Alberto Casarin

4.0k total citations · 2 hit papers
28 papers, 2.7k citations indexed

About

Alberto Casarin is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Alberto Casarin has authored 28 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Clinical Biochemistry. Recurrent topics in Alberto Casarin's work include Mitochondrial Function and Pathology (6 papers), Coenzyme Q10 studies and effects (5 papers) and Metabolism and Genetic Disorders (5 papers). Alberto Casarin is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), Coenzyme Q10 studies and effects (5 papers) and Metabolism and Genetic Disorders (5 papers). Alberto Casarin collaborates with scholars based in Italy, United States and Spain. Alberto Casarin's co-authors include Leonardo Salviati, Vanessa Pertegato, Marco Spinazzi, C. Angelini, Luca Scorrano, Christian Frezza, Sara Cogliati, Rubén Quintana–Cabrera, Ester Perales‐Clemente and Lígia C. Gomes and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Neurology.

In The Last Decade

Alberto Casarin

28 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mitochondrial Cristae Shape Determines Respiratory Chain Supercomplexes Assembly and Respiratory Efficiency

2013 957 citations Sara Cogliati, Christian Frezza et al. Cell profile →
Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells

2012 753 citations Marco Spinazzi, Alberto Casarin et al. profile →

Peers

Countries citing papers authored by Alberto Casarin

Since Specialization

Citations

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

Fields of papers citing papers by Alberto Casarin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alberto Casarin

