Carl Sikkema

651 total citations
18 papers, 495 citations indexed

About

Carl Sikkema is a scholar working on Cellular and Molecular Neuroscience, Behavioral Neuroscience and Physiology. According to data from OpenAlex, Carl Sikkema has authored 18 papers receiving a total of 495 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Cellular and Molecular Neuroscience, 6 papers in Behavioral Neuroscience and 6 papers in Physiology. Recurrent topics in Carl Sikkema's work include Stress Responses and Cortisol (6 papers), Neuroscience and Neuropharmacology Research (5 papers) and Neuroendocrine regulation and behavior (4 papers). Carl Sikkema is often cited by papers focused on Stress Responses and Cortisol (6 papers), Neuroscience and Neuropharmacology Research (5 papers) and Neuroendocrine regulation and behavior (4 papers). Carl Sikkema collaborates with scholars based in United States and Spain. Carl Sikkema's co-authors include Charles W. Wilkinson, Patricia Szot, Murray A. Raskind, Elaine R. Peskind, Elisabeth J. Van Bockstaele, Beverly A.S. Reyes, Cristina Miguélez, Luisa Ugedo, Steven Falowski and Ashwini Sharan and has published in prestigious journals such as Biological Psychiatry, Neuroscience and Neurosurgery.

In The Last Decade

Carl Sikkema

18 papers receiving 489 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carl Sikkema United States 15 163 128 94 92 87 18 495
Baek‐Vin Lim South Korea 15 159 1.0× 81 0.6× 116 1.2× 55 0.6× 88 1.0× 19 513
Cüneyt Demiralay Germany 13 72 0.4× 54 0.4× 65 0.7× 60 0.7× 116 1.3× 33 516
Hiroyuki Hashiguchi Japan 13 231 1.4× 102 0.8× 115 1.2× 73 0.8× 175 2.0× 24 551
Giuseppe Di Iorio Italy 19 132 0.8× 106 0.8× 59 0.6× 139 1.5× 59 0.7× 39 899
Erick Singley United States 10 380 2.3× 58 0.5× 91 1.0× 97 1.1× 103 1.2× 13 589
J. Bryce Ortiz United States 16 150 0.9× 94 0.7× 65 0.7× 150 1.6× 273 3.1× 35 684
Tatsuya Kakigi Japan 10 120 0.7× 118 0.9× 57 0.6× 96 1.0× 70 0.8× 23 486
Sang-Seo Park South Korea 17 131 0.8× 42 0.3× 199 2.1× 79 0.9× 95 1.1× 37 611
John Kealy Ireland 10 184 1.1× 87 0.7× 91 1.0× 151 1.6× 56 0.6× 14 632
James Peoples United States 8 245 1.5× 48 0.4× 73 0.8× 161 1.8× 125 1.4× 10 570

Countries citing papers authored by Carl Sikkema

Since Specialization
Citations

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

Fields of papers citing papers by Carl Sikkema

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carl Sikkema

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

All Works

18 of 18 papers shown
1.
Edwards, Melise M., Tami Wolden‐Hanson, Tomasz Wietecha, et al.. (2024). Sympathetic innervation of interscapular brown adipose tissue is not a predominant mediator of oxytocin-elicited reductions of body weight and adiposity in male diet-induced obese mice. Frontiers in Endocrinology. 15. 1440070–1440070. 2 indexed citations
2.
Wolden‐Hanson, Tami, James L. Graham, Tomasz Wietecha, et al.. (2024). Sympathetic Innervation of Interscapular Brown Adipose Tissue Is Not a Predominant Mediator of Oxytocin-Induced Brown Adipose Tissue Thermogenesis in Female High Fat Diet-Fed Rats. Current Issues in Molecular Biology. 46(10). 11394–11424. 1 indexed citations
3.
Hendrickson, Rebecca C., Murray A. Raskind, Steven P. Millard, et al.. (2018). Evidence for altered brain reactivity to norepinephrine in Veterans with a history of traumatic stress. Neurobiology of Stress. 8. 103–111. 26 indexed citations
4.
Colasurdo, Elizabeth A., et al.. (2018). Chronic Hypopituitarism Associated with Increased Postconcussive Symptoms Is Prevalent after Blast-Induced Mild Traumatic Brain Injury. Frontiers in Neurology. 9. 72–72. 37 indexed citations
5.
Raskind, Murray A., Charles W. Wilkinson, Jane B. Shofer, et al.. (2018). Associations between CSF cortisol and CSF norepinephrine in cognitively normal controls and patients with amnestic MCI and AD dementia. International Journal of Geriatric Psychiatry. 33(5). 763–768. 22 indexed citations
6.
Sikkema, Carl, et al.. (2017). DOPA Decarboxylase Modulates Tau Toxicity. Biological Psychiatry. 83(5). 438–446. 15 indexed citations
7.
Schindler, Abigail G., Kathleen F. Pagulayan, Rebecca C. Hendrickson, et al.. (2017). Blast–related disinhibition and risk seeking in mice and combat Veterans: Potential role for dysfunctional phasic dopamine release. Neurobiology of Disease. 106. 23–34. 27 indexed citations
8.
Ben‐Hamo, Miriam, et al.. (2016). Circadian Forced Desynchrony of the Master Clock Leads to Phenotypic Manifestation of Depression in Rats. eNeuro. 3(6). ENEURO.0237–16.2016. 47 indexed citations
10.
Hanscom, Brett, Ge Li, Steven P. Millard, et al.. (2013). Cerebrospinal fluid norepinephrine and cognition in subjects across the adult age span. Neurobiology of Aging. 34(10). 2287–2292. 27 indexed citations
11.
Reyes, Beverly A.S., et al.. (2012). Stress-induced sensitization of cortical adrenergic receptors following a history of cannabinoid exposure. Experimental Neurology. 236(2). 327–335. 27 indexed citations
12.
Szot, Patricia, Allyn Franklin, Carl Sikkema, Charles W. Wilkinson, & Murray A. Raskind. (2012). Sequential Loss of LC Noradrenergic and Dopaminergic Neurons Results in a Correlation of Dopaminergic Neuronal Number to Striatal Dopamine Concentration. Frontiers in Pharmacology. 3. 184–184. 22 indexed citations
14.
Falowski, Steven, Ashwini Sharan, Beverly A.S. Reyes, et al.. (2011). An Evaluation of Neuroplasticity and Behavior After Deep Brain Stimulation of the Nucleus Accumbens in an Animal Model of Depression. Neurosurgery. 69(6). 1281–1290. 65 indexed citations
15.
Szot, Patricia, Cristina Miguélez, Sylvia S. White, et al.. (2010). A comprehensive analysis of the effect of DSP4 on the locus coeruleus noradrenergic system in the rat. Neuroscience. 166(1). 279–291. 55 indexed citations
16.
Raskind, Murray A., Elaine R. Peskind, Marcella Pascualy, et al.. (1995). The effects of normal aging on cortisol and adrenocorticotropin responses to hypertonic saline infusion. Psychoneuroendocrinology. 20(6). 637–644. 12 indexed citations
17.
Peskind, Elaine R., Murray A. Raskind, Dane Wingerson, et al.. (1995). Enhanced Hypothalamic-Pituitary-Adrenocortical Axis Responses to Physostigmine in Normal Aging. The Journals of Gerontology Series A. 50A(2). M114–M120. 29 indexed citations
18.
Peskind, Elaine R., Allen D. Radant, Dorcas J. Dobie, et al.. (1993). Hypertonic saline infusion increases plasma norepinephrine concentrations in normal men. Psychoneuroendocrinology. 18(2). 103–113. 16 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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