Luísa Diogo

3.0k total citations
71 papers, 1.4k citations indexed

About

Luísa Diogo is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Luísa Diogo has authored 71 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Clinical Biochemistry, 38 papers in Molecular Biology and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Luísa Diogo's work include Metabolism and Genetic Disorders (46 papers), Mitochondrial Function and Pathology (16 papers) and Neonatal Health and Biochemistry (13 papers). Luísa Diogo is often cited by papers focused on Metabolism and Genetic Disorders (46 papers), Mitochondrial Function and Pathology (16 papers) and Neonatal Health and Biochemistry (13 papers). Luísa Diogo collaborates with scholars based in Portugal, Netherlands and Italy. Luísa Diogo's co-authors include Paula Garcia, Manuela Grazina, Catarina R. Oliveira, Guiomar Oliveira, Luís Borges, Carla Marques, Assunção Ataíde, Esmeralda Martins, Elisa Leão Teles and Laura Vilarinho and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Biochemical and Biophysical Research Communications.

In The Last Decade

Luísa Diogo

66 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luísa Diogo Portugal 20 790 622 304 201 185 71 1.4k
Thomas Opladen Germany 24 782 1.0× 860 1.4× 478 1.6× 128 0.6× 191 1.0× 84 1.9k
Mercedes Serrano Spain 24 611 0.8× 504 0.8× 308 1.0× 58 0.3× 159 0.9× 80 1.4k
Paula Garcia Portugal 16 344 0.4× 272 0.4× 195 0.6× 136 0.7× 162 0.9× 49 774
Birgit Assmann Germany 23 870 1.1× 789 1.3× 299 1.0× 29 0.1× 214 1.2× 51 1.7k
Ivo Barić Croatia 25 1.1k 1.4× 980 1.6× 255 0.8× 48 0.2× 240 1.3× 81 1.8k
S. Lane Rutledge United States 19 844 1.1× 519 0.8× 252 0.8× 40 0.2× 104 0.6× 31 1.3k
Concetta Meli Italy 15 460 0.6× 573 0.9× 140 0.5× 82 0.4× 181 1.0× 45 874
Annette Feigenbaum Canada 28 1.7k 2.1× 1.1k 1.8× 252 0.8× 30 0.1× 192 1.0× 61 2.3k
Johanna Uusimaa Finland 24 1.3k 1.7× 747 1.2× 194 0.6× 26 0.1× 145 0.8× 82 1.8k
Pilar Rodríguez‐Pombo Spain 22 870 1.1× 730 1.2× 171 0.6× 19 0.1× 131 0.7× 57 1.3k

Countries citing papers authored by Luísa Diogo

Since Specialization
Citations

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

Fields of papers citing papers by Luísa Diogo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luísa Diogo

