Marcello Morgutti

565 total citations
27 papers, 372 citations indexed

About

Marcello Morgutti is a scholar working on Molecular Biology, Sensory Systems and Immunology. According to data from OpenAlex, Marcello Morgutti has authored 27 papers receiving a total of 372 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Sensory Systems and 7 papers in Immunology. Recurrent topics in Marcello Morgutti's work include Hearing, Cochlea, Tinnitus, Genetics (7 papers), Reproductive System and Pregnancy (5 papers) and Connexins and lens biology (4 papers). Marcello Morgutti is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (7 papers), Reproductive System and Pregnancy (5 papers) and Connexins and lens biology (4 papers). Marcello Morgutti collaborates with scholars based in Italy, Brazil and France. Marcello Morgutti's co-authors include Sérgio Crovella, Annalisa Fabris, Ludovica Segat, Eulalia Catamo, Paolo Gasparini, Massimiliano Bicego, Paola D’Andrea, Doroti Pirulli, Luca Ronfani and Luiz Cláudio Arraes and has published in prestigious journals such as Radiology, Biochemical and Biophysical Research Communications and The American Journal of Gastroenterology.

In The Last Decade

Marcello Morgutti

27 papers receiving 362 citations

Peers

Marcello Morgutti

IMMUN

GENET

PHEOH

Eulalia Catamo Italy

Friedrich Goetz Germany

Elene Haralambous United Kingdom

Jeff Herbert United Kingdom

Kelly A. Metcalf Pate United States

Jordi Gouilly France

Patrick Stauffer United States

Bingjie Li China

Andrew N. Vaughan United Kingdom

John D. Scarborough United States

Eulalia Catamo Italy

Marcello Morgutti

173 ×1.5

337 ×2.8

IMMUN

61 ×0.8

50 ×1.3

GENET

92 ×2.6

PHEOH

Citations per year, relative to Marcello Morgutti Marcello Morgutti (= 1×) peers Eulalia Catamo

Countries citing papers authored by Marcello Morgutti

Since Specialization

Citations

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

Fields of papers citing papers by Marcello Morgutti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marcello Morgutti

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

All Works

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20 of 20 papers shown

Lenarduzzi, Stefania, Anna Morgan, Flavio Faletra, et al.. (2019). Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss. Hearing Research. 381. 107769–107769. 8 indexed citations

Morgan, Anna, Stefania Lenarduzzi, Stefania Cappellani, et al.. (2018). Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations. Frontiers in Genetics. 9. 681–681. 25 indexed citations

Lenarduzzi, Stefania, Diego Vozzi, Anna Morgan, et al.. (2015). Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis. Hearing Research. 320. 18–23. 22 indexed citations

Lenarduzzi, Stefania, Marcello Morgutti, Sérgio Crovella, Alessandra Coiana, & Maria Cristina Rosatelli. (2014). Short Communication Novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients. Genetics and Molecular Research. 13(4). 9636–9641. 1 indexed citations

Segat, Ludovica, et al.. (2012). A Real-Time Polymerase Chain Reaction-Based Protocol for Low/Medium-Throughput Y-Chromosome Microdeletions Analysis. Genetic Testing and Molecular Biomarkers. 16(12). 1349–1355. 3 indexed citations

Catamo, Eulalia, et al.. (2012). CD14 polymorphisms correlate with an augmented risk for celiac disease in Italian patients. Genes and Immunity. 13(6). 489–495. 4 indexed citations

Ricci, Giuseppe, Leo Fischer-Tamaro, Elena Giolo, et al.. (2011). Factor V Leiden and prothrombin gene G20210A mutation and in vitro fertilization: prospective cohort study. Human Reproduction. 26(11). 3068–3077. 33 indexed citations

Fabris, Annalisa, et al.. (2010). HLA-G 14 bp Deletion/Insertion Polymorphism in Celiac Disease. The American Journal of Gastroenterology. 106(1). 139–144. 15 indexed citations

Segat, Ludovica, Eulalia Catamo, Annalisa Fabris, et al.. (2010). HLA-G*0105N allele is associated with augmented risk for HIV infection in white female patients. AIDS. 24(12). 1961–1964. 13 indexed citations

10.

Segat, Ludovica, Marcello Morgutti, Emmanouil Athanasakis, et al.. (2010). Analysis of DEFB1 regulatory SNPs in cystic fibrosis patients from North‐Eastern Italy. International Journal of Immunogenetics. 37(3). 169–175. 9 indexed citations

11.

Guerci, Veronica Ileana, Antonella Fabretto, Flavio Faletra, et al.. (2009). Detection of Epidermal Thickening inGJB2Carriers with Epidermal US. Radiology. 251(1). 280–286. 17 indexed citations

12.

Segat, Ludovica, et al.. (2009). HLA-G 3′ UTR haplotypes and HIV vertical transmission. AIDS. 23(14). 1916–1918. 17 indexed citations

13.

Fabris, Annalisa, Eulalia Catamo, Ludovica Segat, et al.. (2008). Association between HLA-G 3′UTR 14-bp polymorphism and HIV vertical transmission in Brazilian children. AIDS. 23(2). 177–182. 44 indexed citations

14.

Milanese, Michele, Ludovica Segat, Francesco De Seta, et al.. (2008). ORIGINAL ARTICLE: MBL2 Genetic Screening in Patients with Recurrent Vaginal Infections. American Journal of Reproductive Immunology. 59(2). 146–151. 34 indexed citations

15.

Bicego, Massimiliano, Victor H. Hernández, Marcello Morgutti, et al.. (2006). Selective defects in channel permeability associated with Cx32 mutations causing X-linked Charcot–Marie–Tooth disease. Neurobiology of Disease. 21(3). 607–617. 26 indexed citations

16.

Trevisiol, Chiara, Michele Boniotto, L. Giglio, et al.. (2005). MBL2 polymorphisms screening in a regional Italian CF Center. Journal of Cystic Fibrosis. 4(3). 189–191. 17 indexed citations

17.

Melchionda, Salvatore, Massimiliano Bicego, Elio Marciano, et al.. (2005). Functional characterization of a novel Cx26 (T55N) mutation associated to non-syndromic hearing loss. Biochemical and Biophysical Research Communications. 337(3). 799–805. 25 indexed citations

18.

Pirulli, Doroti, Michele Boniotto, Sérgio Crovella, et al.. (2001). Polymorphisms in the promoter region and at codon 54 of the MBL2 gene are not associated with IgA nephropathy. Nephrology Dialysis Transplantation. 16(4). 759–764. 9 indexed citations

19.

Morgutti, Marcello, et al.. (2001). Genomic organization and chromosome mapping of the human homeobox gene HHEX. Cytogenetic and Genome Research. 94(1-2). 30–32. 8 indexed citations

20.

Crovella, Sérgio, Nicola Marziliano, Silvia Garagna, et al.. (1999). MFASAT: A new alphoid DNA sequence isolated from Macaca fascicularis (Cercopithecidae, Primates). Genome. 42(6). 1066–1070. 4 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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