Marco Crimi

1.9k total citations
33 papers, 1.3k citations indexed

About

Marco Crimi is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Marco Crimi has authored 33 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 11 papers in Clinical Biochemistry and 6 papers in Genetics. Recurrent topics in Marco Crimi's work include Mitochondrial Function and Pathology (16 papers), Metabolism and Genetic Disorders (11 papers) and Genomics and Rare Diseases (4 papers). Marco Crimi is often cited by papers focused on Mitochondrial Function and Pathology (16 papers), Metabolism and Genetic Disorders (11 papers) and Genomics and Rare Diseases (4 papers). Marco Crimi collaborates with scholars based in Italy, United States and Greece. Marco Crimi's co-authors include Giacomo P. Comi, Nereo Bresolin, Andreina Bordoni, Sara Galbiati, Roberto Del Bo, Monica Sciacco, Douglas C. Wallace, Chun Shi Lin, Paolo Sassone‐Corsi and Katrina G. Waymire and has published in prestigious journals such as Cell, Hepatology and Neurology.

In The Last Decade

Marco Crimi

31 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marco Crimi Italy 18 930 383 144 138 134 33 1.3k
Bruno Maranda Canada 23 714 0.8× 260 0.7× 93 0.6× 394 2.9× 113 0.8× 57 1.4k
Mohammed Al‐Owain Saudi Arabia 25 1.1k 1.2× 267 0.7× 110 0.8× 595 4.3× 157 1.2× 87 2.0k
Jimmy Huynh United States 16 872 0.9× 26 0.1× 98 0.7× 207 1.5× 102 0.8× 25 1.3k
Silvia Palmeri Italy 18 557 0.6× 98 0.3× 78 0.5× 105 0.8× 187 1.4× 47 1.1k
Nadine Gigarel France 18 1.8k 2.0× 711 1.9× 119 0.8× 282 2.0× 194 1.4× 39 2.2k
Devon S. Svoboda Canada 9 784 0.8× 53 0.1× 85 0.6× 113 0.8× 120 0.9× 13 1.2k
Jukka S. Moilanen Finland 19 1.2k 1.3× 503 1.3× 37 0.3× 386 2.8× 159 1.2× 61 1.6k
Franco Carrara Italy 20 1.6k 1.7× 894 2.3× 30 0.2× 126 0.9× 144 1.1× 28 1.8k
M. Pilar Bayona‐Bafaluy Spain 16 1.4k 1.5× 612 1.6× 53 0.4× 96 0.7× 88 0.7× 37 1.6k
Manir Ali United Kingdom 24 654 0.7× 67 0.2× 105 0.7× 277 2.0× 53 0.4× 61 1.4k

Countries citing papers authored by Marco Crimi

Since Specialization
Citations

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

Fields of papers citing papers by Marco Crimi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marco Crimi

