Nancy Bubula

570 total citations
19 papers, 425 citations indexed

About

Nancy Bubula is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Nancy Bubula has authored 19 papers receiving a total of 425 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Cellular and Molecular Neuroscience, 7 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Nancy Bubula's work include Neurotransmitter Receptor Influence on Behavior (16 papers), Neuroscience and Neuropharmacology Research (11 papers) and Receptor Mechanisms and Signaling (6 papers). Nancy Bubula is often cited by papers focused on Neurotransmitter Receptor Influence on Behavior (16 papers), Neuroscience and Neuropharmacology Research (11 papers) and Receptor Mechanisms and Signaling (6 papers). Nancy Bubula collaborates with scholars based in United States, United Kingdom and Bulgaria. Nancy Bubula's co-authors include Paul Vezina, Alfred Heller, Lisa Won, David Weinshenker, Darlene A. Mitrano, Jason P. Schroeder, Yoland Smith, Jessica A. Loweth, Bryan F. Singer and Dongdong Li and has published in prestigious journals such as Journal of Neuroscience, Annals of the New York Academy of Sciences and Journal of Neurochemistry.

In The Last Decade

Nancy Bubula

19 papers receiving 416 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nancy Bubula United States 12 288 146 74 72 44 19 425
Shu‐E Yan United States 9 322 1.1× 169 1.2× 54 0.7× 58 0.8× 36 0.8× 11 426
Monika Vrajová Czechia 9 264 0.9× 132 0.9× 93 1.3× 36 0.5× 64 1.5× 12 428
Tracy M. Reed United States 8 198 0.7× 167 1.1× 67 0.9× 63 0.9× 107 2.4× 8 370
Hannah G. Sexton United States 12 192 0.7× 130 0.9× 83 1.1× 44 0.6× 50 1.1× 18 385
Alberto Casti Italy 11 233 0.8× 99 0.7× 46 0.6× 35 0.5× 156 3.5× 17 429
Björn Steiniger‐Brach Denmark 15 250 0.9× 140 1.0× 99 1.3× 94 1.3× 63 1.4× 21 523
Christina M. Ruiz United States 9 214 0.7× 105 0.7× 53 0.7× 34 0.5× 122 2.8× 12 383
Evan N. Graf United States 10 241 0.8× 90 0.6× 76 1.0× 46 0.6× 50 1.1× 12 464
Concepción Vaquero‐Lorenzo Spain 11 146 0.5× 103 0.7× 65 0.9× 27 0.4× 72 1.6× 18 433
Shohreh M. Rezazadeh United States 12 299 1.0× 141 1.0× 65 0.9× 19 0.3× 25 0.6× 18 407

Countries citing papers authored by Nancy Bubula

Since Specialization
Citations

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

Fields of papers citing papers by Nancy Bubula

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nancy Bubula

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

All Works

19 of 19 papers shown
1.
Baker, Lorinda K., et al.. (2022). Conditioned inhibition of amphetamine sensitization. Neurobiology of Learning and Memory. 192. 107636–107636. 7 indexed citations
2.
Mascia, Paola, et al.. (2018). Exposure to conditions of uncertainty promotes the pursuit of amphetamine. Neuropsychopharmacology. 44(2). 274–280. 34 indexed citations
4.
Steidl, Stephan, et al.. (2017). Operant responding for optogenetic excitation of LDTg inputs to the VTA requires D1 and D2 dopamine receptor activation in the NAcc. Behavioural Brain Research. 333. 161–170. 19 indexed citations
5.
Singer, Bryan F., et al.. (2016). Drug-Paired Contextual Stimuli Increase Dendritic Spine Dynamics in Select Nucleus Accumbens Neurons. Neuropsychopharmacology. 41(8). 2178–2187. 8 indexed citations
6.
Wang, Qiang, Nancy Bubula, Jason Brown, et al.. (2016). PKC phosphorylates residues in the N-terminal of the DA transporter to regulate amphetamine-induced DA efflux. Neuroscience Letters. 622. 78–82. 18 indexed citations
7.
Singer, Bryan F., et al.. (2016). Stimuli associated with the presence or absence of amphetamine regulate cytoskeletal signaling and behavior. European Neuropsychopharmacology. 26(11). 1836–1842. 2 indexed citations
8.
Singer, Bryan F., et al.. (2014). Locomotor conditioning by amphetamine requires cyclin-dependent kinase 5 signaling in the nucleus accumbens. Neuropharmacology. 85. 243–252. 9 indexed citations
9.
Mitrano, Darlene A., Jason P. Schroeder, Yoland Smith, et al.. (2012). Alpha-1 Adrenergic Receptors are Localized on Presynaptic Elements in the Nucleus Accumbens and Regulate Mesolimbic Dopamine Transmission. Neuropsychopharmacology. 37(9). 2161–2172. 83 indexed citations
10.
Li, Dongdong, Nancy Bubula, Elena Nikitina, et al.. (2011). Casein kinase 1 enables nucleus accumbens amphetamine‐induced locomotion by regulating AMPA receptor phosphorylation. Journal of Neurochemistry. 118(2). 237–247. 32 indexed citations
11.
Loweth, Jessica A., Bryan F. Singer, Lorinda K. Baker, et al.. (2010). Transient Overexpression of α-Ca2+/Calmodulin-Dependent Protein Kinase II in the Nucleus Accumbens Shell Enhances Behavioral Responding to Amphetamine. Journal of Neuroscience. 30(3). 939–949. 60 indexed citations
12.
Heller, Alfred, et al.. (2004). Long-chain fatty acids increase cellular dopamine in an immortalized cell line (MN9D) derived from mouse mesencephalon. Neuroscience Letters. 376(1). 35–39. 16 indexed citations
14.
Heller, Alfred, et al.. (2003). Dopaminergic Stimulatory Polypeptides from Immortalized Striatal Cells. Annals of the New York Academy of Sciences. 991(1). 339–341. 1 indexed citations
15.
Won, Lisa, Nancy Bubula, & Alfred Heller. (2002). Fetal exposure to (±)-methylenedioxymethamphetamine in utero enhances the development and metabolism of serotonergic neurons in three-dimensional reaggregate tissue culture. Developmental Brain Research. 137(1). 67–73. 14 indexed citations
16.
Heller, Alfred, Nancy Bubula, Robert Lew, Bárbara Heller, & Lisa Won. (2001). Gender-Dependent Enhanced Adult Neurotoxic Response to Methamphetamine following Fetal Exposure to the Drug. Journal of Pharmacology and Experimental Therapeutics. 298(2). 769–779. 37 indexed citations
17.
Won, Lisa, Nancy Bubula, & Alfred Heller. (2001). Fetal exposure to methamphetamine in utero stimulates development of serotonergic neurons in three‐dimensional reaggregate tissue culture. Synapse. 43(2). 139–144. 7 indexed citations
18.
Heller, Alfred, et al.. (2001). Elevation of fetal dopamine following exposure to methamphetamine in utero. Developmental Brain Research. 130(1). 139–142. 14 indexed citations
19.
Won, Lisa, et al.. (2001). Methamphetamine concentrations in fetal and maternal brain following prenatal exposure. Neurotoxicology and Teratology. 23(4). 349–354. 48 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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