Alexander Jaïs

3.6k total citations · 3 hit papers
23 papers, 1.7k citations indexed

About

Alexander Jaïs is a scholar working on Endocrine and Autonomic Systems, Molecular Biology and Physiology. According to data from OpenAlex, Alexander Jaïs has authored 23 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Endocrine and Autonomic Systems, 8 papers in Molecular Biology and 7 papers in Physiology. Recurrent topics in Alexander Jaïs's work include Regulation of Appetite and Obesity (8 papers), Neurobiology and Insect Physiology Research (5 papers) and Adipose Tissue and Metabolism (5 papers). Alexander Jaïs is often cited by papers focused on Regulation of Appetite and Obesity (8 papers), Neurobiology and Insect Physiology Research (5 papers) and Adipose Tissue and Metabolism (5 papers). Alexander Jaïs collaborates with scholars based in Germany, Austria and United Kingdom. Alexander Jaïs's co-authors include Jens C. Brüning, Motoharu Awazawa, Sarah M. Turpin-Nolan, Philipp Hammerschmidt, Harald Esterbauer, Catarina C. F. Homem, Victoria Steinmann, Juergen A. Knoblich, Thomas R. Burkard and Thomas Langer and has published in prestigious journals such as Cell, Journal of Clinical Investigation and Endocrine Reviews.

In The Last Decade

Alexander Jaïs

21 papers receiving 1.7k citations

Hit Papers

Hypothalamic inflammation in obesity and metabolic disease 2017 2026 2020 2023 2017 2021 2021 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexander Jaïs Germany 15 724 523 410 253 180 23 1.7k
Juxue Li China 17 559 0.8× 444 0.8× 453 1.1× 152 0.6× 149 0.8× 36 1.7k
Yizhe Tang United States 12 625 0.9× 428 0.8× 371 0.9× 168 0.7× 122 0.7× 23 1.5k
Akiko Satoh United States 14 762 1.1× 1.1k 2.1× 296 0.7× 687 2.7× 210 1.2× 21 2.9k
Bengt‐Frederik Belgardt Germany 15 976 1.3× 735 1.4× 871 2.1× 494 2.0× 199 1.1× 28 2.4k
Jonathan M. Beckel United States 22 633 0.9× 312 0.6× 385 0.9× 282 1.1× 208 1.2× 65 2.0k
Bénédicte Dehouck France 17 560 0.8× 624 1.2× 1.1k 2.8× 180 0.7× 267 1.5× 23 2.5k
Aijun Hao China 26 824 1.1× 304 0.6× 325 0.8× 186 0.7× 310 1.7× 60 2.4k
Anton B. Tonchev Bulgaria 27 881 1.2× 375 0.7× 182 0.4× 326 1.3× 642 3.6× 97 2.3k
Ryoichi Banno Japan 18 312 0.4× 298 0.6× 392 1.0× 174 0.7× 74 0.4× 66 1.0k
Manuel Ros Spain 31 1.2k 1.6× 946 1.8× 583 1.4× 581 2.3× 328 1.8× 77 2.7k

Countries citing papers authored by Alexander Jaïs

Since Specialization
Citations

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

Fields of papers citing papers by Alexander Jaïs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander Jaïs

