Henrik Gezelius

1.5k total citations
17 papers, 1.0k citations indexed

About

Henrik Gezelius is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Henrik Gezelius has authored 17 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cellular and Molecular Neuroscience, 8 papers in Molecular Biology and 5 papers in Cognitive Neuroscience. Recurrent topics in Henrik Gezelius's work include Neuroscience and Neuropharmacology Research (7 papers), Axon Guidance and Neuronal Signaling (5 papers) and Photoreceptor and optogenetics research (3 papers). Henrik Gezelius is often cited by papers focused on Neuroscience and Neuropharmacology Research (7 papers), Axon Guidance and Neuronal Signaling (5 papers) and Photoreceptor and optogenetics research (3 papers). Henrik Gezelius collaborates with scholars based in Sweden, Spain and Germany. Henrik Gezelius's co-authors include Klas Kullander, Anders Enjin, Guillermina López‐Bendito, Katarina E. Leão, Anders Eriksson, Åsa Wallén‐Mackenzie, Sanja Mikulovic, Anna Vallstedt, Richardson N. Leão and Fatima Memic and has published in prestigious journals such as Science, Nature Communications and Neuron.

In The Last Decade

Henrik Gezelius

16 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Henrik Gezelius Sweden 14 674 376 370 200 183 17 1.0k
Hiroyuki Ichijo Japan 12 667 1.0× 522 1.4× 210 0.6× 159 0.8× 162 0.9× 27 1.2k
Christopher A. Hinckley United States 14 350 0.5× 308 0.8× 189 0.5× 322 1.6× 193 1.1× 16 888
Gayane Aramuni Germany 9 904 1.3× 841 2.2× 408 1.1× 317 1.6× 172 0.9× 10 1.6k
Karla E. Hirokawa United States 10 451 0.7× 649 1.7× 283 0.8× 87 0.4× 175 1.0× 11 1.1k
Tetsushi Sadakata Japan 17 431 0.6× 566 1.5× 264 0.7× 251 1.3× 173 0.9× 48 1.1k
Nathalie Dehorter Australia 14 633 0.9× 384 1.0× 356 1.0× 53 0.3× 259 1.4× 21 1.1k
Alexis M. Hattox United States 7 742 1.1× 477 1.3× 567 1.5× 64 0.3× 216 1.2× 7 1.2k
Noriaki Ohkawa Japan 16 544 0.8× 357 0.9× 390 1.1× 156 0.8× 163 0.9× 34 1.1k
Nikolai Chub United States 15 608 0.9× 308 0.8× 243 0.7× 264 1.3× 135 0.7× 19 815
Floor J. Stam United States 11 501 0.7× 341 0.9× 183 0.5× 172 0.9× 236 1.3× 11 937

Countries citing papers authored by Henrik Gezelius

Since Specialization
Citations

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

Fields of papers citing papers by Henrik Gezelius

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Henrik Gezelius

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

All Works

17 of 17 papers shown
1.
Gezelius, Henrik, Anders Lundmark, Claes Andersson, et al.. (2025). Ex vivo drug responses and molecular profiles of 597 pediatric acute lymphoblastic leukemia patients. HemaSphere. 9(7). e70176–e70176.
2.
Bunikis, Ignas, Anders Lundmark, Amanda Raine, et al.. (2024). A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing. Life Science Alliance. 7(8). e202302481–e202302481. 2 indexed citations
3.
Gezelius, Henrik, Anders Lundmark, Amanda Raine, et al.. (2024). Comparison of high-throughput single-cell RNA-seq methods for ex vivo drug screening. NAR Genomics and Bioinformatics. 6(1). lqae001–lqae001. 5 indexed citations
4.
Kitazawa, Taro, Onkar Joshi, Hubertus Kohler, et al.. (2021). A unique bipartite Polycomb signature regulates stimulus-response transcription during development. Nature Genetics. 53(3). 379–391. 17 indexed citations
5.
Antón-Bolaños, Noelia, Teresa Guillamón-Vivancos, Francisco J. Martini, et al.. (2019). Prenatal activity from thalamic neurons governs the emergence of functional cortical maps in mice. Science. 364(6444). 987–990. 104 indexed citations
6.
Enjin, Anders, Markus M. Hilscher, Martin Larhammar, et al.. (2017). Developmental Disruption of Recurrent Inhibitory Feedback Results in Compensatory Adaptation in the Renshaw Cell–Motor Neuron Circuit. Journal of Neuroscience. 37(23). 5634–5647. 19 indexed citations
7.
Moreno‐Juan, Verónica, Anton Filipchuk, Noelia Antón-Bolaños, et al.. (2017). Prenatal thalamic waves regulate cortical area size prior to sensory processing. Nature Communications. 8(1). 14172–14172. 103 indexed citations
8.
Gezelius, Henrik, Verónica Moreno‐Juan, Cecilia Mezzera, et al.. (2016). Genetic Labeling of Nuclei-Specific Thalamocortical Neurons Reveals Putative Sensory-Modality Specific Genes. Cerebral Cortex. 27(11). 5054–5069. 13 indexed citations
9.
Gezelius, Henrik & Guillermina López‐Bendito. (2016). Thalamic neuronal specification and early circuit formation. Developmental Neurobiology. 77(7). 830–843. 19 indexed citations
10.
Gezelius, Henrik, Martin Larhammar, Markus M. Hilscher, et al.. (2015). Firing properties of Renshaw cells defined by Chrna2 are modulated by hyperpolarizing and small conductance ion currents Ih and ISK. European Journal of Neuroscience. 41(7). 889–900. 23 indexed citations
11.
Bernhardt, Nadine, Fatima Memic, Henrik Gezelius, et al.. (2012). DCC mediated axon guidance of spinal interneurons is essential for normal locomotor central pattern generator function. Developmental Biology. 366(2). 279–289. 34 indexed citations
12.
Leão, Richardson N., Sanja Mikulovic, Katarina E. Leão, et al.. (2012). OLM interneurons differentially modulate CA3 and entorhinal inputs to hippocampal CA1 neurons. Nature Neuroscience. 15(11). 1524–1530. 250 indexed citations
13.
Enjin, Anders, Stan T. Nakanishi, Anna Vallstedt, et al.. (2010). Identification of novel spinal cholinergic genetic subtypes disclose Chodl and Pitx2 as markers for fast motor neurons and partition cells. The Journal of Comparative Neurology. 518(12). 2284–2304. 89 indexed citations
14.
Gezelius, Henrik, et al.. (2009). Netrin-1-Dependent Spinal Interneuron Subtypes Are Required for the Formation of Left-Right Alternating Locomotor Circuitry. Journal of Neuroscience. 29(50). 15642–15649. 54 indexed citations
15.
Wegmeyer, Heike, Joaquim Egea, Henrik Gezelius, et al.. (2007). EphA4-Dependent Axon Guidance Is Mediated by the RacGAP α2-Chimaerin. Neuron. 55(5). 756–767. 115 indexed citations
16.
Gezelius, Henrik, Åsa Wallén‐Mackenzie, Anders Enjin, Malin C. Lagerström, & Klas Kullander. (2006). Role of glutamate in locomotor rhythm generating neuronal circuitry. Journal of Physiology-Paris. 100(5-6). 297–303. 21 indexed citations
17.
Wallén‐Mackenzie, Åsa, Henrik Gezelius, Muriel Thoby‐Brisson, et al.. (2006). Vesicular Glutamate Transporter 2 Is Required for Central Respiratory Rhythm Generation But Not for Locomotor Central Pattern Generation. Journal of Neuroscience. 26(47). 12294–12307. 159 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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