Adalberto Vieyra

2.8k total citations
130 papers, 2.1k citations indexed

About

Adalberto Vieyra is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Nutrition and Dietetics. According to data from OpenAlex, Adalberto Vieyra has authored 130 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 28 papers in Pediatrics, Perinatology and Child Health and 18 papers in Nutrition and Dietetics. Recurrent topics in Adalberto Vieyra's work include Ion Transport and Channel Regulation (28 papers), Birth, Development, and Health (21 papers) and Hormonal Regulation and Hypertension (15 papers). Adalberto Vieyra is often cited by papers focused on Ion Transport and Channel Regulation (28 papers), Birth, Development, and Health (21 papers) and Hormonal Regulation and Hypertension (15 papers). Adalberto Vieyra collaborates with scholars based in Brazil, Czechia and France. Adalberto Vieyra's co-authors include Marcelo Einicker‐Lamas, Lucienne S. Lara, Rafael Soares Lindoso, Celso Caruso‐Neves, Federica Collino, Leopoldo de Meis, Helena M. Scofano, J.R. Meyer-Fernandes, Paulo A. Silva and Jennifer Lowe and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Adalberto Vieyra

126 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Adalberto Vieyra Brazil	27	1.2k	312	284	218	212	130	2.1k
Laura Cole Canada	23	1.0k 0.8×	155 0.5×	162 0.6×	161 0.7×	94 0.4×	43	2.1k
Kathleen T. Shiverick United States	30	959 0.8×	402 1.3×	214 0.8×	139 0.6×	116 0.5×	88	2.7k
Daniel G. Fuster Switzerland	25	1.1k 0.9×	329 1.1×	82 0.3×	305 1.4×	206 1.0×	94	2.1k
Edward Karpinski Canada	26	1.1k 0.9×	185 0.6×	292 1.0×	196 0.9×	97 0.5×	98	2.4k
Núria M. Pastor‐Soler United States	36	2.2k 1.8×	181 0.6×	232 0.8×	487 2.2×	217 1.0×	65	3.4k
Luis Michea Chile	32	1.3k 1.1×	240 0.8×	465 1.6×	507 2.3×	288 1.4×	73	2.9k
Osamu Nakajima Japan	29	1.9k 1.6×	305 1.0×	264 0.9×	177 0.8×	154 0.7×	128	3.4k
Astrid Hammer Austria	37	1.0k 0.8×	194 0.6×	78 0.3×	404 1.9×	165 0.8×	76	3.1k
Georgios Scheiner‐Bobis Germany	25	1.5k 1.2×	78 0.3×	166 0.6×	195 0.9×	118 0.6×	69	2.3k
John H. Schwartz United States	35	2.2k 1.7×	278 0.9×	190 0.7×	297 1.4×	259 1.2×	124	4.0k

Countries citing papers authored by Adalberto Vieyra

Since Specialization

Citations

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

Fields of papers citing papers by Adalberto Vieyra

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adalberto Vieyra

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

Almeida, Fernando, Giovane G. Tortelote, Rafael Garrett, et al.. (2025). Characterization of Ceramide Kinase from Basolateral Membranes of Kidney Proximal Tubules: Kinetics, Physicochemical Requirements, and Physiological Relevance. International Journal of Molecular Sciences. 26(21). 10373–10373.

Paixão, Ana D.O., et al.. (2024). Reactive oxygen species impair Na+ transport and renal components of the renin-angiotensin-aldosterone system after paraquat poisoning. Anais da Academia Brasileira de Ciências. 96(1). e20230971–e20230971. 1 indexed citations

Fernandes, Aline Marie, et al.. (2022). Sphingosine 1‐Phosphate Prevents Human Embryonic Stem Cell Death Following Ischemic Injury. European Journal of Lipid Science and Technology. 124(7). 1 indexed citations

Vieyra, Adalberto, et al.. (2021). Angiotensin-(3-4) modulates the overweight- and undernutrition-induced ACE2 downregulation in renal proximal tubule cells: implications for COVID-19?. SHILAP Revista de lepidopterología. 2 indexed citations

Lara, Lucienne S., et al.. (2021). Undernutrition – thirty years of the Regional Basic Diet: the legacy of Naíde Teodósio in different fields of knowledge. Nutritional Neuroscience. 25(9). 1973–1994. 5 indexed citations

