Anwar Baban

3.2k total citations
76 papers, 1.2k citations indexed

About

Anwar Baban is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Anwar Baban has authored 76 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 27 papers in Cardiology and Cardiovascular Medicine and 20 papers in Genetics. Recurrent topics in Anwar Baban's work include Congenital heart defects research (22 papers), Congenital Heart Disease Studies (16 papers) and Cardiomyopathy and Myosin Studies (13 papers). Anwar Baban is often cited by papers focused on Congenital heart defects research (22 papers), Congenital Heart Disease Studies (16 papers) and Cardiomyopathy and Myosin Studies (13 papers). Anwar Baban collaborates with scholars based in Italy, Netherlands and United States. Anwar Baban's co-authors include M. Cristina Digilio, Bruno Dallapiccola, Bruno Marino, Antonio Novelli, Paolo Versacci, Francesca Romana Lepri, Fabrizio Drago, Rossella Capolino, Giulio Calcagni and Maria Lisa Dentici and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and European Heart Journal.

In The Last Decade

Anwar Baban

74 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anwar Baban Italy 20 621 313 283 265 262 76 1.2k
Inge B. Mathijssen Netherlands 17 379 0.6× 192 0.6× 113 0.4× 84 0.3× 143 0.5× 30 740
Giorgio Adriano Paskulin Brazil 17 351 0.6× 344 1.1× 195 0.7× 33 0.1× 195 0.7× 89 899
Rocio Moran United States 16 324 0.5× 378 1.2× 73 0.3× 117 0.4× 128 0.5× 27 854
Antonio Pérez Aytés Spain 15 369 0.6× 341 1.1× 28 0.1× 37 0.1× 147 0.6× 45 795
Kunitaka Joo Japan 11 1.5k 2.5× 513 1.6× 900 3.2× 263 1.0× 322 1.2× 25 1.9k
Reuven Sharony Israel 20 215 0.3× 254 0.8× 88 0.3× 30 0.1× 184 0.7× 79 1.0k
Tamar Katz Israel 11 362 0.6× 52 0.2× 92 0.3× 93 0.4× 126 0.5× 24 685
Marek Niekrasz United States 16 157 0.3× 408 1.3× 127 0.4× 187 0.7× 830 3.2× 45 1.2k
Nanette Sarioglu Germany 14 321 0.5× 282 0.9× 166 0.6× 30 0.1× 166 0.6× 40 941
Lesa Nelson United States 17 205 0.3× 247 0.8× 108 0.4× 226 0.9× 303 1.2× 31 1.3k

