A Single Bout of High-intensity Interval Exercise Increases Corticospinal Excitability, Brain-derived Neurotrophic Factor, and Uncarboxylated Osteolcalcin in Sedentary, Healthy Males

The assessment and analysis of handedness: The Edinburgh inventory

Oldfield, R. C. (1971) · Neuropsychologia · doi:10.1016/0028-3932(71)90067-4 · Cited by 35,900 · see citing works

Exercise training increases size of hippocampus and improves memory

Erickson, K. I., Voss, M. W., Prakash, R. S., Basak, C., Szabo, A., Chaddock, L., Kim, J. S., Heo, S., Alves, H., White, S. M., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1015950108 · Cited by 4,855 · see citing works

A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis

Boström, P., Wu, J., Jedrychowski, M. P., Korde, A., Ye, L., Lo, J. C., Rasbach, K. A., Boström, E. A., Choi, J. H., Long, J. Z., et al. (2012) · Nature · doi:10.1038/nature10777 · Cited by 4,810 · see citing works

Neurotrophins: Roles in Neuronal Development and Function

Huang, E. J., & Reichardt, L. F. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.677 · Cited by 4,394 · see citing works

Be smart, exercise your heart: Exercise effects on brain and cognition

Hillman, C. H., Erickson, K. I., & Kramer, A. F. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2298 · Cited by 3,563 · see citing works

Muscles, exercise and obesity: skeletal muscle as a secretory organ

Pedersen, B. K., & Febbraio, M. A. (2012) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2012.49 · Cited by 2,909 · see citing works

Exercise: a behavioral intervention to enhance brain health and plasticity

Cotman, C. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02143-4 · Cited by 2,739 · see citing works

Exercise builds brain health: key roles of growth factor cascades and inflammation

Cotman, C. W., Berchtold, N. C., & Christie, L.-A. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.06.011 · Cited by 2,268 · see citing works

Neurotrophin regulation of neural circuit development and function

Park, H., & Poo, M.-M. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3379 · Cited by 2,060 · see citing works

Detecting outliers when fitting data with nonlinear regression – a new method based on robust nonlinear regression and the false discovery rate

Motulsky, H. J., & Brown, R. E. (2006) · BMC Bioinformatics · doi:10.1186/1471-2105-7-123 · Cited by 1,616 · see citing works

Exercise induces hippocampal BDNF through a PGC-1α/FNDC5 pathway

Wrann, C. D., White, J. P., Salogiannnis, J., Laznik-Bogoslavski, D., Wu, J., Ma, D., Lin, J. D., Greenberg, M. E., & Spiegelman, B. M. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.09.008 · Cited by 1,440 · see citing works

BDNF function in adult synaptic plasticity: The synaptic consolidation hypothesis

Bramham, C. R., & Messaoudi, E. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.06.003 · Cited by 1,193 · see citing works

Effects of antiepileptic drugs on motor cortex excitability in humans: A transcranial magnetic stimulation study

Ziemann, U., Lönnecker, S., Steinhoff, B. J., & Paulus, W. (1996) · Annals of Neurology · doi:10.1002/ana.410400306 · Cited by 1,136 · see citing works

Insulin signaling in osteoblasts integrates bone remodeling and energy metabolism

Ferron, M., Wei, J., Yoshizawa, T., Del Fattore, A., DePinho, R. A., Teti, A., Ducy, P., & Karsenty, G. (2010) · Cell · doi:10.1016/j.cell.2010.06.003 · Cited by 1,123 · see citing works

Autophosphorylation at Thr ²⁸⁶ of the α Calcium-Calmodulin Kinase II in LTP and Learning

Giese, K. P., Fedorov, N. B., Filipkowski, R. K., & Silva, A. J. (1998) · Science · doi:10.1126/science.279.5352.870 · Cited by 1,055 · see citing works

Circulating Insulin-Like Growth Factor I Mediates Exercise-Induced Increases in the Number of New Neurons in the Adult Hippocampus

Trejo, J. L., Carro, E., & Torres-Alemán, I. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-05-01628.2001 · Cited by 1,017 · see citing works

Exercise-linked FNDC5/irisin rescues synaptic plasticity and memory defects in Alzheimer’s models

Lourenco, M. V., Frozza, R. L., de Freitas, G. B., Zhang, H., Kincheski, G. C., Ribeiro, F. C., Gonçalves, R. A., Clarke, J. R., Beckman, D., Staniszewski, A., et al. (2019) · Nature Medicine · doi:10.1038/s41591-018-0275-4 · Cited by 935 · see citing works

A Review of the Effects of Physical Activity and Exercise on Cognitive and Brain Functions in Older Adults

Bherer, L., Erickson, K. I., & Liu-Ambrose, T. (2013) · Journal of Aging Research · doi:10.1155/2013/657508 · Cited by 899 · see citing works

Differential effects on motorcortical inhibition induced by blockade of GABA uptake in humans

Werhahn, K. J., Kunesch, E., Noachtar, S., Benecke, R., & Classen, J. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.0591t.x · Cited by 887 · see citing works

The effect of acute exercise on serum brain-derived neurotrophic factor levels and cognitive function.

FERRIS, L. T., WILLIAMS, J. S., & SHEN, C.-L. (2007) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e31802f04c7 · Cited by 849 · see citing works

Low-volume high-intensity interval training reduces hyperglycemia and increases muscle mitochondrial capacity in patients with type 2 diabetes

Little, J. P., Gillen, J. B., Percival, M. E., Safdar, A., Tarnopolsky, M. A., Punthakee, Z., Jung, M. E., & Gibala, M. J. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00921.2011 · Cited by 787 · see citing works

Running-induced systemic cathepsin B secretion is associated with memory function

Moon, H. Y., Becke, A., Berron, D., Becker, B., Sah, N., Benoni, G., Janke, E., Lubejko, S. T., Greig, N. H., Mattison, J. A., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.05.025 · Cited by 628 · see citing works

New insights into the biology of osteocalcin

Zoch, M. L., Clemens, T. L., & Riddle, R. C. (2015) · Bone · doi:10.1016/j.bone.2015.05.046 · Cited by 612 · see citing works

Acute effects of moderate aerobic exercise on specific aspects of executive function in different age and fitness groups: A meta‐analysis

Ludyga, S., Gerber, M., Brand, S., Holsboer‐Trachsler, E., & Pühse, U. (2016) · Psychophysiology · doi:10.1111/psyp.12736 · Cited by 589 · see citing works

The effects of acute and chronic exercise on <scp>PGC</scp> ‐1α, irisin and browning of subcutaneous adipose tissue in humans

Norheim, F., Langleite, T. M., Hjorth, M., Holen, T., Kielland, A., Stadheim, H. K., Gulseth, H. L., Birkeland, K. I., Jensen, J., & Drevon, C. A. (2014) · The FEBS Journal · doi:10.1111/febs.12619 · Cited by 563 · see citing works