This figure shows the co-authorship network connecting the top 25 collaborators of Luísa Diogo. A scholar is included among the top collaborators of Luísa Diogo 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 Luísa Diogo. Luísa Diogo 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.
Ferreira, Helena Beatriz, Luísa Diogo, Laura Goracci, et al.. (2025). Lipidomic Profiling of Red Blood Cells in the Mitochondrial Fatty Acid β-oxidation Disorder MCADD Reveals Phospholipid and Sphingolipid Dysregulation. Journal of Proteome Research. 24(9). 4631–4642.
2.
Ferreira, Helena Beatriz, Luísa Diogo, Laura Goracci, et al.. (2024). Plasma lipidomics analysis reveals altered profile of triglycerides and phospholipids in children with Medium‐Chain Acyl‐CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 47(4). 731–745. 3 indexed citations
3.
Alves, Ana Catarina, et al.. (2023). Rare primary dyslipidaemias associated with low LDL and HDL cholesterol values in Portugal. Frontiers in Genetics. 13. 1088040–1088040. 3 indexed citations
4.
Ferreira, Helena Beatriz, Tânia Melo, Hugo Rocha, et al.. (2022). Mitochondrial Fatty Acid β-Oxidation Disorders: From Disease to Lipidomic Studies—A Critical Review. International Journal of Molecular Sciences. 23(22). 13933–13933. 43 indexed citations
5.
González‐Meneses, Antonio, et al.. (2021). Description of the molecular and clinical characteristics of the mucopolysaccharidosis type VII Iberian cohort. Orphanet Journal of Rare Diseases. 16(1). 445–445. 6 indexed citations
6.
Garcia, Paula, et al.. (2020). Experience on statin therapy in paediatric age: retrospective study in a Portuguese referral centre. Cardiology in the Young. 30(6). 840–851. 1 indexed citations
7.
Garcia, Paula, et al.. (2019). Ketogenic Diet for Refractory Childhood Epilepsy: Beyond Seizures Control, the Experience of a Portuguese Pediatric Centre. Acta Médica Portuguesa. 32(12). 760–766. 14 indexed citations
8.
Garcia, Paula, et al.. (2017). Fallo hepático aguda asociado a enfermedades metabólicas hereditarias en niños pequeños. Anales de Pediatría. 88(2). 69–74. 10 indexed citations
9.
Ferdinandusse, Sacha, Liesbeth Keldermans, Dulce Quelhas, et al.. (2017). Galactose Epimerase Deficiency: Expanding the Phenotype. JIMD Reports. 37. 19–25. 6 indexed citations
10.
Pratas, João, Carolina Ribeiro, Maria João Santos, et al.. (2016). In silico analysis for predicting pathogenicity of five unclassified mitochondrial DNA mutations associated with mitochondrial cytopathies' phenotypes. European Journal of Medical Genetics. 60(3). 172–177. 9 indexed citations
11.
Loureiro, Susana, et al.. (2014). Défice cognitivo por defeito da síntese de creatina. SHILAP Revista de lepidopterología. 41(3). 131–131.
12.
Oliveira, Renata L. de, Paula Garcia, Isabel Fineza, et al.. (2013). Pyridoxine‐dependent epilepsy due to antiquitin deficiency: achieving a favourable outcome. Epileptic Disorders. 15(4). 400–406. 18 indexed citations
13.
Garcia, Paula, et al.. (2010). Skeletal complications in mucopolysaccharidosis VI patients: Case reports. Journal of Pediatric Rehabilitation Medicine. 3(1). 63–69. 11 indexed citations
14.
Diogo, Luísa, Miguel Cordeiro, Paula Garcia, et al.. (2010). Value of Brain Magnetic Resonance Imaging in Mitochondrial Respiratory Chain Disorders. Pediatric Neurology. 42(3). 196–200. 9 indexed citations
15.
Diogo, Luísa, Manuela Grazina, Paula Garcia, et al.. (2009). Pediatric Mitochondrial Respiratory Chain Disorders in the Centro Region of Portugal. Pediatric Neurology. 40(5). 351–356. 18 indexed citations
16.
Jones, John G., Paula Garcia, Cristina Barosa, Teresa C. Delgado, & Luísa Diogo. (2009). Hepatic anaplerotic outflow fluxes are redirected from gluconeogenesis to lactate synthesis in patients with Type 1a glycogen storage disease. Metabolic Engineering. 11(3). 155–162. 15 indexed citations
17.
Nogueira, Célia, Chiara Aiello, R. Cerone, et al.. (2008). Spectrum of MMACHC mutations in Italian and Portuguese patients with combined methylmalonic aciduria and homocystinuria, cblC type. Molecular Genetics and Metabolism. 93(4). 475–480. 72 indexed citations
18.
Ruiter, Jos P.N., Lodewijk IJlst, C. C. P. Aires, et al.. (2007). In vivo and in vitro studies on the interaction of valproic acid and metabolites with the leucine oxidative metabolism. Journal of Inherited Metabolic Disease. 30. 42–42. 1 indexed citations
19.
Grazina, Manuela, et al.. (2007). Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation—A case report. European Journal of Paediatric Neurology. 11(2). 115–118. 26 indexed citations
20.
Azevedo, Luı́sa, Laura Vilarinho, Elisa Leão Teles, et al.. (2006). Mutational Spectrum and Linkage Disequilibrium Patterns at the Ornithine Transcarbamylase Gene (OTC). Annals of Human Genetics. 70(6). 797–801. 5 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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