Beáta Búzás

1.8k total citations
25 papers, 1.1k citations indexed

About

Beáta Búzás is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Beáta Búzás has authored 25 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 6 papers in Physiology. Recurrent topics in Beáta Búzás's work include Receptor Mechanisms and Signaling (16 papers), Neuropeptides and Animal Physiology (16 papers) and Neurotransmitter Receptor Influence on Behavior (5 papers). Beáta Búzás is often cited by papers focused on Receptor Mechanisms and Signaling (16 papers), Neuropeptides and Animal Physiology (16 papers) and Neurotransmitter Receptor Influence on Behavior (5 papers). Beáta Búzás collaborates with scholars based in United States, United Kingdom and Hungary. Beáta Búzás's co-authors include Brian M. Cox, John Rosenberger, David Goldman, György Petrovics, Daniel S. Pine, Sari Izenwasser, Colin A. Hodgkinson, Jennifer Y. F. Lau, Monique Ernst and Eric E. Nelson and has published in prestigious journals such as Journal of Neuroscience, NeuroImage and Biological Psychiatry.

In The Last Decade

Beáta Búzás

25 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
Beáta Búzás United States 20 649 505 185 179 113 25 1.1k
Arnauld Belmer Australia 21 626 1.0× 404 0.8× 178 1.0× 197 1.1× 150 1.3× 47 1.3k
Carrie L. Wade United States 12 557 0.9× 295 0.6× 368 2.0× 114 0.6× 74 0.7× 15 1.0k
Valérie Compan France 21 853 1.3× 539 1.1× 180 1.0× 210 1.2× 163 1.4× 39 1.4k
Hilary R. Smith United States 19 1.2k 1.8× 510 1.0× 80 0.4× 459 2.6× 79 0.7× 38 1.5k
Masahiro Nankai Japan 17 498 0.8× 313 0.6× 72 0.4× 147 0.8× 103 0.9× 25 932
Daniel I. Brierley United Kingdom 14 677 1.0× 400 0.8× 267 1.4× 395 2.2× 150 1.3× 16 1.5k
Haruo Shibuya Japan 17 675 1.0× 489 1.0× 167 0.9× 99 0.6× 64 0.6× 32 1.1k
Tomo Okochi Japan 23 465 0.7× 481 1.0× 168 0.9× 223 1.2× 104 0.9× 58 1.5k
Carrol D’Sa United States 14 772 1.2× 430 0.9× 151 0.8× 197 1.1× 78 0.7× 15 1.6k
Jonathan D. Hommel United States 16 535 0.8× 590 1.2× 449 2.4× 254 1.4× 187 1.7× 36 1.9k

