Maria Pennuto

6.8k total citations
81 papers, 3.0k citations indexed

About

Maria Pennuto is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Maria Pennuto has authored 81 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 58 papers in Cellular and Molecular Neuroscience and 32 papers in Genetics. Recurrent topics in Maria Pennuto's work include Genetic Neurodegenerative Diseases (49 papers), Neurogenetic and Muscular Disorders Research (32 papers) and Muscle Physiology and Disorders (30 papers). Maria Pennuto is often cited by papers focused on Genetic Neurodegenerative Diseases (49 papers), Neurogenetic and Muscular Disorders Research (32 papers) and Muscle Physiology and Disorders (30 papers). Maria Pennuto collaborates with scholars based in Italy, United States and United Kingdom. Maria Pennuto's co-authors include Flavia Valtorta, Fabio Benfenati, Dario Bonanomi, Fabio Sambataro, Isabella Palazzolo, Kenneth H. Fischbeck, J. Paul Taylor, Manuela Basso, M. Laura Feltri and Angelo Poletti and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Neuron.

In The Last Decade

Maria Pennuto

75 papers receiving 3.0k citations

Peers

Maria Pennuto

CMN

GENET

NEURO

Rebecca Schüle Germany

Lisa M. Stanek United States

Marie‐Françoise Belin France

Maria K. Lehtinen United States

Vikram G. Shakkottai United States

Amber L. Southwell Canada

Pratap Meera United States

Kevin L. Seburn United States

Carlos Vicario‐Abejón Spain

Mercedes F. Paredes United States

Rebecca Schüle Germany

Maria Pennuto

1.2k ×0.6

1.8k ×1.1

CMN

581 ×0.8

GENET

540 ×1.0

600 ×1.1

NEURO

Citations per year, relative to Maria Pennuto Maria Pennuto (= 1×) peers Rebecca Schüle

Countries citing papers authored by Maria Pennuto

Since Specialization

Citations

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

Fields of papers citing papers by Maria Pennuto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Pennuto

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Pennuto. A scholar is included among the top collaborators of Maria Pennuto 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 Maria Pennuto. Maria Pennuto 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

Gorgoglione, Domenico, Giovanni Minervini, Chiara Romualdi, et al.. (2025). RYR1-Related Myopathies Involve More than Calcium Dysregulation: Insights from Transcriptomic Profiling. Biomolecules. 15(11). 1599–1599.

Giorgio, Valentina, Chiara Leoni, Donato Rigante, et al.. (2024). Clarifying main nutritional aspects and resting energy expenditure in children with Smith-Magenis syndrome. European Journal of Pediatrics. 183(10). 4563–4571. 1 indexed citations

Carletti, Rose Mary, Isabella Torrente, Serena Lattante, et al.. (2024). Generation of induced pluripotent stem cells (CSSi017-A)(12862) from an ALS patient carrying a repeat expansion in the C9orf72 gene. Stem Cell Research. 77. 103412–103412.

Torrente, Isabella, Francesco Nicita, Davide Tonduti, et al.. (2024). Production of an induced pluripotent stem cell line CSSi018-A (14192) from a patient with hypomyelinating leukodystrophy 7 (HLD7) carrying biallelic variants of POLR3A (c.1802 T > A; c.4072G > A). Stem Cell Research. 78. 103468–103468.

Querin, Giorgia, Ilaria Martinelli, Cinzia Bertolin, et al.. (2023). The value of serum creatinine as biomarker of disease progression in spinal and bulbar muscular atrophy (SBMA). Scientific Reports. 13(1). 17311–17311. 6 indexed citations

Zuccaro, Emanuela, et al.. (2022). Skeletal Muscle Pathogenesis in Polyglutamine Diseases. Cells. 11(13). 2105–2105. 1 indexed citations

Zuccaro, Emanuela, et al.. (2021). Motor Neuron Diseases and Neuroprotective Peptides: A Closer Look to Neurons. Frontiers in Aging Neuroscience. 13. 723871–723871. 8 indexed citations

