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Filomena Cariola

Observed names: Cariola, F., F CARIOLA, F Cariola, F. Cariola
OpenAlex ID: A5024437133
Prenatal diagnosis of chromosome 4 mosaicism: Prognostic role of cytogenetic, molecular, and ultrasound/MRI characterization
2005 · Mattia Gentile, Paolo Volpe, et al. · American Journal of Medical Genetics Part A · 83
PD-L1 expression in colorectal cancer defines three subsets of tumor immune microenvironments
2018 · Anna Maria Valentini, Federica Di Pinto, et al. · Oncotarget · 77
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Lapine rotaviruses of the genotype P[22] are widespread in Italian rabbitries
2005 · V. Martella, M. Ciarlet, et al. · Veterinary Microbiology · 32
Adipokine profile in celiac patients: differences in comparison with patients suffering from diarrhea-predominant IBS and healthy subjects
2013 · Francesco Russo, Guglielmina Chimienti, et al. · Scandinavian Journal of Gastroenterology · 30
Low presence of p53 abnormalities in H. pylori -infected gastric mucosa and in gastric adenocarcinoma
2003 · Pasquale Berloco, Francesco Russo, et al. · Journal of Gastroenterology · 25
Oestrogen receptors and microsatellite instability in colorectal carcinoma patients
2001 · Maria Notarnicola, Roberto Gristina, et al. · Cancer Letters · 25
Missense mutation in exon 7 of TRPS1 gene in an Italian family with a mild form of trichorhinophalangeal syndrome type I
2007 · A. Rossi, V. Devirgiliis, et al. · British Journal of Dermatology · 24
Identification of two new mutations in TRPS 1 gene leading to the tricho‐rhino‐phalangeal syndrome type I and III
2009 · Maria Piccione, Marcello Niceta, et al. · American Journal of Medical Genetics Part A · 23
Holt–Oram syndrome associated with anomalies of the feet
2008 · L. Garavelli, D. De Brasi, et al. · American Journal of Medical Genetics Part A · 22
Molecular and cytogenetic characterization of an azoospermic male with a de-novo Y;14 translocation and alternate centromere inactivation
2002 · A.L. Buonadonna, F. Cariola, et al. · Human Reproduction · 22
Serotonin gene polymorphisms and lifetime mood disorders in predicting interferon-induced depression in chronic hepatitis C
2015 · Raffaele Cozzolongo, Piero Porcelli, et al. · Journal of Affective Disorders · 18
Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with APC mutation at the extreme 3′-end
2019 · Vittoria Disciglio, Candida Fasano, et al. · Journal of Medical Genetics · 17
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A novel mutation in exon 7 in a family with mild tricho–rhino–phalangeal syndrome type I
2003 · M Gentile, P Fiorente, et al. · Clinical Genetics · 16
Nine novel APC mutations in Italian FAP patients
2001 · N. Resta, A. Stella, et al. · Human Mutation · 15
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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)
1999 · Mattia Gentile, Antonia L Buonadonna, et al. · Journal of Medical Genetics · 12
Genetic Associations of Alexithymia in Predicting Interferon-Induced Depression in Chronic Hepatitis C
2015 · Piero Porcelli, Raffaele Cozzolongo, et al. · Psychopathology · 10
FISH approach to determine cat eye syndrome chromosome breakpoints of a patient with cat eye syndrome type II
2005 · M. Gentile, S. De Sanctis, et al. · European Journal of Medical Genetics · 9
Clinical, cytogenetic, and molecular characterization of a patient with a de novo interstitial 22q12 duplication
2004 · M. Gentile, W. Wuyts, et al. · American Journal of Medical Genetics Part A · 8
Tumor Testing and Genetic Analysis to Identify Lynch Syndrome Patients in an Italian Colorectal Cancer Cohort
2023 · Antonino Pantaleo, Giovanna Forte, et al. · Cancers · 7
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A novel STK11 gene mutation (c.388dupG, p.Glu130Glyfs∗33) in a Peutz-Jeghers family and evidence of higher gastric cancer susceptibility associated with alterations in STK11 region aa 107-170
2021 · Giovanna Forte, Filomena Cariola, et al. · Genes & Diseases · 7
APC Splicing Mutations Leading to In-Frame Exon 12 or Exon 13 Skipping Are Rare Events in FAP Pathogenesis and Define the Clinical Outcome
2021 · Vittoria Disciglio, Giovanna Forte, et al. · Genes · 7
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Characterization of a rare variant (c.2635-2A>G) of the MSH2 gene in a family with Lynch syndrome
2018 · Filomena Cariola, Vittoria Disciglio, et al. · The International Journal of Biological Markers · 6
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Clinical and Molecular Characterization of SMAD4 Splicing Variants in Patients with Juvenile Polyposis Syndrome
2024 · Giovanna Forte, Antonia Lucia Buonadonna, et al. · International Journal of Molecular Sciences · 5
Identification and Somatic Characterization of the Germline PTEN Promoter Variant rs34149102 in a Family with Gastrointestinal and Breast Tumors
2022 · Vittoria Disciglio, Paola Sanese, et al. · Genes · 5
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Molecular cytogenetic characterization and genotype/phenotype analysis in a patient with a de novo 8p23.2p23.3 deletion/12p13.31p13.33 duplication
2012 · Lucia Margari, Maria Luisa Di Cosola, et al. · American Journal of Medical Genetics Part A · 5
Works count: 41
Citation count: 526
H-index: 14
I10-index: 16
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