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

#	Work	Indexed citations
1	Vitamin K2 cannot substitute Coenzyme Q10 as electron carrier in the mitochondrial respiratory chain of mammalian cells 2019 ·Scientific Reports ·Cristina Cerqua, Alberto Casarin, Fabien Pierrel, Luis Vázquez-Fonseca, Giampietro Viola, Leonardo Salviati, Eva Trevisson	18
2	Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure 2015 ·European Journal of Human Genetics ·María Andrea Desbats, Annalisa Vetro, Ivan Limongelli, (unknown), Alberto Casarin, Mara Doimo, Marco Spinazzi, C. Angelini, Giovanna Cenacchi, Alberto Burlina, María Hernández, Lino Chiandetti, Maurizio Clementi, Eva Trevisson, Plácido Navas, Orsetta Zuffardi, Leonardo Salviati	39
3	Molecular characterization of the human COQ5 C-methyltransferase in coenzyme Q10 biosynthesis 2014 ·Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids ·Theresa Nguyen, Alberto Casarin, María Andrea Desbats, Mara Doimo, Eva Trevisson, Carlos Santos‐Ocaña, Plácido Navas, Catherine F. Clarke, Leonardo Salviati	47
4	Complexity of the 5′UTR region of the CLCN5gene: eleven 5′UTR ends are differentially expressed in the human kidney 2014 ·BMC Medical Genomics ·(unknown), Alberto Casarin, Leonardo Salviati, Alessandra Familiari, John C. Lieske, Franca Anglani	8
5	Mitochondrial Cristae Shape Determines Respiratory Chain Supercomplexes Assembly and Respiratory Efficiency breakdown → 2013 ·Cell ·Sara Cogliati, Christian Frezza, María Eugenia Soriano, Tatiana Varanita, Rubén Quintana–Cabrera, Mauro Corrado, Sara Cipolat, Veronica Costa, Alberto Casarin, Lígia C. Gomes, Ester Perales‐Clemente, Leonardo Salviati, Patricio Fernández‐Silva, José Antonio Enrı́quez, Luca Scorrano	957
6	The FSHD2 Gene SMCHD1 Is a Modifier of Disease Severity in Families Affected by FSHD1 2013 ·The American Journal of Human Genetics ·Sabrina Sacconi, Richard J.L.F. Lemmers, Judit Balog, Patrick J. van der Vliet, (unknown), (unknown), Kirsten R. Straasheijm, (unknown), (unknown), Leonardo Salviati, Alberto Casarin, Elena Pegoraro, Rabi Tawil, Egbert Bakker, Stephen J. Tapscott, Claude Desnuelle, Silvère M. van der Maarel	119
7	Haploinsufficiency of COQ4 causes coenzyme Q₁₀ deficiency 2012 ·Journal of Medical Genetics ·Leonardo Salviati, Eva Trevisson, María Hernández, Alberto Casarin, Vanessa Pertegato, Mara Doimo, Matteo Cassina, Caterina Agosto, María Andrea Desbats, Geppo Sartori, Sabrina Sacconi, Luigi Memo, Orsetta Zuffardi, Rafael Artuch, Catarina M. Quinzii, Salvatore DiMauro, Michio Hirano, Carlos Santos‐Ocaña, Plácido Navas	85
8	Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with sco2 mutations 2012 ·Orphanet Journal of Rare Diseases ·Alberto Casarin, (unknown), Vanessa Pertegato, Roberta Siviero, Cristina Cerqua, Mara Doimo, Giuseppe Basso, Sabrina Sacconi, Matteo Cassina, Rosario Rizzuto, Sonja Brosel, Mercy M. Davidson, Salvatore DiMauro, Eric A. Schon, Maurizio Clementi, Eva Trevisson, Leonardo Salviati	26
9	Optimization of respiratory chain enzymatic assays in muscle for the diagnosis of mitochondrial disorders 2011 ·Mitochondrion ·Marco Spinazzi, Alberto Casarin, Vanessa Pertegato, Mario Ermani, Leonardo Salviati, C. Angelini	50
10	Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage? 2011 ·The Journal of Headache and Pain ·Irene Toldo, Alice Bruson, Alberto Casarin, Leonardo Salviati, Clementina Boniver, Stefano Sartori, Pasquale Montagna, Pier Antonio Battistella, Maurizio Clementi	4
11	Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A 2011 ·Seizure ·Marilena Vecchi, Matteo Cassina, Alberto Casarin, Chiara Rigon, Paola Drigo, Luca De Palma, Maurizio Clementi	18
12	X‐linked brachytelephalangic chondrodysplasia punctata: A simple trait that is not so simple 2009 ·American Journal of Medical Genetics Part A ·Alberto Casarin, (unknown), Mara Doimo, Eva Trevisson, Silvia Carraro, Maurizio Clementi, Romano Tenconi, Eugenio Baraldi, Leonardo Salviati	9
13	Is CFTR 621+3 A>G a cystic fibrosis causing mutation? 2009 ·Journal of Human Genetics ·Monica Forzan, Leonardo Salviati, Vanessa Pertegato, Alberto Casarin, Alice Bruson, Eva Trevisson, Elena Di Gianantonio, Maurizio Clementi	13
14	Functional Complementation in Yeast Allows Molecular Characterization of Missense Argininosuccinate Lyase Mutations 2009 ·Journal of Biological Chemistry ·Eva Trevisson, Alberto Burlina, Mara Doimo, Vanessa Pertegato, Alberto Casarin, Luca Cesaro, Plácido Navas, Giuseppe Basso, Geppo Sartori, Leonardo Salviati	27
15	Functional characterization of human COQ4, a gene required for Coenzyme Q10 biosynthesis 2008 ·Biochemical and Biophysical Research Communications ·Alberto Casarin, (unknown), Eva Trevisson, Vanessa Pertegato, Mara Doimo, (unknown), Sara Abbadi, Rafael Artuch, Catarina M. Quinzii, (unknown), Giuseppe Basso, Carlos Santos‐Ocaña, Plácido Navas, Leonardo Salviati	43
16	Argininosuccinate lyase deficiency: mutational spectrum in Italian patients and identification of a novelASLpseudogene 2007 ·Human Mutation ·Eva Trevisson, Leonardo Salviati, (unknown), Irene Toldo, Alberto Casarin, Sabrina Sacconi, Luca Cesaro, Giuseppe Basso, Alberto Burlina	39
17	LETM1, deleted in Wolf Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability 2007 ·Human Molecular Genetics ·Kai Stefan Dimmer, (unknown), Alberto Casarin, Eva Trevisson, Sabine Endele, Andreas Winterpacht, Leonardo Salviati, Luca Scorrano	152
18	Molecular analysis of two uncharacterized sequence variants of the VHL gene 2006 ·Journal of Human Genetics ·Maddalena Martella, Leonardo Salviati, Alberto Casarin, Eva Trevisson, Giuseppe Opocher, Roberta Polli, David J. Gross, Alessandra Murgia	14
19	Low frequency of VHL gene mutations in young individuals with polycythemia and high serum erythropoietin. 2005 ·PubMed ·Maria Luigia Randi, Alessandra Murgia, Maria Caterina Putti, Maddalena Martella, Alberto Casarin, Giuseppe Opocher, Fabrizio Fabris	16
20	MOLECULAR BASES AND ETIOOGICAL DIAGNOSIS OF PHEOCHROMOCYTOMA/PARAGANGLIOMA IN GENETIC SYNDROMES AND ISOLATED CASES 2005 ·Pediatric Blood & Cancer ·Maddalena Martella, Francesca Schiavi, Alberto Casarin, Antonio Toniato, Giovanni Cecchetto, Giorgio Perilongo, Giuseppe Opocher	1

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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