Filomena Cariola

449 total citations
22 papers, 285 citations indexed

About

Filomena Cariola is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Filomena Cariola has authored 22 papers receiving a total of 285 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 8 papers in Pathology and Forensic Medicine. Recurrent topics in Filomena Cariola's work include Genetic factors in colorectal cancer (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and Congenital Ear and Nasal Anomalies (4 papers). Filomena Cariola is often cited by papers focused on Genetic factors in colorectal cancer (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and Congenital Ear and Nasal Anomalies (4 papers). Filomena Cariola collaborates with scholars based in Italy, United States and Belgium. Filomena Cariola's co-authors include Mattia Gentile, Maria Lucia Caruso, Anna Maria Valentini, M Pirrelli, Vito Guerra, Gianluigi Giannelli, Francesco Russo, Alfredo Di Leo, Antonio Di Carlo and Piero Porcelli and has published in prestigious journals such as International Journal of Molecular Sciences, Journal of Affective Disorders and Cancer Letters.

In The Last Decade

Filomena Cariola

21 papers receiving 267 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Filomena Cariola Italy 12 83 79 76 68 60 22 285
Xingguang Ye China 11 64 0.8× 92 1.2× 29 0.4× 24 0.4× 22 0.4× 25 296
Miki Miura Japan 10 69 0.8× 103 1.3× 41 0.5× 9 0.1× 100 1.7× 29 334
Julie Salomon France 9 101 1.2× 80 1.0× 47 0.6× 22 0.3× 175 2.9× 17 396
D. Piancatelli Italy 14 47 0.6× 62 0.8× 79 1.0× 34 0.5× 48 0.8× 43 478
Doran Khamis United Kingdom 5 40 0.5× 209 2.6× 54 0.7× 17 0.3× 52 0.9× 7 339
Andrea Fuhrer Switzerland 6 92 1.1× 124 1.6× 83 1.1× 6 0.1× 62 1.0× 11 433
Andrew Higham United Kingdom 8 43 0.5× 55 0.7× 105 1.4× 11 0.2× 122 2.0× 11 287
Korri Weldon United States 10 70 0.8× 142 1.8× 106 1.4× 21 0.3× 22 0.4× 16 327
Marianna Lo Pizzo Italy 11 19 0.2× 51 0.6× 18 0.2× 39 0.6× 40 0.7× 22 285
Tatsuo Oyake Japan 10 18 0.2× 91 1.2× 76 1.0× 14 0.2× 40 0.7× 34 338

Countries citing papers authored by Filomena Cariola

Since Specialization
Citations

This map shows the geographic impact of Filomena Cariola's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Filomena Cariola with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Filomena Cariola more than expected).

Fields of papers citing papers by Filomena Cariola

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Filomena Cariola. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Filomena Cariola. The network helps show where Filomena Cariola may publish in the future.

