João Leandro

684 total citations
32 papers, 465 citations indexed

About

João Leandro is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, João Leandro has authored 32 papers receiving a total of 465 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Clinical Biochemistry, 24 papers in Molecular Biology and 5 papers in Rheumatology. Recurrent topics in João Leandro's work include Metabolism and Genetic Disorders (25 papers), Biochemical and Molecular Research (8 papers) and Folate and B Vitamins Research (5 papers). João Leandro is often cited by papers focused on Metabolism and Genetic Disorders (25 papers), Biochemical and Molecular Research (8 papers) and Folate and B Vitamins Research (5 papers). João Leandro collaborates with scholars based in Portugal, United States and Norway. João Leandro's co-authors include Sander M. Houten, Paula Leandro, Ania C. Muntau, Felix P. Mayer, Søren W. Gersting, Torgeir Flatmark, Isabel Tavares de Almeida, Jaakko Saraste, Tetyana Dodatko and Chunli Yu and has published in prestigious journals such as Journal of Biological Chemistry, Biochemistry and Scientific Reports.

In The Last Decade

João Leandro

32 papers receiving 464 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
João Leandro Portugal	13	325	213	88	70	57	32	465
Bárbara J. Henriques Portugal	13	360 1.1×	185 0.9×	43 0.5×	69 1.0×	55 1.0×	22	576
Piero Leone Italy	10	249 0.8×	128 0.6×	55 0.6×	87 1.2×	64 1.1×	18	417
Teresa Anna Giancaspero Italy	15	519 1.6×	243 1.1×	124 1.4×	80 1.1×	101 1.8×	18	725
Carmen Brizio Italy	15	604 1.9×	302 1.4×	158 1.8×	71 1.0×	98 1.7×	20	763
Brendan P. Norman United Kingdom	12	382 1.2×	204 1.0×	99 1.1×	91 1.3×	10 0.2×	37	554
Jan A. M. Smeitink Netherlands	13	523 1.6×	222 1.0×	36 0.4×	88 1.3×	58 1.0×	18	651
Isla Ogilvie United States	10	945 2.9×	351 1.6×	42 0.5×	57 0.8×	26 0.5×	11	1.1k
Siobhan E. Moriarty-Craige United States	7	327 1.0×	34 0.2×	203 2.3×	59 0.8×	54 0.9×	7	618
R. D. Scholem Australia	11	389 1.2×	423 2.0×	191 2.2×	81 1.2×	54 0.9×	12	589
N. Chamoles Argentina	11	302 0.9×	230 1.1×	48 0.5×	120 1.7×	66 1.2×	20	498

Countries citing papers authored by João Leandro

Since Specialization

Citations

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

Fields of papers citing papers by João Leandro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of João Leandro

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

Webb, Bryn D., Sara M. Nowinski, Ashley Solmonson, et al.. (2023). Recessive pathogenic variants in MCAT cause combined oxidative phosphorylation deficiency. eLife. 12. 4 indexed citations

Leandro, Paula, João Leandro, Mariana Amaro, et al.. (2023). Isothermal denaturation fluorimetry vs differential scanning fluorimetry as tools for screening of stabilizers for protein freeze-drying: Human phenylalanine hydroxylase as the case study. European Journal of Pharmaceutics and Biopharmaceutics. 187. 1–11. 2 indexed citations

Houten, Sander M., Tetyana Dodatko, Sara Violante, et al.. (2023). Acyl‐CoA dehydrogenase substrate promiscuity: Challenges and opportunities for development of substrate reduction therapy in disorders of valine and isoleucine metabolism. Journal of Inherited Metabolic Disease. 46(5). 931–942. 1 indexed citations

Nemeria, Natalia S., Bálint Nagy, Roberto Sánchez, et al.. (2022). Functional Versatility of the Human 2-Oxoadipate Dehydrogenase in the L-Lysine Degradation Pathway toward Its Non-Cognate Substrate 2-Oxopimelic Acid. International Journal of Molecular Sciences. 23(15). 8213–8213. 7 indexed citations