The role of GABAB receptors in intracortical inhibition in the human motor cortex

McDonnell, M. N., Orekhov, Y., & Ziemann, U. (2006) · Experimental Brain Research · doi:10.1007/s00221-006-0365-2 · Cited by 558 · see citing works

Insulin-like growth factor I interfaces with brain-derived neurotrophic factor-mediated synaptic plasticity to modulate aspects of exercise-induced cognitive function

Ding, Q., Vaynman, S., Akhavan, M., Ying, Z., & Gomez-Pinilla, F. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.02.084 · Cited by 555 · see citing works

Aerobic exercise improves hippocampal function and increases BDNF in the serum of young adult males

Griffin, É. W., Mullally, S. L., Foley, C., Warmington, S. A., O’Mara, S. M., & Kelly, A. M. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.06.005 · Cited by 543 · see citing works

Maternal and Offspring Pools of Osteocalcin Influence Brain Development and Functions

Oury, F., Khrimian, L., Denny, C. A., Gardin, A., Chamouni, A., Goeden, N., Huang, Y.-Y., Lee, H., Srinivas, P., Gao, X.-B., et al. (2013) · Cell · doi:10.1016/j.cell.2013.08.042 · Cited by 484 · see citing works

MC4R-dependent suppression of appetite by bone-derived lipocalin 2

Mosialou, I., Shikhel, S., Liu, J., Maurizi, A., Luo, N., He, Z., Huang, Y., Zong, H., Friedman, R. A., Barasch, J. M., et al. (2017) · Nature · doi:10.1038/nature21697 · Cited by 457 · see citing works

Osteocalcin Signaling in Myofibers Is Necessary and Sufficient for Optimum Adaptation to Exercise

Mera, P., Laue, K., Ferron, M., Confavreux, C. B., Wei, J., Galán-Díez, M., Lacampagne, A., Mitchell, S. J., Mattison, J. A., Chen, Y., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.05.004 · Cited by 429 · see citing works

Intense exercise increases circulating endocannabinoid and BDNF levels in humans–possible implications for reward and depression

Heyman, E., Gamelin, F.-X., Goekint, M., Piscitelli, F., Roelands, B., Leclair, E., Di Marzo, V., & Meeusen, R. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.09.017 · Cited by 427 · see citing works

Exercise-induced irisin secretion is independent of age or fitness level and increased irisin may directly modulate muscle metabolism through AMPK activation

Huh, J. Y., Mougios, V., Kabasakalis, A., Fatouros, I., Siopi, A., Douroudos, I. I., Filippaios, A., Panagiotou, G., Park, K. H., & Mantzoros, C. S. (2014) · The Journal of Clinical Endocrinology &amp; Metabolism · doi:10.1210/jc.2014-1437 · Cited by 363 · see citing works

Promoting Neuroplasticity for Motor Rehabilitation After Stroke: Considering the Effects of Aerobic Exercise and Genetic Variation on Brain-Derived Neurotrophic Factor

Mang, C. S., Campbell, K. L., Ross, C. J., & Boyd, L. A. (2013) · Physical Therapy · doi:10.2522/ptj.20130053 · Cited by 352 · see citing works

A Necessity for MAP Kinase Activation in Mammalian Spatial Learning

Selcher, J. C., Atkins, C. M., Trzaskos, J. M., Paylor, R., & Sweatt, J. D. (1999) · Learning &amp; Memory · doi:10.1101/lm.6.5.478 · Cited by 341 · see citing works

Acute exercise improves motor memory: exploring potential biomarkers.

Skriver, K., Roig, M., Lundbye-Jensen, J., Pingel, J., Helge, J. W., Kiens, B., & Nielsen, J. B. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.08.004 · Cited by 326 · see citing works

Aerobic Exercise Improves Cognition and Motor Function Poststroke

Quaney, B. M., Boyd, L. A., McDowd, J. M., Zahner, L. H., He, J., Mayo, M. S., & Macko, R. F. (2009) · Neurorehabilitation and neural repair · doi:10.1177/1545968309338193 · Cited by 324 · see citing works

Gpr158 mediates osteocalcin’s regulation of cognition

Khrimian, L., Obri, A., Ramos-Brossier, M., Rousseaud, A., Moriceau, S., Nicot, A.-S., Mera, P., Kosmidis, S., Karnavas, T., Saudou, F., et al. (2017) · Journal of Experimental Medicine · doi:10.1084/jem.20171320 · Cited by 308 · see citing works

Basal serum levels and reactivity of nerve growth factor and brain-derived neurotrophic factor to standardized acute exercise in multiple sclerosis and controls

Gold, S. M., Schulz, K., Hartmann, S., Mladek, M., Lang, U. E., Hellweg, R., Reer, R., Braumann, K.-M., & Heesen, C. (2003) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(03)00121-8 · Cited by 300 · see citing works

Are skeletal muscle <i>FNDC5</i> gene expression and irisin release regulated by exercise and related to health?

Pekkala, S., Wiklund, P. K., Hulmi, J. J., Ahtiainen, J. P., Horttanainen, M., Pöllänen, E., Mäkelä, K. A., Kainulainen, H., Häkkinen, K., Nyman, K., et al. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2013.263707 · Cited by 292 · see citing works

Exercise counteracts declining hippocampal function in aging and Alzheimer's disease

Intlekofer, K. A., & Cotman, C. W. (2012) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.06.011 · Cited by 286 · see citing works

Acute effect of brief low- and high-intensity exercise on circulating insulin-like growth factor (IGF) I, II, and IGF-binding protein-3 and its proteolysis in young healthy men

Schwarz, A. J., Brasel, J. A., Hintz, R. L., Mohan, S., & Cooper, D. M. (1996) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.81.10.8855791 · Cited by 284 · see citing works

Bone and Muscle Endocrine Functions: Unexpected Paradigms of Inter-organ Communication

Karsenty, G., & Olson, E. N. (2016) · Cell · doi:10.1016/j.cell.2016.02.043 · Cited by 274 · see citing works

Influence of exercise on serum brain-derived neurotrophic factor concentrations in healthy human subjects

Tang, S. W., Chu, E., Hui, T. C. K., Helmeste, D. M., & Law, C. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.11.019 · Cited by 247 · see citing works

High-intensity interval training evokes larger serum BDNF levels compared with intense continuous exercise

Marquez, C. M. S., Vanaudenaerde, B. M., Troosters, T., & Wenderoth, N. (2015) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00126.2015 · Cited by 243 · see citing works

Segregating two inhibitory circuits in human motor cortex at the level of GABAA receptor subtypes: A TMS study

