Andrés Berardo

777 total citations
16 papers, 384 citations indexed

About

Andrés Berardo is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Andrés Berardo has authored 16 papers receiving a total of 384 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 4 papers in Clinical Biochemistry. Recurrent topics in Andrés Berardo's work include Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Andrés Berardo is often cited by papers focused on Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Andrés Berardo collaborates with scholars based in United States, Argentina and Finland. Andrés Berardo's co-authors include Michio Hirano, Salvatore DiMauro, Catarina M. Quinzii, Ali Naini, Valentina Emmanuele, Bing Wen, Martha Solomon, Luís C. López, Saba Tadesse and Olimpia Musumeci and has published in prestigious journals such as Experimental Neurology, Journal of Neurology and Journal of Inherited Metabolic Disease.

In The Last Decade

Andrés Berardo

15 papers receiving 376 citations

Peers

Andrés Berardo

EEE

CMN

BIOCH

Helene Bruhn Sweden

Aya Ohkuma Japan

Anna Rubegni Italy

Joanne F. Garbincius United States

Yo-ichi Suzuki Japan

Manabu Hirasawa Japan

Takanori Hazama Japan

Elena Berezhnaya Russia

Victoria Dardov United States

Maya Ando Japan

Helene Bruhn Sweden

Andrés Berardo

346 ×1.2

127 ×1.4

33 ×0.4

EEE

24 ×0.3

CMN

42 ×0.8

BIOCH

Citations per year, relative to Andrés Berardo Andrés Berardo (= 1×) peers Helene Bruhn

Countries citing papers authored by Andrés Berardo

Since Specialization

Citations

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

Fields of papers citing papers by Andrés Berardo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrés Berardo

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

All Works

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16 of 16 papers shown

Berardo, Andrés, et al.. (2023). Blockade of Rho-associated kinase prevents inhibition of axon regeneration of peripheral nerves induced by anti-ganglioside antibodies. Neural Regeneration Research. 19(4). 895–899. 2 indexed citations

Berardo, Andrés, Cristina Domínguez‐González, Kristin Engelstad, & Michio Hirano. (2022). Advances in Thymidine Kinase 2 Deficiency: Clinical Aspects, Translational Progress, and Emerging Therapies. Journal of Neuromuscular Diseases. 9(2). 225–235. 16 indexed citations

Berardo, Andrés & Catarina M. Quinzii. (2020). Redefining infantile-onset multisystem phenotypes of coenzyme Q10-deficiency in the next-generation sequencing era. PubMed. 4. 22–35. 9 indexed citations

Hirano, Michio, Andrés Berardo, Emanuele Barca, et al.. (2020). Regulatory environment for novel therapeutic development in mitochondrial diseases. Journal of Inherited Metabolic Disease. 44(2). 292–300. 1 indexed citations

Berardo, Andrés, Valentina Emmanuele, Wendy Vargas, et al.. (2019). Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6. Journal of Neurology. 267(3). 823–829. 15 indexed citations

Berardo, Andrés, Xavière Lornage, Mridul Johari, et al.. (2019). HNRNPDL-related muscular dystrophy: expanding the clinical, morphological and MRI phenotypes. Journal of Neurology. 266(10). 2524–2534. 19 indexed citations

Palmio, Johanna, Sabrina Sacconi, Maria Flavia Savarese, et al.. (2017). Expanding importance of HMERF titinopathy: new mutations and clinical aspects. Neuromuscular Disorders. 27. S237–S237. 3 indexed citations

Manole, Andreea, Viorica Chelban, Nourelhoda A. Haridy, et al.. (2016). Severe axonal neuropathy is a late manifestation of SPG11. Journal of Neurology. 263(11). 2278–2286. 12 indexed citations

Berardo, Andrés, et al.. (2016). Anti-glycan antibodies halt axon regeneration in a model of Guillain Barrè Syndrome axonal neuropathy by inducing microtubule disorganization via RhoA–ROCK-dependent inactivation of CRMP-2. Experimental Neurology. 278. 42–53. 17 indexed citations

10.

Berardo, Andrés, et al.. (2016). Caracterización clínica, electrofisiológica y molecular en un paciente con parálisis periódica hipocalémica tipo 2, nueva mutación en SCN4A. Neurología Argentina. 8(4). 277–282.

11.

Emmanuele, Valentina, Luís C. López, Andrés Berardo, et al.. (2012). Heterogeneity of Coenzyme Q₁₀Deficiency. Archives of Neurology. 69(8). 978–83. 155 indexed citations

12.

Berardo, Andrés, et al.. (2012). Nueva mutación en C10Orf2 (PEO1) en paciente con oftalmoplejía crónica progresiva mitocondrial dominante (adCPEO), primer caso argentino. Neurología Argentina. 4(3). 157–161. 1 indexed citations

13.

Berardo, Andrés. (2011). El espectro clínico de las mutaciones en POLG. Neurología Argentina. 3(2). 106–112. 1 indexed citations

14.

Berardo, Andrés, Olimpia Musumeci, & Antonio Toscano. (2011). Cardiological manifestations of mitochondrial respiratory chain disorders.. PubMed. 30(1). 9–15. 25 indexed citations

15.

Berardo, Andrés, Salvatore DiMauro, & Michio Hirano. (2010). A Diagnostic Algorithm for Metabolic Myopathies. Current Neurology and Neuroscience Reports. 10(2). 118–126. 93 indexed citations

16.

Berardo, Andrés, Jorida Çoku, Bülent Kurt, Salvatore DiMauro, & Michio Hirano. (2010). A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO). Neuromuscular Disorders. 20(3). 204–206. 15 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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