Thomas Bozza

3.1k total citations
25 papers, 2.3k citations indexed

About

Thomas Bozza is a scholar working on Sensory Systems, Cellular and Molecular Neuroscience and Nutrition and Dietetics. According to data from OpenAlex, Thomas Bozza has authored 25 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Sensory Systems, 23 papers in Cellular and Molecular Neuroscience and 18 papers in Nutrition and Dietetics. Recurrent topics in Thomas Bozza's work include Olfactory and Sensory Function Studies (24 papers), Neurobiology and Insect Physiology Research (23 papers) and Biochemical Analysis and Sensing Techniques (18 papers). Thomas Bozza is often cited by papers focused on Olfactory and Sensory Function Studies (24 papers), Neurobiology and Insect Physiology Research (23 papers) and Biochemical Analysis and Sensing Techniques (18 papers). Thomas Bozza collaborates with scholars based in United States, United Kingdom and Philippines. Thomas Bozza's co-authors include Peter Mombaerts, Paul Feinstein, Dmitry Rinberg, Iván Rodríguez, Zheng Chen, Rodrigo Pacifico, Matt Wachowiak, John P. McGann, Anne Vassalli and Adam Dewan and has published in prestigious journals such as Nature, Cell and Nature Communications.

In The Last Decade

Thomas Bozza

25 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Bozza United States 19 1.9k 1.7k 1.2k 450 202 25 2.3k
Roberto Tirindelli Italy 26 1.7k 0.9× 1.4k 0.8× 1.2k 1.0× 259 0.6× 300 1.5× 54 2.3k
Johannes Reisert United States 28 1.8k 1.0× 1.8k 1.0× 1.1k 0.9× 452 1.0× 604 3.0× 53 2.5k
Minghong Ma United States 32 1.8k 1.0× 1.6k 0.9× 1.2k 1.0× 525 1.2× 362 1.8× 71 2.7k
Takashi Kurahashi Japan 23 1.4k 0.8× 1.5k 0.9× 878 0.7× 411 0.9× 437 2.2× 43 2.0k
Hitoshi Sakano Japan 20 1.3k 0.7× 1.1k 0.6× 831 0.7× 293 0.7× 181 0.9× 48 1.8k
Reiko Kobayakawa Japan 14 1.1k 0.6× 989 0.6× 633 0.5× 235 0.5× 128 0.6× 20 1.6k
Shin Nagayama Japan 18 1.0k 0.5× 1.0k 0.6× 528 0.4× 350 0.8× 355 1.8× 29 1.7k
Ko Kobayakawa Japan 16 947 0.5× 842 0.5× 554 0.4× 214 0.5× 190 0.9× 26 1.5k
Xavier Grosmaître France 16 797 0.4× 676 0.4× 553 0.4× 234 0.5× 66 0.3× 29 1.1k
Nathan E. Schoppa United States 22 1.5k 0.8× 2.0k 1.2× 738 0.6× 371 0.8× 1.1k 5.7× 34 2.8k

