Michela Ranieri

712 total citations
8 papers, 350 citations indexed

About

Michela Ranieri is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Michela Ranieri has authored 8 papers receiving a total of 350 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Neurology and 3 papers in Genetics. Recurrent topics in Michela Ranieri's work include Neurogenetic and Muscular Disorders Research (3 papers), Mitochondrial Function and Pathology (3 papers) and ATP Synthase and ATPases Research (3 papers). Michela Ranieri is often cited by papers focused on Neurogenetic and Muscular Disorders Research (3 papers), Mitochondrial Function and Pathology (3 papers) and ATP Synthase and ATPases Research (3 papers). Michela Ranieri collaborates with scholars based in Italy, United States and United Kingdom. Michela Ranieri's co-authors include Nereo Bresolin, Giacomo P. Comi, Stefania Corti, Giulietta Riboldi, Dario Ronchi, Francesca Magri, Simona Brajkovic, Federica Rizzo, Roberto Del Bo and Monica Sciacco and has published in prestigious journals such as Brain, Neurobiology of Aging and Journal of the Neurological Sciences.

In The Last Decade

Michela Ranieri

8 papers receiving 348 citations

Peers

Michela Ranieri

MB

NEURO

GENET

CB

PHYSI

Samira Ait-El-Mkadem France

Amar Mubaidin Jordan

Allison R. Hanaford United States

F Valsecchi Italy

Akihiko Miyauchi Japan

Tim M. Strom Germany

Motoki Sano Japan

Anna Marcé‐Grau Spain

Hannah E. Steele United Kingdom

Kathrin Jeltsch Germany

Samira Ait-El-Mkadem France

Michela Ranieri

278 ×1.3

MB

64 ×0.4

NEURO

29 ×0.4

GENET

66 ×0.9

CB

66 ×1.4

PHYSI

Citations per year, relative to Michela Ranieri Michela Ranieri (= 1×) peers Samira Ait-El-Mkadem

Countries citing papers authored by Michela Ranieri

Since Specialization

Citations

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

Fields of papers citing papers by Michela Ranieri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michela Ranieri

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

All Works

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8 of 8 papers shown

1.

Riboldi, Giulietta, Chiara Zanetta, Michela Ranieri, et al.. (2014). Antisense Oligonucleotide Therapy for the Treatment of C9ORF72 ALS/FTD Diseases. Molecular Neurobiology. 50(3). 721–732. 46 indexed citations

2.

Bersano, Anna, Michela Ranieri, Andrea Ciammola, et al.. (2013). Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variant.. PubMed. 27(4). 247–52. 16 indexed citations

3.

Ranieri, Michela, Simona Brajkovic, Giulietta Riboldi, et al.. (2013). Mitochondrial Fusion Proteins and Human Diseases. Neurology Research International. 2013. 1–11. 86 indexed citations

4.

Ronchi, Dario, Caterina Garone, Andrea Bordoni, et al.. (2012). Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions. Brain. 135(11). 3404–3415. 73 indexed citations

5.

Riboldi, Giulietta, Roberto Del Bo, Michela Ranieri, et al.. (2011). Tyr78Phe Transthyretin Mutation with Predominant Motor Neuropathy as the Initial Presentation. Case Reports in Neurology. 3(1). 62–68. 15 indexed citations

6.

Ranieri, Michela, Roberto Del Bo, Andreina Bordoni, et al.. (2011). Optic atrophy plus phenotype due to mutations in the OPA1 gene: Two more Italian families. Journal of the Neurological Sciences. 315(1-2). 146–149. 20 indexed citations

7.

Bo, Roberto Del, Serena Ghezzi, Stefania Corti, et al.. (2009). TARDBP (TDP‐43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations. European Journal of Neurology. 16(6). 727–732. 81 indexed citations

8.

Bo, Roberto Del, Stefania Corti, Domenico Santoro, et al.. (2009). No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort. Neurobiology of Aging. 32(6). 1157–1158. 13 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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