Joaquim Calado

1.3k total citations
31 papers, 824 citations indexed

About

Joaquim Calado is a scholar working on Molecular Biology, Surgery and Rheumatology. According to data from OpenAlex, Joaquim Calado has authored 31 papers receiving a total of 824 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 8 papers in Surgery and 7 papers in Rheumatology. Recurrent topics in Joaquim Calado's work include Ion Transport and Channel Regulation (8 papers), Biomedical Research and Pathophysiology (6 papers) and Diabetes Treatment and Management (6 papers). Joaquim Calado is often cited by papers focused on Ion Transport and Channel Regulation (8 papers), Biomedical Research and Pathophysiology (6 papers) and Diabetes Treatment and Management (6 papers). Joaquim Calado collaborates with scholars based in Portugal, France and United States. Joaquim Calado's co-authors include René Santer, José Rueff, Carla Clemente, Sophie Saunier, Corinne Antignac, Flora Silbermann, France Benessy, Roland Heilig, Jean Weissenbach and Karina Soto and has published in prestigious journals such as SHILAP Revista de lepidopterología, FEBS Letters and International Journal of Molecular Sciences.

In The Last Decade

Joaquim Calado

31 papers receiving 798 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joaquim Calado Portugal 12 461 453 325 151 131 31 824
Amanda Mather Australia 8 506 1.1× 274 0.6× 270 0.8× 234 1.5× 36 0.3× 22 804
Sara Watutantrige‐Fernando Italy 18 456 1.0× 163 0.4× 139 0.4× 46 0.3× 80 0.6× 32 717
Kikuko Amo Japan 7 221 0.5× 276 0.6× 153 0.5× 268 1.8× 76 0.6× 9 765
Thor Tejada United States 10 100 0.2× 366 0.8× 219 0.7× 170 1.1× 64 0.5× 14 725
Chizuru Watanabe Japan 12 240 0.5× 196 0.4× 144 0.4× 37 0.2× 74 0.6× 19 594
Fabio Gianiorio Italy 9 94 0.2× 220 0.5× 101 0.3× 211 1.4× 63 0.5× 10 706
Yosuke Nagai Japan 12 194 0.4× 230 0.5× 93 0.3× 205 1.4× 32 0.2× 19 615
Chenzhong Li China 9 287 0.6× 174 0.4× 133 0.4× 160 1.1× 35 0.3× 20 605
Taishan Zheng China 14 207 0.4× 344 0.8× 214 0.7× 37 0.2× 207 1.6× 32 662

