Denny Schanze

2.9k total citations
55 papers, 749 citations indexed

About

Denny Schanze is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Denny Schanze has authored 55 papers receiving a total of 749 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 19 papers in Genetics and 11 papers in Immunology. Recurrent topics in Denny Schanze's work include Ocular Disorders and Treatments (10 papers), Protein Tyrosine Phosphatases (7 papers) and Galectins and Cancer Biology (6 papers). Denny Schanze is often cited by papers focused on Ocular Disorders and Treatments (10 papers), Protein Tyrosine Phosphatases (7 papers) and Galectins and Cancer Biology (6 papers). Denny Schanze collaborates with scholars based in Germany, United States and United Kingdom. Denny Schanze's co-authors include Martin Zenker, Alexander Link, Ina Schanze, Peter Malfertheiner, Juozas Kupčinskas, Rūta Steponaitienė, Claudia Marini, Anna Fejtová, Carolina Montenegro‐Venegas and André Reis and has published in prestigious journals such as Nature Communications, The EMBO Journal and Scientific Reports.

In The Last Decade

Denny Schanze

52 papers receiving 736 citations

Peers

Denny Schanze

GENET

SURGE

IMMUN

Bartolomeo Augello Italy

Jakob V. Nielsen Denmark

Yafei Zhang China

Ok‐Hee Jeon South Korea

Khushnooda Ramzan Saudi Arabia

Jonathan Lim United States

Vimla S. Aggarwal United States

Bahareh Rabbani Iran

Sami S. Amr United States

Michele Salemi Italy

Bartolomeo Augello Italy

Denny Schanze

439 ×1.1

199 ×0.9

GENET

63 ×0.6

SURGE

62 ×0.6

184 ×2.1

IMMUN

Citations per year, relative to Denny Schanze Denny Schanze (= 1×) peers Bartolomeo Augello

Countries citing papers authored by Denny Schanze

Since Specialization

Citations

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

Fields of papers citing papers by Denny Schanze

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Denny Schanze

This figure shows the co-authorship network connecting the top 25 collaborators of Denny Schanze. A scholar is included among the top collaborators of Denny Schanze 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 Denny Schanze. Denny Schanze is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Vilchez‐Vargas, Ramiro, Albrecht Hoffmeister, Jürgen Feisthammel, et al.. (2024). Prediction of anastomotic insufficiency based on the mucosal microbiome prior to colorectal surgery: a proof-of-principle study. Scientific Reports. 14(1). 15335–15335. 4 indexed citations

Mengoni, Miriam, Andreas Braun, Evi Kostenis, et al.. (2024). Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice. Cancer Gene Therapy. 31(6). 884–893. 1 indexed citations

Keßler, T., B. Liesfeld, Simon von Ameln, et al.. (2023). Impact of cfDNA Reference Materials on Clinical Performance of Liquid Biopsy NGS Assays. Cancers. 15(20). 5024–5024. 5 indexed citations

Lingel, Holger, Denny Schanze, Martin Zenker, et al.. (2023). Bifidobacteria shape antimicrobial T-helper cell responses during infancy and adulthood. Nature Communications. 14(1). 5943–5943. 11 indexed citations

Schanze, Denny, et al.. (2023). Happle‐Tinschert syndrome variable phenotype as part of the mosaic hedgehog spectrum: Report of three cases. Pediatric Dermatology. 40(4). 691–694. 2 indexed citations

Zepeda‐Romero, Luz Consuelo, Martin Zenker, Denny Schanze, et al.. (2022). Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndrome. European Journal of Medical Genetics. 65(12). 104653–104653. 4 indexed citations

Vilchez‐Vargas, Ramiro, Jurgita Skiecevičienė, Denny Schanze, et al.. (2022). Gut microbial similarity in twins is driven by shared environment and aging. EBioMedicine. 79. 104011–104011. 22 indexed citations

Bassi, Andrea, Friedrich Kapp, Ilse Wieland, et al.. (2022). Cutis marmorata telangiectatica congenita being caused by postzygotic GNA11 mutations. European Journal of Medical Genetics. 65(5). 104472–104472. 5 indexed citations

Metzger, Patrick, Martin Boeker, Till Acker, et al.. (2020). Requirements Analysis and Specification for a Molecular Tumor Board Platform Based on cBioPortal. Diagnostics. 10(2). 93–93. 25 indexed citations

10.

Wong, Jasmine C., Pedro A. Pérez–Mancera, Joaquím Grego‐Bessa, et al.. (2020). KrasP34R and KrasT58I mutations induce distinct RASopathy phenotypes in mice. JCI Insight. 5(21). 8 indexed citations

11.

Martinelli, Simone, Luca Pannone, Christina Lißewski, et al.. (2020). Pathogenic PTPN11 variants involving the poly‐glutamine Gln ²⁵⁵ ‐Gln ²⁵⁶ ‐Gln ²⁵⁷ stretch highlight the relevance of helix B in SHP2's functional regulation. Human Mutation. 41(6). 1171–1182. 1 indexed citations

12.

Kunz, Felix, Hülya Kayserili, Alina T. Midro, et al.. (2020). Characteristic dental pattern with hypodontia and short roots in Fraser syndrome. American Journal of Medical Genetics Part A. 182(7). 1681–1689. 7 indexed citations

13.

Zenker, Martin, Sigrid Tinschert, Ilse Wieland, Denny Schanze, & Rudolf Happle. (2018). A Postzygotic SMO Mutation Caused the Original Case of Happle–Tinschert Syndrome. Acta Dermato Venereologica. 98(5). 534–535. 6 indexed citations

14.

Lingel, Holger, Josef Wissing, Denny Schanze, et al.. (2017). CTLA-4-mediated posttranslational modifications direct cytotoxic T-lymphocyte differentiation. Cell Death and Differentiation. 24(10). 1739–1749. 35 indexed citations

15.

Pothula, Santosh, Saeideh Nakhaei‐Rad, Carolina Montenegro‐Venegas, et al.. (2017). Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy. PLoS Genetics. 13(3). e1006684–e1006684. 20 indexed citations

16.

Dahlmann, Julia, Sönke Weinert, Martin Möckel, et al.. (2017). In Vitro Modeling of Congenital Hypertrophic Cardiomyopathy using Induced Pluripotent Stem Cell-Derived Cardiomyocytes. The Thoracic and Cardiovascular Surgeon. 65(S 01). S1–S110. 1 indexed citations

17.

Ivanova, Daniela, Carolina Montenegro‐Venegas, Cornelia Schöne, et al.. (2015). Synaptic activity controls localization and function of Ct BP 1 via binding to B assoon and P iccolo. The EMBO Journal. 34(8). 1056–1077. 46 indexed citations

18.

Richter, Anni, Marc Guitart‐Masip, Gusalija Behnisch, et al.. (2014). Valenced action/inhibition learning in humans is modulated by a genetic variant linked to dopamine D2 receptor expression. Frontiers in Systems Neuroscience. 8. 140–140. 18 indexed citations

19.

Mitter, Diana, Denny Schanze, Ina Sterker, et al.. (2012). MOTA Syndrome: Molecular Genetic Confirmation of the Diagnosis in a Newborn with Previously Unreported Clinical Features. Molecular Syndromology. 3(3). 136–139. 9 indexed citations

20.

Goecke, Tamme W., Arif B. Ekici, Beate Niesler, et al.. (2009). Two naturally occurring variants of the serotonin receptor geneHTR3Care associated with nausea in pregnancy. Acta Obstetricia Et Gynecologica Scandinavica. 89(1). 7–14. 19 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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