Iris Salecker

2.7k total citations
30 papers, 2.0k citations indexed

About

Iris Salecker is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Genetics. According to data from OpenAlex, Iris Salecker has authored 30 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Cellular and Molecular Neuroscience, 21 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Iris Salecker's work include Neurobiology and Insect Physiology Research (24 papers), Developmental Biology and Gene Regulation (15 papers) and Axon Guidance and Neuronal Signaling (7 papers). Iris Salecker is often cited by papers focused on Neurobiology and Insect Physiology Research (24 papers), Developmental Biology and Gene Regulation (15 papers) and Axon Guidance and Neuronal Signaling (7 papers). Iris Salecker collaborates with scholars based in United Kingdom, United States and Germany. Iris Salecker's co-authors include S Lawrence Zipursky, Holger Apitz, Dafni Hadjieconomou, Paul Garrity, George R. Jackson, Peter W. Faber, Marcy E. MacDonald, Norman Arnheim, Xiang Yao and Xinzhong Dong and has published in prestigious journals such as Cell, Nature Communications and Neuron.

In The Last Decade

Iris Salecker

30 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Iris Salecker United Kingdom 21 1.5k 1.3k 371 173 155 30 2.0k
Jasprina N. Noordermeer Netherlands 22 1.2k 0.9× 1.4k 1.0× 540 1.5× 178 1.0× 149 1.0× 36 2.1k
A. Pejmun Haghighi United States 21 1.5k 1.0× 2.0k 1.5× 770 2.1× 251 1.5× 121 0.8× 33 3.0k
Ulrich Thomas Germany 25 1.2k 0.9× 1.6k 1.2× 888 2.4× 234 1.4× 144 0.9× 59 2.4k
Thomas Osterwalder Switzerland 14 738 0.5× 840 0.6× 376 1.0× 182 1.1× 169 1.1× 14 1.7k
Vanessa J. Auld Canada 27 1.8k 1.2× 2.0k 1.5× 540 1.5× 154 0.9× 245 1.6× 52 2.8k
Steven Robinow United States 16 1.1k 0.8× 1.2k 0.9× 302 0.8× 282 1.6× 346 2.2× 19 2.0k
Susan Younger United States 14 833 0.6× 811 0.6× 571 1.5× 129 0.7× 175 1.1× 16 1.5k
Alicia Hidalgo United Kingdom 25 1.1k 0.8× 1.5k 1.1× 391 1.1× 293 1.7× 352 2.3× 60 2.4k
Bing Ye United States 22 1.2k 0.8× 1.3k 1.0× 871 2.3× 256 1.5× 182 1.2× 57 2.4k
Motojiro Yoshihara United States 19 1.1k 0.8× 1.2k 0.9× 681 1.8× 175 1.0× 104 0.7× 27 1.8k

Countries citing papers authored by Iris Salecker

Since Specialization
Citations

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

Fields of papers citing papers by Iris Salecker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Iris Salecker

This figure shows the co-authorship network connecting the top 25 collaborators of Iris Salecker. A scholar is included among the top collaborators of Iris Salecker 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 Iris Salecker. Iris Salecker 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
2.
Apitz, Holger & Iris Salecker. (2018). Spatio-temporal relays control layer identity of direction-selective neuron subtypes in Drosophila. Nature Communications. 9(1). 2295–2295. 43 indexed citations
3.
Salecker, Iris, et al.. (2017). Lapsyn controls branch extension and positioning of astrocyte-like glia in the Drosophila optic lobe. Nature Communications. 8(1). 317–317. 21 indexed citations
4.
Apitz, Holger & Iris Salecker. (2016). Retinal determination genes coordinate neuroepithelial specification and neurogenesis modes in the Drosophila optic lobe. Development. 143(13). 2431–2442. 10 indexed citations
5.
Apitz, Holger & Iris Salecker. (2014). A Challenge of Numbers and Diversity: Neurogenesis in theDrosophilaOptic Lobe. Journal of Neurogenetics. 28(3-4). 233–249. 46 indexed citations
6.
Apitz, Holger & Iris Salecker. (2014). A region-specific neurogenesis mode requires migratory progenitors in the Drosophila visual system. Nature Neuroscience. 18(1). 46–55. 53 indexed citations
7.
Apitz, Holger, et al.. (2012). Regulation of locomotion and motoneuron trajectory selection and targeting by the Drosophila homolog of Olig family transcription factors. Developmental Biology. 369(2). 261–276. 23 indexed citations
8.
Hadjieconomou, Dafni, et al.. (2012). Localized Netrins Act as Positional Cues to Control Layer-Specific Targeting of Photoreceptor Axons in Drosophila. Neuron. 75(1). 80–93. 75 indexed citations
9.
Hadjieconomou, Dafni, Shay Rotkopf, Cyrille Alexandre, et al.. (2011). Flybow: genetic multicolor cell labeling for neural circuit analysis in Drosophila melanogaster. Nature Methods. 8(3). 260–266. 162 indexed citations
10.
Salecker, Iris, et al.. (2007). Glial cell development and function in the Drosophila visual system. PubMed. 3(1). 17–25. 50 indexed citations
11.
Bazigou, Eleni, Holger Apitz, Jana H. Johansson, et al.. (2007). Anterograde Jelly belly and Alk Receptor Tyrosine Kinase Signaling Mediates Retinal Axon Targeting in Drosophila. Cell. 128(5). 961–975. 123 indexed citations
12.
Salecker, Iris, et al.. (2004). Neurons and glia: team players in axon guidance. Trends in Neurosciences. 27(11). 655–661. 80 indexed citations
13.
Poeck, Burkhard, et al.. (2001). Glial Cells Mediate Target Layer Selection of Retinal Axons in the Developing Visual System of Drosophila. Neuron. 29(1). 99–113. 139 indexed citations
14.
Garrity, Paul, et al.. (1999). Retinal Axon Target Selection in Drosophila Is Regulated by a Receptor Protein Tyrosine Phosphatase. Neuron. 22(4). 707–717. 130 indexed citations
15.
Salecker, Iris, et al.. (1999). Quantitative morphological analysis of embryonic cockroach ( Periplaneta americana) brain neurons developing in vitro. Cell and Tissue Research. 299(1). 129–143. 6 indexed citations
16.
Salecker, Iris, Thomas R. Clandinin, & S Lawrence Zipursky. (1998). Hedgehog and Spitz. Cell. 95(5). 587–590. 11 indexed citations
17.
Garrity, Paul, Yong Rao, Iris Salecker, et al.. (1996). Drosophila Photoreceptor Axon Guidance and Targeting Requires the Dreadlocks SH2/SH3 Adapter Protein. Cell. 85(5). 639–650. 226 indexed citations
18.
Salecker, Iris & J. Boeckh. (1996). Influence of receptor axons on the formation of olfactory glomeruli in a hemimetabolous insect, the cockroachPeriplaneta americana. The Journal of Comparative Neurology. 370(2). 262–279. 19 indexed citations
19.
Salecker, Iris & Jürgen Boeckh. (1995). Embryonic development of the antennal lobes of a hemimetabolous insect, the cockroach periplaneta americana: Light and electron microscopic observations. The Journal of Comparative Neurology. 352(1). 33–54. 33 indexed citations
20.
Salecker, Iris & Paul G. Distler. (1990). Serotonin-immunoreactive neurons in the antennal lobes of the American cockroach Periplaneta americana: light- and electron-microscopic observations. Histochemistry and Cell Biology. 94(5). 463–473. 60 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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