Nemeria, Natalia S., João Leandro, Jieyu Zhou, et al.. (2021). Toward an Understanding of the Structural and Mechanistic Aspects of Protein-Protein Interactions in 2-Oxoacid Dehydrogenase Complexes. Life. 11(5). 407–407. 16 indexed citations

Leandro, João, Aaron Bender, Tetyana Dodatko, et al.. (2021). Glutaric aciduria type 3 is a naturally occurring biochemical trait in inbred mice of 129 substrains. Molecular Genetics and Metabolism. 132(2). 139–145. 4 indexed citations

Leandro, João, Tetyana Dodatko, Jan Aten, et al.. (2020). DHTKD1 and OGDH display substrate overlap in cultured cells and form a hybrid 2-oxo acid dehydrogenase complex in vivo. Human Molecular Genetics. 29(7). 1168–1179. 20 indexed citations

Zhang, Xu, Natalia S. Nemeria, João Leandro, et al.. (2020). Structure–function analyses of the G729R 2-oxoadipate dehydrogenase genetic variant associated with a disorder of l-lysine metabolism. Journal of Biological Chemistry. 295(23). 8078–8095. 7 indexed citations

Leandro, João & Sander M. Houten. (2020). The lysine degradation pathway: Subcellular compartmentalization and enzyme deficiencies. Molecular Genetics and Metabolism. 131(1-2). 14–22. 71 indexed citations

10.

Leandro, João, Tetyana Dodatko, Robert J. DeVita, et al.. (2020). Deletion of 2‐aminoadipic semialdehyde synthase limits metabolite accumulation in cell and mouse models for glutaric aciduria type 1. Journal of Inherited Metabolic Disease. 43(6). 1154–1164. 19 indexed citations

11.

Sousa, Pedro M. F., Mariana Amaro, João Leandro, et al.. (2019). Author Correction: Structure of full-length wild-type human phenylalanine hydroxylase by small angle X-ray scattering reveals substrate-induced conformational stability. Scientific Reports. 9(1). 17513–17513. 1 indexed citations

12.

Sousa, Pedro M. F., Mariana Amaro, João Leandro, et al.. (2019). Structure of full-length wild-type human phenylalanine hydroxylase by small angle X-ray scattering reveals substrate-induced conformational stability. Scientific Reports. 9(1). 13615–13615. 14 indexed citations

13.

Leandro, João, Sara Violante, Carmen Argmann, et al.. (2019). Mild inborn errors of metabolism in commonly used inbred mouse strains. Molecular Genetics and Metabolism. 126(4). 388–396. 10 indexed citations

14.

Morais, Maurício, João Leandro, Lurdes Gano, et al.. (2017). Albumin-binding domain from Streptococcus zooepidemicus protein Zag as a novel strategy to improve the half-life of therapeutic proteins. Journal of Biotechnology. 253. 23–33. 15 indexed citations

15.

Leandro, João, Jaakko Saraste, Paula Leandro, & Torgeir Flatmark. (2011). The G46S-hPAH mutant protein: A model to study the rescue of aggregation-prone PKU mutations by chaperones. Molecular Genetics and Metabolism. 104. S40–S44. 8 indexed citations

16.

Leandro, João, Paula Leandro, & Torgeir Flatmark. (2011). Heterotetrameric forms of human phenylalanine hydroxylase: Co-expression of wild-type and mutant forms in a bicistronic system. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1812(5). 602–612. 26 indexed citations

17.

Leandro, João, et al.. (2010). Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1812(1). 106–120. 28 indexed citations

18.

Leandro, João, et al.. (2008). Modulation of the Activity of Newly Synthesized Human Phenylalanine Hydroxylase Mutant Proteins by Low-Molecular-Weight Compounds. The Protein Journal. 27(6). 392–400. 16 indexed citations

19.

Leandro, João, et al.. (2006). Co-expression of different subunits of human phenylalanine hydroxylase: Evidence of negative interallelic complementation. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1762(5). 544–550. 31 indexed citations

20.

Nascimento, Cairo Lúcio, et al.. (2005). Biochemical characterization of chimerical mutant forms of human phenylalanine hydroxylase. FEBS Journal. 272. 382–383. 1 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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