Peripheral antioxidant markers are associated with total hippocampal and CA3/dentate gyrus volume in MDD and healthy controls—Preliminary findings

Whole Brain Segmentation

Fischl, B., Salat, D. H., Busa, E., Albert, M., Dieterich, M., Haselgrove, C., van der Kouwe, A., Killiany, R., Kennedy, D., Klaveness, S., et al. (2002) · Neuron · doi:10.1016/s0896-6273(02)00569-x · Cited by 8,610 · see citing works

Adjusting for multiple testing—when and how?

Bender, R., & Lange, S. (2001) · Journal of Clinical Epidemiology · doi:10.1016/s0895-4356(00)00314-0 · Cited by 3,060 · see citing works

What you see may not be what you get: a brief, nontechnical introduction to overfitting in regression-type models

Babyak, M. A. (2004) · Psychosomatic Medicine · doi:10.1097/01.psy.0000127692.23278.a9 · Cited by 2,061 · see citing works

Apoptosis in neurodegenerative disorders

Mattson, M. P. (2000) · Nature Reviews Molecular Cell Biology · doi:10.1038/35040009 · Cited by 1,605 · see citing works

Glutathione Peroxidase-1 in Health and Disease: From Molecular Mechanisms to Therapeutic Opportunities

Lubos, E., Loscalzo, J., & Handy, D. E. (2011) · Antioxidants & Redox Signaling · doi:10.1089/ars.2010.3586 · Cited by 1,280 · see citing works

Oxidative stress in psychiatric disorders: evidence base and therapeutic implications

Ng, F., Berk, M., Dean, O., & Bush, A. I. (2008) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145707008401 · Cited by 1,069 · see citing works

A meta-analysis examining clinical predictors of hippocampal volume in patients with major depressive disorder

McKinnon, M. C., Yucel, K., Nazarov, A., & MacQueen, G. M. (2009) · Journal of Psychiatry and Neuroscience · doi:10.1139/jpn.0905 · Cited by 742 · see citing works

Glutathione Pathways in the Brain

Dringen, R., & Hirrlinger, J. (2003) · Biological Chemistry · doi:10.1515/bc.2003.059 · Cited by 597 · see citing works

Decreased levels of glutathione, the major brain antioxidant, in post-mortem prefrontal cortex from patients with psychiatric disorders

Gawryluk, J. W., Wang, J.-F., Andreazza, A. C., Shao, L., & Young, L. T. (2011) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145710000805 · Cited by 594 · see citing works

Free radicals in brain metabolism and pathology

Evans, P. H. (1993) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a072632 · Cited by 446 · see citing works

Reduced hippocampal volumes and memory loss in patients with early- and late-onset depression

Hickie, I., Naismith, S., Ward, P. B., Turner, K., Scott, E., Mitchell, P., Wilhelm, K., & Parker, G. (2005) · British Journal of Psychiatry · doi:10.1192/bjp.186.3.197 · Cited by 437 · see citing works

Leukocyte Telomere Length in Major Depression: Correlations with Chronicity, Inflammation and Oxidative Stress - Preliminary Findings

Wolkowitz, O. M., Mellon, S. H., Epel, E. S., Lin, J., Dhabhar, F. S., Su, Y., Reus, V. I., Rosser, R., Burke, H. M., Kupferman, E., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017837 · Cited by 421 · see citing works

Hippocampal atrophy patterns in mild cognitive impairment and Alzheimer's disease

Mueller, S. G., Schuff, N., Yaffe, K., Madison, C., Miller, B., & Weiner, M. W. (2010) · Human Brain Mapping · doi:10.1002/hbm.20934 · Cited by 361 · see citing works

Measurement of hippocampal subfields and age-related changes with high resolution MRI at 4T

Mueller, S. G., Stables, L. A., Du, A., Schuff, N. W., Truran, D., Cashdollar, N. M., & Weiner, M. W. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.03.007 · Cited by 266 · see citing works

Dysregulated relationship of inflammation and oxidative stress in major depression

Rawdin, B. J., Mellon, S. H., Dhabhar, F. S., Epel, E. S., Puterman, E., Su, Y., Burke, H. M., Reus, V. I., Rosser, R., Hamilton, S. P., et al. (2013) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2012.11.011 · Cited by 255 · see citing works

Low serum IL-10 concentrations and loss of regulatory association between IL-6 and IL-10 in adults with major depression

