Luı́sa Azevedo

2.3k total citations · 1 hit paper
63 papers, 1.2k citations indexed

About

Luı́sa Azevedo is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Luı́sa Azevedo has authored 63 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 21 papers in Genetics and 17 papers in Clinical Biochemistry. Recurrent topics in Luı́sa Azevedo's work include Metabolism and Genetic Disorders (17 papers), Amino Acid Enzymes and Metabolism (11 papers) and Genomics and Rare Diseases (9 papers). Luı́sa Azevedo is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Amino Acid Enzymes and Metabolism (11 papers) and Genomics and Rare Diseases (9 papers). Luı́sa Azevedo collaborates with scholars based in Portugal, United Kingdom and Belgium. Luı́sa Azevedo's co-authors include António Amorim, D.N. Cooper, Matthew Mort, Peter D. Stenson, Edward V. Ball, David Millar, Matthew Hayden, Sally Heywood, Andrew D. Phillips and Raquel M. Silva and has published in prestigious journals such as PLoS ONE, Scientific Reports and Biochemical and Biophysical Research Communications.

In The Last Decade

Luı́sa Azevedo

59 papers receiving 1.2k citations

Hit Papers

The Human Gene Mutation Database (HGMD®): optimizing its ... 2020 2026 2022 2024 2020 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luı́sa Azevedo Portugal 17 770 393 153 83 83 63 1.2k
Radek Szklarczyk Netherlands 23 1.3k 1.7× 133 0.3× 334 2.2× 77 0.9× 74 0.9× 36 1.6k
Bryce A. Mendelsohn United States 16 561 0.7× 184 0.5× 50 0.3× 157 1.9× 117 1.4× 28 1.0k
F Quan United States 16 672 0.9× 208 0.5× 106 0.7× 210 2.5× 160 1.9× 20 1.0k
Jukka Kallijärvi Finland 19 753 1.0× 126 0.3× 87 0.6× 84 1.0× 95 1.1× 41 1.1k
Claire Redin France 10 888 1.2× 482 1.2× 97 0.6× 79 1.0× 82 1.0× 18 1.3k
Mizuki Ohno Japan 20 1.1k 1.4× 338 0.9× 50 0.3× 52 0.6× 44 0.5× 32 1.6k
Isha H. Jain United States 13 844 1.1× 151 0.4× 175 1.1× 57 0.7× 72 0.9× 24 1.1k
Lucia Cavelier Sweden 22 1.0k 1.3× 208 0.5× 169 1.1× 115 1.4× 22 0.3× 63 1.7k
Narasimhan Nagan United States 21 1.3k 1.7× 235 0.6× 106 0.7× 103 1.2× 113 1.4× 27 2.0k
Joseph G. Vockley United States 19 730 0.9× 457 1.2× 230 1.5× 28 0.3× 65 0.8× 31 1.4k

Countries citing papers authored by Luı́sa Azevedo

Since Specialization
Citations

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

Fields of papers citing papers by Luı́sa Azevedo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luı́sa Azevedo

This figure shows the co-authorship network connecting the top 25 collaborators of Luı́sa Azevedo. A scholar is included among the top collaborators of Luı́sa Azevedo 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 Luı́sa Azevedo. Luı́sa Azevedo 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.
Azevedo, Luı́sa, et al.. (2025). The role of crustacean zooplankton in water quality monitoring: Findings from two Portuguese reservoirs. Ecohydrology & Hydrobiology. 25(4). 100646–100646. 1 indexed citations
2.
Azevedo, Luı́sa, et al.. (2025). Changes in Regional Practices and Their Effects on the Water Quality of Portuguese Reservoirs. Earth. 6(2). 29–29. 2 indexed citations
3.
Azevedo, Luı́sa, et al.. (2024). A Comprehensive Approach to the Diagnosis of Leigh Syndrome Spectrum. Diagnostics. 14(19). 2133–2133.
4.
Azevedo, Luı́sa, et al.. (2024). Naturally occurring genetic diseases caused by de novo variants in domestic animals. Animal Genetics. 55(3). 319–327. 1 indexed citations
5.
Lopes‐Marques, Mónica, Maria João Peixoto, D.N. Cooper, et al.. (2024). Polymorphic pseudogenes in the human genome - a comprehensive assessment. Human Genetics. 143(12). 1465–1479. 1 indexed citations
6.
Oliveira, Manuela, Luı́sa Azevedo, David Ballard, Wojciech Branicki, & António Amorim. (2023). Using plants in forensics: State-of-the-art and prospects. Plant Science. 336. 111860–111860. 6 indexed citations
7.
Lopes‐Marques, Mónica, Maria João Peixoto, António Amorim, et al.. (2021). Common polymorphic OTC variants can act as genetic modifiers of enzymatic activity. Human Mutation. 42(8). 978–989. 4 indexed citations
8.
Stenson, Peter D., Matthew Mort, Edward V. Ball, et al.. (2020). The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting. Human Genetics. 139(10). 1197–1207. 410 indexed citations breakdown →
9.
Lopes‐Marques, Mónica, Renato Salazar, Susana Seixas, et al.. (2020). GBA3: a polymorphic pseudogene in humans that experienced repeated gene loss during mammalian evolution. Scientific Reports. 10(1). 11565–11565. 4 indexed citations
10.
Carvalho, R., et al.. (2018). Evaluation of InnoQuant® HY and InnoTyper® 21 kits in the DNA analysis of rootless hair samples. Forensic Science International Genetics. 39. 61–65. 10 indexed citations
12.
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
13.
Moreira, Cláudia, Bárbara van Asch, Luís Fonseca, et al.. (2013). The mitochondrial genome of the pinewood nematode (Bursaphelenchus xylophilus) lineage introduced in Europe. Mitochondrial DNA. 25(6). 420–421. 3 indexed citations
14.
Pereira‐Castro, Isabel, Luís Teixeira da Costa, António Amorim, & Luı́sa Azevedo. (2012). Transcriptional regulation of the human mitochondrial peptide deformylase (PDF). Biochemical and Biophysical Research Communications. 421(4). 825–831. 5 indexed citations
15.
Lopes‐Marques, Mónica, Isabel Pereira‐Castro, António Amorim, & Luı́sa Azevedo. (2011). Characterization of the Human Ornithine Transcarbamylase 3′ Untranslated Regulatory Region. DNA and Cell Biology. 31(4). 427–433. 6 indexed citations
16.
Azevedo, Luı́sa, et al.. (2010). Comparative analyses of the Conserved Oligomeric Golgi (COG) complex in vertebrates. BMC Evolutionary Biology. 10(1). 212–212. 8 indexed citations
17.
Almeida, Teresa, Isabel Alonso, Sandra Martins, et al.. (2009). Ancestral Origin of the ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10 (SCA10). PLoS ONE. 4(2). e4553–e4553. 39 indexed citations
18.
Azevedo, Luı́sa, et al.. (2009). Epistatic interactions modulate the evolution of mammalian mitochondrial respiratory complex components. BMC Genomics. 10(1). 266–266. 30 indexed citations
19.
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
20.
Azevedo, Luı́sa, Consuelo Climent, Laura Vilarinho, Francesc Calafell, & António Amorim. (2004). Evidence for mutational cis-acting factors affecting mutagenesis in the ornithine transcarbamylase gene. Human Mutation. 24(3). 273–273. 3 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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