Sigmar Stricker

5.6k total citations
74 papers, 3.5k citations indexed

About

Sigmar Stricker is a scholar working on Molecular Biology, Genetics and Developmental Biology. According to data from OpenAlex, Sigmar Stricker has authored 74 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Molecular Biology, 23 papers in Genetics and 15 papers in Developmental Biology. Recurrent topics in Sigmar Stricker's work include Congenital limb and hand anomalies (15 papers), Muscle Physiology and Disorders (12 papers) and Connective tissue disorders research (12 papers). Sigmar Stricker is often cited by papers focused on Congenital limb and hand anomalies (15 papers), Muscle Physiology and Disorders (12 papers) and Connective tissue disorders research (12 papers). Sigmar Stricker collaborates with scholars based in Germany, United States and France. Sigmar Stricker's co-authors include Stefan Mundlos, Florian Witte, Reinald Fundele, Andrea Vortkamp, Jochen Hecht, Peter N. Robinson, Petra Seemann, Janine Dokas, Uwe Kornak and Alexandra Schambony and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Sigmar Stricker

72 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sigmar Stricker Germany 36 2.6k 825 422 316 313 74 3.5k
Douglas P. Mortlock United States 29 2.0k 0.8× 740 0.9× 277 0.7× 363 1.1× 218 0.7× 52 3.3k
Joaquín Rodríguez‐León Spain 26 2.4k 0.9× 533 0.6× 307 0.7× 169 0.5× 161 0.5× 44 3.0k
Dmitry A. Ovchinnikov Australia 23 1.9k 0.8× 542 0.7× 367 0.9× 149 0.5× 338 1.1× 67 2.9k
Peter Meinecke Germany 31 2.5k 1.0× 1.9k 2.3× 238 0.6× 319 1.0× 217 0.7× 105 4.0k
Juan M. Hurlé Spain 41 3.4k 1.3× 968 1.2× 577 1.4× 249 0.8× 368 1.2× 139 5.2k
Javier López-Rı́os Switzerland 22 2.3k 0.9× 662 0.8× 260 0.6× 217 0.7× 158 0.5× 30 3.0k
Y. Gañán Spain 24 1.9k 0.8× 604 0.7× 390 0.9× 155 0.5× 129 0.4× 41 2.6k
Pao‐Tien Chuang United States 34 4.2k 1.7× 1.5k 1.8× 207 0.5× 244 0.8× 203 0.6× 52 5.1k
Rong Mo Canada 31 4.5k 1.8× 1.6k 2.0× 153 0.4× 230 0.7× 246 0.8× 40 5.4k
Andrew T. Dudley United States 22 2.9k 1.1× 681 0.8× 468 1.1× 168 0.5× 140 0.4× 44 4.3k

Countries citing papers authored by Sigmar Stricker

Since Specialization
Citations

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

Fields of papers citing papers by Sigmar Stricker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sigmar Stricker

