Franco Stanzial

1.8k total citations
21 papers, 311 citations indexed

About

Franco Stanzial is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Franco Stanzial has authored 21 papers receiving a total of 311 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Rheumatology. Recurrent topics in Franco Stanzial's work include RNA regulation and disease (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Connective tissue disorders research (2 papers). Franco Stanzial is often cited by papers focused on RNA regulation and disease (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Connective tissue disorders research (2 papers). Franco Stanzial collaborates with scholars based in Italy, Germany and Switzerland. Franco Stanzial's co-authors include Francesco Benedicenti, J I Maiztegui, António Francisco Ambrósio, Silvana Levis, Delia Enría, Enrico Bertini, Guido Mazzoleni, Bernd Wissinger, Silvana Pilotti and Eberhart Zrenner and has published in prestigious journals such as PLoS ONE, Clinical Cancer Research and International Journal of Molecular Sciences.

In The Last Decade

Franco Stanzial

21 papers receiving 299 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Franco Stanzial Italy 10 133 77 53 52 33 21 311
Sunila Jain India 9 141 1.1× 17 0.2× 8 0.2× 23 0.4× 32 1.0× 42 422
Ruth Cordoba-Rodriguez United States 7 195 1.5× 46 0.6× 5 0.1× 61 1.2× 24 0.7× 11 354
Vedrana Bali United States 8 166 1.2× 48 0.6× 13 0.2× 69 1.3× 21 0.6× 13 308
Björn E. Wenzel Germany 11 158 1.2× 117 1.5× 4 0.1× 14 0.3× 19 0.6× 17 619
Jason Evans United States 5 111 0.8× 37 0.5× 9 0.2× 49 0.9× 17 0.5× 8 357
Satoshi Tamahara Japan 11 90 0.7× 54 0.7× 6 0.1× 45 0.9× 41 1.2× 26 351
Kristin Hartmann Germany 10 125 0.9× 58 0.8× 16 0.3× 46 0.9× 55 1.7× 17 330
Uroš Hladnik Italy 12 191 1.4× 84 1.1× 4 0.1× 30 0.6× 24 0.7× 24 361
M Lacour United Kingdom 9 85 0.6× 54 0.7× 3 0.1× 8 0.2× 48 1.5× 26 486
N Ionescu Romania 5 167 1.3× 34 0.4× 92 1.7× 31 0.6× 136 4.1× 20 443

