Treatment of depression with low-strength transcranial pulsed electromagnetic fields: A mechanistic point of view

From inflammation to sickness and depression: when the immune system subjugates the brain

Dantzer, R., O'Connor, J. C., Freund, G. G., Johnson, R. W., & Kelley, K. W. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2297 · Cited by 7,395 · see citing works

Acute and longer-term outcomes in depressed outpatients requiring one or several treatment steps: a STAR*D report

Rush, A. J., Trivedi, M. H., Wisniewski, S. R., Nierenberg, A. A., Stewart, J. W., Warden, D., Niederehe, G., Thase, M. E., Lavori, P. W., Lebowitz, B. D., et al. (2006) · American Journal of Psychiatry · doi:10.1176/ajp.2006.163.11.1905 · Cited by 5,643 · see citing works

A Meta-Analysis of Cytokines in Major Depression

Dowlati, Y., Herrmann, N., Swardfager, W., Liu, H., Sham, L., Reim, E. K., & Lanctôt, K. L. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.09.033 · Cited by 4,729 · see citing works

NON-INVASIVE MAGNETIC STIMULATION OF HUMAN MOTOR CORTEX

Barker, A. T., Jalinous, R., & Freeston, I. L. (1985) · The Lancet · doi:10.1016/s0140-6736(85)92413-4 · Cited by 4,466 · see citing works

Coordination of circadian timing in mammals

Reppert, S. M., & Weaver, D. R. (2002) · Nature · doi:10.1038/nature00965 · Cited by 4,379 · see citing works

Inflammation and Its Discontents: The Role of Cytokines in the Pathophysiology of Major Depression

Miller, A. H., Maletic, V., & Raison, C. L. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.11.029 · Cited by 3,848 · see citing works

Personal Communication

D.Watson, L., & Hoefer, R. A. (2014) · Sage eBooks · doi:10.4135/9781483388007.n5 · Cited by 3,823 · see citing works

Burden of depressive disorders by country, sex, age, and year: findings from the Global Burden of Disease Study 2010

Ferrari, A. J., Charlson, F. J., Norman, R. E., Patten, S. B., Freedman, G., Murray, C. J. L., Vos, T., & Whiteford, H. A. (2013) · PLoS Medicine · doi:10.1371/journal.pmed.1001547 · Cited by 3,115 · see citing works

Transcranial direct current stimulation: State of the art 2008

Nitsche, M. A., Cohen, L. G., Wassermann, E. M., Priori, A., Lang, N., Antal, A., Paulus, W., Hummel, F., Boggio, P. S., Fregni, F., et al. (2008) · Brain Stimulation · doi:10.1016/j.brs.2008.06.004 · Cited by 3,057 · see citing works

Associations of depression with C-reactive protein, IL-1, and IL-6: a meta-analysis.

Howren, M. B., Lamkin, D. M., & Suls, J. (2009) · Psychosomatic Medicine · doi:10.1097/psy.0b013e3181907c1b · Cited by 2,766 · see citing works

Seasonal Affective Disorder: A Description of the Syndrome and Preliminary Findings With Light Therapy

Rosenthal, N. E. (1984) · Archives of General Psychiatry · doi:10.1001/archpsyc.1984.01790120076010 · Cited by 2,385 · see citing works

Efficacy and safety of electroconvulsive therapy in depressive disorders: a systematic review and meta-analysis

(2003) · The Lancet · doi:10.1016/s0140-6736(03)12705-5 · Cited by 1,706 · see citing works

Clinical research with transcranial direct current stimulation (tDCS): challenges and future directions

Brunoni, A. R., Nitsche, M. A., Bolognini, N., Bikson, M., Wagner, T., Merabet, L., Edwards, D. J., Valero-Cabre, A., Rotenberg, A., Pascual-Leone, A., et al. (2012) · Brain stimulation · doi:10.1016/j.brs.2011.03.002 · Cited by 1,445 · see citing works

Molecular analysis of mammalian circadian rhythms

Reppert, S. M., & Weaver, D. R. (2001) · Annual Review of Physiology · doi:10.1146/annurev.physiol.63.1.647 · Cited by 1,444 · see citing works

Mammalian Cry1 and Cry2 are essential for maintenance of circadian rhythms

Horst, G. T. J. V. D., Muijtjens, M., Kobayashi, K., Takano, R., Kanno, S.-I., Takao, M., Wit, J. D., Verkerk, A., Eker, A. P. M., Leenen, D. V., et al. (1999) · Nature · doi:10.1038/19323 · Cited by 1,402 · see citing works