Countries citing papers authored by Beáta Búzás

Since Specialization
Citations

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

Fields of papers citing papers by Beáta Búzás

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beáta Búzás

This figure shows the co-authorship network connecting the top 25 collaborators of Beáta Búzás. A scholar is included among the top collaborators of Beáta Búzás 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 Beáta Búzás. Beáta Búzás 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.
Lau, Jennifer Y. F., David Goldman, Beáta Búzás, et al.. (2009). BDNF gene polymorphism (Val66Met) predicts amygdala and anterior hippocampus responses to emotional faces in anxious and depressed adolescents. NeuroImage. 53(3). 952–961. 92 indexed citations
2.
Srivastava, Vibhuti, Beáta Búzás, Reza Momenan, et al.. (2009). Association of SOD2, a Mitochondrial Antioxidant Enzyme, with Gray Matter Volume Shrinkage in Alcoholics. Neuropsychopharmacology. 35(5). 1120–1128. 20 indexed citations
3.
Mellman, Thomas A., Tanya N. Alim, Elena Gorodetsky, et al.. (2009). Serotonin polymorphisms and posttraumatic stress disorder in a trauma exposed African American population. Depression and Anxiety. 26(11). 993–997. 49 indexed citations
4.
Lau, Jennifer Y. F., David Goldman, Beáta Búzás, et al.. (2008). Amygdala Function and 5-HTT Gene Variants in Adolescent Anxiety and Major Depressive Disorder. Biological Psychiatry. 65(4). 349–355. 89 indexed citations
5.
Marsh, Abigail A., Elizabeth Finger, Beáta Búzás, et al.. (2006). Impaired recognition of fear facial expressions in 5-HTTLPR S-polymorphism carriers following tryptophan depletion. Psychopharmacology. 189(3). 387–394. 41 indexed citations
6.
Finger, Elizabeth, Abigail A. Marsh, Beáta Búzás, et al.. (2006). The Impact of Tryptophan Depletion and 5-HTTLPR Genotype on Passive Avoidance and Response Reversal Instrumental Learning Tasks. Neuropsychopharmacology. 32(1). 206–215. 66 indexed citations
7.
Marti, Matteo, F Mela, Martina Fantin, et al.. (2005). Blockade of Nociceptin/Orphanin FQ Transmission Attenuates Symptoms and Neurodegeneration Associated with Parkinson's Disease. Journal of Neuroscience. 25(42). 9591–9601. 98 indexed citations
8.
Belfer, Inna, Beáta Búzás, Heather S. Hipp, et al.. (2004). Haplotype structure of the beta adrenergic receptor genes in US Caucasians and African Americans. European Journal of Human Genetics. 13(3). 341–351. 33 indexed citations
9.
Belfer, Inna, Beáta Búzás, Heather S. Hipp, et al.. (2004). Haplotype-based analysis of alpha 2A, 2B, and 2C adrenergic receptor genes captures information on common functional loci at each gene. Journal of Human Genetics. 50(1). 12–20. 45 indexed citations
10.
Búzás, Beáta, et al.. (2002). Inflammatory mediators increase the expression of nociceptin/orphanin FQ in rat astrocytes in culture. Glia. 39(3). 237–246. 43 indexed citations
11.
Búzás, Beáta. (2002). Regulation of nociceptin/orphanin FQ gene expression in astrocytes by ceramide. Neuroreport. 13(14). 1707–1710. 15 indexed citations
12.
Búzás, Beáta, et al.. (1999). Regulation of Nociceptin/Orphanin FQ Gene Expression by Neuropoietic Cytokines and Neurotrophic Factors in Neurons and Astrocytes. Journal of Neurochemistry. 72(5). 1882–1889. 45 indexed citations
13.
Búzás, Beáta, John Rosenberger, & Brian M. Cox. (1998). Activity and Cyclic AMP‐Dependent Regulation of Nociceptin/Orphanin FQ Gene Expression in Primary Neuronal and Astrocyte Cultures. Journal of Neurochemistry. 71(2). 556–563. 33 indexed citations
14.
Búzás, Beáta, John Rosenberger, & Brian M. Cox. (1998). Ca2+/Calmodulin‐Dependent Transcriptional Activation of δ‐Opioid Receptor Gene Expression Induced by Membrane Depolarization in NG108‐15 Cells. Journal of Neurochemistry. 70(1). 105–112. 14 indexed citations
15.
Búzás, Beáta, John Rosenberger, & Brian M. Cox. (1997). Regulation of δ‐Opioid Receptor mRNA Levels by Receptor‐Mediated and Direct Activation of the Adenylyl Cyclase‐Protein Kinase A Pathway. Journal of Neurochemistry. 68(2). 610–615. 14 indexed citations
16.
Búzás, Beáta, John Rosenberger, & Brian M. Cox. (1996). Mu and delta opioid receptor gene expression after chronic treatment with opioid agonist. Neuroreport. 7(9). 1505–1508. 48 indexed citations
17.
Azaryan, Anahit V., et al.. (1996). Effect of Chronic Cocaine Treatment on μ‐ and δ‐Opioid Receptor mRNA Levels in Dopaminergically Innervated Brain Regions. Journal of Neurochemistry. 66(2). 443–448. 74 indexed citations
18.
Búzás, Beáta, et al.. (1994). Evidence for delta opioid receptor subtypes regulating adenylyl cyclase activity in rat brain. Life Sciences. 54(7). PL101–PL106. 42 indexed citations
19.
Búzás, Beáta, et al.. (1993). Highly potent novel opioid receptor agonist in the 14-alkoxymetopon series. European Journal of Pharmacology. 236(2). 209–215. 45 indexed citations
20.
Horváth, Gábor, et al.. (1992). Impact of the stringency of cell selection on plastid segregation in protoplast fusion-derived Nicotiana regenerates. Theoretical and Applied Genetics. 84-84(7-8). 866–873. 7 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026