normal of Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families
Tabolacci E, Pietrobono R, Maneri G, Remondini L, Nobile V, Monica M, et al.
Genes (Basel)
. 2020 Mar;
11(3).
PMID: 32111011
Fragile X syndrome (FXS) is mostly due to the expansion and subsequent methylation of a polymorphic CGG repeat in the 5' UTR of the gene. Full mutation alleles (FM) have...