Serum Brain-Derived Neurotrophic Factor, Depression, and Antidepressant Medications: Meta-Analyses and Implications

Sen, S., Duman, R., & Sanacora, G. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.05.005 · Cited by 1,232 · see citing works

Rapid-rate transcranial magnetic stimulation of left dorsolateral prefrontal cortex in drug-resistant depression

Pascual-Leone, A., Rubio, B., Pallardó, F., & Catalá, M. D. (1996) · The Lancet · doi:10.1016/s0140-6736(96)01219-6 · Cited by 1,229 · see citing works

Neuroimaging and neuropathological studies of depression: implications for the cognitive-emotional features of mood disorders

Drevets, W. C. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00203-8 · Cited by 1,146 · see citing works

Evidence for an immune response in major depression: A review and hypothesis

Maes, M. (1995) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/0278-5846(94)00101-m · Cited by 1,003 · see citing works

A systematic review and meta-analysis of clinical studies on major depression and BDNF levels: implications for the role of neuroplasticity in depression

Brunoni, A. R., Lopes, M., & Fregni, F. (2008) · International Journal of Neuropsychopharmacology · doi:10.1017/s1461145708009309 · Cited by 972 · see citing works

Effect of Anti-inflammatory Treatment on Depression, Depressive Symptoms, and Adverse Effects: A Systematic Review and Meta-analysis of Randomized Clinical Trials

Köhler, O., Benros, M. E., Nordentoft, M., Farkouh, M. E., Iyengar, R. L., Mors, O., & Krogh, J. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.1611 · Cited by 941 · see citing works

CRY, a Drosophila clock and light-regulated cryptochrome, is a major contributor to circadian rhythm resetting and photosensitivity

Emery, P., So, W. V., Kaneko, M., Hall, J. C., & Rosbash, M. (1998) · Cell · doi:10.1016/s0092-8674(00)81637-2 · Cited by 912 · see citing works

The cryptochromes: blue light photoreceptors in plants and animals

Chaves, I., Pokorny, R., Byrdin, M., Hoang, N., Ritz, T., Brettel, K., Essen, L.-O., van der Horst, G. T. J., Batschauer, A., & Ahmad, M. (2011) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042110-103759 · Cited by 845 · see citing works

Changes in Regional Brain Glucose Metabolism Measured With Positron Emission Tomography After Paroxetine Treatment of Major Depression

Kennedy, S. H., Evans, K. R., Krüger, S., Mayberg, H. S., Meyer, J. H., McCann, S., Arifuzzman, A. I., Houle, S., & Vaccarino, F. J. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.6.899 · Cited by 710 · see citing works

Serum BDNF concentrations as peripheral manifestations of depression: evidence from a systematic review and meta-analyses on 179 associations (N=9484)

Molendijk, M. L., Spinhoven, P., Polak, M., Bus, B. A. A., Penninx, B. W. J. H., & Elzinga, B. M. (2014) · Molecular Psychiatry · doi:10.1038/mp.2013.105 · Cited by 702 · cited 4× · see citing works

The new ‘5-HT’ hypothesis of depression: Cell-mediated immune activation induces indoleamine 2,3-dioxygenase, which leads to lower plasma tryptophan and an increased synthesis of detrimental tryptophan catabolites (TRYCATs), both of which contribute to the onset of depression

Maes, M., Leonard, B. E., Myint, A. M., Kubera, M., & Verkerk, R. (2011) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2010.12.017 · Cited by 700 · see citing works

Differential regulation of mammalian <i>Period</i> genes and circadian rhythmicity by cryptochromes 1 and 2

Vitaterna, M. H., Selby, C. P., Todo, T., Niwa, H., Thompson, C., Fruechte, E. M., Hitomi, K., Thresher, R. J., Ishikawa, T., Miyazaki, J., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.21.12114 · Cited by 690 · see citing works

Circadian genes, rhythms and the biology of mood disorders

McClung, C. A. (2007) · Pharmacology &amp; Therapeutics · doi:10.1016/j.pharmthera.2007.02.003 · Cited by 666 · see citing works

Light-Independent Role of CRY1 and CRY2 in the Mammalian Circadian Clock

Griffin, E. A., Staknis, D., & Weitz, C. J. (1999) · Science · doi:10.1126/science.286.5440.768 · Cited by 646 · see citing works

Ephaptic coupling of cortical neurons

Anastassiou, C. A., Perin, R., Markram, H., & Koch, C. (2011) · Nature Neuroscience · doi:10.1038/nn.2727 · Cited by 628 · see citing works

Pathophysiology of depression: do we have any solid evidence of interest to clinicians?