This figure shows the co-authorship network connecting the top 25 collaborators of Sigmar Stricker. A scholar is included among the top collaborators of Sigmar Stricker 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 Sigmar Stricker. Sigmar Stricker 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.
Shonka, Nicole, et al.. (2025). Methotrexate-induced acute neurotoxicity in patients with osteosarcoma: a case report. Journal of Medical Case Reports. 19(1). 473–473.
2.
Qazi, Taimoor H., Christian H. Bucher, Hafsa Zahid, et al.. (2023). Odd skipped-related 1 controls the pro-regenerative response of fibro-adipogenic progenitors. npj Regenerative Medicine. 8(1). 13 indexed citations
3.
Hirsinger, Estelle, Shinichiro Hayashi, Sandra Swist, et al.. (2023). Inhibitory SMAD6 interferes with BMP dependent generation of muscle progenitor cells and perturbs proximodistal pattern of murine limb muscles. Development. 150(11). 3 indexed citations
4.
Fernández-Pérez, Daniel, Fabrizia Marullo, Roberta Maggio, et al.. (2021). Prdm16-mediated H3K9 methylation controls fibro-adipogenic progenitors identity during skeletal muscle repair. Science Advances. 7(23). 44 indexed citations
5.
Comai, Glenda, Markéta Tesařová, Valérie Dupé, et al.. (2020). Local retinoic acid signaling directs emergence of the extraocular muscle functional unit. PLoS Biology. 18(11). e3000902–e3000902. 22 indexed citations
6.
Wei, Xiaoyan, Julia Franke, Mario Ost, et al.. (2020). Cell autonomous requirement of neurofibromin (Nf1) for postnatal muscle hypertrophic growth and metabolic homeostasis. Journal of Cachexia Sarcopenia and Muscle. 11(6). 1758–1778. 6 indexed citations
7.
Chen, Feng, Wilson Cheuk Wing Chan, Xue Wang, et al.. (2019). Lgr5 and Col22a1 Mark Progenitor Cells in the Lineage toward Juvenile Articular Chondrocytes. Stem Cell Reports. 13(4). 713–729. 39 indexed citations
8.
Orgeur, Mickael, Marvin Martens, Sonya Nassari, et al.. (2018). Genome-wide strategies identify downstream target genes of chick connective tissue-associated transcription factors. Development. 145(7). 42 indexed citations
9.
Orgeur, Mickael, Marvin Martens, Stefan T. Börno, et al.. (2017). A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model. Biology Open. 7(1). 7 indexed citations
10.
Vallecillo-García, Pedro, Mickael Orgeur, Jürgen Stumm, et al.. (2017). Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development. Nature Communications. 8(1). 1218–1218. 88 indexed citations
11.
Kuss, Pia, Katerina Kraft, Jürgen Stumm, et al.. (2013). Regulation of cell polarity in the cartilage growth plate and perichondrium of metacarpal elements by HOXD13 and WNT5A. Developmental Biology. 385(1). 83–93. 57 indexed citations
12.
Ott, Claus‐Eric, Silke B. Lohan, Jeannette Hoogeboom, et al.. (2012). Microduplications upstream ofMSX2are associated with a phenocopy of cleidocranial dysplasia. Journal of Medical Genetics. 49(7). 437–441. 12 indexed citations
13.
Stricker, Sigmar, Susanne Mathia, Julia Haupt, et al.. (2011). Odd-Skipped Related Genes Regulate Differentiation of Embryonic Limb Mesenchyme and Bone Marrow Mesenchymal Stromal Cells. Stem Cells and Development. 21(4). 623–633. 33 indexed citations
14.
Kossler, Nadine, Sigmar Stricker, Christian Rödelsperger, et al.. (2011). Neurofibromin (Nf1) is required for skeletal muscle development. Human Molecular Genetics. 20(14). 2697–2709. 47 indexed citations
15.
Liška, František, Sigmar Stricker, Claudia Gösele, et al.. (2010). Impairment of Sox9 Expression in Limb Buds of Rats Homozygous for Hypodactyly Mutation. Folia Biologica. 56(2). 58–65. 1 indexed citations
16.
Brancati, Francesco, Paola Fortugno, Irene Bottillo, et al.. (2010). Mutations in PVRL4, Encoding Cell Adhesion Molecule Nectin-4, Cause Ectodermal Dysplasia-Syndactyly Syndrome. The American Journal of Human Genetics. 87(2). 265–273. 91 indexed citations
17.
Witte, Florian, et al.. (2009). The LIM domain protein Wtip interacts with the receptor tyrosine kinase Ror2 and inhibits canonical Wnt signalling. Biochemical and Biophysical Research Communications. 390(2). 211–216. 16 indexed citations
18.
Gao, Bo, Jianxin Hu, Sigmar Stricker, et al.. (2009). A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range. Nature. 458(7242). 1196–1200. 78 indexed citations
19.
Hoffmann, Katrin, Juliane Müller, Sigmar Stricker, et al.. (2006). Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit. The American Journal of Human Genetics. 79(2). 303–312. 100 indexed citations
20.
Sammar, Marei, Sigmar Stricker, Georg C. Schwabe, et al.. (2004). Modulation of GDF5/BRI‐b signalling through interaction with the tyrosine kinase receptor Ror2. Genes to Cells. 9(12). 1227–1238. 85 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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