Luís Negrão

679 total citations
34 papers, 365 citations indexed

About

Luís Negrão is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Luís Negrão has authored 34 papers receiving a total of 365 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 8 papers in Neurology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Luís Negrão's work include Muscle Physiology and Disorders (11 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Genetic Neurodegenerative Diseases (6 papers). Luís Negrão is often cited by papers focused on Muscle Physiology and Disorders (11 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Genetic Neurodegenerative Diseases (6 papers). Luís Negrão collaborates with scholars based in Portugal, Spain and France. Luís Negrão's co-authors include Olinda Rebelo, Luciano Almendra, Ana Fernández‐Marmiesse, Tânia Santiago, Isabel Fineza, António Guimarães, Paula Borralho, Francisco Laranjeira, Ana María Fortuna and Mónica Mendes Sousa and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Annals of Neurology.

In The Last Decade

Luís Negrão

32 papers receiving 359 citations

Peers

Luís Negrão

CMN

CCM

GENET

PHYSI

Masakazu Kawajiri Japan

Alessia Perna Italy

Justin D. Wagner Canada

Ziad Rifai United States

Takekazu Ohi Japan

J. Bautista Spain

Gianni Losano Italy

Robert‐Yves Carlier France

Sarah Goodrich United States

Lorenzo Peverelli Italy

Masakazu Kawajiri Japan

Luís Negrão

176 ×0.9

81 ×1.0

CMN

93 ×1.3

CCM

28 ×0.6

GENET

37 ×0.8

PHYSI

Citations per year, relative to Luís Negrão Luís Negrão (= 1×) peers Masakazu Kawajiri

Countries citing papers authored by Luís Negrão

Since Specialization

Citations

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

Fields of papers citing papers by Luís Negrão

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luís Negrão

This figure shows the co-authorship network connecting the top 25 collaborators of Luís Negrão. A scholar is included among the top collaborators of Luís Negrão 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 Luís Negrão. Luís Negrão 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

Negrão, Luís, et al.. (2025). Enhancing diagnostic sensitivity in Myasthenia Gravis: The combined role of CMAP area and amplitude decrements in repetitive nerve stimulation. Clinical Neurophysiology. 174. 169–172.

Gouveia, Sofía, M.E. Vázquez-Mosquera, Emiliano González‐Vioque, et al.. (2022). Rapid Molecular Diagnosis of Genetically Inherited Neuromuscular Disorders Using Next-Generation Sequencing Technologies. Journal of Clinical Medicine. 11(10). 2750–2750. 4 indexed citations

Martins, Ana Inês, et al.. (2022). A 6-month trial of memantine for nystagmus and associated phenomena in oculopalatal tremor. Frontiers in Neurology. 13. 921341–921341. 2 indexed citations

Coelho, Teresa, T. Moreno, Luís Negrão, et al.. (2022). POSA102 Burden of Disease and Cost of Illness of Spinal Muscular Atrophy in Portugal. Value in Health. 25(1). S53–S53. 2 indexed citations

Rebelo, Olinda, Inês Baldeiras, Luciano Almendra, et al.. (2021). Vasculitic peripheral neuropathy in deficiency of adenosine deaminase 2. Neuromuscular Disorders. 31(9). 891–895. 1 indexed citations

Pinto‐Basto, Jorge, et al.. (2019). The first Portuguese family with NEFL-related Charcot-Marie-Tooth type 2 disease.. PubMed. 38(3). 180–183. 1 indexed citations

Almendra, Luciano, Francisco Laranjeira, Ana Fernández‐Marmiesse, & Luís Negrão. (2018). SIGMAR1 gene mutation causing Distal Hereditary Motor Neuropathy in a Portuguese family.. PubMed. 37(1). 2–4. 17 indexed citations

Tábuas‐Pereira, Miguel, Luciano Almendra, Maria Rosário Almeida, et al.. (2018). Increased risk of melanoma in C9ORF72 repeat expansion carriers: A case–control study. Muscle & Nerve. 59(3). 362–365. 2 indexed citations

Rebelo, Olinda, et al.. (2018). Novel mosaic mutation in the dystrophin gene causing distal asymmetric muscle weakness of the upper limbs and dilated cardiomyopathy.. PubMed. 37(2). 117–120. 5 indexed citations

10.

Martins, Ana Inês, et al.. (2017). Bethlem myopathy in a Portuguese patient - case report.. PubMed. 36(3). 178–181. 6 indexed citations

11.

Almeida, Vânia, Isabel Conceição, Isabel Fineza, et al.. (2017). Screening for Pompe disease in a Portuguese high risk population. Neuromuscular Disorders. 27(8). 777–781. 11 indexed citations

12.

Sousa, Inês, Patrícia Abrantes, Gilberto Teixeira, et al.. (2016). Multicentric Genome-Wide Association Study for Primary Spontaneous Pneumothorax. PLoS ONE. 11(5). e0156103–e0156103. 6 indexed citations

13.

Oliveira, Jorge, Luís Negrão, Isabel Fineza, et al.. (2015). New splicing mutation in the choline kinase beta (CHKB) gene causing a muscular dystrophy detected by whole-exome sequencing. Journal of Human Genetics. 60(6). 305–312. 31 indexed citations

14.

Santiago, Tânia, et al.. (2014). Macrophagic myofasciitis and vaccination: Consequence or coincidence?. Rheumatology International. 35(1). 189–192. 25 indexed citations

15.

Negrão, Luís, et al.. (2014). Charcot-Marie-Tooth 4B2 caused by a novel mutation in the MTMR13/SBF2 gene in two related Portuguese families.. PubMed. 33(3). 144–8. 3 indexed citations

16.

Baets, Jonathan, M. Zimoń, Margarida Venâncio, et al.. (2013). Autosomal Recessive Axonal Neuropathy With Neuromyotonia: A Rare Entity. Pediatric Neurology. 50(1). 104–107. 17 indexed citations

17.

Oliveira, Jorge, Martin Krahn, Rosário Santos, et al.. (2011). Novel ancestral Dysferlin splicing mutation which migrated from the Iberian peninsula to South America. Neuromuscular Disorders. 21(5). 328–337. 9 indexed citations

18.

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

19.

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

20.

Negrão, Luís, et al.. (1994). Community-based stroke prevention: a Portuguese challenge.. PubMed. 6(1). 189–95. 7 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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