Lúcia Lacerda

1.6k total citations
39 papers, 936 citations indexed

About

Lúcia Lacerda is a scholar working on Physiology, Cell Biology and Molecular Biology. According to data from OpenAlex, Lúcia Lacerda has authored 39 papers receiving a total of 936 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Physiology, 18 papers in Cell Biology and 16 papers in Molecular Biology. Recurrent topics in Lúcia Lacerda's work include Lysosomal Storage Disorders Research (30 papers), Cellular transport and secretion (18 papers) and Carbohydrate Chemistry and Synthesis (11 papers). Lúcia Lacerda is often cited by papers focused on Lysosomal Storage Disorders Research (30 papers), Cellular transport and secretion (18 papers) and Carbohydrate Chemistry and Synthesis (11 papers). Lúcia Lacerda collaborates with scholars based in Portugal, Spain and Netherlands. Lúcia Lacerda's co-authors include Clara Sá-Miranda, Sandra Alves, Maria Francisca Coutinho, Olga Amaral, Rui Pinto, G. Ribeiro, Eugénia Pinto, Lurdes Lopes, Helena Ribeiro and Isaura Ribeiro and has published in prestigious journals such as SHILAP Revista de lepidopterología, British Journal of Haematology and Clinica Chimica Acta.

In The Last Decade

Lúcia Lacerda

38 papers receiving 909 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lúcia Lacerda Portugal 16 745 294 286 282 197 39 936
Helena Poupětová Czechia 17 932 1.3× 272 0.9× 302 1.1× 407 1.4× 196 1.0× 40 1.1k
Alison McVie‐Wylie United States 14 742 1.0× 124 0.4× 575 2.0× 238 0.8× 178 0.9× 20 1.2k
E. Young United Kingdom 15 664 0.9× 179 0.6× 175 0.6× 281 1.0× 138 0.7× 23 768
Monica Cardone Italy 10 405 0.5× 174 0.6× 330 1.2× 313 1.1× 85 0.4× 13 817
R J Desnick United States 12 778 1.0× 205 0.7× 245 0.9× 309 1.1× 198 1.0× 20 941
Robert Dobrovolný Czechia 13 640 0.9× 208 0.7× 154 0.5× 302 1.1× 190 1.0× 17 753
Roscoe O. Brady United States 10 426 0.6× 164 0.6× 317 1.1× 99 0.4× 141 0.7× 10 713
Marieke Biegstraaten Netherlands 17 1.1k 1.5× 386 1.3× 259 0.9× 410 1.5× 316 1.6× 29 1.3k
Motomichi Kosuga Japan 19 500 0.7× 89 0.3× 239 0.8× 223 0.8× 88 0.4× 54 839
Cordula Steglich Germany 16 609 0.8× 132 0.4× 226 0.8× 358 1.3× 158 0.8× 24 805

Countries citing papers authored by Lúcia Lacerda

Since Specialization
Citations

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

Fields of papers citing papers by Lúcia Lacerda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lúcia Lacerda

