The hypothalamus

Sleep state switching

Saper, C. B., Fuller, P. M., Pedersen, N. P., Lu, J., & Scammell, T. E. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.032 · Cited by 1,404 · see citing works

Neurobiology of food intake in health and disease

Morton, G. J., Meek, T. H., & Schwartz, M. W. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3745 · Cited by 748 · see citing works

Central Neural Regulation of Brown Adipose Tissue Thermogenesis and Energy Expenditure

Morrison, S. F., Madden, C. J., & Tupone, D. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.02.007 · Cited by 427 · see citing works

Neural circuitry engaged by prostaglandins during the sickness syndrome

Saper, C. B., Romanovsky, A. A., & Scammell, T. E. (2012) · Nature Neuroscience · doi:10.1038/nn.3159 · Cited by 285 · see citing works

Optogenetics, Sex, and Violence in the Brain: Implications for Psychiatry

Anderson, D. J. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.11.012 · Cited by 127 · see citing works

2010 Carl Ludwig Distinguished Lectureship of the APS Neural Control and Autonomic Regulation Section: Central neural pathways for thermoregulatory cold defense

Morrison, S. F. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01227.2010 · Cited by 111 · see citing works

A high-resolution transcriptomic and spatial atlas of cell types in the whole mouse brain

Yao, Z., van Velthoven, C. T. J., Kunst, M., Zhang, M., McMillen, D., Lee, C., Jung, W., Goldy, J., Abdelhak, A., Aitken, M., et al. (2023) · Nature · doi:10.1038/s41586-023-06812-z · Cited by 1,194 · see citing works

Ventromedial hypothalamic neurons control a defensive emotion state

Kunwar, P. S., Zelikowsky, M., Remedios, R., Cai, H., Balban, M. Y., Meister, M., & Anderson, D. J. (2015) · eLife · doi:10.7554/elife.06633 · Cited by 1,112 · see citing works

Neural circuits of interoception

Berntson, G. G., & Khalsa, S. S. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.09.011 · Cited by 419 · see citing works

The Basal Ganglia Over 500 Million Years

Grillner, S. E., & Robertson, B. (2016) · Current Biology · doi:10.1016/j.cub.2016.06.041 · Cited by 350 · see citing works

HypoMap—a unified single-cell gene expression atlas of the murine hypothalamus

Steuernagel, L., Lam, B. Y. H., Klemm, P., Dowsett, G. K. C., Bauder, C. A., Tadross, J. A., Hitschfeld, T. S., del Rio Martin, A., Chen, W., de Solis, A. J., et al. (2022) · Nature Metabolism · doi:10.1038/s42255-022-00657-y · Cited by 267 · see citing works

Multimodal analysis of cell types in a hypothalamic node controlling social behavior

Kim, D.-W., Yao, Z., Graybuck, L. T., Kim, T. K., Nguyen, T. N., Smith, K. A., Fong, O., Yi, L., Koulena, N., Pierson, N., et al. (2019) · Cell · doi:10.1016/j.cell.2019.09.020 · Cited by 259 · see citing works

A hypothalamic novelty signal modulates hippocampal memory

Chen, S., He, L., Huang, A. J. Y., Boehringer, R., Robert, V., Wintzer, M. E., Polygalov, D., Weitemier, A. Z., Tao, Y., Gu, M., et al. (2020) · Nature · doi:10.1038/s41586-020-2771-1 · Cited by 258 · see citing works

Hypothalamic control of energy expenditure and thermogenesis

Tran, L. T., Park, S., Kim, S. K., Lee, J. S., Kim, K. W., & Kwon, O. (2022) · Experimental & Molecular Medicine · doi:10.1038/s12276-022-00741-z · Cited by 208 · see citing works

Behavioral state coding by molecularly defined paraventricular hypothalamic cell type ensembles

Xu, S., Yang, H., Menon, V., Lemire, A. L., Wang, L., Henry, F. E., Turaga, S. C., & Sternson, S. M. (2020) · Science · doi:10.1126/science.abb2494 · Cited by 197 · see citing works

A hypothalamus-habenula circuit controls aversion

Lazaridis, I., Tzortzi, O., Weglage, M., Märtin, A., Xuan, Y., Parent, M. A., Johansson, Y., Fuzik, J., Fürth, D., Fenno, L. E., et al. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0369-5 · Cited by 180 · see citing works

