Henry Roehl

2.8k total citations
31 papers, 2.0k citations indexed

About

Henry Roehl is a scholar working on Molecular Biology, Cell Biology and Cancer Research. According to data from OpenAlex, Henry Roehl has authored 31 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 9 papers in Cell Biology and 5 papers in Cancer Research. Recurrent topics in Henry Roehl's work include Developmental Biology and Gene Regulation (8 papers), Congenital heart defects research (7 papers) and Fibroblast Growth Factor Research (4 papers). Henry Roehl is often cited by papers focused on Developmental Biology and Gene Regulation (8 papers), Congenital heart defects research (7 papers) and Fibroblast Growth Factor Research (4 papers). Henry Roehl collaborates with scholars based in United Kingdom, United States and Germany. Henry Roehl's co-authors include Christiane Nüsslein‐Volhard, Judith Kimble, Peter I. Croucher, Philip M. Elks, Nan Li, Matthias Hammerschmidt, Melissa Rusch, Scott B. Selleck, Chi‐Bin Chien and Jennifer K. Grenier and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Henry Roehl

31 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Henry Roehl United Kingdom 20 1.4k 551 312 179 152 31 2.0k
Pamela C. Yelick United States 26 1.5k 1.0× 409 0.7× 585 1.9× 164 0.9× 119 0.8× 54 2.3k
Gerrit Begemann Germany 26 1.9k 1.3× 490 0.9× 437 1.4× 261 1.5× 170 1.1× 57 2.4k
Ira L. Blitz United States 29 2.3k 1.6× 337 0.6× 500 1.6× 163 0.9× 192 1.3× 47 2.7k
Marie‐Andrée Akimenko Canada 22 1.9k 1.3× 708 1.3× 476 1.5× 100 0.6× 223 1.5× 38 2.5k
Naoya Takeda Japan 26 1.6k 1.1× 329 0.6× 415 1.3× 270 1.5× 107 0.7× 47 3.5k
Jeffrey M. Gross United States 30 1.6k 1.1× 577 1.0× 327 1.0× 210 1.2× 85 0.6× 77 2.0k
Thierry Lepage France 28 2.6k 1.8× 632 1.1× 374 1.2× 247 1.4× 226 1.5× 45 3.5k
Edwin L. Ferguson United States 25 3.2k 2.2× 610 1.1× 451 1.4× 401 2.2× 107 0.7× 31 4.1k
Ela W. Knapik United States 28 1.7k 1.2× 970 1.8× 763 2.4× 166 0.9× 249 1.6× 45 2.6k
Gregory M. Kelly Canada 23 1.3k 0.9× 519 0.9× 229 0.7× 164 0.9× 171 1.1× 61 1.8k

Countries citing papers authored by Henry Roehl

Since Specialization
Citations

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

Fields of papers citing papers by Henry Roehl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Henry Roehl