Co-authorship network of co-authors of Filomena Cariola

This figure shows the co-authorship network connecting the top 25 collaborators of Filomena Cariola. A scholar is included among the top collaborators of Filomena Cariola based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Filomena Cariola. Filomena Cariola is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Forte, Giovanna, Rossella Donghia, Martina Lepore Signorile, et al.. (2024). Exploring the Relationship of rs2802292 with Diabetes and NAFLD in a Southern Italian Cohort—Nutrihep Study. International Journal of Molecular Sciences. 25(17). 9512–9512. 1 indexed citations
2.
Forte, Giovanna, Valentina Grossi, Filomena Cariola, et al.. (2023). Identification of a novel germline APC N-terminal pathogenic variant associated with attenuated familial adenomatous polyposis. Genes & Diseases. 11(6). 101078–101078.
3.
Disciglio, Vittoria, Candida Fasano, Filomena Cariola, et al.. (2019). Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with APC mutation at the extreme 3′-end. Journal of Medical Genetics. 57(5). 356–360. 12 indexed citations
4.
Valentini, Anna Maria, Filomena Cariola, Vito Guerra, et al.. (2018). PD-L1 expression in colorectal cancer defines three subsets of tumor immune microenvironments. Oncotarget. 9(9). 8584–8596. 49 indexed citations
5.
Cariola, Filomena, Vittoria Disciglio, Anna Maria Valentini, et al.. (2018). Characterization of a rare variant (c.2635-2A>G) of the MSH2 gene in a family with Lynch syndrome. The International Journal of Biological Markers. 33(4). 534–539. 5 indexed citations
6.
Porcelli, Piero, Raffaele Cozzolongo, Filomena Cariola, et al.. (2015). Genetic Associations of Alexithymia in Predicting Interferon-Induced Depression in Chronic Hepatitis C. Psychopathology. 48(6). 417–420. 6 indexed citations
7.
Cozzolongo, Raffaele, Piero Porcelli, Filomena Cariola, et al.. (2015). Serotonin gene polymorphisms and lifetime mood disorders in predicting interferon-induced depression in chronic hepatitis C. Journal of Affective Disorders. 183. 90–97. 14 indexed citations
8.
Russo, Francesco, Guglielmina Chimienti, Caterina Clemente, et al.. (2013). Adipokine profile in celiac patients: differences in comparison with patients suffering from diarrhea-predominant IBS and healthy subjects. Scandinavian Journal of Gastroenterology. 48(12). 1377–1385. 26 indexed citations
9.
Margari, Lucia, Maura Buttiglione, Francesco Craig, et al.. (2012). Molecular cytogenetic characterization and genotype/phenotype analysis in a patient with a de novo 8p23.2p23.3 deletion/12p13.31p13.33 duplication. American Journal of Medical Genetics Part A. 158A(7). 1713–1718. 4 indexed citations
10.
Piccione, Maria, Marcello Niceta, Vincenzo Antona, et al.. (2009). Identification of two new mutations in TRPS 1 gene leading to the tricho‐rhino‐phalangeal syndrome type I and III. American Journal of Medical Genetics Part A. 149A(8). 1837–1841. 20 indexed citations
11.
Garavelli, Livia, Daniele De Brasi, Filomena Cariola, et al.. (2008). Holt–Oram syndrome associated with anomalies of the feet. American Journal of Medical Genetics Part A. 146A(9). 1185–1189. 11 indexed citations
12.
Rossi, Alfredo, Vincenzo Panasiti, Riccardo G. Borroni, et al.. (2007). Missense mutation in exon 7 of TRPS1 gene in an Italian family with a mild form of trichorhinophalangeal syndrome type I. British Journal of Dermatology. 157(5). 1021–1024. 19 indexed citations
13.
Martella, Vito, Max Ciarlet, Antonio Lavazza, et al.. (2005). Lapine rotaviruses of the genotype P[22] are widespread in Italian rabbitries. Veterinary Microbiology. 111(1-2). 117–124. 23 indexed citations
14.
Gentile, Mattia, et al.. (2005). Prenatal diagnosis of chromosome 4 mosaicism: Prognostic role of cytogenetic, molecular, and ultrasound/MRI characterization. American Journal of Medical Genetics Part A. 136A(1). 66–70. 21 indexed citations
15.
Gentile, Mattia, et al.. (2005). FISH approach to determine cat eye syndrome chromosome breakpoints of a patient with cat eye syndrome type II. European Journal of Medical Genetics. 48(1). 33–39. 6 indexed citations
16.
Gentile, Mattia, Wim Wuyts, Antonio Di Carlo, et al.. (2004). Clinical, cytogenetic, and molecular characterization of a patient with a de novo interstitial 22q12 duplication. American Journal of Medical Genetics Part A. 127A(2). 186–190. 8 indexed citations
17.
Berloco, P.B., Francesco Russo, Filomena Cariola, et al.. (2003). Low presence of p53 abnormalities in H. pylori -infected gastric mucosa and in gastric adenocarcinoma. Journal of Gastroenterology. 38(1). 28–36. 20 indexed citations
18.
Resta, Nicoletta, Alessandro Stella, Francesco Susca, et al.. (2001). Nine novel APC mutations in Italian FAP patients. Human Mutation. 17(5). 434–435. 11 indexed citations
19.
Notarnicola, Maria, Roberto Gristina, Caterina Messa, et al.. (2001). Oestrogen receptors and microsatellite instability in colorectal carcinoma patients. Cancer Letters. 168(1). 65–70. 19 indexed citations
20.
Stella, Alessandro, Nicoletta Resta, Angela Polizzi, et al.. (1998). The familial adenomatous polyposis region exhibits many different haplotypes. Human Genetics. 102(6). 624–628. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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