Manuela Grazina

1.4k total citations
45 papers, 847 citations indexed

About

Manuela Grazina is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Manuela Grazina has authored 45 papers receiving a total of 847 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 20 papers in Clinical Biochemistry and 7 papers in Genetics. Recurrent topics in Manuela Grazina's work include Mitochondrial Function and Pathology (25 papers), Metabolism and Genetic Disorders (19 papers) and ATP Synthase and ATPases Research (10 papers). Manuela Grazina is often cited by papers focused on Mitochondrial Function and Pathology (25 papers), Metabolism and Genetic Disorders (19 papers) and ATP Synthase and ATPases Research (10 papers). Manuela Grazina collaborates with scholars based in Portugal, United States and Spain. Manuela Grazina's co-authors include Catarina R. Oliveira, Luísa Diogo, Paula Garcia, Luís Borges, Carla Marques, Guiomar Oliveira, Assunção Ataíde, João Pratas, Isabel Santana and Sandra M. Cardoso and has published in prestigious journals such as SHILAP Revista de lepidopterología, NeuroImage and Human Molecular Genetics.

In The Last Decade

Manuela Grazina

42 papers receiving 816 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manuela Grazina Portugal 15 443 232 209 164 99 45 847
Jean‐Baptiste Roullet United States 16 371 0.8× 75 0.3× 67 0.3× 113 0.7× 167 1.7× 52 901
Adnan Yüksel Türkiye 17 314 0.7× 127 0.5× 38 0.2× 77 0.5× 112 1.1× 62 971
Irene B. Hopkins United States 15 482 1.1× 43 0.2× 47 0.2× 157 1.0× 394 4.0× 19 962
Pierluigi Sebastiani Italy 12 178 0.4× 36 0.2× 38 0.2× 109 0.7× 103 1.0× 28 586
Mei‐Mei Gao China 16 319 0.7× 164 0.7× 78 0.4× 14 0.1× 50 0.5× 33 644
Maneesh Gupta United States 17 385 0.9× 52 0.2× 31 0.1× 245 1.5× 205 2.1× 34 903
Núria Brandi Spain 11 289 0.7× 89 0.4× 23 0.1× 193 1.2× 83 0.8× 14 529
C. Jakobs Netherlands 17 680 1.5× 84 0.4× 26 0.1× 621 3.8× 171 1.7× 39 1.1k
Talin Gulesserian Austria 18 436 1.0× 88 0.4× 33 0.2× 18 0.1× 89 0.9× 31 836

Countries citing papers authored by Manuela Grazina

Since Specialization
Citations

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

Fields of papers citing papers by Manuela Grazina

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Grazina

This figure shows the co-authorship network connecting the top 25 collaborators of Manuela Grazina. A scholar is included among the top collaborators of Manuela Grazina 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 Manuela Grazina. Manuela Grazina 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.
Silva, Roberto, et al.. (2024). Homozygosity for a Rare FASTKD2 Variant Resulting in an Adult Onset Autosomal Recessive Mitochondrial Podocytopathy. American Journal of Kidney Diseases. 85(1). 119–123.
2.
Jacinto, Sandra, Patrícia Guerreiro, Rita Machado de Oliveira, et al.. (2021). MPV17 Mutations Are Associated With a Quiescent Energetic Metabolic Profile. Frontiers in Cellular Neuroscience. 15. 641264–641264. 14 indexed citations
3.
Faria, Pedro, et al.. (2021). MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal. Acta Médica Portuguesa. 34(9). 586–591.
4.
Rodrigues‐Soares, Fernanda, Eva Peñas‐Lledó, Eduardo Tarazona‐Santos, et al.. (2019). Genomic Ancestry,CYP2D6,CYP2C9, andCYP2C19Among Latin Americans. Clinical Pharmacology & Therapeutics. 107(1). 257–268. 38 indexed citations
5.
Ribeiro, Carolina, Patrícia A. T. Martins, & Manuela Grazina. (2017). Genotyping CYP2D6 by three different methods: advantages and disadvantages. Drug Metabolism and Personalized Therapy. 32(1). 33–37. 3 indexed citations
6.
Rocha, Mariana C., Steven Hardy, Amy E. Vincent, et al.. (2017). Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant. Neuromuscular Disorders. 28(4). 350–360. 8 indexed citations
7.
Santos, Diana, Maria João Santos, Miguel Alves‐Ferreira, et al.. (2017). mtDNA copy number associated with age of onset in familial amyloid polyneuropathy. Journal of Neurology Neurosurgery & Psychiatry. 89(3). 300–304. 18 indexed citations
8.
Pratas, João, Carolina Ribeiro, Maria João Santos, et al.. (2016). In silico analysis for predicting pathogenicity of five unclassified mitochondrial DNA mutations associated with mitochondrial cytopathies' phenotypes. European Journal of Medical Genetics. 60(3). 172–177. 9 indexed citations
9.
Costa, Beatriz, et al.. (2016). Argininemia and plasma arginine bioavailability – predictive factors of mortality in the severe trauma patients?. Nutrition & Metabolism. 13(1). 60–60. 8 indexed citations
10.
Macário, Carmo, João Pratas, Maria João Santos, et al.. (2016). Identification of a novel deletion in SURF1 gene: Heterogeneity in Leigh syndrome with COX deficiency. Mitochondrion. 31. 84–88. 6 indexed citations
11.
Reis, Aldina, et al.. (2013). Long term cortical plasticity in visual retinotopic areas in humans with silent retinal ganglion cell loss. NeuroImage. 81. 222–230. 22 indexed citations
12.
Arduíno, Daniela M., A. Raquel Esteves, Luísa Cortes, et al.. (2012). Mitochondrial metabolism in Parkinson's disease impairs quality control autophagy by hampering microtubule-dependent traffic. Human Molecular Genetics. 21(21). 4680–4702. 67 indexed citations
13.
Grazina, Manuela. (2011). Mitochondrial Respiratory Chain: Biochemical Analysis and Criterion for Deficiency in Diagnosis. Methods in molecular biology. 837. 73–91. 12 indexed citations
14.
Diogo, Luísa, Miguel Cordeiro, Paula Garcia, et al.. (2010). Value of Brain Magnetic Resonance Imaging in Mitochondrial Respiratory Chain Disorders. Pediatric Neurology. 42(3). 196–200. 9 indexed citations
15.
Ferreira, Ildete L., Márcio Ribeiro, Sandra Almeida, et al.. (2010). Mitochondrial-dependent apoptosis in Huntington's disease human cybrids. Experimental Neurology. 222(2). 243–255. 50 indexed citations
16.
Diogo, Luísa, Manuela Grazina, Paula Garcia, et al.. (2009). Pediatric Mitochondrial Respiratory Chain Disorders in the Centro Region of Portugal. Pediatric Neurology. 40(5). 351–356. 18 indexed citations
17.
Grazina, Manuela, et al.. (2007). Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation—A case report. European Journal of Paediatric Neurology. 11(2). 115–118. 26 indexed citations
18.
Grazina, Manuela, F.S. Silva, Isabel Santana, et al.. (2005). Mitochondrial DNA Variants in a Portuguese Population of Patients with Alzheimer’s Disease. European Neurology. 53(3). 121–124. 8 indexed citations
19.
20.
Oliveira‐Brett, Ana Maria, et al.. (1993). A study of the electrochemical oxidation of Navelbine. Journal of Pharmaceutical and Biomedical Analysis. 11(3). 203–206. 12 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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