Marta Unolt

1.1k total citations
26 papers, 311 citations indexed

About

Marta Unolt is a scholar working on Molecular Biology, Epidemiology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Marta Unolt has authored 26 papers receiving a total of 311 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 18 papers in Epidemiology and 13 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Marta Unolt's work include Congenital heart defects research (21 papers), Congenital Heart Disease Studies (17 papers) and Coronary Artery Anomalies (9 papers). Marta Unolt is often cited by papers focused on Congenital heart defects research (21 papers), Congenital Heart Disease Studies (17 papers) and Coronary Artery Anomalies (9 papers). Marta Unolt collaborates with scholars based in Italy, United States and Canada. Marta Unolt's co-authors include Bruno Marino, M. Cristina Digilio, Paolo Versacci, Giulio Calcagni, Anwar Baban, Carolina Putotto, Elaine H. Zackai, Donna M. McDonald‐McGinn, T. Blaine Crowley and Antonio Baldini and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and The Journal of Pediatrics.

In The Last Decade

Marta Unolt

25 papers receiving 310 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marta Unolt Italy 11 202 196 115 86 51 26 311
Carolina Putotto Italy 11 129 0.6× 156 0.8× 66 0.6× 53 0.6× 55 1.1× 38 288
Sharon Edman United States 5 154 0.8× 126 0.6× 74 0.6× 51 0.6× 32 0.6× 7 191
Avery C. Rossidis United States 11 95 0.5× 193 1.0× 134 1.2× 104 1.2× 91 1.8× 19 413
Jacoba Louw Belgium 11 165 0.8× 99 0.5× 275 2.4× 239 2.8× 63 1.2× 20 479
Fahad Alhabshan Saudi Arabia 11 173 0.9× 58 0.3× 131 1.1× 80 0.9× 23 0.5× 39 291
Flaminia Pugnaloni Italy 10 94 0.5× 71 0.4× 79 0.7× 84 1.0× 20 0.4× 32 188
Henriëtte ter Heide Netherlands 10 133 0.7× 38 0.2× 80 0.7× 64 0.7× 31 0.6× 17 229
Barbara E. Coons United States 8 27 0.1× 186 0.9× 61 0.5× 54 0.6× 92 1.8× 17 344
Sikha Singh United States 10 42 0.2× 58 0.3× 39 0.3× 51 0.6× 62 1.2× 16 247
P Corone France 9 212 1.0× 98 0.5× 147 1.3× 116 1.3× 54 1.1× 42 330

Countries citing papers authored by Marta Unolt

Since Specialization
Citations

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

Fields of papers citing papers by Marta Unolt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marta Unolt