HASLER, G. (2010) · World Psychiatry · doi:10.1002/j.2051-5545.2010.tb00298.x · Cited by 604 · see citing works

Efficacy of ECT in Depression: A Meta-Analytic Review

Pagnin, D., de Queiroz, V., Pini, S., & Cassano, G. B. (2004) · Journal of Ect · doi:10.1097/00124509-200403000-00004 · Cited by 515 · see citing works

Brain polarization in humans: a reappraisal of an old tool for prolonged non-invasive modulation of brain excitability

Priori, A. (2003) · Clinical Neurophysiology · doi:10.1016/s1388-2457(02)00437-6 · Cited by 507 · see citing works

Treatment of depression with transcranial direct current stimulation (tDCS): A Review

Nitsche, M. A., Boggio, P. S., Fregni, F., & Pascual-Leone, A. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.03.038 · Cited by 498 · see citing works

PET measurements of brain glucose metabolism and blood flow in major depressive disorder: a critical review

Videbech, P. (2000) · Acta Psychiatrica Scandinavica · doi:10.1034/j.1600-0447.2000.101001011.x · Cited by 419 · see citing works

Transcranial direct current stimulation for acute major depressive episodes: meta-analysis of individual patient data

Brunoni, A. R., Moffa, A. H., Fregni, F., Palm, U., Padberg, F., Blumberger, D. M., Daskalakis, Z. J., Bennabi, D., Haffen, E., Alonzo, A., et al. (2016) · British Journal of Psychiatry · doi:10.1192/bjp.bp.115.164715 · Cited by 414 · see citing works

Modulation of cortical excitability induced by repetitive transcranial magnetic stimulation: Influence of timing and geometrical parameters and underlying mechanisms

Pell, G. S., Roth, Y., & Zangen, A. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.10.003 · Cited by 410 · see citing works

Role of Mouse Cryptochrome Blue-Light Photoreceptor in Circadian Photoresponses

Thresher, R., Vitaterna, M. H., Miyamoto, Y., Kazantsev, A. G., Hsu, D. S., Petit, C. R., Selby, C. P., Dawut, L., Smithies, O., Takahashi, J. S., et al. (1998) · Science · doi:10.1126/science.282.5393.1490 · Cited by 401 · see citing works

Depressed new Neurons?—Adult hippocampal neurogenesis and a cellular plasticity hypothesis of major depression

Kempermann, G., & Kronenberg, G. (2003) · Biological Psychiatry · doi:10.1016/s0006-3223(03)00319-6 · Cited by 392 · see citing works

The role of inflammatory mediators in the biology of major depression: Central nervous system cytokines modulate the biological substrate of depressive symptoms, regulate stress-responsive systems, and contribute to neurotoxicity and neuroprotection

Licinio, J., & Wong, M.-L. (1999) · Molecular Psychiatry · doi:10.1038/sj.mp.4000586 · Cited by 380 · see citing works

Complex Interaction of the Sleep-Wake Cycle and Circadian Phase Modulates Mood in Healthy Subjects

Boivin, D. B. (1997) · Archives of General Psychiatry · doi:10.1001/archpsyc.1997.01830140055010 · Cited by 378 · see citing works

Magnetically sensitive light-induced reactions in cryptochrome are consistent with its proposed role as a magnetoreceptor

Maeda, K., Robinson, A. J., Henbest, K. B., Hogben, H. J., Biskup, T., Ahmad, M., Schleicher, E., Weber, S., Timmel, C. R., & Hore, P. J. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1118959109 · Cited by 374 · see citing works

How does transcranial magnetic stimulation modify neuronal activity in the brain? Implications for studies of cognition

Siebner, H. R., Hartwigsen, G., Kassuba, T., & Rothwell, J. C. (2009) · Cortex · doi:10.1016/j.cortex.2009.02.007 · Cited by 345 · see citing works

The immune system, depression and the action of antidepressants

Leonard, B. E. (2001) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(01)00155-5 · Cited by 333 · see citing works

Serotonin and Hippocampal Neurogenesis

Gould, E. (1999) · Neuropsychopharmacology · doi:10.1016/s0893-133x(99)00045-7 · Cited by 328 · see citing works

Pro- and Anti-Inflammatory Cytokine Balance in Major Depression: Effect of Sertraline Therapy

Sutcigil, L., Oktenli, C., Musabak, U., Bozkurt, A., Cansever, A., Uzun, O., Sanisoglu, S. Y., Yesilova, Z., Ozmenler, N., Ozsahin, A., et al. (2007) · Clinical and Developmental Immunology · doi:10.1155/2007/76396 · Cited by 315 · see citing works

