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D. Loconte · SciRah

Researcher profile · Semantic Scholar

D. Loconte

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D. Loconte — researcher profile on SciRah

h-index: 9
Works: 23
Citations: 543

Most-cited papers

Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.
N. Resta, D. Pierannunzio, G. M. Lenato, A. Stella +26 more
2013Digestive and Liver Disease157 citations Open access
Semantic Scholar
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS)
C. Ranieri, S. Di Tommaso, D. Loconte, V. Grossi +17 more
2018Neurogenetics84 citations Open access
Semantic Scholar
Molecular and Functional Characterization of Three Different Postzygotic Mutations in PIK3CA-Related Overgrowth Spectrum (PROS) Patients: Effects on PI3K/AKT/mTOR Signaling and Sensitivity to PIK3 Inhibitors
D. Loconte, V. Grossi, C. Bozzao, G. Forte +14 more
2015PLoS ONE77 citations Open access
Semantic Scholar
The longevity SNP rs2802292 uncovered: HSF1 activates stress-dependent expression of FOXO3 through an intronic enhancer
V. Grossi, G. Forte, P. Sanese, A. Peserico +9 more
2018Nucleic Acids Research67 citations Open access
Semantic Scholar
Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants
A. Mussa, C. Leoni, M. Iacoviello, D. Carli +36 more
2022Journal of Medical Genetics37 citations Open access
Semantic Scholar
Loss of STK11 expression is an early event in prostate carcinogenesis and predicts therapeutic response to targeted therapy against MAPK/p38
V. Grossi, G. Lucarelli, G. Forte, A. Peserico +16 more
2015Autophagy35 citations Open access
Semantic Scholar
Accurate Classification of NF1 Gene Variants in 84 Italian Patients with Neurofibromatosis Type 1
A. Stella, P. Lastella, D. Loconte, N. Bukvic +7 more
2018Genes26 citations Open access
Semantic Scholar
Stat3-positive tumor cells contribute to vessels neoformation in primary central nervous system lymphoma
Simona Ruggieri, R. Tamma, N. Resta, F. Albano +9 more
2017OncoTarget14 citations Open access
Semantic Scholar
Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes
G. Forte, V. Grossi, V. Celestini, G. Lucisano +12 more
2014BMC Cancer14 citations Open access
Semantic Scholar
A rare MSH2 mutation causes defective binding to hMSH6, normal hMSH2 staining, and loss of hMSH6 at advanced cancer stage.
D. Loconte, M. Patruno, P. Lastella, C. di Gregorio +8 more
2014Human Pathology9 citations
Semantic Scholar
Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers
Antonella Turchiano, D. Loconte, R. De Nola, F. Arezzo +16 more
2022Cancers8 citations Open access
Semantic Scholar
A prospective multicentric study of risk-reducing salpingo-oophorectomy in BRCA mutation patients
Vera Loizzi, E. Cicinelli, V. Del Vecchio, F. Arezzo +9 more
2021Acta bio-medica : Atenei Parmensis5 citations
Semantic Scholar
Prenatal overgrowth and polydramnios: Would you think about Noonan syndrome?
B. Beltrami, Jacopo Cerasani, A. Consales, R. Villa +8 more
2022Clinical Case Reports3 citations Open access
Semantic Scholar
Gait disturbance and lower limb pain in a patient with PIK3CA-related disorder.
G. Cappuccio, M. Alagia, M. D'Anna, C. Ranieri +11 more
2017European Journal of Medical Genetics3 citations
Semantic Scholar
401 Loss of LKB1/STK11 expression is an early event in prostate cancer development and predicts therapeutic response to p38α inhibitor
V. Grossi, G. Lucarelli, A. Matrone, G. Forte +14 more
20152 citations
Semantic Scholar
Functional evidence of mTORβ splice variant involvement in the pathogenesis of congenital heart defects
M. Gentile, C. Ranieri, D. Loconte, Emanuela Ponzi +11 more
2020Clinical Genetics1 citations
Semantic Scholar
Vitrificazione dell'ovocita equino: esperienze preliminari
T. Nervo, C. Semita, R. Cota, D. Loconte
20061 citations
Semantic Scholar
A new era for transplant-ineligible R/R LBCL patients: what’s changing?
G. Tarantini, R. Miccolis, E. Arcuti, C. Buquicchio +13 more
2026Leukemia and Lymphoma0 citations Open access
Semantic Scholar
A focus on LBCL patients in partial remission in the CAR-T era
G. Tarantini, E. Arcuti, C. Buquicchio, Vera Carluccio +9 more
2025Frontiers in Hematology0 citations Open access
Semantic Scholar
Author response for "Functional evidence of mTORβ splice variant involvement in the pathogenesis of congenital heart defects"
M. Gentile, C. Ranieri, D. Loconte, Emanuela Ponzi +11 more
20200 citations Open access
Semantic Scholar
Author response for "Functional evidence of mTORβ splice variant involvement in the pathogenesis of congenital heart defects"
M. Gentile, C. Ranieri, D. Loconte, Emanuela Ponzi +11 more
20200 citations Open access
Semantic Scholar
Characterization of the rs2802292 SNP identifies FOXO3Aas a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes
G. Forte, V. Grossi, V. Celestini, G. Lucisano +12 more
2014BMC Cancer0 citations Open access
Semantic Scholar
Vitrification of equine oocyte: first trials.
T. Nervo, Carlo Semita, R. Cota, D. Loconte
20070 citations
Semantic Scholar

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