Molecular design of hypothalamus development

Romanov, R. A., Tretiakov, E. O., Kastriti, M. E., Zupančič, M., Häring, M., Korchynska, S., Popadin, K. Y., Benevento, M., Rebernik, P., Lallemend, F., et al. (2020) · Nature · doi:10.1038/s41586-020-2266-0 · Cited by 172 · see citing works

The Paraventricular Nucleus of the Hypothalamus: Development, Function, and Human Diseases

Qin, C., Li, J., & Tang, K. (2018) · Endocrinology · doi:10.1210/en.2018-00453 · Cited by 164 · see citing works

Stress and central autonomic network

Lamotte, G. J., Shouman, K., & Benarroch, E. E. (2021) · Autonomic Neuroscience · doi:10.1016/j.autneu.2021.102870 · Cited by 148 · see citing works

Connectional architecture of a mouse hypothalamic circuit node controlling social behavior

Lo, L., Yao, S., Kim, D., Cetin, A. H., Harris, J. A., Zeng, H., Anderson, D. J., & Weissbourd, B. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1817503116 · Cited by 138 · see citing works

A high-resolution in vivo magnetic resonance imaging atlas of the human hypothalamic region

Neudorfer, C., Germann, J., Elias, G. J. B., Gramer, R., Boutet, A., & Lozano, A. M. (2020) · Scientific Data · doi:10.1038/s41597-020-00644-6 · Cited by 136 · see citing works

An approximate line attractor in the hypothalamus encodes an aggressive state

Nair, A., Karigo, T., Yang, B., Ganguli, S., Schnitzer, M. J., Linderman, S. W., Anderson, D. J., & Kennedy, A. (2023) · Cell · doi:10.1016/j.cell.2022.11.027 · Cited by 143 · see citing works

Neural Circuits for Emotion

Malézieux, M., Klein, A. S., & Gogolla, N. (2023) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-111020-103314 · Cited by 131 · see citing works

Development of the Neuroendocrine Hypothalamus

Burbridge, S., Stewart, I. D., & Placzek, M. (2016) · Comprehensive physiology · doi:10.1002/cphy.c150023 · Cited by 115 · see citing works

Oxytocin-receptor-expressing neurons in the parabrachial nucleus regulate fluid intake

Ryan, P. J., Ross, S. I., Campos, C., Derkach, V. A., & Palmiter, R. D. (2017) · Nature Neuroscience · doi:10.1038/s41593-017-0014-z · Cited by 113 · see citing works

Multiple convergent hypothalamus–brainstem circuits drive defensive behavior

Lovett-Barron, M., Chen, R., Bradbury, S., Andalman, A. S., Wagle, M. D., Guo, S., & Deisseroth, K. A. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0655-1 · Cited by 110 · see citing works

The Brain–to–Pancreatic Islet Neuronal Map Reveals Differential Glucose Regulation From Distinct Hypothalamic Regions

Rosario, W., Singh, I., Wautlet, A., Patterson, C., Flak, J., Becker, T., Ali, A. F., Tamarina, N., Philipson, L., Enquist, L., et al. (2016) · Diabetes · doi:10.2337/db15-0629 · Cited by 98 · see citing works

The structural and functional complexity of the integrative hypothalamus

Fong, H., Zheng, J., & Kurrasch, D. M. (2023) · Science · doi:10.1126/science.adh8488 · Cited by 103 · see citing works

The Structural Connectome of the Human Central Homeostatic Network

Edlow, B. L., McNab, J. A., Witzel, T., & Kinney, H. C. (2015) · Brain Connectivity · doi:10.1089/brain.2015.0378 · Cited by 99 · see citing works

Cellular activity in insular cortex across seconds to hours: Sensations and predictions of bodily states

Livneh, Y., & Andermann, M. L. (2021) · Neuron · doi:10.1016/j.neuron.2021.08.036 · Cited by 106 · see citing works

Skeletal interoception in bone homeostasis and pain

Lv, X., Gao, F., & Cao, X. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.09.025 · Cited by 93 · see citing works

A GABAergic neural circuit in the ventromedial hypothalamus mediates chronic stress–induced bone loss

Yang, F., Liu, Y., Chen, S., Dai, Z., Yang, D., Gao, D., Shao, J., Wang, Y., Wang, T., Zhang, Z., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci136105 · Cited by 86 · see citing works

