Bruno Marino

12.4k total citations · 1 hit paper
183 papers, 5.5k citations indexed

About

Bruno Marino is a scholar working on Molecular Biology, Epidemiology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Bruno Marino has authored 183 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 112 papers in Molecular Biology, 85 papers in Epidemiology and 66 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Bruno Marino's work include Congenital heart defects research (89 papers), Congenital Heart Disease Studies (85 papers) and Coronary Artery Anomalies (38 papers). Bruno Marino is often cited by papers focused on Congenital heart defects research (89 papers), Congenital Heart Disease Studies (85 papers) and Coronary Artery Anomalies (38 papers). Bruno Marino collaborates with scholars based in Italy, United States and Australia. Bruno Marino's co-authors include M. Cristina Digilio, Bruno Dallapiccola, Anna Sárközy, Donna M. McDonald‐McGinn, Ann Swillen, Anne S. Bassett, Nicole Philip, Jacob Vorstman, Kathleen E. Sullivan and Aldo Giannotti and has published in prestigious journals such as The Lancet, Circulation and Nature Genetics.

In The Last Decade

Bruno Marino

174 papers receiving 5.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

22q11.2 deletion syndrome

2015 791 citations Donna M. McDonald‐McGinn, Kathleen E. Sullivan et al. profile →

Peers

Bruno Marino

EPIDE

GENET

PRM

SURGE

Mary Ella Pierpont United States

David I. Wilson United Kingdom

B P Wordsworth United Kingdom

Anne‐Lise Delezoide France

Homa Adle‐Biassette France

Donald F. Patterson United States

Rebekka K. Schneider Germany

Kerstin Hansson Sweden

Tarra L. McDowell United Kingdom

Toshiyuki Yamamoto Japan

Mary Ella Pierpont United States

Bruno Marino

3.9k ×1.1

1.6k ×0.7

EPIDE

1.6k ×1.1

GENET

834 ×0.6

PRM

1.2k ×1.1

SURGE

Citations per year, relative to Bruno Marino Bruno Marino (= 1×) peers Mary Ella Pierpont

Countries citing papers authored by Bruno Marino

Since Specialization

Citations

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

Fields of papers citing papers by Bruno Marino

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bruno Marino

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Goldmuntz, Elizabeth, Anne S. Bassett, Erik Boot, et al.. (2024). Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation. Prenatal Diagnosis. 44(6-7). 804–814. 2 indexed citations

Calcagni, Giulio, Federica Ferrigno, Maria Lisa Dentici, et al.. (2024). Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome. Diagnostics. 14(6). 594–594. 1 indexed citations

Pugnaloni, Flaminia, et al.. (2023). Gender differences in congenital heart defects: a narrative review. Translational Pediatrics. 12(9). 1753–1764. 10 indexed citations

Frascarelli, Marianna, F. Ghezzi, Georgios D. Kotzalidis, et al.. (2023). Social cognition and real‐life functioning in patient samples with 22q11.2 deletion syndrome with or without psychosis, compared to a large sample of patients with schizophrenia only and healthy controls. Journal of Neuropsychology. 17(3). 564–583.

Blagowidow, Natalie, Beata Nowakowska, Erica Schindewolf, et al.. (2023). Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes. 14(1). 160–160. 15 indexed citations

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

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

Onesimo, Roberta, Paolo Versacci, Angelica Bibiana Delogu, et al.. (2021). Smith–Magenis syndrome: Report of morphological and new functional cardiac findings with review of the literature. American Journal of Medical Genetics Part A. 185(7). 2003–2011. 5 indexed citations

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

10.

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

11.

Baban, Anwar, Nicoletta Cantarutti, Rachele Adorisio, et al.. (2018). Long-term survival and phenotypic spectrum in heterotaxy syndrome: A 25-year follow-up experience. International Journal of Cardiology. 268. 100–105. 25 indexed citations

12.

Bellomo, Rinaldo, Bruno Marino, Scott Alan Carson, et al.. (2016). Direct cerebral perfusion and cooling in experimental cardiac arrest. Critical Care and Resuscitation. 18(4). 255–260.

13.

Marino, Bruno, et al.. (2014). Patient with Ebstein anomaly and Downsyndrome. Strange combination. SHILAP Revista de lepidopterología. 1 indexed citations

14.

Putotto, Carolina, et al.. (2013). Le cardiopatie congenite nel sesso femminile. Giornale italiano di cardiologia. 14(2). 120–5. 1 indexed citations

15.

Bellomo, Rinaldo, Satoshi Suzuki, Bruno Marino, et al.. (2012). Normothermic extracorporeal perfusion of isolated porcine liver after warm ischaemia: a preliminary report. Critical Care and Resuscitation. 14(3). 173–176. 14 indexed citations

16.

Sárközy, Anna, et al.. (2006). Noonan's syndrome and related disorders: Clinical-molecular update and guidelines. The Italian Journal of Pediatrics/Italian journal of pediatrics. 32(3). 145–155. 3 indexed citations

17.

Amati, Francesca, Rita Carsetti, Silvia Placidi, et al.. (2006). A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice. Cardiovascular Pathology. 15(4). 194–202. 26 indexed citations

18.

Sárközy, Anna, Emanuela Conti, M. Cristina Digilio, et al.. (2005). ZFPM2/FOG2 andHEY2 genes analysis in nonsyndromic tricuspid atresia. American Journal of Medical Genetics Part A. 133A(1). 68–70. 11 indexed citations

19.

Digilio, Maria Cristina, et al.. (1998). Congenital heart defect in sibs with discordant karyotypes. American Journal of Medical Genetics. 80(2). 169–172. 8 indexed citations

20.

Puddu, Paolo Emilio, et al.. (1997). Analisi univariata su potenziali fattori di rischio della mortalità precoce (entro 28 giorni) dopo bypass aortocoronarico in Italia. Gruppo di Studio OP-RISK.. 42(9). 957–969. 1 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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