Cecilia Mancini

2.2k total citations
51 papers, 760 citations indexed

About

Cecilia Mancini is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Cecilia Mancini has authored 51 papers receiving a total of 760 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 13 papers in Genetics and 7 papers in Neurology. Recurrent topics in Cecilia Mancini's work include Mitochondrial Function and Pathology (9 papers), RNA modifications and cancer (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Cecilia Mancini is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), RNA modifications and cancer (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Cecilia Mancini collaborates with scholars based in Italy, United States and Russia. Cecilia Mancini's co-authors include Alfredo Brusco, Mirca Lazzaretti, Simona Colla, Nicola Giuliani, Simona Cavalieri, Alessandro Brussino, Elisa Giorgio, Eleonora Di Gregorio, Emanuela Garelli and Adriana Carando and has published in prestigious journals such as The Journal of Immunology, JNCI Journal of the National Cancer Institute and Scientific Reports.

In The Last Decade

Cecilia Mancini

48 papers receiving 747 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Cecilia Mancini Italy	17	421	103	100	96	84	51	760
Tomoko Okamoto Japan	18	636 1.5×	86 0.8×	162 1.6×	60 0.6×	169 2.0×	85	1.9k
Emily Kistner‐Griffin United States	20	338 0.8×	101 1.0×	140 1.4×	24 0.3×	31 0.4×	37	753
Zarko Manojlovic United States	11	284 0.7×	60 0.6×	69 0.7×	35 0.4×	88 1.0×	25	555
Yafei Zhang China	14	453 1.1×	182 1.8×	78 0.8×	35 0.4×	25 0.3×	24	737
Tzipora C. Falik‐Zaccai Israel	19	326 0.8×	191 1.9×	116 1.2×	44 0.5×	78 0.9×	56	809
Ayushi Jain India	15	267 0.6×	32 0.3×	137 1.4×	23 0.2×	73 0.9×	55	878
Hoa Le Canada	13	419 1.0×	145 1.4×	63 0.6×	21 0.2×	49 0.6×	28	914
Kathy White United States	9	135 0.3×	72 0.7×	98 1.0×	192 2.0×	63 0.8×	19	608
Mark D. Potter United States	16	611 1.5×	367 3.6×	147 1.5×	167 1.7×	79 0.9×	23	1.3k
Imma Hernán Spain	16	386 0.9×	95 0.9×	64 0.6×	12 0.1×	63 0.8×	31	712

Countries citing papers authored by Cecilia Mancini

Since Specialization

Citations

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

Fields of papers citing papers by Cecilia Mancini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cecilia Mancini

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

Stellacci, Emilia, Marcello Niceta, Alessandro Bruselles, et al.. (2024). Whole Genome Sequencing Solves an Atypical Form of Bardet–Biedl Syndrome: Identification of Novel Pathogenic Variants of BBS9. International Journal of Molecular Sciences. 25(15). 8313–8313.

Galosi, Serena, Cecilia Mancini, Paolo Calligari, et al.. (2024). Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome. Movement Disorders. 39(7). 1225–1231. 2 indexed citations

Accardi, Fabrizio, Benedetta Dalla Palma, Cecilia Mancini, et al.. (2023). P58 LOW CD38 EXPRESSION BY PLASMA CELLS IN EXTRAMEDULLARY DISEASE IN MULTIPLE MYELOMA PATIENTS. HemaSphere. 7(S2). 42–43.

Niceta, Marcello, Simone Pizzi, Francesca Clementina Radio, et al.. (2023). Case report: Novel compound heterozygosity for pathogenic variants in MED23 in a syndromic patient with postnatal microcephaly. Frontiers in Neurology. 14. 1090082–1090082. 1 indexed citations

Pollazzon, Marzia, Cecilia Mancini, Simone Pizzi, et al.. (2023). Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures. Frontiers in Neurology. 14. 1207176–1207176. 3 indexed citations

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

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

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

Pozzi, Elisa, Elisa Giorgio, Cecilia Mancini, et al.. (2020). In vitro dexamethasone treatment does not induce alternative ATM transcripts in cells from Ataxia–Telangiectasia patients. Scientific Reports. 10(1). 20182–20182. 2 indexed citations

10.

Richter, Uwe, Fumi Suomi, Paula Marttinen, et al.. (2019). Mitochondrial stress response triggered by defects in protein synthesis quality control. Life Science Alliance. 2(1). e201800219–e201800219. 33 indexed citations

11.

Cagnoli, Claudia, Alessandro Brussino, Cecilia Mancini, et al.. (2018). Spinocerebellar Ataxia Tethering PCR. Journal of Molecular Diagnostics. 20(3). 289–297. 15 indexed citations

12.

Rubino, Elisa, Cecilia Mancini, Silvia Boschi, et al.. (2018). ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementia. Neurobiology of Aging. 73. 231.e7–231.e9. 21 indexed citations

13.

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

14.

Biamino, Elisa, Eleonora Di Gregorio, Elga Fabia Belligni, et al.. (2015). A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(2). 290–299. 25 indexed citations

15.

Gregorio, Eleonora Di, Giovanni Botta, Alessandro Calcia, et al.. (2015). Array-Comparative Genomic Hybridization Analysis in Fetuses with Major Congenital Malformations Reveals that 24% of Cases Have Pathogenic Deletions/Duplications. Cytogenetic and Genome Research. 147(1). 10–16. 2 indexed citations

16.

Squadrone, Stefania, Paola Brizio, Cecilia Mancini, et al.. (2015). Blood metal levels and related antioxidant enzyme activities in patients with ataxia telangiectasia. Neurobiology of Disease. 81. 162–167. 11 indexed citations

17.

Storti, Paola, Marina Bolzoni, Gaetano Donofrío, et al.. (2013). Hypoxia-inducible factor (HIF)-1α suppression in myeloma cells blocks tumoral growth in vivo inhibiting angiogenesis and bone destruction. Leukemia. 27(8). 1697–1706. 89 indexed citations

18.

Garelli, Emanuela, Alfredo Brusco, Adriana Carando, et al.. (2012). High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assay. Haematologica. 97(12). 1813–1817. 44 indexed citations

19.

Mancini, Cecilia, et al.. (2011). Gene-targeted embryonic stem cells: real-time PCR assay for estimation of the number of neomycin selection cassettes. Biological Procedures Online. 13(1). 10–10. 10 indexed citations

20.

Russo, Alessandro, Marco Falcone, Antonio Vena, et al.. (2011). Invasive Pulmonary Aspergillosis in Non-Neutropenic Patients: Analysis of a 14-Month Prospective Clinical Experience. Journal of Chemotherapy. 23(5). 290–294. 21 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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