Giorgio Lagna

6.4k total citations · 3 hit papers
41 papers, 5.3k citations indexed

About

Giorgio Lagna is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Cancer Research. According to data from OpenAlex, Giorgio Lagna has authored 41 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 11 papers in Pulmonary and Respiratory Medicine and 8 papers in Cancer Research. Recurrent topics in Giorgio Lagna's work include TGF-β signaling in diseases (10 papers), Pulmonary Hypertension Research and Treatments (10 papers) and MicroRNA in disease regulation (8 papers). Giorgio Lagna is often cited by papers focused on TGF-β signaling in diseases (10 papers), Pulmonary Hypertension Research and Treatments (10 papers) and MicroRNA in disease regulation (8 papers). Giorgio Lagna collaborates with scholars based in United States, United Kingdom and Japan. Giorgio Lagna's co-authors include Akiko Hata, Brandi N. Davis‐Dusenbery, Ali Hemmati‐Brivanlou, Joan Massagué, Peter Nguyen, Atsushi Suzuki, Paul A. Wilson, Mun Chun Chan, David Wotton and Roger S. Lo and has published in prestigious journals such as Nature, Cell and Nucleic Acids Research.

In The Last Decade

Giorgio Lagna

39 papers receiving 5.3k citations

Hit Papers

SMAD proteins control DROSHA-mediated microRNA matur... 1996 2026 2006 2016 2008 1996 1998 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Giorgio Lagna United States 24 4.5k 1.8k 573 446 406 41 5.3k
Carlos le Sage Netherlands 24 5.3k 1.2× 4.2k 2.3× 568 1.0× 196 0.4× 389 1.0× 31 6.4k
Klaas Kok Netherlands 38 2.9k 0.6× 1.3k 0.7× 1.0k 1.8× 766 1.7× 977 2.4× 128 4.4k
Jitesh Pratap United States 34 3.2k 0.7× 943 0.5× 1.4k 2.5× 278 0.6× 387 1.0× 67 4.1k
Nathan Bucay United States 19 3.7k 0.8× 912 0.5× 1.6k 2.7× 502 1.1× 507 1.2× 30 5.0k
Marko Rehn Finland 30 2.0k 0.4× 790 0.4× 742 1.3× 310 0.7× 260 0.6× 53 3.2k
Carl‐Henrik Heldin Sweden 23 4.0k 0.9× 664 0.4× 1.3k 2.3× 508 1.1× 417 1.0× 29 5.7k
Anita Morén Sweden 25 2.6k 0.6× 450 0.2× 716 1.2× 239 0.5× 421 1.0× 33 3.3k
L E Gentry United States 28 2.8k 0.6× 662 0.4× 900 1.6× 240 0.5× 453 1.1× 44 4.0k
Jacqueline Doody United States 23 5.2k 1.2× 552 0.3× 1.6k 2.7× 419 0.9× 403 1.0× 34 6.5k
Marta Garcia Del Barrio Spain 6 2.5k 0.6× 629 0.3× 1.4k 2.4× 309 0.7× 332 0.8× 6 3.4k

