Andrea Ciolfi

5.9k total citations
55 papers, 1.7k citations indexed

About

Andrea Ciolfi is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Andrea Ciolfi has authored 55 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 18 papers in Genetics and 8 papers in Cell Biology. Recurrent topics in Andrea Ciolfi's work include Plant Molecular Biology Research (8 papers), Genomics and Rare Diseases (7 papers) and Light effects on plants (7 papers). Andrea Ciolfi is often cited by papers focused on Plant Molecular Biology Research (8 papers), Genomics and Rare Diseases (7 papers) and Light effects on plants (7 papers). Andrea Ciolfi collaborates with scholars based in Italy, United States and Germany. Andrea Ciolfi's co-authors include Giorgio Morelli, Monica Carabelli, Marco Possenti, Ida Ruberti, Giovanna Sessa, Massimiliano Sassi, Marco Tartaglia, Jörg D. Becker, Viviana Caputo and Marcello Niceta and has published in prestigious journals such as Nature Communications, Genes & Development and PLANT PHYSIOLOGY.

In The Last Decade

Andrea Ciolfi

53 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrea Ciolfi Italy 21 983 787 255 143 112 55 1.7k
Rebecca Favaro Italy 20 1.9k 2.0× 657 0.8× 331 1.3× 146 1.0× 117 1.0× 27 2.6k
Mark W. Kankel United States 16 1.8k 1.8× 488 0.6× 166 0.7× 310 2.2× 273 2.4× 18 2.4k
Christophe Houbron France 16 1.4k 1.4× 160 0.2× 299 1.2× 219 1.5× 186 1.7× 24 2.0k
Christine Fauth Austria 22 1.5k 1.5× 522 0.7× 790 3.1× 49 0.3× 234 2.1× 66 2.3k
Maximina H. Yun Germany 15 972 1.0× 238 0.3× 114 0.4× 59 0.4× 155 1.4× 30 1.5k
Vered Raz Netherlands 26 2.0k 2.1× 1.8k 2.3× 174 0.7× 127 0.9× 117 1.0× 77 3.0k
Niels Vandamme Belgium 17 1.0k 1.1× 305 0.4× 72 0.3× 68 0.5× 175 1.6× 37 2.0k
Susan Gribble United Kingdom 18 579 0.6× 349 0.4× 765 3.0× 96 0.7× 41 0.4× 29 1.2k
Juliane Ramser Germany 20 934 1.0× 240 0.3× 376 1.5× 85 0.6× 133 1.2× 54 1.8k
Steve Bilodeau Canada 23 3.1k 3.1× 379 0.5× 508 2.0× 76 0.5× 146 1.3× 39 3.9k

Countries citing papers authored by Andrea Ciolfi

Since Specialization
Citations

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

Fields of papers citing papers by Andrea Ciolfi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Ciolfi

