Mario Bengala

523 total citations
17 papers, 185 citations indexed

About

Mario Bengala is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Mario Bengala has authored 17 papers receiving a total of 185 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Rheumatology. Recurrent topics in Mario Bengala's work include Congenital heart defects research (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Mario Bengala is often cited by papers focused on Congenital heart defects research (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Mario Bengala collaborates with scholars based in Italy, Canada and United States. Mario Bengala's co-authors include Giuseppe Novelli, Francesca Amati, Bruno Dallapiccola, Emanuela Conti, Aldo Giannotti, Bruno Marino, Orazio Gabrielli, Antonio Novelli, M. Cristina Digilio and Federica Sangiuolo and has published in prestigious journals such as Gene, European Journal of Human Genetics and Frontiers in Genetics.

In The Last Decade

Mario Bengala

17 papers receiving 181 citations

Peers

Mario Bengala
María Gabriela Obregón Argentina
Kristen L. Sund United States
Gabriela Ferraz Leal Brazil
Magdalena Socha Poland
Jeannette Connerney United States
Fernando Santos Spain
Xingbo Cheng China
Angeline Lai Singapore
Eriko Nishi Japan
Stefano Petrocchi Italy
María Gabriela Obregón Argentina
Mario Bengala
Citations per year, relative to Mario Bengala Mario Bengala (= 1×) peers María Gabriela Obregón

Countries citing papers authored by Mario Bengala

Since Specialization
Citations

This map shows the geographic impact of Mario Bengala'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 Mario Bengala with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mario Bengala more than expected).

Fields of papers citing papers by Mario Bengala

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mario Bengala. 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 Mario Bengala. The network helps show where Mario Bengala may publish in the future.

Co-authorship network of co-authors of Mario Bengala

This figure shows the co-authorship network connecting the top 25 collaborators of Mario Bengala. A scholar is included among the top collaborators of Mario Bengala 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 Mario Bengala. Mario Bengala is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Albanese, Maria, Francesca Pescini, Luigi Francesco Iannone, et al.. (2024). Long-Term Treatment with the Calcitonin Gene-Related Peptide Receptor Antagonist Erenumab in CADASIL: Two Case Reports. Journal of Clinical Medicine. 13(7). 1870–1870. 1 indexed citations
2.
Carriero, Miriam Lucia, Flavio Pozzi, Aikaterini Andreadi, et al.. (2024). Genetic Variability of SOX10-Related Disorders within an Italian Family: Straddling the Line between Kallmann and Waardenburg Syndrome. Molecular Syndromology. 15(4). 339–346. 1 indexed citations
3.
Carriero, Miriam Lucia, Mario Bengala, Silvia Lai, et al.. (2024). A Novel COL4A5 Pathogenic Variant Joins the Dots in a Family with a Synchronous Diagnosis of Alport Syndrome and Polycystic Kidney Disease. Genes. 15(5). 597–597. 1 indexed citations
4.
Sgrulletti, Mayla, Cristina Cifaldi, Silvia Di Cesare, et al.. (2023). Case Report: Crossing a rugged road in a primary immune regulatory disorder. Frontiers in Pediatrics. 10. 1055091–1055091. 1 indexed citations
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Conte, Chiara, et al.. (2023). A likely pathogenic ACTG1 variant in a child showing partial phenotypic overlap with Baraitser‐Winter syndrome. American Journal of Medical Genetics Part A. 191(6). 1565–1569. 1 indexed citations
7.
8.
Botta, Annalisa, Paola Bisceglia, Mario Bengala, et al.. (2021). A 14-Year Italian Experience in DM2 Genetic Testing: Frequency and Distribution of Normal and Premutated CNBP Alleles. Frontiers in Genetics. 12. 668094–668094. 3 indexed citations
9.
Alesi, Viola, Silvia Di Tommaso, Mario Bengala, et al.. (2021). 1p36 Deletion Syndrome and the Aorta: A Report of Three New Patients and a Literature Review. Journal of Cardiovascular Development and Disease. 8(11). 159–159. 3 indexed citations
10.
Diomedi, Marina, Ziv Gan‐Or, Fabio Placidi, et al.. (2016). A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegia. European Journal of Medical Genetics. 59(11). 564–568. 8 indexed citations
11.
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Graziani, Simona, Caterina Cancrini, Andrea Finocchi, et al.. (2012). The Impact of TACI Mutations: From Hypogammaglobulinemia in Infancy to Autoimmunity in Adulthood. International Journal of Immunopathology and Pharmacology. 25(2). 407–414. 16 indexed citations
13.
D’Apice, Maria Rosaria, Stefano Gambardella, Mario Bengala, et al.. (2004). Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate among the affected population in Central Italy. BMC Medical Genetics. 5(1). 8–8. 20 indexed citations
14.
Pizzuti, Antonio, Giuseppe Novelli, Antonia Ratti, et al.. (1999). Isolation and Characterization of a Novel Transcript Embedded within HIRA, a Gene Deleted in DiGeorge Syndrome. Molecular Genetics and Metabolism. 67(3). 227–235. 16 indexed citations
15.
Amati, Francesca, Emanuela Conti, Antonio Novelli, et al.. (1999). Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome. European Journal of Human Genetics. 7(8). 903–909. 66 indexed citations
16.
Novelli, Giuseppe, Aldo Mari, Francesca Amati, et al.. (1998). Structure and expression of the human ubiquitin fusion–degradation gene (UFD1L). Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1396(2). 158–162. 18 indexed citations
17.
Man, Adrian, Francesca Amati, Eugenia Conti, et al.. (1998). A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region. Clinical Genetics. 53(3). 226–227. 6 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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