Reciprocal activity of AgRP and POMC neurons governs coordinated control of feeding and metabolism

Solís, A. J. D., Río-Martín, A. D., Radermacher, J., Chen, W., Steuernagel, L., Bauder, C. A., Eggersmann, F. R., Morgan, D. A., Lena, C. A., Sue, M. W., et al. (2024) · Nature Metabolism · doi:10.1038/s42255-024-00987-z · Cited by 91 · see citing works

The self on its axis: a framework for understanding depression

Davey, C. G., & Harrison, B. J. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01790-8 · Cited by 85 · see citing works

Histamine and the striatum

Bolam, J. P., & Ellender, T. J. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.08.013 · Cited by 83 · see citing works

Non-Contact Infrared Thermometers and Thermal Scanners for Human Body Temperature Monitoring: A Systematic Review

Zhao, Y., & Bergmann, J. (2023) · Sensors · doi:10.3390/s23177439 · Cited by 82 · see citing works

Neurogenetic basis for circadian regulation of metabolism by the hypothalamusPreprint

Cedernaes, J., Waldeck, N. J., & Bass, J. T. (2019) · Genes & Development · doi:10.1101/gad.328633.119 · Cited by 84 · see citing works

Cellular taxonomy and spatial organization of the murine ventral posterior hypothalamus

Mickelsen, L. E., Flynn, W. F., Springer, K., Wilson, L., Beltrami, E. J., Bolisetty, M. T., Robson, P., & Jackson, A. C. (2020) · eLife · doi:10.7554/elife.58901 · Cited by 78 · see citing works

Pivotal role of median eminence tanycytes for hypothalamic function and neurogenesis

Rizzoti, K., & Lovell-Badge, R. H. (2016) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.08.020 · Cited by 79 · see citing works

Cellular and molecular properties of neural progenitors in the developing mammalian hypothalamus

Zhou, X., Zhong, S., Peng, H., Liu, J., Ding, W., Sun, L., Ma, Q., Liu, Z., Chen, R., Wu, Q., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17890-2 · Cited by 77 · see citing works

The anterior hypothalamus in cluster headache

Arkink, E. B., Schmitz, N., Schoonman, G. G., van Vliet, J. A., Haan, J., van Buchem, M. A., Ferrari, M. D., & Kruit, M. C. (2016) · Cephalalgia · doi:10.1177/0333102416660550 · Cited by 76 · see citing works

Molecular and Neural Functions of Rai1 , the Causal Gene for Smith-Magenis Syndrome

Huang, W., Guenthner, C. J., Xu, J., Nguyen, T., Schwarz, L. A., Wilkinson, A. W., Gozani, O., Chang, H. Y., Shamloo, M., & Luo, L. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.019 · Cited by 72 · see citing works

The forgotten effects of thyrotropin-releasing hormone: Metabolic functions and medical applications

Fröhlich, E., & Wahl, R. (2018) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2018.06.006 · Cited by 72 · see citing works

The neural basis of sex differences in sexual behavior: A quantitative meta-analysis

Poeppl, T. B., Langguth, B., Rupprecht, R., Safron, A., Bzdok, D., Laird, A. R., & Eickhoff, S. B. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.10.001 · Cited by 69 · see citing works

Metabolic Crosstalk between Liver and Brain: From Diseases to Mechanisms

Yang, X., Qiu, K., Jiang, Y., Huang, Y., Zhang, Y., & Liao, Y. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25147621 · Cited by 69 · see citing works

Imaging the Limbic System in Parkinson’s Disease—A Review of Limbic Pathology and Clinical Symptoms

Banwinkler, M., Theis, H., Prange, S., & van Eimeren, T. (2022) · Brain Sciences · doi:10.3390/brainsci12091248 · Cited by 66 · see citing works

Homeodomain protein Otp affects developmental neuropeptide switching in oxytocin neurons associated with a long-term effect on social behavior

Wircer, E., Blechman, J., Borodovsky, N., Tsoory, M., Nunes, A. R., Oliveira, R. F., & Levkowitz, G. (2017) · eLife · doi:10.7554/elife.22170 · Cited by 60 · see citing works

Orexins/Hypocretins: Key Regulators of Energy Homeostasis

Milbank, E., & López, M. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00830 · Cited by 62 · see citing works