Countries citing papers authored by Giorgio Lagna

Since Specialization
Citations

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

Fields of papers citing papers by Giorgio Lagna

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giorgio Lagna

This figure shows the co-authorship network connecting the top 25 collaborators of Giorgio Lagna. A scholar is included among the top collaborators of Giorgio Lagna 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 Giorgio Lagna. Giorgio Lagna 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.
Prabhakar, Amit, Meetu Wadhwa, Rahul Kumar, et al.. (2024). Mechanisms underlying age-associated exacerbation of pulmonary veno-occlusive disease. JCI Insight. 9(19). 4 indexed citations
2.
Prabhakar, Amit, Rahul Kumar, Meetu Wadhwa, et al.. (2024). Reply to the letter to the editor entitled “Bridging the species divide: The limits of rat models in capturing human PVOD mechanisms” by Perros F. et al.. Pulmonary Circulation. 14(4). e70015–e70015.
3.
Prabhakar, Amit, Rahul Kumar, Meetu Wadhwa, et al.. (2024). Reversal of pulmonary veno-occlusive disease phenotypes by inhibition of the integrated stress response. Nature Cardiovascular Research. 3(7). 799–818. 5 indexed citations
4.
Prabhakar, Amit, et al.. (2023). Essential role of the amino-terminal region of Drosha for the Microprocessor function. iScience. 26(10). 107971–107971. 1 indexed citations
5.
Jiang, Xuan, Amit Prabhakar, Barbara Celona, et al.. (2021). Control of ribosomal protein synthesis by the Microprocessor complex. Science Signaling. 14(671). 7 indexed citations
6.
Hata, Akiko & Giorgio Lagna. (2019). Deregulation of Drosha in the pathogenesis of hereditary hemorrhagic telangiectasia. Current Opinion in Hematology. 26(3). 161–169. 5 indexed citations
7.
Jiang, Xuan, Whitney Wooderchak‐Donahue, Jamie McDonald, et al.. (2018). Inactivating mutations in Drosha mediate vascular abnormalities similar to hereditary hemorrhagic telangiectasia. Science Signaling. 11(513). 22 indexed citations
8.
Kashima, Risa, Patrick Redmond, Sougata Roy, et al.. (2017). Hyperactive locomotion in a Drosophila model is a functional readout for the synaptic abnormalities underlying fragile X syndrome. Science Signaling. 10(477). 32 indexed citations
9.
Chang, Jonathan, Brandi N. Davis‐Dusenbery, Risa Kashima, et al.. (2013). Acetylation of p53 stimulates miRNA processing and determines cell survival following genotoxic stress. The EMBO Journal. 32(24). 3192–3205. 31 indexed citations
10.
Wang, Dahai, Peter Nguyen, Brandi N. Davis‐Dusenbery, et al.. (2012). Bone Morphogenetic Protein Signaling in Vascular Disease. Journal of Biological Chemistry. 287(33). 28067–28077. 34 indexed citations
11.
Kang, Hara, Alexandra S. Weisman, Jessica Sheu‐Gruttadauria, et al.. (2012). Inhibition of MicroRNA-302 (miR-302) by Bone Morphogenetic Protein 4 (BMP4) Facilitates the BMP Signaling Pathway. Journal of Biological Chemistry. 287(46). 38656–38664. 47 indexed citations
12.
Kang, Hara, Brandi N. Davis‐Dusenbery, Peter Nguyen, et al.. (2011). Bone Morphogenetic Protein 4 Promotes Vascular Smooth Muscle Contractility by Activating MicroRNA-21 (miR-21), which Down-regulates Expression of Family of Dedicator of Cytokinesis (DOCK) Proteins. Journal of Biological Chemistry. 287(6). 3976–3986. 84 indexed citations
13.
Chan, Mun Chun, Brandi N. Davis‐Dusenbery, Nicholas S. Hill, et al.. (2009). Molecular basis for antagonism between PDGF and the TGFβ family of signalling pathways by control of miR‐24 expression. The EMBO Journal. 29(3). 559–573. 170 indexed citations
14.
Schnitzler, Gavin R., et al.. (2009). The Four-and-a-half LIM Domain Protein 2 Regulates Vascular Smooth Muscle Phenotype and Vascular Tone. Journal of Biological Chemistry. 284(19). 13202–13212. 29 indexed citations
15.
Davis‐Dusenbery, Brandi N., et al.. (2008). SMAD proteins control DROSHA-mediated microRNA maturation. Nature. 454(7200). 56–61. 1049 indexed citations breakdown →
16.
Chan, Mun Chun, Peter Nguyen, Brandi N. Davis‐Dusenbery, et al.. (2007). A Novel Regulatory Mechanism of the Bone Morphogenetic Protein (BMP) Signaling Pathway Involving the Carboxyl-Terminal Tail Domain of BMP Type II Receptor. Molecular and Cellular Biology. 27(16). 5776–5789. 108 indexed citations
17.
Lagna, Giorgio, et al.. (2007). Control of Phenotypic Plasticity of Smooth Muscle Cells by Bone Morphogenetic Protein Signaling through the Myocardin-related Transcription Factors. Journal of Biological Chemistry. 282(51). 37244–37255. 142 indexed citations
18.
Hata, Akiko, et al.. (2000). OAZ Uses Distinct DNA- and Protein-Binding Zinc Fingers in Separate BMP-Smad and Olf Signaling Pathways. Cell. 100(2). 229–240. 361 indexed citations
19.
Lagna, Giorgio & Ali Hemmati‐Brivanlou. (1997). 4 Use of Dominant Negative Constructs to Modulate Gene Expression. Current topics in developmental biology. 36. 75–98. 9 indexed citations
20.
Lagna, Giorgio, Akiko Hata, Ali Hemmati‐Brivanlou, & Joan Massagué. (1996). Partnership between DPC4 and SMAD proteins in TGF-β signalling pathways. Nature. 383(6603). 832–836. 792 indexed citations breakdown →

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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