Florence Gizard

2.2k total citations
32 papers, 1.8k citations indexed

About

Florence Gizard is a scholar working on Molecular Biology, Immunology and Physiology. According to data from OpenAlex, Florence Gizard has authored 32 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 10 papers in Immunology and 8 papers in Physiology. Recurrent topics in Florence Gizard's work include Peroxisome Proliferator-Activated Receptors (8 papers), Estrogen and related hormone effects (6 papers) and Adipokines, Inflammation, and Metabolic Diseases (5 papers). Florence Gizard is often cited by papers focused on Peroxisome Proliferator-Activated Receptors (8 papers), Estrogen and related hormone effects (6 papers) and Adipokines, Inflammation, and Metabolic Diseases (5 papers). Florence Gizard collaborates with scholars based in France, United States and Canada. Florence Gizard's co-authors include Dennis Bruemmer, Elizabeth B. Heywood, Karrie L. Jones, Bart Staels, Takashi Nomiyama, Hannes M. Findeisen, Ryuzo Kawamori, Yue Zhao, Philippe Monget and Joëlle Dupont and has published in prestigious journals such as Journal of Biological Chemistry, Circulation and Journal of Clinical Investigation.

In The Last Decade

Florence Gizard

32 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Florence Gizard France 24 861 464 362 320 276 32 1.8k
Hiroji Oida Japan 14 654 0.8× 349 0.8× 286 0.8× 162 0.5× 235 0.9× 19 2.1k
Bhavapriya Vaitheesvaran United States 17 1.2k 1.4× 598 1.3× 190 0.5× 575 1.8× 255 0.9× 20 2.3k
Susan Gray United States 19 1.4k 1.6× 427 0.9× 173 0.5× 240 0.8× 94 0.3× 21 2.1k
Cong Tang China 15 916 1.1× 431 0.9× 267 0.7× 137 0.4× 114 0.4× 30 1.6k
Bong Sook Jhun United States 25 1.5k 1.8× 382 0.8× 150 0.4× 246 0.8× 180 0.7× 51 2.2k
Yan Ge China 26 805 0.9× 167 0.4× 317 0.9× 190 0.6× 111 0.4× 88 1.9k
Frédéric Leprêtre France 21 690 0.8× 460 1.0× 155 0.4× 473 1.5× 94 0.3× 47 1.8k
Man‐Wook Hur South Korea 26 1.4k 1.6× 269 0.6× 184 0.5× 131 0.4× 106 0.4× 77 2.0k
Rongrong Cui China 25 885 1.0× 198 0.4× 125 0.3× 290 0.9× 202 0.7× 59 1.8k
Shoichiro Ikuyama Japan 27 796 0.9× 272 0.6× 202 0.6× 206 0.6× 120 0.4× 66 1.9k

Countries citing papers authored by Florence Gizard

Since Specialization
Citations

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

Fields of papers citing papers by Florence Gizard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florence Gizard

