Francesca Madia

4.6k total citations
62 papers, 1.0k citations indexed

About

Francesca Madia is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Francesca Madia has authored 62 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Neurology, 17 papers in Molecular Biology and 17 papers in Genetics. Recurrent topics in Francesca Madia's work include Peripheral Neuropathies and Disorders (12 papers), Hereditary Neurological Disorders (12 papers) and Genetics and Neurodevelopmental Disorders (12 papers). Francesca Madia is often cited by papers focused on Peripheral Neuropathies and Disorders (12 papers), Hereditary Neurological Disorders (12 papers) and Genetics and Neurodevelopmental Disorders (12 papers). Francesca Madia collaborates with scholars based in Italy, United States and United Kingdom. Francesca Madia's co-authors include Mario Sabatelli, Federico Zara, Pasquale Striano, Amelia Conte, Marco Luigetti, Carlo Minetti, Alessandra Del Grande, Elena Di Gennaro, P. Tonali and P. Tonali and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Epilepsia.

In The Last Decade

Francesca Madia

60 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 Madia Italy 18 438 351 292 290 180 62 1.0k
Vincenzo Salpietro Italy 22 245 0.6× 481 1.4× 387 1.3× 199 0.7× 150 0.8× 89 1.2k
Salah Omer United Kingdom 11 769 1.8× 390 1.1× 312 1.1× 217 0.7× 89 0.5× 17 1.2k
Makoto Hara Japan 20 838 1.9× 218 0.6× 178 0.6× 247 0.9× 82 0.5× 105 1.4k
S. Binelli Italy 20 188 0.4× 209 0.6× 109 0.4× 185 0.6× 387 2.1× 43 926
Rick van Minkelen Netherlands 20 472 1.1× 292 0.8× 150 0.5× 68 0.2× 108 0.6× 36 878
J. C. Antoine France 15 1.3k 2.9× 331 0.9× 210 0.7× 578 2.0× 41 0.2× 28 1.6k
H.-M. Meinck Germany 13 952 2.2× 362 1.0× 215 0.7× 553 1.9× 35 0.2× 18 1.4k
Hideji Hashida Japan 19 434 1.0× 672 1.9× 81 0.3× 520 1.8× 45 0.3× 49 1.2k
Hillary Lipe United States 24 600 1.4× 593 1.7× 110 0.4× 945 3.3× 85 0.5× 40 1.5k
Karine Lascelles United Kingdom 16 143 0.3× 295 0.8× 183 0.6× 136 0.5× 109 0.6× 25 858

Countries citing papers authored by Francesca Madia

Since Specialization
Citations

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

Fields of papers citing papers by Francesca Madia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Madia

