Robert L. Jakab

2.0k total citations
29 papers, 1.6k citations indexed

About

Robert L. Jakab is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Robert L. Jakab has authored 29 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cellular and Molecular Neuroscience, 13 papers in Molecular Biology and 7 papers in Cognitive Neuroscience. Recurrent topics in Robert L. Jakab's work include Neuroscience and Neuropharmacology Research (13 papers), Neurotransmitter Receptor Influence on Behavior (8 papers) and Memory and Neural Mechanisms (5 papers). Robert L. Jakab is often cited by papers focused on Neuroscience and Neuropharmacology Research (13 papers), Neurotransmitter Receptor Influence on Behavior (8 papers) and Memory and Neural Mechanisms (5 papers). Robert L. Jakab collaborates with scholars based in United States, Japan and Hungary. Robert L. Jakab's co-authors include Patricia S. Goldman‐Rakic, Anne Collaco, Nadia A. Ameen, Patricia S. Goldman‐Rakic, Frederick Naftolin, Csaba Léránth, Tamás L. Horváth, Jacques Balthazart, Csaba Leranth and Scott M. Belcher and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Robert L. Jakab

29 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Robert L. Jakab United States	20	878	600	309	222	154	29	1.6k
Hisayuki Funahashi Japan	26	455 0.5×	445 0.7×	943 3.1×	93 0.4×	122 0.8×	47	3.3k
Jana Velı́šková United States	37	2.2k 2.5×	920 1.5×	453 1.5×	449 2.0×	123 0.8×	111	3.8k
Shane T. Hentges United States	26	651 0.7×	605 1.0×	391 1.3×	127 0.6×	132 0.9×	51	2.4k
Shuichi Koda Japan	13	683 0.8×	431 0.7×	541 1.8×	82 0.4×	241 1.6×	18	2.9k
W. John Sheward United Kingdom	28	1.5k 1.7×	802 1.3×	301 1.0×	130 0.6×	626 4.1×	42	2.7k
Eleftheria Maratos‐Flier United States	13	322 0.4×	524 0.9×	871 2.8×	135 0.6×	100 0.6×	15	3.3k
Johan Alsiö United Kingdom	25	678 0.8×	549 0.9×	526 1.7×	220 1.0×	205 1.3×	43	2.0k
Jarlath M.H. ffrench‐Mullen United States	16	535 0.6×	597 1.0×	104 0.3×	128 0.6×	77 0.5×	18	1.4k
Ross A. McDevitt United States	19	1.0k 1.2×	694 1.2×	477 1.5×	81 0.4×	227 1.5×	47	1.9k
Henning Fenselau Germany	16	350 0.4×	466 0.8×	397 1.3×	82 0.4×	228 1.5×	27	2.0k

Countries citing papers authored by Robert L. Jakab

Since Specialization

Citations

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

Fields of papers citing papers by Robert L. Jakab

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert L. Jakab. 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 Robert L. Jakab. The network helps show where Robert L. Jakab may publish in the future.

Co-authorship network of co-authors of Robert L. Jakab

This figure shows the co-authorship network connecting the top 25 collaborators of Robert L. Jakab. A scholar is included among the top collaborators of Robert L. Jakab 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 Robert L. Jakab. Robert L. Jakab 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

Collaco, Anne, et al.. (2013). Regulated traffic of anion transporters in mammalian Brunner's glands: a role for water and fluid transport. American Journal of Physiology-Gastrointestinal and Liver Physiology. 305(3). G258–G275. 30 indexed citations

Jakab, Robert L., Anne Collaco, & Nadia A. Ameen. (2012). Cell-specific effects of luminal acid, bicarbonate, cAMP, and carbachol on transporter trafficking in the intestine. American Journal of Physiology-Gastrointestinal and Liver Physiology. 303(8). G937–G950. 21 indexed citations

Jakab, Robert L., Anne Collaco, & Nadia A. Ameen. (2012). Lubiprostone Targets Prostanoid Signaling and Promotes Ion Transporter Trafficking, Mucus Exocytosis, and Contractility. Digestive Diseases and Sciences. 57(11). 2826–2845. 41 indexed citations

Jakab, Robert L., Anne Collaco, & Nadia A. Ameen. (2010). Physiological relevance of cell-specific distribution patterns of CFTR, NKCC1, NBCe1, and NHE3 along the crypt-villus axis in the intestine. American Journal of Physiology-Gastrointestinal and Liver Physiology. 300(1). G82–G98. 108 indexed citations

Fang, Hong, Weida Tong, Leming Shi, Robert L. Jakab, & John F. Bowyer. (2004). Classification of cDNA Array Genes That Have a Highly Significant Discriminative Power Due to Their Unique Distribution in Four Brain Regions. DNA and Cell Biology. 23(10). 661–674. 3 indexed citations