Cytokine imbalance in the pathophysiology of major depressive disorder

Kim, Y., Na, K.-S., Shin, K.-H., Jung, H., Choi, S., & Kim, J.-B. (2007) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2007.03.004 · Cited by 312 · see citing works

The Expanding Evidence Base for rTMS Treatment of Depression

George, M., Taylor, J. J., & Short, E. (2013) · Current Opinion in Psychiatry · doi:10.1097/yco.0b013e32835ab46d · Cited by 276 · see citing works

Molecular Clock Genes in Man and Lower Animals Possible Implications for Circadian Abnormalities in Depression

Bunney, W. E. (2000) · Neuropsychopharmacology · doi:10.1016/s0893-133x(99)00145-1 · Cited by 268 · see citing works

Cryptochrome Mediates Light-Dependent Magnetosensitivity of Drosophila's Circadian Clock

Yoshii, T., Ahmad, M., & Helfrich-Förster, C. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000086 · Cited by 232 · see citing works

Lifetime prevalence estimates of major depression: An indirect estimation method and a quantification of recall bias

Kruijshaar, M. E., Barendregt, J. J., Vos, T., de Graaf, R., Spijker, J., & Andrews, G. (2005) · European Journal of Epidemiology · doi:10.1007/s10654-004-1009-0 · Cited by 216 · see citing works

Human cryptochrome exhibits light-dependent magnetosensitivity

Foley, L. E., Gegear, R. J., & Reppert, S. M. (2011) · Nature Communications · doi:10.1038/ncomms1364 · Cited by 214 · see citing works

Staging methods for treatment resistant depression. A systematic review

Ruhé, H. G., van Rooijen, G., Spijker, J., Peeters, F. P. M. L., & Schene, A. H. (2012) · Journal of Affective Disorders · doi:10.1016/j.jad.2011.02.020 · Cited by 210 · see citing works

Is impaired neurogenesis relevant to the affective symptoms of depression?

Sapolsky, R. M. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.04.012 · Cited by 188 · see citing works

The circadian basis of mood disorders: Recent developments and treatment implications

Monteleone, P., & Maj, M. (2008) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2008.06.007 · Cited by 185 · see citing works

When Clocks Go Bad: Neurobehavioural Consequences of Disrupted Circadian Timing

Barnard, A. R., & Nolan, P. M. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000040 · Cited by 181 · see citing works

Circadian rhythms and mood regulation: insights from pre-clinical models

McClung, C. A. (2011) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2011.07.008 · Cited by 169 · see citing works

Chronotherapeutics in a psychiatric ward

Benedetti, F., Barbini, B., Colombo, C., & Smeraldi, E. (2007) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2007.06.004 · Cited by 167 · see citing works

Composition of brain oscillations in ongoing EEG during major depression disorder

Fingelkurts, A. A., Fingelkurts, A. A., Rytsälä, H. J., Suominen, K. H., Isometsä, E. T., & Kähkönen, S. (2006) · Neuroscience Research · doi:10.1016/j.neures.2006.06.006 · Cited by 158 · see citing works

How Does Electroconvulsive Therapy Work? Theories on its Mechanism

Bolwig, T. G. (2011) · The Canadian Journal of Psychiatry · doi:10.1177/070674371105600104 · Cited by 153 · see citing works

Evolving applications of light therapy

Terman, M. (2007) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2007.06.003 · Cited by 152 · see citing works

The effects of low-intensity pulsed ultrasound and pulsed electromagnetic fields bone growth stimulation in acute fractures: A systematic review and meta-analysis of randomized controlled trials

Hannemann, P. F. W., Mommers, E. H. H., Schots, J. P. M., Brink, P. R. G., & Poeze, M. (2014) · Archives of Orthopaedic and Trauma Surgery · doi:10.1007/s00402-014-2014-8 · Cited by 151 · see citing works

The relationship between brain oscillatory activity and therapeutic effectiveness of transcranial magnetic stimulation in the treatment of major depressive disorder

Leuchter, A. F., Cook, I. A., Jin, Y., & Phillips, B. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00037 · Cited by 139 · see citing works

Transcranial Low Voltage Pulsed Electromagnetic Fields in Patients with Treatment-Resistant Depression

Martiny, K., Lunde, M., & Bech, P. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.02.017 · Cited by 137 · see citing works

Neuroplasticity in Depressed Individuals Compared with Healthy Controls

Player, M. J., Taylor, J. L., Weickert, C. S., Alonzo, A., Sachdev, P., Martin, D., Mitchell, P. B., & Loo, C. K. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.126 · Cited by 127 · see citing works