Countries citing papers authored by Franco Stanzial

Since Specialization
Citations

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

Fields of papers citing papers by Franco Stanzial

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Franco Stanzial

This figure shows the co-authorship network connecting the top 25 collaborators of Franco Stanzial. A scholar is included among the top collaborators of Franco Stanzial 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 Franco Stanzial. Franco Stanzial 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.
Parmeggiani, Lucio, Franco Stanzial, Elisabetta Menna, et al.. (2023). Early onset developmental and epileptic encephalopathy and Rett-like phenotype in a 15-year-old girl affected by Cornelia de Lange syndrome type 2 due to a SMC1A gene mutation. Epilepsy & Behavior Reports. 24. 100634–100634. 1 indexed citations
2.
Leva, Francesca Di, Francesco Benedicenti, Franco Stanzial, et al.. (2022). Induced Pluripotent Stem Cell (iPSC) Lines from a Family with Resistant Epileptic Encephalopathy Caused by Compound Heterozygous Mutations in SZT2 Gene. International Journal of Molecular Sciences. 23(21). 13095–13095. 2 indexed citations
3.
Lanzafame, Manuela, Tiziana Nardò, Roberta Ricotti, et al.. (2022). TFIIH stabilization recovers the DNA repair and transcription dysfunctions in thermo‐sensitive trichothiodystrophy. Human Mutation. 43(12). 2222–2233. 5 indexed citations
4.
Romaniello, Romina, Chiara Gagliardi, Livio Provenzi, et al.. (2021). Challenges and resources in adult life with Joubert syndrome: issues from an international classification of functioning (ICF) perspective. Disability and Rehabilitation. 44(18). 4966–4973. 4 indexed citations
5.
Bettella, Elisa, Roberta Polli, Emanuela Leonardi, et al.. (2020). Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotype. Journal of Human Genetics. 65(10). 855–864. 9 indexed citations
6.
Domingues, Francisco S., Christine Schwienbacher, Cláudia B. Volpato, et al.. (2018). Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly. Seizure. 66. 81–85. 11 indexed citations
7.
Zobor, Ditta, Annette Werner, Franco Stanzial, et al.. (2017). The Clinical Phenotype of CNGA3 -Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial. Investigative Ophthalmology & Visual Science. 58(2). 821–821. 39 indexed citations
8.
Gasparotto, Daniela, Sabrina Rossi, Maurizio Polano, et al.. (2016). Quadruple-Negative GIST Is a Sentinel for Unrecognized Neurofibromatosis Type 1 Syndrome. Clinical Cancer Research. 23(1). 273–282. 60 indexed citations
9.
Nicchia, Elena, Francesco Benedicenti, Daniela De Rocco, et al.. (2015). Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencing. Birth Defects Research Part A Clinical and Molecular Teratology. 103(12). 1003–1010. 5 indexed citations
10.
Zobor, Ditta, Franco Stanzial, Ulrich Kellner, et al.. (2014). Retinal structure and function in Achromatopsia: the CNGA3 phenotype. 55(13). 346–346. 1 indexed citations
11.
Novara, Francesca, Franco Stanzial, Elena Rossi, et al.. (2014). Defining the phenotype associated with microduplication reciprocal to Sotos syndrome microdeletion. American Journal of Medical Genetics Part A. 164(8). 2084–2090. 28 indexed citations
12.
Mauri, Lucia, Alessandra Longo, Elena Piozzi, et al.. (2013). SLC45A2 mutation frequency in Oculocutaneous Albinism Italian patients doesn't differ from other European studies. Gene. 533(1). 398–402. 7 indexed citations
13.
Zampieri, Stefania, Camillo Rosano, Charles Marques Lourenço, et al.. (2012). Sequence and Copy Number Analyses of HEXB Gene in Patients Affected by Sandhoff Disease: Functional Characterization of 9 Novel Sequence Variants. PLoS ONE. 7(7). e41516–e41516. 19 indexed citations
14.
Grossi, Serena, Stefano Regis, Roberta Biancheri, et al.. (2011). Molecular Genetic Analysis of the PLP1 Gene in 38 Families with PLP1-related disorders: Identification and Functional Characterization of 11 Novel PLP1 Mutations. Orphanet Journal of Rare Diseases. 6(1). 40–40. 32 indexed citations
15.
Unger, Sheila, Ekkehart Lausch, Franco Stanzial, et al.. (2011). Fetal akinesia in metatropic dysplasia: The combined phenotype of chondrodysplasia and neuropathy?. American Journal of Medical Genetics Part A. 155(11). 2860–2864. 26 indexed citations
16.
Origone, Paola, Carlo Bellini, Barbara Banelli, et al.. (2003). Neurofibromatosis eurofibromatosis type 1 (NF1): Identification of eight unreported mutations in NF1 gene in Italian patients. Human Mutation. 22(2). 179–180. 5 indexed citations
17.
18.
Stanzial, Franco, et al.. (1994). Cancer registration: a feasibility study in northern Italy. European Journal of Cancer. 30(8). 1128–1133. 1 indexed citations
19.
Valli, Maurizia, Francesca Zolezzi, Monica Mottes, et al.. (1993). Gly85 to Val substitution in proα1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion. European Journal of Biochemistry. 217(1). 77–82. 14 indexed citations
20.
Enría, Delia, et al.. (1986). Current status of the treatment of Argentine Hemorrhagic Fever. Medical Microbiology and Immunology. 175(2-3). 173–176. 27 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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