Heinrich Jasper

12.0k total citations · 2 hit papers
84 papers, 7.7k citations indexed

About

Heinrich Jasper is a scholar working on Immunology, Molecular Biology and Aging. According to data from OpenAlex, Heinrich Jasper has authored 84 papers receiving a total of 7.7k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Immunology, 40 papers in Molecular Biology and 37 papers in Aging. Recurrent topics in Heinrich Jasper's work include Invertebrate Immune Response Mechanisms (42 papers), Genetics, Aging, and Longevity in Model Organisms (37 papers) and Neurobiology and Insect Physiology Research (29 papers). Heinrich Jasper is often cited by papers focused on Invertebrate Immune Response Mechanisms (42 papers), Genetics, Aging, and Longevity in Model Organisms (37 papers) and Neurobiology and Insect Physiology Research (29 papers). Heinrich Jasper collaborates with scholars based in United States, Germany and France. Heinrich Jasper's co-authors include Benoît Biteau, Dirk Bohmann, Jason Karpac, Meng C. Wang, Hongjie Li, Yanyan Qi, Joana Neves, Bruno Lemaître, Irene Miguel‐Aliaga and Pedro Sousa‐Victor and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Heinrich Jasper

82 papers receiving 7.7k citations

Hit Papers

Anatomy and Physiology of... 2018 2026 2020 2023 2018 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
Heinrich Jasper United States 48 3.7k 2.7k 2.0k 1.9k 1.3k 84 7.7k
Hugo Stocker Switzerland 30 4.3k 1.2× 1.1k 0.4× 2.4k 1.2× 1.9k 1.0× 666 0.5× 83 7.7k
Rolf Bodmer United States 55 5.6k 1.5× 971 0.4× 2.9k 1.5× 1.7k 0.9× 520 0.4× 161 9.1k
Dirk Bohmann United States 49 7.7k 2.1× 1.8k 0.6× 1.4k 0.7× 1.0k 0.5× 381 0.3× 84 10.6k
Thomas P. Neufeld United States 43 6.1k 1.7× 1.1k 0.4× 1.4k 0.7× 700 0.4× 364 0.3× 66 10.9k
Ronald Ellis United States 29 3.5k 1.0× 862 0.3× 468 0.2× 2.1k 1.1× 176 0.1× 49 6.1k
Shohei Mitani Japan 49 4.9k 1.3× 547 0.2× 714 0.4× 3.1k 1.6× 95 0.1× 160 7.7k
Douglas R. Cavener United States 49 5.6k 1.5× 1.3k 0.5× 1.1k 0.5× 207 0.1× 378 0.3× 111 10.5k
Jin Jiang United States 52 9.1k 2.5× 1.4k 0.5× 1.1k 0.6× 241 0.1× 386 0.3× 127 11.8k
Gábor Juhász Hungary 37 2.5k 0.7× 701 0.3× 546 0.3× 369 0.2× 314 0.2× 107 6.1k
Richard A. Lockshin United States 38 3.4k 0.9× 832 0.3× 791 0.4× 150 0.1× 421 0.3× 91 5.8k

