Philippe Gascard

13.8k total citations · 1 hit paper
57 papers, 2.4k citations indexed

About

Philippe Gascard is a scholar working on Physiology, Molecular Biology and Cell Biology. According to data from OpenAlex, Philippe Gascard has authored 57 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Physiology, 30 papers in Molecular Biology and 14 papers in Cell Biology. Recurrent topics in Philippe Gascard's work include Erythrocyte Function and Pathophysiology (31 papers), Blood properties and coagulation (8 papers) and Cellular transport and secretion (7 papers). Philippe Gascard is often cited by papers focused on Erythrocyte Function and Pathophysiology (31 papers), Blood properties and coagulation (8 papers) and Cellular transport and secretion (7 papers). Philippe Gascard collaborates with scholars based in United States, France and Japan. Philippe Gascard's co-authors include Thea D. Tlsty, Narla Mohandas, John G. Conboy, Loren D. Walensky, Cindy Cohen, Solomon H. Snyder, Françoise Giraud, Joel Anne Chasis, Yuichi Takakuwa and Jean‐Claude Sulpice and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Philippe Gascard

57 papers receiving 2.3k citations

Hit Papers

Carcinoma-associated fibroblasts: orchestrating the compo... 2016 2026 2019 2022 2016 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philippe Gascard United States 27 1.4k 675 575 542 360 57 2.4k
Jeffrey E. DeClue United States 29 1.6k 1.2× 878 1.3× 528 0.9× 428 0.8× 381 1.1× 43 2.9k
Deniz Toksoz United States 30 1.8k 1.3× 223 0.3× 459 0.8× 432 0.8× 339 0.9× 49 2.9k
Nina Jones Canada 30 2.1k 1.5× 203 0.3× 440 0.8× 379 0.7× 199 0.6× 59 3.3k
Anders Eriksson Sweden 19 1.2k 0.9× 215 0.3× 316 0.5× 247 0.5× 186 0.5× 36 2.1k
Rónán C. O’Hagan United States 18 2.2k 1.7× 410 0.6× 1.1k 1.9× 323 0.6× 191 0.5× 30 3.1k
Marta Barradas Spain 11 2.2k 1.7× 1.2k 1.7× 1.1k 1.9× 246 0.5× 200 0.6× 15 3.1k
John P. O’Bryan United States 35 2.3k 1.7× 397 0.6× 708 1.2× 968 1.8× 208 0.6× 77 3.9k
Pedro A. Pérez–Mancera United Kingdom 24 2.1k 1.5× 446 0.7× 1.0k 1.8× 295 0.5× 225 0.6× 38 3.1k
Rita Falcioni Italy 32 1.6k 1.2× 175 0.3× 745 1.3× 780 1.4× 151 0.4× 64 3.1k
Mary L. Stracke United States 32 2.7k 2.0× 296 0.4× 605 1.1× 1.3k 2.4× 138 0.4× 52 3.7k

Countries citing papers authored by Philippe Gascard

Since Specialization
Citations

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

Fields of papers citing papers by Philippe Gascard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philippe Gascard