Di Lazzaro, V., Pilato, F., Dileone, M., Profice, P., Ranieri, F., Ricci, V., Bria, P., Tonali, P. A., & Ziemann, U. (2007) · Clinical Neurophysiology · doi:10.1016/j.clinph.2007.07.005 · Cited by 240 · see citing works

Osteocalcin—A Versatile Bone-Derived Hormone

Moser, S. C., & van der Eerden, B. C. J. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00794 · Cited by 234 · see citing works

Inhibitory circuits and the nature of their interactions in the human motor cortex – a pharmacological TMS study

Müller‐Dahlhaus, J. F. M., Liu, Y., & Ziemann, U. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.142059 · Cited by 230 · see citing works

A single bout of high-intensity aerobic exercise facilitates response to paired associative stimulation and promotes sequence-specific implicit motor learning

Mang, C. S., Snow, N. J., Campbell, K. L., Ross, C. J., & Boyd, L. A. (2014) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00498.2014 · Cited by 224 · see citing works

Plasma irisin levels progressively increase in response to increasing exercise workloads in young, healthy, active subjects

Daskalopoulou, S. S., Cooke, A. B., Sandoval, Y.-H. G., Mutter, A. F., Filippaios, A., Mesfum, E. T., & Mantzoros, C. S. (2014) · European Journal of Endocrinology · doi:10.1530/eje-14-0204 · Cited by 216 · see citing works

Serum Irisin Levels Are Regulated by Acute Strenuous Exercise

Löffler, D., Müller, U., Scheuermann, K., Friebe, D., Gesing, J. K., Bielitz, J., Erbs, S., Landgraf, K., Wagner, I. V., Kieß, W., et al. (2015) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-2932 · Cited by 213 · see citing works

Irisin in response to exercise in humans with and without metabolic syndrome

Huh, J. Y., Siopi, A., Mougios, V., Park, K. H., & Mantzoros, C. S. (2015) · The Journal of Clinical Endocrinology &amp; Metabolism · doi:10.1210/jc.2014-2416 · Cited by 210 · see citing works

Brain-derived neurotrophic factor mechanisms and function in adult synaptic plasticity: new insights and implications for therapy.

Kuipers, S. D., & Bramham, C. R. (2006) · PubMed · Cited by 209 · see citing works

Resistance exercise induces a greater irisin response than endurance exercise

Tsuchiya, Y., Ando, D., Takamatsu, K., & Goto, K. (2015) · Metabolism · doi:10.1016/j.metabol.2015.05.010 · Cited by 207 · see citing works

Motor cortex plasticity induced by paired associative stimulation is enhanced in physically active individuals

Cirillo, J., Lavender, A. P., Ridding, M. C., & Semmler, J. G. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.181834 · Cited by 199 · see citing works

Effect of brief exercise on circulating insulin-like growth factor I

Cappon, J. P., Brasel, J. A., Mohan, S., & Cooper, D. M. (1994) · Journal of Applied Physiology · doi:10.1152/jappl.1994.76.6.2490 · Cited by 190 · see citing works

Circulating Irisin in Healthy, Young Individuals: Day-Night Rhythm, Effects of Food Intake and Exercise, and Associations With Gender, Physical Activity, Diet, and Body Composition

Anastasilakis, A. D., Pοlyzos, S. A., Saridakis, Z. G., Kynigopoulos, G., Skouvaklidou, E. C., Molyvas, D., Vasiloglou, M. F., Apostolou, A., Karagiozoglou‐Lampoudi, Τ., Siopi, A., et al. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-1367 · Cited by 186 · see citing works

A Transient Elevated Irisin Blood Concentration in Response to Prolonged, Moderate Aerobic Exercise in Young Men and Women

Kraemer, R. R., Shockett, P. E., Webb, N., Shah, U. R., & Castracane, V. D. (2013) · Hormone and Metabolic Research · doi:10.1055/s-0033-1355381 · Cited by 181 · see citing works

High-intensity exercise causes greater irisin response compared with low-intensity exercise under similar energy consumption

Tsuchiya, Y., Ando, D., Goto, K., Kiuchi, M., Yamakita, M., & Koyama, K. (2014) · The Tohoku Journal of Experimental Medicine · doi:10.1620/tjem.233.135 · Cited by 176 · see citing works

A single bout of aerobic exercise promotes motor cortical neuroplasticity

McDonnell, M. N., Buckley, J. D., Opie, G. M., Ridding, M. C., & Semmler, J. G. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01378.2012 · Cited by 170 · see citing works

Mitogen‐activated protein kinase/extracellular regulated kinase signalling and memory stabilization: a review

Davis, S., & Laroche, S. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00230.x · Cited by 164 · see citing works

On the Run for Hippocampal PlasticityPreprint

Cooper, C. P., Moon, H. Y., & van Praag, H. (2017) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a029736 · Cited by 160 · see citing works

The influence of exercise on brain aging and dementia

Lautenschlager, N. T., Cox, K. L., & Cyarto, E. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.07.010 · Cited by 157 · see citing works

Bone As An Endocrine Organ

Guntur, A. R., & Rosen, C. J. (2012) · Endocrine Practice · doi:10.4158/ep12141.ra · Cited by 150 · see citing works

The influence of a single bout of aerobic exercise on short-interval intracortical excitability

Smith, A. E., Goldsworthy, M. R., Garside, T., Wood, F. M., & Ridding, M. C. (2014) · Experimental Brain Research · doi:10.1007/s00221-014-3879-z · Cited by 147 · see citing works

Aerobic exercise modulates intracortical inhibition and facilitation in a nonexercised upper limb muscle

Singh, A. M., Duncan, R. E., Neva, J. L., & Staines, R. W. (2014) · BMC Sports Science Medicine and Rehabilitation · doi:10.1186/2052-1847-6-23 · Cited by 145 · see citing works

Effects of acute resistance exercise on cognition in late middle-aged adults: General or specific cognitive improvement?

