Thomas E. Willnow

20.4k total citations · 3 hit papers
179 papers, 14.7k citations indexed

About

Thomas E. Willnow is a scholar working on Molecular Biology, Physiology and Cell Biology. According to data from OpenAlex, Thomas E. Willnow has authored 179 papers receiving a total of 14.7k indexed citations (citations by other indexed papers that have themselves been cited), including 105 papers in Molecular Biology, 45 papers in Physiology and 33 papers in Cell Biology. Recurrent topics in Thomas E. Willnow's work include Alzheimer's disease research and treatments (35 papers), Cellular transport and secretion (19 papers) and Renal and related cancers (14 papers). Thomas E. Willnow is often cited by papers focused on Alzheimer's disease research and treatments (35 papers), Cellular transport and secretion (19 papers) and Renal and related cancers (14 papers). Thomas E. Willnow collaborates with scholars based in Germany, Denmark and United States. Thomas E. Willnow's co-authors include Anders Nykjær, Joachim Herz, Christian Jacobsen, Joachim Herz, Erik Christensen, Olav M. Andersen, Robert E. Hammer, Søren K. Moestrup, Henrik Vorum and Jan Hilpert and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Thomas E. Willnow

175 papers receiving 14.5k citations

Hit Papers

An Endocytic Pathway Essential for Renal Uptake and Activ... 1999 2026 2008 2017 1999 2004 2005 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas E. Willnow Germany 69 6.8k 3.2k 2.7k 2.4k 1.5k 179 14.7k
Anders Nykjær Denmark 56 5.3k 0.8× 2.7k 0.8× 2.3k 0.8× 3.4k 1.4× 1.0k 0.7× 134 12.7k
Ken Inoki United States 56 12.9k 1.9× 3.0k 0.9× 2.4k 0.9× 764 0.3× 1.9k 1.2× 92 17.9k
Masato Koike Japan 61 6.6k 1.0× 3.0k 0.9× 2.7k 1.0× 1.6k 0.7× 1.5k 1.0× 215 16.4k
Allen M. Spiegel United States 79 10.0k 1.5× 1.6k 0.5× 2.1k 0.8× 2.7k 1.1× 2.1k 1.4× 294 19.0k
Kevin R. Lynch United States 71 10.7k 1.6× 2.5k 0.8× 2.2k 0.8× 2.2k 0.9× 1.0k 0.7× 202 16.0k
Gary E. Shull United States 78 13.4k 2.0× 1.7k 0.5× 1.5k 0.5× 2.3k 0.9× 2.6k 1.7× 213 17.6k
Michael Leitges United States 66 7.2k 1.1× 1.3k 0.4× 1.3k 0.5× 1.1k 0.5× 1.2k 0.8× 237 12.7k
Markus A. Rüegg Switzerland 70 10.0k 1.5× 2.4k 0.8× 2.8k 1.0× 3.4k 1.4× 1.0k 0.7× 184 14.8k
Thomas Meitinger Germany 69 11.2k 1.6× 1.3k 0.4× 1.1k 0.4× 1.7k 0.7× 1.2k 0.8× 319 19.1k
Tomoichiro Asano Japan 69 10.3k 1.5× 2.9k 0.9× 2.4k 0.9× 827 0.3× 4.1k 2.7× 313 17.8k

Countries citing papers authored by Thomas E. Willnow

Since Specialization
Citations

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

Fields of papers citing papers by Thomas E. Willnow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas E. Willnow. 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 Thomas E. Willnow. The network helps show where Thomas E. Willnow may publish in the future.

