B. W. Ache

2.1k total citations
46 papers, 1.8k citations indexed

About

B. W. Ache is a scholar working on Cellular and Molecular Neuroscience, Sensory Systems and Nutrition and Dietetics. According to data from OpenAlex, B. W. Ache has authored 46 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Cellular and Molecular Neuroscience, 37 papers in Sensory Systems and 16 papers in Nutrition and Dietetics. Recurrent topics in B. W. Ache's work include Neurobiology and Insect Physiology Research (44 papers), Olfactory and Sensory Function Studies (36 papers) and Biochemical Analysis and Sensing Techniques (16 papers). B. W. Ache is often cited by papers focused on Neurobiology and Insect Physiology Research (44 papers), Olfactory and Sensory Function Studies (36 papers) and Biochemical Analysis and Sensing Techniques (16 papers). B. W. Ache collaborates with scholars based in United States, Germany and New Zealand. B. W. Ache's co-authors include W. C. Michel, Debra Ann Fadool, Timothy S. McClintock, Manfred Schmidt, Matt Wachowiak, Hanns Hatt, A.B. Zhainazarov, Yuriy V. Bobkov, Charles D. Derby and Ingrid Boekhoff and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Neuron.

In The Last Decade

B. W. Ache

46 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
B. W. Ache United States	25	1.5k	995	469	394	258	46	1.8k
Timothy S. McClintock United States	28	1.1k 0.8×	994 1.0×	664 1.4×	149 0.4×	160 0.6×	61	1.9k
John H. Teeter United States	29	977 0.7×	1.2k 1.2×	1.0k 2.2×	164 0.4×	263 1.0×	59	2.3k
Barry W. Ache United States	32	2.2k 1.5×	1.2k 1.2×	536 1.1×	652 1.7×	783 3.0×	83	3.0k
John Caprio United States	34	1.5k 1.0×	1.7k 1.7×	1.3k 2.8×	121 0.3×	443 1.7×	87	3.1k
Heather L. Eisthen United States	19	670 0.5×	660 0.7×	381 0.8×	56 0.1×	111 0.4×	30	1.3k
David G. Moulton United States	22	697 0.5×	1.3k 1.3×	599 1.3×	140 0.4×	100 0.4×	33	1.9k
Lynne A. Oland United States	20	1.0k 0.7×	529 0.5×	225 0.5×	206 0.5×	56 0.2×	40	1.2k
DeForest Mellon United States	24	1.1k 0.7×	206 0.2×	56 0.1×	253 0.6×	569 2.2×	66	1.6k
Anupama Dahanukar United States	26	2.8k 1.9×	507 0.5×	811 1.7×	1.5k 3.9×	270 1.0×	44	3.5k
W. Daniel Tracey United States	21	1.7k 1.2×	446 0.4×	106 0.2×	512 1.3×	285 1.1×	36	2.6k

Countries citing papers authored by B. W. Ache

Since Specialization

Citations

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

Fields of papers citing papers by B. W. Ache

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by B. W. Ache. 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 B. W. Ache. The network helps show where B. W. Ache may publish in the future.

Co-authorship network of co-authors of B. W. Ache

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

All Works

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20 of 20 papers shown

Ukhanov, Kirill, Yuriy V. Bobkov, Elizabeth A. Corey, & B. W. Ache. (2014). Ligand-selective activation of heterologously-expressed mammalian olfactory receptor. Cell Calcium. 56(4). 245–256. 5 indexed citations

Bobkov, Yuriy V., Elizabeth A. Corey, & B. W. Ache. (2014). An inhibitor of Na+/Ca2+ exchange blocks activation of insect olfactory receptors. Biochemical and Biophysical Research Communications. 450(2). 1104–1109. 6 indexed citations

Ukhanov, Kirill, Yuriy V. Bobkov, & B. W. Ache. (2011). Imaging ensemble activity in arthropod olfactory receptor neurons in situ. Cell Calcium. 49(2). 100–107. 17 indexed citations