Low-Field Magnetic Stimulation in Bipolar Depression Using an MRI-Based Stimulator

Rohan, M., Parow, A., Stoll, A. L., Demopulos, C., Friedman, S., Dager, S., Hennen, J., Cohen, B. M., & Renshaw, P. F. (2004) · American Journal of Psychiatry · doi:10.1176/appi.ajp.161.1.93 · Cited by 125 · see citing works

Decrypting Cryptochrome: Revealing the Molecular Identity of the Photoactivation Reaction

Solov’yov, I. A., Domratcheva, T. M., Shahi, A. R. M., & Schulten, K. J. (2012) · Journal of the American Chemical Society · doi:10.1021/ja3074819 · Cited by 121 · see citing works

Left prefrontal-repetitive transcranial magnetic stimulation (rTMS) and regional cerebral glucose metabolism in normal volunteers

Kimbrell, T. A., Dunn, R. T., George, M. S., Danielson, A., Willis, M. W., Repella, J. D., Benson, B. E., Herscovitch, P., Post, R. M., & Wassermann, E. M. (2002) · Psychiatry Research Neuroimaging · doi:10.1016/s0925-4927(02)00041-0 · Cited by 114 · see citing works

Elucidating the mechanisms and loci of neuronal excitation by Transcranial Magnetic Stimulation using a finite element model of a cortical sulcus

Silva, S., Basser, P., & Miranda, P. C. (2008) · Clinical Neurophysiology · doi:10.1016/j.clinph.2008.07.248 · Cited by 114 · see citing works

Effects of pulsed electromagnetic field on knee osteoarthritis: a systematic review

We, S. R., Koog, Y. H., Jeong, K.-I., & Wi, H. (2012) · Lara D. Veeken · doi:10.1093/rheumatology/kes063 · Cited by 109 · see citing works

Extremely low frequency electromagnetic field and wound healing: implication of cytokines as biological mediators

Pesce, M., Patruno, A., Speranza, L., & Reale, M. (2013) · European Cytokine Network · doi:10.1684/ecn.2013.0332 · Cited by 108 · see citing works

Effects of Pulsed Electromagnetic Fields on Interleukin-1β and Postoperative Pain: A Double-Blind, Placebo-Controlled, Pilot Study in Breast Reduction Patients

Rohde, C. H., Chiang, A. L., Adipoju, O., Casper, D., & Pilla, A. A. (2010) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0b013e3181c9f6d3 · Cited by 107 · see citing works

Cytokines as a stressor: implications for depressive illness

Anisman, H., Hayley, S. P., Turrin, N. P., & Merali, Z. (2002) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145702003097 · Cited by 106 · see citing works

A Randomized, Double‐Blind, Placebo‐Controlled Clinical Trial Using a Low‐Frequency Magnetic Field in the Treatment of Musculoskeletal Chronic Pain

Thomas, A. W., Graham, K., Prato, F. S., et al. (2007) · Pain Research and Management · doi:10.1155/2007/626072 · Cited by 101 · see citing works

Repetitive Transcranial Magnetic Stimulation Increases the Corticospinal Inhibition and the Brain-Derived Neurotrophic Factor in Chronic Myofascial Pain Syndrome: An Explanatory Double-Blinded, Randomized, Sham-Controlled Trial

Dall’Agnol, L., Medeiros, L. F., Torres, I. L. D. S., Deitos, A., Brietzke, A. P., Laste, G., de Souza, A., Vieira, J. L., Fregni, F., & Caumo, W. (2014) · Journal of Pain · doi:10.1016/j.jpain.2014.05.001 · Cited by 99 · see citing works

Antinociceptive effects of a pulsed magnetic field in the land snail, Cepaea nemoralis

Thomas, A. W., Kavaliers, M., Prato, F. S., et al. (1997) · Neuroscience Letters · doi:10.1016/s0304-3940(97)13359-6 · Cited by 99 · see citing works

Stimulation of Bone Formation and Fracture Healing with Pulsed Electromagnetic Fields: Biologic Responses and Clinical Implications

Chalidis, B. E., Sachinis, N. P., Assiotis, A., Maccauro, G., & Graziani, F. (2011) · International Journal of Immunopathology and Pharmacology · doi:10.1177/03946320110241s204 · Cited by 97 · see citing works

Rapid Mood-Elevating Effects of Low Field Magnetic Stimulation in Depression

Rohan, M. L., Yamamoto, R. T., Ravichandran, C. T., Cayetano, K. R., Morales, O. G., Olson, D. P., Vitaliano, G., Paul, S. M., & Cohen, B. M. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.10.024 · Cited by 97 · see citing works

