Francesco Benedicenti

1.7k total citations
21 papers, 417 citations indexed

About

Francesco Benedicenti is a scholar working on Molecular Biology, Genetics and Dermatology. According to data from OpenAlex, Francesco Benedicenti has authored 21 papers receiving a total of 417 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 2 papers in Dermatology. Recurrent topics in Francesco Benedicenti's work include RNA regulation and disease (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic and rare skin diseases. (2 papers). Francesco Benedicenti is often cited by papers focused on RNA regulation and disease (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic and rare skin diseases. (2 papers). Francesco Benedicenti collaborates with scholars based in Italy, Germany and France. Francesco Benedicenti's co-authors include B Bellemin, Elisabeth Robert, Maxime Cournot, Minke Reuvers, P Mastroiacovo, Christof Schaefer, Antonio Addis, Judy Arnon, Elena Di Gianantonio and Maurizio Clementi and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Francesco Benedicenti

21 papers receiving 396 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Francesco Benedicenti Italy	10	165	123	77	66	47	21	417
Naoaki Hori Japan	10	191 1.2×	131 1.1×	61 0.8×	110 1.7×	11 0.2×	24	425
Elisabetta Pelo Italy	11	216 1.3×	80 0.7×	88 1.1×	29 0.4×	6 0.1×	36	480
Gita Tan-Sindhunata Netherlands	8	189 1.1×	172 1.4×	18 0.2×	213 3.2×	18 0.4×	12	439
Kemal O. Yariz United States	8	212 1.3×	90 0.7×	17 0.2×	25 0.4×	17 0.4×	9	346
Cecilie F. Rustad Norway	11	210 1.3×	116 0.9×	10 0.1×	37 0.6×	34 0.7×	18	491
Martina Klempt Germany	12	235 1.4×	86 0.7×	25 0.3×	29 0.4×	5 0.1×	18	397
A. David France	13	326 2.0×	230 1.9×	8 0.1×	115 1.7×	31 0.7×	42	579
Harsh Vaidya United Kingdom	6	212 1.3×	60 0.5×	70 0.9×	62 0.9×	3 0.1×	6	548
Mona L. Essawi Egypt	10	232 1.4×	120 1.0×	34 0.4×	29 0.4×	5 0.1×	45	331
Gülen Eda Ütine Türkiye	14	367 2.2×	373 3.0×	21 0.3×	66 1.0×	5 0.1×	114	715

Countries citing papers authored by Francesco Benedicenti

Since Specialization

Citations

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

Fields of papers citing papers by Francesco Benedicenti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesco Benedicenti

This figure shows the co-authorship network connecting the top 25 collaborators of Francesco Benedicenti. A scholar is included among the top collaborators of Francesco Benedicenti 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 Francesco Benedicenti. Francesco Benedicenti 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

Wischmeijer, Anita, Laurence Perrin, Duccio Maria Cordelli, et al.. (2024). Olfactory bulb anomalies in KBG syndrome mouse model and patients. BMC Medicine. 22(1). 158–158. 2 indexed citations

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

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

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

Pichler, Maria, et al.. (2020). Metastatic cylindrocarcinoma in Brooke‐Spiegler Syndrome – Report of a case and review of the literature. JDDG Journal der Deutschen Dermatologischen Gesellschaft. 19(1). 125–128. 3 indexed citations

Benedicenti, Francesco, et al.. (2020). Clinical aspects of Hyaline Fibromatosis Syndrome and identification of a novel mutation. Molecular Genetics & Genomic Medicine. 8(6). e1203–e1203. 9 indexed citations

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

Mehrjouy, Mana M., Nadja Ehmke, Giorgio Adriano Paskulin, et al.. (2017). Regulatory variants of FOXG1 in the context of its topological domain organisation. European Journal of Human Genetics. 26(2). 186–196. 16 indexed citations

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

10.

Loconte, Daria Carmela, Valentina Grossi, Cristina Bozzao, et al.. (2015). Molecular and Functional Characterization of Three Different Postzygotic Mutations in PIK3CA-Related Overgrowth Spectrum (PROS) Patients: Effects on PI3K/AKT/mTOR Signaling and Sensitivity to PIK3 Inhibitors. PLoS ONE. 10(4). e0123092–e0123092. 52 indexed citations

11.

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

12.

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

13.

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

14.

Malvestiti, Francesca, Francesco Benedicenti, Simona De Toffol, et al.. (2013). Recombinant Chromosome 4 from a Familial Pericentric Inversion: Prenatal and Adulthood Wolf-Hirschhorn Phenotypes. SHILAP Revista de lepidopterología. 2013. 1–4. 4 indexed citations

15.

Pedace, Lucia, A. Amantea, Giovanna Zambruno, et al.. (2011). Molecular characterization of 11 Italian patients with Darier Disease. European Journal of Dermatology. 21(3). 334–338. 9 indexed citations

16.

Nishimura, Gen, Jin Dai, Ekkehart Lausch, et al.. (2010). Spondylo‐epiphyseal dysplasia, Maroteaux type (pseudo‐Morquio syndrome type 2), and parastremmatic dysplasia are caused by TRPV4 mutations. American Journal of Medical Genetics Part A. 152A(6). 1443–1449. 58 indexed citations

17.

Botta, Elena, Tiziana Nardò, Donata Orioli, et al.. (2008). Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in theXPDgene. Human Mutation. 30(3). 438–445. 21 indexed citations

18.

Benedicenti, Francesco, et al.. (2003). Utilization of genetic counseling by parents of a child or fetus with congenital malformation in North‐East Italy. American Journal of Medical Genetics Part A. 121A(3). 214–218. 5 indexed citations

19.

Gianantonio, Elena Di, Christof Schaefer, P Mastroiacovo, et al.. (2001). Adverse effects of prenatal methimazole exposure. Teratology. 64(5). 262–266. 127 indexed citations

20.

Clementi, Massimo, Sebastiano Bianca, Francesco Benedicenti, & Romano Tenconi. (1999). Down Syndrome and Parity. Public Health Genomics. 2(1). 18–22. 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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