Andreas Kispert

25.2k total citations · 3 hit papers
178 papers, 16.4k citations indexed

About

Andreas Kispert is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Andreas Kispert has authored 178 papers receiving a total of 16.4k indexed citations (citations by other indexed papers that have themselves been cited), including 161 papers in Molecular Biology, 39 papers in Genetics and 29 papers in Surgery. Recurrent topics in Andreas Kispert's work include Congenital heart defects research (65 papers), Renal and related cancers (53 papers) and Developmental Biology and Gene Regulation (33 papers). Andreas Kispert is often cited by papers focused on Congenital heart defects research (65 papers), Renal and related cancers (53 papers) and Developmental Biology and Gene Regulation (33 papers). Andreas Kispert collaborates with scholars based in Germany, United States and Netherlands. Andreas Kispert's co-authors include Bernhard G. Herrmann, Andrew P. McMahon, Jörg Stappert, Andreas Bauer, Seppo Vainio, Hermann Aberle, Vincent M. Christoffels, Minna Heikkilä, Bénédicte Haenig and Carsten Rudat and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Andreas Kispert

178 papers receiving 16.1k citations

Hit Papers

β-catenin is a target for the ubiquitin–proteasome pathway 1994 2026 2004 2015 1997 1999 1994 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andreas Kispert Germany 62 13.4k 4.0k 1.9k 1.5k 1.2k 178 16.4k
Andreas Schedl France 52 9.6k 0.7× 4.3k 1.1× 1.3k 0.7× 1.1k 0.7× 575 0.5× 116 13.4k
Cynthia C. Morton United States 73 8.7k 0.6× 2.9k 0.7× 1.3k 0.7× 1.5k 1.0× 575 0.5× 281 18.9k
Virginia E. Papaioannou United States 62 12.6k 0.9× 4.0k 1.0× 1.4k 0.7× 937 0.6× 592 0.5× 176 17.8k
Thomas Doetschman United States 63 13.8k 1.0× 3.3k 0.8× 2.4k 1.3× 1.5k 1.0× 2.9k 2.4× 134 19.5k
Marina Gertsenstein Canada 30 13.1k 1.0× 2.1k 0.5× 1.5k 0.8× 1.1k 0.7× 631 0.5× 130 16.3k
Haruhiko Koseki Japan 90 19.2k 1.4× 4.3k 1.1× 1.2k 0.6× 680 0.4× 387 0.3× 388 29.9k
Elizabeth J. Robertson United States 80 20.8k 1.5× 6.7k 1.7× 2.5k 1.4× 940 0.6× 447 0.4× 171 26.4k
Jan Kitajewski United States 76 11.6k 0.9× 1.4k 0.3× 1.9k 1.0× 1.3k 0.8× 462 0.4× 180 17.7k
Christof Niehrs Germany 74 20.3k 1.5× 3.8k 0.9× 1.4k 0.8× 805 0.5× 484 0.4× 204 24.2k
Richard P. Harvey Australia 76 13.8k 1.0× 2.6k 0.7× 3.0k 1.6× 1.4k 0.9× 3.4k 2.8× 240 18.6k

Countries citing papers authored by Andreas Kispert

Since Specialization
Citations

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

Fields of papers citing papers by Andreas Kispert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Kispert

