Laura Vilarinho

5.3k total citations
157 papers, 2.5k citations indexed

About

Laura Vilarinho is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, Laura Vilarinho has authored 157 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 95 papers in Clinical Biochemistry, 82 papers in Molecular Biology and 36 papers in Rheumatology. Recurrent topics in Laura Vilarinho's work include Metabolism and Genetic Disorders (94 papers), Mitochondrial Function and Pathology (46 papers) and Folate and B Vitamins Research (32 papers). Laura Vilarinho is often cited by papers focused on Metabolism and Genetic Disorders (94 papers), Mitochondrial Function and Pathology (46 papers) and Folate and B Vitamins Research (32 papers). Laura Vilarinho collaborates with scholars based in Portugal, Italy and Spain. Laura Vilarinho's co-authors include Filippo M. Santorelli, Esmeralda Martins, Hugo Rocha, Maria Luı́s Cardoso, Célia Nogueira, Lígia S. Almeida, Jorge Machado, Elisa Leão Teles, Carlo Dionisi‐Vici and Ana Marcão and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Laura Vilarinho

145 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Laura Vilarinho Portugal	25	1.5k	1.4k	479	232	224	157	2.5k
Xuefan Gu China	27	1.4k 0.9×	888 0.7×	515 1.1×	419 1.8×	170 0.8×	217	2.5k
Majid Alfadhel Saudi Arabia	28	1.4k 0.9×	625 0.5×	254 0.5×	301 1.3×	218 1.0×	157	2.5k
Lee-Jun Wong United States	28	1.8k 1.2×	1.1k 0.8×	117 0.2×	203 0.9×	99 0.4×	59	2.6k
Timothy Wai France	24	4.3k 2.8×	1.3k 0.9×	229 0.5×	304 1.3×	334 1.5×	39	5.4k
Charles P. Venditti United States	37	2.2k 1.4×	1.6k 1.2×	891 1.9×	407 1.8×	165 0.7×	102	4.1k
David Watkins Canada	30	1.6k 1.1×	1.1k 0.8×	1.9k 3.9×	298 1.3×	83 0.4×	99	3.0k
Antonella Spinazzola United Kingdom	33	3.5k 2.2×	1.8k 1.4×	146 0.3×	95 0.4×	106 0.5×	57	3.9k
Garry K. Brown United Kingdom	39	2.8k 1.8×	2.2k 1.6×	144 0.3×	210 0.9×	148 0.7×	91	3.8k
Valérie Serre France	26	1.9k 1.2×	703 0.5×	89 0.2×	90 0.4×	157 0.7×	47	2.6k
M. T. Zabot France	25	826 0.5×	423 0.3×	154 0.3×	136 0.6×	121 0.5×	54	1.6k

Countries citing papers authored by Laura Vilarinho

Since Specialization

Citations

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

Fields of papers citing papers by Laura Vilarinho

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Vilarinho

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

Marcão, Ana, Teresa Faria, Ana Rita Coimbra Motta-Castro, et al.. (2025). Newborn Screening for Sickle Cell Disease: Results from a Pilot Study in the Portuguese Population. International Journal of Neonatal Screening. 11(1). 10–10. 1 indexed citations

Marcão, Ana, et al.. (2024). Portuguese Neonatal Screening Program: A Cohort Study of 18 Years Using MS/MS. International Journal of Neonatal Screening. 10(1). 25–25. 3 indexed citations

Costeira, María José, et al.. (2024). History of Neonatal Screening of Congenital Hypothyroidism in Portugal. International Journal of Neonatal Screening. 10(1). 16–16. 3 indexed citations

Roque, Susana, Tim I.M. Korevaar, Ana Machado, et al.. (2024). Iodineminho Study: Iodine Supplementation and Prevalence of Iodine Deficiency In Pregnant Women. The Journal of Clinical Endocrinology & Metabolism. 109(11). e2065–e2074. 1 indexed citations

Azevedo, Luı́sa, et al.. (2024). A Comprehensive Approach to the Diagnosis of Leigh Syndrome Spectrum. Diagnostics. 14(19). 2133–2133.

