Zac Pujic

2.8k total citations
38 papers, 1.1k citations indexed

About

Zac Pujic is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Zac Pujic has authored 38 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 20 papers in Cellular and Molecular Neuroscience and 17 papers in Cell Biology. Recurrent topics in Zac Pujic's work include Axon Guidance and Neuronal Signaling (13 papers), Neuroscience and Neuropharmacology Research (9 papers) and Neurogenesis and neuroplasticity mechanisms (9 papers). Zac Pujic is often cited by papers focused on Axon Guidance and Neuronal Signaling (13 papers), Neuroscience and Neuropharmacology Research (9 papers) and Neurogenesis and neuroplasticity mechanisms (9 papers). Zac Pujic collaborates with scholars based in Australia, United States and United Kingdom. Zac Pujic's co-authors include Geoffrey J. Goodhill, Jarema Malicki, Duncan Mortimer, Hakryul Jo, Linda J. Richards, Thomas Fothergill, Irina Vetter, Julia Feldner, Peter A. Wilce and Lilach Avitan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and Trends in Neurosciences.

In The Last Decade

Zac Pujic

37 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zac Pujic Australia 20 512 490 420 142 136 38 1.1k
Chuansheng Zhang China 15 447 0.9× 391 0.8× 197 0.5× 118 0.8× 74 0.5× 53 994
S R Heidemann United States 23 845 1.7× 844 1.7× 1.7k 4.0× 190 1.3× 284 2.1× 24 2.4k
Hideru Togashi Japan 15 721 1.4× 516 1.1× 394 0.9× 92 0.6× 53 0.4× 34 1.2k
Cora S. Thiel Germany 20 588 1.1× 244 0.5× 239 0.6× 92 0.6× 101 0.7× 42 2.2k
Max A. Tischfield United States 17 812 1.6× 454 0.9× 325 0.8× 114 0.8× 14 0.1× 27 1.6k
Jason R. Meyers United States 13 999 2.0× 259 0.5× 464 1.1× 182 1.3× 103 0.8× 15 1.7k
Yoshito Masamizu Japan 15 984 1.9× 393 0.8× 150 0.4× 86 0.6× 50 0.4× 20 1.5k
Stephen G. Turney United States 12 484 0.9× 393 0.8× 275 0.7× 67 0.5× 118 0.9× 17 960
Sylvie Gory‐Fauré France 18 608 1.2× 293 0.6× 406 1.0× 72 0.5× 66 0.5× 28 1.1k
Andrew Prendergast United States 16 356 0.7× 244 0.5× 415 1.0× 160 1.1× 41 0.3× 24 920

Countries citing papers authored by Zac Pujic

Since Specialization
Citations

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

Fields of papers citing papers by Zac Pujic

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zac Pujic

This figure shows the co-authorship network connecting the top 25 collaborators of Zac Pujic. A scholar is included among the top collaborators of Zac Pujic 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 Zac Pujic. Zac Pujic 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.
Zhu, Shuyu, et al.. (2023). fmr1Mutation Alters the Early Development of Sensory Coding and Hunting and Social Behaviors in Larval Zebrafish. Journal of Neuroscience. 43(7). 1211–1224. 6 indexed citations
2.
Avitan, Lilach, et al.. (2020). Behavioral Signatures of a Developing Neural Code. Current Biology. 30(17). 3352–3363.e5. 15 indexed citations
3.
Pujic, Zac, et al.. (2020). Model-based decoupling of evoked and spontaneous neural activity in calcium imaging data. PLoS Computational Biology. 16(11). e1008330–e1008330. 15 indexed citations
4.
Avitan, Lilach, et al.. (2020). Behavioral Signatures of a Developing Neural Code. Current Biology. 30(17). 3491–3493.
5.
Bicknell, Brendan A., Zac Pujic, Julia Feldner, Irina Vetter, & Geoffrey J. Goodhill. (2018). Chemotactic responses of growing neurites to precisely controlled gradients of nerve growth factor. Scientific Data. 5(1). 180183–180183. 8 indexed citations
6.
Bicknell, Brendan A., Zac Pujic, Peter Dayan, & Geoffrey J. Goodhill. (2018). Control of neurite growth and guidance by an inhibitory cell-body signal. PLoS Computational Biology. 14(6). e1006218–e1006218. 10 indexed citations
7.
Avitan, Lilach, Zac Pujic, Biao Sun, et al.. (2017). Spontaneous Activity in the Zebrafish Tectum Reorganizes over Development and Is Influenced by Visual Experience. Current Biology. 27(16). 2407–2419.e4. 55 indexed citations
8.
Pujic, Zac, et al.. (2014). Calcium signaling in axon guidance. Trends in Neurosciences. 37(8). 424–432. 60 indexed citations
9.
Thompson, Andrew W., Zac Pujic, Linda J. Richards, & Geoffrey J. Goodhill. (2011). Cyclic nucleotide-dependent switching of mammalian axon guidance depends on gradient steepness. Molecular and Cellular Neuroscience. 47(1). 45–52. 16 indexed citations
10.
Pujic, Zac, et al.. (2008). Analysis of the growth cone turning assay for studying axon guidance. Journal of Neuroscience Methods. 170(2). 220–228. 39 indexed citations
11.
Mortimer, Duncan, Thomas Fothergill, Zac Pujic, Linda J. Richards, & Geoffrey J. Goodhill. (2008). Growth cone chemotaxis. Trends in Neurosciences. 31(2). 90–98. 120 indexed citations
12.
Pujic, Zac, Yoshihiro Omori, Motokazu Tsujikawa, et al.. (2006). Reverse genetic analysis of neurogenesis in the zebrafish retina. Developmental Biology. 293(2). 330–347. 43 indexed citations
13.
Malicki, Jarema, Hakryul Jo, & Zac Pujic. (2003). Zebrafish N-cadherin, encoded by the glass onion locus, plays an essential role in retinal patterning. Developmental Biology. 259(1). 95–108. 102 indexed citations
14.
Malicki, Jarema, Zac Pujic, Christine Thisse, Bernard Thisse, & Xiangyun Wei. (2002). Forward and reverse genetic approaches to the analysis of eye development in zebrafish. Vision Research. 42(4). 527–533. 29 indexed citations
16.
Goodenough, Sharon, Wenbin Chen, Alison M. Beckmann, et al.. (1997). Immediate Early Gene Expression and Delayed Cell Death in Limbic Areas of the Rat Brain after Kainic Acid Treatment and Recovery in the Cold. Experimental Neurology. 145(2). 451–461. 25 indexed citations
17.
Savage, NW, et al.. (1997). Immunohistochemical localization of mast cells and mast cell‐nerve interactions in oral lichen planus. Oral Diseases. 3(2). 71–76. 39 indexed citations
18.
19.
Pujic, Zac, Izuru Matsumoto, & Peter A. Wilce. (1995). Expression of the Genes Coding for Ornithine Decarboxylase and Its Regulatory Protein Antizyme in the Developing Rat Brain. Developmental Neuroscience. 17(5-6). 286–291. 5 indexed citations
20.
Pujic, Zac, Izuru Matsumoto, & Peter A. Wilce. (1993). Expression of the gene coding for the NR1 subunit of the NMDA receptor during rat brain development. Neuroscience Letters. 162(1-2). 67–70. 27 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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