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Kispert. A scholar is included among the top collaborators of Andreas Kispert 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 Andreas Kispert. Andreas Kispert 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.
Beckers, Anja, et al.. (2025). Interplay of SHH, WNT and BMP4 signaling regulates the development of the lamina propria in the murine ureter. Development. 152(3). 2 indexed citations
2.
Martens, Helge, Frank Brand, Mark‐Oliver Trowe, et al.. (2024). Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract. European Journal of Human Genetics. 33(1). 44–55. 2 indexed citations
3.
Weiss, Anna‐Carina, et al.. (2023). Permissive ureter specification by TBX18-mediated repression of metanephric gene expression. Development. 150(6). 5 indexed citations
4.
Kurz, Jennifer, Anna‐Carina Weiss, Timo H. Lüdtke, et al.. (2022). GATA6 is a crucial factor for Myocd expression in the visceral smooth muscle cell differentiation program of the murine ureter. Development. 149(15). 6 indexed citations
5.
Thiesler, Hauke, et al.. (2022). Mesenchymal FGFR1 and FGFR2 control patterning of the ureteric mesenchyme by balancing SHH and BMP4 signaling. Development. 149(17). 4 indexed citations
6.
Lüdtke, Timo H., et al.. (2022). TBX2 specifies and maintains inner hair and supporting cell fate in the Organ of Corti. Nature Communications. 13(1). 7628–7628. 27 indexed citations
7.
Rudat, Carsten, Timo H. Lüdtke, Vincent M. Christoffels, et al.. (2021). Regulation of otocyst patterning by Tbx2 and Tbx3 is required for inner ear morphogenesis in the mouse. Development. 148(8). 33 indexed citations
8.
Lüdtke, Timo H., Carsten Rudat, Jennifer Kurz, et al.. (2019). Mesothelial mobilization in the developing lung and heart differs in timing, quantity, and pathway dependency. American Journal of Physiology-Lung Cellular and Molecular Physiology. 316(5). L767–L783. 9 indexed citations
9.
Cordero, Julio, Yong Wang, Andrea Grund, et al.. (2019). Inactivation of Sox9 in fibroblasts reduces cardiac fibrosis and inflammation. JCI Insight. 4(15). 56 indexed citations
10.
Albers, Iris, Andreas Kispert, Stephen Tomlinson, et al.. (2018). Sialic acid is a critical fetal defense against maternal complement attack. Journal of Clinical Investigation. 129(1). 422–436. 55 indexed citations
11.
Greulich, Franziska, Mark‐Oliver Trowe, Andreas Leffler, et al.. (2016). Misexpression of Tbx18 in cardiac chambers of fetal mice interferes with chamber-specific developmental programs but does not induce a pacemaker-like gene signature. Journal of Molecular and Cellular Cardiology. 97. 140–149. 14 indexed citations
12.
Braun, Ursula, Norbert Roos, Shaohua Li, et al.. (2013). Phenotypical Analysis of Atypical PKCs In Vivo Function Display a Compensatory System at Mouse Embryonic Day 7.5. PLoS ONE. 8(5). e62756–e62756. 28 indexed citations
14.
Loges, Niki T., Heike Olbrich, Anita Becker-Heck, et al.. (2009). Deletions and Point Mutations of LRRC50 Cause Primary Ciliary Dyskinesia Due to Dynein Arm Defects. The American Journal of Human Genetics. 85(6). 883–889. 144 indexed citations
15.
Lüdtke, Timo H., et al.. (2009). Expression and requirement of T-box transcription factors Tbx2 and Tbx3 during secondary palate development in the mouse. Developmental Biology. 336(2). 145–155. 38 indexed citations
16.
Winkler, M, Christina Mauritz, Stephanie Groos, et al.. (2008). Serum-Free Differentiation of Murine Embryonic Stem Cells into Alveolar Type II Epithelial Cells. Cloning and Stem Cells. 10(1). 49–64A. 29 indexed citations
17.
Lausch, Ekkehart, Pia Hermanns, Henner F. Farin, et al.. (2008). TBX15 Mutations Cause Craniofacial Dysmorphism, Hypoplasia of Scapula and Pelvis, and Short Stature in Cousin Syndrome. The American Journal of Human Genetics. 83(5). 649–655. 46 indexed citations
18.
Goering, Lisa M., et al.. (2003). An interacting network of T-box genes directs gene expression and fate in the zebrafish mesoderm. Proceedings of the National Academy of Sciences. 100(16). 9410–9415. 69 indexed citations
19.
Haenig, Bénédicte, et al.. (1998). sFRP-2 is a target of the Wnt-4 signaling pathway in the developing metanephric kidney. Developmental Dynamics. 213(4). 440–451. 107 indexed citations
20.
Haenig, Bénédicte, et al.. (1998). sFRP2 is a target of the Wnt‐4 signaling pathway in the developing metanephric kidney. Developmental Dynamics. 213(4). 440–451. 4 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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