Chang, Y., Tsai, C., Huang, C., Wang, C., & Chu, I. (2013) · Journal of science and medicine in sport · doi:10.1016/j.jsams.2013.02.007 · Cited by 145 · see citing works

Irisin in Blood Increases Transiently after Single Sessions of Intense Endurance Exercise and Heavy Strength Training

Nygaard, H., Slettaløkken, G., Vegge, G., Hollan, I., Whist, J. E., Strand, T. A., Rønnestad, B. R., & Ellefsen, S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0121367 · Cited by 141 · see citing works

A role for FNDC5/Irisin in the beneficial effects of exercise on the brain and in neurodegenerative diseases

Young, M. F., Valaris, S., & Wrann, C. D. (2019) · Progress in Cardiovascular Diseases · doi:10.1016/j.pcad.2019.02.007 · Cited by 136 · see citing works

Exercise improves object recognition memory and induces BDNF expression and cell proliferation in cognitively enriched rats

Bechara, R. G., & Kelly, A. M. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.02.018 · Cited by 132 · see citing works

The concentrations of serum, plasma and platelet BDNF are all increased by treadmill VO2max performance in healthy college men

Hyun-Chul, C., Kim, J., Kim, S.-Y., Son, Y. H., Lee, N., & Jung, S. H. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.05.025 · Cited by 128 · see citing works

High-intensity Interval Exercise Promotes Motor Cortex Disinhibition and Early Motor Skill Consolidation

Stavrinos, E. L., & Coxon, J. P. (2016) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01078 · Cited by 125 · see citing works

No exercise-induced increase in serum BDNF after cycling near a major traffic road

Bos, I., Jacobs, L., Nawrot, T. S., de Geus, B., Torfs, R., Panis, L. I., Degraeuwe, B., & MEEUSEN, R. R. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.06.019 · Cited by 124 · see citing works

Molecular bases of the crosstalk between bone and muscle

Karsenty, G., & Mera, P. (2017) · Bone · doi:10.1016/j.bone.2017.04.006 · Cited by 116 · see citing works

Irisin in response to acute and chronic whole-body vibration exercise in humans

Huh, J. Y., Mougios, V., Skraparlis, A. N., Kabasakalis, A., & Mantzoros, C. S. (2014) · Metabolism · doi:10.1016/j.metabol.2014.04.001 · Cited by 112 · see citing works

Acute exercise enhances the response to paired associative stimulation-induced plasticity in the primary motor cortex

Singh, A. M., Neva, J. L., & Staines, R. W. (2014) · Experimental Brain Research · doi:10.1007/s00221-014-4049-z · Cited by 112 · see citing works

Intensity Matters: High-intensity Interval Exercise Enhances Motor Cortex Plasticity More Than Moderate Exercise

Andrews, S. C., Curtin, D., Hawi, Z., Wongtrakun, J., Stout, J. C., & Coxon, J. P. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz075 · Cited by 109 · see citing works

Active and resting motor threshold are efficiently obtained with adaptive threshold hunting

Sen, C. B. A., Fassett, H. J., El‐Sayes, J., Turco, C. V., Hameer, M. M., & Nelson, A. J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0186007 · Cited by 107 · see citing works

Local Effects of BDNF on Dendritic Growth

Horch, H. W. (2004) · Reviews in the Neurosciences · doi:10.1515/revneuro.2004.15.2.117 · Cited by 103 · see citing works

The effect of acute exercise on undercarboxylated osteocalcin and insulin sensitivity in obese men

Levinger, I., Jerums, G., Stepto, N. K., Parker, L., Serpiello, F. R., McConell, G. K., Anderson, M., Hare, D. L., Byrnes, E., Ebeling, P. R., et al. (2014) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2285 · Cited by 101 · see citing works

A Practical and Time-Efficient High-Intensity Interval Training Program Modifies Cardio-Metabolic Risk Factors in Adults with Risk Factors for Type II Diabetes

Phillips, B. E., Kelly, B. M., Lilja, M. R., Ponce‐González, J. G., Brogan, R. J., Morris, D. L., Gustafsson, T. P., Kraus, W. E., Atherton, P. J., Vollaard, N. B. J., et al. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00229 · Cited by 98 · see citing works

Physical activity levels determine exercise-induced changes in brain excitability

Lulic-Kuryllo, T., El‐Sayes, J., Fassett, H. J., & Nelson, A. J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0173672 · Cited by 97 · see citing works

Novel insights into CaMKII function and regulation during memory formation

Lucchesi, W., Mizuno, K., & Giese, K.-P. (2010) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2010.10.009 · Cited by 95 · see citing works

Higher Serum Undercarboxylated Osteocalcin and Other Bone Turnover Markers Are Associated With Reduced Diabetes Risk and Lower Estradiol Concentrations in Older Men

Yeap, B. B., Alfonso, H. S., Chubb, S. A. P., Gauci, R., Byrnes, E., Beilby, J. P., Ebeling, P. R., Handelsman, D. J., Allan, C. A., Grossmann, M., et al. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-3019 · Cited by 94 · see citing works

The effect of perspiration on the sEMG amplitude and power spectrum

Abdoli-Eramaki, M., Damecour, C., Christenson, J., & Stevenson, J. M. (2012) · Journal of Electromyography and Kinesiology · doi:10.1016/j.jelekin.2012.04.009 · Cited by 87 · see citing works

The effect of acute exercise on undercarboxylated osteocalcin in obese men

Levinger, I., Zebaze, R., Jerums, G., Hare, D. L., Selig, S. E., & Seeman, E. (2010) · Osteoporosis International · doi:10.1007/s00198-010-1370-7 · Cited by 79 · see citing works

The relationship between brain-derived neurotrophic factor, irisin and cognitive skills of endurance athletes

Belviranlı, M., Okudan, N., Kabak, B., Erdoğan, M., & Karanfılcı, M. (2016) · The Physician and Sportsmedicine · doi:10.1080/00913847.2016.1196125 · Cited by 76 · see citing works

Fatiguing intermittent lower limb exercise influences corticospinal and corticocortical excitability in the nonexercised upper limb

Takahashi, K., Maruyama, A., Hirakoba, K., Maeda, M., Etoh, S., Kawahira, K., & Rothwell, J. C. (2010) · Brain stimulation · doi:10.1016/j.brs.2010.07.001 · Cited by 71 · see citing works

Acute aerobic exercise modulates primary motor cortex inhibition

Mooney, R. A., Coxon, J. P., Cirillo, J., Glenny, H., Gant, N., & Byblow, W. D. (2016) · Experimental Brain Research · doi:10.1007/s00221-016-4767-5 · Cited by 69 · see citing works

No Influence of Noradrenaline Manipulation on Acute Exercise-Induced Increase of Brain-Derived Neurotrophic Factor

Goekint, M., Heyman, E., Roelands, B., Njemini, R., Bautmans, I., Mets, T. F., & MEEUSEN, R. R. (2008) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e31817eee85 · Cited by 62 · see citing works

Reference Intervals for Bone Turnover Markers and Their Association With Incident Hip Fractures in Older Men: The Health In Men Study

Chubb, S. A. P., Byrnes, E., Manning, L. A., Beilby, J. P., Ebeling, P. R., Vasikaran, S. D., Golledge, J., Flicker, L. A., & Yeap, B. B. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-2646 · Cited by 57 · see citing works

Brain-Derived Neurotrophic Factor: the Link Between Amyloid-β and Memory Loss

Fahnestock, M. L. (2011) · Future Neurology · doi:10.2217/fnl.11.44 · Cited by 55 · see citing works

