Dario Balestra

793 citations

33 papers · 634 indexed · h-index 16

Co-authors: Mirko Pinotti Francesco Bernardi Nicola Cavallari Daniela Perrone Alessio Branchini Malgorzata Ewa Rogalska Saverio Marchi Paolo Pinton
Topics: Hemophilia Treatment and Research (14 papers)RNA Research and Splicing (13 papers)Neurogenetic and Muscular Disorders Research (9 papers)
Cited by: Hematology Genetics Molecular Biology
Journals: SHILAP Revista de lepidopterologíaBlood International Journal of Molecular Sciences
Partner nations: Italy Netherlands United States

In The Last Decade

Dario Balestra

29 papers receiving 633 citations

Peers

Countries citing papers authored by Dario Balestra

Since Specialization

Citations

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

Fields of papers citing papers by Dario Balestra

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dario Balestra

This figure shows the co-authorship network connecting the top 25 collaborators of Dario Balestra. A scholar is included among the top collaborators of Dario Balestra 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 Dario Balestra. Dario Balestra 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	Pharmacokinetics of extended half-life albumin-fused factor IX and heterogeneous <i>F9</i> variants in hemophilia B: a retrospective cohort study 2026 ·SHILAP Revista de lepidopterología ·(unknown),Massimo Morfini,(unknown),Dario Balestra,Alessio Branchini,(unknown),Donata Belvini,(unknown),(unknown),(unknown),(unknown)	0
2	BPS2025 - Respiratory complex I mutation alters mitochondrial bioenergetics in Apennine brown bears 2025 ·Biophysical Journal ·(unknown),Emiliano Trucchi,Silvia Fuselli,Simone Patergnani,Alberto Danese,Dario Balestra,Emidio Capriotti,(unknown),Paolo Pinton,Giorgio Bertorelle	0
3	Rescue of a panel of Hemophilia A-causing 5’ss splicing mutations by unique Exon-specific U1snRNA variants 2025 ·Molecular Medicine ·(unknown),(unknown),P. Ferraresi,Dario Balestra,Mirko Pinotti	0
4	DNA base editing corrects common hemophilia A mutations and restores factor VIII expression in in vitro and ex vivo models 2024 ·Journal of Thrombosis and Haemostasis ·(unknown),Alessia Cucci,Antonia Follenzi,(unknown),Mirko Pinotti,Dario Balestra	1
5	Whole-Exome Sequencing in a Family with an Unexplained Tendency for Venous Thromboembolism: Multicomponent Prediction of Low-Frequency Variant Deleteriousness and of Individual Protein Interaction 2023 ·International Journal of Molecular Sciences ·Barbara Lunghi,Nicole Ziliotto,Dario Balestra,(unknown),Patrizia Della Valle,Pasquale Pignatelli,Mirko Pinotti,Armando D’Angelo,Giovanna Marchetti,Francesco Bernardi	0
6	Counteracting the Common Shwachman–Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing 2023 ·International Journal of Molecular Sciences ·(unknown),(unknown),Iva Maestri,Valentino Bezzerri,Roberto Valli,Marco Cipolli,Mirko Pinotti,Dario Balestra	7
7	OTC intron 4 variations mediate pathogenic splicing patterns caused by the c.386G>A mutation in humans and spfash mice, and govern susceptibility to RNA-based therapies 2021 ·Molecular Medicine ·(unknown),(unknown),Francisco E. Baralle,Iva Maestri,Francesca Tassi,Francesco Bernardi,Stan F.J. van de Graaf,(unknown),Mirko Pinotti,Dario Balestra	4
8	An advanced method for the small-scale production of high-quality minicircle DNA 2021 ·International Journal of Pharmaceutics ·(unknown),(unknown),(unknown),Maria Francesca Testa,(unknown),Dario Balestra,Mirko Pinotti,Alexander Weng	1
9	An Altered Splicing Registry Explains the Differential ExSpeU1-Mediated Rescue of Splicing Mutations Causing Haemophilia A 2019 ·Frontiers in Genetics ·Dario Balestra,Iva Maestri,Alessio Branchini,(unknown),Francesco Bernardi,Mirko Pinotti	10
10	C6orf10 Low-Frequency and Rare Variants in Italian Multiple Sclerosis Patients 2019 ·Frontiers in Genetics ·Nicole Ziliotto,Giovanna Marchetti,Chiara Scapoli,Matteo Bovolenta,(unknown),Andrea Benazzo,Barbara Lunghi,Dario Balestra,(unknown),(unknown),(unknown),Fabrizio Salvi,Sofía Straudi,Donato Gemmati,Erica Menegatti,Paolo Zamboni,Francesco Bernardi	10
