Christian M. Moya

714 total citations
18 papers, 540 citations indexed

About

Christian M. Moya is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Christian M. Moya has authored 18 papers receiving a total of 540 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Endocrinology, Diabetes and Metabolism and 3 papers in Genetics. Recurrent topics in Christian M. Moya's work include Thyroid Disorders and Treatments (9 papers), Ion channel regulation and function (6 papers) and RNA and protein synthesis mechanisms (5 papers). Christian M. Moya is often cited by papers focused on Thyroid Disorders and Treatments (9 papers), Ion channel regulation and function (6 papers) and RNA and protein synthesis mechanisms (5 papers). Christian M. Moya collaborates with scholars based in Argentina, Spain and United States. Christian M. Moya's co-authors include Héctor M. Targovnik, Pilar Santisteban, Lucas C. González-Matías, Federico Mallo, E. Vigo, Marina Romaní‐Pérez, Viviana Varela, Fernando Mendive, Geraldo Medeiros‐Neto and Sabina Domené and has published in prestigious journals such as Journal of Clinical Oncology, The Journal of Clinical Endocrinology & Metabolism and Endocrinology.

In The Last Decade

Christian M. Moya

17 papers receiving 523 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christian M. Moya Argentina 11 346 245 138 87 60 18 540
Vita Rovīte Latvia 13 105 0.3× 180 0.7× 70 0.5× 50 0.6× 48 0.8× 43 461
Xuming Sun United States 15 147 0.4× 185 0.8× 157 1.1× 54 0.6× 24 0.4× 34 542
G Consoli Italy 10 235 0.7× 125 0.5× 51 0.4× 20 0.2× 52 0.9× 27 481
Mikiya Usukura Japan 12 236 0.7× 120 0.5× 18 0.1× 26 0.3× 149 2.5× 20 442
Hisakazu Nakajima Japan 11 77 0.2× 112 0.5× 86 0.6× 21 0.2× 61 1.0× 43 389
Catalina Norman United States 10 182 0.5× 95 0.4× 21 0.2× 33 0.4× 48 0.8× 16 419
Roberto Queiroga Lautner Brazil 7 105 0.3× 156 0.6× 71 0.5× 34 0.4× 23 0.4× 13 369
Heidi Fodstad Finland 15 83 0.2× 454 1.9× 73 0.5× 10 0.1× 20 0.3× 26 673

Countries citing papers authored by Christian M. Moya

Since Specialization
Citations

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

Fields of papers citing papers by Christian M. Moya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christian M. Moya. 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 Christian M. Moya. The network helps show where Christian M. Moya may publish in the future.

Co-authorship network of co-authors of Christian M. Moya

This figure shows the co-authorship network connecting the top 25 collaborators of Christian M. Moya. A scholar is included among the top collaborators of Christian M. Moya 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 Christian M. Moya. Christian M. Moya is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Masotto, Bárbara, et al.. (2023). Case report: A novel SON mutation in a Colombian patient with ZTTK syndrome. Frontiers in Genetics. 14. 1183362–1183362. 1 indexed citations
2.
Toscano, Marta A., et al.. (2022). Testing of mutations on thyroid nodules with indeterminate cytology: A prospective study of 112 patients in Argentina. Endocrinología Diabetes y Nutrición (English ed ). 69(2). 122–130. 3 indexed citations
3.
Toscano, Marta A., et al.. (2021). Testeo de mutaciones en nódulos tiroideos con citología indeterminada: estudio prospectivo de 112 pacientes en Argentina. Endocrinología Diabetes y Nutrición. 69(2). 122–130.
4.
Citterio, Cintia E., et al.. (2020). p.L571P in the linker domain of rat thyroglobulin causes intracellular retention. Molecular and Cellular Endocrinology. 505. 110719–110719. 4 indexed citations
5.
Cantalapiedra, Diego, Ignacio Durán, Oriol Calvete, et al.. (2018). The application of cognitive computing technology in genomics in precision oncological medicine: The Sistemas Genomicos Experience.. Journal of Clinical Oncology. 36(15_suppl). e18544–e18544. 3 indexed citations
6.
Moya, Christian M., Carmen Luna, Rogelio Simón, et al.. (2017). TAZ/WWTR1 Mediates the Pulmonary Effects of NKX2-1 Mutations in Brain-Lung-Thyroid Syndrome. The Journal of Clinical Endocrinology & Metabolism. 103(3). 839–852. 10 indexed citations
7.
Romaní‐Pérez, Marina, Christian M. Moya, Pilar Santisteban, et al.. (2015). Activation of the GLP-1 Receptor by Liraglutide Increases ACE2 Expression, Reversing Right Ventricle Hypertrophy, and Improving the Production of SP-A and SP-B in the Lungs of Type 1 Diabetes Rats. Endocrinology. 156(10). 3559–3569. 144 indexed citations
8.
García-Martínez, José Manuel, Ana Chocarro‐Calvo, Christian M. Moya, & Custodia García‐Jiménez. (2009). WNT/β-catenin increases the production of incretins by entero-endocrine cells. Diabetologia. 52(9). 1913–1924. 33 indexed citations
9.
Moya, Christian M., Guiomar Pérez de Nanclares, Luís Castaño, et al.. (2006). Functional Study of a Novel Single Deletion in theTITF1/NKX2.1Homeobox Gene That Produces Congenital Hypothyroidism and Benign Chorea But Not Pulmonary Distress. The Journal of Clinical Endocrinology & Metabolism. 91(5). 1832–1841. 63 indexed citations
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Moya, Christian M., et al.. (2005). [The thyroid as a model for molecular mechanisms in genetic diseases].. PubMed. 65(3). 257–67. 9 indexed citations
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Caron, Philippe, et al.. (2003). Compound Heterozygous Mutations in the Thyroglobulin Gene (1143delC and 6725G→A [R2223H]) Resulting in Fetal Goitrous Hypothyroidism. The Journal of Clinical Endocrinology & Metabolism. 88(8). 3546–3553. 60 indexed citations
14.
Esperante, Sebastián, Laura Gruñeiro‐Papendieck, Ana Chiesa, et al.. (2003). Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect. Human Mutation. 22(3). 259–259. 39 indexed citations
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Targovnik, Héctor M., et al.. (2001). Congenital Goiter with Hypothyroidism Caused by a 5′ Splice Site Mutation in the Thyroglobulin Gene. Thyroid. 11(7). 685–690. 47 indexed citations
18.
Moya, Christian M., et al.. (2000). Genomic organization of the 5' region of the human thyroglobulin gene. European Journal of Endocrinology. 143(6). 789–798. 24 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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