Sodium bicarbonate ingestion augments the increase in PGC-1α mRNA expression during recovery from intense interval exercise in human skeletal muscle

Percival, M. E., Martin, B. J., Gillen, J. B., Skelly, L. E., MacInnis, M. J., Green, A. E., Tarnopolsky, M. A., & Gibala, M. J. (2015) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00048.2015 · Cited by 50 · see citing works

Acute Exercise at Different Intensities Influences Corticomotor Excitability and Performance of a Ballistic Thumb Training Task

Opie, G. M., & Semmler, J. G. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.05.049 · Cited by 48 · see citing works

The Effect of Aerobic Exercise on Neuroplasticity within the Motor Cortex following Stroke

Murdoch, K., Buckley, J. D., & McDonnell, M. N. (2016) · PLoS ONE · doi:10.1371/journal.pone.0152377 · Cited by 45 · see citing works

Fibroblast growth factor 23 as a phosphotropic hormone and beyond

Fukumoto, S., & Shimizu, Y. (2011) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-011-0298-0 · Cited by 44 · see citing works

No changes in corticospinal excitability, biochemical markers, and working memory after six weeks of high‐intensity interval training in sedentary males

Nicolini, C., Toepp, S. L., Harasym, D., Michalski, B., Fahnestock, M. L., Gibala, M. J., & Nelson, A. J. (2019) · Physiological Reports · doi:10.14814/phy2.14140 · Cited by 42 · see citing works

The Effects of Biological Sex and Ovarian Hormones on Exercise-Induced Neuroplasticity

El‐Sayes, J., Turco, C. V., Skelly, L. E., Nicolini, C., Fahnestock, M. L., Gibala, M. J., & Nelson, A. J. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.04.054 · Cited by 40 · see citing works

Proportion of Undercarboxylated Osteocalcin and Serum P1NP Predict Incidence of Myocardial Infarction in Older Men

Yeap, B. B., Alfonso, H. S., Chubb, S. A. P., Byrnes, E., Beilby, J. P., Ebeling, P. R., Allan, C. A., Schultz, C. J., Hankey, G. J., Golledge, J., et al. (2015) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2015-1899 · Cited by 31 · see citing works

The effects of upper limb posture and a sub-maximal gripping task on corticospinal excitability to muscles of the forearm

Forman, D. A., Baarbé, J. K., Daligadu, J., Murphy, B. A., & Holmes, M. W. R. (2016) · Journal of Electromyography and Kinesiology · doi:10.1016/j.jelekin.2016.02.005 · Cited by 29 · see citing works

Mitogen-Activated Protein Kinase Phosphatase-2 Deletion Impairs Synaptic Plasticity and Hippocampal-Dependent Memory

Rahman, N. Z. A., Greenwood, S. M., Brett, R. R., Tossell, K., Ungless, M. A., Plevin, R. J., & Bushell, T. J. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3825-15.2016 · Cited by 28 · see citing works

Intensity of acute aerobic exercise but not aerobic fitness impacts on corticospinal excitability

MacDonald, M., Khan, H., Kraeutner, S. N., Usai, F., Rogers, E. A., Kimmerly, D. S., Dechman, G., & Boe, S. G. (2019) · Applied Physiology Nutrition and Metabolism · doi:10.1139/apnm-2018-0643 · Cited by 24 · see citing works

Acute high-intensity and moderate-intensity interval exercise do not change corticospinal excitability in low fit, young adults

El‐Sayes, J., Turco, C. V., Skelly, L. E., Locke, M. B., Gibala, M. J., & Nelson, A. J. (2020) · PLoS ONE · doi:10.1371/journal.pone.0227581 · Cited by 21 · see citing works

Exerkines in health, resilience and disease

Chow, L. S., Gerszten, R. E., Taylor, J. M., Pedersen, B. K., van Praag, H., Trappe, S., Febbraio, M. A., Galis, Z. S., Gao, Y., Haus, J. M., et al. (2022) · Nature Reviews Endocrinology · doi:10.1038/s41574-022-00641-2 · Cited by 927 · see citing works

Effects of Aerobic Exercise Training on Systemic Biomarkers and Cognition in Late Middle-Aged Adults at Risk for Alzheimer’s Disease

Gaitán, J. M., Moon, H. Y., Stremlau, M., Dubal, D. B., Cook, D. B., Okonkwo, O. C., & van Praag, H. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.660181 · Cited by 160 · see citing works

Exerkines and long-term synaptic potentiation: Mechanisms of exercise-induced neuroplasticity

Vints, W. A. J., Levin, O., Fujiyama, H., Verbunt, J., & Masiulis, N. (2022) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2022.100993 · Cited by 114 · see citing works

Immediate effect of high-intensity exercise on brain-derived neurotrophic factor in healthy young adults: A systematic review and meta-analysis

Fernández‐Rodríguez, R., Álvarez‐Bueno, C., Martínez-Ortega, I. A., Martínez‐Vizcaíno, V., Mesas, A. E., & Notario‐Pacheco, B. (2021) · Journal of sport and health science/Journal of Sport and Health Science · doi:10.1016/j.jshs.2021.08.004 · Cited by 102 · see citing works

The Combined Influences of Exercise, Diet and Sleep on Neuroplasticity

Pickersgill, J. W., Turco, C. V., Ramdeo, K. R., Rehsi, R. S., Foglia, S. D., & Nelson, A. J. (2022) · Frontiers in Psychology · doi:10.3389/fpsyg.2022.831819 · Cited by 88 · see citing works

Mechanisms of the Beneficial Effects of Exercise on Brain-Derived Neurotrophic Factor Expression in Alzheimer’s Disease

Jaberi, S., & Fahnestock, M. L. (2023) · Biomolecules · doi:10.3390/biom13111577 · Cited by 74 · see citing works

Understanding the Neurophysiological and Molecular Mechanisms of Exercise-Induced Neuroplasticity in Cortical and Descending Motor Pathways: Where Do We Stand?