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander Jaïs. A scholar is included among the top collaborators of Alexander Jaïs 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 Alexander Jaïs. Alexander Jaïs 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.
Hoffmann, Anne, Adhideb Ghosh, Christian Wolfrum, et al.. (2025). B cell-derived nociceptin/orphanin FQ contributes to impaired glucose tolerance and insulin resistance in obesity. iScience. 28(7). 112819–112819.
2.
Backes, Heiko, Anna Lena Cremer, Paul Klemm, et al.. (2025). Reduced Notch signaling in hypothalamic endothelial cells mediates obesity-induced alterations in glucose uptake and insulin signaling. Cell Reports. 44(4). 115522–115522.
3.
Sotelo-Hitschfeld, Tamara, Paul Klemm, Alexander Jaïs, et al.. (2024). GABAergic disinhibition from the BNST to PNOCARC neurons promotes HFD-induced hyperphagia. Cell Reports. 43(6). 114343–114343. 6 indexed citations
4.
Jaïs, Alexander, et al.. (2022). Reciprocal signaling between adipose tissue depots and the central nervous system. Frontiers in Cell and Developmental Biology. 10. 979251–979251. 7 indexed citations
5.
Willenborg, Sebastian, David E. Sanin, Alexander Jaïs, et al.. (2021). Mitochondrial metabolism coordinates stage-specific repair processes in macrophages during wound healing. Cell Metabolism. 33(12). 2398–2414.e9. 183 indexed citations breakdown →
6.
Cremer, Anna Lena, Paul Klemm, Lukas Steuernagel, et al.. (2021). Insulin signalling in tanycytes gates hypothalamic insulin uptake and regulation of AgRP neuron activity. Nature Metabolism. 3(12). 1662–1679. 59 indexed citations
7.
Jaïs, Alexander & Jens C. Brüning. (2021). Arcuate Nucleus-Dependent Regulation of Metabolism—Pathways to Obesity and Diabetes Mellitus. Endocrine Reviews. 43(2). 314–328. 148 indexed citations breakdown →
8.
Ding, Xiaolei, Sebastian Willenborg, Wilhelm Bloch, et al.. (2019). Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation. Journal of Allergy and Clinical Immunology. 145(1). 283–300.e8. 28 indexed citations
9.
Hammerschmidt, Philipp, Hendrik Nolte, Mathias J. Gerl, et al.. (2019). CerS6-Derived Sphingolipids Interact with Mff and Promote Mitochondrial Fragmentation in Obesity. Cell. 177(6). 1536–1552.e23. 216 indexed citations
10.
Turpin-Nolan, Sarah M., Philipp Hammerschmidt, Weiyi Chen, et al.. (2019). CerS1-Derived C18:0 Ceramide in Skeletal Muscle Promotes Obesity-Induced Insulin Resistance. Cell Reports. 26(1). 1–10.e7. 138 indexed citations
11.
Schüler, Rita, Martin Osterhoff, A. Veronica Witte, et al.. (2018). VEGF and GLUT1 are highly heritable, inversely correlated and affected by dietary fat intake: Consequences for cognitive function in humans. Molecular Metabolism. 11. 129–136. 42 indexed citations
12.
Timper, Katharina, Lars Paeger, Luis Varela, et al.. (2018). Mild Impairment of Mitochondrial OXPHOS Promotes Fatty Acid Utilization in POMC Neurons and Improves Glucose Homeostasis in Obesity. Cell Reports. 25(2). 383–397.e10. 27 indexed citations
13.
Jaïs, Alexander & Jens C. Brüning. (2017). Hypothalamic inflammation in obesity and metabolic disease. Journal of Clinical Investigation. 127(1). 24–32. 344 indexed citations breakdown →
14.
Jaïs, Alexander, Maite Solas, Heiko Backes, et al.. (2016). Myeloid-Cell-Derived VEGF Maintains Brain Glucose Uptake and Limits Cognitive Impairment in Obesity. Cell. 165(4). 882–895. 198 indexed citations
15.
Homem, Catarina C. F., Victoria Steinmann, Thomas R. Burkard, et al.. (2014). Ecdysone and Mediator Change Energy Metabolism to Terminate Proliferation in Drosophila Neural Stem Cells. Cell. 158(4). 874–888. 168 indexed citations
16.
Todoric, Jelena, Birgit Strobl, Alexander Jaïs, et al.. (2011). Cross-Talk Between Interferon-γ and Hedgehog Signaling Regulates Adipogenesis. Diabetes. 60(6). 1668–1676. 36 indexed citations
17.
Tauber, Stefanie, Alexander Jaïs, Sandra Haider, et al.. (2010). Transcriptome analysis of human cancer reveals a functional role of Heme Oxygenase-1 in tumor cell adhesion. Molecular Cancer. 9(1). 200–200. 46 indexed citations
18.
Jaïs, Alexander, Dieter Klein, Birgitt Wolfesberger, & Ingrid Walter. (2010). Gene expression profile of vascular endothelial growth factor (VEGF) and its receptors in various cell types of the canine lymph node using laser capture microdissection (LCM). Veterinary Immunology and Immunopathology. 140(3-4). 207–214. 11 indexed citations
19.
Jaïs, Alexander, G.A. Kerkut, & Robert Walker. (1984). The ionic mechanisms associated with the excitatory response of kainate, l-glutamate, quisqualate, ibotenate, AMPA and methyltetrahydrofolate on leech retzius cells. Comparative Biochemistry and Physiology Part C Comparative Pharmacology. 77(1). 115–126. 23 indexed citations
20.
Jaïs, Alexander, G.A. Kerkut, & R.J. Walker. (1983). The ionic mechanism associated with the biphasic glutamate response on leech retzius cells. Comparative Biochemistry and Physiology Part C Comparative Pharmacology. 74(2). 425–432. 18 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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