Giancarlo Deidda

1.3k total citations
24 papers, 971 citations indexed

About

Giancarlo Deidda is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Giancarlo Deidda has authored 24 papers receiving a total of 971 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Giancarlo Deidda's work include Muscle Physiology and Disorders (12 papers), Hemoglobinopathies and Related Disorders (7 papers) and Cardiomyopathy and Myosin Studies (7 papers). Giancarlo Deidda is often cited by papers focused on Muscle Physiology and Disorders (12 papers), Hemoglobinopathies and Related Disorders (7 papers) and Cardiomyopathy and Myosin Studies (7 papers). Giancarlo Deidda collaborates with scholars based in Italy, Netherlands and Egypt. Giancarlo Deidda's co-authors include L. Felicetti, S. Cacurri, Eliana Vigneti, Enzo Ricci, Giuliana Galluzzi, Luca Colantoni, Barbara Merico, Silvère M. van der Maarel, Paola Grisanti and Serenella Servidei and has published in prestigious journals such as Journal of Clinical Investigation, Nature Biotechnology and Annals of Neurology.

In The Last Decade

Giancarlo Deidda

24 papers receiving 945 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Giancarlo Deidda Italy 15 733 365 260 210 125 24 971
Jeffrey Murray United Kingdom 7 605 0.8× 141 0.4× 90 0.3× 100 0.5× 19 0.2× 8 766
G K Suthers Australia 11 587 0.8× 107 0.3× 65 0.3× 112 0.5× 13 0.1× 18 717
Claudia Castiglioni Chile 15 320 0.4× 125 0.3× 99 0.4× 111 0.5× 27 0.2× 47 566
Patrick J. van der Vliet Netherlands 16 1.2k 1.6× 332 0.9× 337 1.3× 219 1.0× 6 0.0× 24 1.3k
P N Ray Canada 13 643 0.9× 136 0.4× 102 0.4× 116 0.6× 6 0.0× 17 783
Andoni Urtizberea France 15 555 0.8× 155 0.4× 129 0.5× 203 1.0× 5 0.0× 27 796
Mike Pike United Kingdom 8 472 0.6× 119 0.3× 85 0.3× 80 0.4× 8 0.1× 12 692
Mark A. Mynhier United States 8 313 0.4× 140 0.4× 65 0.3× 77 0.4× 35 0.3× 8 580
Danielle A. Griffin United States 16 908 1.2× 207 0.6× 255 1.0× 112 0.5× 6 0.0× 23 1.0k
Takao Hijikata Japan 17 654 0.9× 49 0.1× 208 0.8× 89 0.4× 8 0.1× 35 1.0k

Countries citing papers authored by Giancarlo Deidda

Since Specialization
Citations

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

Fields of papers citing papers by Giancarlo Deidda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giancarlo Deidda

This figure shows the co-authorship network connecting the top 25 collaborators of Giancarlo Deidda. A scholar is included among the top collaborators of Giancarlo Deidda 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 Giancarlo Deidda. Giancarlo Deidda 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.
Cascella, Raffaella, Claudia Strafella, Valerio Caputo, et al.. (2018). Digenic Inheritance of Shortened Repeat Units of the D4Z4 Region and a Loss-of-Function Variant in SMCHD1 in a Family With FSHD. Frontiers in Neurology. 9. 1027–1027. 10 indexed citations
2.
Pellegrino, Marsha, Sabrina Sacconi, Isabella Cascino, et al.. (2017). Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity. Journal of Clinical Investigation. 127(4). 1531–1545. 51 indexed citations
3.
Cascino, Isabella, Richard J.L.F. Lemmers, Giuliana Galluzzi, et al.. (2016). Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2. Journal of Medical Genetics. 53(5). 348–355. 48 indexed citations
4.
Putti, Sabrina, et al.. (2013). Highly efficient, in vivo optimized, archaeal endonuclease for controlled RNA splicing in mammalian cells. The FASEB Journal. 27(9). 3466–3477. 2 indexed citations
5.
Deidda, Giancarlo, et al.. (2010). ARCHAEA‐ExPRESs targeting of α‐tubulin 4 mRNA: a model for high‐specificity trans‐splicing. The FASEB Journal. 24(8). 2976–2984. 3 indexed citations
6.
Deidda, Giancarlo, et al.. (2003). An archaeal endoribonuclease catalyzes cis- and trans- nonspliceosomal splicing in mouse cells. Nature Biotechnology. 21(12). 1499–1504. 22 indexed citations
7.
Maarel, Silvère M. van der, Giancarlo Deidda, Richard J.L.F. Lemmers, et al.. (2000). De Novo Facioscapulohumeral Muscular Dystrophy: Frequent Somatic Mosaicism, Sex-Dependent Phenotype, and the Role of Mitotic Transchromosomal Repeat Interaction between Chromosomes 4 and 10. The American Journal of Human Genetics. 66(1). 26–35. 116 indexed citations
8.
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
9.
10.
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
11.
Bianco, I, et al.. (1998). Phenotypes of individuals with a beta thal classical allele associated either with a beta thal silent allele or with alpha globin gene triplication.. PubMed. 82(5). 513–25. 18 indexed citations
12.
Deidda, Giancarlo, et al.. (1997). Detection of alpha-globin gene disorders by a simple PCR methodology.. PubMed. 81(5). 387–96. 42 indexed citations
13.
Bianco, I, et al.. (1997). Silent thalassemias: genotypes and phenotypes.. PubMed. 82(3). 269–80. 36 indexed citations
14.
15.
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
16.
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
17.
Deidda, Giancarlo, et al.. (1991). A new β‐thalassaemia frameshift mutation detected by PCR after selective hybridization to immobilized oligonucleotides. British Journal of Haematology. 79(1). 90–92. 6 indexed citations
18.
Deidda, Giancarlo, Andrea Novelletto, Mohamed Hafez, et al.. (1990). A New β-Thalassemia Mutation Produced by a Single Nucleotide Substitution in the Conserved Dinucleotide Sequence of the IVS-I Consensus Acceptor Site (Ag→AA). Hemoglobin. 14(4). 431–440. 17 indexed citations
19.
Novelletto, Andrea, Mohamed Hafez, Giancarlo Deidda, et al.. (1990). Molecular characterization of β-thalassemia mutations in Egypt. Human Genetics. 85(3). 272–274. 39 indexed citations
20.
Novelletto, Andrea, et al.. (1989). Frequency and molecular types of deletional α-thalassemia in Egypt. Human Genetics. 81(3). 211–213. 8 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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