Winfried Edelmann

15.5k total citations · 1 hit paper
140 papers, 11.3k citations indexed

About

Winfried Edelmann is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Cancer Research. According to data from OpenAlex, Winfried Edelmann has authored 140 papers receiving a total of 11.3k indexed citations (citations by other indexed papers that have themselves been cited), including 95 papers in Molecular Biology, 76 papers in Pathology and Forensic Medicine and 40 papers in Cancer Research. Recurrent topics in Winfried Edelmann's work include Genetic factors in colorectal cancer (74 papers), DNA Repair Mechanisms (53 papers) and Cancer Genomics and Diagnostics (27 papers). Winfried Edelmann is often cited by papers focused on Genetic factors in colorectal cancer (74 papers), DNA Repair Mechanisms (53 papers) and Cancer Genomics and Diagnostics (27 papers). Winfried Edelmann collaborates with scholars based in United States, Germany and Canada. Winfried Edelmann's co-authors include Raju Kucherlapati, Burkhard Kneitz, Kan Yang, Harry Hou, Uwe Werling, Martin Lipkin, Matthew D. Scharff, Yongwei Zhang, Xiao Lan Zhang and Michael P. Lisanti and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Winfried Edelmann

140 papers receiving 11.1k citations

Hit Papers

Caveolin-1 Null Mice Are ... 2001 2026 2009 2017 2001 250 500 750

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Winfried Edelmann 7.9k 2.8k 2.0k 1.9k 1.9k 140 11.3k
Vladimír Kořínek 10.4k 1.3× 1.6k 0.6× 2.6k 1.3× 1.2k 0.6× 1.7k 0.9× 72 12.8k
Hein te Riele 6.0k 0.8× 1.6k 0.6× 2.3k 1.1× 550 0.3× 1.5k 0.8× 108 8.2k
Elena Sancho 6.7k 0.9× 1.1k 0.4× 4.7k 2.3× 1.2k 0.6× 1.5k 0.8× 28 10.3k
Dos D. Sarbassov 12.8k 1.6× 1.0k 0.4× 1.8k 0.9× 1.9k 1.0× 810 0.4× 53 16.1k
Karen C. Arden 11.6k 1.5× 999 0.4× 2.1k 1.0× 1.0k 0.5× 1.3k 0.7× 77 15.0k
Piotr Siciński 10.2k 1.3× 831 0.3× 6.6k 3.3× 2.5k 1.3× 1.5k 0.8× 106 15.6k
Pierre Dubus 5.3k 0.7× 1.1k 0.4× 4.0k 2.0× 1.7k 0.9× 637 0.3× 163 9.7k
Bart O. Williams 11.2k 1.4× 743 0.3× 5.6k 2.8× 1.5k 0.8× 2.3k 1.2× 148 15.5k
Robert H. Costa 10.1k 1.3× 1.0k 0.4× 1.8k 0.9× 1.2k 0.6× 2.5k 1.3× 132 13.5k
Anthony E. Oro 7.5k 0.9× 811 0.3× 2.1k 1.1× 979 0.5× 3.3k 1.8× 100 11.4k

Countries citing papers authored by Winfried Edelmann

Since Specialization
Citations

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

Fields of papers citing papers by Winfried Edelmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Winfried Edelmann

