Luca Sbaiz

1.4k total citations
28 papers, 530 citations indexed

About

Luca Sbaiz is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Luca Sbaiz has authored 28 papers receiving a total of 530 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Genetics and 10 papers in Neurology. Recurrent topics in Luca Sbaiz's work include Amyotrophic Lateral Sclerosis Research (10 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Iron Metabolism and Disorders (6 papers). Luca Sbaiz is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (10 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Iron Metabolism and Disorders (6 papers). Luca Sbaiz collaborates with scholars based in Italy, United States and United Kingdom. Luca Sbaiz's co-authors include Clara Camaschella, Gabriella Restagno, Adriano Chiò, Antonella Roetto, Andrea Calvo, Cristina Moglia, Maura Brunetti, Bryan J. Traynor, Paolo Fortina and Paolo Gasparini and has published in prestigious journals such as Hepatology, Neurology and Annals of Neurology.

In The Last Decade

Luca Sbaiz

28 papers receiving 521 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luca Sbaiz Italy 14 309 176 160 154 110 28 530
Bhavya S. Doshi United States 11 62 0.2× 22 0.1× 271 1.7× 227 1.5× 49 0.4× 28 518
Francesca Bertola Italy 10 68 0.2× 38 0.2× 76 0.5× 66 0.4× 50 0.5× 20 291
Hongkuan Yang China 11 40 0.1× 43 0.2× 69 0.4× 149 1.0× 69 0.6× 18 342
Sharan Goobie Canada 15 88 0.3× 17 0.1× 41 0.3× 162 1.1× 3 0.0× 29 504
Ljiljana Luković Serbia 10 48 0.2× 8 0.0× 43 0.3× 106 0.7× 9 0.1× 20 327
Amir Jahić Germany 9 51 0.2× 35 0.2× 20 0.1× 63 0.4× 6 0.1× 13 252
Shu-Chuan Chiang Taiwan 10 135 0.4× 22 0.1× 21 0.1× 208 1.4× 3 0.0× 20 721
Andrea Zito Italy 7 32 0.1× 13 0.1× 66 0.4× 97 0.6× 20 0.2× 12 390
Sarah Moustafa United States 6 23 0.1× 23 0.1× 39 0.2× 61 0.4× 27 0.2× 13 320
Brenda L. Court United States 4 11 0.0× 29 0.2× 15 0.1× 251 1.6× 89 0.8× 5 437

Countries citing papers authored by Luca Sbaiz

Since Specialization
Citations

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

Fields of papers citing papers by Luca Sbaiz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luca Sbaiz