Chivet, Mathilde, Marco Pirazzini, Chiara Scaramuzzino, et al.. (2020). Polyglutamine-Expanded Androgen Receptor Alteration of Skeletal Muscle Homeostasis and Myonuclear Aggregation Are Affected by Sex, Age and Muscle Metabolism. Cells. 9(2). 325–325. 24 indexed citations

Yu, Zhigang, Samuel T. Jones, Gianni Sorarú, et al.. (2020). MEF2 impairment underlies skeletal muscle atrophy in polyglutamine disease. Acta Neuropathologica. 140(1). 63–80. 23 indexed citations

10.

Casci, Ian, Karthik Krishnamurthy, Sukhleen Kour, et al.. (2019). Muscleblind acts as a modifier of FUS toxicity by modulating stress granule dynamics and SMN localization. Nature Communications. 10(1). 5583–5583. 24 indexed citations

11.

Meroni, M., V. Crippa, Riccardo Cristofani, et al.. (2019). Transforming growth factor beta 1 signaling is altered in the spinal cord and muscle of amyotrophic lateral sclerosis mice and patients. Neurobiology of Aging. 82. 48–59. 14 indexed citations

12.

Manzano, Raquel, Gianni Sorarú, Christopher Grunseich, et al.. (2018). Beyond motor neurons: expanding the clinical spectrum in Kennedy’s disease. Journal of Neurology Neurosurgery & Psychiatry. 89(8). 808–812. 40 indexed citations

13.

Sambataro, Fabio & Maria Pennuto. (2017). Post-translational Modifications and Protein Quality Control in Motor Neuron and Polyglutamine Diseases. Frontiers in Molecular Neuroscience. 10. 82–82. 43 indexed citations

14.

Basso, Manuela & Maria Pennuto. (2015). Serine phosphorylation and arginine methylation at the crossroads to neurodegeneration. Experimental Neurology. 271. 77–83. 27 indexed citations

15.

Aggarwal, Tanya, María José Polanco, Chiara Scaramuzzino, et al.. (2014). Androgens affect muscle, motor neuron, and survival in a mouse model of SOD1-related amyotrophic lateral sclerosis. Neurobiology of Aging. 35(8). 1929–1938. 31 indexed citations

16.

Sambataro, Fabio, Maria Pennuto, & Robert Christian Wolf. (2012). Catechol-O-Methyl Transferase Modulates Cognition in Late Life: Evidence and Implications for Cognitive Enhancement. CNS & Neurological Disorders - Drug Targets. 11(3). 195–208. 12 indexed citations

17.

Pennuto, Maria, Elisa Tinelli, Ubaldo Del Carro, et al.. (2008). Ablation of the UPR-Mediator CHOP Restores Motor Function and Reduces Demyelination in Charcot-Marie-Tooth 1B Mice. Neuron. 57(3). 393–405. 211 indexed citations

18.

Valtorta, Flavia, Maria Pennuto, Dario Bonanomi, & Fabio Benfenati. (2004). Synaptophysin: leading actor or walk‐on role in synaptic vesicle exocytosis?. BioEssays. 26(4). 445–453. 288 indexed citations

19.

Pennuto, Maria, David Dunlap, Andrea Contestabile, Fabio Benfenati, & Flavia Valtorta. (2002). Fluorescence Resonance Energy Transfer Detection of Synaptophysin I and Vesicle-associated Membrane Protein 2 Interactions during Exocytosis from Single Live Synapses. Molecular Biology of the Cell. 13(8). 2706–2717. 53 indexed citations

20.

Rocco, Giuliana Di, Maria Pennuto, Barbara Illi, et al.. (1997). Interplay of the E Box, the Cyclic AMP Response Element, and HTF4/HEB in Transcriptional Regulation of the Neurospecific, Neurotrophin-Inducible vgf Gene†. Molecular and Cellular Biology. 17(3). 1244–1253. 30 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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