Nogueira, Célia, Patrícia Janeiro, Charles Marques Lourenço, et al.. (2023). Leigh Syndrome Spectrum: A Portuguese Population Cohort in an Evolutionary Genetic Era. Genes. 14(8). 1536–1536. 2 indexed citations

Vilarinho, Laura, et al.. (2023). Maternal Urinary Iodine Concentration during Pregnancy and Its Impact on Child Growth and Neurodevelopment: An 11-Year Follow-Up Study. Nutrients. 15(20). 4447–4447. 1 indexed citations

Nogueira‐Ferreira, Rita, Hugo Rocha, José Alberto Duarte, et al.. (2022). Exercise training counteracts the cardiac metabolic remodelling induced by experimental pulmonary arterial hypertension. Archives of Biochemistry and Biophysics. 730. 109419–109419. 1 indexed citations

Janeiro, Patrícia, et al.. (2022). Acquired Vitamin B12 Deficiency in Newborns: Positive Impact on Newborn Health through Early Detection. Nutrients. 14(20). 4397–4397. 7 indexed citations

10.

Nogueira, Célia, Ana Marcão, Hugo Rocha, et al.. (2021). Role of RNA in Molecular Diagnosis of MADD Patients. Biomedicines. 9(5). 507–507. 5 indexed citations

11.

Encarnação, Marisa, Maria Francisca Coutinho, Isaura Ribeiro, et al.. (2020). NPC1 silent variant induces skipping of exon 11 (p.V562V) and unfolded protein response was found in a specific Niemann‐Pick type C patient. Molecular Genetics & Genomic Medicine. 8(11). e1451–e1451. 12 indexed citations

12.

Navarro, David, Sílvia Sequeira, Ana Carina Ferreira, et al.. (2018). Atypical adult-onset methylmalonic acidemia and homocystinuria presenting as hemolytic uremic syndrome. CEN Case Reports. 7(1). 73–76. 5 indexed citations

13.

Mota, Conceição, et al.. (2018). <i>CTNS</i> Molecular Genetics Profile in a Portuguese Cystinosis Population. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 8(4). 91–100. 2 indexed citations

14.

Azevedo, Luı́sa, et al.. (2016). 3-Methylcrotonyl-CoA carboxylase deficiency: Mutational spectrum derived from comprehensive newborn screening. Gene. 594(2). 203–210. 15 indexed citations

15.

Vanzin, Camila Simioni, Caroline Paula Mescka, Bruna Donida, et al.. (2015). Lipid, Oxidative and Inflammatory Profile and Alterations in the Enzymes Paraoxonase and Butyrylcholinesterase in Plasma of Patients with Homocystinuria Due CBS Deficiency: The Vitamin B12 and Folic Acid Importance. Cellular and Molecular Neurobiology. 35(6). 899–911. 18 indexed citations

16.

Nogueira, Célia, Lígia S. Almeida, Claudia Nesti, et al.. (2014). Syndromes associated with mitochondrial DNA depletion. The Italian Journal of Pediatrics/Italian journal of pediatrics. 40(1). 34–34. 37 indexed citations

17.

Vilarinho, Laura, et al.. (2012). Programa Nacional de Diagnóstico Precoce: Relatório 2011. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 1–51. 2 indexed citations

18.

Aguiar, Tatiana Quinta, et al.. (2008). Cadeia Respiratória Mitocondrial Aspectos Clínicos, Bioquímicos, Enzimáticos e Moleculares Associados ao Déﬁce do Complexo I. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 22. 49–56. 3 indexed citations

19.

Nogueira, Célia, João Paulo Silva Nunes, Teresinha Evangelista, et al.. (2007). A new mtDNA–tRNAGlu mutation (14728T>C) presenting a late-onset mitochondrial encephalomyopathy. Mitochondrion. 7(6). 396–398. 6 indexed citations

20.

Cardoso, Maria Luı́s, Esmeralda Martins, Luís Nunes, et al.. (2005). Molecular studies in Portuguese patients with Smith–Lemli–Opitz syndrome and report of three new mutations in DHCR7. Molecular Genetics and Metabolism. 85(3). 228–235. 8 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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