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G. Fortunato · SciRah

Researcher profile · Semantic Scholar

G. Fortunato

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G. Fortunato — researcher profile on SciRah

h-index: 29
Works: 105
Citations: 2,320

Most-cited papers

Refinement of variant selection for the LDL-C genetic risk score in the diagnosis of the polygenic form of clinical Familial Hypercholesterolemia and replication in samples from six countries
M. Futema, Sonia H. Shah, J. Cooper, Ka-Wah Li +22 more
2014Clinical Chemistry204 citations Open access
Semantic Scholar
Galectin-3 in Cardiovascular Diseases
V. Blanda, U. Bracale, M. D. Di Taranto, G. Fortunato
2020International Journal of Molecular Sciences169 citations Open access
Semantic Scholar
Paraoxonase and superoxide dismutase gene polymorphisms and noise-induced hearing loss.
G. Fortunato, E. Marciano, F. Zarrilli, C. Mazzaccara +7 more
2004Clinical Chemistry114 citations Open access
Semantic Scholar
Recent advances in the diagnosis of malignant hyperthermia susceptibility: How confident can we be of genetic testing?
R. Robinson, M. Anetseder, Virginia Brancadoro, C. van Broekhoven +17 more
2003European Journal of Human Genetics101 citations
Semantic Scholar
Familial hypercholesterolemia: A complex genetic disease with variable phenotypes.
M. D. Di Taranto, C. Giacobbe, G. Fortunato
2019European Journal of Medical Genetics73 citations
Semantic Scholar
Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study.
M. Casula, E. Olmastroni, A. Pirillo, A. Catapano +102 more
2018Atherosclerosis69 citations Open access
Semantic Scholar
Multivariate discriminant function based on six biochemical markers in blood can predict the cirrhotic evolution of chronic hepatitis.
G. Fortunato, Giuseppe Castaldo, G. Oriani, R. Cerini +7 more
2001Clinical Chemistry67 citations
Semantic Scholar
Measurement of spleen volume by ultrasound scanning in patients with thrombocytosis: a prospective study.
M. Picardi, V. Martinelli, R. Ciancia, E. Soscia +4 more
2002Blood60 citations
Semantic Scholar
A paraoxonase gene polymorphism, PON 1 (55), as an independent risk factor for increased carotid intima-media thickness in middle-aged women.
G. Fortunato, P. Rubba, S. Panico, D. Trono +7 more
2003Atherosclerosis59 citations
Semantic Scholar
Identification and functional characterization of malignant hyperthermia mutation T1354S in the outer pore of the Cavalpha1S-subunit.
A. Pirone, Johann Schredelseker, P. Tuluc, E. Gravino +5 more
2010American Journal of Physiology - Cell Physiology56 citations Open access
Semantic Scholar
Comparative Characteristics of Mesenchymal Stem Cells from Human Bone Marrow and Placenta: CD10, CD49d, and CD56 Make a Difference
E. Mariotti, P. Mirabelli, G. Abate, M. Schiattarella +4 more
2008Stem Cells and Development54 citations
Semantic Scholar
Multiple Sclerosis and Hepatitis C Virus Infection Are Associated with Single Nucleotide Polymorphisms in Interferon Pathway Genes
G. Fortunato, G. Calcagno, Vincenzo Brescia-Morra, E. Salvatore +8 more
2008Journal of Interferon and Cytokine Research54 citations
Semantic Scholar
Prevalence and long-term course of macro-aspartate aminotransferase in children.
M. Caropreso, G. Fortunato, S. Lenta, D. Palmieri +4 more
2009Jornal de Pediatria51 citations
Semantic Scholar
Decreased Paraoxonase-2 Expression in Human Carotids During the Progression of Atherosclerosis
G. Fortunato, M. D. Di Taranto, U. Bracale, L. del Guercio +9 more
2008Arteriosclerosis, Thrombosis and Vascular Biology45 citations
Semantic Scholar
Endothelial function improvement in patients with familial hypercholesterolemia receiving PCSK-9 inhibitors on top of maximally tolerated lipid lowering therapy.
A. Di Minno, M. Gentile, G. Iannuzzo, I. Calcaterra +8 more
2020Thrombosis Research42 citations
Semantic Scholar
Identification and in vitro characterization of two new PCSK9 Gain of Function variants found in patients with Familial Hypercholesterolemia
M. D. Di Taranto, A. Benito-Vicente, C. Giacobbe, K. Uribe +6 more
2017Scientific Reports42 citations Open access
Semantic Scholar
Functional characterization of ryanodine receptor (RYR1) sequence variants using a metabolic assay in immortalized B‐lymphocytes