Brain glucose metabolism difference between bipolar and unipolar mood disorders in depressed and euthymic states

Hosokawa, T., Momose, T., & Kasai, K. (2008) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2008.11.014 · Cited by 94 · see citing works

Human exposure to a specific pulsed magnetic field: effects on thermal sensory and pain thresholds

Shupak, N. M., Prato, F. S., & Thomas, A. W. (2004) · Neuroscience Letters · doi:10.1016/j.neulet.2004.03.069 · Cited by 90 · see citing works

Pain perception and electromagnetic fields

Seppia, C. D., Ghione, S., Luschi, P., Ossenkopp, K., Choleris, E., & Kavaliers, M. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.01.003 · Cited by 90 · see citing works

Exposure to a Specific Pulsed Low‐Frequency Magnetic Field: A Double‐Blind Placebo‐Controlled Study of Effects on Pain Ratings in Rheumatoid Arthritis and Fibromyalgia Patients

Shupak, N. M., McKay, J. C., Nielson, W. R., Rollman, G. B., Prato, F. S., & Thomas, A. W. (2006) · Pain Research and Management · doi:10.1155/2006/842162 · Cited by 80 · see citing works

Biomarker Approaches in Major Depressive Disorder Evaluated in the Context of Current Hypotheses

Jentsch, M., van Buel, E. M., Bosker, F. J., Gladkevich, A. V., Klein, H. C., Voshaar, R. C. O., Ruhé, H. G., Eisel, U. L., & Schoevers, R. A. (2015) · Biomarkers in Medicine · doi:10.2217/bmm.14.114 · Cited by 79 · see citing works

Effect of transcranial magnetic stimulation on the expression of c-Fos and brain-derived neurotrophic factor of the cerebral cortex in rats with cerebral infarct

Zhang, X., Yuanwu, M., Liu, C., et al. (2007) · Journal of Huazhong University of Science and Technology [Medical Sciences] · doi:10.1007/s11596-007-0416-3 · Cited by 75 · see citing works

Transcranial Magnetic Stimulation in the Management of Mood Disorders

Allan, C., Herrmann, L. L., & Ebmeier, K. P. (2011) · Neuropsychobiology · doi:10.1159/000328951 · Cited by 74 · see citing works

Pulsed electromagnetic field enhances brain-derived neurotrophic factor expression through L-type voltage-gated calcium channel- and Erk-dependent signaling pathways in neonatal rat dorsal root ganglion neurons

Li, Y., Yan, X., Liu, J., Li, L., Hu, X., Sun, H., & Tian, J. (2014) · Neurochemistry International · doi:10.1016/j.neuint.2014.06.004 · Cited by 67 · see citing works

Human circadian rhythms under the influence of weak electric fields and the different aspects of these studies

Wever, R. (1973) · International Journal of Biometeorology · doi:10.1007/bf01804614 · Cited by 63 · see citing works

Attenuation of interleukin-1beta by pulsed electromagnetic fields after traumatic brain injury

Rasouli, J. J., Lekhraj, R., White, N. M., Flamm, E. S., Pilla, A. A., Strauch, B., & Casper, D. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.03.089 · Cited by 62 · see citing works

Pulsed electromagnetic fields decrease proinflammatory cytokine secretion (IL-1β and TNF-α) on human fibroblast-like cell culture

Gómez-Ochoa, I., Gómez-Ochoa, P., Gómez-Casal, F., Cativiela, E., & Larrad-Mur, L. (2010) · Rheumatology International · doi:10.1007/s00296-010-1488-0 · Cited by 60 · see citing works

Effects of Low-Field Magnetic Stimulation on Brain Glucose Metabolism

Volkow, N., Tomasi, D., Wang, G.-J., Fowler, J., Telang, F., Wang, R., Alexoff, D., Logan, J., Wong, C. T., Pradhan, K., et al. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.02.015 · Cited by 58 · see citing works

Pathophysiological mechanism of seasonal affective disorder

Lee, T. M. C., Blashko, C. A., Janzen, H. L., Paterson, J. G., & Chan, C. C. H. (1997) · Journal of Affective Disorders · doi:10.1016/s0165-0327(97)00076-1 · Cited by 58 · see citing works

Antidepressant-like effects of cranial stimulation within a low-energy magnetic field in rats

Carlezon, W. A., Rohan, M. L., Mague, S. D., Meloni, E. G., Parsegian, A., Cayetano, K. R., Tomasiewicz, H. C., Rouse, E. D., Cohen, B. M., & Renshaw, P. F. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.12.011 · Cited by 54 · see citing works