Countries citing papers authored by Joaquim Calado

Since Specialization
Citations

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

Fields of papers citing papers by Joaquim Calado

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joaquim Calado

This figure shows the co-authorship network connecting the top 25 collaborators of Joaquim Calado. A scholar is included among the top collaborators of Joaquim Calado 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 Joaquim Calado. Joaquim Calado 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.
Jorge, Cristina, et al.. (2025). Autosomal Dominant Polycystic Kidney Disease Inflammation Biomarkers in the Tolvaptan Era. International Journal of Molecular Sciences. 26(3). 1121–1121. 1 indexed citations
2.
Quinodoz, Mathieu, Marc Folcher, Siying Lin, et al.. (2024). Bi-allelic variants in COQ8B, a gene involved in the biosynthesis of coenzyme Q10, lead to non-syndromic retinitis pigmentosa. The American Journal of Human Genetics. 111(10). 2299–2306. 1 indexed citations
3.
Fonseca, Nuno Moreira, Ana Faria, Emília C. Monteiro, et al.. (2023). Oxalate (dys)Metabolism: Person-to-Person Variability, Kidney and Cardiometabolic Toxicity. Genes. 14(9). 1719–1719. 9 indexed citations
4.
Barata, Rui, Marc Fila, Paula Santos Nunes, et al.. (2023). Performance of the ACMG‐AMP criteria in a large familial renal glucosuria cohort with identified SLC5A2 sequence variants. Clinical Genetics. 104(5). 582–586. 1 indexed citations
5.
Morelló, Judit, Joaquim Calado, Alexandra M. M. Antunes, et al.. (2022). Cysteine as a Multifaceted Player in Kidney, the Cysteine-Related Thiolome and Its Implications for Precision Medicine. Molecules. 27(4). 1416–1416. 23 indexed citations
6.
Nolasco, Fernando, et al.. (2021). Zebrafish Model as a Screen to Prevent Cyst Inflation in Autosomal Dominant Polycystic Kidney Disease. International Journal of Molecular Sciences. 22(16). 9013–9013. 2 indexed citations
7.
Messias, Ana, Joaquim Calado, Helena Viana, & Fernando Nolasco. (2020). Nephrotic syndrome in a patient with metastatic melanoma: beyond the obvious. Repository of the Hospital Center of Central Lisbon (Hospital Center of Central Lisbon). 33(4). 1 indexed citations
8.
Menezes, Maria Do Mar, et al.. (2019). An Atypical Presentation of Thrombotic Microangiopathy After Lung Transplant: A Case Report. Transplantation Proceedings. 51(5). 1633–1635. 2 indexed citations
9.
Monteiro, Pedro, Carlos Aguíar, José Silva‐Nunes, et al.. (2019). Effect of empagliflozin beyond glycemic control: Cardiovascular benefit in patients with type 2 diabetes and established cardiovascular disease. SHILAP Revista de lepidopterología. 38(10). 721–735. 3 indexed citations
10.
Monteiro, Pedro, Carlos Aguíar, José Silva‐Nunes, et al.. (2019). Efeito da empagliflozina para além do controlo glicémico: benefício cardiovascular em doentes com DMT2 e doença cardiovascular estabelecida. Revista Portuguesa de Cardiologia. 38(10). 721–735. 4 indexed citations
11.
Navarro, David, Sílvia Sequeira, Ana Carina Ferreira, et al.. (2018). Atypical adult-onset methylmalonic acidemia and homocystinuria presenting as hemolytic uremic syndrome. CEN Case Reports. 7(1). 73–76. 5 indexed citations
12.
Calado, Joaquim, Ana Rita Santos, Inês Aires, et al.. (2018). The Na+‐coupled glucose transporter SGLT2 interacts with its accessory unit MAP17 in vitro and their expressions overlap in the renal proximal tubule. FEBS Letters. 592(19). 3317–3326. 5 indexed citations
13.
Viana, Helena, et al.. (2015). Anti-Phospholipase A2 Receptor Antibodies in the Diagnosis of Idiopathic Membranous Nephropathy. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 29(1). 44–47. 1 indexed citations
14.
Aires, Inês, et al.. (2013). Hypouricaemia and hyperuricosuria in familial renal glucosuria. Clinical Kidney Journal. 6(5). 523–525. 7 indexed citations
15.
Calado, Joaquim. (2009). Dapagliflozin, an oral sodium glucose cotransporter type 2 inhibitor for the treatment of type 2 diabetes mellitus.. PubMed. 12(12). 785–98. 7 indexed citations
16.
Calado, Joaquim, Yves Sznajer, Daniel L. Metzger, et al.. (2008). Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion. Nephrology Dialysis Transplantation. 23(12). 3874–3879. 78 indexed citations
17.
Calado, Joaquim, Onur Sakallıoğlu, Faysal Gök, et al.. (2006). Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting. Kidney International. 69(5). 852–855. 69 indexed citations
18.
Calado, Joaquim, et al.. (2004). Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria. Human Genetics. 114(3). 314–316. 56 indexed citations
19.
Saunier, Sophie, Joaquim Calado, France Benessy, et al.. (2000). Characterization of the NPHP1 Locus: Mutational Mechanism Involved in Deletions in Familial Juvenile Nephronophthisis. The American Journal of Human Genetics. 66(3). 778–789. 86 indexed citations
20.
Konrad, Moira, Sophie Saunier, Joaquim Calado, et al.. (1998). Familial juvenile nephronophthisis. Journal of Molecular Medicine. 76(5). 310–316. 19 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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