Co-authorship network of co-authors of Thomas E. Willnow

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas E. Willnow. A scholar is included among the top collaborators of Thomas E. Willnow 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 Thomas E. Willnow. Thomas E. Willnow 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.
Schmidt, Vanessa, Ewa Żurawska-Płaksej, Johan Palmfeldt, et al.. (2025). Astrocytes distress triggers brain pathology through induction of δ secretase in a murine model of Alzheimer’s disease. Nature Communications. 16(1). 9653–9653.
2.
Juul‐Madsen, Kristian, Narasimha Swamy Telugu, Fabia Febbraro, et al.. (2025). Familial Alzheimer's disease mutation identifies novel role of SORLA in release of neurotrophic exosomes. Alzheimer s & Dementia. 21(9). e70591–e70591.
3.
Bolduan, Felix, Natália Alenina, Michael Bäder, et al.. (2024). Elevated sortilin expression discriminates functional from non-functional neuroendocrine tumors and enables therapeutic targeting. Frontiers in Endocrinology. 15. 1331231–1331231.
4.
Margineanu, Anca, Camille Boutin, Mireille Montcouquiol, et al.. (2023). LRP2 contributes to planar cell polarity-dependent coordination of motile cilia function. Cell and Tissue Research. 392(2). 535–551. 2 indexed citations
5.
Bakun, Magdalena, Tymon Rubel, Michał Dadlez, et al.. (2021). ApoE4 disrupts interaction of sortilin with fatty acid-binding protein 7 essential to promote lipid signaling. Journal of Cell Science. 134(20). 20 indexed citations
6.
7.
Christ, Annabel, et al.. (2020). LRP2 controls sonic hedgehog-dependent differentiation of cardiac progenitor cells during outflow tract formation. Human Molecular Genetics. 29(19). 3183–3196. 13 indexed citations
8.
Huang, Anfei, Prashant V. Shinde, Jun Huang, et al.. (2019). Progranulin prevents regulatory NK cell cytotoxicity against antiviral T cells. JCI Insight. 4(17). 9 indexed citations
9.
Thelen, Melanie, Kerstin Cornils, Michaela Schweizer, et al.. (2015). Lrp1/ LDL Receptor Play Critical Roles in Mannose 6‐Phosphate‐Independent Lysosomal Enzyme Targeting. Traffic. 16(7). 743–759. 51 indexed citations
10.
Schmidt, Vanessa & Thomas E. Willnow. (2015). Protein sorting gone wrong – VPS10P domain receptors in cardiovascular and metabolic diseases. Atherosclerosis. 245. 194–199. 32 indexed citations
11.
Hartl, Daniela, Stephan Klatt, Zoltán Konthur, et al.. (2013). Soluble Alpha-APP (sAPPalpha) Regulates CDK5 Expression and Activity in Neurons. PLoS ONE. 8(6). e65920–e65920. 30 indexed citations
12.
Breiderhoff, Tilman, Nina Himmerkus, Marchel Stuiver, et al.. (2012). Deletion of claudin-10 ( Cldn10 ) in the thick ascending limb impairs paracellular sodium permeability and leads to hypermagnesemia and nephrocalcinosis. Proceedings of the National Academy of Sciences. 109(35). 14241–14246. 121 indexed citations
13.
Christ, Annabel, Esther Kur, Oleg Lioubinski, et al.. (2012). LRP2 Is an Auxiliary SHH Receptor Required to Condition the Forebrain Ventral Midline for Inductive Signals. Developmental Cell. 22(2). 268–278. 86 indexed citations
14.
Rohe, Michael, Anne-Sophie Carlo, Henning Breyhan, et al.. (2008). Sortilin-related Receptor with A-type Repeats (SORLA) Affects the Amyloid Precursor Protein-dependent Stimulation of ERK Signaling and Adult Neurogenesis. Journal of Biological Chemistry. 283(21). 14826–14834. 84 indexed citations
15.
Jansen, Pernille, Klaus M. Giehl, Jens Randel Nyengaard, et al.. (2007). Roles for the pro-neurotrophin receptor sortilin in neuronal development, aging and brain injury. Nature Neuroscience. 10(11). 1449–1457. 230 indexed citations
16.
Hammes, Annette, Thomas K. Andreassen, Robert Spoelgen, et al.. (2005). Role of Endocytosis in Cellular Uptake of Sex Steroids. Cell. 122(5). 751–762. 299 indexed citations
17.
Willnow, Thomas E., Anders Nykjær, & Claus Munck Petersen. (2005). p75 NTR ¿ live or let die. Current Opinion in Neurobiology. 49–57. 15 indexed citations
18.
Lisi, Simonetta, Aldo Pinchera, Robert T. McCluskey, et al.. (2003). Preferential megalin-mediated transcytosis of low-hormonogenic thyroglobulin: A control mechanism for thyroid hormone release. Proceedings of the National Academy of Sciences. 100(25). 14858–14863. 44 indexed citations
19.
Sinnis, Photini, Thomas E. Willnow, Marcelo R. S. Briones, Joachim Herz, & Victor Nussenzweig. (1996). Remnant lipoproteins inhibit malaria sporozoite invasion of hepatocytes.. The Journal of Experimental Medicine. 184(3). 945–954. 83 indexed citations
20.
Willnow, Thomas E. & Joachim Herz. (1995). Animal models for disorders of hepatic lipoprotein metabolism. Journal of Molecular Medicine. 73(5). 213–20. 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.

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