Manfred Blessing

5.9k total citations · 1 hit paper
47 papers, 4.9k citations indexed

About

Manfred Blessing is a scholar working on Molecular Biology, Immunology and Oncology. According to data from OpenAlex, Manfred Blessing has authored 47 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 18 papers in Immunology and 9 papers in Oncology. Recurrent topics in Manfred Blessing's work include TGF-β signaling in diseases (11 papers), Immune Cell Function and Interaction (8 papers) and T-cell and B-cell Immunology (7 papers). Manfred Blessing is often cited by papers focused on TGF-β signaling in diseases (11 papers), Immune Cell Function and Interaction (8 papers) and T-cell and B-cell Immunology (7 papers). Manfred Blessing collaborates with scholars based in Germany, United States and United Kingdom. Manfred Blessing's co-authors include Peter R. Galle, Markus F. Neurath, Peter Schirmacher, Stefan Wirtz, Christoph Becker, Amrit Mann, Hans A. Lehr, Christoph Schramm, Ansgar W. Lohse and Samuel Huber and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Manfred Blessing

47 papers receiving 4.8k citations

Hit Papers

TGF-β Suppresses Tumor Progression in Colon Cancer by Inh... 2004 2026 2011 2018 2004 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manfred Blessing Germany 35 1.7k 1.6k 990 767 679 47 4.9k
Elena Fattori Italy 30 1.5k 0.9× 1.8k 1.2× 1.1k 1.1× 663 0.9× 869 1.3× 43 4.7k
Giorgio Senaldi United States 37 2.2k 1.3× 1.8k 1.1× 858 0.9× 633 0.8× 247 0.4× 106 5.1k
T Hirano Japan 36 2.9k 1.7× 1.4k 0.9× 1.9k 2.0× 510 0.7× 423 0.6× 117 6.1k
Dianne Grail Australia 25 2.7k 1.5× 1.7k 1.1× 1.6k 1.6× 447 0.6× 448 0.7× 30 5.5k
Chen Varol Israel 24 3.4k 2.0× 1.3k 0.8× 657 0.7× 592 0.8× 353 0.5× 48 5.5k
Yuqiong Liang United States 28 3.7k 2.1× 1.8k 1.1× 899 0.9× 970 1.3× 434 0.6× 36 6.2k
Dagmar Scheel‐Toellner United Kingdom 35 2.5k 1.4× 1.9k 1.2× 1.0k 1.0× 462 0.6× 269 0.4× 63 5.4k
Pierre Graber Switzerland 34 2.2k 1.3× 1.5k 1.0× 532 0.5× 504 0.7× 281 0.4× 87 4.7k
Irina A. Udalova United Kingdom 43 3.9k 2.3× 1.9k 1.2× 864 0.9× 1.0k 1.3× 545 0.8× 93 6.8k
Julie Lekstrom-Himes United States 28 1.6k 0.9× 1.6k 1.0× 438 0.4× 531 0.7× 515 0.8× 51 4.5k