Underlying Susceptibility to Eating Disorders and Drug Abuse: Genetic and Pharmacological Aspects of Dopamine D4 Receptors

Botticelli, L., Bonaventura, E. M. D., Bello, F. D., Giorgioni, G., Piergentili, A., Romano, A., Quaglia, W., Cifani, C., & Bonaventura, M. V. M. D. (2020) · Nutrients · doi:10.3390/nu12082288 · Cited by 61 · see citing works

Deciphering the spatial-temporal transcriptional landscape of human hypothalamus development

Zhou, X., Lu, Y., Zhao, F., Dong, J., Ma, W., Zhong, S., Wang, M., Wang, B., Zhao, Y., Shi, Y., et al. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.11.009 · Cited by 58 · see citing works

Single-cell genomics reveals region-specific developmental trajectories underlying neuronal diversity in the human hypothalamus

Herb, B. R., Glover, H. J., Bhaduri, A., Colantuoni, C., Bale, T. L., Siletti, K., Linnarsson, S., Hodge, R. D., Lein, E. S., Kriegstein, A. R., et al. (2023) · Science Advances · doi:10.1126/sciadv.adf6251 · Cited by 55 · see citing works

The Role of the Human Hypothalamus in Food Intake Networks: An MRI Perspective

Roger, C., Lasbleiz, A., Guye, M., Dutour, A., Gaborit, B., & Ranjeva, J. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2021.760914 · Cited by 55 · see citing works

Anatomy, development, and plasticity of the neurosecretory hypothalamus in zebrafish

Nagpal, J. K., Herget, U., Choi, M. K., & Ryu, S. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2900-4 · Cited by 52 · see citing works

Construction of complex memories via parallel distributed cortical–subcortical iterative integration

McNaughton, N., & Vann, S. D. (2022) · Trends in Neurosciences · doi:10.1016/j.tins.2022.04.006 · Cited by 52 · see citing works

Hypothalamic expression of inflammatory mediators in an animal model of binge eating

Alboni, S., Bonaventura, M. V. M. D., Benatti, C., Giusepponi, M. E., Brunello, N., & Cifani, C. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.10.044 · Cited by 54 · see citing works

Hypothalamic dysfunction is related to sleep impairment and CSF biomarkers in Alzheimer’s disease

Liguori, C., Chiaravalloti, A., Nuccetelli, M., Izzi, F., Sancesario, G., Cimini, A., Bernardini, S., Schillaci, O., Mercuri, N. B., & Placidi, F. (2017) · Journal of Neurology · doi:10.1007/s00415-017-8613-x · Cited by 52 · see citing works

Glutamatergic neurons of the paraventricular nucleus are critical contributors to the development of neurogenic hypertension

Basting, T. M., Xu, J., Mukerjee, S., Epling, J. P., Fuchs, R., Sriramula, S., & Lazartigues, E. D. (2018) · The Journal of Physiology · doi:10.1113/jp276229 · Cited by 51 · see citing works

Cellular populations and thermosensing mechanisms of the hypothalamic thermoregulatory center

Siemens, J., & Kamm, G. B. (2018) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-017-2101-0 · Cited by 50 · see citing works

Craniopharyngiomas Primarily Involving the Hypothalamus: A Model of Neurosurgical Lesions to Elucidate the Neurobiological Basis of Psychiatric Disorders

Pascual, J. M., Prieto, R., Castro-Dufourny, I., Mongardi, L., Rosdolsky, M., Strauss, S., Carrasco, R., & Barrios, L. (2018) · World Neurosurgery · doi:10.1016/j.wneu.2018.09.053 · Cited by 50 · see citing works

The hypothalamus at the crossroads of psychopathology and neurosurgery

Barbosa, D. A. N., de Oliveira‐Souza, R., Santo, F. M., Faria, A. C. D. O., Gorgulho, A. A., & Salles, A. A. F. D. (2017) · Neurosurgical FOCUS · doi:10.3171/2017.6.focus17256 · Cited by 47 · see citing works

The neuroscience of adaptive thermoregulation

Angilletta, M. J., Youngblood, J. P., Neel, L. K., & VandenBrooks, J. M. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.10.046 · Cited by 47 · see citing works

The Role of Brown Adipose Tissue and Energy Metabolism in Mammalian Thermoregulation during the Perinatal Period

