Clara Sá-Miranda

6.3k total citations
123 papers, 4.7k citations indexed

About

Clara Sá-Miranda is a scholar working on Physiology, Molecular Biology and Epidemiology. According to data from OpenAlex, Clara Sá-Miranda has authored 123 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 85 papers in Physiology, 73 papers in Molecular Biology and 23 papers in Epidemiology. Recurrent topics in Clara Sá-Miranda's work include Lysosomal Storage Disorders Research (76 papers), Peroxisome Proliferator-Activated Receptors (27 papers) and Trypanosoma species research and implications (23 papers). Clara Sá-Miranda is often cited by papers focused on Lysosomal Storage Disorders Research (76 papers), Peroxisome Proliferator-Activated Receptors (27 papers) and Trypanosoma species research and implications (23 papers). Clara Sá-Miranda collaborates with scholars based in Portugal, United States and France. Clara Sá-Miranda's co-authors include Jorge E. Azevedo, Andreia F. Carvalho, Márcia E. Oliveira, Cláudia P. Grou, Alexandra Gouveia, Manuel P. Pinto, Marc Fransen, Olga Amaral, Rui Pinto and Carlos Reguenga and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Blood.

In The Last Decade

Clara Sá-Miranda

121 papers receiving 4.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Clara Sá-Miranda Portugal	41	2.6k	2.4k	1.1k	813	665	123	4.7k
Tadao Orii Japan	48	4.2k 1.7×	2.7k 1.1×	1.9k 1.7×	820 1.0×	1.1k 1.7×	251	7.1k
Amelia Morrone Italy	29	1.7k 0.7×	1.6k 0.7×	568 0.5×	528 0.6×	414 0.6×	145	3.4k
David F. Bishop United States	40	1.5k 0.6×	2.6k 1.1×	682 0.6×	478 0.6×	452 0.7×	86	4.2k
Michael Cantz Germany	29	1.3k 0.5×	1.9k 0.8×	291 0.3×	697 0.9×	506 0.8×	79	3.2k
Norio Sakai Japan	26	1.1k 0.4×	678 0.3×	465 0.4×	403 0.5×	180 0.3×	104	2.0k
Robert Steinfeld Germany	29	820 0.3×	1.6k 0.7×	325 0.3×	655 0.8×	84 0.1×	56	2.8k
Wendy Westbroek United States	29	997 0.4×	1.3k 0.5×	312 0.3×	1.3k 1.6×	285 0.4×	57	3.0k
George E. Tiller United States	22	709 0.3×	884 0.4×	324 0.3×	316 0.4×	182 0.3×	46	2.4k
R Gitzelmann Switzerland	35	642 0.3×	1.3k 0.6×	284 0.3×	469 0.6×	172 0.3×	141	3.8k
Shigeki Sugii Singapore	26	944 0.4×	1.4k 0.6×	491 0.4×	322 0.4×	95 0.1×	50	2.6k

Countries citing papers authored by Clara Sá-Miranda

Since Specialization

Citations

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

Fields of papers citing papers by Clara Sá-Miranda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Clara Sá-Miranda. 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 Clara Sá-Miranda. The network helps show where Clara Sá-Miranda may publish in the future.

Co-authorship network of co-authors of Clara Sá-Miranda

This figure shows the co-authorship network connecting the top 25 collaborators of Clara Sá-Miranda. A scholar is included among the top collaborators of Clara Sá-Miranda 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 Clara Sá-Miranda. Clara Sá-Miranda 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

Loucera, Carlos, Rosario Carmona, Josefa Salgado, et al.. (2020). SMN1 copy‐number and sequence variant analysis from next‐generation sequencing data. Human Mutation. 41(12). 2073–2077. 12 indexed citations

Hoogeveen‐Westerveld, Marianne, Marian A. Kroos, Sirpa Ala‐Mello, et al.. (2019). Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays. European Journal of Human Genetics. 27(6). 919–927. 8 indexed citations

Mar, Fernando Milhazes, Tiago Ferreira da Silva, Daniel Rodrigues, et al.. (2015). Myelin Lipids Inhibit Axon Regeneration Following Spinal Cord Injury: a Novel Perspective for Therapy. Molecular Neurobiology. 53(2). 1052–1064. 24 indexed citations

Azevedo, Olga, et al.. (2011). Left Ventricular Noncompaction in a Patient with Fabry Disease: Overdiagnosis, Morphological Manifestation of Fabry Disease or Two Unrelated Rare Conditions in the Same Patient?. Cardiology. 119(3). 155–159. 17 indexed citations

