Supawadee Sukseree

6.6k total citations
23 papers, 440 citations indexed

About

Supawadee Sukseree is a scholar working on Molecular Biology, Epidemiology and Cell Biology. According to data from OpenAlex, Supawadee Sukseree has authored 23 papers receiving a total of 440 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Epidemiology and 10 papers in Cell Biology. Recurrent topics in Supawadee Sukseree's work include Autophagy in Disease and Therapy (10 papers), Skin and Cellular Biology Research (7 papers) and Plant Reproductive Biology (3 papers). Supawadee Sukseree is often cited by papers focused on Autophagy in Disease and Therapy (10 papers), Skin and Cellular Biology Research (7 papers) and Plant Reproductive Biology (3 papers). Supawadee Sukseree collaborates with scholars based in Austria, Thailand and United States. Supawadee Sukseree's co-authors include Leopold Eckhart, Erwin Tschachler, Heidemarie Rossiter, Ramida Watanapokasin, Veronika Mlitz, Флориан Грубер, Maria Buchberger, Lorenzo Alibardi, Johannes Pammer and Michael Mildner and has published in prestigious journals such as PLoS ONE, Scientific Reports and Biochemical and Biophysical Research Communications.

In The Last Decade

Supawadee Sukseree

22 papers receiving 433 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Supawadee Sukseree Austria 14 198 166 144 58 56 23 440
Ruth Pofahl Germany 9 176 0.9× 112 0.7× 29 0.2× 67 1.2× 21 0.4× 10 435
Lamia Azzi‐Martin France 13 284 1.4× 48 0.3× 52 0.4× 61 1.1× 141 2.5× 24 632
Hai‐Ying Jin China 14 351 1.8× 120 0.7× 26 0.2× 55 0.9× 18 0.3× 33 582
C.M.L.J. Tilli Netherlands 6 231 1.2× 104 0.6× 92 0.6× 157 2.7× 58 1.0× 6 456
Michelle L. Kerns United States 11 426 2.2× 367 2.2× 129 0.9× 265 4.6× 39 0.7× 21 853
Minhee Kim South Korea 12 356 1.8× 242 1.5× 38 0.3× 38 0.7× 32 0.6× 27 537
Vladimir U. Emelianov Russia 10 183 0.9× 91 0.5× 48 0.3× 205 3.5× 13 0.2× 22 577
Rossana Tiberio Italy 9 115 0.6× 52 0.3× 49 0.3× 58 1.0× 8 0.1× 16 313
Pierre Carraux Switzerland 16 242 1.2× 239 1.4× 62 0.4× 471 8.1× 35 0.6× 29 801
Constantinos Vouthounis United States 6 221 1.1× 100 0.6× 31 0.2× 183 3.2× 16 0.3× 8 675

