Paolo Forleo

1.2k total citations
25 papers, 730 citations indexed

About

Paolo Forleo is a scholar working on Physiology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Paolo Forleo has authored 25 papers receiving a total of 730 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Physiology, 11 papers in Molecular Biology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Paolo Forleo's work include Alzheimer's disease research and treatments (12 papers), Cholinesterase and Neurodegenerative Diseases (4 papers) and Dementia and Cognitive Impairment Research (4 papers). Paolo Forleo is often cited by papers focused on Alzheimer's disease research and treatments (12 papers), Cholinesterase and Neurodegenerative Diseases (4 papers) and Dementia and Cognitive Impairment Research (4 papers). Paolo Forleo collaborates with scholars based in Italy. Paolo Forleo's co-authors include Sandro Sorbi, Luigi Amaducci, Benedetta Nacmias, Silvia Piacentini, Stefania Latorraca, Marinella Marinoni, Andrea Tedde, M. Ida Gobbini, Elena Cellini and Laura Bracco and has published in prestigious journals such as Neurology, Annals of Neurology and Biological Psychiatry.

In The Last Decade

Paolo Forleo

24 papers receiving 710 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paolo Forleo Italy 15 387 252 154 154 151 25 730
Y. Robitaille Canada 18 605 1.6× 408 1.6× 226 1.5× 129 0.8× 212 1.4× 26 1.1k
T. Bird United States 12 358 0.9× 305 1.2× 128 0.8× 173 1.1× 286 1.9× 16 904
Guiqiong He China 6 375 1.0× 232 0.9× 87 0.6× 69 0.4× 74 0.5× 7 644
Kevin P. Koster United States 11 395 1.0× 236 0.9× 135 0.9× 78 0.5× 49 0.3× 17 697
Yuetiva Deming United States 15 631 1.6× 329 1.3× 80 0.5× 222 1.4× 102 0.7× 40 1.3k
Martha Foiani United Kingdom 18 408 1.1× 312 1.2× 153 1.0× 211 1.4× 256 1.7× 23 855
Catherine Joachim United Kingdom 11 426 1.1× 176 0.7× 113 0.7× 212 1.4× 469 3.1× 16 921
Giada Mascio Italy 14 242 0.6× 283 1.1× 185 1.2× 99 0.6× 99 0.7× 28 828
Amber Nolan United States 14 251 0.6× 166 0.7× 68 0.4× 167 1.1× 236 1.6× 31 727
Adriana Cardozo Spain 16 294 0.8× 214 0.8× 222 1.4× 63 0.4× 403 2.7× 27 832

Countries citing papers authored by Paolo Forleo

Since Specialization
Citations

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

Fields of papers citing papers by Paolo Forleo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paolo Forleo