Countries citing papers authored by Heinrich Jasper

Since Specialization
Citations

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

Fields of papers citing papers by Heinrich Jasper

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heinrich Jasper

This figure shows the co-authorship network connecting the top 25 collaborators of Heinrich Jasper. A scholar is included among the top collaborators of Heinrich Jasper 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 Heinrich Jasper. Heinrich Jasper 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.
Yun, Jina, Simon Hansen, Otto Morris, et al.. (2023). Senescent cells perturb intestinal stem cell differentiation through Ptk7 induced noncanonical Wnt and YAP signaling. Nature Communications. 14(1). 156–156. 41 indexed citations
2.
Katheder, Nadja Sandra, Diana Chang, Ann De Mazière, et al.. (2023). Nicotinic acetylcholine receptor signaling maintains epithelial barrier integrity. eLife. 12. 5 indexed citations
3.
Rodriguez‐Fernandez, Imilce A., Jason A. Hackney, Michał Pawlak, et al.. (2021). Age-related changes in polycomb gene regulation disrupt lineage fidelity in intestinal stem cells. eLife. 10. 30 indexed citations
4.
Kramer, Joshua, et al.. (2021). Dpp/TGFβ-superfamily play a dual conserved role in mediating the damage response in the retina. PLoS ONE. 16(10). e0258872–e0258872.
5.
Neves, Joana, Kathleen R. Chirco, Shereen Chew, et al.. (2020). MANF delivery improves retinal homeostasis and cell replacement therapies in ageing mice. Experimental Gerontology. 134. 110893–110893. 12 indexed citations
6.
Sousa‐Victor, Pedro, Joana Neves, Patrick Ventura, et al.. (2019). MANF regulates metabolic and immune homeostasis in ageing and protects against liver damage. Nature Metabolism. 1(2). 276–290. 97 indexed citations
7.
Akagi, Kazutaka, Kenneth A. Wilson, Subhash D. Katewa, et al.. (2018). Dietary restriction improves intestinal cellular fitness to enhance gut barrier function and lifespan in D. melanogaster. PLoS Genetics. 14(11). e1007777–e1007777. 46 indexed citations
8.
Neves, Joana, Pedro Sousa‐Victor, & Heinrich Jasper. (2017). Rejuvenating Strategies for Stem Cell-Based Therapies in Aging. Cell stem cell. 20(2). 161–175. 119 indexed citations
9.
Jasper, Heinrich, et al.. (2017). Tis11 mediated mRNA decay promotes the reacquisition of Drosophila intestinal stem cell quiescence. Developmental Biology. 426(1). 8–16. 11 indexed citations
10.
Ayyaz, Arshad, Hongjie Li, & Heinrich Jasper. (2015). Haemocytes control stem cell activity in the Drosophila intestine. Nature Cell Biology. 17(6). 736–748. 109 indexed citations
11.
Jasper, Heinrich. (2014). Exploring the physiology and pathology of aging in the intestine ofDrosophila melanogaster. Invertebrate Reproduction & Development. 59(sup1). 51–58. 27 indexed citations
12.
Wang, Lifen, Jason Karpac, & Heinrich Jasper. (2013). Promoting longevity by maintaining metabolic and proliferative homeostasis. Journal of Experimental Biology. 217(1). 109–118. 67 indexed citations
13.
Li, Hongjie, Yanyan Qi, & Heinrich Jasper. (2013). Dpp Signaling Determines Regional Stem Cell Identity in the Regenerating Adult Drosophila Gastrointestinal Tract. Cell Reports. 4(1). 10–18. 60 indexed citations
14.
Ayyaz, Arshad & Heinrich Jasper. (2013). Intestinal inflammation and stem cell homeostasis in aging Drosophila melanogaster. Frontiers in Cellular and Infection Microbiology. 3. 98–98. 65 indexed citations
15.
Luo, Xi, et al.. (2012). Schnurri regulates hemocyte function to promote tissue recovery after DNA damage. Journal of Cell Science. 125(Pt 6). 1393–400. 21 indexed citations
16.
Biteau, Benoît & Heinrich Jasper. (2011). EGF signaling regulates the proliferation of intestinal stem cells in Drosophila. Development. 138(6). 1045–1055. 228 indexed citations
17.
Biteau, Benoît, et al.. (2010). Lifespan Extension by Preserving Proliferative Homeostasis in Drosophila. PLoS Genetics. 6(10). e1001159–e1001159. 278 indexed citations
18.
Luo, Xi, et al.. (2006). Foxo and Fos regulate the decision between cell death and survival in response to UV irradiation. The EMBO Journal. 26(2). 380–390. 111 indexed citations
19.
Etter, Paul D., Radhakrishnan Narayanan, Zaneta Navratilova, et al.. (2005). Synaptic and genomic responses to JNK and AP-1 signaling in Drosophilaneurons. 1 indexed citations
20.
Jasper, Heinrich & Dirk Bohmann. (2002). Drosophila Innate Immunity. Molecular Cell. 10(5). 967–969. 6 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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