Romina Combi

1.7k total citations
38 papers, 1.1k citations indexed

About

Romina Combi is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Psychiatry and Mental health. According to data from OpenAlex, Romina Combi has authored 38 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 18 papers in Cellular and Molecular Neuroscience and 10 papers in Psychiatry and Mental health. Recurrent topics in Romina Combi's work include Neuroscience and Neuropharmacology Research (17 papers), Ion channel regulation and function (12 papers) and Nicotinic Acetylcholine Receptors Study (9 papers). Romina Combi is often cited by papers focused on Neuroscience and Neuropharmacology Research (17 papers), Ion channel regulation and function (12 papers) and Nicotinic Acetylcholine Receptors Study (9 papers). Romina Combi collaborates with scholars based in Italy, United States and France. Romina Combi's co-authors include Chiara Villa, Luigi Ferini‐Strambi, Maria Luisa Tenchini, L. Dalpr�, Marialuisa Lavitrano, Leda Dalprà, Andrea Galbiati, Serena Redaelli, Elena Salvatore and Veronica Sansoni and has published in prestigious journals such as PLoS ONE, Neurology and Oncogene.

In The Last Decade

Romina Combi

37 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Romina Combi Italy 19 496 375 349 155 150 38 1.1k
Kanehiro Hayashi Japan 19 549 1.1× 505 1.3× 248 0.7× 92 0.6× 194 1.3× 31 1.4k
Stanley F. Nelson United States 12 391 0.8× 145 0.4× 245 0.7× 197 1.3× 168 1.1× 16 1.1k
Emanuele Zurolo Netherlands 15 666 1.3× 534 1.4× 438 1.3× 59 0.4× 160 1.1× 16 1.6k
Luisa P. Cacheaux United States 9 510 1.0× 436 1.2× 315 0.9× 60 0.4× 98 0.7× 12 1.2k
Ida Manna Italy 23 510 1.0× 331 0.9× 310 0.9× 67 0.4× 162 1.1× 52 1.2k
Laura A. Jansen United States 14 512 1.0× 266 0.7× 221 0.6× 78 0.5× 316 2.1× 18 1.0k
Angelika Mühlebner Netherlands 24 497 1.0× 394 1.1× 792 2.3× 114 0.7× 340 2.3× 59 1.7k
David A. Rempe United States 16 559 1.1× 503 1.3× 167 0.5× 185 1.2× 67 0.4× 20 1.2k
Michelle Apperson United States 15 678 1.4× 450 1.2× 101 0.3× 89 0.6× 69 0.5× 25 1.2k
Michael P. Starkey United Kingdom 7 629 1.3× 209 0.6× 204 0.6× 143 0.9× 305 2.0× 11 1.2k

Countries citing papers authored by Romina Combi

Since Specialization
Citations

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

Fields of papers citing papers by Romina Combi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Romina Combi