Countries citing papers authored by Manfred Blessing

Since Specialization
Citations

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

Fields of papers citing papers by Manfred Blessing

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manfred Blessing

This figure shows the co-authorship network connecting the top 25 collaborators of Manfred Blessing. A scholar is included among the top collaborators of Manfred Blessing 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 Manfred Blessing. Manfred Blessing 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.
Reifenberg, Kurt, Fei Cheng, Elena Wiese, et al.. (2013). T Cell-Specific Overexpression of TGFß1 Fails to Influence Atherosclerosis in ApoE-Deficient Mice. PLoS ONE. 8(12). e81444–e81444. 6 indexed citations
2.
Schreier, Barbara, Sindy Rabe, Bettina Schneider, et al.. (2011). Aldosterone/NaCl-induced renal and cardiac fibrosis is modulated by TGF-β responsiveness of T cells. Hypertension Research. 34(5). 623–629. 28 indexed citations
3.
Huber, Samuel, Felix R. Stahl, Jörg Schrader, et al.. (2009). Activin A Promotes the TGF-β-Induced Conversion of CD4+CD25− T Cells into Foxp3+ Induced Regulatory T Cells. The Journal of Immunology. 182(8). 4633–4640. 98 indexed citations
4.
Stenzel, Werner, Uwe Müller, Gabriele Köhler, et al.. (2009). IL-4/IL-13-Dependent Alternative Activation of Macrophages but Not Microglial Cells Is Associated with Uncontrolled Cerebral Cryptococcosis. American Journal Of Pathology. 174(2). 486–496. 80 indexed citations
5.
Müller, Uwe, Werner Stenzel, Gabriele Köhler, et al.. (2008). A Gene‐Dosage Effect for Interleukin‐4 Receptor α‐Chain Expression Has an Impact on Th2‐Mediated Allergic Inflammation during Bronchopulmonary Mycosis. The Journal of Infectious Diseases. 198(11). 1714–1721. 29 indexed citations
6.
Müller, Uwe, Werner Stenzel, Gabriele Köhler, et al.. (2007). IL-13 Induces Disease-Promoting Type 2 Cytokines, Alternatively Activated Macrophages and Allergic Inflammation during Pulmonary Infection of Mice with Cryptococcus neoformans. The Journal of Immunology. 179(8). 5367–5377. 220 indexed citations
7.
Klopcic, Borut, T Maass, Erik Meyer, et al.. (2007). TGF-β superfamily signaling is essential for tooth and hair morphogenesis and differentiation. European Journal of Cell Biology. 86(11-12). 781–799. 41 indexed citations
8.
Mann, Amrit, et al.. (2006). Granulocyte–Macrophage Colony-Stimulating Factor Is Essential for Normal Wound Healing. Journal of Investigative Dermatology Symposium Proceedings. 11(1). 87–92. 45 indexed citations
9.
Huber, Samuel, Christoph Schramm, Hans A. Lehr, et al.. (2004). Cutting Edge: TGF-β Signaling Is Required for the In Vivo Expansion and Immunosuppressive Capacity of Regulatory CD4+CD25+ T Cells. The Journal of Immunology. 173(11). 6526–6531. 328 indexed citations
10.
Becker, Christoph, Massimo Claudio Fantini, Christoph Schramm, et al.. (2004). TGF-β Suppresses Tumor Progression in Colon Cancer by Inhibition of IL-6 trans-Signaling. Immunity. 21(4). 491–501. 590 indexed citations breakdown →
11.
Postina, Rolf, Anja Schroeder, Ilse Dewachter, et al.. (2004). A disintegrin-metalloproteinase prevents amyloid plaque formation and hippocampal defects in an Alzheimer disease mouse model. Journal of Clinical Investigation. 113(10). 1456–1464. 499 indexed citations
12.
Becker, Christoph, Stefan Wirtz, Manfred Blessing, et al.. (2003). Constitutive p40 promoter activation and IL-23 production in the terminal ileum mediated by dendritic cells. Journal of Clinical Investigation. 112(5). 693–706. 276 indexed citations
13.
Siebler, Jürgen, Stefan Wirtz, Martina Protschka, et al.. (2003). A Key Pathogenic Role for the Stat1/T–Bet Signaling Pathway in T–Cell-Mediated Liver Inflammation. Hepatology. 38(6). 1573–1580. 61 indexed citations
16.
Schirmacher, Peter, Amrit Mann, Kai Breuhahn, & Manfred Blessing. (2001). Keratinocyte-Derived Granulocyte-Macrophage Colony Stimulating Factor Accelerates Wound Healing: Stimulation of Keratinocyte Proliferation, Granulation Tissue Formation, and Vascularization. Journal of Investigative Dermatology. 117(6). 1382–1390. 141 indexed citations
17.
Kanzler, Stephan, Erik Meyer, Ansgar W. Lohse, et al.. (2001). Hepatocellular expression of a dominant-negative mutant TGF-β type II receptor accelerates chemically induced hepatocarcinogenesis. Oncogene. 20(36). 5015–5024. 55 indexed citations
18.
Wirtz, Stefan, Susetta Finotto, Stephan Kanzler, et al.. (1999). Cutting Edge: Chronic Intestinal Inflammation in STAT-4 Transgenic Mice: Characterization of Disease and Adoptive Transfer by TNF- Plus IFN-γ-Producing CD4+ T Cells That Respond to Bacterial Antigens. The Journal of Immunology. 162(4). 1884–1888. 107 indexed citations
19.
Schirmacher, Peter, et al.. (1998). Induction of Bone Morphogenetic Protein-6 in Skin Wounds. Delayed Reepitheliazation and Scar Formation in BMP-6 Overexpressing Transgenic Mice. Journal of Investigative Dermatology. 111(6). 1145–1152. 51 indexed citations
20.
Blessing, Manfred, Lillian B. Nanney, Lloyd E. King, & Brigid L.M. Hogan. (1995). Chemical skin carcinogenesis is prevented in mice by the induced expression of a TGF‐β related transgene. Teratogenesis Carcinogenesis and Mutagenesis. 15(1). 11–21. 33 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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