Nicolini, C., Fahnestock, M. L., Gibala, M. J., & Nelson, A. J. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.12.013 · Cited by 50 · see citing works

Comparative Impact of Various Exercises on Circulating Irisin in Healthy Subjects: A Systematic Review and Network Meta-Analysis

Kazeminasab, F., Sadeghi, E., & Afshari-Safavi, A. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/8235809 · Cited by 43 · see citing works

Cellular and Molecular Regulation of Exercise—A Neuronal Perspective

Reddy, I., Yadav, Y., & Dey, C. S. (2022) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-022-01272-x · Cited by 41 · see citing works

Exercise, exerkines, and cardiometabolic health: from individual players to a team sport

Robbins, J., & Gerszten, R. E. (2023) · Journal of Clinical Investigation · doi:10.1172/jci168121 · Cited by 41 · see citing works

Musculoskeletal Deficits and Cognitive Impairment: Epidemiological Evidence and Biological Mechanisms

Sui, S. X., Balanta‐Melo, J., Pasco, J. A., & Plotkin, L. I. (2022) · Current Osteoporosis Reports · doi:10.1007/s11914-022-00736-9 · Cited by 34 · see citing works

High Intensity Acute Aerobic Exercise Elicits Alterations in Circulating and Skeletal Muscle Tissue Expression of Neuroprotective Exerkines

Mazo, C. E., Miranda, E. R., Shadiow, J., Vesia, M., & Haus, J. M. (2022) · Brain Plasticity · doi:10.3233/bpl-220137 · Cited by 29 · see citing works

Exercise and Dietary Factors Mediate Neural Plasticity Through Modulation of BDNF Signaling

Fakhoury, M., Eid, F., Ahmad, P. E., Khoury, R. E., Mezher, A., Masri, D. E., Haddad, Z. L., Zoghby, Y. E., Ghayad, L. M., Sleiman, S. F., et al. (2022) · Brain Plasticity · doi:10.3233/bpl-220140 · Cited by 29 · see citing works

Time-dependent cortical plasticity during moderate-intensity continuous training versus high-intensity interval training in rats

Hugues, N., Pin-Barre, C., Pellegrino, C., Rivera, C., Berton, É., & Laurin, J. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab451 · Cited by 28 · see citing works

Exercise, Neuroprotective Exerkines, and Parkinson’s Disease: A Narrative Review

Mitchell, A. K., Bliss, R. R., & Church, F. (2024) · Biomolecules · doi:10.3390/biom14101241 · Cited by 32 · see citing works

Resilience by design: How nature, nurture, environment, and microbiome mitigate stress and allostatic load

Chbeir, S., & Carrión, V. (2023) · World Journal of Psychiatry · doi:10.5498/wjp.v13.i5.144 · Cited by 25 · see citing works

Effects of exercise on brain-derived neurotrophic factor in Alzheimer's disease models: A systematic review and meta-analysis

Zhang, S., Gu, B., Zhen, K., Du, L., Lv, Y., & Yu, L. (2024) · Archives of Gerontology and Geriatrics · doi:10.1016/j.archger.2024.105538 · Cited by 25 · see citing works

The Effect of Two Somatic-Based Practices Dance and Martial Arts on Irisin, BDNF Levels and Cognitive and Physical Fitness in Older Adults: A Randomized Control Trial

Hola, V., Polanská, H., Jandova, T., Dytrtová, J. J., Weinerová, J., Šteffl, M., Kramperová, V., Daďová, K., Durkalec‐Michalski, K., & Bartoš, A. (2024) · Clinical Interventions in Aging · doi:10.2147/cia.s482479 · Cited by 27 · see citing works

Exercise Factors Released by the Liver, Muscle, and Bones Have Promising Therapeutic Potential for Stroke

Stephan, J. S., & Sleiman, S. F. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.600365 · Cited by 23 · see citing works

Transcranial Magnetic Stimulation to Assess Exercise-Induced Neuroplasticity

Turco, C. V., & Nelson, A. J. (2021) · Frontiers in Neuroergonomics · doi:10.3389/fnrgo.2021.679033 · Cited by 23 · see citing works

Running from stress: a perspective on the potential benefits of exercise-induced small extracellular vesicles for individuals with major depressive disorder

Khoury, R., & Nagy, C. (2023) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2023.1154872 · Cited by 18 · see citing works

Acute Exercise Modulates the Excitability of Specific Interneurons in Human Motor Cortex

Neva, J. L., Brown, K. E., Peters, S., Feldman, S. J., Mahendran, N., Boisgontier, M. P., & Boyd, L. A. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.08.032 · Cited by 18 · see citing works

Neurophysiological effects of acute aerobic exercise in young adults: a systematic review and meta-analysis

Youssef, L., Harroum, N., Francisco, B. A., Johnson, L. G., Arvisais, D., Pageaux, B., Romain, A. J., Hayward, K. S., & Neva, J. L. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105811 · Cited by 17 · see citing works

Exercise Intervention for Alzheimer’s Disease: Unraveling Neurobiological Mechanisms and Assessing Effects

Ren, J., & Xiao, H. (2023) · Life · doi:10.3390/life13122285 · Cited by 16 · see citing works

Neuroplasticity to autophagy cross-talk in a therapeutic effect of physical exercises and irisin in ADHD

Abdulghani, A., Poghosyan, M., Mehren, A., Philipsen, A., & Anderzhanova, E. A. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.997054 · Cited by 15 · see citing works

Investigation of Brain Function-Related Myokine Secretion by Using Contractile 3D-Engineered Muscle

Sugimoto, T., Nakamura, T., YOKOYAMA, S., Fujisato, T., Konishi, S., & Hashimoto, T. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105723 · Cited by 14 · see citing works

Enhanced motor learning and motor savings after acute intermittent hypoxia are associated with a reduction in metabolic cost

Bogard, A. T., Hemmerle, M. R., Smith, A. C., & Tan, A. Q. (2023) · The Journal of Physiology · doi:10.1113/jp285425 · Cited by 13 · see citing works

Charting the Molecular Terrain of Exercise: Energetics, Exerkines, and the Future of Multiomic Mapping

Katz, D. H., Lindholm, M. E., & Ashley, E. A. (2024) · Physiology · doi:10.1152/physiol.00024.2024 · Cited by 12 · see citing works

Myokines and osteokines in aging-related degenerative diseases: Regulatory networks in the muscle-bone-brain axis

Gao, S., Li, N., Qi, L., Li, X., Zhang, J., Zhang, Z., Xu, Z., Liang, S., Zhu, W., & Liu, W. (2025) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2025.09.001 · Cited by 12 · see citing works

Cathepsin B and Muscular Strength are Independently Associated with Cognitive Control

Kim, J., McKenna, C. F., Salvador, A. F., Scaroni, S. E., Askow, A. T., Cerna, J., Cannavale, C. N., Paluska, S. A., Lisio, M. D., Petruzzello, S. J., et al. (2022) · Brain Plasticity · doi:10.3233/bpl-210136 · Cited by 11 · see citing works

Current Methodological Pitfalls and Caveats in the Assessment of Exercise-Induced Changes in Peripheral Brain-Derived Neurotrophic Factor: How Result Reproducibility Can Be Improved

Nicolini, C., & Nelson, A. J. (2021) · Frontiers in Neuroergonomics · doi:10.3389/fnrgo.2021.678541 · Cited by 8 · see citing works

Impact of Acute High-intensity Interval Training on Cortical Excitability, M1-related Cognitive Functions, and Myokines: A Randomized Crossover Study