Countries citing papers authored by Thomas Bozza

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Bozza

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Bozza

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Bozza. A scholar is included among the top collaborators of Thomas Bozza 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 Thomas Bozza. Thomas Bozza 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.
Wachowiak, Matt, et al.. (2025). Recalibrating Olfactory Neuroscience to the Range of Naturally Occurring Odor Concentrations. Journal of Neuroscience. 45(10). e1872242024–e1872242024. 2 indexed citations
2.
Shah, Ami N., et al.. (2021). Olfactory expression of trace amine-associated receptors requires cooperative cis-acting enhancers. Nature Communications. 12(1). 3797–3797. 13 indexed citations
3.
Tsukahara, Tatsuya, David H. Brann, Stan L. Pashkovski, et al.. (2021). A transcriptional rheostat couples past activity to future sensory responses. Cell. 184(26). 6326–6343.e32. 42 indexed citations
4.
Shor, Erez, Adam Dewan, Ilke Uguz, et al.. (2021). Sensitive and robust chemical detection using an olfactory brain-computer interface. Biosensors and Bioelectronics. 195. 113664–113664. 11 indexed citations
5.
Rabinowitz, Neil C., et al.. (2018). Stimulus dependent diversity and stereotypy in the output of an olfactory functional unit. Nature Communications. 9(1). 1347–1347. 27 indexed citations
6.
Braubach, Oliver, et al.. (2018). Sparsened neuronal activity in an optogenetically activated olfactory glomerulus. Scientific Reports. 8(1). 14955–14955. 4 indexed citations
7.
Dewan, Adam, Annika Cichy, Jingji Zhang, et al.. (2018). Single olfactory receptors set odor detection thresholds. Nature Communications. 9(1). 2887–2887. 60 indexed citations
8.
Zhang, Jingji, et al.. (2013). Ultrasensitive Detection of Amines by a Trace Amine-Associated Receptor. Journal of Neuroscience. 33(7). 3228–3239. 68 indexed citations
9.
Dewan, Adam, et al.. (2013). Non-redundant coding of aversive odours in the main olfactory pathway. Nature. 497(7450). 486–489. 132 indexed citations
10.
Smear, Matthew C., et al.. (2013). Multiple perceptible signals from a single olfactory glomerulus. Nature Neuroscience. 16(11). 1687–1691. 90 indexed citations
11.
Pacifico, Rodrigo, et al.. (2012). An Olfactory Subsystem that Mediates High-Sensitivity Detection of Volatile Amines. Cell Reports. 2(1). 76–88. 97 indexed citations
12.
Zhang, Jingji, et al.. (2012). Uncoupling stimulus specificity and glomerular position in the mouse olfactory system. Molecular and Cellular Neuroscience. 51(3-4). 79–88. 31 indexed citations
13.
Rajapaksha, Tharinda W., William A. Eimer, Thomas Bozza, & Robert Vassar. (2011). The Alzheimer's β-secretase enzyme BACE1 is required for accurate axon guidance of olfactory sensory neurons and normal glomerulus formation in the olfactory bulb. Molecular Neurodegeneration. 6(1). 88–88. 84 indexed citations
14.
Smear, Matthew C., Roman Shusterman, Rodney P. O’Connor, Thomas Bozza, & Dmitry Rinberg. (2011). Perception of sniff phase in mouse olfaction. Nature. 479(7373). 397–400. 172 indexed citations
15.
Bozza, Thomas, Anne Vassalli, Stefan H. Fuss, et al.. (2009). Mapping of Class I and Class II Odorant Receptors to Glomerular Domains by Two Distinct Types of Olfactory Sensory Neurons in the Mouse. Neuron. 61(2). 220–233. 151 indexed citations
16.
Feinstein, Paul, Thomas Bozza, Iván Rodríguez, Anne Vassalli, & Peter Mombaerts. (2004). Axon Guidance of Mouse Olfactory Sensory Neurons by Odorant Receptors and the β2 Adrenergic Receptor. Cell. 117(6). 833–846. 237 indexed citations
17.
Bozza, Thomas, John P. McGann, Peter Mombaerts, & Matt Wachowiak. (2004). In Vivo Imaging of Neuronal Activity by Targeted Expression of a Genetically Encoded Probe in the Mouse. Neuron. 42(1). 9–21. 274 indexed citations
18.
Bozza, Thomas & Peter Mombaerts. (2001). Olfactory coding: Revealing intrinsic representations of odors. Current Biology. 11(17). R687–R690. 27 indexed citations
19.
Zheng, Chen, Paul Feinstein, Thomas Bozza, Iván Rodríguez, & Peter Mombaerts. (2000). Peripheral Olfactory Projections Are Differentially Affected in Mice Deficient in a Cyclic Nucleotide-Gated Channel Subunit. Neuron. 26(1). 81–91. 206 indexed citations
20.
Alkasab, Tarik K., Thomas Bozza, Thomas A. Cleland, et al.. (1999). Characterizing complex chemosensors: information-theoretic analysis of olfactory systems. Trends in Neurosciences. 22(3). 102–108. 18 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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