| Class III β-tubulin overexpression is a prominent mechanism of paclitaxel resistance in ovarian cancer patients S Mozzetti, C Ferlini, P Concolino, F Filippetti, G Raspaglio, S Prislei, ... Clinical Cancer Research 11 (1), 298-305, 2005 | 476 | 2005 |
| Multiple endocrine neoplasia type 1 (MEN1): an update of 208 new germline variants reported in the last nine years P Concolino, A Costella, E Capoluongo Cancer genetics 209 (1-2), 36-41, 2016 | 134 | 2016 |
| Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification MT Parsons, E Tudini, H Li, E Hahnen, B Wappenschmidt, L Feliubadaló, ... Human mutation 40 (9), 1557-1578, 2019 | 123 | 2019 |
| Congenital Adrenal Hyperplasia (CAH) due to 21-Hydroxylase Deficiency: A Comprehensive Focus on 233 Pathogenic Variants of CYP21A2 Gene P Concolino, A Costella Molecular diagnosis & therapy 22, 261-280, 2018 | 93 | 2018 |
| Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in congenital adrenal hyperplasia: first technical report P Concolino, E Mello, V Toscano, F Ameglio, C Zuppi, E Capoluongo Clinica chimica acta 402 (1-2), 164-170, 2009 | 84 | 2009 |
| Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations P Concolino, E Mello, C Zuppi, E Capoluongo Clinical chemistry and laboratory medicine 48 (8), 1057-1062, 2010 | 78 | 2010 |
| Serum levels of seven cytokines in premature ventilated newborns: correlations with old and new forms of bronchopulmonary dysplasia G Vento, E Capoluongo, P G Matassa, P Concolino, V Vendettuoli, ... Intensive care medicine 32, 723-730, 2006 | 78 | 2006 |
| Association between cutaneous melanoma, Breslow thickness and vitamin D receptor BsmI polymorphism C Santonocito, R Capizzi, P Concolino, MM Lavieri, A Paradisi, ... British Journal of Dermatology 156 (2), 277-282, 2007 | 76 | 2007 |
| Functional effect of Saffron supplementation and risk genotypes in early age-related macular degeneration: a preliminary report D Marangoni, B Falsini, M Piccardi, L Ambrosio, AM Minnella, ... Journal of translational medicine 11, 1-11, 2013 | 68 | 2013 |
| Slight association between type 1 diabetes and “ff” VDR FokI genotype in patients from the Italian Lazio Region. Lack of association with diabetes complications E Capoluongo, D Pitocco, P Concolino, C Santonocito, E Di Stasio, ... Clinical biochemistry 39 (9), 888-892, 2006 | 62 | 2006 |
| A new CYP21A1P/CYP21A2chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form P Concolino, E Mello, A Minucci, E Giardina, C Zuppi, V Toscano, ... BMC medical genetics 10, 1-7, 2009 | 56 | 2009 |
| Rapid UGT1A1 (TA) n genotyping by high resolution melting curve analysis for Gilbert's syndrome diagnosis A Minucci, P Concolino, B Giardina, C Zuppi, E Capoluongo Clinica Chimica Acta 411 (3-4), 246-249, 2010 | 49 | 2010 |
| Epithelial lining fluid free IGF-I-to-PAPP-A ratio is associated with bronchopulmonary dysplasia in preterm infants E Capoluongo, F Ameglio, P Lulli, A Minucci, C Santonocito, P Concolino, ... American Journal of Physiology-Endocrinology and Metabolism 292 (1), E308-E313, 2007 | 45 | 2007 |
| GSTM1-null polymorphism as possible risk marker for hypertension: results from the aging and longevity study in the Sirente Geographic Area (ilSIRENTE study) E Capoluongo, G Onder, P Concolino, A Russo, C Santonocito, ... Clinica Chimica Acta 399 (1-2), 92-96, 2009 | 42 | 2009 |
| Radioanatomical study of the pedicle of the superficial circumflex iliac perforator flap S Gentileschi, M Servillo, F De Bonis, R Albanese, V Pino, ... Journal of Reconstructive Microsurgery 35 (09), 669-676, 2019 | 40 | 2019 |
| A comprehensive BRCA1/2 NGS pipeline for an immediate Copy Number Variation (CNV) detection in breast and ovarian cancer molecular diagnosis P Concolino, R Rizza, F Mignone, A Costella, D Guarino, I Carboni, ... Clinica Chimica Acta 480, 173-179, 2018 | 39 | 2018 |
| Vitamin D Receptor Polymorphisms and Falls Among Older Adults Living in the Community: Results From the ilSIRENTE Study G Onder, E Capoluongo, P Danese, S Settanni, A Russo, P Concolino, ... Journal of bone and mineral research 23 (7), 1031-1036, 2008 | 38 | 2008 |
| Association of periodontitis with GSTM1/GSTT1-null variants—A pilot study P Concolino, F Cecchetti, C D'Autilia, C Santonocito, E Di Stasio, C Zuppi, ... Clinical Biochemistry 40 (13-14), 939-945, 2007 | 35 | 2007 |
| Reverse-hybridization assay for rapid detection of common CYP21A2 mutations in dried blood spots from newborns with elevated 17-OH progesterone S Németh, S Riedl, G Kriegshäuser, S Baumgartner-Parzer, P Concolino, ... Clinica Chimica Acta 414, 211-214, 2012 | 33 | 2012 |
| Advanced tools for BRCA1/2 mutational screening: comparison between two methods for large genomic rearrangements (LGRs) detection P Concolino, E Mello, A Minucci, C Santonocito, G Scambia, B Giardina, ... Clinical Chemistry and Laboratory Medicine (CCLM) 52 (8), 1119-1127, 2014 | 32 | 2014 |
