Fernando López‐Casillas

6.1k total citations · 2 hit papers
82 papers, 4.8k citations indexed

About

Fernando López‐Casillas is a scholar working on Molecular Biology, Cell Biology and Physiology. According to data from OpenAlex, Fernando López‐Casillas has authored 82 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 17 papers in Cell Biology and 9 papers in Physiology. Recurrent topics in Fernando López‐Casillas's work include TGF-β signaling in diseases (31 papers), Biotin and Related Studies (9 papers) and Adipose Tissue and Metabolism (9 papers). Fernando López‐Casillas is often cited by papers focused on TGF-β signaling in diseases (31 papers), Biotin and Related Studies (9 papers) and Adipose Tissue and Metabolism (9 papers). Fernando López‐Casillas collaborates with scholars based in Mexico, United States and Canada. Fernando López‐Casillas's co-authors include Joan Massagué, Jeffrey L. Wrana, Sela Cheifetz, Valentı́n Mendoza, Janet Andres, William S. Lane, Jacqueline Doody, Liliana Attisano, Ki-Han Kim and Joaquı́n Arribas and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Fernando López‐Casillas

80 papers receiving 4.7k citations

Hit Papers

Betaglycan presents ligan... 1991 2026 2002 2014 1993 1991 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fernando López‐Casillas Mexico 35 3.3k 839 681 530 483 82 4.8k
Jacques Bertoglio France 41 3.1k 0.9× 1.0k 1.2× 888 1.3× 516 1.0× 499 1.0× 118 6.1k
Paul W. Kincade United States 59 3.0k 0.9× 1.2k 1.4× 827 1.2× 746 1.4× 494 1.0× 155 9.6k
Thomas A. Ferguson United States 43 3.3k 1.0× 606 0.7× 353 0.5× 454 0.9× 624 1.3× 84 8.4k
Adam B. Glick United States 47 4.6k 1.4× 1.6k 1.9× 903 1.3× 590 1.1× 893 1.8× 109 7.4k
Roberto Testi Italy 47 4.2k 1.3× 795 0.9× 704 1.0× 217 0.4× 442 0.9× 113 7.4k
Ottmar Janßen Germany 42 2.3k 0.7× 1.1k 1.3× 428 0.6× 460 0.9× 490 1.0× 135 5.6k
Ann Ranger United States 24 2.9k 0.9× 1.0k 1.2× 342 0.5× 230 0.4× 644 1.3× 46 6.0k
D J McKean United States 40 2.3k 0.7× 832 1.0× 388 0.6× 346 0.7× 329 0.7× 114 6.4k
T Sudo Japan 33 2.9k 0.9× 1.1k 1.3× 552 0.8× 230 0.4× 517 1.1× 80 5.6k
Peter Adamson United Kingdom 43 2.9k 0.9× 594 0.7× 808 1.2× 922 1.7× 294 0.6× 99 5.8k

Countries citing papers authored by Fernando López‐Casillas

Since Specialization
Citations

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

Fields of papers citing papers by Fernando López‐Casillas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fernando López‐Casillas. 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 Fernando López‐Casillas. The network helps show where Fernando López‐Casillas may publish in the future.

