Federica Invernizzi

4.5k total citations
72 papers, 2.7k citations indexed

About

Federica Invernizzi is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Federica Invernizzi has authored 72 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 28 papers in Clinical Biochemistry and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in Federica Invernizzi's work include Mitochondrial Function and Pathology (35 papers), Metabolism and Genetic Disorders (28 papers) and ATP Synthase and ATPases Research (15 papers). Federica Invernizzi is often cited by papers focused on Mitochondrial Function and Pathology (35 papers), Metabolism and Genetic Disorders (28 papers) and ATP Synthase and ATPases Research (15 papers). Federica Invernizzi collaborates with scholars based in Italy, United Kingdom and Germany. Federica Invernizzi's co-authors include Massimo Zeviani, Eleonora Lamantea, Graziella Uziel, Daniele Ghezzi, Juan Manuel Falomir‐Pichastor, Barbara Garavaglia, Isabella Moroni, F. Carrara, Laura Farina and Holger Prokisch and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Federica Invernizzi

72 papers receiving 2.6k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Federica Invernizzi Italy 27 1.9k 1.1k 299 260 241 72 2.7k
John Guy United States 34 2.1k 1.1× 413 0.4× 533 1.8× 184 0.7× 293 1.2× 121 3.7k
Nicole I. Wolf Netherlands 41 3.1k 1.6× 1.1k 1.0× 411 1.4× 664 2.6× 594 2.5× 169 4.8k
Mitsuko Nakashima Japan 39 2.5k 1.3× 262 0.2× 152 0.5× 332 1.3× 404 1.7× 191 4.4k
Louise Nicholson New Zealand 36 1.8k 0.9× 237 0.2× 524 1.8× 526 2.0× 960 4.0× 88 3.5k
Mária Judit Molnár Hungary 24 992 0.5× 233 0.2× 377 1.3× 220 0.8× 279 1.2× 142 1.9k
Maggie C. Walter Germany 32 1.8k 0.9× 128 0.1× 280 0.9× 439 1.7× 558 2.3× 122 2.9k
Stavit A. Shalev Israel 29 1.8k 0.9× 287 0.3× 76 0.3× 175 0.7× 211 0.9× 88 2.6k
William Seltzer United States 26 976 0.5× 101 0.1× 614 2.1× 262 1.0× 604 2.5× 80 2.5k
Eric Schmitt United States 24 1.4k 0.7× 547 0.5× 21 0.1× 92 0.4× 75 0.3× 68 2.0k
Sampath Arepalli United States 18 1.2k 0.6× 80 0.1× 374 1.3× 296 1.1× 230 1.0× 23 1.9k

Countries citing papers authored by Federica Invernizzi

Since Specialization
Citations

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

Fields of papers citing papers by Federica Invernizzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Federica Invernizzi

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

All Works

20 of 20 papers shown
1.
Invernizzi, Federica, Barbara Castellotti, Chiara Reale, et al.. (2024). CLN6‐related continuum phenotype caused by aberrant splicing. Epilepsia Open. 10(1). 348–354. 1 indexed citations
2.
Panteghini, Celeste, et al.. (2023). Sex distribution and classification of GBA1 variants in an Italian cohort of Parkinson's disease patients analyzed over the last seventeen years. Parkinsonism & Related Disorders. 117. 105919–105919. 3 indexed citations
3.
Invernizzi, Federica, Andrea Legati, Nadia Zanetti, et al.. (2023). NGS-Based Genetic Analysis in a Cohort of Italian Patients with Suspected Inherited Myopathies and/or HyperCKemia. Genes. 14(7). 1393–1393. 3 indexed citations
4.
Devigili, Grazia, Giulia Straccia, Emanuele Cereda, et al.. (2023). Unraveling Autonomic Dysfunction in GBA‐Related Parkinson's Disease. Movement Disorders Clinical Practice. 10(11). 1620–1638. 7 indexed citations
5.
Marchet, Silvia, Federica Invernizzi, Flavia Blàsevich, et al.. (2019). Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene. Mitochondrion. 47. 24–29. 10 indexed citations
6.
Invernizzi, Federica, Celeste Panteghini, Luisa Chiapparini, et al.. (2017). Thiamine-responsive disease due to mutation of tpk1 : Importance of avoiding misdiagnosis. Neurology. 89(8). 870–871. 13 indexed citations
7.
Legati, Andrea, Aurelio Reyes, Alessia Nasca, et al.. (2016). New genes and pathomechanisms in mitochondrial disorders unraveled by NGS technologies. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1857(8). 1326–1335. 71 indexed citations
8.
Carecchio, Miryam, Chiara Reale, Federica Invernizzi, et al.. (2016). DYT2 screening in early-onset isolated dystonia. European Journal of Paediatric Neurology. 21(2). 269–271. 9 indexed citations
9.
Ardissone, Anna, Eleonora Lamantea, Federica Invernizzi, et al.. (2014). Mitochondrial Diseases in Childhood. Current Molecular Medicine. 14(8). 1069–1078. 2 indexed citations
10.
Invernizzi, Federica, Anna Ardissone, Eleonora Lamantea, et al.. (2014). Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutations. Frontiers in Genetics. 5. 412–412. 40 indexed citations
11.
Lamperti, Costanza, Mingyan Fang, Federica Invernizzi, et al.. (2012). A novel homozygous mutation in SUCLA2 gene identified by exome sequencing. Molecular Genetics and Metabolism. 107(3). 403–408. 31 indexed citations
12.
Invernizzi, Federica, Ilaria D’Amato, Per Bo Jensen, et al.. (2012). Microscale oxygraphy reveals OXPHOS impairment in MRC mutant cells. Mitochondrion. 12(2). 328–335. 77 indexed citations
13.
Galassi, Giuliana, Eleonora Lamantea, Federica Invernizzi, et al.. (2008). Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathy. Neuromuscular Disorders. 18(6). 465–470. 29 indexed citations
14.
Puoti, Gianfranco, Simone Sampaolo, F. Carrara, et al.. (2003). Brain cysts associated with mutation in the Aristaless related homeobox gene, ARX. Journal of Medical Genetics. 40(11). 863–863. 2 indexed citations
15.
Falomir‐Pichastor, Juan Manuel, et al.. (2002). Social influence on intention to quit smoking: the effect of the rhetoric of an identity relevant message. Archive ouverte UNIGE (University of Geneva). 11 indexed citations
16.
Falomir‐Pichastor, Juan Manuel, et al.. (2000). Normative-related discrepancies and social discrimination change in an experimental group setting. Archive ouverte UNIGE (University of Geneva). 9 indexed citations
17.
Invernizzi, Federica, Barbara Garavaglia, Antònia Ribes, et al.. (2000). Clinical and molecular heterogeneity in carnitine-acylcarnitine translocase deficiency.. Journal of Inherited Metabolic Disease. 23. 121. 6 indexed citations
18.
Pons, Roser, Patrizia Cavadini, Silvia Baratta, et al.. (2000). Clinical and molecular heterogeneity in very–long-chain acyl-coenzyme a dehydrogenase deficiency. Pediatric Neurology. 22(2). 98–105. 31 indexed citations
19.
20.
Minetti, Carlo, Barbara Garavaglia, M. Bado, et al.. (1998). Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria. Neuromuscular Disorders. 8(1). 3–6. 20 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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