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Paola Concolino

Class III beta-tubulin overexpression is a prominent mechanism of paclitaxel resistance in ovarian cancer patients.
2005 · Simona Mozzetti, Cristiano Ferlini, et al. · PubMed · 323
Class III β-Tubulin Overexpression Is a Prominent Mechanism of Paclitaxel Resistance in Ovarian Cancer Patients
2005 · Simona Mozzetti, Cristiano Ferlini, et al. · Clinical Cancer Research · 303
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Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
2019 · Michael T. Parsons, Emma Tudini, et al. · Human Mutation · 145
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Functional effect of Saffron supplementation and risk genotypes in early age-related macular degeneration: a preliminary report
2013 · Dario Marangoni, Benedetto Falsini, et al. · Journal of Translational Medicine · 71
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Association between cutaneous melanoma, Breslow thickness and vitamin D receptor BsmI polymorphism
2006 · C. Santonocito, R. Capizzi, et al. · British Journal of Dermatology · 71
Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in Congenital Adrenal Hyperplasia: First technical report
2009 · Paola Concolino, Enrica Mello, et al. · Clinica Chimica Acta · 64
Serum levels of seven cytokines in premature ventilated newborns: correlations with old and new forms of bronchopulmonary dysplasia
2006 · Giovanni Vento, Ettore Capoluongo, et al. · Intensive Care Medicine · 62
Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations
2010 · Paola Concolino, Enrica Mello, et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 48
A new CYP21A1P/CYP21A2chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form
2009 · Paola Concolino, Enrica Mello, et al. · BMC Medical Genetics · 47
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BRCA Mutation Status in Triple-Negative Breast Cancer Patients Treated with Neoadjuvant Chemotherapy: A Pivotal Role for Treatment Decision-Making
2022 · Francesco Pavese, Ettore Domenico Capoluongo, et al. · Cancers · 44
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GSTM1-null polymorphism as possible risk marker for hypertension: Results from the aging and longevity study in the Sirente Geographic Area (ilSIRENTE study)
2008 · Ettore Capoluongo, Graziano Onder, et al. · Clinica Chimica Acta · 42
Slight association between type 1 diabetes and “ff” VDR FokI genotype in patients from the Italian Lazio Region. Lack of association with diabetes complications
2006 · E. Capoluongo, D. Pitocco, et al. · Clinical Biochemistry · 41
Vitamin D Receptor Polymorphisms and Falls Among Older Adults Living in the Community: Results From the ilSIRENTE Study
2008 · Graziano Onder, Ettore Capoluongo, et al. · Journal of Bone and Mineral Research · 38
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Rapid UGT1A1 (TA)n genotyping by high resolution melting curve analysis for Gilbert's syndrome diagnosis
2009 · Angelo Minucci, Paola Concolino, et al. · Clinica Chimica Acta · 33
Identification of RFLP G6PD mutations by using microcapillary electrophoretic chips (ExperionTM)
2008 · Angelo Minucci, Elisabetta Delibato, et al. · Journal of Separation Science · 30
Mutational Landscape of Resistance to Thyroid Hormone Beta (RTHβ)
2019 · Paola Concolino, Alessandra Costella, et al. · Molecular Diagnosis & Therapy · 29
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study
2007 · Ettore Capoluongo, Giovanni Vento, et al. · Intensive Care Medicine · 27
Epithelial lining fluid free IGF-I-to-PAPP-A ratio is associated with bronchopulmonary dysplasia in preterm infants
2006 · Ettore Capoluongo, Franco Ameglio, et al. · American Journal of Physiology-Endocrinology and Metabolism · 27
Association of periodontitis with GSTM1/GSTT1-null variants—A pilot study
2007 · Paola Concolino, Francesco Cecchetti, et al. · Clinical Biochemistry · 25
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100B, LDH, NSE biochemical markers
2005 · Concetta Santonocito, Paola Concolino, et al. · Clinica Chimica Acta · 25
Glucose-6-phosphate dehydrogenase Buenos Aires: A novel de novo missense mutation associated with severe enzyme deficiency
2007 · Angelo Minucci, Paola Concolino, et al. · Clinical Biochemistry · 23
Insight into a Novel p53 Single Point Mutation (G389E) by Molecular Dynamics Simulations
2010 · Davide Pirolli, Cristiana Carelli Alinovi, et al. · International Journal of Molecular Sciences · 22
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Genes, pseudogenes and like genes: The case of 21-hydroxylase in Italian population
2013 · Paola Concolino, Enrica Mello, et al. · Clinica Chimica Acta · 21
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Multiplex Ligation-Dependent Probe Amplification Analysis Is Useful for Diagnosing Congenital Adrenal Hyperplasia but Requires a Deep Knowledge of CYP21A2 Genetics
2011 · Paola Concolino, Enrica Mello, et al. · Clinical Chemistry · 21
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Reverse-hybridization assay for rapid detection of common CYP21A2 mutations in dried blood spots from newborns with elevated 17-OH progesterone
2012 · Stefan Németh, Stefan Riedl, et al. · Clinica Chimica Acta · 20
Works count: 82
Citation count: 1,981
H-index: 22
I10-index: 41
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