Co-authorship network of co-authors of Fernando López‐Casillas

This figure shows the co-authorship network connecting the top 25 collaborators of Fernando López‐Casillas. A scholar is included among the top collaborators of Fernando López‐Casillas 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 Fernando López‐Casillas. Fernando López‐Casillas 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.
Wieteska, Łukasz, Alexander B. Taylor, Jonathan A. Coleman, et al.. (2025). Structures of TGF-β with betaglycan and signaling receptors reveal mechanisms of complex assembly and signaling. Nature Communications. 16(1). 1778–1778. 7 indexed citations
2.
Mendoza, Valentı́n, et al.. (2023). Betaglycan promoter activity is differentially regulated during myogenesis in zebrafish embryo somites. Developmental Dynamics. 252(9). 1162–1179. 1 indexed citations
3.
Kim, Sun Kyung, Matthew J. Whitley, Troy C. Krzysiak, et al.. (2019). Structural Adaptation in Its Orphan Domain Engenders Betaglycan with an Alternate Mode of Growth Factor Binding Relative to Endoglin. Structure. 27(9). 1427–1442.e4. 10 indexed citations
4.
Alemán-Muench, Germán Rodrigo, Valentı́n Mendoza, Kaye L. Stenvers, et al.. (2012). Betaglycan (TβRIII) Is Expressed in the Thymus and Regulates T Cell Development by Protecting Thymocytes from Apoptosis. PLoS ONE. 7(8). e44217–e44217. 9 indexed citations
5.
Mata‐Espinosa, Dulce, et al.. (2008). Therapeutic Effect of Recombinant Adenovirus Encoding Interferon-γ in a Murine Model of Progressive Pulmonary Tuberculosis. Molecular Therapy. 16(6). 1065–1072. 21 indexed citations
6.
Juárez, M. Patricia, María Magdalena Vilchis‐Landeros, José Ponce‐Coria, et al.. (2006). Soluble betaglycan reduces renal damage progression indb/dbmice. American Journal of Physiology-Renal Physiology. 292(1). F321–F329. 46 indexed citations
7.
Crescenzo, Grégory De, Cynthia S. Hinck, Zhanyong Shu, et al.. (2005). Three Key Residues Underlie the Differential Affinity of the TGFβ Isoforms for the TGFβ Type II Receptor. Journal of Molecular Biology. 355(1). 47–62. 65 indexed citations
8.
García‐Sáinz, J. Adolfo, María Magdalena Vilchis‐Landeros, Patricia Juárez, et al.. (2003). Receptores y funciones del TGF-beta, una citocina crucial en la cicatrización.. Gaceta Médica de México. 139(2). 126–143. 1 indexed citations
9.
López‐Casillas, Fernando & Joan Massagué. (2003). Gaceta Medica de Mexico. 65 indexed citations
10.
Juárez, M. Patricia, Victoria Ramírez, Norma Uribe, et al.. (2003). Therapeutic benefit of spironolactone in experimental chronic cyclosporine A nephrotoxicity. Kidney International. 63(1). 43–52. 123 indexed citations
11.
Xavier, Gabriela da Silva, Frédérique Diraison, Chao Zhao, et al.. (2002). Stimulation of Acetyl-CoA Carboxylase Gene Expression by Glucose Requires Insulin Release and Sterol Regulatory Element Binding Protein 1c in Pancreatic MIN6 β-Cells. Diabetes. 51(8). 2536–2545. 51 indexed citations
12.
Sciutto, Edda, Gladis Fragoso, Karen Manoutcharian, et al.. (2002). New Approaches to Improve a Peptide Vaccine Against Porcine Taenia solium Cysticercosis. Archives of Medical Research. 33(4). 371–378. 26 indexed citations
13.
Toledo, Andrea, Carlos Larralde, Gladis Fragoso, et al.. (1999). Towards aTaenia soliumCysticercosis Vaccine: an Epitope Shared byTaenia crassicepsandTaenia soliumProtects Mice against Experimental Cysticercosis. Infection and Immunity. 67(5). 2522–2530. 81 indexed citations
14.
Ponce-Castañeda, M. Verónica, et al.. (1998). Murine betaglycan primary structure, expression and glycosaminoglycan attachment sites. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1384(2). 189–196. 12 indexed citations
15.
Wrana, Jeffrey L., Juan M. Cárcamo, Liliana Attisano, et al.. (1992). The Type II TGF-  Receptor Signals Diverse Responses in Cooperation with the Type I Receptor. Cold Spring Harbor Symposia on Quantitative Biology. 57(0). 81–86. 28 indexed citations
16.
López‐Casillas, Fernando, et al.. (1991). The 5′ untranslated regions of acetyl‐coenzyme A carboxylase mRNA provide specific translational control in vitro. European Journal of Biochemistry. 201(1). 119–127. 21 indexed citations
17.
López‐Casillas, Fernando, M. Verónica Ponce-Castañeda, & Ki-Han Kim. (1991). In VivoRegulation of the Activity of the Two Promoters of the Rat Acetyl Coenzyme-A Carboxylase Gene*. Endocrinology. 129(2). 1049–1058. 59 indexed citations
18.
Pape, Michael E., Fernando López‐Casillas, & Ki-Han Kim. (1988). Physiological regulation of acetyl-CoA carboxylase gene expression: Effects of diet, diabetes, and lactation on acetyl-CoA carboxylase mRNA. Archives of Biochemistry and Biophysics. 267(1). 104–109. 111 indexed citations
19.
Milatovich, Athena, et al.. (1988). Localization of the gene for acetyl-CoA carboxylase to human chromosome 17. Cytogenetic and Genome Research. 48(3). 190–192. 8 indexed citations
20.
López‐Casillas, Fernando, Michael E. Pape, Dong-Hoon Bai, et al.. (1987). Preparation of functional acetyl-CoA carboxylase mRNA from rat mammary gland. Archives of Biochemistry and Biophysics. 257(1). 63–68. 18 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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