António Guimarães

1.1k total citations
22 papers, 819 citations indexed

About

António Guimarães is a scholar working on Molecular Biology, Physiology and Clinical Biochemistry. According to data from OpenAlex, António Guimarães has authored 22 papers receiving a total of 819 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 6 papers in Physiology and 5 papers in Clinical Biochemistry. Recurrent topics in António Guimarães's work include Amyloidosis: Diagnosis, Treatment, Outcomes (7 papers), Alzheimer's disease research and treatments (6 papers) and Mitochondrial Function and Pathology (5 papers). António Guimarães is often cited by papers focused on Amyloidosis: Diagnosis, Treatment, Outcomes (7 papers), Alzheimer's disease research and treatments (6 papers) and Mitochondrial Function and Pathology (5 papers). António Guimarães collaborates with scholars based in Portugal, United States and France. António Guimarães's co-authors include Maria João Saraiva, Mónica Mendes Sousa, Rui Fernandes, Isabel Cardoso, Shi Du Yan, David Stern, Barbas do Amaral, Mie Kuroiwa, Clara Barbot and Robert Kisilevsky and has published in prestigious journals such as Journal of Clinical Oncology, Journal of Neuroscience and SHILAP Revista de lepidopterología.

In The Last Decade

António Guimarães

19 papers receiving 812 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
António Guimarães Portugal 12 677 239 203 91 88 22 819
Taro Yamashita Japan 16 552 0.8× 200 0.8× 78 0.4× 41 0.5× 23 0.3× 48 745
Annett Böddrich Germany 11 356 0.5× 166 0.7× 78 0.4× 49 0.5× 19 0.2× 12 737
Gaetano Arcuri Italy 16 403 0.6× 100 0.4× 88 0.4× 165 1.8× 29 0.3× 19 710
Angela Cassese Italy 14 381 0.6× 133 0.6× 79 0.4× 43 0.5× 69 0.8× 17 657
Nathalie Danièle France 18 742 1.1× 215 0.9× 159 0.8× 97 1.1× 10 0.1× 27 1.1k
Silvia Nerini‐Molteni Italy 10 282 0.4× 73 0.3× 130 0.6× 43 0.5× 34 0.4× 13 643
J Willmer Canada 8 581 0.9× 358 1.5× 170 0.8× 17 0.2× 31 0.4× 10 746
Sripriya Ranganathan United States 10 455 0.7× 312 1.3× 233 1.1× 79 0.9× 8 0.1× 13 945
Ayse G. Kayali United States 14 413 0.6× 157 0.7× 119 0.6× 45 0.5× 11 0.1× 26 821
Yann Nouët France 8 607 0.9× 112 0.5× 84 0.4× 24 0.3× 20 0.2× 8 829