This figure shows the co-authorship network connecting the top 25 collaborators of Lúcia Lacerda. A scholar is included among the top collaborators of Lúcia Lacerda 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 Lúcia Lacerda. Lúcia Lacerda 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.
Lacerda, Lúcia, et al.. (2023). Amino Acid Profiles in the Biological Fluids and Tumor Tissue of CRC Patients. Cancers. 16(1). 69–69. 4 indexed citations
2.
Silva, Jorge Diogo Da, Isaura Ribeiro, Eugénia Pinto, et al.. (2023). Impact of Structural GLA Protein Changes on Peripheral GLA Activity and Substrate Accumulation in Fabry Disease Patients. Endocrine Metabolic & Immune Disorders - Drug Targets. 24(16). 3–3. 1 indexed citations
3.
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
4.
Laranjeira, Francisco, et al.. (2019). Genotype‐phenotype correlations and BH4 estimated responsiveness in patients with phenylketonuria from Rio de Janeiro, Southeast Brazil. Molecular Genetics & Genomic Medicine. 7(5). e610–e610. 8 indexed citations
5.
Laranjeira, Francisco, et al.. (2018). Mutation analysis of the PAH gene in phenylketonuria patients from Rio de Janeiro, Southeast Brazil. Molecular Genetics & Genomic Medicine. 6(4). 575–591. 13 indexed citations
6.
Nascimento, João, et al.. (2015). D-Bifunctional Protein Deficiency: A Cause of Neonatal Onset Seizures and Hypotonia. Pediatric Neurology. 52(5). 539–543. 11 indexed citations
7.
Durães, João, et al.. (2015). Adolescent-onset Krabbe disease with an initial diagnosis of multiple sclerosis and a novel mutation. BMJ Case Reports. 2015. bcr2015210625–bcr2015210625. 10 indexed citations
8.
Rocha, Júlio César, Manuela Almeida, Esmeralda Martins, et al.. (2015). Infantile Refsum Disease: Influence of Dietary Treatment on Plasma Phytanic Acid Levels. JIMD Reports. 26. 53–60. 6 indexed citations
9.
Fernández‐Marmiesse, Ana, Mercè Pineda, Jesús Manuel Eirís Puñal, et al.. (2014). Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders. Orphanet Journal of Rare Diseases. 9(1). 59–59. 38 indexed citations
10.
Garcia, Paula, et al.. (2013). Doença de Pompe Juvenil: Estudo Retrospetivo de Casuística Clínica. Acta Médica Portuguesa. 26(4). 361–370. 3 indexed citations
11.
Coutinho, Maria Francisca, Lúcia Lacerda, Sandra Macedo‐Ribeiro, et al.. (2011). Lysosomal multienzymatic complex‐related diseases: a genetic study among Portuguese patients. Clinical Genetics. 81(4). 379–393. 10 indexed citations
12.
Coutinho, Maria Francisca, Lúcia Lacerda, Flemming Wibrand, et al.. (2011). Alu-Alu Recombination Underlying the First Large Genomic Deletion in GlcNAc-Phosphotransferase Alpha/Beta (GNPTAB) Gene in a MLII Alpha/Beta Patient. JIMD Reports. 4. 117–124. 7 indexed citations
13.
Nogueira, Célia, Maria João Prata, Lúcia Lacerda, et al.. (2008). Molecular analysis of mucopolysaccharidosis type IIIB in Portugal: evidence of a single origin for a common mutation (R234C) in the Iberian Peninsula. Clinical Genetics. 73(3). 251–256. 15 indexed citations
14.
Bessa, Carlos, Carla Andreia Teixeira, Ana Cristi Basile Dias, et al.. (2007). CLN2/TPP1 deficiency: The novel mutation IVS7-10A>G causes intron retention and is associated with a mild disease phenotype. Molecular Genetics and Metabolism. 93(1). 66–73. 27 indexed citations
15.
Alves, Sandra, Maria João Prata, G. Ribeiro, et al.. (2006). Molecular characterization of Portuguese patients with mucopolysaccharidosis type II shows evidence that the IDS gene is prone to splicing mutations. Journal of Inherited Metabolic Disease. 29(6). 743–754. 31 indexed citations
16.
Pinto, Rui, Manuela Nascimento de Lemos, Lurdes Lopes, et al.. (2003). Prevalence of lysosomal storage diseases in Portugal. European Journal of Human Genetics. 12(2). 87–92. 243 indexed citations
17.
Lacerda, Lúcia, Fernando A. Arosa, Rosa Lacerda, et al.. (1999). T Cell Numbers Relate to Bone Involvement in Gaucher Disease. Blood Cells Molecules and Diseases. 25(2). 130–138. 40 indexed citations
18.
Amaral, Olga, et al.. (1996). Type 1 Gaucher disease: Identification of N396T and prevalence of glucocerebrosidase mutations in the Portuguese. Human Mutation. 8(3). 280–281. 3 indexed citations
19.
Lacerda, Lúcia, Olga Amaral, Rui Pinto, Johannes M. F. G. Aerts, & Clara Sá-Miranda. (1993). Identification of Gaucher Disease Carriers: Glucocerebrosidase Antigen and DNA Analysis. Biochemical Medicine and Metabolic Biology. 50(2). 190–196. 3 indexed citations
20.
Sá-Miranda, Clara, Johannes M. F. G. Aerts, Rui Pinto, et al.. (1990). Activity of glucocerebrosidase in extracts of different cell types from type 1 Gaucher disease patients. Clinical Genetics. 38(3). 218–227. 22 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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