Dhabhar, F. S., Burke, H. M., Epel, E. S., Mellon, S. H., Rosser, R., Reus, V. I., & Wolkowitz, O. M. (2009) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2009.05.010 · Cited by 225 · see citing works

Preclinical and Clinical Evidence of Antioxidant Effects of Antidepressant Agents: Implications for the Pathophysiology of Major Depressive Disorder

Behr, G. A., Moreira, J. C. F., & Frey, B. N. (2012) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2012/609421 · Cited by 205 · see citing works

Redox Dysregulation Affects the Ventral But Not Dorsal Hippocampus: Impairment of Parvalbumin Neurons, Gamma Oscillations, and Related Behaviors

Steullet, P., Cabungcal, J.-H., Kulak, A., Kraftsik, R., Chen, Y., Dalton, T. P., Cuenod, M., & Do, K. Q. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3857-09.2010 · Cited by 202 · see citing works

High-Dimensional Mapping of the Hippocampus in Depression

Posener, J. A., Wang, L., Price, J. L., Gado, M. H., Province, M. A., Miller, M. I., Babb, C. M., & Csernansky, J. G. (2002) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.1.83 · Cited by 200 · see citing works

Glutathione: a novel treatment target in psychiatry

Berk, M., Ng, F., Dean, O., Dodd, S., & Bush, A. I. (2008) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2008.05.001 · Cited by 183 · see citing works

Structural changes in hippocampal subfields in major depressive disorder: a high-field magnetic resonance imaging study

Huang, Y., Coupland, N. J., Lebel, R. M., Carter, R., Seres, P., Wilman, A. H., & Malykhin, N. V. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.01.005 · Cited by 179 · see citing works

Oxidative stress and adult neurogenesis—Effects of radiation and superoxide dismutase deficiency

Huang, T., Zou, Y., & Corniola, R. S. (2012) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2012.04.003 · Cited by 164 · see citing works

Oxidative damage to RNA but not DNA in the hippocampus of patients with major mental illness

Che, Y., Wang, J.-F., Shao, L., & Young, L. T. (2010) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.090083 · Cited by 155 · see citing works

Die Glutathionperoxidase: Enzymologie und biologische Aspekte

Floh�, L. (1971) · Journal of Molecular Medicine · doi:10.1007/bf01487101 · Cited by 136 · see citing works

Ascorbate transport by primary cultured neurons and its role in neuronal function and protection against excitotoxicity

Qiu, S., Li, L., Weeber, E. J., & May, J. M. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21204 · Cited by 133 · see citing works

Resting leukocyte telomerase activity is elevated in major depression and predicts treatment response

Wolkowitz, O. M., Mellon, S. H., Epel, E. S., Lin, J., Reus, V. I., Rosser, R., Burke, H., Compagnone, M., Nelson, J. C., Dhabhar, F. S., et al. (2011) · Molecular Psychiatry · doi:10.1038/mp.2010.133 · Cited by 125 · see citing works

Antioxidant protection: A promising therapeutic intervention in neurodegenerative disease

Ghosh, N., Ghosh, R. B., & Mandal, S. C. (2011) · Free Radical Research · doi:10.3109/10715762.2011.574290 · Cited by 116 · see citing works

Vitamin C deficiency in early postnatal life impairs spatial memory and reduces the number of hippocampal neurons in guinea pigs

Tveden‐Nyborg, P., Jensen, L. K., Raida, Z., Villumsen, C. K., Larsen, J. O., & Lykkesfeldt, J. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2009.27954 · Cited by 104 · see citing works

Ascorbate‐induced differentiation of embryonic cortical precursors into neurons and astrocytes

Lee, J., Chang, M., Park, C., Kim, H., Kim, J., Son, H., Lee, Y., & Lee, S. (2003) · Journal of Neuroscience Research · doi:10.1002/jnr.10647 · Cited by 77 · see citing works

PROPELLER MRI visualizes detailed pathology of hippocampal sclerosis

Eriksson, S. H., Thom, M., Bartlett, P. A., Symms, M. R., McEvoy, A. W., Sisodiya, S. M., & Duncan, J. S. (2007) · Epilepsia · doi:10.1111/j.1528-1167.2007.01277.x · Cited by 64 · see citing works

Ascorbic acid ameliorates oxidative damage induced by maternal low-level lead exposure in the hippocampus of rat pups during gestation and lactation

Chang, B., Jang, B.-J., Son, T. G., Cho, I., Quan, F.-S., Choe, N., Nahm, S., & Lee, J. (2011) · Food and Chemical Toxicology · doi:10.1016/j.fct.2011.09.043 · Cited by 60 · see citing works

