Anne Schohl

1.1k total citations
26 papers, 797 citations indexed

About

Anne Schohl is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Anne Schohl has authored 26 papers receiving a total of 797 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Cellular and Molecular Neuroscience, 19 papers in Molecular Biology and 4 papers in Neurology. Recurrent topics in Anne Schohl's work include Neuroscience and Neuropharmacology Research (13 papers), Retinal Development and Disorders (10 papers) and Photoreceptor and optogenetics research (8 papers). Anne Schohl is often cited by papers focused on Neuroscience and Neuropharmacology Research (13 papers), Retinal Development and Disorders (10 papers) and Photoreceptor and optogenetics research (8 papers). Anne Schohl collaborates with scholars based in Canada, Germany and United States. Anne Schohl's co-authors include François Fagotto, Edward S. Ruthazer, Neil Schwartz, Nicola Wiechens, Ludwig Englmeier, Perry W.E. Spratt, Delphine Gobert, Martin Munz, Marc Adélard Tremblay and Jessie Poquérusse and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Anne Schohl

26 papers receiving 787 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne Schohl Canada 13 579 296 134 73 57 26 797
Magali Mondin France 12 376 0.6× 360 1.2× 91 0.7× 88 1.2× 48 0.8× 20 690
Matthew B. Veldman United States 16 454 0.8× 233 0.8× 235 1.8× 49 0.7× 89 1.6× 25 776
Patrick W. Keeley United States 16 588 1.0× 394 1.3× 105 0.8× 44 0.6× 33 0.6× 41 721
Vedakumar Tatavarty United States 10 290 0.5× 217 0.7× 83 0.6× 88 1.2× 44 0.8× 10 483
Matteo Fossati Italy 11 320 0.6× 157 0.5× 149 1.1× 39 0.5× 24 0.4× 19 558
Nina Wittenmayer Germany 11 306 0.5× 262 0.9× 248 1.9× 38 0.5× 32 0.6× 13 536
Olaya Llano Finland 5 212 0.4× 284 1.0× 175 1.3× 31 0.4× 60 1.1× 5 448
Louis C. Leung United States 12 400 0.7× 224 0.8× 298 2.2× 100 1.4× 102 1.8× 17 688
Iván J. Cajigas Germany 9 761 1.3× 250 0.8× 126 0.9× 60 0.8× 47 0.8× 10 929
Karen Perez de Arce United States 9 287 0.5× 266 0.9× 116 0.9× 40 0.5× 51 0.9× 10 561

Countries citing papers authored by Anne Schohl

Since Specialization
Citations

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

Fields of papers citing papers by Anne Schohl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Schohl

This figure shows the co-authorship network connecting the top 25 collaborators of Anne Schohl. A scholar is included among the top collaborators of Anne Schohl 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 Anne Schohl. Anne Schohl 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.
Kutsarova, Elena, Anne Schohl, Martin Munz, et al.. (2023). BDNF signaling in correlation-dependent structural plasticity in the developing visual system. PLoS Biology. 21(4). e3002070–e3002070. 2 indexed citations
2.
Schohl, Anne, et al.. (2023). The effects of the NMDAR co-agonist d-serine on the structure and function of optic tectal neurons in the developing visual system. Scientific Reports. 13(1). 13383–13383. 1 indexed citations
3.
Schohl, Anne, et al.. (2022). Topographic map formation and the effects of NMDA receptor blockade in the developing visual system. Proceedings of the National Academy of Sciences. 119(8). 8 indexed citations
4.
Aufmkolk, Sarah, et al.. (2021). Activity‐dependent alteration of early myelin ensheathment in a developing sensory circuit. The Journal of Comparative Neurology. 530(6). 871–885. 2 indexed citations
5.
Farooqi, Nasr, et al.. (2021). Early Inflammation Dysregulates Neuronal Circuit Formation In Vivo via Upregulation of IL-1β. Journal of Neuroscience. 41(29). 6353–6366. 9 indexed citations
6.
Schohl, Anne, et al.. (2021). Sodium-calcium exchanger mediates sensory-evoked glial calcium transients in the developing retinotectal system. Cell Reports. 37(1). 109791–109791. 11 indexed citations
7.
Qian, Yong, Danielle M. Cosio, Kiryl D. Piatkevich, et al.. (2020). Improved genetically encoded near-infrared fluorescent calcium ion indicators for in vivo imaging. PLoS Biology. 18(11). e3000965–e3000965. 64 indexed citations
8.
Schohl, Anne, et al.. (2020). Postsynaptic and Presynaptic NMDARs Have Distinct Roles in Visual Circuit Development. Cell Reports. 32(4). 107955–107955. 13 indexed citations
9.
Schohl, Anne, et al.. (2020). A Simple and Efficient Method for Visualizing Individual Cells in vivo by Cre-Mediated Single-Cell Labeling by Electroporation (CREMSCLE). Frontiers in Neural Circuits. 14. 47–47. 9 indexed citations
10.
Miraucourt, Loïs S., Jennifer Tsui, Delphine Gobert, et al.. (2016). Endocannabinoid signaling enhances visual responses through modulation of intracellular chloride levels in retinal ganglion cells. eLife. 5. 18 indexed citations
11.
Ruthazer, Edward S., et al.. (2013). Bulk Electroporation of Retinal Ganglion Cells in Live Xenopus Tadpoles. Cold Spring Harbor Protocols. 2013(8). pdb.prot076471–pdb.prot076471. 11 indexed citations
12.
Ruthazer, Edward S., et al.. (2013). Labeling Individual Neurons in the Brains of Live Xenopus Tadpoles by Electroporation of Dyes or DNA. Cold Spring Harbor Protocols. 2013(9). pdb.prot077149–pdb.prot077149. 2 indexed citations
13.
Schwartz, Neil, Anne Schohl, & Edward S. Ruthazer. (2011). Activity-Dependent Transcription of BDNF Enhances Visual Acuity during Development. Neuron. 70(3). 455–467. 31 indexed citations
14.
Tremblay, Marc Adélard, Vincent Fugère, Jennifer Tsui, et al.. (2009). Regulation of Radial Glial Motility by Visual Experience. Journal of Neuroscience. 29(45). 14066–14076. 31 indexed citations
15.
Pedraza, Liliana, et al.. (2009). N‐cadherin prodomain cleavage regulates synapse formation in vivo. Developmental Neurobiology. 69(8). 518–529. 22 indexed citations
16.
Schwartz, Neil, Anne Schohl, & Edward S. Ruthazer. (2009). Neural Activity Regulates Synaptic Properties and Dendritic Structure In Vivo through Calcineurin/NFAT Signaling. Neuron. 62(5). 655–669. 80 indexed citations
17.
Wiechens, Nicola, et al.. (2004). Nucleo-cytoplasmic Shuttling of Axin, a Negative Regulator of the Wnt-β-Catenin Pathway. Journal of Biological Chemistry. 279(7). 5263–5267. 70 indexed citations
18.
Schohl, Anne. (2003). A role for maternal  -catenin in early mesoderm induction in Xenopus. The EMBO Journal. 22(13). 3303–3313. 63 indexed citations
19.
Schohl, Anne, Guillermo Barreto, Thomas Joos, & Christine Dreyer. (2002). Oocytes and embryos of Xenopus laevis express two different isoforms of germ cell nuclear factor (GCNF, NR6A1). Mechanisms of Development. 118(1-2). 261–264. 3 indexed citations
20.
Schohl, Anne & François Fagotto. (2002). β-catenin, MAPK and Smad signaling during earlyXenopusdevelopment. Development. 129(1). 37–52. 220 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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