This figure shows the co-authorship network connecting the top 25 collaborators of Luca Sbaiz. A scholar is included among the top collaborators of Luca Sbaiz 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 Luca Sbaiz. Luca Sbaiz 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.
Moglia, Cristina, Andrea Calvo, Antonio Canosa, et al.. (2024). Cognitive and Behavioral Features of Patients With Amyotrophic Lateral Sclerosis Who Are Carriers of the TARDBP Pathogenic Variant. Neurology. 102(4). e208082–e208082. 6 indexed citations
2.
Calvo, Andrea, Cristina Moglia, Antonio Canosa, et al.. (2024). High Frequency of Cognitive and Behavioral Impairment in Amyotrophic Lateral Sclerosis Patients with SOD1 Pathogenic Variants. Annals of Neurology. 96(1). 150–158. 5 indexed citations
3.
Canosa, Antonio, Andrea Calvo, Cristina Moglia, et al.. (2022). Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changes. European Journal of Nuclear Medicine and Molecular Imaging. 49(7). 2242–2250. 14 indexed citations
4.
Fenoglio, Roberta, Simone Baldovino, Antonella Barreca, et al.. (2022). Renal Involvement in Transthyretin Amyloidosis: The Double Presentation of Transthyretin Amyloidosis Deposition Disease. ˜The œNephron journals/Nephron journals. 146(5). 481–488. 6 indexed citations
5.
Grassano, Maurizio, Andrea Calvo, Cristina Moglia, et al.. (2022). Systematic evaluation of genetic mutations in ALS: a population-based study. Journal of Neurology Neurosurgery & Psychiatry. 93(11). 1190–1193. 29 indexed citations
6.
Iazzolino, Barbara, Laura Peotta, Jean Pierre Zucchetti, et al.. (2020). Differential Neuropsychological Profile of Patients With Amyotrophic Lateral Sclerosis With and Without C9orf72 Mutation. Neurology. 96(1). e141–e152. 17 indexed citations
7.
Grassano, Maurizio, Andrea Calvo, Cristina Moglia, et al.. (2020). Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort. Neurology. 96(4). e600–e609. 21 indexed citations
8.
Minelli, Antonella, Andrea Guala, Gabriella Restagno, et al.. (2011). Mechanism of origin in two cases of chimerism. Open Journal of Pediatrics. 1(4). 79–86. 6 indexed citations
9.
Chiò, Adriano, Andrea Calvo, Cristina Moglia, et al.. (2010). A de novo missense mutation of the FUS gene in a “true” sporadic ALS case. Neurobiology of Aging. 32(3). 553.e23–553.e26. 61 indexed citations
10.
Galbiati, Silvia, Barbara Foglieni, Cristina Curcio, et al.. (2008). Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of  -thalassemia. Haematologica. 93(4). 610–614. 32 indexed citations
11.
Restagno, Gabriella, Federica Lombardo, Luca Sbaiz, et al.. (2008). The rare G93D mutation causes a slowly progressing lower motor neuron disease. Amyotrophic Lateral Sclerosis. 9(1). 35–39. 16 indexed citations
12.
Cagnoli, Claudia, Alessandro Brussino, Luca Sbaiz, et al.. (2008). A previously undiagnosed case of Gerstmann‐Sträussler‐Scheinker disease revealed by PRNP gene analysis in patients with adult‐onset ataxia. Movement Disorders. 23(10). 1468–1471. 9 indexed citations
13.
Stenirri, Stefania, Gabriella Restagno, Giovanni Battista Ferrero, et al.. (2007). Integrated Strategy for Fast and Automated Molecular Characterization of Genes Involved in Craniosynostosis. Clinical Chemistry. 53(10). 1767–1774. 13 indexed citations
14.
Galbiati, Silvia, Gabriella Restagno, Barbara Foglieni, et al.. (2006). Different Approaches for Noninvasive Prenatal Diagnosis of Genetic Diseases Based on PNA‐Mediated Enriched PCR. Annals of the New York Academy of Sciences. 1075(1). 137–143. 12 indexed citations
15.
Acutis, Pier Luigi, Simone Peletto, Luca Sbaiz, et al.. (2005). Analysis of the polymorphism of the prion protein gene in indigenous sheep breeds in the Piedmont.. Large animals review. 11(3). 39–43. 1 indexed citations
16.
Restagno, Gabriella, Ana M. Gómez, Luca Sbaiz, et al.. (2000). A Pilot C282Y Hemochromatosis Screening in Italian Newborns by TaqMan™ Technology. Genetic Testing. 4(2). 177–181. 23 indexed citations
17.
Restagno, Gabriella, Luca Sbaiz, Paolo Fortina, et al.. (1999). Screening of the C282Y mutation in the HFE gene in Italy by Taqman technology.. The American Journal of Human Genetics. 65. 2 indexed citations
18.
Camaschella, Clara, Antonios Kattamis, Antonella Roetto, et al.. (1997). Different hematological phenotypes caused by the interaction of triplicated α-globin genes and heterozygous β-thalassemia. American Journal of Hematology. 55(2). 83–88. 49 indexed citations
19.
Roetto, Antonella, Luca Sbaiz, S. Bosio, et al.. (1997). A recombination event close to HFE gene in hereditary hemochromatosis.. PubMed. 40(3). 150–3. 2 indexed citations
20.
Totaro, Antonio, A. Grifa, Antonella Roetto, et al.. (1995). New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE). Human Genetics. 95(4). 429–434. 13 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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