Aída Lemes

700 total citations
11 papers, 71 citations indexed

About

Aída Lemes is a scholar working on Clinical Biochemistry, Physiology and Genetics. According to data from OpenAlex, Aída Lemes has authored 11 papers receiving a total of 71 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Clinical Biochemistry, 5 papers in Physiology and 4 papers in Genetics. Recurrent topics in Aída Lemes's work include Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (3 papers) and Diet and metabolism studies (3 papers). Aída Lemes is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (3 papers) and Diet and metabolism studies (3 papers). Aída Lemes collaborates with scholars based in Uruguay, Chile and Spain. Aída Lemes's co-authors include Mara Lúcia Schmitz Ferreira Santos, Angelina Xavier Acosta, Juan Francisco Cabello, Ana Maria Martins, Norberto Guelbert, Hernán Amartino, Roberto Giugliani, Carlos Robello, Martín Graña and Gonzalo Greif and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Medical Genetics and Journal of Inherited Metabolic Disease.

In The Last Decade

Aída Lemes

9 papers receiving 68 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aída Lemes Uruguay	5	37	26	19	13	12	11	71
Mary Ann R. Abacan Philippines	5	45 1.2×	24 0.9×	20 1.1×	25 1.9×	18 1.5×	14	81
A. Valiente Chile	5	40 1.1×	36 1.4×	15 0.8×	36 2.8×	23 1.9×	9	99
Shaun Bolton United Kingdom	5	23 0.6×	27 1.0×	11 0.6×	5 0.4×	4 0.3×	5	119
Iulia-Elena Simina Romania	5	31 0.8×	10 0.4×	9 0.5×	5 0.4×	13 1.1×	11	64
María Pérez-Poyato Spain	5	55 1.5×	20 0.8×	21 1.1×	3 0.2×	13 1.1×	6	83
Eulalia Turón‐Viñas Spain	6	15 0.4×	23 0.9×	16 0.8×	3 0.2×	7 0.6×	14	75
Jennifer C. Kelley United States	5	21 0.6×	14 0.5×	15 0.8×	2 0.2×	3 0.3×	9	85
Isabella Batten Ireland	5	10 0.3×	14 0.5×	8 0.4×	5 0.4×	5 0.4×	9	84
Anri Hayashi Japan	7	19 0.5×	47 1.8×	3 0.2×	28 2.2×	6 0.5×	17	128
Inmaculada Rueda Spain	4	9 0.2×	23 0.9×	5 0.3×	33 2.5×	10 0.8×	7	56

Countries citing papers authored by Aída Lemes

Since Specialization

Citations

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

Fields of papers citing papers by Aída Lemes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aída Lemes

This figure shows the co-authorship network connecting the top 25 collaborators of Aída Lemes. A scholar is included among the top collaborators of Aída Lemes 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 Aída Lemes. Aída Lemes is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

1.

Alonso, Martina, Daniela Lens, Martín Graña, et al.. (2021). Blood cell respiration rates and mtDNA copy number: A promising tool for the diagnosis of mitochondrial disease. Mitochondrion. 61. 31–43. 7 indexed citations

2.

Spangenberg, Lucía, Martín Graña, Gonzalo Greif, et al.. (2016). 3697G>A in MT-ND1 is a causative mutation in mitochondrial disease. Mitochondrion. 28. 54–59. 11 indexed citations

3.

Lemes, Aída, et al.. (2014). Care model for phenylketonuria (PKU) in Uruguay. SHILAP Revista de lepidopterología.

4.

Giugliani, Roberto, Norberto Guelbert, Ana Maria Martins, et al.. (2014). Guidelines for diagnosis and treatment of Hunter Syndrome for clinicians in Latin America. Genetics and Molecular Biology. 37(2). 315–329. 36 indexed citations

5.

Queijo, Cecilia, et al.. (2011). Déficit de acetil CoA deshidrogenasa de cadena media detectado por pesquisa neonatal en Uruguay. Acta bioquímica clínica latinoamericana. 45(1). 87–93. 1 indexed citations

6.

Lemes, Aída, et al.. (2006). Tres casos de enfermedad de Gaucher tipo I Clínica, diagnóstico, genética molecular y tratamiento actual. Revista Médica del Uruguay. 22(1). 73–77.

7.

Lemes, Aída, et al.. (2006). Succinic semialdehyde dehydrogenase (SSADH) deficiency: Molecular analysis in a South American family. Journal of Inherited Metabolic Disease. 29(4). 587–587. 6 indexed citations

8.

Lemes, Aída. (2003). Errores congénitos del metabolismo. 74(1). 33–36. 2 indexed citations

9.

Gutiérrez, Carmen, et al.. (2003). Muerte inesperada del lactante: Diagnóstico de situación en la ciudad de Montevideo. Revista chilena de pediatría. 74(2). 3 indexed citations

10.

Gutiérrez, Carmen, et al.. (2001). Muerte inesperada del lactante: Diagnóstico de situación en la ciudad de Montevideo. Scientific Electronic Library Online (Scientific Electronic Library Online). 72(3). 185–197. 4 indexed citations

11.

Quadrelli, Roberto, Alicia Vaglio, Aída Lemes, et al.. (2000). Uruguay facio-cardio-musculo-skeletal syndrome: A novel X-linked recessive disorder. American Journal of Medical Genetics. 95(3). 247–265. 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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