Countries citing papers authored by Anwar Baban

Since Specialization
Citations

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

Fields of papers citing papers by Anwar Baban

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anwar Baban

This figure shows the co-authorship network connecting the top 25 collaborators of Anwar Baban. A scholar is included among the top collaborators of Anwar Baban 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 Anwar Baban. Anwar Baban 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.
Gnazzo, Maria, et al.. (2024). Usmani‐Riazuddin syndrome can have a recognizable phenotype: Report of a novel AP1G1 variant. Clinical Genetics. 106(1). 109–113.
2.
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
3.
Gnazzo, Maria, Silvia Genovese, Massimo Stefano Silvetti, et al.. (2024). Copy Number Variants in Cardiac Channelopathies: Still a Missed Part in Routine Arrhythmic Diagnostics. Biomolecules. 14(11). 1450–1450. 2 indexed citations
4.
Baban, Anwar, Marianna Cicenia, Antonino Romanzo, et al.. (2024). Unique Features of Cardiovascular Involvement and Progression in Children with Marfan Syndrome Justify Dedicated Multidisciplinary Care. Journal of Cardiovascular Development and Disease. 11(4). 114–114. 1 indexed citations
5.
Picciolli, Irene, Berardo Rinaldi, Anwar Baban, et al.. (2024). Biallelic NEXN variants and fetal onset dilated cardiomyopathy: two independent case reports and revision of literature. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 50(1). 156–156. 1 indexed citations
6.
Baban, Anwar, Viola Alesi, Silvia Genovese, et al.. (2022). Cardiovascular Involvement in Pediatric FLNC Variants: A Case Series of Fourteen Patients. Journal of Cardiovascular Development and Disease. 9(10). 332–332. 4 indexed citations
7.
Silvetti, Massimo Stefano, Rachele Adorisio, May El Hachem, et al.. (2022). Cardiomyopathies in Children and Systemic Disorders When Is It Useful to Look beyond the Heart?. Journal of Cardiovascular Development and Disease. 9(2). 47–47. 14 indexed citations
8.
Calcagni, Giulio, Camilla Calvieri, Anwar Baban, et al.. (2022). Syndromic and Non-Syndromic Patients with Repaired Tetralogy of Fallot: Does It Affect the Long-Term Outcome?. Journal of Clinical Medicine. 11(3). 850–850. 5 indexed citations
9.
Silvetti, Massimo Stefano, Nicoletta Cantarutti, Marianna Cicenia, et al.. (2022). ICD Outcome in Pediatric Cardiomyopathies. Journal of Cardiovascular Development and Disease. 9(2). 33–33. 5 indexed citations
10.
Baban, Anwar, Marianna Cicenia, Lorena Travaglini, et al.. (2022). Remember Friedreich ataxia even in a toddler with apparently isolated dilated (not hypertrophic!) cardiomyopathy. Revisited. Minerva Pediatrics. 75(1). 117–123. 2 indexed citations
11.
Calvieri, Camilla, Corrado Di Mambro, Anwar Baban, et al.. (2021). Clinical characteristics and risk of arrhythmic events in patients younger than 12 years diagnosed with Brugada syndrome. Heart Rhythm. 18(10). 1691–1697. 5 indexed citations
12.
Caiazza, Martina, Michele Lioncino, Emanuele Monda, et al.. (2021). Troponin T Mutation as a Cause of Left Ventricular Systolic Dysfunction in a Young Patient with Previous Surgical Correction of Aortic Coarctation. Biomolecules. 11(5). 696–696. 3 indexed citations
13.
Baban, Anwar, Corrado Di Mambro, Rachele Adorisio, et al.. (2021). Myocardial and Arrhythmic Spectrum of Neuromuscular Disorders in Children. Biomolecules. 11(11). 1578–1578. 6 indexed citations
14.
Mambro, Corrado Di, Massimo Stefano Silvetti, Anwar Baban, et al.. (2020). Progressive involvement of cardiac conduction system in paediatric patients with Kearns–Sayre syndrome: how to predict occurrence of complete heart block and sudden cardiac death?. EP Europace. 23(6). 948–957. 16 indexed citations
15.
Kühnisch, Jirko, Manuel Holtgrewe, Anwar Baban, et al.. (2019). Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3. Clinical Genetics. 96(6). 549–559. 30 indexed citations
16.
Guerra, Liliana, Anwar Baban, Corrado Di Mambro, et al.. (2019). Palmoplantar Keratoderma and Woolly Hair Revealing Asymptomatic Arrhythmogenic Cardiomyopathy. Acta Dermato Venereologica. 99(9). 831–832. 3 indexed citations
17.
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
18.
Morlino, Silvia, Viola Alesi, Francesca Romana Lepri, et al.. (2018). LTBP2‐related “Marfan‐like” phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant. American Journal of Medical Genetics Part A. 179(1). 104–112. 15 indexed citations
19.
Baban, Anwar & Marco Castori. (2018). Pharmacological resources, diagnostic approach and coordination of care in joint hypermobility-related disorders. Expert Review of Clinical Pharmacology. 11(7). 689–703. 6 indexed citations
20.
Baban, Anwar, Alex V. Postma, Monica Marini, et al.. (2014). Identification of TBX5 mutations in a series of 94 patients with Tetralogy of Fallot. American Journal of Medical Genetics Part A. 164(12). 3100–3107. 41 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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