This figure shows the co-authorship network connecting the top 25 collaborators of Marco Crimi. A scholar is included among the top collaborators of Marco Crimi 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 Marco Crimi. Marco Crimi 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.
Crimi, Marco, et al.. (2025). Preparing hospitals and health organizations for AI: practical guidelines for the required infrastructure. Frontiers in Digital Health. 7. 1605006–1605006.
2.
Hartman, Adam L., Gareth Baynam, Lara Bloom, et al.. (2024). Telehealth for rare disease care, research, and education across the globe: A review of the literature by the IRDiRC telehealth task force. European Journal of Medical Genetics. 72. 104977–104977. 2 indexed citations
3.
Li, Peining, Barbara R. DuPont, Qiping Hu, et al.. (2022). The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes. Human Genetics and Genomics Advances. 3(4). 100139–100139. 5 indexed citations
4.
Crimi, Marco, et al.. (2022). The genetic counseling in a patient affected by congenital polyneuropathy after a “diagnostic odyssey” recently solved with WES approach. European Journal of Translational Myology. 32(1). 2 indexed citations
5.
Crimi, Marco, et al.. (2022). Genome access and other web-based IT solutions: Genetic counseling in the digital era. Frontiers in Public Health. 10. 1035316–1035316. 4 indexed citations
6.
Baldelli, Ilaria, Fabio Gallo, Marco Crimi, et al.. (2019). Experiences of patients with Poland syndrome of diagnosis and care in Italy: a pilot survey. Orphanet Journal of Rare Diseases. 14(1). 269–269. 11 indexed citations
7.
Monaco, Lucía, Marco Crimi, & Chiuhui Mary Wang. (2014). The Challenge for a European Network of Biobanks for Rare Diseases Taken up by RD-Connect. Pathobiology. 81(5-6). 231–236. 22 indexed citations
8.
Sharpley, Mark S., Kristin Eckel‐Mahan, Meagan J. McManus, et al.. (2012). Heteroplasmy of Mouse mtDNA Is Genetically Unstable and Results in Altered Behavior and Cognition. Cell. 151(2). 333–343. 281 indexed citations
9.
Marabita, Francesco, Alessio Aghemo, Stella De Nicola, et al.. (2011). Genetic variation in the interleukin - 28B gene is not associated with fibrosis progression in patients with chronic hepatitis C and known date of infection. Hepatology. 54(4). 1127–1134. 103 indexed citations
10.
Bosè, Francesca, Lorenzo Raeli, Marco Crimi, et al.. (2011). Dual role of anti-TNF therapy: Enhancement of TCR-mediated T cell activation in peripheral blood and inhibition of inflammation in target tissues. Clinical Immunology. 139(2). 164–176. 35 indexed citations
11.
Corti, Stefania, Federica Locatelli, Dimitra Papadimitriou, et al.. (2005). Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1. Human Molecular Genetics. 15(2). 167–187. 80 indexed citations
12.
Bo, Roberto Del, Marina Scarlato, Serena Ghezzi, et al.. (2005). Vascular endothelial growth factor gene variability is associated with increased risk for AD. Annals of Neurology. 57(3). 373–380. 100 indexed citations
13.
Crimi, Marco, Sean F. O’Hearn, Douglas C. Wallace, & Giacomo P. Comi. (2005). Molecular research technologies in mitochondrial diseases: The microarray approach. IUBMB Life. 57(12). 811–818. 15 indexed citations
14.
Sciacco, Monica, A. Prelle, Gigliola Fagiolari, et al.. (2005). A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsy. Journal of the Neurological Sciences. 239(1). 21–24. 12 indexed citations
15.
Crimi, Marco, Alexandros Papadimitriou, Sara Galbiati, et al.. (2004). A New Mitochondrial DNA Mutation in ND3 Gene Causing Severe Leigh Syndrome with Early Lethality. Pediatric Research. 55(5). 842–846. 61 indexed citations
16.
Salani, Sabrina, Sabrina Lucchiari, Francesco Fortunato, et al.. (2004). Developmental and tissue‐specific regulation of a novel dysferlin isoform. Muscle & Nerve. 30(3). 366–374. 15 indexed citations
17.
Crimi, Marco, Roberto Del Bo, Sara Galbiati, et al.. (2003). Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion. European Journal of Human Genetics. 11(11). 896–898. 17 indexed citations
18.
Crimi, Marco, Sara Galbiati, Isabella Moroni, et al.. (2003). A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome. Neurology. 60(11). 1857–1861. 59 indexed citations
19.
Fonzo, Alessio Di, Andreina Bordoni, Marco Crimi, et al.. (2003). POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions. Human Mutation. 22(6). 498–499. 79 indexed citations
20.
Bo, Roberto Del, Andreina Bordoni, Filippo Martinelli Boneschi, et al.. (2002). Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients. Journal of the Neurological Sciences. 202(1-2). 85–91. 35 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Bruno Maranda Breakdown of academic impact, for papers by Mohammed Al‐Owain Breakdown of academic impact, for papers by Jimmy Huynh Breakdown of academic impact, for papers by Silvia Palmeri Breakdown of academic impact, for papers by Nadine Gigarel Breakdown of academic impact, for papers by Devon S. Svoboda Breakdown of academic impact, for papers by Jukka S. Moilanen Breakdown of academic impact, for papers by Franco Carrara Breakdown of academic impact, for papers by M. Pilar Bayona‐Bafaluy Breakdown of academic impact, for papers by Manir Ali
Rankless by CCL
2026