Flávia Piazzon

605 total citations
21 papers, 135 citations indexed

About

Flávia Piazzon is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Flávia Piazzon has authored 21 papers receiving a total of 135 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Flávia Piazzon's work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (6 papers) and Metabolism and Genetic Disorders (5 papers). Flávia Piazzon is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (6 papers) and Metabolism and Genetic Disorders (5 papers). Flávia Piazzon collaborates with scholars based in Brazil, Belgium and United Kingdom. Flávia Piazzon's co-authors include Leslie Domenici Kulikowski, María Helena Vaisbich, Fernando Kok, Chong Ae Kim, Maria Isabel Melaragno, Clarissa Bueno, Darius J. Adams, François Feillet, Turgay Coşkun and Yin‐Hsiu Chien and has published in prestigious journals such as Scientific Reports, Gene and Journal of the Neurological Sciences.

In The Last Decade

Flávia Piazzon

20 papers receiving 123 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Flávia Piazzon Brazil 6 74 56 56 26 26 21 135
Mari‐Anne Vals Estonia 9 100 1.4× 22 0.4× 74 1.3× 51 2.0× 18 0.7× 14 177
Shawn Fayer United States 7 95 1.3× 37 0.7× 166 3.0× 47 1.8× 7 0.3× 13 241
William L. Macken United Kingdom 6 106 1.4× 31 0.6× 40 0.7× 6 0.2× 16 0.6× 11 146
Guangping Fu China 7 203 2.7× 27 0.5× 85 1.5× 24 0.9× 21 0.8× 17 280
V. Reid Sutton United States 5 120 1.6× 109 1.9× 36 0.6× 29 1.1× 19 0.7× 11 167
William Lee Australia 7 261 3.5× 67 1.2× 29 0.5× 34 1.3× 13 0.5× 11 295
Ping Chun Wu United States 5 91 1.2× 41 0.7× 24 0.4× 8 0.3× 37 1.4× 8 171
Vibha Patil Australia 4 251 3.4× 23 0.4× 46 0.8× 36 1.4× 22 0.8× 6 296
Amy Hietala United States 4 113 1.5× 94 1.7× 15 0.3× 15 0.6× 18 0.7× 7 137
Takuya Fushimi Japan 9 259 3.5× 143 2.6× 30 0.5× 9 0.3× 13 0.5× 23 299

Countries citing papers authored by Flávia Piazzon

Since Specialization
Citations

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

Fields of papers citing papers by Flávia Piazzon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Flávia Piazzon

This figure shows the co-authorship network connecting the top 25 collaborators of Flávia Piazzon. A scholar is included among the top collaborators of Flávia Piazzon 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 Flávia Piazzon. Flávia Piazzon 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.
Dangouloff, Tamara, Kristine Hovhannesyan, Frédéric Minner, et al.. (2024). Feasibility and Acceptability of a Newborn Screening Program Using Targeted Next-Generation Sequencing in One Maternity Hospital in Southern Belgium. Children. 11(8). 926–926. 2 indexed citations
2.
Barcelos, Isabella Peixoto de, Clarissa Bueno, Luís Filipe de Souza Godoy, et al.. (2023). Subacute Partially Reversible Leukoencephalopathy Expands the Aicardi–Goutières Syndrome Phenotype. Brain Sciences. 13(8). 1169–1169. 1 indexed citations
3.
Dangouloff, Tamara, Kristine Hovhannesyan, Flávia Piazzon, et al.. (2023). Baby detect: Universal genomic newborn screening for early, treatable, and severe conditions. Journal of the Neurological Sciences. 455. 121259–121259. 1 indexed citations
4.
Dangouloff, Tamara, et al.. (2023). O10 Universal genomic newborn screening for early, treatable, and severe conditions- including 33 genes of NMD: Baby Detect. Neuromuscular Disorders. 33. S130–S131. 3 indexed citations
5.
6.
Santos, Bibiana Alves dos, et al.. (2022). Allan-Herndon-Dudley syndrome in a female patient and related mechanisms. Molecular Genetics and Metabolism Reports. 31. 100879–100879. 4 indexed citations
7.
Cola, Paula Cristina, et al.. (2022). CEDNIK syndrome in a Brazilian patient with compound heterozygous pathogenic variants. European Journal of Medical Genetics. 65(3). 104440–104440. 1 indexed citations
8.
Piazzon, Flávia, et al.. (2022). Pseudohipoaldosteronism Type 1: a case report supported by a literature review. International Journal of Nutrology. 15(3).
9.
Piazzon, Flávia, et al.. (2020). Electrical storm treated successfully in a patient with TANGO2 gene mutation and long QT syndrome: A case report. HeartRhythm Case Reports. 6(5). 256–260. 7 indexed citations
10.
Muntau, Ania C., Darius J. Adams, Amaya Bélanger-Quintana, et al.. (2019). International best practice for the evaluation of responsiveness to sapropterin dihydrochloride in patients with phenylketonuria. Molecular Genetics and Metabolism. 127(1). 1–11. 43 indexed citations
11.
Ceroni, José Ricardo Magliocco, Rachel Sayuri Honjo, Juan Clinton Llerena, et al.. (2018). A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability. Scientific Reports. 8(1). 13382–13382. 1 indexed citations
12.
Vaisbich, María Helena, et al.. (2017). Thrombotic microangiopathy caused by methionine synthase deficiency: diagnosis and treatment pitfalls. Pediatric Nephrology. 32(6). 1089–1092. 15 indexed citations
13.
14.
Piazzon, Flávia, et al.. (2016). Subtelomeric Copy Number Variations: The Importance of 4p/4q Deletions in Patients with Congenital Anomalies and Developmental Disability. Cytogenetic and Genome Research. 149(4). 241–246. 5 indexed citations
15.
Piazzon, Flávia, Cíntia Milani, Regina Schultz, et al.. (2016). Post-mortem cytogenomic investigations in patients with congenital malformations. Experimental and Molecular Pathology. 101(1). 116–123. 4 indexed citations
16.
Piazzon, Flávia, et al.. (2015). Rare genomic rearrangement in a boy with Williams–Beuren syndrome associated to XYY syndrome and intriguing behavior. American Journal of Medical Genetics Part A. 167(12). 3197–3203. 2 indexed citations
17.
Christofolini, Denise Maria, Flávia Piazzon, Fernanda Mafra, et al.. (2014). Complex small supernumerary marker chromosome with a 15q/16p duplication: clinical implications. Molecular Cytogenetics. 7(1). 29–29. 3 indexed citations
18.
Piazzon, Flávia, et al.. (2014). Complex structural rearrangement features suggesting chromoanagenesis mechanism in a case of 1p36 deletion syndrome. Molecular Genetics and Genomics. 289(6). 1037–1043. 11 indexed citations
19.
20.
Belangero, Síntia, Fernanda T. Bellucco, Denise Maria Christofolini, et al.. (2012). Wide Clinical Variability in Cat Eye Syndrome Patients: Four Non-Related Patients and Three Patients from the Same Family. Cytogenetic and Genome Research. 138(1). 5–10. 16 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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