This figure shows the co-authorship network connecting the top 25 collaborators of Henry Roehl. A scholar is included among the top collaborators of Henry Roehl 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 Henry Roehl. Henry Roehl 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.
Greaves, Sarah, et al.. (2022). Tetraspanin Cd9b plays a role in fertility in zebrafish. PLoS ONE. 17(11). e0277274–e0277274. 4 indexed citations
2.
Greaves, Sarah, Harsha Mahabaleshwar, Henry Roehl, et al.. (2021). Tetraspanin Cd9b and Cxcl12a/Cxcr4b have a synergistic effect on the control of collective cell migration. PLoS ONE. 16(11). e0260372–e0260372. 4 indexed citations
3.
Roehl, Henry. (2018). Linking wound response and inflammation to regeneration in the zebrafish larval fin. The International Journal of Developmental Biology. 62(6-7-8). 473–477. 19 indexed citations
4.
Roehl, Henry, et al.. (2018). Damage-induced reactive oxygen species enable zebrafish tail regeneration by repositioning of Hedgehog expressing cells. Nature Communications. 9(1). 4010–4010. 54 indexed citations
5.
Roehl, Henry, et al.. (2017). Tetraspanins in zebrafish development. Mechanisms of Development. 145. S64–S65. 1 indexed citations
6.
Elks, Philip M., et al.. (2015). Expression of osterix Is Regulated by FGF and Wnt/β-Catenin Signalling during Osteoblast Differentiation. PLoS ONE. 10(12). e0144982–e0144982. 46 indexed citations
7.
Madan, Sanjeev, James A. Fernandes, Frank H. Ebetino, et al.. (2013). Can Bisphosphonates extend Life Span? Effects on Stem Cell survival, DNA Repair and Tissue Regeneration. Journal of Bone and Mineral Research. 28. 1 indexed citations
8.
Wiweger, Małgorzata, et al.. (2012). HSPG-Deficient Zebrafish Uncovers Dental Aspect of Multiple Osteochondromas. PLoS ONE. 7(1). e29734–e29734. 27 indexed citations
9.
Monk, Peter N., et al.. (2011). Regulation of Zebrafish Hatching by Tetraspanin cd63. PLoS ONE. 6(5). e19683–e19683. 50 indexed citations
10.
Knight, Robert, et al.. (2011). Ret signalling integrates a craniofacial muscle module during development. Development. 138(10). 2015–2024. 14 indexed citations
11.
Thompson, Mark J., Steven Ferrara, Matthew P. Jackson, et al.. (2011). Discovery of 6-substituted indole-3-glyoxylamides as lead antiprion agents with enhanced cell line activity, improved microsomal stability and low toxicity. European Journal of Medicinal Chemistry. 46(9). 4125–4132. 20 indexed citations
12.
Croucher, Peter I., et al.. (2010). Hedgehog signalling is required for perichondral osteoblast differentiation in zebrafish. Mechanisms of Development. 128(1-2). 141–152. 18 indexed citations
13.
Roehl, Henry & Maurizio Pacifici. (2010). Shop talk: Sugars, bones, and a disease called multiple hereditary exostoses. Developmental Dynamics. 239(6). 1901–1904. 9 indexed citations
14.
Li, Nan, et al.. (2009). Tracking gene expression during zebrafish osteoblast differentiation. Developmental Dynamics. 238(2). 459–466. 151 indexed citations
15.
Knight, Robert, Katharina Mebus, & Henry Roehl. (2008). Mandibular arch muscle identity is regulated by a conserved molecular process during vertebrate development. Journal of Experimental Zoology Part B Molecular and Developmental Evolution. 310B(4). 355–369. 19 indexed citations
16.
Clément, Aurélie, Małgorzata Wiweger, Melissa Rusch, et al.. (2008). Regulation of Zebrafish Skeletogenesis by ext2/dackel and papst1/pinscher. PLoS Genetics. 4(7). e1000136–e1000136. 99 indexed citations
17.
Lee, Jeong-Soo, Melissa Rusch, Sally E. Stringer, et al.. (2004). Axon Sorting in the Optic Tract Requires HSPG Synthesis by ext2 (dackel) and extl3 (boxer). Neuron. 44(6). 947–960. 129 indexed citations
18.
Roehl, Henry & Christiane Nüsslein‐Volhard. (2001). Zebrafish pea3 and erm are general targets of FGF8 signaling. Current Biology. 11(7). 503–507. 220 indexed citations
19.
Panganiban, Grace, Christopher J. Lowe, Henry Roehl, et al.. (1997). The origin and evolution of animal appendages. Proceedings of the National Academy of Sciences. 94(10). 5162–5166. 300 indexed citations
20.
Roehl, Henry, Marcus Bosenberg, Robert Blelloch, & Judith Kimble. (1996). Roles of the RAM and ANK domains in signaling by the C. elegans GLP-1 receptor.. The EMBO Journal. 15(24). 7002–7012. 75 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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