Decker, Celeste, Zi‐Fan Yu, Roberto Giugliani, et al.. (2010). Enzyme replacement therapy for mucopolysaccharidosis VI: Growth and pubertal development in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase. Journal of Pediatric Rehabilitation Medicine. 3(2). 89–100. 52 indexed citations

Svarch, Eva, et al.. (2010). Clinical, biochemical and molecular features and the treatment of two patients presenting with Gaucher's disease. Revista Cubana de Hematología, Inmunología y Hemoterapia. 26(1). 54–61. 1 indexed citations

Svarch, Eva, et al.. (2010). Aspectos clínicos, bioquímicos, moleculares y tratamiento de 2 pacientes con enfermedad de Gaucher. Revista Cubana de Hematología, Inmunología y Hemoterapia. 26(1). 54–61.

Pinto, Manuel P., Cláudia P. Grou, Marc Fransen, Clara Sá-Miranda, & Jorge E. Azevedo. (2009). The cytosolic domain of PEX3, a protein involved in the biogenesis of peroxisomes, binds membrane lipids. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1793(11). 1669–1675. 22 indexed citations

Turkia, Hadhami Ben, Néji Tebib, Olga Amaral, et al.. (2007). [Mutation spectrum of Gaucher disease in Tunisia: high frequency of N370S/Rec NciI compound heterozygous].. PubMed. 84(1-4). 65–70. 5 indexed citations

10.

Sá-Miranda, Clara, JA Silva, Hiromu Aoyama, et al.. (2007). Purification, characterization and application of laccase from Trametes versicolor for colour and phenolic removal of olive mill wastewater in the presence of 1- hydroxybenzotriazole. AFRICAN JOURNAL OF BIOTECHNOLOGY. 6(10). 1248–1254. 67 indexed citations

11.

Sá-Miranda, Clara, JA Silva, Hiromu Aoyama, et al.. (2007). Purification, characterization and application of laccase from Trametes versicolor for colour and phenolic removal of olive mill wastewater in the presence of 1-hydroxybenzotriazole. Americanae (AECID Library). 1 indexed citations

12.

Santamaría, Raül, Amparo Chabás, María Josep Coll, et al.. (2006). Twenty-one novel mutations in the GLB1 gene identified in a large group of GM1-gangliosidosis and Morquio B patients: possible common origin for the prevalent p.R59H mutation among gypsies. Human Mutation. 27(10). 1060–1060. 52 indexed citations

13.

Teixeira, Carla Andreia, Simon Lin, Carlos Bessa, et al.. (2006). Gene expression profiling in vLINCL CLN6-deficient fibroblasts: Insights into pathobiology. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1762(7). 637–646. 11 indexed citations

14.

Guimarães, Carla P., Pedro Domíngues, Patrick Aubourg, et al.. (2004). Mouse liver PMP70 and ALDP: homomeric interactions prevail in vivo. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1689(3). 235–243. 45 indexed citations

15.

Gouveia, Alexandra, et al.. (2003). Characterization of the Peroxisomal Cycling Receptor Pex5p Import Pathway. Advances in experimental medicine and biology. 544. 219–220. 15 indexed citations

16.

Díaz, George A., Bruce D. Gelb, Neil Risch, et al.. (2000). Gaucher Disease: The Origins of the Ashkenazi Jewish N370S and 84GG Acid β-Glucosidase Mutations. The American Journal of Human Genetics. 66(6). 1821–1832. 52 indexed citations

17.

Pérez, Luis Francisco, et al.. (1999). Characterization of the Isoenzyme Profile of β-N-Acetylhexosaminidase in the Urine of Newborns. Clinical Chemistry and Laboratory Medicine (CCLM). 37(7). 765–769. 1 indexed citations

18.

Pérez, Luis Francisco, Helena Margarida Ribeiro, J. Casal, et al.. (1999). Thermodynamic characterisation of the mutated isoenzyme A of β-N-acetylhexosaminidase in GM2-gangliosidosis B1 variant. Clinica Chimica Acta. 285(1-2). 45–51. 9 indexed citations

19.

Amaral, Olga, et al.. (1997). Distinct Haplotype in Non-Ashkenazi Gaucher Patients with N370S Mutation. Blood Cells Molecules and Diseases. 23(3). 415–416. 8 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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