Bienboire‐Frosini, C., Wang, D., Marcet‐Rius, M., Villanueva‐García, D., Gazzano, A., Domínguez-Oliva, A., Olmos-Hernández, A. S., Hernández-Ávalos, I., Lezama-García, K., Verduzco-Mendoza, A., et al. (2023) · Animals · doi:10.3390/ani13132173 · Cited by 46 · see citing works

Endocannabinoids in Body Weight Control

Horn, H., Böhme, B., Dietrich, L., & Koch, M. (2018) · Pharmaceuticals · doi:10.3390/ph11020055 · Cited by 46 · see citing works

High-fat Diet and Physical Exercise Differentially Modulate Adult Neurogenesis in the Mouse Hypothalamus

Klein, C., Jonas, W., Wiedmer, P., Schreyer, S., Akyüz, L., Spranger, J., Hellweg, R., & Steiner, B. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.12.037 · Cited by 46 · see citing works

Metabolic Surgery to Treat Obesity in Diabetic Kidney Disease, Chronic Kidney Disease, and End-Stage Kidney Disease; What Are the Unanswered Questions?

Martin, W. P., White, J. P., López-Hernández, F. J., Docherty, N. G., & le Roux, C. W. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00289 · Cited by 48 · see citing works

A novel endoscopic classification for craniopharyngioma based on its origin

Tang, B., Xie, S., Li, X., Huang, G. L., Wang, Z. G., Yang, L., Yang, X., Xu, S., Chen, Y. Y., Ji, Y., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-28282-4 · Cited by 46 · see citing works

Skeletal interoception in osteoarthritis

Yang, D., Xu, J., Xu, K., & Xu, P. (2024) · Bone Research · doi:10.1038/s41413-024-00328-6 · Cited by 45 · see citing works

Decoding neuronal composition and ontogeny of individual hypothalamic nuclei

Ma, T., Wong, S. Z. H., Lee, B., Ming, G., & Song, H. (2021) · Neuron · doi:10.1016/j.neuron.2021.01.026 · Cited by 40 · see citing works

Hypothalamic neuropeptides and neurocircuitries in Prader Willi syndrome

Corrêa‐da‐Silva, F., Fliers, E., Swaab, D. F., & Yi, C. (2021) · Journal of Neuroendocrinology · doi:10.1111/jne.12994 · Cited by 39 · see citing works

Loss of transient receptor potential channel 5 causes obesity and postpartum depression

Li, Y., Cacciottolo, T. M., Yin, N., He, Y., Liu, H., Liu, H., Yang, Y., Henning, E., Keogh, J. M., Lawler, K., et al. (2024) · Cell · doi:10.1016/j.cell.2024.06.001 · Cited by 41 · see citing works

Flexible neural control of transition points within the egg-laying behavioral sequence in Drosophila

Cury, K. M., & Axel, R. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01332-5 · Cited by 40 · see citing works

Neuronal cAMP/PKA Signaling and Energy Homeostasis

Yang, L. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-1286-1_3 · Cited by 39 · see citing works

Cancer as a homeostatic challenge: the role of the hypothalamus

Francis, N., & Borniger, J. C. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.08.008 · Cited by 39 · see citing works

Sex difference in thermal preference of adult mice does not depend on presence of the gonads

Kaikaew, K., Steenbergen, J., Themmen, A. P. N., Visser, J. A., & Grefhorst, A. (2017) · Biology of Sex Differences · doi:10.1186/s13293-017-0145-7 · Cited by 40 · see citing works

Cerebrospinal fluid dynamics along the optic nerve

Sheng, J., Li, Q., Liu, T., & Wang, X. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.931523 · Cited by 41 · see citing works

Single-cell analysis of early chick hypothalamic development reveals that hypothalamic cells are induced from prethalamic-like progenitors

Kim, D. W., Place, E., Chinnaiya, K., Manning, E., Sun, C., Dai, W., Groves, I., Ohyama, K., Burbridge, S., Placzek, M., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110251 · Cited by 36 · see citing works

Exercise and the hypothalamic–pituitary–adrenal axis: a special focus on acute cortisol and growth hormone responses

Anderson, T., Berry, N. T., & Wideman, L. (2019) · Current Opinion in Endocrine and Metabolic Research · doi:10.1016/j.coemr.2019.08.002 · Cited by 35 · see citing works