Gökçe, E., Adıgüzel, E., Koçak, Ö. K., Kılınç, H., Langeard, A., Boran, H. E., & Çengiz, B. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2024.05.032 · Cited by 7 · see citing works

Modulating Brain Excitability with Cardiovascular Exercise in Chronic Stroke: A Randomized Controlled Trial

Rodrigues, L., Moncion, K., Heras, B. D. L., Cristini, J., Khalili, R., Eng, J. J., Fung, J., MacKay-Lyons, M. J., Thiel, A., Tang, A., et al. (2025) · Neurorehabilitation and neural repair · doi:10.1177/15459683251351883 · Cited by 7 · see citing works

Use-dependent corticospinal excitability is associated with resilience and physical performance during simulated military operational stress

Proessl, F., Canino, M. C., Beckner, M. E., Conkright, W. R., LaGoy, A. D., Sinnott, A. M., Eagle, S. R., Martin, B. J., Sterczala, A. J., Roma, P. G., et al. (2021) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00628.2021 · Cited by 6 · see citing works

Effect of Single Bout of Moderate and High Intensity Interval Exercise on Brain Derived Neurotrophic Factor and Working Memory in Young Adult Females

Shah, Z., Ahmad, F., Zahra, M., Zulfiqar, F., Aziz, S., & Mahmood, A. (2022) · Brain Plasticity · doi:10.3233/bpl-210130 · Cited by 6 · see citing works

The Effects of Electrical Stimulation on a 3D Osteoblast Cell Model

Mahadeo, C., Shahin‐Shamsabadi, A., Khodamoradi, M., Fahnestock, M. L., & Selvaganapathy, P. R. (2025) · Cells · doi:10.3390/cells14060396 · Cited by 5 · see citing works

Investigating the mediating effect of myokines on exercise-induced cognitive changes in older adults: A living systematic review and meta-analysis

Vints, W. A. J., Gökçe, E., Langeard, A., Павлова, Ю., Çevik, Ö. S., Ziaaldini, M. M., Todri, J., Lena, O., Shalom, S. B., Jak, S., et al. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106381 · Cited by 5 · see citing works

Bone-brain crosstalk: emerging roles of osteocalcin in central nervous system disorders

Chen, H., Zhang, Z., Yi, W., Wang, N., Dong, X., Xing, Y., Liu, Q., Wu, Y., & Ma, X. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.12.028 · Cited by 6 · see citing works

The Effects of Exercise on Synaptic Plasticity in Individuals With Mild Cognitive Impairment: Protocol for a Pilot Intervention Study

Ramdeo, K. R., Fahnestock, M. L., Gibala, M. J., Selvaganapathy, P. R., Lee, J., & Nelson, A. J. (2023) · JMIR Research Protocols · doi:10.2196/50030 · Cited by 5 · see citing works

Reducing motor evoked potential amplitude variability through normalization

Viana, F. F., Cotovio, G., da Silva, D. R., Seybert, C., Pereira, P., Silva, A., Carvalho, F., & Oliveira-Maia, A. J. (2024) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2024.1279072 · Cited by 4 · see citing works

Research Progress on the Effects of Different Exercise Modes on the Secretion of Exerkines After Spinal Cord Injury

Li, Q., Li, C., & Zhang, X. (2024) · Cellular and molecular neurobiology · doi:10.1007/s10571-024-01497-y · Cited by 5 · see citing works

Exercise and its beneficial impacts on mood disorders and neurodegeneration: a novel mechanistic perspective of the exosomes involvement

Wang, J., Fan, S., & Wang, J. (2025) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-025-05357-1 · Cited by 3 · see citing works

Motor cortical excitability and inhibition are differentially modulated by aerobic exercise intensity

Harroum, N., O’Farrell, A., Youssef, L., Bohbot, L., Maati, H., Joubert, M., Pageaux, B., & Neva, J. L. (2025) · Cerebral Cortex · doi:10.1093/cercor/bhaf230 · Cited by 6 · see citing works

High-Velocity, Accentuated Eccentric, or Maximal Elastic Band Resistance Training? Effects of Resistance Training Modalities on Bone Health, Isokinetic Strength, and Systemic Biomarkers in Sedentary Older Adults: A Comparative Study

Saez-Berlanga, Á., Gené‐Morales, J., Teixeira, A. M., Castuera, R. J., Gené‐Sampedro, A., Juesas, Á., Gargallo, P., Caballero, O., Garrido, J. F., Alix‐Fages, C., et al. (2025) · Healthcare · doi:10.3390/healthcare13233129 · Cited by 3 · see citing works

Motor cortex plasticity is greater in endurance-trained cyclists following acute exercise

Hand, B. J., Opie, G. M., Sidhu, S. K., & Semmler, J. G. (2022) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00213.2022 · Cited by 3 · see citing works

Comparing the effect of high-intensity interval exercise and voluntary exercise training on cognitive functions in rats

Sezer, T., Okudan, N., & Belviranlı, M. (2024) · Neuroscience Letters · doi:10.1016/j.neulet.2024.137993 · Cited by 3 · see citing works

High-intensity training and irisin response: A possible molecular cross-talk for irisin response

Li, P., Tong, L., & Bi, X. (2025) · Current Research in Physiology · doi:10.1016/j.crphys.2025.100163 · Cited by 4 · see citing works

Exercise-induced neuroplasticity

Neva, J. L. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00218-7 · Cited by 3 · see citing works

Global multi-omics analysis of exerkines in progressive treadmill-exercised rodentsPreprint

Taha, H. B. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.08.627439 · Cited by 3 · see citing works

Acute exercise after motor practice enhances generalized skill learning, corticospinal excitability and intermuscular coherence in older adults

Bjørndal, J. R., Jespersen, L., Wiedemann, R. D., Therkildsen, E. R., Karabanov, A. N., & Lundbye‐Jensen, J. (2025) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2025.108107 · Cited by 2 · see citing works

Irisin at the Croasroad of Autophagy and BNDF Signaling for Neuroplasticity Regulation

Anderzhanova, E. A., & Воронина, Т. А. (2023) · Neurochemical Journal · doi:10.1134/s1819712423020034 · Cited by 2 · see citing works

Unraveling of Molecular Mechanisms of Cognitive Frailty in Chronic Kidney Disease: How Exercise Makes a Difference

Michou, V., Tsamos, G., Vasdeki, D., Deligiannis, A. P., & Kouidi, E. J. (2024) · Journal of Clinical Medicine · doi:10.3390/jcm13195698 · Cited by 2 · see citing works

Could aerobic exercise applied before constraint-induced movement therapy change circulating molecular biomarkers in chronic post-stroke?

