Josephine Jüttner

1.5k total citations
11 papers, 770 citations indexed

About

Josephine Jüttner is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cognitive Neuroscience. According to data from OpenAlex, Josephine Jüttner has authored 11 papers receiving a total of 770 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 5 papers in Cognitive Neuroscience. Recurrent topics in Josephine Jüttner's work include Retinal Development and Disorders (9 papers), Photoreceptor and optogenetics research (7 papers) and Neural dynamics and brain function (4 papers). Josephine Jüttner is often cited by papers focused on Retinal Development and Disorders (9 papers), Photoreceptor and optogenetics research (7 papers) and Neural dynamics and brain function (4 papers). Josephine Jüttner collaborates with scholars based in Switzerland, United States and Germany. Josephine Jüttner's co-authors include Botond Roska, Dániel Hillier, Karl Farrow, Antonia Drinnenberg, Volker Busskamp, Péter Hantz, Andreas Hierlemann, Stuart Trenholm, Keisuke Yonehara and Pamela S. Lagali and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Neuron.

In The Last Decade

Josephine Jüttner

11 papers receiving 766 citations

Peers

Josephine Jüttner

CMN

GENET

Mingna Liu United States

Brigitte Gross Scherf Switzerland

Julia Veit Switzerland

Gerrit Hilgen United Kingdom

Y. Kate Hong United States

Frans Vinberg United States

Whitney E. Heavner United States

Haibo Zhou China

Alexandra Erven United Kingdom

Mitra Cowan Canada

Mingna Liu United States

Josephine Jüttner

433 ×0.8

286 ×0.6

CMN

241 ×1.1

96 ×1.6

GENET

46 ×0.8

Citations per year, relative to Josephine Jüttner Josephine Jüttner (= 1×) peers Mingna Liu

Countries citing papers authored by Josephine Jüttner

Since Specialization

Citations

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

Fields of papers citing papers by Josephine Jüttner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Josephine Jüttner

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

All Works

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11 of 11 papers shown

Micheli, Pietro, Andrés González-Guerra, Gioia De Franceschi, et al.. (2025). Pupil size modulation drives retinal activity in mice and shapes human perception. Nature Communications. 16(1). 7334–7334. 1 indexed citations

Morikawa, Rei, Tiago M. Rodrigues, Helene M. Schreyer, et al.. (2024). The sodium-bicarbonate cotransporter Slc4a5 mediates feedback at the first synapse of vision. Neuron. 112(22). 3715–3733.e9. 2 indexed citations

Drinnenberg, Antonia, Felix Franke, Rei Morikawa, et al.. (2018). How Diverse Retinal Functions Arise from Feedback at the First Visual Synapse. Neuron. 99(1). 117–134.e11. 37 indexed citations

Mager, Thomas, Katrin Feldbauer, Christian Wrobel, et al.. (2018). High frequency neural spiking and auditory signaling by ultrafast red-shifted optogenetics. Nature Communications. 9(1). 1750–1750. 117 indexed citations

Hillier, Dániel, Michele Fiscella, Antonia Drinnenberg, et al.. (2017). Causal evidence for retina-dependent and -independent visual motion computations in mouse cortex. Nature Neuroscience. 20(7). 960–968. 71 indexed citations

Hartl, Dominik, Arnaud Krebs, Josephine Jüttner, Botond Roska, & Dirk Schübeler. (2017). Cis-regulatory landscapes of four cell types of the retina. Nucleic Acids Research. 45(20). 11607–11621. 23 indexed citations

Yonehara, Keisuke, Michele Fiscella, Antonia Drinnenberg, et al.. (2015). Congenital Nystagmus Gene FRMD7 Is Necessary for Establishing a Neuronal Circuit Asymmetry for Direction Selectivity. Neuron. 89(1). 177–193. 99 indexed citations

Szikra, Tamás, Stuart Trenholm, Antonia Drinnenberg, et al.. (2014). Rods in daylight act as relay cells for cone-driven horizontal cell–mediated surround inhibition. Nature Neuroscience. 17(12). 1728–1735. 54 indexed citations

Cronin, Thérèse, Luk H. Vandenberghe, Péter Hantz, et al.. (2014). Efficient transduction and optogenetic stimulation of retinal bipolar cells by a synthetic adeno‐associated virus capsid and promoter. EMBO Molecular Medicine. 6(9). 1175–1190. 146 indexed citations

10.

Busskamp, Volker, Jacek Król, Tamás Szikra, et al.. (2014). miRNAs 182 and 183 Are Necessary to Maintain Adult Cone Photoreceptor Outer Segments and Visual Function. Neuron. 83(3). 586–600. 110 indexed citations

11.

Yonehara, Keisuke, Karl Farrow, Alexander Ghanem, et al.. (2013). The First Stage of Cardinal Direction Selectivity Is Localized to the Dendrites of Retinal Ganglion Cells. Neuron. 79(6). 1078–1085. 110 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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