This figure shows the co-authorship network connecting the top 25 collaborators of Marta Unolt. A scholar is included among the top collaborators of Marta Unolt 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 Marta Unolt. Marta Unolt 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.
Mambro, Corrado Di, Ugo Giordano, Marta Unolt, et al.. (2024). Long-term incidence of arrhythmias in extracardiac conduit Fontan and comparison between systemic left and right ventricle. EP Europace. 26(5). 7 indexed citations
2.
Putotto, Carolina, Flaminia Pugnaloni, Marta Unolt, et al.. (2024). Laterality, heterotaxy, and isolated congenital heart defects. Genome Medicine. 16(1). 100–100. 1 indexed citations
3.
Crowley, T. Blaine, Yichuan Liu, Marta Unolt, et al.. (2022). Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study. Genes. 14(1). 62–62. 7 indexed citations
4.
Calcagni, Giulio, Silvia Anaclerio, Flaminia Pugnaloni, et al.. (2022). Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes—A report of 74 cases with systematic review of the literature. American Journal of Medical Genetics Part A. 188(8). 2351–2359. 3 indexed citations
5.
Putotto, Carolina, Federica Pulvirenti, Flaminia Pugnaloni, et al.. (2022). Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study. Genes. 13(12). 2334–2334. 3 indexed citations
6.
Putotto, Carolina, Flaminia Pugnaloni, Marta Unolt, et al.. (2022). 22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects. Children. 9(6). 772–772. 12 indexed citations
7.
Putotto, Carolina, Marta Unolt, Silvia Anaclerio, et al.. (2022). Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease. European Journal of Medical Genetics. 66(1). 104651–104651. 1 indexed citations
8.
Silvetti, Massimo Stefano, Marta Unolt, Carolina D’Anna, et al.. (2020). Left ventricular (LV) pacing in newborns and infants: Echo assessment of LV systolic function and synchrony at 5‐year follow‐up. Pacing and Clinical Electrophysiology. 43(6). 535–541. 10 indexed citations
9.
Fanella, Martina, Marianna Frascarelli, Alessandra Morano, et al.. (2019). Myoclonic epilepsy, parkinsonism, schizophrenia and left-handedness as common neuropsychiatric features in 22q11.2 deletion syndrome. Journal of Medical Genetics. 57(3). 151–159. 9 indexed citations
10.
Unolt, Marta, Molka Kammoun, Beata Nowakowska, et al.. (2019). Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition. Genetics in Medicine. 22(2). 326–335. 7 indexed citations
11.
Calcagni, Giulio, Paolo Versacci, Carolina Putotto, et al.. (2019). Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice. PLoS ONE. 14(4). e0211170–e0211170. 10 indexed citations
12.
Drago, Fabrizio, Camilla Calvieri, Silvia Placidi, et al.. (2018). Use of a Pediatric Syncope Unit Improves Diagnosis and Lowers Costs: A Hospital-Based Experience. The Journal of Pediatrics. 201. 184–189.e2. 3 indexed citations
13.
Unolt, Marta, M. Cristina Digilio, Bruno Marino, et al.. (2018). Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome. European Journal of Medical Genetics. 61(7). 411–415. 3 indexed citations
14.
Cohen, Jennifer L., T. Blaine Crowley, Daniel E. McGinn, et al.. (2018). 22q and two: 22q11.2 deletion syndrome and coexisting conditions. American Journal of Medical Genetics Part A. 176(10). 2203–2214. 21 indexed citations
15.
Unolt, Marta, Paolo Versacci, Silvia Anaclerio, et al.. (2018). Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well‐established knowledge to new frontiers. American Journal of Medical Genetics Part A. 176(10). 2087–2098. 43 indexed citations
16.
Putotto, Carolina, Giulio Calcagni, Marta Unolt, et al.. (2018). Impact of genetic studies on comprehension and treatment of congenital heart disease. Progress in Pediatric Cardiology. 51. 31–36.
17.
Unolt, Marta, Lori J. Howell, Stefanie B. Kasperski, et al.. (2016). Congenital diaphragmatic hernia in 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A. 173(1). 135–142. 16 indexed citations
18.
Radio, Francesca Clementina, M. Cristina Digilio, Rossella Capolino, et al.. (2015). Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo–Cardio–Facial) syndrome. American Journal of Medical Genetics Part A. 170(3). 661–664. 1 indexed citations
19.
Putotto, Carolina, et al.. (2013). Le cardiopatie congenite nel sesso femminile. Giornale italiano di cardiologia. 14(2). 120–5. 1 indexed citations
20.
Unolt, Marta. (2013). Transposition of great arteries: new insights into the pathogenesis. Frontiers in Pediatrics. 1. 11–11. 50 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Carolina Putotto Breakdown of academic impact, for papers by Sharon Edman Breakdown of academic impact, for papers by Avery C. Rossidis Breakdown of academic impact, for papers by Jacoba Louw Breakdown of academic impact, for papers by Fahad Alhabshan Breakdown of academic impact, for papers by Flaminia Pugnaloni Breakdown of academic impact, for papers by Henriëtte ter Heide Breakdown of academic impact, for papers by Barbara E. Coons Breakdown of academic impact, for papers by Sikha Singh Breakdown of academic impact, for papers by P Corone
Rankless by CCL
2026