P. Tarantino

413 total citations
13 papers, 252 citations indexed

About

P. Tarantino is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, P. Tarantino has authored 13 papers receiving a total of 252 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Cellular and Molecular Neuroscience, 5 papers in Neurology and 3 papers in Molecular Biology. Recurrent topics in P. Tarantino's work include Parkinson's Disease Mechanisms and Treatments (5 papers), Nuclear Receptors and Signaling (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). P. Tarantino is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (5 papers), Nuclear Receptors and Signaling (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). P. Tarantino collaborates with scholars based in Italy. P. Tarantino's co-authors include Vittoria Rago, Amalia Carpino, L. Siciliano, Grazia Annesi, Concetta De Stefano, Aldo Quattrone, Ferdinanda Annesi, Giuseppe Nicoletti, Antonio Cerasa and Donatella Civitelli and has published in prestigious journals such as Neurology, Neuroscience and Neuroscience Letters.

In The Last Decade

P. Tarantino

12 papers receiving 239 citations

Peers

P. Tarantino
Özlem Akman Türkiye
P. Tarantino
Citations per year, relative to P. Tarantino P. Tarantino (= 1×) peers Özlem Akman

Countries citing papers authored by P. Tarantino

Since Specialization
Citations

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

Fields of papers citing papers by P. Tarantino

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. Tarantino

This figure shows the co-authorship network connecting the top 25 collaborators of P. Tarantino. A scholar is included among the top collaborators of P. Tarantino 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 P. Tarantino. P. Tarantino is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
1.
Tremolizzo, Lucio, L. Marzorati, Francesca Lanzani, et al.. (2011). Early-onset SCA17 with 43 TBP repeats: expanding the phenotype?. Neurological Sciences. 32(5). 941–943. 4 indexed citations
2.
Annesi, Ferdinanda, Elvira Valeria De Marco, Alessandra Nicoletti, et al.. (2011). Association study between the LINGO1 gene and Parkinson’s disease in the Italian population. Parkinsonism & Related Disorders. 17(8). 638–641. 10 indexed citations
3.
Nicoletti, Giuseppe, Ferdinanda Annesi, Donatella Civitelli, et al.. (2010). Novel human pathological mutations. Gene symbol: PINK1. Disease: Parkinson disease.. PubMed. 127(4). 464–464.
4.
Cerasa, Antonio, Andrea Cherubini, Aldo Quattrone, et al.. (2010). Met158 variant of the catechol-O-methyltransferase genotype is associated with thicker cortex in adult brain. Neuroscience. 167(3). 809–814. 32 indexed citations
5.
Tarantino, P., Ferdinanda Annesi, Elvira Valeria De Marco, et al.. (2010). Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson disease.. PubMed. 127(4). 463–463. 5 indexed citations
6.
Annesi, Grazia, P. Tarantino, Giuseppe Nicoletti, et al.. (2009). DJ‐1 is a Parkinson's disease susceptibility gene in southern Italy. Clinical Genetics. 77(2). 183–188. 21 indexed citations
7.
Cerasa, Antonio, Maria Cecilia Gioia, P. Tarantino, et al.. (2009). The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individuals. Genes Brain & Behavior. 8(4). 459–463. 25 indexed citations
8.
Marco, Elvira Valeria De, P. Tarantino, Giovanni Provenzano, et al.. (2007). Alpha‐synuclein promoter haplotypes and dementia in Parkinson's Disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(3). 403–407. 15 indexed citations
9.
Carrideo, Sara, P. Tarantino, Giovanni Provenzano, et al.. (2007). Novel human pathological mutations. Gene symbol: MEN1. Disease: MEN1, Multiple endocrine neoplasia, type 1.. PubMed. 122(3-4). 415–415. 2 indexed citations
10.
Carpino, Amalia, P. Tarantino, Vittoria Rago, Vincenzo De Sanctis, & L. Siciliano. (2004). Antioxidant Capacity in Seminal Plasma of Transfusion-Dependent β-Thalassemic Patients. Experimental and Clinical Endocrinology & Diabetes. 112(3). 131–134. 10 indexed citations
11.
Pugliese, Pierfrancesco, Grazia Annesi, Nunzio Cutuli, et al.. (2004). The fragile X premutation presenting as postprandial hypotension. Neurology. 63(11). 2188–2189. 15 indexed citations
12.
Spadafora, Patrizia, Grazia Annesi, Angela Aurora Pasqua, et al.. (2003). NACP-REP1 polymorphism is not involved in Parkinson's disease: a case-control study in a population sample from southern Italy. Neuroscience Letters. 351(2). 75–78. 38 indexed citations
13.
Siciliano, L., et al.. (2001). Impaired Seminal Antioxidant Capacity in Human Semen With Hyperviscosity or Oligoasthenozoospermia. Journal of Andrology. 22(5). 798–803. 75 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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