Paola Prandini

1.6k total citations
15 papers, 1.0k citations indexed

About

Paola Prandini is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Paola Prandini has authored 15 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Cardiology and Cardiovascular Medicine and 4 papers in Genetics. Recurrent topics in Paola Prandini's work include Muscle Physiology and Disorders (6 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Antiplatelet Therapy and Cardiovascular Diseases (3 papers). Paola Prandini is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Antiplatelet Therapy and Cardiovascular Diseases (3 papers). Paola Prandini collaborates with scholars based in Italy, United States and France. Paola Prandini's co-authors include Silvia Torelli, S. Brown, Martin Brockington, Eugenio Mercuri, Francesco Muntoni, Caroline A. Sewry, Pascale Guicheney, Derek J. Blake, Norma B. Romero and Thomas Voit and has published in prestigious journals such as Journal of the American College of Cardiology, Neurology and The American Journal of Human Genetics.

In The Last Decade

Paola Prandini

15 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paola Prandini Italy 11 799 212 189 152 144 15 1.0k
Emma Clement United Kingdom 16 968 1.2× 294 1.4× 245 1.3× 187 1.2× 141 1.0× 37 1.3k
Aliana Egeo Italy 12 691 0.9× 101 0.5× 139 0.7× 84 0.6× 319 2.2× 15 842
Kinji Kobayashi Japan 10 647 0.8× 129 0.6× 114 0.6× 125 0.8× 51 0.4× 18 779
Isabelle Nelson France 24 1.3k 1.6× 113 0.5× 83 0.4× 249 1.6× 53 0.4× 49 1.5k
Carol Saunders United States 22 744 0.9× 635 3.0× 119 0.6× 93 0.6× 95 0.7× 59 1.3k
Pilar Camaño Spain 11 1.1k 1.3× 119 0.6× 254 1.3× 183 1.2× 60 0.4× 22 1.3k
Pagon Ra United States 6 450 0.6× 260 1.2× 57 0.3× 82 0.5× 44 0.3× 291 791
Marco Savarese Finland 20 983 1.2× 197 0.9× 477 2.5× 224 1.5× 166 1.2× 72 1.3k
Jeroen Vreijling Netherlands 12 527 0.7× 107 0.5× 45 0.2× 85 0.6× 55 0.4× 19 844
Chooi‐May Lai Australia 21 1.2k 1.5× 305 1.4× 21 0.1× 149 1.0× 63 0.4× 38 1.6k

Countries citing papers authored by Paola Prandini

Since Specialization
Citations

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

Fields of papers citing papers by Paola Prandini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paola Prandini

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

All Works

15 of 15 papers shown
1.
Rimessi, Alessandro, Valentino Bezzerri, Francesca Salvatori, et al.. (2018). PLCB3 Loss of Function Reduces Pseudomonas aeruginosa –Dependent IL-8 Release in Cystic Fibrosis. American Journal of Respiratory Cell and Molecular Biology. 59(4). 428–436. 15 indexed citations
2.
Prandini, Paola, et al.. (2014). Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs. Molecular and Cellular Probes. 28(5-6). 242–245. 5 indexed citations
3.
Prandini, Paola, Alessandra Pasquali, Giovanni Malerba, et al.. (2012). The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families. Psychiatric Genetics. 22(4). 177–181. 26 indexed citations
4.
Angiolillo, Dominick J., Esther Bernardo, David Vivas, et al.. (2011). Impact of Insulin Receptor Substrate-1 Genotypes on Platelet Reactivity and Cardiovascular Outcomes in Patients With Type 2 Diabetes Mellitus and Coronary Artery Disease. Journal of the American College of Cardiology. 58(1). 30–39. 45 indexed citations
5.
Costantini, Silvia, Paola Prandini, Massimiliano Corradi, et al.. (2011). A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype. Diabetes Research and Clinical Practice. 92(1). e23–e26. 6 indexed citations
6.
Angiolillo, Dominick J., Esther Bernardo, Piera Capranzano, et al.. (2010). IMPACT OF IRS-1 GENOTYPES ON PLATELET REACTIVITY AND CARDIOVASCULAR OUTCOMES IN TYPE 2 DIABETES MELLITUS PATIENTS WITH CORONARY ARTERY DISEASE. Journal of the American College of Cardiology. 55(10). A207.E1953–A207.E1953. 1 indexed citations
7.
Pereira, Patricia Lopes, Laetitia Magnol, Ignasi Sahún, et al.. (2009). A new mouse model for the trisomy of the Abcg1–U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome. Human Molecular Genetics. 18(24). 4756–4769. 92 indexed citations
8.
Trabetti, Elisabetta, Paola Prandini, Dominick J. Angiolillo, et al.. (2008). Role of the C1236T (rs1128503) polymorphism of the MDR-1 gene on clopidogrel responsiveness. 4 indexed citations
9.
Prandini, Paola, Samuel Deutsch, Robert Lyle, et al.. (2007). Natural Gene-Expression Variation in Down Syndrome Modulates the Outcome of Gene-Dosage Imbalance. The American Journal of Human Genetics. 81(2). 252–263. 145 indexed citations
10.
Brockington, Martin, Silvia Torelli, Paola Prandini, et al.. (2005). Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy. Human Molecular Genetics. 14(5). 657–665. 78 indexed citations
11.
Melacini, Paola, Andrea Vianello, Paola Prandini, et al.. (2005). Clinical and Molecular Characterization of Patients With Limb-Girdle Muscular Dystrophy Type 2I. Archives of Neurology. 62(12). 1894–1894. 65 indexed citations
12.
Prandini, Paola, Angela Berardinelli, Frank A. Morello, et al.. (2004). LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy. Neurology. 63(6). 1118–1121. 18 indexed citations
13.
Težak, Živana, Paola Prandini, Marco Boscaro, et al.. (2003). Clinical and molecular study in congenital muscular dystrophy with partial laminin ?2 (LAMA2) deficiency. Human Mutation. 21(2). 103–111. 36 indexed citations
14.
Pegoraro, Elena, Paola Prandini, Francesco Mari, et al.. (2002). Integrin α7β1 in Muscular Dystrophy/Myopathy of Unknown Etiology. American Journal Of Pathology. 160(6). 2135–2143. 42 indexed citations
15.
Brockington, Martin, Derek J. Blake, Paola Prandini, et al.. (2001). Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan. The American Journal of Human Genetics. 69(6). 1198–1209. 452 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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