Grazia Annesi

9.0k total citations
94 papers, 2.7k citations indexed

About

Grazia Annesi is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Grazia Annesi has authored 94 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Neurology, 42 papers in Cellular and Molecular Neuroscience and 34 papers in Molecular Biology. Recurrent topics in Grazia Annesi's work include Parkinson's Disease Mechanisms and Treatments (38 papers), Neurological disorders and treatments (21 papers) and Genetic Neurodegenerative Diseases (16 papers). Grazia Annesi is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (38 papers), Neurological disorders and treatments (21 papers) and Genetic Neurodegenerative Diseases (16 papers). Grazia Annesi collaborates with scholars based in Italy, United States and Canada. Grazia Annesi's co-authors include Aldo Quattrone, Antonio Gambardella, Ferdinanda Annesi, Giuseppe Nicoletti, Patrizia Tarantino, Donatella Civitelli, Enzo Wanke, Mario Zappia, Elvira Valeria De Marco and Sara Carrideo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Grazia Annesi

89 papers receiving 2.7k citations

Peers

Grazia Annesi

CMN

NEURO

PMH

GENET

Yvonne Weber Germany

Jean‐Marc Burgunder Switzerland

Ornit Chiba‐Falek United States

Pau Pástor Spain

Christiane Penet France

M. Ben Hamida Tunisia

Jan K. Teller United States

Mario Ezquerra Spain

Björn Holmberg Sweden

Olof Sydow Sweden

Yvonne Weber Germany

Grazia Annesi

816 ×0.7

CMN

354 ×0.3

NEURO

1.2k ×1.1

867 ×1.4

PMH

677 ×1.5

GENET

Citations per year, relative to Grazia Annesi Grazia Annesi (= 1×) peers Yvonne Weber

Countries citing papers authored by Grazia Annesi

Since Specialization

Citations

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

Fields of papers citing papers by Grazia Annesi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Grazia Annesi

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

All Works

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20 of 20 papers shown

Gagliardi, Monica, Francesco Fortunato, Anna Caterina Procopio, et al.. (2024). Two Novel Variants in the CHRNA2 and SCN2A Genes in Italian Patients with Febrile Seizures. Genes. 15(11). 1407–1407.

Gagliardi, Monica, Andrea Quattrone, Gennarina Arabia, et al.. (2023). ANXA1 mutation analysis in Italian patients with early onset PD. Neurobiology of Aging. 125. 123–124. 1 indexed citations

Salsone, Maria, Gennarina Arabia, Grazia Annesi, et al.. (2021). Aceruloplasminemia: a multimodal imaging study in an Italian family with a novel mutation. Neurological Sciences. 43(3). 1791–1797. 4 indexed citations

Gagliardi, Monica, Marco D’Amelio, Laura Brighina, et al.. (2020). DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB. Neurobiology of Aging. 93. 143.e5–143.e7. 3 indexed citations

Bonapace, Giuseppe, Daniela Concolino, Monica Gagliardi, et al.. (2019). Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by fragile X tremor ataxia syndrome. Heliyon. 5(6). e01954–e01954. 6 indexed citations

Gagliardi, Monica, et al.. (2018). Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria. Journal of the Neurological Sciences. 390. 209–211. 5 indexed citations

Gagliardi, Monica, et al.. (2016). Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria. Neurobiology of Aging. 50. 169.e5–169.e6. 6 indexed citations

Gagliardi, Monica, Maurizio Morelli, Grazia Annesi, et al.. (2015). A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification. Gene. 568(1). 109–111. 12 indexed citations

Gagliardi, Monica, Grazia Annesi, Patrizia Tarantino, et al.. (2014). PCDH19 mutations in female patients from Southern Italy. Seizure. 24. 118–120. 7 indexed citations

10.

Nicoletti, Alessandra, Giuseppe Nicoletti, Gennarina Arabia, et al.. (2011). Reproductive factors and Parkinson's disease: A multicenter case–control study. Movement Disorders. 26(14). 2563–2566. 29 indexed citations

11.

Nicoletti, Giuseppe, Ferdinanda Annesi, Donatella Civitelli, et al.. (2010). Novel human pathological mutations. Gene symbol: PINK1. Disease: Parkinson disease.. PubMed. 127(4). 464–464.

12.

Nicoletti, Alessandra, Pierfrancesco Pugliese, Giuseppe Nicoletti, et al.. (2010). Voluptuary habits and clinical subtypes of Parkinson's disease: The FRAGAMP case–control study. Movement Disorders. 25(14). 2387–2394. 34 indexed citations

13.

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

14.

Quattrone, Aldo, Grazia Annesi, Fabiana Novellino, et al.. (2007). Myocardial ¹²³metaiodobenzylguanidine uptake in genetic Parkinson's disease. Movement Disorders. 23(1). 21–27. 49 indexed citations

15.

Mantegazza, Massimo, Antonio Gambardella, Raffaella Rusconi, et al.. (2005). Identification of an Na _v 1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures. Proceedings of the National Academy of Sciences. 102(50). 18177–18182. 154 indexed citations

16.

Toscano, António, Sonia Messina, Giuseppe M. Campo, et al.. (2005). Oxidative stress in myotonic dystrophy type 1. Free Radical Research. 39(7). 771–776. 45 indexed citations

17.

Annesi, Grazia, Giuseppe Nicoletti, Patrizia Tarantino, et al.. (2004). FRAXE intermediate alleles are associated with Parkinson’s disease. Neuroscience Letters. 368(1). 21–24. 13 indexed citations

18.

Uncini, Antonino, Maria Vittoria De Angelis, Patrizia Di Fulvio, et al.. (2004). Wide expressivity variation and high but no gender‐related penetrance in two dopa‐responsive dystonia families with a novel GCH‐I mutation. Movement Disorders. 19(10). 1139–1145. 15 indexed citations

19.

Gambardella, Antonio, Demetrio Messina, Emilio Le Piane, et al.. (2000). Familial temporal lobe epilepsy. Epilepsy Research. 38(2-3). 127–132. 43 indexed citations

20.

Gambardella, Antonio, Paola Valentino, Grazia Annesi, et al.. (1999). Hyperekplexia in a patient with a brainstem vascular anomaly. Acta Neurologica Scandinavica. 99(4). 255–259. 10 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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