Martin Gajewski

857 total citations
17 papers, 698 citations indexed

About

Martin Gajewski is a scholar working on Molecular Biology, Cell Biology and Paleontology. According to data from OpenAlex, Martin Gajewski has authored 17 papers receiving a total of 698 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 4 papers in Cell Biology and 3 papers in Paleontology. Recurrent topics in Martin Gajewski's work include Developmental Biology and Gene Regulation (12 papers), Congenital heart defects research (8 papers) and Zebrafish Biomedical Research Applications (4 papers). Martin Gajewski is often cited by papers focused on Developmental Biology and Gene Regulation (12 papers), Congenital heart defects research (8 papers) and Zebrafish Biomedical Research Applications (4 papers). Martin Gajewski collaborates with scholars based in Germany, Singapore and Argentina. Martin Gajewski's co-authors include Diethard Tautz, Dirk Sieger, Günter Plickert, Klaus Röhr, Thomas Leitz, Andrew C. Oates, Suma Choorapoikayil, Christian Schröter, Stefan Hans and Christoph Winkler and has published in prestigious journals such as PLoS ONE, Development and Annals of the New York Academy of Sciences.

In The Last Decade

Martin Gajewski

17 papers receiving 692 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin Gajewski Germany 16 590 171 99 79 67 17 698
Birgit L. Aerne United Kingdom 14 739 1.3× 307 1.8× 96 1.0× 73 0.9× 86 1.3× 20 925
Linda L. Runft United States 7 476 0.8× 156 0.9× 92 0.9× 88 1.1× 76 1.1× 10 953
Jennifer B. Phillips United States 12 577 1.0× 292 1.7× 49 0.5× 102 1.3× 36 0.5× 19 850
Charisios D. Tsiairis Switzerland 11 456 0.8× 147 0.9× 175 1.8× 41 0.5× 73 1.1× 17 648
Juan Pascual‐Anaya Spain 17 564 1.0× 97 0.6× 93 0.9× 142 1.8× 78 1.2× 27 800
Ann Grens United States 9 498 0.8× 214 1.3× 306 3.1× 49 0.6× 42 0.6× 9 719
Yoshitaka Kobayakawa Japan 14 395 0.7× 159 0.9× 234 2.4× 60 0.8× 60 0.9× 29 749
Brock Roberts United States 10 405 0.7× 139 0.8× 57 0.6× 78 1.0× 17 0.3× 13 675
Ildikó Somorjai United Kingdom 16 611 1.0× 81 0.5× 64 0.6× 114 1.4× 37 0.6× 31 909
Mary‐Lee Dequéant United States 7 1.0k 1.7× 151 0.9× 48 0.5× 179 2.3× 148 2.2× 12 1.2k

Countries citing papers authored by Martin Gajewski

Since Specialization
Citations

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

Fields of papers citing papers by Martin Gajewski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Gajewski

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

All Works

17 of 17 papers shown
1.
Wagh, Vasant, Michael Xavier Doss, Davood Sabour, et al.. (2014). Fam40b is required for lineage commitment of murine embryonic stem cells. Cell Death and Disease. 5(7). e1320–e1320. 17 indexed citations
2.
Holder, Maxine V., et al.. (2012). The elongation rate of RNA polymerase II in zebrafish and its significance in the somite segmentation clock. Development. 140(2). 444–453. 46 indexed citations
3.
Choorapoikayil, Suma, et al.. (2012). Analysis of her1 and her7 Mutants Reveals a Spatio Temporal Separation of the Somite Clock Module. PLoS ONE. 7(6). e39073–e39073. 21 indexed citations
4.
Schröter, Christian, Saúl Ares, Luis G. Morelli, et al.. (2012). Topology and Dynamics of the Zebrafish Segmentation Clock Core Circuit. PLoS Biology. 10(7). e1001364–e1001364. 100 indexed citations
5.
Gajewski, Martin, Johannes Winkler, Shuhua Chen, et al.. (2009). Somitovasculin, a Novel Endothelial-Specific Transcript Involved in the Vasculature Development. Arteriosclerosis Thrombosis and Vascular Biology. 29(11). 1823–1829. 6 indexed citations
6.
Shankaran, Sunita S., Dirk Sieger, Christian Schröter, et al.. (2007). Completing the set of h/E(spl) cyclic genes in zebrafish: her12 and her15 reveal novel modes of expression and contribute to the segmentation clock. Developmental Biology. 304(2). 615–632. 41 indexed citations
7.
Gajewski, Martin, et al.. (2006). Comparative analysis of her genes during fish somitogenesis suggests a mouse/chick-like mode of oscillation in medaka. Development Genes and Evolution. 216(6). 315–332. 31 indexed citations
8.
Sieger, Dirk, et al.. (2006). her1 and her13.2 are jointly required for somitic border specification along the entire axis of the fish embryo. Developmental Biology. 293(1). 242–251. 24 indexed citations
9.
Sieger, Dirk, Diethard Tautz, & Martin Gajewski. (2004). her11 is involved in the somitogenesis clock in zebrafish. Development Genes and Evolution. 214(8). 393–406. 37 indexed citations
10.
Sieger, Dirk, Diethard Tautz, & Martin Gajewski. (2003). The role of Suppressor of Hairless in Notch mediated signalling during zebrafish somitogenesis. Mechanisms of Development. 120(9). 1083–1094. 46 indexed citations
11.
Plickert, Günter, et al.. (2003). The role of alpha-amidated neuropeptides in hydroid development--LWamides and metamorphosis in Hydractinia echinata. The International Journal of Developmental Biology. 47(6). 439–450. 30 indexed citations
12.
Gajewski, Martin, Dirk Sieger, Stefan Hans, et al.. (2003). Anterior and posterior waves of cyclicher1gene expression are differentially regulated in the presomitic mesoderm of zebrafish. Development. 130(18). 4269–4278. 84 indexed citations
13.
Gajewski, Martin, et al.. (2002). Comparative analysis of somitogenesis related genes of the hairy/Enhancer of split class in Fugu and zebrafish. BMC Genomics. 3(1). 21–21. 27 indexed citations
14.
Gajewski, Martin, et al.. (2001). Homologues of c-hairy1 (her9) and lunatic fringe in zebrafish are expressed in the developing central nervous system, but not in the presomitic mesoderm. Development Genes and Evolution. 211(10). 493–500. 49 indexed citations
15.
Gajewski, Martin, Cornelia Schmutzler, & Günter Plickert. (1998). Structure of Neuropeptide Precursors in Cnidaria. Annals of the New York Academy of Sciences. 839(1). 311–315. 15 indexed citations
16.
Plickert, G., et al.. (1997). Automated in situ detection (AISD) of biomolecules. Development Genes and Evolution. 207(5). 362–367. 42 indexed citations
17.
Gajewski, Martin, et al.. (1996). LWamides from Cnidaria constitute a novel family of neuropeptides with morphogenetic activity. Development Genes and Evolution. 205(5-6). 232–242. 82 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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