A brainstem–hypothalamus neuronal circuit reduces feeding upon heat exposure

Benevento, M., Alpár, A., Gundacker, A., Afjehi, L., Balueva, K., Hevesi, Z., Hanics, J., Rehman, S., Pollak, D. D., Lübec, G., et al. (2024) · Nature · doi:10.1038/s41586-024-07232-3 · Cited by 35 · see citing works

Emerging roles for hypothalamic microglia as regulators of physiological homeostasis

Rosin, J. M., & Kurrasch, D. M. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100748 · Cited by 35 · see citing works

Developmental Genes and Malformations in the Hypothalamus

Dı́az, C., & Puelles, L. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.607111 · Cited by 33 · see citing works

Distinct temporal requirements for Sonic hedgehog signaling in development of the tuberal hypothalamus

Corman, T. S., Zevallos, S. E., & Epstein, D. J. (2018) · Development · doi:10.1242/dev.167379 · Cited by 32 · see citing works

Effect of short and long-term treatment with antipsychotics on orexigenic/anorexigenic neuropeptides expression in the rat hypothalamus

Rojczyk, E., Pałasz, A., & Wiaderkiewicz, R. (2015) · Neuropeptides · doi:10.1016/j.npep.2015.04.001 · Cited by 34 · see citing works

Adult Neurogenesis in Sheep: Characterization and Contribution to Reproduction and Behavior

Lévy, F., Batailler, M., Meurisse, M., & Migaud, M. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00570 · Cited by 34 · see citing works

Interoception and Obsessive-Compulsive Disorder: A Review of Current Evidence and Future Directions

Bragdon, L. B., Eng, G. K., Belanger, A., Collins, K. A., & Stern, E. R. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.686482 · Cited by 35 · see citing works

A hypothalamic dopamine locus for psychostimulant-induced hyperlocomotion in mice

Korchynska, S., Rebernik, P., Pende, M., Boi, L., Alpár, A., Tasan, R. O., Becker, K., Balueva, K., Saghafi, S., Wulff, P., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33584-3 · Cited by 33 · see citing works

Heart–Brain Axis: A Narrative Review of the Interaction between Depression and Arrhythmia

Fang, S., & Zhang, W. Y. (2024) · Biomedicines · doi:10.3390/biomedicines12081719 · Cited by 37 · see citing works

The effects of graded levels of calorie restriction: VI. Impact of short-term graded calorie restriction on transcriptomic responses of the hypothalamic hunger and circadian signaling pathways

Derous, D., Mitchell, S. E., Green, C. L., Chen, L., Han, J. J., Wang, Y., Promislow, D., Lusseau, D., Speakman, J. R., & Douglas, A. (2016) · Aging · doi:10.18632/aging.100895 · Cited by 32 · see citing works

Hypocretin/orexin neurons encode social discrimination and exhibit a sex-dependent necessity for social interaction

Dawson, M., Terstege, D. J., Jamani, N. F., Tsutsui, M., Pavlov, D., Bugescu, R., Epp, J. R., Leinninger, G. M., & Sargin, D. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112815 · Cited by 31 · see citing works

Altered Bioenergetics and Metabolic Homeostasis in Amyotrophic Lateral Sclerosis

Nelson, A. T., & Trotti, D. (2022) · Neurotherapeutics · doi:10.1007/s13311-022-01262-3 · Cited by 31 · see citing works

Neuropeptides in Cancer: Friend and Foe?

Wu, Y., Berisha, A., & Borniger, J. C. (2022) · Advanced Biology · doi:10.1002/adbi.202200111 · Cited by 30 · see citing works

Maternal fat-soluble vitamins, brain development, and regulation of feeding behavior: an overview of research

Sánchez‐Hernández, D., Anderson, G. H., Poon, A. N., Pannia, E., Cho, C. E., Huot, P. S. P., & Kubant, R. (2016) · Nutrition Research · doi:10.1016/j.nutres.2016.09.009 · Cited by 30 · see citing works

Hypothalamic MCH Neurons: From Feeding to Cognitive Control

Concetti, C., Peleg-Raibstein, D., & Burdakov, D. (2023) · Function · doi:10.1093/function/zqad059 · Cited by 28 · see citing works

A Neural Model of Empathic States in Attachment-Based Psychotherapy

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