This figure shows the co-authorship network connecting the top 25 collaborators of Philippe Gascard. A scholar is included among the top collaborators of Philippe Gascard 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 Philippe Gascard. Philippe Gascard 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.
Bons, Joanna, Filipe C. Lourenço, Samah Shah, et al.. (2024). Extracellular Matrix Orchestration of Tissue Remodeling in the Chronically Inflamed Mouse Colon. Cellular and Molecular Gastroenterology and Hepatology. 17(4). 639–656. 3 indexed citations
2.
Shimshoni, Elee, Viktor J. Horváth, Joseph A. Caruso, et al.. (2023). Epithelial-Stromal Interactions in Barrett’s Esophagus Modeled in Human Organ Chips. SHILAP Revista de lepidopterología. 2(5). 676–680. 7 indexed citations
3.
Murrow, Lyndsay M., Robert J. Weber, Christopher S. McGinnis, et al.. (2022). Mapping hormone-regulated cell-cell interaction networks in the human breast at single-cell resolution. Cell Systems. 13(8). 644–664.e8. 16 indexed citations
4.
Pan, Deng, et al.. (2016). SOX2, OCT3/4 and NANOG expression and cellular plasticity in rare human somatic cells requires CD73. Cellular Signalling. 28(12). 1923–1932. 7 indexed citations
5.
Keating, Mark, et al.. (2015). Novel insights from 3D models: the pivotal role of physical symmetry in epithelial organization. Scientific Reports. 5(1). 15153–15153. 9 indexed citations
6.
Nunomura, Wataru, Philippe Gascard, Hideki Wakui, & Yuichi Takakuwa. (2014). Phosphatidylinositol-4,5 bisphosphate (PIP2) inhibits apo-calmodulin binding to protein 4.1. Biochemical and Biophysical Research Communications. 446(2). 434–440. 2 indexed citations
7.
Gascard, Philippe, Nancy Dumont, Jian‐xin Zhao, et al.. (2013). Rare somatic cells from human breast tissue exhibit extensive lineage plasticity. Proceedings of the National Academy of Sciences. 110(12). 4598–4603. 71 indexed citations
8.
Andarawewa, Kumari L., Anna Erickson, William Chou, et al.. (2007). Ionizing Radiation Predisposes Nonmalignant Human Mammary Epithelial Cells to Undergo Transforming Growth Factor β–Induced Epithelial to Mesenchymal Transition. Cancer Research. 67(18). 8662–8670. 135 indexed citations
9.
Rivera, Alicia, Lucia De Franceschi, Luanne L. Peters, et al.. (2006). Effect of complete protein 4.1R deficiency on ion transport properties of murine erythrocytes. American Journal of Physiology-Cell Physiology. 291(5). C880–C886. 26 indexed citations
10.
Puttini, Stefania, Antoine Ouvrard‐Pascaud, Gaël Palais, et al.. (2005). Development of a targeted transgenesis strategy in highly differentiated cells: a powerful tool for functional genomic analysis. Journal of Biotechnology. 116(2). 145–151. 6 indexed citations
11.
Gascard, Philippe, Marilyn Parra, Zhiyong Zhao, et al.. (2004). Putative tumor suppressor protein 4.1B is differentially expressed in kidney and brain via alternative promoters and 5′ alternative splicing. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1680(2). 71–82. 17 indexed citations
12.
Blot‐Chabaud, Marcel, Françoise Cluzeaud, Michael Patterson, et al.. (2003). Distinct distribution of specific members of protein 4.1 gene family in the mouse nephron. Kidney International. 63(4). 1321–1337. 48 indexed citations
13.
Robb, Victoria A., Wen Li, Philippe Gascard, et al.. (2003). Identification of a third Protein 4.1 tumor suppressor, Protein 4.1R, in meningioma pathogenesis. Neurobiology of Disease. 13(3). 191–202. 68 indexed citations
14.
An, Xiuli, Yuichi Takakuwa, Sumie Manno, et al.. (2001). Structural and Functional Characterization of Protein 4.1R-Phosphatidylserine Interaction. Journal of Biological Chemistry. 276(38). 35778–35785. 43 indexed citations
15.
Parra, Marilyn, Philippe Gascard, Loren D. Walensky, et al.. (2000). Molecular and Functional Characterization of Protein 4.1B, a Novel Member of the Protein 4.1 Family with High Level, Focal Expression in Brain. Journal of Biological Chemistry. 275(5). 3247–3255. 114 indexed citations
16.
Mohandas, Narla & Philippe Gascard. (1999). What do mouse gene knockouts tell us about the structure and function of the red cell membrane?. Best Practice & Research Clinical Haematology. 12(4). 605–620. 6 indexed citations
17.
Gascard, Philippe, Wataru Nunomura, Gloria Lee, et al.. (1999). Deciphering the Nuclear Import Pathway for the Cytoskeletal Red Cell Protein 4.1R. Molecular Biology of the Cell. 10(6). 1783–1798. 39 indexed citations
18.
Parra, Mireya, Philippe Gascard, Loren D. Walensky, et al.. (1998). Cloning and Characterization of 4.1G (EPB41L2), a New Member of the Skeletal Protein 4.1 (EPB41) Gene Family. Genomics. 49(2). 298–306. 97 indexed citations
19.
Gascard, Philippe, Tadeusz Pawełczyk, John M. Lowenstein, & Carl M. Cohen. (1993). The role of inositol phospholipids in the association of band 4.1 with the human erythrocyte membrane. European Journal of Biochemistry. 211(3). 671–681. 29 indexed citations
20.
Gascard, Philippe, Dien Tran, Jean‐Claude Sulpice, et al.. (1991). Asymmetric distribution of phosphoinositides and phosphatidic acid in the human erythrocyte membrane. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1069(1). 27–36. 72 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026