Carole Sztalryd

12.7k total citations · 3 hit papers
60 papers, 7.0k citations indexed

About

Carole Sztalryd is a scholar working on Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Carole Sztalryd has authored 60 papers receiving a total of 7.0k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Biochemistry, 28 papers in Physiology and 26 papers in Molecular Biology. Recurrent topics in Carole Sztalryd's work include Lipid metabolism and biosynthesis (40 papers), Adipose Tissue and Metabolism (27 papers) and Research in Cotton Cultivation (14 papers). Carole Sztalryd is often cited by papers focused on Lipid metabolism and biosynthesis (40 papers), Adipose Tissue and Metabolism (27 papers) and Research in Cotton Cultivation (14 papers). Carole Sztalryd collaborates with scholars based in United States, Sweden and China. Carole Sztalryd's co-authors include Alan R. Kimmel, Constantine Londos, Dawn Brasaemle, John T. Tansey, Fredric B. Kraemer, Hong Wang, Guoheng Xu, Da‐Wei Gong, Heidi Dorward and Juan Antonio Rojas‐Contreras and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Carole Sztalryd

60 papers receiving 6.9k citations

Hit Papers

Perilipin ablation results in a lean mouse with aberrant ... 2001 2026 2009 2017 2001 2017 2018 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
Carole Sztalryd United States 37 4.2k 3.3k 3.3k 1.1k 1.1k 60 7.0k
Dawn Brasaemle United States 33 5.0k 1.2× 3.0k 0.9× 3.6k 1.1× 1.5k 1.4× 1.0k 0.9× 39 7.4k
Perry E. Bickel United States 27 2.2k 0.5× 2.5k 0.8× 3.1k 1.0× 1.5k 1.4× 690 0.6× 36 5.8k
Martina Schweiger Austria 33 2.6k 0.6× 3.1k 0.9× 2.0k 0.6× 795 0.7× 912 0.8× 53 5.4k
Juliane Gertrude Bogner‐Strauß Austria 29 2.2k 0.5× 2.2k 0.7× 1.9k 0.6× 605 0.5× 788 0.7× 48 4.6k
Jesús Balsinde Spain 59 2.0k 0.5× 1.3k 0.4× 6.1k 1.9× 1.2k 1.1× 1.0k 0.9× 147 9.1k
Rajat Singh United States 37 1.7k 0.4× 2.0k 0.6× 3.4k 1.1× 1.7k 1.5× 898 0.8× 60 9.4k
David Pan Australia 33 708 0.2× 2.9k 0.9× 3.8k 1.2× 927 0.8× 1.6k 1.4× 46 7.2k
Ruth E. Gimeno United States 42 1.1k 0.3× 2.9k 0.9× 3.7k 1.1× 1.2k 1.1× 1.2k 1.1× 48 7.5k
Petra C. Kienesberger Canada 30 1.4k 0.3× 1.5k 0.4× 1.6k 0.5× 554 0.5× 513 0.5× 58 3.4k
Charles Harris United States 29 876 0.2× 1.5k 0.5× 2.3k 0.7× 428 0.4× 433 0.4× 53 5.1k

Countries citing papers authored by Carole Sztalryd

Since Specialization
Citations

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

Fields of papers citing papers by Carole Sztalryd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carole Sztalryd

