Giorgio Casari

31.6k total citations · 3 hit papers
144 papers, 10.5k citations indexed

About

Giorgio Casari is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Giorgio Casari has authored 144 papers receiving a total of 10.5k indexed citations (citations by other indexed papers that have themselves been cited), including 88 papers in Molecular Biology, 40 papers in Cellular and Molecular Neuroscience and 24 papers in Genetics. Recurrent topics in Giorgio Casari's work include Mitochondrial Function and Pathology (25 papers), Neurological diseases and metabolism (20 papers) and Hereditary Neurological Disorders (16 papers). Giorgio Casari is often cited by papers focused on Mitochondrial Function and Pathology (25 papers), Neurological diseases and metabolism (20 papers) and Hereditary Neurological Disorders (16 papers). Giorgio Casari collaborates with scholars based in Italy, United States and Germany. Giorgio Casari's co-authors include Andrea Ballabio, Maurizio De Fusco, Laura Silvestri, Paolo Aridon, Luigia Atorino, Luca Rampoldi, Alberto Bettinelli, Giacomo Colussi, Roberto Marconi and Francesca Morgante and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Giorgio Casari

143 papers receiving 10.2k 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.

Paracellin-1, a Renal Tight Junction Protein Required for Paracellular Mg ²⁺ Resorption

1999 819 citations Giorgio Casari, Alberto Bettinelli et al. profile →
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2

2003 710 citations Maurizio De Fusco, Laura Silvestri et al. profile →
Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease

1998 586 citations Giorgio Casari, Maurizio De Fusco et al. profile →

Peers

Countries citing papers authored by Giorgio Casari

Since Specialization

Citations

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

Fields of papers citing papers by Giorgio Casari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giorgio Casari

