Francesca Menni

1.6k total citations
46 papers, 1.0k citations indexed

About

Francesca Menni is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Francesca Menni has authored 46 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Clinical Biochemistry and 13 papers in Rheumatology. Recurrent topics in Francesca Menni's work include Metabolism and Genetic Disorders (13 papers), Lysosomal Storage Disorders Research (6 papers) and Glycogen Storage Diseases and Myoclonus (6 papers). Francesca Menni is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Lysosomal Storage Disorders Research (6 papers) and Glycogen Storage Diseases and Myoclonus (6 papers). Francesca Menni collaborates with scholars based in Italy, United Kingdom and Germany. Francesca Menni's co-authors include Susanna Esposito, Donatella Milani, Pascale de Lonlay, Caroline Sevin, Valérie Barbier, Jean-Marie Saudubray, Guy Touati, Claire Nihoul‐Feketé, Sophie Guez and Rossella Parini and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and Journal of Hepatology.

In The Last Decade

Francesca Menni

45 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Francesca Menni Italy 17 271 253 208 173 173 46 1.0k
Katarina Trebušak Podkrajšek Slovenia 22 373 1.4× 255 1.0× 160 0.8× 257 1.5× 119 0.7× 92 1.2k
Isabelle Fajardy France 20 301 1.1× 184 0.7× 153 0.7× 259 1.5× 180 1.0× 44 1.5k
Todor Arsov Australia 18 255 0.9× 139 0.5× 226 1.1× 86 0.5× 98 0.6× 41 1.1k
Anna Elsa Maria Allegri Italy 18 285 1.1× 336 1.3× 108 0.5× 131 0.8× 63 0.4× 43 830
N. Sörensen Germany 20 397 1.5× 556 2.2× 233 1.1× 297 1.7× 50 0.3× 62 1.5k
J Coll Spain 17 415 1.5× 57 0.2× 239 1.1× 122 0.7× 204 1.2× 46 1.1k
Tatsuro Izumi Japan 16 225 0.8× 59 0.2× 79 0.4× 184 1.1× 50 0.3× 70 895
Ayfer Alikaşifoğlu Türkiye 20 381 1.4× 502 2.0× 91 0.4× 167 1.0× 77 0.4× 99 1.2k
Uta Tacke Germany 13 329 1.2× 55 0.2× 472 2.3× 96 0.6× 127 0.7× 27 1.3k
S. Variend United Kingdom 20 426 1.6× 47 0.2× 85 0.4× 137 0.8× 124 0.7× 49 1.2k

Countries citing papers authored by Francesca Menni

Since Specialization
Citations

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

Fields of papers citing papers by Francesca Menni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Menni