Alberto Zullo, W. Klingler, Claudia De Sarno, Marina Ferrara +8 more
2009Human Mutation40 citations Open access
Semantic Scholar
Carotid artery remodeling in middle-aged women with the metabolic syndrome (from the "Progetto ATENA" study).
A. Iannuzzi, M. de Michele, M. Bond, L. Sacchetti +5 more
2005American Journal of Cardiology39 citations
Semantic Scholar
Genetic Heterogeneity of Familial Hypercholesterolemia: Repercussions for Molecular Diagnosis
M. D. Di Taranto, G. Fortunato
2023International Journal of Molecular Sciences38 citations Open access
Semantic Scholar
Association of USF1 and APOA5 polymorphisms with familial combined hyperlipidemia in an Italian population.
M. D. Di Taranto, A. Staiano, M. D'Agostino, Antonietta D'Angelo +6 more
2015Molecular and Cellular Probes37 citations
Semantic Scholar
A multilayer perceptron neural network-based approach for the identification of responsiveness to interferon therapy in multiple sclerosis patients
G. Calcagno, A. Staiano, G. Fortunato, Vincenzo Brescia-Morra +6 more
2010Information Sciences37 citations
Semantic Scholar
Identification and functional characterization of LDLR mutations in familial hypercholesterolemia patients from Southern Italy.
Maria Romano, M. D. Di Taranto, M. D'Agostino, G. Marotta +7 more
2010Atherosclerosis35 citations
Semantic Scholar
Homocysteine levels and sustained virological response to pegylated‐interferon α2b plus ribavirin therapy for chronic hepatitis C: a prospective study
G. Borgia, I. Gentile, G. Fortunato, F. Borrelli +9 more
2009Liver international (Print)35 citations Open access
Semantic Scholar
An improved method on stimulated T-lymphocytes to functionally characterize novel and known LDLR mutations[S]
Maria Romano, M. D. Di Taranto, P. Mirabelli, M. D'Agostino +8 more
2011Journal of Lipid Research33 citations Open access
Semantic Scholar
Rapid detection of mycoplasma in continuous cell lines using a selective biochemical test.
E. Mariotti, P. Mirabelli, R. Di Noto, G. Fortunato +1 more
2008Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis33 citations
Semantic Scholar
Causative mutations and premature cardiovascular disease in patients with heterozygous familial hypercholesterolaemia
P. Rubba, M. Gentile, G. Marotta, A. Iannuzzi +7 more
2017European Journal of Preventive Cardiology31 citations
Semantic Scholar
Altered expression of inflammation-related genes in human carotid atherosclerotic plaques.
M. D. Di Taranto, A. Morgante, U. Bracale, F. D'Armiento +4 more
2012Atherosclerosis31 citations
Semantic Scholar
Genetic spectrum of familial hypercholesterolemia and correlations with clinical expression: Implications for diagnosis improvement
M. D. Di Taranto, C. Giacobbe, D. Palma, G. Iannuzzo +6 more
2021Clinical Genetics29 citations Open access
Semantic Scholar
Prenatal diagnosis of inherited diseases: 20 years’ experience of an Italian Regional Reference Centre
G. Maruotti, G. Frisso, G. Calcagno, G. Fortunato +4 more
2013Clinical Chemistry and Laboratory Medicine29 citations
Semantic Scholar
Cardiac troponin T and amino-terminal pro-natriuretic peptide concentrations in fetuses in the second trimester and in healthy neonates
G. Fortunato, Patrizia Carandente Giarrusso, P. Martinelli, G. Sglavo +4 more
2006Clinical Chemistry and Laboratory Medicine28 citations
Semantic Scholar
Long-term efficacy of lipoprotein apheresis and lomitapide in the treatment of homozygous familial hypercholesterolemia (HoFH): a cross-national retrospective survey
L. D'Erasmo, A. Gallo, A. Cefalù, A. Di Costanzo +31 more
2021Orphanet Journal of Rare Diseases27 citations Open access
Semantic Scholar
A Real-World Experience of Clinical, Biochemical and Genetic Assessment of Patients with Homozygous Familial Hypercholesterolemia
M. D. Di Taranto, C. Giacobbe, A. Buonaiuto, I. Calcaterra +6 more
2020Journal of Clinical Medicine26 citations Open access
Semantic Scholar
Cerebrotendinous xanthomatosis, a metabolic disease with different neurological signs: two case reports
M. D. Di Taranto, M. Gelzo, C. Giacobbe, M. Gentile +5 more
2016Metabolic brain disease25 citations
Semantic Scholar
