Paula Faustino

2.7k total citations
67 papers, 1.9k citations indexed

About

Paula Faustino is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Paula Faustino has authored 67 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 37 papers in Hematology and 20 papers in Molecular Biology. Recurrent topics in Paula Faustino's work include Hemoglobinopathies and Related Disorders (39 papers), Iron Metabolism and Disorders (37 papers) and Trace Elements in Health (12 papers). Paula Faustino is often cited by papers focused on Hemoglobinopathies and Related Disorders (39 papers), Iron Metabolism and Disorders (37 papers) and Trace Elements in Health (12 papers). Paula Faustino collaborates with scholars based in Portugal, Mozambique and United States. Paula Faustino's co-authors include Bruno Silva, Jack S. Cohen, Robbe C. Lyon, Peter F. Daly, Luı́sa Romão, João Lavinha, Ofer Kaplan, James J. Pekar, Chrit Moonen and Peter C. van Zijl and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Paula Faustino

63 papers receiving 1.8k citations

Peers

Paula Faustino
Michael H. Creer United States
Orla Cunningham United States
Fritz Sieber United States
John F. Healey United States
Martha P. Mims United States
Takako Furukawa Japan
B Hecquet France
Joëlle Thillet France
Arineh Khechaduri United States
Daruka Mahadevan United States
Michael H. Creer United States
Paula Faustino
Citations per year, relative to Paula Faustino Paula Faustino (= 1×) peers Michael H. Creer

Countries citing papers authored by Paula Faustino

Since Specialization
Citations

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

Fields of papers citing papers by Paula Faustino

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paula Faustino

This figure shows the co-authorship network connecting the top 25 collaborators of Paula Faustino. A scholar is included among the top collaborators of Paula Faustino 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 Paula Faustino. Paula Faustino 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.
Faustino, Paula, et al.. (2024). Analysis of Genes Involved in Oxidative Stress and Iron Metabolism in Heart Failure: A Step Forward in Risk Stratification. Cureus. 16(5). e60707–e60707. 1 indexed citations
2.
3.
Vargas, Sofía, et al.. (2021). VCAM1, HMOX1 and NOS3 differential endothelial expression may impact sickle cell anemia vasculopathy. Blood Cells Molecules and Diseases. 93. 102639–102639. 3 indexed citations
4.
Santos, Brígida, et al.. (2020). Co-Inheritance of alpha-thalassemia and sickle cell disease in a cohort of Angolan pediatric patients. Molecular Biology Reports. 47(7). 5397–5402. 11 indexed citations
5.
Kislaya, Irina, Mafalda Sousa‐Uva, Vânia Gaio, et al.. (2020). Prevalence of anemia in the Portuguese adult population: results from the first National Health Examination Survey (INSEF 2015). Journal of Public Health. 30(4). 1033–1040.
6.
Vargas, Sofía, et al.. (2020). Biomarkers and genetic modulators of cerebral vasculopathy in sub-Saharan ancestry children with sickle cell anemia. Blood Cells Molecules and Diseases. 83. 102436–102436. 8 indexed citations
7.
David, Susana, Liliana Antunes, Paula Faustino, et al.. (2017). Population genetics of IFITM3 in Portugal and Central Africa reveals a potential modifier of influenza severity. Immunogenetics. 70(3). 169–177. 19 indexed citations
8.
Monteiro, Estela, et al.. (2017). Widening the spectrum of deletions and molecular mechanisms underlying alpha-thalassemia. Annals of Hematology. 96(11). 1921–1929. 6 indexed citations
9.
Marques, Oriana, Paula Faustino, Alexandra Rêma, et al.. (2016). HFE Variants and the Expression of Iron-Related Proteins in Breast Cancer-Associated Lymphocytes and Macrophages. Cancer Microenvironment. 9(2-3). 85–91. 3 indexed citations
10.
Silva, Bruno, Ângela C. Crespo, Sónia Costa, et al.. (2015). Decrease in APP and CP mRNA expression supports impairment of iron export in Alzheimer's disease patients. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1852(10). 2116–2122. 19 indexed citations
11.
Silva, Bruno & Paula Faustino. (2015). An overview of molecular basis of iron metabolism regulation and the associated pathologies. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1852(7). 1347–1359. 233 indexed citations
12.
Silva, Bruno, et al.. (2014). The soluble form of HFE protein regulates hephaestin mRNA expression in the duodenum through an endocytosis-dependent mechanism. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(11). 2298–2305. 4 indexed citations
13.
Martins, Rute, et al.. (2011). Differential HFE Gene Expression Is Regulated by Alternative Splicing in Human Tissues. PLoS ONE. 6(3). e17542–e17542. 15 indexed citations
14.
Bettencourt, Andreia, Ernestina Santos, Saint Clair Gomes, et al.. (2010). HFE gene polymorphisms and severity in Portuguese patients with multiple sclerosis. European Journal of Neurology. 18(4). 663–666. 9 indexed citations
15.
Martins, Rute, et al.. (2008). Early modification of sickle cell disease clinical course by UDP-glucuronosyltransferase 1A1 gene promoter polymorphism. Journal of Human Genetics. 53(6). 524–528. 12 indexed citations
16.
Alves, Maria Teresa de Seixas, et al.. (2007). Mutational spectrum of delta‐globin gene in the Portuguese population. European Journal Of Haematology. 79(5). 422–428. 26 indexed citations
17.
Silva, Maria do Céu, et al.. (2006). Human α2‐globin nonsense‐mediated mRNA decay induced by a novel α‐thalassaemia frameshift mutation at codon 22. British Journal of Haematology. 133(1). 98–102. 15 indexed citations
18.
Silva, Ana Luísa, Jian Kong, Rute Martins, et al.. (2006). The canonical UPF1-dependent nonsense-mediated mRNA decay is inhibited in transcripts carrying a short open reading frame independent of sequence context. RNA. 12(12). 2160–2170. 37 indexed citations
19.
20.
Lyon, Robbe C., et al.. (1987). Metabolic changes associated with drug resistance in human breast cancer cells monitored by magnetic resonance spectroscopy mrs. 28. 293. 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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