García-Salazar, L. F., Pereira, N. D., da Silva, E. S. M., Ribeiro, J. A. M., Ocamoto, G. N., Zambetta, R. M., Oliveira, S. G., Catai, A. M., Borstad, A. L., & Russo, T. L. (2024) · Physiotherapy Theory and Practice · doi:10.1080/09593985.2024.2411311 · Cited by 2 · see citing works

Motor cortical circuits are uniquely impacted by different exercise intensitiesPreprint

Harroum, N., O’Farrell, A., Youssef, L., Bohbot, L., Maati, H., Joubert, M., Pageaux, B., & Neva, J. L. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.24.634315 · Cited by 2 · see citing works

High intensity interval exercise maintains irisin level and reduces body fat in overweight women

Karimullah, A., Wibowo, N. F., Devi, A. I., Ilmi, S. Z., Yosnengsih, Azmy, U., Irwadi, I., Mohamed, M. N. A., Kusnanik, N. W., Purwanto, B., et al. (2023) · Comparative Exercise Physiology · doi:10.1163/17552559-20230030 · Cited by 1 · see citing works

Short-term moderate-intensity treadmill running may confer a greater benefit to bone strength than high-intensity treadmill running in 12-month-old C57BL/6 mice

Chan, A. S., Zare, N., Blank, M. A., Broatch, J. R., Bishop, D. J., Sims, N. A., Lynch, G. S., & Levinger, I. (2025) · Bone · doi:10.1016/j.bone.2025.117615 · Cited by 1 · see citing works

Cross-Platform Transcriptomic Analysis of 40 Human and Rodent Skeletal Muscle Exerkines

Taha, H. B., Robbins, N., Zoha, F.-S., Zhu, S., Vivek, N., & Bogoniewski, A. (2026) · Muscles · doi:10.3390/muscles5010015 · Cited by 1 · see citing works

Sports-Related Concussion Assessment: A New Physiological, Biomechanical, and Cognitive Methodology Incorporating a Randomized Controlled Trial Study Protocol

Irwin, G., Rogatzki, M. J., Wiltshire, H., Williams, G., Gu, Y., Ash, G. I., Tao, D., & Baker, J. S. (2023) · Biology · doi:10.3390/biology12081089 · Cited by 1 · see citing works

Irisin at the Crossroad of Autophagy and BNDF Signaling for Neuroplasticity Regulation

Андяржанова, Э. А., & Воронина, Т. А. (2023) · Нейрохимия · doi:10.31857/s1027813323020036 · Cited by 1 · see citing works

Effects of Physical Activity-Induced Myocytokines on Alzheimer's Disease

He, Q. (2022) · Journal of Quality in Health Care & Economics · doi:10.23880/jqhe-16000255

High intensity exercise may be needed to change Levels of Biomarkers related to Neuroplasticity

Murphy, B. A. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.04.012 · Cited by 1 · see citing works

Efecto de la osteocalcina y el ejercicio físico, sobre la función cognitiva en adultos y adultos mayores: una revisión sistemática

Morales, V. J., Ledesma-Amaya, L. I., Vázquez-Moreno, A., Delgado‐Olivares, L., Lerma, A., & Bosques-Brugada, L. E. (2024) · Revista Argentina de Ciencias del Comportamiento ( RACC ) · doi:10.32348/1852.4206.v16.n4.45118

Eccentric cycling enhances primary motor cortex excitabilityPreprint

Youssef, L., O’Farrell, A., Harroum, N., Bakhta, Y., Cohen, L., Pageaux, B., & Neva, J. L. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.04.663236

Gating of Neuroplasticity: Effects and Mechanisms of Acute Aerobic Exercise as a Brain Stimulation for the Sensorimotor Cortex

Yamazaki, Y., Sato, D., & Yamashiro, K. (2025) · Advances in neurobiology · doi:10.1007/978-981-95-0066-6_22

Amelioration of emotional processing deficits in individuals with high trait anxiety following high-intensity interval training

Li, C., Che, X., Yu, J., Yan, F., Yu, F., Zhao, P., Zhang, J., Zhao, L., & Xia, X. (2025) · BMC Psychology · doi:10.1186/s40359-025-03413-5

Aerobic Exercise Intensity: A Dose-Response Effect on Motor Adaptation and LearningPreprint

Harroum, N., Mahrez, Y., Pageaux, B., & Neva, J. L. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.28.680122

Étude des effets de programmes d’entrainement en endurance sur la performance, les fonctions cognitives et sensorimotrices ainsi que sur la plasticité cérébrale chez le rat sain et ayant subi une ischémie cérébrale

Hugues, N. (2023) · theses.fr (ABES) · doi:10.70675/3c52cc4bze9dfz499cza28az42945d38cbd6

Motor cortical excitability is differentially modulated by HIIT and strength exercise

Rostami, M., Lee, A., Frazer, A. K., Akalu, Y., Siddique, U., Walker, S., Tallent, J., & Kidgell, D. J. (2026) · Journal of Sports Sciences · doi:10.1080/02640414.2026.2705072

Brain-Derived Neurotrophic Factor in Neurodegenerative Diseases: Biomarker Evidence and Therapeutic Perspectives

Turčić, M., & Vurušić, K. (2026) · Galician Medical Journal · doi:10.21802/e-gmj2026-a24

No changes in corticospinal excitability, biochemical markers, and working memory after six weeks of high‐intensity interval training in sedentary males

Nicolini, C., Toepp, S. L., Harasym, D., Michalski, B., Fahnestock, M. L., Gibala, M. J., & Nelson, A. J. (2019) · Physiological Reports · doi:10.14814/phy2.14140 · Cited by 42 · see citing works

Acute Effects of High-Intensity Aerobic Exercise on Motor Cortical Excitability and Inhibition in Sedentary Adults

Hendy, A. M., Andrushko, J. W., Gatta, P. A. D., & Teo, W. (2022) · Frontiers in Psychology · doi:10.3389/fpsyg.2022.814633 · Cited by 29 · see citing works

Acute high-intensity and moderate-intensity interval exercise do not change corticospinal excitability in low fit, young adults

El‐Sayes, J., Turco, C. V., Skelly, L. E., Locke, M. B., Gibala, M. J., & Nelson, A. J. (2020) · PLoS ONE · doi:10.1371/journal.pone.0227581 · Cited by 21 · see citing works

A single bout of aerobic exercise promotes motor cortical neuroplasticity

McDonnell, M. N., Buckley, J. D., Opie, G. M., Ridding, M. C., & Semmler, J. G. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01378.2012 · Cited by 170 · see citing works

Interleukin-6, undercarboxylated osteocalcin, and brain-derived neurotrophic factor responses to single and repeated sessions of high-intensity interval exercise

Aktitiz, S., ATAKAN, M. M., Turnagöl, H. H., & Koşar, Ş. N. (2022) · Peptides · doi:10.1016/j.peptides.2022.170864 · Cited by 8 · see citing works