The percentage of CD133+ cells in human colorectal cancer cell lines is influenced by Mycoplasma hyorhinis infection
E. Mariotti, Marica Gemei, P. Mirabelli, F. D'Alessio +3 more
2010BMC Cancer25 citations Open access
Semantic Scholar
Changes in carotid stiffness in patients with familial hypercholesterolemia treated with Evolocumab®: A prospective cohort study.
M. D. Di Minno, M. Gentile, A. Di Minno, G. Iannuzzo +6 more
2020NMCD. Nutrition Metabolism and Cardiovascular Diseases24 citations
Semantic Scholar
The Arg499His gain-of-function mutation in the C-terminal domain of PCSK9.
R. Sánchez-Hernández, M. D. Di Taranto, A. Benito-Vicente, K. Uribe +10 more
2019Atherosclerosis23 citations Open access
Semantic Scholar
Lipid profile and genetic status in a familial hypercholesterolemia pediatric population: exploring the LDL/HDL ratio
M. D. Di Taranto, R. de Falco, O. Guardamagna, G. Massini +7 more
2019Clinical Chemistry and Laboratory Medicine21 citations
Semantic Scholar
Investigation of Single Nucleotide Polymorphisms Associated to Familial Combined Hyperlipidemia with Random Forests
A. Staiano, M. D. Di Taranto, Elena Bloise, M. D'Agostino +7 more
2012Italian Workshop on Neural Nets21 citations
Semantic Scholar
Do Selective Estrogen Receptor Modulators Treat Cervical Precancer and Cancer? Time to Pool Data from Relevant Trials
Marica Gemei, P. Mirabelli, R. di Noto, G. Fortunato +1 more
2011International Journal of Cancer21 citations Open access
Semantic Scholar
The novel variant p.Ser465Leu in the PCSK9 gene does not account for the decreased LDLR activity in members of a FH family
A. Ruótolo, M. D. Di Taranto, M. D'Agostino, G. Marotta +7 more
2014Clinical Chemistry and Laboratory Medicine20 citations
Semantic Scholar
A case of discordance between genotype and phenotype in a malignant hyperthermia family
G. Fortunato, A. Carsana, N. Tinto, V. Brancadoro +2 more
1999European Journal of Human Genetics18 citations Open access
Semantic Scholar
Genetic Typing of Corallium rubrum
D. del Gaudio, G. Fortunato, M. Borriello, J. Gili +4 more
2004Marine Biotechnology17 citations
Semantic Scholar
Polychromatic flow cytometry analysis of CD34+ hematopoietic stem cells in cryopreserved early preterm human cord blood samples
F. D'Alessio, P. Mirabelli, Marisa Gorrese, G. Scalia +7 more
2011Cytometry Part A16 citations
Semantic Scholar
Sequence Analysis of the UCP1 Gene in a Severe Obese Population from Southern Italy
G. Labruna, F. Pasanisi, G. Fortunato, C. Nardelli +4 more
2011Journal of Obesity16 citations Open access
Semantic Scholar
Polymorphisms and the expression of genes encoding enzymes involved in cardiovascular diseases.
G. Fortunato, M. D. Di Taranto
2007Clinica chimica acta; international journal of clinical chemistry16 citations
Semantic Scholar
Identification of a novel mutation in the ryanodine receptor gene (RYR1) in a malignant hyperthermia Italian family
G. Fortunato, Renata Berruti, V. Brancadoro, M. Fattore +2 more
2000European Journal of Human Genetics16 citations
Semantic Scholar
Allele frequency distributions at several variable number of tandem repeat (VNTR) and short tandem repeat (STR) loci in a restricted Caucasian population from south Italy and their evaluation for paternity and forensic use.
L. Pastore, Emilia Vuttariello, C. Sarrantonio, I. Coto +4 more
1996Molecular and Cellular Probes14 citations
Semantic Scholar
Association between causative mutations and response to PCSK9 inhibitor therapy in subjects with familial hypercholesterolemia: A single center real-world study.
G. Iannuzzo, A. Buonaiuto, I. Calcaterra, M. Gentile +7 more
2021NMCD. Nutrition Metabolism and Cardiovascular Diseases13 citations
Semantic Scholar
Targeting Nanostrategies for Imaging of Atherosclerosis
Angela Costagliola di Polidoro, Agnese Grassia, Francesca De Sarno, P. Bevilacqua +8 more
2021Contrast Media & Molecular Imaging13 citations Open access
Semantic Scholar
B-Type Natriuretic Peptides and High-Sensitive Troponin I as COVID-19 Survival Factors: Which One Is the Best Performer?
R. de Falco, M. Vargas, D. Palma, Marcella Savoia +6 more
2021Journal of Clinical Medicine13 citations Open access
Semantic Scholar

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