This figure shows the co-authorship network connecting the top 25 collaborators of Francesca Madia. A scholar is included among the top collaborators of Francesca Madia 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 Madia. Francesca Madia 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.
Scala, Marcello, Yu Zhang, Mariasavina Severino, et al.. (2025). A hypomorphic FLVCR2 variant resulting in moderate transport deficiency causes hydranencephaly syndrome with brain calcifications. European Journal of Human Genetics. 34(3). 324–332. 1 indexed citations
2.
Scala, Marcello, Patrizia De Marco, Marzia Ognibene, et al.. (2023). Somatic Double Inactivation of NF1 Associated with NF1-Related Pectus Excavatum Deformity. Human Mutation. 2023. 1–7. 3 indexed citations
3.
Scala, Marcello, Francesca Madia, Diego Vozzi, et al.. (2023). MYT1L variant inherited by a mosaic father in a case of severe developmental and epileptic encephalopathy. Epileptic Disorders. 25(6). 874–879.
4.
Amadori, Elisabetta, Francesca Madia, Mariasavina Severino, et al.. (2023). Case Report: Novel biallelic moderately damaging variants in RTTN in a patient with cerebellar dysplasia. Frontiers in Pediatrics. 11. 1326552–1326552. 2 indexed citations
5.
Accogli, Andrea, Ana Filipa Geraldo, Gianluca Piccolo, et al.. (2022). Diagnostic Approach to Macrocephaly in Children. Frontiers in Pediatrics. 9. 794069–794069. 25 indexed citations
6.
Marengo, Barbara, Alessandra Pulliero, Maria Valeria Corrias, et al.. (2021). Potential Role of miRNAs in the Acquisition of Chemoresistance in Neuroblastoma. Journal of Personalized Medicine. 11(2). 107–107. 5 indexed citations
7.
Luigetti, Marco, Ângela Romano, Andrea Di Paolantonio, et al.. (2020). Pathological Findings in Chronic Inflammatory Demyelinating Polyradiculoneuropathy: A Single-Center Experience. Brain Sciences. 10(6). 383–383. 7 indexed citations
8.
Luigetti, Marco, Andrea Di Paolantonio, Giulia Bisogni, et al.. (2019). Sural nerve biopsy in peripheral neuropathies: 30-year experience from a single center. Neurological Sciences. 41(2). 341–346. 12 indexed citations
9.
Traverso, Monica, Stefania Assereto, Michele Iacomino, et al.. (2018). Clinical and molecular consequences of exon 78 deletion in DMD gene. Journal of Human Genetics. 63(6). 761–764. 7 indexed citations
10.
Bernardo, Pia, Francesca Madia, Lia Santulli, et al.. (2016). 17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome. Brain and Development. 38(7). 663–668. 7 indexed citations
11.
Luigetti, Marco, Amelia Conte, Nicola Montano, et al.. (2012). Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy. Journal of the Neurological Sciences. 319(1-2). 75–80. 17 indexed citations
12.
Sabatelli, Mario, Marcella Zollino, Marco Luigetti, et al.. (2011). Uncovering amyotrophic lateral sclerosis phenotypes: Clinical features and long-term follow-up of upper motor neuron-dominant ALS. Amyotrophic Lateral Sclerosis. 12(4). 278–282. 31 indexed citations
13.
Grande, Alessandra Del, Amelia Conte, Serena Lattante, et al.. (2011). D11Y SOD1 mutation and benign ALS: A consistent genotype-phenotype correlation. Journal of the Neurological Sciences. 309(1-2). 31–33. 7 indexed citations
14.
Luigetti, Marco, Antonio Pizzuti, Stefano Bartoletti, et al.. (2010). Triple A syndrome: A novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. Journal of the Neurological Sciences. 290(1-2). 150–152. 11 indexed citations
15.
Luigetti, Marco, Gian Maria Fabrizi, Francesca Madia, et al.. (2010). A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. Journal of the Neurological Sciences. 298(1-2). 114–117. 38 indexed citations
16.
Canafoglia, Laura, Elisa Visani, Ferruccio Panzica, et al.. (2010). Short and long interval cortical inhibition in patients with Unverricht-Lundborg and Lafora body disease. Epilepsy Research. 89(2-3). 232–237. 28 indexed citations
17.
Luigetti, Marco, Francesca Madia, Amelia Conte, et al.. (2009). SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis. 10(5-6). 479–482. 10 indexed citations
18.
Striano, Pasquale, Antonietta Coppola, Francesca Madia, et al.. (2007). Life‐Threatening Status Epilepticus Following Gabapentin Administration in a Patient with Benign Adult Familial Myoclonic Epilepsy. Epilepsia. 48(10). 1995–1998. 27 indexed citations
19.
Baykan, Betül, Francesca Madia, Nerses Bebek, et al.. (2004). Autosomal Recessive Idiopathic Epilepsy in an Inbred Family from Turkey: Identification of a Putative Locus on Chromosome 9q32‐33. Epilepsia. 45(5). 479–487. 9 indexed citations
20.
Padua, Luca, Pietro Caliandro, Irene Aprile, et al.. (2004). Occurrence of nerve entrapment lesion in chronic inflammatory demyelinating polyneuropathy. Clinical Neurophysiology. 115(5). 1140–1144. 8 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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