S. Cacurri

646 total citations
6 papers, 507 citations indexed

About

S. Cacurri is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, S. Cacurri has authored 6 papers receiving a total of 507 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Cardiology and Cardiovascular Medicine and 3 papers in Genetics. Recurrent topics in S. Cacurri's work include Cardiomyopathy and Myosin Studies (6 papers), Muscle Physiology and Disorders (6 papers) and Neurogenetic and Muscular Disorders Research (3 papers). S. Cacurri is often cited by papers focused on Cardiomyopathy and Myosin Studies (6 papers), Muscle Physiology and Disorders (6 papers) and Neurogenetic and Muscular Disorders Research (3 papers). S. Cacurri collaborates with scholars based in Italy and Netherlands. S. Cacurri's co-authors include Giancarlo Deidda, L. Felicetti, Eliana Vigneti, Giuliana Galluzzi, Luca Colantoni, Enzo Ricci, Barbara Merico, Serenella Servidei, P. Tonali and Francesca Mangiola and has published in prestigious journals such as Annals of Neurology, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

S. Cacurri

6 papers receiving 498 citations

Peers

S. Cacurri

MB

CCM

CMN

GENET

Luca Colantoni Italy

G Danieli Italy

Mariëlle Wohlgemuth Netherlands

Barbara Merico Italy

L. Specht United States

Ebe Pastorello Italy

J.C. van den Bergen Netherlands

Luigia Passamano Italy

P.F. Ippel Netherlands

M. Chevallay France

Luca Colantoni Italy

S. Cacurri

474 ×1.0

MB

147 ×0.8

CCM

150 ×1.1

CMN

126 ×0.9

GENET

69 ×1.3

GENET

Citations per year, relative to S. Cacurri S. Cacurri (= 1×) peers Luca Colantoni

Countries citing papers authored by S. Cacurri

Since Specialization

Citations

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

Fields of papers citing papers by S. Cacurri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Cacurri

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

All Works

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6 of 6 papers shown

1.

Ricci, Enzo, Giuliana Galluzzi, Giancarlo Deidda, et al.. (1999). Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype. Annals of Neurology. 45(6). 751–757. 232 indexed citations

2.

Galluzzi, Giuliana, Giancarlo Deidda, S. Cacurri, et al.. (1999). Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease. Neuromuscular Disorders. 9(3). 190–198. 24 indexed citations

3.

Cacurri, S., Giancarlo Deidda, Eliana Vigneti, et al.. (1998). Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy. The American Journal of Human Genetics. 63(1). 181–190. 48 indexed citations

4.

Deidda, Giancarlo, et al.. (1996). Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD).. Journal of Medical Genetics. 33(5). 361–365. 113 indexed citations

5.

Deidda, Giancarlo, et al.. (1995). Physical Mapping Evidence for a Duplicated Region on Chromosome 10qter Showing High Homology with the Facioscapulohumeral Muscular Dystrophy Locus on Chromosome 4qter. European Journal of Human Genetics. 3(3). 155–167. 78 indexed citations

6.

Cacurri, S., Giancarlo Deidda, Andrea Novelletto, et al.. (1994). Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral musculatur dystrophy (FSHD). Human Genetics. 94(4). 367–374. 12 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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