This figure shows the co-authorship network connecting the top 25 collaborators of Winfried Edelmann. A scholar is included among the top collaborators of Winfried Edelmann 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 Winfried Edelmann. Winfried Edelmann 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.
Smith, Edward J., Christian Landles, Georgina F Osborne, et al.. (2024). A CAG repeat threshold for therapeutics targeting somatic instability in Huntington's disease. Brain. 147(5). 1784–1798. 21 indexed citations
2.
Tosti, Elena, et al.. (2023). Vaccination and Microbiota Manipulation Approaches for Colon Cancer Prevention in Rodent Models. Cancer Prevention Research. 16(8). 429–438. 3 indexed citations
3.
Tosti, Elena, Karl J. Shaffer, Peter C. Tyler, et al.. (2023). Combined inhibition of MTAP and MAT2a mimics synthetic lethality in tumor models via PRMT5 inhibition. Journal of Biological Chemistry. 300(1). 105492–105492. 15 indexed citations
4.
Wang, Shanzhi, Stephen Gray, Yongwei Zhang, et al.. (2022). Role of EXO1 nuclease activity in genome maintenance, the immune response and tumor suppression in Exo1D173A mice. Nucleic Acids Research. 50(14). 8093–8106. 12 indexed citations
5.
Holloway, J. Kim, Yongwei Zhang, Bo Jin, et al.. (2019). Mutation of the ATPase Domain of MutS Homolog-5 (MSH5) Reveals a Requirement for a Functional MutSγ Complex for All Crossovers in Mammalian Meiosis. G3 Genes Genomes Genetics. 9(6). 1839–1850. 18 indexed citations
6.
Zhang, Yongliang, Jennifer T. Fox, Young-Un Park, et al.. (2016). A Novel Chemotherapeutic Agent to Treat Tumors with DNA Mismatch Repair Deficiencies. Cancer Research. 76(14). 4183–4191. 20 indexed citations
7.
Eso, Yuji, Atsushi Takai, Tomonori Matsumoto, et al.. (2016). MSH2 Dysregulation Is Triggered by Proinflammatory Cytokine Stimulation and Is Associated with Liver Cancer Development. Cancer Research. 76(15). 4383–4393. 24 indexed citations
8.
He, Shuying, Rebecca McGreal, Qing Xie, et al.. (2016). Chromatin remodeling enzyme Snf2h regulates embryonic lens differentiation and denucleation. Development. 143(11). 1937–1947. 43 indexed citations
9.
Dietlein, Felix, Lisa Thelen, Mladen Jokić, et al.. (2014). A Functional Cancer Genomics Screen Identifies a Druggable Synthetic Lethal Interaction between MSH3 and PRKDC. Cancer Discovery. 4(5). 592–605. 53 indexed citations
10.
Campregher, Christoph, Michaela Lang, Vineeta Khare, et al.. (2014). Mesalazine and thymoquinone attenuate intestinal tumour development in Msh2 loxP/loxP Villin-Cre mice. Gut. 64(12). 1905–1912. 26 indexed citations
11.
McIlhatton, Michael A., Jessica K. Tyler, Laura A. Kerepesi, et al.. (2011). Aspirin and Low-Dose Nitric Oxide–Donating Aspirin Increase Life Span in a Lynch Syndrome Mouse Model. Cancer Prevention Research. 4(5). 684–693. 34 indexed citations
12.
Kadyrov, Farid A., et al.. (2009). A possible mechanism for exonuclease 1-independent eukaryotic mismatch repair. Proceedings of the National Academy of Sciences. 106(21). 8495–8500. 112 indexed citations
13.
Kucherlapati, Melanie H., Andrew Nguyen, Allan Clark, et al.. (2009). An Msh2 Conditional Knockout Mouse for Studying Intestinal Cancer and Testing Anticancer Agents. Gastroenterology. 138(3). 993–1002.e1. 77 indexed citations
14.
Yang, Kan, Naoto Kurihara, Kunhua Fan, et al.. (2008). Dietary Induction of Colonic Tumors in a Mouse Model of Sporadic Colon Cancer. Cancer Research. 68(19). 7803–7810. 85 indexed citations
15.
Roa, Sergio, Elena Avdievich, Jonathan U. Peled, et al.. (2008). Ubiquitylated PCNA plays a role in somatic hypermutation and class-switch recombination and is required for meiotic progression. Proceedings of the National Academy of Sciences. 105(42). 16248–16253. 94 indexed citations
16.
Yang, Kan, Н. В. Попова, Wancai Yang, et al.. (2008). Interaction of Muc2 and Apc on Wnt Signaling and in Intestinal Tumorigenesis: Potential Role of Chronic Inflammation. Cancer Research. 68(18). 7313–7322. 88 indexed citations
17.
Lin, Diana P., Yuxun Wang, Stefan Scherer, et al.. (2004). An Msh2 Point Mutation Uncouples DNA Mismatch Repair and Apoptosis. Cancer Research. 64(2). 517–522. 151 indexed citations
18.
Pretlow, Theresa P., Theresa P. Pretlow, Winfried Edelmann, et al.. (2003). Spontaneous Aberrant Crypt Foci in Apc1638N Mice with a Mutant Apc Allele. American Journal Of Pathology. 163(5). 1757–1763. 18 indexed citations
19.
Wiesendanger, Margrit, Burkhard Kneitz, Winfried Edelmann, & Matthew D. Scharff. (2000). Somatic Hypermutation in Muts Homologue (Msh)3-, Msh6-, and Msh3/Msh6-Deficient Mice Reveals a Role for the Msh2–Msh6 Heterodimer in Modulating the Base Substitution Pattern. The Journal of Experimental Medicine. 191(3). 579–584. 159 indexed citations
20.
Liedtke, Wolfgang, et al.. (1998). Experimental autoimmune encephalomyelitis in mice lacking glial fibrillary acidic protein is characterized by a more severe clinical course and an infiltrative central nervous system lesion.. Europe PMC (PubMed Central). 152(1). 251–9. 114 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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