11	Next-generation sequencing and recombinant expression characterized aberrant splicing mechanisms and provided correction strategies in factor VII deficiency 2019 ·Haematologica ·P. Ferraresi,Dario Balestra,Caroline Guittard,(unknown),(unknown),Iva Maestri,Roula Farah,Mirko Pinotti,Muriel Giansily‐Blaizot	17
12	The somatic FAH C.1061C>A change counteracts the frequent FAH c.1062+5G>A mutation and permits U1snRNA-based splicing correction 2018 ·Journal of Human Genetics ·(unknown),(unknown),Francesco Bernardi,Mirko Pinotti,Stan F.J. van de Graaf,Dario Balestra	17
13	The carboxyl-terminal region of human coagulation factor X as a natural linker for fusion strategies 2018 ·Thrombosis Research ·(unknown),(unknown),(unknown),Dario Balestra,Francesco Bernardi,Mirko Pinotti,Alessio Branchini	7
14	The chaperone‐like sodium phenylbutyrate improves factor IX intracellular trafficking and activity impaired by the frequent p.R294Q mutation 2018 ·Journal of Thrombosis and Haemostasis ·(unknown),(unknown),(unknown),Saverio Marchi,(unknown),Dario Balestra,Paolo Pinton,Francesco Bernardi,Mirko Pinotti,Alessio Branchini	15
15	Molecular Basis and Therapeutic Strategies to Rescue Factor IX Variants That Affect Splicing and Protein Function 2016 ·PLoS Genetics ·Mojca Tajnik,Malgorzata Ewa Rogalska,Erica Bussani,Elena Barbon,Dario Balestra,Mirko Pinotti,(unknown)	33
16	An Exon-Specific U1snRNA Induces a Robust Factor IX Activity in Mice Expressing Multiple Human FIX Splicing Mutants 2016 ·Molecular Therapy — Nucleic Acids ·Dario Balestra,(unknown),(unknown),Malgorzata Ewa Rogalska,(unknown),Francesco Bernardi,Mirko Pinotti	25
17	Exploring Splicing-Switching Molecules For Seckel Syndrome Therapy 2016 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·(unknown),Dario Balestra,(unknown),Matteo Bovolenta,Daniela Perrone,Francesco Bernardi,Stefano Campaner,Mirko Pinotti	20
18	Regulation of a strongF9cryptic 5′ss by intrinsic elements and by combination of tailored U1snRNAs with antisense oligonucleotides 2015 ·Human Molecular Genetics ·Dario Balestra,Elena Barbon,(unknown),Nicola Cavallari,Daniela Perrone,(unknown),Francesco Bernardi,Mirko Pinotti	26
19	Activation of a cryptic splice site in a potentially lethal coagulation defect accounts for a functional protein variant 2012 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Nicola Cavallari,Dario Balestra,Alessio Branchini,Iva Maestri,(unknown),Werasak Sasanakul,Guglielmo Mariani,(unknown),Francesco Bernardi,Mirko Pinotti	19
20	An exon-specific U1 small nuclear RNA (snRNA) strategy to correct splicing defects 2012 ·Human Molecular Genetics ·(unknown),Mirko Pinotti,Andrea Dal Mas,Dario Balestra,Nicola Cavallari,Malgorzata Ewa Rogalska,Francesco Bernardi,(unknown)	88

About Dario Balestra

Dario Balestra is a scholar working on Hematology, Genetics and Molecular Biology, having authored 33 papers that have together received 634 indexed citations. Recurring topics across this work include Hemophilia Treatment and Research (14 papers), RNA Research and Splicing (13 papers) and Neurogenetic and Muscular Disorders Research (9 papers). The work is most often cited by research in Hematology (133 citations), Genetics (118 citations) and Molecular Biology (505 citations). Dario Balestra has collaborated with scholars based in Italy, Netherlands and United States. Frequent co-authors include Mirko Pinotti, Francesco Bernardi, Nicola Cavallari, Daniela Perrone, Alessio Branchini, Malgorzata Ewa Rogalska, Saverio Marchi, Paolo Pinton, Iva Maestri and Carlotta Giorgi. Their work appears in journals such as SHILAP Revista de lepidopterología, Blood and International Journal of Molecular Sciences.

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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