Galina, Antônio, Christina Maeda Takiya, Rafael Soares Lindoso, et al.. (2020). Type 2 diabetes mellitus alters cardiac mitochondrial content and function in a non-obese mice model. Anais da Academia Brasileira de Ciências. 92(2). e20191340–e20191340. 5 indexed citations

Silva, Paulo A., et al.. (2020). Angiotensin-(3–4) normalizes blood pressure, decreases Na+ and energy intake, but preserves urinary Na+ excretion in overweight hypertensive rats. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1867(3). 166012–166012. 7 indexed citations

Andrade, Cherley Borba Vieira de, Antônio Carlos Campos de Carvalho, Rafael Soares Lindoso, et al.. (2020). Acute Myocardial Infarction Reduces Respiration in Rat Cardiac Fibers, despite Adipose Tissue Mesenchymal Stromal Cell Transplant. Stem Cells International. 2020. 1–19. 5 indexed citations

Lindoso, Rafael Soares, Renata Binato, Eliana Abdelhay, et al.. (2019). Adipose Mesenchymal Cells-Derived EVs Alleviate DOCA-Salt-Induced Hypertension by Promoting Cardio-Renal Protection. Molecular Therapy — Methods & Clinical Development. 16(11). 63–77. 34 indexed citations

10.

Filho, Leucio Duarte Vieira, et al.. (2018). Perinatal α-tocopherol overload programs alterations in kidney development and renal angiotensin II signaling pathways at birth and at juvenile age: Mechanisms underlying the development of elevated blood pressure. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864(7). 2458–2471. 12 indexed citations

11.

Cuillel, Martine, Elisabeth Mintz, Peggy Charbonnier, et al.. (2016). Modulation of hepatic copper-ATPase activity by insulin and glucagon involves protein kinase A (PKA) signaling pathway. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1862(11). 2086–2097. 19 indexed citations

12.

Lindoso, Rafael Soares, Federica Collino, Stefania Bruno, et al.. (2014). Extracellular Vesicles Released from Mesenchymal Stromal Cells Modulate miRNA in Renal Tubular Cells and Inhibit ATP Depletion Injury. Stem Cells and Development. 23(15). 1809–1819. 113 indexed citations

13.

Silva, Paulo A., Gustavo Monnerat, Lucienne S. Lara, et al.. (2014). Mechanisms Involving Ang II and MAPK/ERK1/2 Signaling Pathways Underlie Cardiac and Renal Alterations during Chronic Undernutrition. PLoS ONE. 9(7). e100410–e100410. 25 indexed citations

14.

Britto‐Borges, Thiago, Jennifer Lowe, Marcelo Einicker‐Lamas, et al.. (2010). Two Serine Residues Control Sequential Steps during Catalysis of the Yeast Copper ATPase through Different Mechanisms That Involve Kinase-mediated Phosphorylations. Journal of Biological Chemistry. 286(9). 6879–6889. 5 indexed citations

15.

Filho, Leucio Duarte Vieira, et al.. (2010). Placental malnutrition changes the regulatory network of renal Na-ATPase in adult rat progeny: Reprogramming by maternal α-tocopherol during lactation. Archives of Biochemistry and Biophysics. 505(1). 91–97. 25 indexed citations

16.

Ferrão, Fernanda M., et al.. (2009). A scrutiny of the biochemical pathways from Ang II to Ang-(3–4) in renal basolateral membranes. Regulatory Peptides. 158(1-3). 47–56. 14 indexed citations

17.

Bernardo, Róbson Roney, et al.. (2004). Diacylglycerol kinase activity in purified basolateral membranes of kidney tubules. The International Journal of Biochemistry & Cell Biology. 37(1). 79–90. 10 indexed citations

18.

Caruso‐Neves, Celso, et al.. (2000). Ouabain-insensitive Na+-ATPase activity is an effector protein for cAMP regulation in basolateral membranes of the proximal tubule. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1468(1-2). 107–114. 30 indexed citations

19.

Hermes‐Lima, Marcelo & Adalberto Vieyra. (1992). Pyrophosphate synthesis from phospho(enol)pyruvate catalyzed by precipitated magnesium phosphate with ?enzyme-like? activity. Journal of Molecular Evolution. 35(4). 277–285. 13 indexed citations

20.

Guilherme, Adı́lson, J.R. Meyer-Fernandes, & Adalberto Vieyra. (1991). Reversible inhibition by 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid of the plasma membrane calcium-magnesium ATPase from kidney proximal tubules. Biochemistry. 30(23). 5700–5706. 30 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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