Bowyer, John F., Robert R. Delongchamp, & Robert L. Jakab. (2004). Glutamate N-methyl-d-aspartate and dopamine receptors have contrasting effects on the limbic versus the somatosensory cortex with respect to amphetamine-induced neurodegeneration. Brain Research. 1030(2). 234–246. 10 indexed citations

Bowyer, John F., Angela J. Harris, Robert R. Delongchamp, et al.. (2003). Selective Changes in Gene Expression in Cortical Regions Sensitive to Amphetamine During the Neurodegenerative Process. NeuroToxicology. 25(4). 555–572. 22 indexed citations

Jakab, Robert L. & John F. Bowyer. (2002). Parvalbumin neuron circuits and microglia in three dopamine-poor cortical regions remain sensitive to amphetamine exposure in the absence of hyperthermia, seizure and stroke. Brain Research. 958(1). 52–69. 25 indexed citations

Bowyer, John F., Keri J Hopkins, Robert L. Jakab, & Sherry A. Ferguson. (2001). l-ephedrine-induced neurodegeneration in the parietal cortex and thalamus of the rat is dependent on hyperthermia and can be altered by the process of in vivo brain microdialysis. Toxicology Letters. 125(1-3). 151–166. 7 indexed citations

10.

Jakab, Robert L., et al.. (2001). Estrogen receptor ? immunoreactivity in differentiating cells of the developing rat cerebellum. The Journal of Comparative Neurology. 430(3). 396–409. 82 indexed citations

11.

Alcantara, Adriana A., Ladislav Mrzljak, Robert L. Jakab, et al.. (2001). Muscarinic m1 and m2 receptor proteins in local circuit and projection neurons of the primate striatum: Anatomical evidence for cholinergic modulation of glutamatergic prefronto‐striatal pathways. The Journal of Comparative Neurology. 434(4). 445–460. 88 indexed citations

12.

Jakab, Robert L. & Patricia S. Goldman‐Rakic. (2000). Segregation of serotonin 5-HT2A and 5-HT3 receptors in inhibitory circuits of the primate cerebral cortex. The Journal of Comparative Neurology. 417(3). 337–348. 141 indexed citations

13.

Hámori, J., et al.. (1997). Morphogenetic Plasticity of Neuronal Elements in Cerebellar Glomeruli during Deafferentation‐Induced Synaptic Reorganization. Neural Plasticity. 6(1). 11–20. 8 indexed citations

14.

Horváth, Tamás L., Lucia Roa‐Peña, Robert L. Jakab, Evan R. Simpson, & Frederick Naftolin. (1997). Aromatase in axonal processes of early postnatal hypothalamic and limbic areas including the cingulate cortex. The Journal of Steroid Biochemistry and Molecular Biology. 61(3-6). 349–357. 32 indexed citations

15.

Jakab, Robert L., Lili‐Naz Hazrati, & Patricia S. Goldman‐Rakic. (1996). Distribution and neurochemical character of substance P receptor (SPR)-immunoreactive striatal neurons of the macaque monkey: Accumulation of SP fibers and SPR neurons and dendrites in ?striocapsules? encircling striosomes. The Journal of Comparative Neurology. 369(1). 137–149. 42 indexed citations

16.

Naftolin, Frederick, et al.. (1996). Aromatase Immunoreactivity in Axon Terminals of the Vertebrate Brain. Neuroendocrinology. 63(2). 149–155. 204 indexed citations

17.

Jakab, Robert L. & Patricia S. Goldman‐Rakic. (1996). Presynaptic and postsynaptic subcellular localization of substance P receptor immunoreactivity in the neostriatum of the rat and rhesus monkey (Macaca mulatta). The Journal of Comparative Neurology. 369(1). 125–136. 41 indexed citations

18.

Jakab, Robert L., Lili‐Naz Hazrati, & Patricia S. Goldman‐Rakic. (1996). Distribution and neurochemical character of substance P receptor (SPR)‐immunoreactive striatal neurons of the macaque monkey: Accumulation of SP fibers and SPR neurons and dendrites in “striocapsules” encircling striosomes. The Journal of Comparative Neurology. 369(1). 137–149. 6 indexed citations

19.

Jakab, Robert L., Nobuhiro Harada, & Frederick Naftolin. (1994). Aromatase- (estrogen synthetase) immunoreactive neurons in the rat septal area. A light and electron microscopic study. Brain Research. 664(1-2). 85–93. 29 indexed citations

20.

Jakab, Robert L. & Csaba Léránth. (1990). Somatospiny neurons in the rat lateral septal area are synaptic targets of hippocamposeptal fibers: A combined EM/Golgi and degejeration study. Synapse. 6(1). 10–22. 31 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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