Fabíola Paoli Monteiro

1.1k total citations
24 papers, 314 citations indexed

About

Fabíola Paoli Monteiro is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Fabíola Paoli Monteiro has authored 24 papers receiving a total of 314 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 18 papers in Genetics and 4 papers in Plant Science. Recurrent topics in Fabíola Paoli Monteiro's work include Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (11 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Fabíola Paoli Monteiro is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (11 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Fabíola Paoli Monteiro collaborates with scholars based in Brazil, United States and Canada. Fabíola Paoli Monteiro's co-authors include Vera Lúcia Gil‐da‐Silva‐Lopes, Társis Paiva Vieira, Fernando Kok, João Paulo Kitajima, Milena Simioni, Josiane Souza, Érika L. Freitas, Isabella Lopes Monlleó, Agnes Cristina Fett‐Conte and Têmis Maria Félix and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Scientific Reports.

In The Last Decade

Fabíola Paoli Monteiro

24 papers receiving 311 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fabíola Paoli Monteiro Brazil 11 198 138 58 58 29 24 314
Cristina da Silva United States 12 225 1.1× 218 1.6× 38 0.7× 38 0.7× 68 2.3× 19 528
Bird Td United States 6 162 0.8× 90 0.7× 26 0.4× 18 0.3× 10 0.3× 244 342
Mefford Hc 6 163 0.8× 90 0.7× 25 0.4× 17 0.3× 11 0.4× 239 337
Patrick A. Lundquist United States 8 130 0.7× 55 0.4× 48 0.8× 50 0.9× 31 1.1× 16 440
Kei Shioda Japan 14 274 1.4× 82 0.6× 42 0.7× 50 0.9× 27 0.9× 25 517
Giuseppe Galvani Italy 13 193 1.0× 193 1.4× 13 0.2× 28 0.5× 14 0.5× 22 367
Luis Rohena United States 12 192 1.0× 154 1.1× 13 0.2× 24 0.4× 18 0.6× 27 383
Luigina Spaccini Italy 13 208 1.1× 159 1.2× 19 0.3× 16 0.3× 29 1.0× 47 455
Marwan Nashabat Saudi Arabia 13 229 1.2× 105 0.8× 21 0.4× 12 0.2× 29 1.0× 25 422
Ilenia Bernascone Italy 10 244 1.2× 69 0.5× 130 2.2× 16 0.3× 10 0.3× 11 473

Countries citing papers authored by Fabíola Paoli Monteiro

Since Specialization
Citations

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

Fields of papers citing papers by Fabíola Paoli Monteiro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fabíola Paoli Monteiro. 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 Fabíola Paoli Monteiro. The network helps show where Fabíola Paoli Monteiro may publish in the future.