This figure shows the co-authorship network connecting the top 25 collaborators of Florence Gizard. A scholar is included among the top collaborators of Florence Gizard 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 Florence Gizard. Florence Gizard 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.
2.
Wouters, Kristiaan, Céline Cudejko, Marion J. Gijbels, et al.. (2012). Bone Marrow p16INK4a-Deficiency Does Not Modulate Obesity, Glucose Homeostasis or Atherosclerosis Development. PLoS ONE. 7(3). e32440–e32440. 11 indexed citations
3.
Findeisen, Hannes M., Kevin J. Pearson, Florence Gizard, et al.. (2011). Oxidative Stress Accumulates in Adipose Tissue during Aging and Inhibits Adipogenesis. PLoS ONE. 6(4). e18532–e18532. 81 indexed citations
4.
Gizard, Florence, Yue Zhao, Hannes M. Findeisen, et al.. (2011). Transcriptional Regulation of S Phase Kinase-associated Protein 2 by NR4A Orphan Nuclear Receptor NOR1 in Vascular Smooth Muscle Cells. Journal of Biological Chemistry. 286(41). 35485–35493. 25 indexed citations
5.
Findeisen, Hannes M., Florence Gizard, Yue Zhao, et al.. (2011). Glutathione Depletion Prevents Diet‐Induced Obesity and Enhances Insulin Sensitivity. Obesity. 19(12). 2429–2432. 36 indexed citations
6.
Zhao, Yue, Deborah A. Howatt, Florence Gizard, et al.. (2010). Deficiency of the NR4A Orphan Nuclear Receptor NOR1 Decreases Monocyte Adhesion and Atherosclerosis. Circulation Research. 107(4). 501–511. 70 indexed citations
7.
Gizard, Florence, Takashi Nomiyama, Yue Zhao, et al.. (2008). The PPARα/p16 INK4a Pathway Inhibits Vascular Smooth Muscle Cell Proliferation by Repressing Cell Cycle–Dependent Telomerase Activation. Circulation Research. 103(10). 1155–1163. 52 indexed citations
8.
9.
Nomiyama, Takashi, Diego Pérez–Tilve, Daisuke Ogawa, et al.. (2007). Osteopontin mediates obesity-induced adipose tissue macrophage infiltration and insulin resistance in mice. Journal of Clinical Investigation. 117(10). 2877–2888. 316 indexed citations
10.
Froment, Pascal, et al.. (2006). Peroxisome proliferator-activated receptors in reproductive tissues: from gametogenesis to parturition. Journal of Endocrinology. 189(2). 199–209. 177 indexed citations
11.
Nomiyama, Takashi, Florence Gizard, Elizabeth B. Heywood, et al.. (2006). The NR4A Orphan Nuclear Receptor NOR1 Is Induced by Platelet-derived Growth Factor and Mediates Vascular Smooth Muscle Cell Proliferation. Journal of Biological Chemistry. 281(44). 33467–33476. 112 indexed citations
12.
Gizard, Florence & Bart Staels. (2006). Rôle protecteur de la voie fibrates/p16INK4Adans les lesions vasculaires occlusives. médecine/sciences. 22(4). 351–353. 1 indexed citations
13.
Gizard, Florence, Carole Amant, Olivier Barbier, et al.. (2005). PPARα inhibits vascular smooth muscle cell proliferation underlying intimal hyperplasia by inducing the tumor suppressor p16INK4a. Journal of Clinical Investigation. 115(11). 3228–3238. 134 indexed citations
14.
15.
Froment, Pascal, Florence Gizard, Bart Staels, Joëlle Dupont, & Philippe Monget. (2005). Un rôle pour PPARγ dans la reproduction ?. médecine/sciences. 21(5). 507–511. 15 indexed citations
16.
Gizard, Florence, Elisabeth Teissier, Isabelle Dufort, et al.. (2004). The transcriptional regulating protein of 132 kDa (TReP-132) differentially influences steroidogenic pathways in human adrenal NCI-H295 cells. Journal of Molecular Endocrinology. 32(2). 557–569. 9 indexed citations
17.
Gizard, Florence, Mohamed Elalfy, Yannick Duguay, et al.. (2002). FUNCTION OF THE TRANSCRIPTIONAL REGULATING PROTEIN OF 132 kDa (TReP-132) ON HUMAN P450scc GENE EXPRESSION. Endocrine Research. 28(4). 559–574. 10 indexed citations
18.
Gizard, Florence, et al.. (2002). The Transcriptional Regulating Protein of 132 kDa (TReP-132) Enhances P450scc Gene Transcription through Interaction with Steroidogenic Factor-1 in Human Adrenal Cells. Journal of Biological Chemistry. 277(42). 39144–39155. 51 indexed citations
19.
Gizard, Florence, et al.. (2001). A Novel Zinc Finger Protein TReP-132 Interacts with CBP/p300 to Regulate Human CYP11A1 Gene Expression. Journal of Biological Chemistry. 276(36). 33881–33892. 42 indexed citations
20.
Vasconcelos, Anne Pereira de, Florence Gizard, Christian Marescaux, & Astrid Nehlig. (2000). Role of Nitric Oxide in Pentylenetetrazol‐Induced Seizures: Age‐Dependent Effects in the Immature Rat. Epilepsia. 41(4). 363–371. 26 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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