This figure shows the co-authorship network connecting the top 25 collaborators of Giorgio Casari. A scholar is included among the top collaborators of Giorgio Casari 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 Giorgio Casari. Giorgio Casari 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	VarGenius-HZD Allows Accurate Detection of Rare Homozygous or Hemizygous Deletions in Targeted Sequencing Leveraging Breadth of Coverage 2021 ·Genes ·Francesco Musacchia, Marianthi Karali, Annalaura Torella, Steven Laurie, (unknown), Mariateresa Pizzo, Sergi Beltrán, Giorgio Casari, Vincenzo Nigro, Sandro Banfi	2
2	Impaired flickering of the permeability transition pore causes SPG7 spastic paraplegia 2020 ·EBioMedicine ·Irene Sambri, (unknown), Francesca Gullo, (unknown), Laura Cassina, Michela Carraro, Giorgia Dina, Angelo Quattrini, (unknown), Annamaria Carissimo, Antonella Iuliano, Filippo M. Santorelli, Franca Codazzi, Fabio Grohovaz, Paolo Bernardi, Andrea Becchetti, Giorgio Casari	32
3	Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activation 2019 ·Journal of Medical Genetics ·(unknown), (unknown), (unknown), Davide Mazza, Franca Codazzi, Tyler Mark Pierson, Alessandro Ambrosi, Dagmar Nolte, Cyril Goizet, Camilo Toro, Jonathan Baets, Tine Deconinck, (unknown), Paola Mandich, Giorgio Casari, Francesca Maltecca	19
4	Upregulation of Peroxiredoxin 3 Protects Afg3l2-KO Cortical Neurons In Vitro from Oxidative Stress: A Paradigm for Neuronal Cell Survival under Neurodegenerative Conditions 2019 ·Oxidative Medicine and Cellular Longevity ·(unknown), Ilaria Pelizzoni, (unknown), Lisa Michelle Restelli, Daniele Zacchetti, Francesca Maltecca, Giorgio Casari, Fabio Grohovaz, Franca Codazzi	9
5	Haploinsufficiency ofAFG3L2, the Gene Responsible for Spinocerebellar Ataxia Type 28, Causes Mitochondria-Mediated Purkinje Cell Dark Degeneration 2009 ·Journal of Neuroscience ·Francesca Maltecca, (unknown), Federica Cerri, Gregory A. Cox, Angelo Quattrini, Giorgio Casari	80
6	Analysis of Uromodulin Polymerization Provides New Insights into the Mechanisms Regulating ZP Domain-mediated Protein Assembly 2008 ·Molecular Biology of the Cell ·Céline Schaeffer, S Santambrogio, (unknown), Giorgio Casari, Luca Rampoldi	73
7	Autosomal dominant hereditary spastic paraplegia: report of a large italian family with R581X spastin mutation 2007 ·Neurological Sciences ·Paolo Aridon, Paolo Ragonese, Maurizio De Fusco, Daniele Lo Coco, Giuseppe Salemi, Giorgio Casari, Giovanni Savettieri	5
8	A Thiazide Test for the Diagnosis of Renal Tubular Hypokalemic Disorders 2007 ·Clinical Journal of the American Society of Nephrology ·Giacomo Colussi, Alberto Bettinelli, Silvana Tedeschi, Maria Elisabetta De Ferrari, (unknown), (unknown), (unknown), Giorgio Casari, Mario G. Bianchetti	90
9	Noncoding RNA synthesis and loss of Polycomb group repression accompanies the colinear activation of the human HOXA cluster 2006 ·RNA ·Luca Sessa, Achim Breiling, G Lavorgna, Laura Silvestri, Giorgio Casari, Valerio Orlando	102
10	Increased Sensitivity of the Neuronal Nicotinic Receptor α2 Subunit Causes Familial Epilepsy with Nocturnal Wandering and Ictal Fear 2006 ·The American Journal of Human Genetics ·Paolo Aridon, Carla Marini, Chiara Di Resta, Elisa Brilli, Maurizio De Fusco, (unknown), Elena Parrini, Irene Manfredi, Tiziana Pisano, Dario Pruna, Giulia Curia, Carlo Cianchetti, Massimo Pasqualetti, Andrea Becchetti, Renzo Guerrini, Giorgio Casari	171
11	Elusive amines and cluster headache: mutational analysis of trace amine receptor cluster on chromosome 6q23 2004 ·Neurological Sciences ·Paolo Aridon, G D’Andrea, (unknown), Massimo Leone, Giorgio Casari, Gennaro Bussone	11
12	Uromodulin storage diseases: Clinical aspects and mechanisms 2004 ·American Journal of Kidney Diseases ·Francesco Scolari, Gianluca Caridi, Luca Rampoldi, Regina Tardanico, Claudia Izzi, Doroti Pirulli, Antonio Amoroso, Giorgio Casari, Gian Marco Ghiggeri	94
13	Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport 2004 ·Journal of Clinical Investigation ·Fátima Ferreirinha, Angelo Quattrini, Marinella Pirozzi, (unknown), Giorgia Dina, Vania Broccoli, Alberto Auricchio, Fiorella Piemonte, Giulia Tozzi, Laura Gaeta, Giorgio Casari, Andrea Ballabio, Elena I. Rugarli	227
14	Towards the identification of (a) gene(s) for autosomal dominant medullary cystic kidney disease 2003 ·Journal of Nephrology ·Francesco Scolari, Battista Fabio Viola, Gian Marco Ghiggeri, Gianluca Caridi, Antonio Amoroso, Luca Rampoldi, Giorgio Casari	8
15	Mapping of MRX81 in Xp11.2‐Xq12 suggests the presence of a new gene involved in nonspecific X‐linked mental retardation 2003 ·American Journal of Medical Genetics Part A ·Ida Annunziata, Carmela Lanzara, Iván Conte, Alberto Zullo, V. Ventruto, Maria Michela Rinaldi, Michele D’Urso, Giorgio Casari, Alfredo Ciccodicola, Maria Giuseppina Miano	10
16	Autosomal dominant restless legs syndrome maps on chromosome 14q 2003 ·Brain ·Maria Teresa Bonati, Luigi Ferini‐Strambi, Paolo Aridon, Alessandro Oldani, Marco Zucconi, Giorgio Casari	193
17	Identification and Characterization of YME1L1, a Novel Paraplegin-Related Gene 2000 ·Genomics ·(unknown), (unknown), Sandro Banfi, Maria Teresa Bassi, Giorgio Casari, Barbara Incerti	75
18	Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: Linkage analysis and clinical findings in a three-generation Sardinian family 2000 ·American Journal of Medical Genetics ·Silvia Russo, Francesca Cogliati, (unknown), (unknown), (unknown), Daniela Toniolo, Giorgio Casari, Lidia Larizza	8
19	Variable phenotype of long QT syndrome patients with the same genetic defect 1998 ·Journal of the American College of Cardiology ·Silvia G. Priori, Carlo Napolitano, Peter J. Schwartz, (unknown), (unknown), Isabelle Denjoy, (unknown), J.A. Towbin, (unknown), Giorgio Casari	3
20	Mutational Analyses Support a Model for the HRV2 2A Proteinase 1997 ·Virology ·Wolfgang Sommergruber, Joachim Seipelt, (unknown), Tim Skern, Hans Liebig, Giorgio Casari	16

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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