Bobkov, Yuriy V., Elizabeth A. Corey, & B. W. Ache. (2010). The pore properties of human nociceptor channel TRPA1 evaluated in single channel recordings. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1808(4). 1120–1128. 28 indexed citations

Brunert, Daniela, et al.. (2010). PI3K -Dependent Signaling in Mouse Olfactory Receptor Neurons. Chemical Senses. 35(4). 301–308. 16 indexed citations

Bobkov, Yuriy V., et al.. (2009). The Na⁺/Ca²⁺Exchanger Inhibitor, KB-R7943, Blocks a Nonselective Cation Channel Implicated in Chemosensory Transduction. Journal of Neurophysiology. 101(3). 1151–1159. 15 indexed citations

Corey, Elizabeth A., et al.. (2009). Odorant-stimulated phosphoinositide signaling in mammalian olfactory receptor neurons. Cellular Signalling. 22(1). 150–157. 25 indexed citations

McClintock, Timothy S., B. W. Ache, & Charles D. Derby. (2006). Lobster olfactory genomics. Integrative and Comparative Biology. 46(6). 940–947. 13 indexed citations

Bobkov, Yuriy V. & B. W. Ache. (2006). Intrinsically Bursting Olfactory Receptor Neurons. Journal of Neurophysiology. 97(2). 1052–1057. 25 indexed citations

10.

Zhainazarov, A.B., Marc Spehr, Christian H. Wetzel, Hanns Hatt, & B. W. Ache. (2004). Modulation of the Olfactory CNG Channel by Ptdlns(3,4,5)P3. The Journal of Membrane Biology. 201(1). 51–57. 52 indexed citations

11.

Wachowiak, Matt, Carol E. Diebel, & B. W. Ache. (1997). Local Interneurons Define Functionally Distinct Regions Within Lobster Olfactory Glomeruli. Journal of Experimental Biology. 200(6). 989–1001. 24 indexed citations

12.

Fadool, Debra Ann, et al.. (1995). Evidence that a G_q-protein Mediates Excitatory Odor Transduction in Lobster Olfactory Receptor Neurons. Chemical Senses. 20(5). 489–498. 31 indexed citations

13.

Michel, W. C. & B. W. Ache. (1994). Odor-evoked inhibition in primary olfactory receptor neurons. Chemical Senses. 19(1). 11–24. 46 indexed citations

14.

Orona, Edward & B. W. Ache. (1992). Physiological and pharmacological evidence for histamine as a neurotransmitter in the olfactory CNS of the spiny lobster. Brain Research. 590(1-2). 136–143. 15 indexed citations

15.

Michel, W. C. & B. W. Ache. (1992). Cyclic nucleotides mediate an odor-evoked potassium conductance in lobster olfactory receptor cells. Journal of Neuroscience. 12(10). 3979–3984. 89 indexed citations

16.

Fadool, Debra Ann, W. C. Michel, & B. W. Ache. (1991). Sustained primary culture of lobster (Panulirus argus) olfactory receptor neurons. Tissue and Cell. 23(5). 719–731. 21 indexed citations

17.

McClintock, Timothy S. & B. W. Ache. (1989). Ionic currents and ion channels of lobster olfactory receptor neurons.. The Journal of General Physiology. 94(6). 1085–1099. 27 indexed citations

18.

Carr, William E. S., B. W. Ache, & Richard A. Gleeson. (1987). Chemoreceptors of crustaceans: similarities to receptors for neuroactive substances in internal tissues.. Environmental Health Perspectives. 71. 31–46. 43 indexed citations

19.

Ache, B. W.. (1987). Insect Chemoreception: Mechanisms in Insect Olfaction.. Science. 236(4799). 341–341. 3 indexed citations

20.

Ache, B. W., Zoltan M. Fuzessery, & William E. S. Carr. (1976). ANTENNULAR CHEMOSENSITIVITY IN THE SPINY LOBSTER, PANULIRUS ARGUS: COMPARATIVE TESTS OF HIGH AND LOW MOLECULAR WEIGHT STIMULANTS. Biological Bulletin. 151(2). 273–282. 28 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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