Co-authorship network of co-authors of Fabíola Paoli Monteiro

This figure shows the co-authorship network connecting the top 25 collaborators of Fabíola Paoli Monteiro. A scholar is included among the top collaborators of Fabíola Paoli Monteiro 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 Fabíola Paoli Monteiro. Fabíola Paoli Monteiro 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.
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
2.
Guindalini, Rodrigo Santa Cruz, João Paulo Kitajima, Rossana Veronica Mendoza López, et al.. (2022). Detection of germline variants in Brazilian breast cancer patients using multigene panel testing. Scientific Reports. 12(1). 4190–4190. 35 indexed citations
3.
Smith, Richard S., Marta Florio, Shyam K. Akula, et al.. (2021). Early role for a Na + ,K + -ATPase ( ATP1A3 ) in brain development. Proceedings of the National Academy of Sciences. 118(25). 28 indexed citations
4.
Ligabue‐Braun, Rodrigo, Carolina Fischinger Moura de Souza, Fabíola Paoli Monteiro, et al.. (2021). The fructose-1,6-bisphosphatase deficiency and the p.(Lys204ArgfsTer72) variant. Genetics and Molecular Biology. 44(2). e20200281–e20200281. 2 indexed citations
5.
Macedo‐Souza, Lúcia Inês, Juliana Gurgel‐Giannetti, Fabíola Paoli Monteiro, et al.. (2021). MECP2-related conditions in males: A systematic literature review and 8 additional cases. European Journal of Paediatric Neurology. 34. 7–13. 9 indexed citations
6.
Macedo‐Souza, Lúcia Inês, et al.. (2020). Additional observation of a de novo pathogenic variant in KCNT2 leading to epileptic encephalopathy with clinical features of frontal lobe epilepsy. Brain and Development. 42(9). 691–695. 9 indexed citations
7.
Monteiro, Fabíola Paoli, et al.. (2020). Application of Whole-Exome Sequencing in Detecting Copy Number Variants in Patients with Developmental Delay and/or Multiple Congenital Malformations. Journal of Molecular Diagnostics. 22(8). 1041–1049. 11 indexed citations
8.
Macedo‐Souza, Lúcia Inês, Fabíola Paoli Monteiro, João Paulo Kitajima, et al.. (2019). Neurodevelopmental disorder associated with de novo SCN3A pathogenic variants: two new cases and review of the literature. Brain and Development. 42(2). 211–216. 15 indexed citations
9.
Monteiro, Fabíola Paoli, et al.. (2019). Testing criteria for 22q11.2 deletion syndrome: preliminary results of a low cost strategy for public health. Orphanet Journal of Rare Diseases. 14(1). 123–123. 10 indexed citations
10.
Monteiro, Fabíola Paoli, Cynthia J. Curry, Robert F. Hevner, et al.. (2019). Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. European Journal of Medical Genetics. 63(1). 103624–103624. 18 indexed citations
11.
Simioni, Milena, et al.. (2018). A Pure 2-Mb 3q26.2 Duplication Proximal to the Critical Region of 3q Duplication Syndrome. Molecular Syndromology. 9(4). 197–204. 2 indexed citations
12.
Simioni, Milena, et al.. (2017). A New Case of the Rare 10q22.3q23.2 Microdeletion Flanked by Low-Copy Repeats 3/4. Molecular Syndromology. 8(3). 161–167. 4 indexed citations
13.
Simioni, Milena, Társis Paiva Vieira, Fabíola Paoli Monteiro, et al.. (2017). Genomic imbalances in syndromic congenital heart disease. Jornal de Pediatria. 93(5). 497–507. 22 indexed citations
14.
Monteiro, Fabíola Paoli, et al.. (2017). Diagnostic Approach to Microdeletion Syndromes Based on 22q11.2 Investigation: Challenges in Four Cases. Molecular Syndromology. 8(5). 244–252. 7 indexed citations
15.
Ng, Bobby G., Kimiyo Raymond, Martin Kircher, et al.. (2015). Expanding the Molecular and Clinical Phenotype of SSR4-CDG. Human Mutation. 36(11). 1048–1051. 25 indexed citations
16.
Monteiro, Fabíola Paoli, et al.. (2015). 8p23.1 Interstitial Deletion in a Patient with Congenital Cardiopathy, Neurobehavioral Disorders, and Minor Signs Suggesting 22q11.2 Deletion Syndrome. Journal of Developmental & Behavioral Pediatrics. 36(7). 544–548. 7 indexed citations
17.
Vieira, Társis Paiva, Fabíola Paoli Monteiro, Josiane Souza, et al.. (2014). Clinical Features in Patients with 22q11.2 Deletion Syndrome Ascertained by Palatal Abnormalities. The Cleft Palate-Craniofacial Journal. 52(4). 411–416. 12 indexed citations
18.
Vieira, Társis Paiva, et al.. (2013). Atypical copy number abnormalities in 22q11.2 region: Report of three cases. European Journal of Medical Genetics. 56(9). 515–520. 14 indexed citations
19.
Monteiro, Fabíola Paoli, Társis Paiva Vieira, Josiane Souza, et al.. (2013). Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature. European Journal of Pediatrics. 172(7). 927–945. 46 indexed citations
20.

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 Cristina da Silva Breakdown of academic impact, for papers by Bird Td Breakdown of academic impact, for papers by Mefford Hc Breakdown of academic impact, for papers by Patrick A. Lundquist Breakdown of academic impact, for papers by Kei Shioda Breakdown of academic impact, for papers by Giuseppe Galvani Breakdown of academic impact, for papers by Luis Rohena Breakdown of academic impact, for papers by Luigina Spaccini Breakdown of academic impact, for papers by Marwan Nashabat Breakdown of academic impact, for papers by Ilenia Bernascone
Rankless by CCL
2026