Countries citing papers authored by António Guimarães

Since Specialization
Citations

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

Fields of papers citing papers by António Guimarães

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of António Guimarães

This figure shows the co-authorship network connecting the top 25 collaborators of António Guimarães. A scholar is included among the top collaborators of António Guimarães 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 António Guimarães. António Guimarães 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.
Rosa, Joaninha Costa, et al.. (2022). A case of scleroderma-like lesions as a cutaneous manifestation of carcinoid syndrome. SHILAP Revista de lepidopterología. 5. 100146–100146. 1 indexed citations
2.
Guimarães, António, et al.. (2022). Leptomeningeal carcinomatosis: Retrospective review of a large series.. Journal of Clinical Oncology. 40(16_suppl). e14005–e14005.
3.
Coelho, Teresa, et al.. (2019). Clinicopathological correlations of sural nerve biopsies in TTR Val30Met familial amyloid polyneuropathy. Brain Communications. 1(1). 17 indexed citations
4.
Taipa, Ricardo, Célia Nogueira, Lígia S. Almeida, et al.. (2017). Clinical, biochemical, molecular, and histological features of 65 Portuguese patients with mitochondrial disorders. Muscle & Nerve. 56(5). 868–872. 3 indexed citations
5.
Silva, Ana, Helena Miranda, Jorge Daniel, et al.. (2013). Domino Liver Transplantation (DLT) and De Novo Familial Amyloid Polyneuropathy (FAP): The Portuguese Experience (S58.004). Neurology. 80(7_supplement).
6.
Santos, Rosário, Jorge Oliveira, Teresa Coelho, et al.. (2010). Private dysferlin exon skipping mutation (c.5492G>A) with a founder effect reveals further alternative splicing involving exons 49–51. Journal of Human Genetics. 55(8). 546–549. 11 indexed citations
7.
Oliveira, Jorge, Isabel Soares‐Silva, Ivo F.A.C. Fokkema, et al.. (2008). Novel synonymous substitution in POMGNT1 promotes exon skipping in a patient with congenital muscular dystrophy. Journal of Human Genetics. 53(6). 565–572. 11 indexed citations
8.
Carrilho, Inês, António Guimarães, João Paulo Teixeira, et al.. (2008). Infantile neuroaxonal dystrophy: What's most important for the diagnosis?. European Journal of Paediatric Neurology. 12(6). 491–500. 43 indexed citations
9.
Nogueira, Célia, Clara Barbot, Alessandra Tessa, et al.. (2007). Identification of a new mtDNA mutation (14724G>A) associated with mitochondrial leukoencephalopathy. Biochemical and Biophysical Research Communications. 354(4). 937–941. 10 indexed citations
10.
Sousa, Mónica Mendes, Rui Fernandes, António Guimarães, et al.. (2004). Deposition and passage of transthyretin through the blood-nerve barrier in recipients of familial amyloid polyneuropathy livers. Laboratory Investigation. 84(7). 865–873. 46 indexed citations
11.
Sousa, Mónica Mendes, Barbas do Amaral, António Guimarães, & Maria João Saraiva. (2004). Up‐regulation of the extracellular matrix remodeling genes, biglycan, neutrophil gelatinase‐associated lipocalin and matrix metalloproteinase‐9 in familial amyloid polyneuropathy. The FASEB Journal. 19(1). 124–126. 62 indexed citations
12.
Teixeira, João Paulo, et al.. (2003). [Merosin-positive congenital muscular dystrophy, white matter abnormalities, and bilateral posterior occipital cortical dysplasia].. PubMed. 16(3). 189–92.
13.
Sousa, Mónica Mendes, Isabel Cardoso, Rui Fernandes, António Guimarães, & Maria João Saraiva. (2001). Deposition of Transthyretin in Early Stages of Familial Amyloidotic Polyneuropathy. American Journal Of Pathology. 159(6). 1993–2000. 266 indexed citations
14.
Barbot, Clara, Paula Coutinho, Rui Chorão, et al.. (2001). Recessive Ataxia With Ocular Apraxia. Archives of Neurology. 58(2). 201–201. 68 indexed citations
15.
Sousa, Mónica Mendes, Shi Du Yan, Rui Fernandes, et al.. (2001). Familial Amyloid Polyneuropathy: Receptor for Advanced Glycation End Products-Dependent Triggering of Neuronal Inflammatory and Apoptotic Pathways. Journal of Neuroscience. 21(19). 7576–7586. 168 indexed citations
16.
Benevides, S. D., et al.. (2000). ESTUDO BIOQUÍMICO E SENSORIAL DO QUEIJO DE COALHO PRODUZIDO COM LEITE CRU E PASTEURIZADO NO ESTADO DO CEARÁ. Boletim do Centro de Pesquisa de Processamento de Alimentos. 18(2). 3 indexed citations
17.
Vilarinho, Laura, Filippo M. Santorelli, Isabel Coelho, et al.. (1999). The mitochondrial DNA A3243G mutation in Portugal: clinical and molecular studies in 5 families. Journal of the Neurological Sciences. 163(2). 168–174. 21 indexed citations
18.
Kuroiwa, Mie, et al.. (1998). Ultrastructure of Familial Amyloid Polyneuropathy Amyloid Fibrils: Examination with High-Resolution Electron Microscopy. Journal of Structural Biology. 124(1). 1–12. 50 indexed citations
19.
Vilarinho, Laura, Filippo M. Santorelli, Maria Luı́s Cardoso, et al.. (1998). Mitochondrial DNA Analysis in Ocular Myopathy. European Neurology. 39(3). 148–153. 8 indexed citations
20.
Barrett, J. Carl, António Guimarães, Jonathan Cullis, & John M. Goldman. (1993). Immunological characterization of the tumor‐specificbcr/abljunction of philadelphia chromosome positive chronic myeloid leukemia. Stem Cells. 11(S3). 104–108. 10 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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