Pulsed electromagnetic field stimulation of bone marrow cells derived from ovariectomized rats affects osteoclast formation and local factor production

Chang, K., Chang, W. H., Yu, Y., et al. (2004) · Bioelectromagnetics · doi:10.1002/bem.10168 · Cited by 54 · see citing works

Reduction of Pain Thresholds in Fibromyalgia after Very Low‐Intensity Magnetic Stimulation: A Double‐Blinded, Randomized Placebo‐Controlled Clinical Trial

Maestú, C., Blanco, M., Nevado, Á., Romero, J., Rodríguez-Rubio, P., Galindo, J., Lorite, J. B., Morenas, F. D. L., & Fernández-Argüelles, P. (2013) · Pain Research and Management · doi:10.1155/2013/270183 · Cited by 53 · see citing works

Resting EEG effects during exposure to a pulsed ELF magnetic field

Cook, C. M., Thomas, A. W., Keenliside, L. D., & Prato, F. S. (2005) · Bioelectromagnetics · doi:10.1002/bem.20113 · Cited by 53 · see citing works

Neuromodulation for treatment-resistant depression

Holtzheimer, P. E., & Mayberg, H. S. (2012) · F1000 Medicine Reports · doi:10.3410/m4-22 · Cited by 53 · see citing works

BDNF blood levels after non-invasive brain stimulation interventions in major depressive disorder: A systematic review and meta-analysis

Brunoni, A. R., Baeken, C., Machado‐Vieira, R., Gattaz, W. F., & Vanderhasselt, M. (2014) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2014.958101 · Cited by 52 · see citing works

Comparing different physical factors on serum TNF-α levels, chondrocyte apoptosis, caspase-3 and caspase-8 expression in osteoarthritis of the knee in rabbits

Guo, H., Luo, Q., Zhang, J., et al. (2011) · Joint Bone Spine · doi:10.1016/j.jbspin.2011.01.009 · Cited by 48 · see citing works

Metabolic changes of cerebrum by repetitive transcranial magnetic stimulation over lateral cerebellum: a study with FDG PET

Cho, S. S., Yoon, E. J., Bang, S. A., Park, H. S., Kim, Y. K., Strafella, A. P., & Kim, S. E. (2012) · The Cerebellum · doi:10.1007/s12311-011-0333-7 · Cited by 46 · see citing works

The effects of electric fields on circadian rhythmicity in men.

Wever, R. (1970) · PubMed · Cited by 46 · see citing works

Changes in human EEG alpha activity following exposure to two different pulsed magnetic field sequences

Cook, C. M., Saucier, D. M., Thomas, A. W., & Prato, F. S. (2008) · Bioelectromagnetics · doi:10.1002/bem.20434 · Cited by 45 · see citing works

A systematic review of the clinical relevance of repetitive transcranial magnetic stimulation

Lepping, P., Schönfeldt‐Lecuona, C., Sambhi, R. S., Lanka, S. V., Lane, S., Whittington, R., Leucht, S., & Poole, R. (2014) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.12276 · Cited by 44 · see citing works

Dose-Dependent Development of Depressive Symptoms During Adjuvant Interferon-α Treatment of Patients With Malignant Melanoma

Friebe, A., Horn, M., Schmidt, F., Janssen, G., Schmid-Wendtner, M.-H., Volkenandt, M., Hauschild, A., Goldsmith, C. H., & Schaefer, M. (2010) · Psychosomatics · doi:10.1016/s0033-3182(10)70738-6 · Cited by 39 · see citing works

Serial repetitive transcranial magnetic stimulation (rTMS) decreases BDNF serum levels in healthy male volunteers

Schaller, G., Sperling, W., Richter‐Schmidinger, T., Mühle, C., Heberlein, A., Maihöfner, C., Kornhuber, J., & Lenz, B. (2013) · Journal of Neural Transmission · doi:10.1007/s00702-013-1102-1 · Cited by 33 · see citing works

Pulsed electromagnetic fields potentiate neurite outgrowth in the dopaminergic MN9D cell line

Lekhraj, R., Cynamon, D. E., DeLuca, S. E., Taub, E. S., Pilla, A. A., & Casper, D. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23361 · Cited by 30 · see citing works

Acute prefrontal cortex transcranial magnetic stimulation in healthy volunteers: No effects on brain-derived neurotrophic factor (BDNF) concentrations in serum

Lang, U. E., Hellweg, R., Gallinat, J., & Bajbouj, M. (2007) · Journal of Affective Disorders · doi:10.1016/j.jad.2007.08.008 · Cited by 29 · see citing works