This figure shows the co-authorship network connecting the top 25 collaborators of Romina Combi. A scholar is included among the top collaborators of Romina Combi 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 Romina Combi. Romina Combi 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.
Villa, Chiara & Romina Combi. (2024). Epigenetics in Alzheimer’s Disease: A Critical Overview. International Journal of Molecular Sciences. 25(11). 5970–5970. 11 indexed citations
2.
Villa, Chiara, Federica Arrigoni, Marialuisa Lavitrano, et al.. (2022). Exome Sequencing in an ADSHE Family: VUS Identification and Limits. International Journal of Environmental Research and Public Health. 19(19). 12548–12548.
3.
Martinelli, Marianna, Chiara Villa, Giovanni Sotgiu, et al.. (2020). Analysis of Human Papillomavirus (HPV) 16 Variants Associated with Cervical Infection in Italian Women. International Journal of Environmental Research and Public Health. 17(1). 306–306. 8 indexed citations
4.
Ferini‐Strambi, Luigi, Andrea Galbiati, & Romina Combi. (2019). Sleep disorder-related headaches. Neurological Sciences. 40(S1). 107–113. 45 indexed citations
5.
Villa, Chiara, et al.. (2019). Potassium channels in the neuronal homeostasis and neurodegenerative pathways underlying Alzheimer’s disease: An update. Mechanisms of Ageing and Development. 185. 111197–111197. 30 indexed citations
6.
Cortini, Francesca, et al.. (2019). Understanding the basis of Ehlers–Danlos syndrome in the era of the next-generation sequencing. Archives of Dermatological Research. 311(4). 265–275. 12 indexed citations
7.
Villa, Chiara, Cecilia Gotti, Milena Moretti, et al.. (2019). CHRNA2 and Nocturnal Frontal Lobe Epilepsy: Identification and Characterization of a Novel Loss of Function Mutation. Frontiers in Molecular Neuroscience. 12. 17–17. 19 indexed citations
8.
Binda, Anna, Ilaria Rivolta, Chiara Villa, et al.. (2018). A Novel KCNJ2 Mutation Identified in an Autistic Proband Affects the Single Channel Properties of Kir2.1. Frontiers in Cellular Neuroscience. 12. 76–76. 18 indexed citations
9.
Villa, Chiara & Romina Combi. (2016). Potassium Channels and Human Epileptic Phenotypes: An Updated Overview. Frontiers in Cellular Neuroscience. 10. 81–81. 103 indexed citations
10.
Nobili, Lino, Paola Proserpio, Romina Combi, et al.. (2014). Nocturnal Frontal Lobe Epilepsy. Current Neurology and Neuroscience Reports. 14(2). 424–424. 45 indexed citations
11.
Sansoni, Veronica, Matilde Forcella, Alessandra Mozzi, et al.. (2013). Functional Characterization of a CRH Missense Mutation Identified in an ADNFLE Family. PLoS ONE. 8(4). e61306–e61306. 17 indexed citations
12.
Sansoni, Veronica, Lino Nobili, Paola Proserpio, Luigi Ferini‐Strambi, & Romina Combi. (2011). A de novo mutation in an Italian sporadic patient affected by nocturnal frontal lobe epilepsy. Journal of Sleep Research. 21(3). 352–353. 10 indexed citations
13.
Combi, Romina, Serena Redaelli, Massimiliano Beghi, et al.. (2010). Clinical and genetic evaluation of a family showing both autism and epilepsy. Brain Research Bulletin. 82(1-2). 25–28. 6 indexed citations
14.
Combi, Romina, et al.. (2009). A rescuable folding defective Nav1.1 (SCN1A) sodium channel mutant causes GEFS+: Common mechanism in Nav1.1 related epilepsies?. Human Mutation. 30(7). E747–E760. 52 indexed citations
15.
Combi, Romina, Luigi Ferini‐Strambi, & Maria Luisa Tenchini. (2008). CHRNA2 mutations are rare in the NFLE population: Evaluation of a large cohort of Italian patients. Sleep Medicine. 10(1). 139–142. 16 indexed citations
16.
Combi, Romina, Elena Sala, Nicoletta Villa, et al.. (2008). Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver–Russell syndrome. Clinical Dysmorphology. 17(1). 35–39. 4 indexed citations
17.
Combi, Romina, Leda Dalprà, Luigi Ferini‐Strambi, & Maria Luisa Tenchini. (2005). Frontal lobe epilepsy and mutations of the corticotropin‐releasing hormone gene. Annals of Neurology. 58(6). 899–904. 36 indexed citations
18.
Combi, Romina, L. Dalpr�, Maria Luisa Tenchini, & Luigi Ferini‐Strambi. (2004). Autosomal dominant nocturnal frontal lobe epilepsy. Journal of Neurology. 251(8). 923–34. 169 indexed citations
19.
Combi, Romina. (2004). Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy. Brain Research Bulletin. 1 indexed citations
20.
Bonati, Maria Teresa, Romina Combi, Rosanna Asselta, et al.. (2002). Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families. Journal of Neurology. 249(8). 967–974. 22 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Kanehiro Hayashi Breakdown of academic impact, for papers by Stanley F. Nelson Breakdown of academic impact, for papers by Emanuele Zurolo Breakdown of academic impact, for papers by Luisa P. Cacheaux Breakdown of academic impact, for papers by Ida Manna Breakdown of academic impact, for papers by Laura A. Jansen Breakdown of academic impact, for papers by Angelika Mühlebner Breakdown of academic impact, for papers by David A. Rempe Breakdown of academic impact, for papers by Michelle Apperson Breakdown of academic impact, for papers by Michael P. Starkey
Rankless by CCL
2026