This figure shows the co-authorship network connecting the top 25 collaborators of Andrea Ciolfi. A scholar is included among the top collaborators of Andrea Ciolfi 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 Andrea Ciolfi. Andrea Ciolfi 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.
Bruselles, Alessandro, Paola D′Ambrosio, Andrea Ciolfi, et al.. (2025). The p.Ile202Thr Substitution in TUBB2B Can Be Associated with Syndromic Presentation of Congenital Fibrosis of the Extraocular Muscles. Genes. 16(10). 1182–1182. 1 indexed citations
2.
3.
Bellomo, Francesco, Sara Cairoli, Cristiano De Stefanis, et al.. (2024). Ketogenic Diet and Progression of Kidney Disease in Animal Models of Nephropathic Cystinosis. Journal of the American Society of Nephrology. 35(11). 1493–1506. 6 indexed citations
4.
Hjortshøj, Tina Duelund, Morten Dunø, Lotte Risom, et al.. (2023). DNA methylation signature classification of rare disorders using publicly available methylation data. Clinical Genetics. 103(6). 688–692. 1 indexed citations
5.
Priolo, Manuela, Francesca Clementina Radio, Andrea Ciolfi, et al.. (2023). Natural history of MRAS‐related Noonan syndrome: Evidence of mild adult‐onset left ventricular hypertrophy and neuropsychiatric features. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 193(2). 160–166.
6.
Priolo, Manuela, Francesca Clementina Radio, Andrea Ciolfi, et al.. (2023). Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variants. European Journal of Human Genetics. 31(7). 805–814. 4 indexed citations
7.
Priolo, Manuela, Andrea Ciolfi, Luca Pannone, et al.. (2022). SHP2 's gain‐of‐function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction. Clinical Genetics. 102(1). 12–21. 2 indexed citations
8.
Ziccardi, Lucia, Marcello Niceta, Emilia Stellacci, et al.. (2022). Biallelic Inactivating TUB Variants Cause Retinal Ciliopathy Impairing Biogenesis and the Structure of the Primary Cilium. International Journal of Molecular Sciences. 23(23). 14656–14656. 2 indexed citations
9.
Leoni, Chiara, Francesca Clementina Radio, Giovanni Chillemi, et al.. (2021). Broadening the phenotypic spectrum of Beta3GalT6 ‐associated phenotypes. American Journal of Medical Genetics Part A. 185(10). 3153–3160. 4 indexed citations
10.
Colletti, Marta, Angela Galardi, Evelina Miele, et al.. (2021). Establishment and Characterization of a Cell Line (S-RMS1) Derived from an Infantile Spindle Cell Rhabdomyosarcoma with SRF-NCOA2 Fusion Transcript. International Journal of Molecular Sciences. 22(11). 5484–5484. 6 indexed citations
11.
Rossi, Sabrina, Sabina Barresi, Stefano Chiaravalli, et al.. (2021). DICER1-associated malignancies mimicking germ cell neoplasms: Report of two cases and review of the literature. Pathology - Research and Practice. 225. 153553–153553. 12 indexed citations
12.
Flex, Elisabetta, Giovanna Carpentieri, Alessandro Bruselles, et al.. (2021). A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in LTBP3. Genes. 12(9). 1406–1406. 3 indexed citations
13.
Dentici, Maria Lisa, Sabina Barresi, Marcello Niceta, et al.. (2019). Expanding the clinical spectrum associated with PACS2 mutations. Clinical Genetics. 95(4). 525–531. 17 indexed citations
14.
Colafati, Giovanna Stefania, Francesca Diomedi‐Camassei, Andrea Ciolfi, et al.. (2019). Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review. Frontiers in Genetics. 10. 391–391. 20 indexed citations
15.
Zanni, Ginevra, Paola De Magistris, Emanuele Bellacchio, et al.. (2019). Biallelic Variants in the Nuclear Pore Complex Protein NUP93 Are Associated with Non-progressive Congenital Ataxia. The Cerebellum. 18(3). 422–432. 10 indexed citations
16.
Sferra, Antonella, Fabiana Fattori, Teresa Rizza, et al.. (2018). Defective kinesin binding of TUBB2A causes progressive spastic ataxia syndrome resembling sacsinopathy. Human Molecular Genetics. 27(11). 1892–1904. 28 indexed citations
17.
Servidei, Tiziana, Daniela Meco, Valentina Muto, et al.. (2017). Novel SEC61G – EGFR Fusion Gene in Pediatric Ependymomas Discovered by Clonal Expansion of Stem Cells in Absence of Exogenous Mitogens. Cancer Research. 77(21). 5860–5872. 20 indexed citations
18.
Giorgio, Elisa, Alessandro Brussino, Elisa Biamino, et al.. (2016). Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes. European Journal of Paediatric Neurology. 21(3). 475–484. 11 indexed citations
19.
Hedberg, Carola, Marcello Niceta, Fabiana Fattori, et al.. (2014). Childhood onset tubular aggregate myopathy associated with de novo STIM1 mutations. Journal of Neurology. 261(5). 870–876. 50 indexed citations
20.
Carabelli, Monica, Marco Possenti, Giovanna Sessa, et al.. (2007). Canopy shade causes a rapid and transient arrest in leaf development through auxin-induced cytokinin oxidase activity. Genes & Development. 21(15). 1863–1868. 179 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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