M.G. Tibiletti

663 total citations
25 papers, 441 citations indexed

About

M.G. Tibiletti is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, M.G. Tibiletti has authored 25 papers receiving a total of 441 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 M.G. Tibiletti's work include Genomic variations and chromosomal abnormalities (7 papers), Genetic factors in colorectal cancer (6 papers) and Prenatal Screening and Diagnostics (6 papers). M.G. Tibiletti is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genetic factors in colorectal cancer (6 papers) and Prenatal Screening and Diagnostics (6 papers). M.G. Tibiletti collaborates with scholars based in Italy, Canada and Germany. M.G. Tibiletti's co-authors include Leda Dalprà, Daniela Furlan, C. Capella, Roberto Taramelli, Massimo Piergiuseppe Franchi, Cristina Riva, Maurizio Trubia, G. Nocera, Monica Taborelli and Paola Queirolo and has published in prestigious journals such as Cancer, Annals of Oncology and International Journal of Cancer.

In The Last Decade

M.G. Tibiletti

25 papers receiving 428 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M.G. Tibiletti Italy 11 142 126 118 102 96 25 441
Thomas A. Lallas United States 11 171 1.2× 93 0.7× 133 1.1× 151 1.5× 85 0.9× 17 435
P. Renwick United Kingdom 7 105 0.7× 61 0.5× 71 0.6× 79 0.8× 36 0.4× 14 464
Jacqueline R. Batanian United States 15 206 1.5× 62 0.5× 82 0.7× 186 1.8× 35 0.4× 56 568
Elisabeth A. McKeen United States 7 71 0.5× 60 0.5× 165 1.4× 37 0.4× 50 0.5× 10 369
Xin-Yan Lu United States 6 321 2.3× 69 0.5× 178 1.5× 157 1.5× 154 1.6× 7 594
Musaffe Tuna United States 13 415 2.9× 96 0.8× 128 1.1× 133 1.3× 217 2.3× 22 673
Stéphanie Struski France 16 264 1.9× 94 0.7× 112 0.9× 106 1.0× 84 0.9× 30 596
Brita Thode Germany 10 102 0.7× 101 0.8× 140 1.2× 95 0.9× 49 0.5× 18 381
Małgorzata Babińska Poland 12 133 0.9× 77 0.6× 94 0.8× 56 0.5× 75 0.8× 20 394
Audrey Basinko France 13 217 1.5× 47 0.4× 32 0.3× 119 1.2× 53 0.6× 33 512

Countries citing papers authored by M.G. Tibiletti

Since Specialization
Citations

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

Fields of papers citing papers by M.G. Tibiletti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.G. Tibiletti. 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 M.G. Tibiletti. The network helps show where M.G. Tibiletti may publish in the future.

Co-authorship network of co-authors of M.G. Tibiletti

This figure shows the co-authorship network connecting the top 25 collaborators of M.G. Tibiletti. A scholar is included among the top collaborators of M.G. Tibiletti 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 M.G. Tibiletti. M.G. Tibiletti 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.
Cini, Giulia, Mara Fornasarig, Franco Armelao, et al.. (2021). Filling the gap: A thorough investigation for the genetic diagnosis of unsolved polyposis patients with monoallelic MUTYH pathogenic variants. Molecular Genetics & Genomic Medicine. 9(12). e1831–e1831. 4 indexed citations
2.
Chiaravalli, Anna Maria, Ileana Carnevali, Nora Sahnane, et al.. (2019). Universal screening to identify Lynch syndrome: two years of experience in a Northern Italian Center. European Journal of Cancer Prevention. 29(4). 281–288. 11 indexed citations
3.
Ghiorzo, Paola, Lorenza Pastorino, Paola Queirolo, et al.. (2012). Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history. Pigment Cell & Melanoma Research. 26(2). 259–262. 66 indexed citations
4.
Beghini, Alessandro, M.G. Tibiletti, Gaia Roversi, et al.. (2001). Germline mutation in the juxtamembrane domain of KIT gene in a family with GISTs and Urticaria Pigmentosa. Cancer. 92(3). 657–662. 3 indexed citations
5.
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
6.
Miozzo, Monica, Leda Dalprà, Paola Riva, et al.. (2000). A tumor suppressor locus in familial and sporadic chordoma maps to 1p36. International Journal of Cancer. 87(1). 68–72. 3 indexed citations
7.
Miozzo, Monica, Leda Dalprà, Paola Riva, et al.. (2000). A tumor suppressor locus in familial and sporadic chordoma maps to 1p36. International Journal of Cancer. 87(1). 68–72. 58 indexed citations
8.
Tibiletti, M.G., Daniela Furlan, Monica Taborelli, et al.. (1999). Microsatellite Instability in Endometrial Cancer: Relation to Histological Subtypes. Gynecologic Oncology. 73(2). 247–252. 49 indexed citations
9.
Bertoni, Francesco, A.M. Codegoni, Daniela Furlan, et al.. (1999). CHK1 frameshift mutations in genetically unstable colorectal and endometrial cancers. European Journal of Cancer. 35. S190–S190. 2 indexed citations
10.
11.
Bernasconi, Barbara, M.G. Tibiletti, Daniela Furlan, et al.. (1996). Early involvement of 6q in epithelial ovarian tumors. Cancer Genetics and Cytogenetics. 91(2). 132–132. 2 indexed citations
12.
Tibiletti, M.G., et al.. (1996). Chromosome 22 marker in a child with Duane syndrome and urogenital abnormalities.. PubMed. 39(3). 168–72. 15 indexed citations
13.
Tibiletti, M.G., Barbara Bernasconi, Daniela Furlan, et al.. (1996). Early involvement of 6q in surface epithelial ovarian tumors.. PubMed. 56(19). 4493–8. 57 indexed citations
14.
Tibiletti, M.G., Monica Taborelli, Barbara Bernasconi, et al.. (1996). Involvement of chromosome 6 in endometrial cancer. Cancer Genetics and Cytogenetics. 91(2). 132–132. 1 indexed citations
15.
Pittalis, Maria Carla, Leda Dalprà, Francesca Torricelli, et al.. (1994). The predictive value of cytogenetic diagnosis after CVS based on 4860 cases with both direct and culture methods. Prenatal Diagnosis. 14(4). 267–278. 58 indexed citations
16.
Dalprà, Leda, et al.. (1993). ‘Late’ chorionic villus sampling: Cytogenetic aspects. Prenatal Diagnosis. 13(4). 239–246. 6 indexed citations
17.
Doneda, Luisa, Ivana Magnani, M.G. Tibiletti, Leda Dalprà, & Lidia Larizza. (1992). Different phenotypes in two cases of an apparently identical familial (Yq;13p) translocation. Human Reproduction. 7(4). 495–499. 9 indexed citations
18.
Dalprà, Leda, et al.. (1983). SCE analysis in children exposed to lead emission from a smelting plant. Mutation Research Letters. 120(4). 249–256. 15 indexed citations
19.
Tibiletti, M.G., et al.. (1982). [48,XXXX syndrome in a 1-year-old girl].. PubMed. 34(13-14). 621–6. 2 indexed citations
20.
Simoni, Giuseppe, L. Dalpr�, G. L. Terzoli, F. Rossella, & M.G. Tibiletti. (1980). The offspring of marriage between two first cousins with the same reciprocal translocation t(2;7)(p11;q31). Human Genetics. 55(2). 199–202. 9 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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