Countries citing papers authored by Supawadee Sukseree

Since Specialization
Citations

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

Fields of papers citing papers by Supawadee Sukseree

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Supawadee Sukseree

This figure shows the co-authorship network connecting the top 25 collaborators of Supawadee Sukseree. A scholar is included among the top collaborators of Supawadee Sukseree 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 Supawadee Sukseree. Supawadee Sukseree 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.
Eckhart, Leopold, Флориан Грубер, & Supawadee Sukseree. (2024). Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages. Cells. 13(20). 1675–1675. 3 indexed citations
2.
Sukseree, Supawadee, et al.. (2023). Iron Metabolism of the Skin: Recycling versus Release. Metabolites. 13(9). 1005–1005. 8 indexed citations
3.
Sukseree, Supawadee, Dragan Copic, Bahar Golabi, et al.. (2023). Heme Oxygenase-1 Is Upregulated during Differentiation of Keratinocytes but Its Expression Is Dispensable for Cornification of Murine Epidermis. Journal of Developmental Biology. 11(1). 12–12. 4 indexed citations
4.
Barresi, Caterina, Heidemarie Rossiter, Maria Buchberger, et al.. (2022). Inactivation of Autophagy in Keratinocytes Reduces Tumor Growth in Mouse Models of Epithelial Skin Cancer. Cells. 11(22). 3691–3691. 5 indexed citations
5.
Sukseree, Supawadee, Latifa Bakiri, Marta Palomo-Irigoyen, et al.. (2021). Sequestosome 1/p62 enhances chronic skin inflammation. Journal of Allergy and Clinical Immunology. 147(6). 2386–2393.e4. 17 indexed citations
6.
Rossiter, Heidemarie, Dragan Copic, Martin Direder, et al.. (2021). Autophagy protects murine preputial glands against premature aging, and controls their sebum phospholipid and pheromone profile. Autophagy. 18(5). 1005–1019. 7 indexed citations
7.
Jaeger, Karin, Supawadee Sukseree, Veronika Mlitz, et al.. (2018). 1344 Keratinocyte cornification requires autophagy for efficient degradation of non-cytoskeletal proteins. Journal of Investigative Dermatology. 138(5). S228–S228. 1 indexed citations
8.
Strasser, Bettina, Supawadee Sukseree, Wolfgang Sipos, et al.. (2018). Comparative Analysis of Epidermal Differentiation Genes of Crocodilians Suggests New Models for the Evolutionary Origin of Avian Feather Proteins. Genome Biology and Evolution. 10(2). 694–704. 28 indexed citations
9.
Jaeger, Karin, Supawadee Sukseree, Brett S. Phinney, et al.. (2018). Cornification of nail keratinocytes requires autophagy for bulk degradation of intracellular proteins while sparing components of the cytoskeleton. APOPTOSIS. 24(1-2). 62–73. 19 indexed citations
10.
Sukseree, Supawadee, Lajos László, Флориан Грубер, et al.. (2018). Filamentous Aggregation of Sequestosome-1/p62 in Brain Neurons and Neuroepithelial Cells upon Tyr-Cre-Mediated Deletion of the Autophagy Gene Atg7. Molecular Neurobiology. 55(11). 8425–8437. 11 indexed citations
11.
Rossiter, Heidemarie, Gerald Stübiger, Marion Gröger, et al.. (2018). Inactivation of autophagy leads to changes in sebaceous gland morphology and function. Experimental Dermatology. 27(10). 1142–1151. 20 indexed citations
12.
Fischer, Heinz, Joan Climent, Eduard Casas, et al.. (2017). Double deficiency of Trex2 and DNase1L2 nucleases leads to accumulation of DNA in lingual cornifying keratinocytes without activating inflammatory responses. Scientific Reports. 7(1). 11902–11902. 14 indexed citations
13.
Sukseree, Supawadee, Ying‐Ting Chen, Maria Laggner, et al.. (2016). Tyrosinase-Cre-Mediated Deletion of the Autophagy Gene Atg7 Leads to Accumulation of the RPE65 Variant M450 in the Retinal Pigment Epithelium of C57BL/6 Mice. PLoS ONE. 11(8). e0161640–e0161640. 13 indexed citations
14.
15.
Strasser, Bettina, Wolfgang Sipos, Heiko A. Schmidt, et al.. (2015). Comparative Genomics Identifies Epidermal Proteins Associated with the Evolution of the Turtle Shell. Molecular Biology and Evolution. 33(3). 726–737. 47 indexed citations
16.
Rossiter, Heidemarie, Ulrich König, Caterina Barresi, et al.. (2013). Epidermal keratinocytes form a functional skin barrier in the absence of Atg7 dependent autophagy. Journal of Dermatological Science. 71(1). 67–75. 53 indexed citations
17.
Sukseree, Supawadee, Heidemarie Rossiter, Michael Mildner, et al.. (2012). Targeted deletion of Atg5 reveals differential roles of autophagy in keratin K5-expressing epithelia. Biochemical and Biophysical Research Communications. 430(2). 689–694. 39 indexed citations
18.
Sukseree, Supawadee, Michael Mildner, Heidemarie Rossiter, et al.. (2012). Autophagy in the Thymic Epithelium Is Dispensable for the Development of Self-Tolerance in a Novel Mouse Model. PLoS ONE. 7(6). e38933–e38933. 41 indexed citations
19.
Watanapokasin, Ramida, Sunit Suksamrarn, Yukio Nakamura, et al.. (2010). Potential of Xanthones from Tropical Fruit Mangosteen as Anti-cancer Agents: Caspase-Dependent Apoptosis Induction In Vitro and in Mice. Applied Biochemistry and Biotechnology. 162(4). 1080–1094. 40 indexed citations
20.

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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