This figure shows the co-authorship network connecting the top 25 collaborators of Francesca Menni. A scholar is included among the top collaborators of Francesca Menni 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 Francesca Menni. Francesca Menni 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.
Bani, Marco, Selena Russo, Serena Gasperini, et al.. (2024). Prevalence and predictors of parental distress at the communication of positivity at newborn screening for metabolic diseases: an Italian longitudinal study. BMJ Paediatrics Open. 8(1). e003103–e003103.
2.
Cattaneo, Valentina, Alessio Caccioppola, Sebastiano Maria Colombo, et al.. (2023). Hyperammonemia Syndrome After Lung Transplantation: A Double-Hit Fatal Syndrome. A Case Report. Transplantation Proceedings. 55(8). 1991–1994. 1 indexed citations
3.
Bani, Marco, Selena Russo, Serena Gasperini, et al.. (2023). Parents' experience of the communication process of positivity at newborn screening for metabolic diseases: A qualitative study. Child Care Health and Development. 49(6). 961–971. 6 indexed citations
4.
Consales, Alessandra, Beatrice Letizia Crippa, Lorenzo Colombo, et al.. (2022). CHARGE syndrome presenting with persistent hypoglycemia: case report and overview of the main genetic syndromes associated with neonatal hypoglycemia. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 48(1). 154–154. 2 indexed citations
5.
Paoletti, Matteo, Anna Pichiecchio, Giovanna Stefania Colafati, et al.. (2020). Multicentric Retrospective Evaluation of Five Classic Infantile Pompe Disease Subjects Under Enzyme Replacement Therapy With Early Infratentorial Involvement. Frontiers in Neurology. 11. 569153–569153. 9 indexed citations
6.
Dilena, Robertino, Sophie Guez, Francesca Menni, et al.. (2019). Pseudotumour cerebri associated with mycoplasma pneumoniae infection and treatment with levofloxacin: a case report. BMC Pediatrics. 19(1). 4–4. 5 indexed citations
7.
Tucci, Arianna, Veronica Saletti, Francesca Menni, et al.. (2017). The absence that makes the difference: choroidal abnormalities in Legius syndrome. Journal of Human Genetics. 62(11). 1001–1004. 5 indexed citations
8.
Ardissino, Gianluigi, Michela Perrone, Francesca Tel, et al.. (2017). Late Onset Cobalamin Disorder and Hemolytic Uremic Syndrome: A Rare Cause of Nephrotic Syndrome. SHILAP Revista de lepidopterología. 2017(1). 2794060–2794060. 10 indexed citations
9.
Milani, Donatella, Francesca Manzoni, Lidia Pezzani, et al.. (2015). Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 41(1). 4–4. 86 indexed citations
10.
Esposito, Susanna, Marta Cerutti, Donatella Milani, Francesca Menni, & Nicola Principi. (2015). Vaccination coverage of children with rare genetic diseases and attitudes of their parents toward vaccines. Human Vaccines & Immunotherapeutics. 12(3). 801–805. 11 indexed citations
11.
Rodríguez, Anabel, et al.. (2014). Evaluación de tecnologías alternativas de manejo para disminuir los daños causados por el viento en frutos de pera cv. Williams, en el alto valle de Río Negro, Argentina. SHILAP Revista de lepidopterología. 2 indexed citations
12.
Rodríguez, Anabel, et al.. (2014). Evaluation of alternative management technologies to reduce wind damage in fruits of pear cv. Williams, Upper Black River Valley, Argentina.. 40(2). 208–212. 1 indexed citations
13.
Diodato, Daria, Federica Invernizzi, Eleonora Lamantea, et al.. (2014). Common and Novel TMEM70 Mutations in a Cohort of Italian Patients with Mitochondrial Encephalocardiomyopathy. JIMD Reports. 15. 71–8. 23 indexed citations
14.
Menni, Francesca, Maria Francesca Bedeschi, Federica Natacci, et al.. (2013). Healthcare transition in patients with rare genetic disorders with and without developmental disability: Neurofibromatosis 1 and williams–beuren syndrome. American Journal of Medical Genetics Part A. 161(7). 1666–1674. 36 indexed citations
15.
Russo, Silvia, et al.. (2013). Think About It. Journal of Child Neurology. 29(9). NP74–NP77. 11 indexed citations
16.
Bergamaschi, S., Claudia Giavoli, Eriselda Profka, et al.. (2012). A particular phenotype in a case of Down-Turner syndrome. 15th International & 14th European Congress of Endocrinology. 29. 2 indexed citations
17.
Milani, Donatella, et al.. (2012). De novo Deletion of 1q31.1–q32.1 in a Patient with Developmental Delay and Behavioral Disorders. Cytogenetic and Genome Research. 136(3). 167–170. 4 indexed citations
18.
19.
Milani, Donatella, Anna Cereda, Marta Cerutti, et al.. (2009). Clinical problems and everyday abilities of a group of Italian adolescent and young adults with Cornelia de Lange syndrome. American Journal of Medical Genetics Part A. 149A(11). 2532–2537. 6 indexed citations
20.
Parini, Rossella, Francesca Furlan, Luigi D. Notarangelo, et al.. (2008). Glucose metabolism and diet-based prevention of liver dysfunction in MPV17 mutant patients. Journal of Hepatology. 50(1). 215–221. 36 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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