This figure shows the co-authorship network connecting the top 25 collaborators of Carole Sztalryd. A scholar is included among the top collaborators of Carole Sztalryd 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 Carole Sztalryd. Carole Sztalryd 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.
Mitchell, Braxton D., Kathleen A. Ryan, Carole Sztalryd, et al.. (2018). Increased usual physical activity is associated with a blunting of the triglyceride response to a high-fat meal. Journal of clinical lipidology. 13(1). 109–114. 8 indexed citations
2.
Benador, Ilan Y., Michaela Veliova, Kiana Mahdaviani, et al.. (2018). Mitochondria Bound to Lipid Droplets Have Unique Bioenergetics, Composition, and Dynamics that Support Lipid Droplet Expansion. Cell Metabolism. 27(4). 869–885.e6. 429 indexed citations breakdown →
3.
Kimmel, Alan R. & Carole Sztalryd. (2014). Perilipin 5, a lipid droplet protein adapted to mitochondrial energy utilization. Current Opinion in Lipidology. 25(2). 110–117. 96 indexed citations
4.
Yerges‐Armstrong, Laura M., Richard B. Horenstein, Toni I. Pollin, et al.. (2014). Null Mutation in Hormone-Sensitive Lipase Gene and Risk of Type 2 Diabetes. New England Journal of Medicine. 370(24). 2307–2315. 151 indexed citations
5.
Wang, Hong, Ming Lei, Ru‐ching Hsia, & Carole Sztalryd. (2013). Analysis of Lipid Droplets in Cardiac Muscle. Methods in cell biology. 116. 129–149. 23 indexed citations
6.
Wang, Hong, et al.. (2013). Role of adipose specific lipid droplet proteins in maintaining whole body energy homeostasis. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(3). 393–401. 103 indexed citations
7.
Wang, Hong, Urmila Sreenivasan, Da‐Wei Gong, et al.. (2013). Cardiomyocyte-specific perilipin 5 overexpression leads to myocardial steatosis and modest cardiac dysfunction. Journal of Lipid Research. 54(4). 953–965. 114 indexed citations
8.
Sun, Zheng, Russell Miller, Rajesh T. Patel, et al.. (2012). Hepatic Hdac3 promotes gluconeogenesis by repressing lipid synthesis and sequestration. Nature Medicine. 18(6). 934–942. 273 indexed citations
9.
Wang, Hong, Hong Hu, Jun Liu, et al.. (2011). Unique Regulation of Adipose Triglyceride Lipase (ATGL) by Perilipin 5, a Lipid Droplet-associated Protein. Journal of Biological Chemistry. 286(18). 15707–15715. 232 indexed citations
10.
Wang, Hong, Hong Hu, Andrew J. Saladino, et al.. (2011). Perilipin 5, a lipid droplet-associated protein, provides physical and metabolic linkage to mitochondria. Journal of Lipid Research. 52(12). 2159–2168. 378 indexed citations
11.
Wang, Hong, Liping Hu, Knut Tomas Dalen, et al.. (2009). Activation of Hormone-sensitive Lipase Requires Two Steps, Protein Phosphorylation and Binding to the PAT-1 Domain of Lipid Droplet Coat Proteins. Journal of Biological Chemistry. 284(46). 32116–32125. 139 indexed citations
12.
Kimmel, Alan R., Dawn Brasaemle, Monica McAndrews-Hill, Carole Sztalryd, & Constantine Londos. (2009). Adoption of PERILIPIN as a unifying nomenclature for the mammalian PAT-family of intracellular lipid storage droplet proteins. Journal of Lipid Research. 51(3). 468–471. 364 indexed citations
13.
Beller, Mathias, Carole Sztalryd, Noel Southall, et al.. (2008). COPI Complex Is a Regulator of Lipid Homeostasis. PLoS Biology. 6(11). e292–e292. 285 indexed citations
14.
Dalen, Knut Tomas, Tuva B. Dahl, Elin Holter, et al.. (2006). LSDP5 is a PAT protein specifically expressed in fatty acid oxidizing tissues. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1771(2). 210–227. 199 indexed citations
15.
Prats, Clara, Morten Donsmark, Klaus Qvortrup, et al.. (2006). Decrease in intramuscular lipid droplets and translocation of HSL in response to muscle contraction and epinephrine. Journal of Lipid Research. 47(11). 2392–2399. 83 indexed citations
16.
Londos, Constantine, Carole Sztalryd, John T. Tansey, & Alan R. Kimmel. (2005). Role of PAT proteins in lipid metabolism. Biochimie. 87(1). 45–49. 217 indexed citations
17.
Tansey, John T., Carole Sztalryd, Erica M. Hlavin, Alan R. Kimmel, & Constantine Londos. (2004). The Central Role of Perilipin A in Lipid Metabolism and Adipocyte Lipolysis. IUBMB Life. 56(7). 379–385. 213 indexed citations
18.
Kraemer, Fredric B., et al.. (1994). Low-density lipoprotein receptors in rat adipocytes: regulation with fasting. American Journal of Physiology-Endocrinology and Metabolism. 266(1). E26–E32. 26 indexed citations
19.
Sztalryd, Carole & Fredric B. Kraemer. (1994). Differences in hormone-sensitive lipase expression in white adipose tissue from various anatomic locations of the rat. Metabolism. 43(2). 241–247. 50 indexed citations
20.
Levacher, Christine, et al.. (1988). Hepatic and Adipose Tissue Lipogenesis as Related to Age and Thyroid Status in the Rat. Hormone and Metabolic Research. 20(7). 395–399. 5 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