| Involvement of PTEN mutations in the genetic pathways of colorectal cancerogenesis G Guanti, N Resta, C Simone, F Cariola, I Demma, P Fiorente, M Gentile Human molecular genetics 9 (2), 283-287, 2000 | 164 | 2000 |
| PD-L1 expression in colorectal cancer defines three subsets of tumor immune microenvironments AM Valentini, F Di Pinto, F Cariola, V Guerra, G Giannelli, ML Caruso, ... Oncotarget 9 (9), 8584, 2018 | 81 | 2018 |
| Identification of two new mutations in TRPS 1 gene leading to the tricho‐rhino‐phalangeal syndrome type I and III M Piccione, M Niceta, V Antona, A Di Fiore, F Cariola, M Gentile, ... American Journal of Medical Genetics Part A 149 (8), 1837-1841, 2009 | 40 | 2009 |
| Low presence of p53 abnormalities in H. pylori-infected gastric mucosa and in gastric adenocarcinoma P Berloco, F Russo, F Cariola, M Gentile, P Giorgio, ML Caruso, ... Journal of gastroenterology 38, 28-36, 2003 | 37 | 2003 |
| Lapine rotaviruses of the genotype P [22] are widespread in Italian rabbitries V Martella, M Ciarlet, A Lavazza, A Camarda, E Lorusso, V Terio, D Ricci, ... Veterinary microbiology 111 (1-2), 117-124, 2005 | 35 | 2005 |
| Oestrogen receptors and microsatellite instability in colorectal carcinoma patients M Notarnicola, R Gristina, C Messa, F Cariola, P Fiorente, ML Caruso, ... Cancer letters 168 (1), 65-70, 2001 | 33 | 2001 |
| Molecular and cytogenetic characterization of an azoospermic male with a de-novo Y; 14 translocation and alternate centromere inactivation AL Buonadonna, F Cariola, E Caroppo, AD Carlo, P Fiorente, ... Human Reproduction 17 (3), 564-569, 2002 | 31 | 2002 |
| Adipokine profile in celiac patients: differences in comparison with patients suffering from diarrhea-predominant IBS and healthy subjects F Russo, G Chimienti, C Clemente, B D’Attoma, M Linsalata, A Orlando, ... Scandinavian Journal of Gastroenterology 48 (12), 1377-1385, 2013 | 30 | 2013 |
| Holt–Oram syndrome associated with anomalies of the feet L Garavelli, D De Brasi, R Verri, E Guareschi, F Cariola, D Melis, ... American journal of medical genetics Part A 146 (9), 1185-1189, 2008 | 29 | 2008 |
| Missense mutation in exon 7 of TRPS1 gene in an Italian family with a mild form of trichorhinophalangeal syndrome type I A Rossi, V Devirgiliis, V Panasiti, RG Borroni, M Carlesimo, M Gentile, ... British Journal of Dermatology 157 (5), 1021-1024, 2007 | 27 | 2007 |
| Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46, XX, r (13)(p11q14)/46, XX, der (13) t (13; 13)(q10; q14) M Gentile, AL Buonadonna, F Cariola, P Fiorente, MC Valenzano, ... Journal of medical genetics 36 (1), 77-82, 1999 | 21 | 1999 |
| Serotonin gene polymorphisms and lifetime mood disorders in predicting interferon-induced depression in chronic hepatitis C R Cozzolongo, P Porcelli, F Cariola, V Giannuzzi, E Lanzilotta, M Gentile, ... Journal of affective disorders 183, 90-97, 2015 | 18 | 2015 |
| A novel mutation in exon 7 in a family with mild tricho–rhino–phalangeal syndrome type I. M Gentile, P Fiorente, AL Buonadonna, F Macina, F Cariola Clinical genetics 63 (2), 2003 | 17 | 2003 |
| Nine novel APC mutations in Italian FAP patients N Resta, A Stella, F Susca, M Montera, M Gentile, F Cariola, F Prete, ... Human mutation 17 (5), 434-435, 2001 | 17 | 2001 |
| Genetic associations of alexithymia in predicting interferon-induced depression in chronic hepatitis C P Porcelli, R Cozzolongo, F Cariola, V Giannuzzi, E Lanzilotta, M Gentile, ... Psychopathology 48 (6), 417-420, 2015 | 15 | 2015 |
| FISH approach to determine cat eye syndrome chromosome breakpoints of a patient with cat eye syndrome type II M Gentile, S De Sanctis, F Cariola, T Spezzi, A Di Carlo, F Tontoli, F Lista, ... European journal of medical genetics 48 (1), 33-39, 2005 | 15 | 2005 |
| Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with APC mutation at the extreme 3′-end V Disciglio, C Fasano, F Cariola, G Forte, V Grossi, P Sanese, ... Journal of Medical Genetics 57 (5), 356-360, 2020 | 14 | 2020 |
| Prenatal diagnosis of chromosome 4 mosaicism: prognostic role of cytogenetic, molecular, and ultrasound/MRI characterization M Gentile, P Volpe, F Cariola, AD Carlo, V Marotta, AL Buonadonna, ... American Journal of Medical Genetics Part A 136 (1), 66-70, 2005 | 13 | 2005 |
| Clinical, cytogenetic, and molecular characterization of a patient with a de novo interstitial 22q12 duplication M Gentile, W Wuyts, S Grittani, A Di Carlo, F Cariola, P Verdyck, L Margari, ... American Journal of Medical Genetics Part A 127 (2), 186-190, 2004 | 9 | 2004 |
| Characterization of a rare variant (c.2635-2A>G) of the MSH2 gene in a family with Lynch syndrome F Cariola, V Disciglio, AM Valentini, C Lotesoriere, C Fasano, G Forte, ... The International journal of biological markers 33 (4), 534-539, 2018 | 7 | 2018 |