Dose-remission of pulsating electromagnetic fields as augmentation in therapy-resistant depression: a randomized, double-blind controlled study

Straasø, B., Lauritzen, L., Lunde, M., Vinberg, M., Lindberg, L., Larsen, E. R., Dissing, S., & Bech, P. (2014) · Acta Neuropsychiatrica · doi:10.1017/neu.2014.5 · Cited by 29 · see citing works

Interactions of Low-Frequency, Pulsed Electromagnetic Fields with Living Tissue: Biochemical Responses and Clinical Results

Rahbek, U. L., Tritsaris, K., & Dissing, S. (2005) · Research at the University of Copenhagen (University of Copenhagen) · Cited by 28 · see citing works

Why do some promising brain-stimulation devices fail the next steps of clinical development?

Edelmuth, R. C. L., Nitsche, M., Battistella, L., & Fregni, F. (2010) · Expert Review of Medical Devices · doi:10.1586/erd.09.64 · Cited by 25 · see citing works

Small-animal repetitive transcranial magnetic stimulation combined with [18F]-FDG microPET to quantify the neuromodulation effect in the rat brain

Parthoens, J., Verhaeghe, J. A. J., Wyckhuys, T., Stroobants, S. G., & Staelens, S. G. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.06.042 · Cited by 23 · see citing works

The detection threshold for extremely low frequency magnetic fields may be below 1000 nT‐Hz in mice

Prato, F. S., Desjardins‐Holmes, D., Keenliside, L. D., et al. (2011) · Bioelectromagnetics · doi:10.1002/bem.20661 · Cited by 20 · see citing works

Antidepressant-like effect of magnetic resonance imaging-based stimulation in mice

Rokni-Yazdi, H., Sotoudeh, H., Akhondzadeh, S., et al. (2007) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2006.11.021 · Cited by 15 · see citing works

Antidepressant-like effects of echo-planar magnetic resonance imaging in mice determined using the forced swimming test

Aksöz, E., Aksöz, T., Bilge, S. S., İlkaya, F., Celik, S., & Diren, B. (2008) · Brain Research · doi:10.1016/j.brainres.2008.08.011 · Cited by 15 · see citing works

A Novel Magnetic Stimulator Increases Experimental Pain Tolerance in Healthy Volunteers - A Double-Blind Sham-Controlled Crossover Study

Kortekaas, R., van Nierop, L. E., Baas, V. G., Konopka, K.-H., Harbers, M., van der Hoeven, J. H., van Wijhe, M., Aleman, A., & Maurits, N. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061926 · Cited by 11 · see citing works

Changes in winter depression phenotype correlate with white blood cell gene expression profiles: A combined metagene and gene ontology approach

Bosker, F. J., Terpstra, P., Gladkevich, A. V., Dijck-Brouwer, J., Meerman, G. T., Nolen, W. A., Schoevers, R. A., & Meesters, Y. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2014.10.015 · Cited by 6 · see citing works

Paying attention to attention in depression

Keller, A. S., Leikauf, J. E., Holt-Gosselin, B., Staveland, B. R., & Williams, L. M. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0616-1 · Cited by 329 · see citing works

Effects of rTMS on the brain: is there value in variability?

Goldsworthy, M. R., Hordacre, B. G., Rothwell, J. C., & Ridding, M. C. (2021) · Cortex · doi:10.1016/j.cortex.2021.02.024 · Cited by 78 · see citing works

Low frequency rTMS: Induction of neuroplastic effects

Hajak, G., Langguth, B., Sand, P. G., et al. (2005) · Pharmacopsychiatry · doi:10.1055/s-2005-918702 · Cited by 2 · see citing works

Spaced Noninvasive Brain Stimulation

Goldsworthy, M. R., Pitcher, J. B., & Ridding, M. C. (2014) · Neurorehabilitation and neural repair · doi:10.1177/1545968314562649 · Cited by 74 · see citing works

Propagation of TMS pulses versus functional brain connectivity

Klooster, D., Vink, J. J. T., van Mierlo, P., Boon, P., Cooke, D., Gedankien, T., Roberts, A., Boucher, P. O., Pascual‐Leone, Á., Fox, M., et al. (2019) · Brain stimulation · doi:10.1016/j.brs.2018.12.461

[Repetitive transcranial magnetic stimulation in depression; stimulation of the brain in order to cure the psyche].

Helmich, R. C. G., Snijders, A. H., Verkes, R., et al. (2004) · PubMed · Cited by 1 · see citing works