Maria Gnazzo

672 total citations
26 papers, 304 citations indexed

About

Maria Gnazzo is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Maria Gnazzo has authored 26 papers receiving a total of 304 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Molecular Biology and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Maria Gnazzo's work include Genomics and Rare Diseases (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Maria Gnazzo is often cited by papers focused on Genomics and Rare Diseases (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Maria Gnazzo collaborates with scholars based in Italy, Netherlands and United Kingdom. Maria Gnazzo's co-authors include M. Cristina Digilio, Francesca Romana Lepri, Bruno Dallapiccola, Rossella Capolino, Adriano Angioni, Maria Lisa Dentici, Elisa Pisaneschi, Anwar Baban, Antonio Novelli and Bruno Marino and has published in prestigious journals such as Atherosclerosis, Archives of Disease in Childhood and BMC Medicine.

In The Last Decade

Maria Gnazzo

25 papers receiving 300 citations

Peers

Maria Gnazzo

GENET

IMMUN

PRM

SURGE

Heide Seidel Germany

María Gabriela Obregón Argentina

Ken L. Jones United States

Eva Maria Cutiongco Philippines

Jaime Sánchez del Pozo Spain

Teresa Vendrell Spain

Victoria C. O׳Reilly Australia

Mitchell W. Dillon United States

Natalia V. Voronova Russia

Serina Huang United States

Heide Seidel Germany

Maria Gnazzo

192 ×1.0

GENET

182 ×1.3

42 ×0.9

IMMUN

36 ×1.1

PRM

45 ×1.5

SURGE

Citations per year, relative to Maria Gnazzo Maria Gnazzo (= 1×) peers Heide Seidel

Countries citing papers authored by Maria Gnazzo

Since Specialization

Citations

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

Fields of papers citing papers by Maria Gnazzo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Gnazzo

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Gnazzo. A scholar is included among the top collaborators of Maria Gnazzo 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 Maria Gnazzo. Maria Gnazzo 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

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.

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

Wischmeijer, Anita, Laurence Perrin, Duccio Maria Cordelli, et al.. (2024). Olfactory bulb anomalies in KBG syndrome mouse model and patients. BMC Medicine. 22(1). 158–158. 2 indexed citations

Leonardi, Lucia, Francesca Conti, Antonio Marzollo, et al.. (2023). Immune dysregulation in Kabuki syndrome: a case report of Evans syndrome and hypogammaglobulinemia. Frontiers in Pediatrics. 11. 1087002–1087002. 2 indexed citations

Mambro, Corrado Di, Maria Gnazzo, Anwar Baban, et al.. (2023). Autosomal Recessive Long QT Syndrome: Clinical Aspects and Therapy. Pediatric Cardiology. 44(8). 1736–1740. 2 indexed citations

Baban, Anwar, Marianna Cicenia, Marco Cirillo, et al.. (2023). Biallelic truncating variants in children with titinopathy represent a recognizable condition with distinctive muscular and cardiac characteristics: a report on five patients. Frontiers in Cardiovascular Medicine. 10. 1210378–1210378. 1 indexed citations

Alfieri, Paolo, Maria Lisa Dentici, M. Cristina Digilio, et al.. (2021). Cognitive and Adaptive Characterization of Children and Adolescents with KBG Syndrome: An Explorative Study. Journal of Clinical Medicine. 10(7). 1523–1523. 2 indexed citations

Buonuomo, Paola Sabrina, Giovanna Leone, Michaela Veronika Gonfiantini, et al.. (2021). Evolocumab in the management of children <10 years of age affected by homozygous familial hypercholesterolemia. Atherosclerosis. 324. 148–150. 2 indexed citations

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

10.

Cicenia, Marianna, Massimo Stefano Silvetti, Sonia Albanese, et al.. (2021). Idiopathic Ventricular Fibrillation: Look for the Hidden Guilty—A case of aborted cardiac death. Pediatric Cardiology. 42(7). 1650–1652. 1 indexed citations

11.

Digilio, M. Cristina, Giulio Calcagni, Maria Gnazzo, et al.. (2021). Congenital heart defects in molecularly confirmed KBG syndrome patients. American Journal of Medical Genetics Part A. 188(4). 1149–1159. 8 indexed citations

12.

Baban, Anwar, Marianna Cicenia, Maria Gnazzo, et al.. (2020). Cardiovascular Involvement in Pediatric Laminopathies. Report of Six Patients and Literature Revision. Frontiers in Pediatrics. 8. 374–374. 8 indexed citations

13.

Gnazzo, Maria, et al.. (2019). A new missense mutation in DPF2 gene related to Coffin Siris syndrome 7: Description of a mild phenotype expanding DPF2-related clinical spectrum and differential diagnosis among similar syndromes epigenetically determined. Brain and Development. 42(2). 192–198. 3 indexed citations

14.

Alfieri, Paolo, Francesco Demaria, M. Cristina Digilio, et al.. (2019). Obsessive Compulsive Symptoms and Psychopathological Profile in Children and Adolescents with KBG Syndrome. Brain Sciences. 9(11). 313–313. 7 indexed citations

15.

Ivanovski, Ivan, Stefano Giuseppe Caraffi, Maria Elisabeth Street, et al.. (2018). Prominent and elongated coccyx, a new manifestation of KBG syndrome associated with novel mutation in ANKRD11. American Journal of Medical Genetics Part A. 176(9). 1991–1995. 4 indexed citations

16.

Billy, Emmanuel de, Luisa Strocchio, Antonella Cacchione, et al.. (2018). Burkitt lymphoma in a patient with Kabuki syndrome carrying a novel KMT2D mutation. American Journal of Medical Genetics Part A. 179(1). 113–117. 10 indexed citations

17.

Sofia, Valentina, Letizia Da Sacco, Cecilia Surace, et al.. (2016). Extensive Molecular Analysis Suggested the Strong Genetic Heterogeneity of Idiopathic Chronic Pancreatitis. Molecular Medicine. 22(1). 300–309. 18 indexed citations

18.

Dentici, Maria Lisa, Francesca Romana Lepri, Maria Gnazzo, et al.. (2014). Kabuki syndrome: clinical and molecular diagnosis in the first year of life. Archives of Disease in Childhood. 100(2). 158–164. 62 indexed citations

19.

Lepri, Francesca Romana, M. Cristina Digilio, Maria Gnazzo, et al.. (2014). Diagnosis of Noonan syndrome and related disorders using target next generation sequencing. BMC Medical Genetics. 15(1). 14–14. 48 indexed citations

20.

Macchiaiolo, Marina, Maurizio Mennini, M. Cristina Digilio, et al.. (2013). Thricho‐rhino‐phalangeal syndrome and severe osteoporosis: A rare association or a feature? An effective therapeutic approach with biphosphonates. American Journal of Medical Genetics Part A. 164(3). 760–763. 7 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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