This figure shows the co-authorship network connecting the top 25 collaborators of Paolo Forleo. A scholar is included among the top collaborators of Paolo Forleo 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 Paolo Forleo. Paolo Forleo 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.
Matà, Sabrina, et al.. (2021). Polyneuropathy and monoclonal gammopathy of undetermined significance (MGUS); update of a clinical experience. Journal of the Neurological Sciences. 423. 117335–117335. 4 indexed citations
2.
Prestipino, Elio, et al.. (2018). A case of Takotsubo syndrome during a multiple sclerosis brainstem relapse. Multiple Sclerosis and Related Disorders. 24. 1–2. 11 indexed citations
3.
Cellini, Elena, Paolo Forleo, Andrea Ginestroni, et al.. (2006). Fragile X Premutation With Atypical Symptoms at Onset. Archives of Neurology. 63(8). 1135–1135. 15 indexed citations
4.
Tedde, Andrea, Benedetta Nacmias, Paolo Forleo, et al.. (2003). Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease. Archives of Neurology. 60(11). 1541–1541. 40 indexed citations
5.
Cellini, Elena, Silvia Piacentini, Benedetta Nacmias, et al.. (2002). A Family With Spinocerebellar Ataxia Type 8 Expansion and Vitamin E Deficiency Ataxia. Archives of Neurology. 59(12). 1952–1952. 10 indexed citations
6.
Sorbi, Sandro, Paolo Forleo, Andrea Tedde, et al.. (2001). Genetic risk factors in familial Alzheimer's disease. Mechanisms of Ageing and Development. 122(16). 1951–1960. 23 indexed citations
7.
Nacmias, Benedetta, Andrea Tedde, Elena Cellini, et al.. (2001). α2-Macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease. Neuroscience Letters. 299(1-2). 9–12. 15 indexed citations
8.
Nacmias, Benedetta, Andrea Tedde, Paolo Forleo, et al.. (2001). Psychosis, serotonin receptor polymorphism and Alzheimer's disease. Archives of Gerontology and Geriatrics. 33. 279–283.
9.
Nacmias, Benedetta, Andrea Tedde, Paolo Forleo, et al.. (2001). Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer’s disease. Biological Psychiatry. 50(6). 472–475. 47 indexed citations
10.
Cellini, Elena, Paolo Forleo, Benedetta Nacmias, et al.. (2001). Clinical and genetic analysis of hereditary and sporadic ataxia in central Italy. Brain Research Bulletin. 56(3-4). 363–366. 5 indexed citations
11.
Sorbi, Sandro, et al.. (2000). Double-Blind, Crossover, Placebo-Controlled Clinical Trial with L-Acetylcarnitine in Patients with Degenerative Cerebellar Ataxia. Clinical Neuropharmacology. 23(2). 114–118. 28 indexed citations
12.
Nacmias, Benedetta, Gabriella Marcon, Andrea Tedde, et al.. (1998). Implication of α1-antichymotrypsin polymorphism in familial Alzheimer's disease. Neuroscience Letters. 244(2). 85–88. 14 indexed citations
13.
Sorbi, Sandro, Benedetta Nacmias, Andrea Tedde, et al.. (1998). No implication of apolipoprotein E polymorphism in Italian schizophrenic patients. Neuroscience Letters. 244(2). 118–120. 20 indexed citations
14.
Sorbi, Sandro, Benedetta Nacmias, Andrea Tedde, et al.. (1997). Presenilin-1 gene intronic polymorphism in sporadic and familial Azheimer's disease. Neuroscience Letters. 222(2). 132–134. 26 indexed citations
15.
Forleo, Paolo, Dominique Couchie, Sandrine Chabas, & Jacques Nunez. (1996). Four repeat high-mol-wt MAP2 forms in rat dorsal root ganglia. Journal of Molecular Neuroscience. 7(3). 193–201. 12 indexed citations
16.
Sorbi, Sandro, Benedetta Nacmias, Paolo Forleo, Silvia Piacentini, & L. Amaducci. (1996). Alzheimer's Disease and Apolipoprotein E in Italya. Annals of the New York Academy of Sciences. 777(1). 260–265. 18 indexed citations
17.
Nacmias, Benedetta, Stefania Latorraca, Paolo Forleo, et al.. (1995). ApoE genotype and familial Alzheimer's disease: a possible influence on age of onset in APP717 Val → Ile mutated families. Neuroscience Letters. 183(1-2). 1–3. 62 indexed citations
18.
Sorbi, Sandro, Benedetta Nacmias, Paolo Forleo, et al.. (1995). Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease. Annals of Neurology. 38(1). 124–127. 84 indexed citations
19.
Sorbi, Sandro, Benedetta Nacmias, Paolo Forleo, et al.. (1994). ApoE allele frequencies in Italian sporadic and familial Alzheimer's disease. Neuroscience Letters. 177(1-2). 100–102. 124 indexed citations
20.
Sorbi, Sandro, Benedetta Nacmias, Marzia Mortilla, et al.. (1994). Molecular genetics of Alzheimer's disease in Italian families. Neurochemistry International. 25(1). 81–84. 2 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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