Antioxidants in Alzheimer's disease-vitamin C delivery to a demanding brain

Quinn, J. F., Suh, J. H., Moore, M. M., Kaye, J. A., & Frei, B. B. (2003) · Journal of Alzheimer s Disease · doi:10.3233/jad-2003-5406 · Cited by 57 · see citing works

Decreased glutathione levels predict loss of brain volume in children and adolescents with first-episode psychosis in a two-year longitudinal study

Fraguas, D., González-Pinto, A. M., Micó, J. A., Reig, S., Parellada, M., Martínez‐Cengotitabengoa, M., Castro‐Fornieles, J., Rapado‐Castro, M., Baeza, I., Janssen, J., et al. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.01.040 · Cited by 57 · see citing works

Altered Hippocampal Morphology in Unmedicated Patients with Major Depressive Illness

Bearden, C. E., Thompson, P. M., Avedissian, C., Klunder, A. D., Nicoletti, M., Dierschke, N. A., Brambilla, P., & Soares, J. C. (2009) · ASN NEURO · doi:10.1042/an20090026 · Cited by 57 · see citing works

Pattern of neuronal loss in the rat hippocampus following experimental cardiac arrest-induced ischemia

Sadowski, M., Wı́sniewski, H. M., Jakubowska-Sadowska, K., Tarnawski, M. J., Łazarewicz, J. W., & Mossakowski, M. J. (1999) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(99)00159-8 · Cited by 52 · see citing works

Liquid chromatographic measurement of l-ascorbic acid and d-ascorbic acid in biological samples

Margolis, S. A., & Schapira, R. M. (1997) · Journal of Chromatography B Biomedical Sciences and Applications · doi:10.1016/s0378-4347(96)00401-x · Cited by 52 · see citing works

Oxidative stress in Alzheimer's disease hippocampus: A topographical study

Cruz-Sánchez, F. F., Gironès, X., Aznar, A. O., Alameda, F., & Lafuente, J. V. (2010) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2010.08.029 · Cited by 49 · see citing works

Age-related changes in apoptosis in rat hippocampus induced by oxidative stress

Uysal, N., Tuğyan, K., Aksu, İ., Özbal, S., Ozdemir, D., Dayı, A., Gönenç, S., & Açıkgöz, O. (2011) · Biotechnic & Histochemistry · doi:10.3109/10520295.2011.556665 · Cited by 24 · see citing works

Early hippocampal oxidative stress is a direct consequence of seizures in the rapid electrical amygdala kindling model

Sashindranath, M., McLean, K. J., Trounce, I. A., Cotton, R. G. H., & Cook, M. J. (2010) · Epilepsy Research · doi:10.1016/j.eplepsyres.2010.06.005 · Cited by 16 · see citing works

The Impact of Stress and Major Depressive Disorder on Hippocampal and Medial Prefrontal Cortex Morphology

Belleau, E. L., Treadway, M. T., & Pizzagalli, D. A. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.09.031 · Cited by 550 · see citing works

Oxidative stress, inflammation and treatment response in major depression

Lindqvist, D., Dhabhar, F. S., James, S. J., Hough, C. M., Jain, F. A., Bersani, F. S., Reus, V. I., Verhoeven, J. E., Epel, E. S., Mahan, L., et al. (2017) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.11.031 · Cited by 473 · see citing works

Pathways Connecting Late-Life Depression and Dementia

Linnemann, C., & Lang, U. E. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00279 · Cited by 212 · see citing works

Hippocampal neuroplasticity in major depressive disorder

Malykhin, N. V., & Coupland, N. J. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.04.047 · Cited by 178 · see citing works

FreeSurfer ‐based segmentation of hippocampal subfields: A review of methods and applications, with a novel quality control procedure for ENIGMA studies and other collaborative efforts

Sämann, P. G., Iglesias, J. E., Gutman, B. A., Grotegerd, D., Leenings, R., Flint, C., Dannlowski, U., Clarke‐Rubright, E. K., Morey, R. A., van Erp, T. G. M., et al. (2020) · Human Brain Mapping · doi:10.1002/hbm.25326 · Cited by 135 · see citing works

Increased hippocampal tail volume predicts depression status and remission to anti-depressant medications in major depression

Maller, J. J., Broadhouse, K., Rush, A. J., Gordon, E., Koslow, S., & Grieve, S. M. (2018) · Molecular Psychiatry · doi:10.1038/mp.2017.224 · Cited by 87 · see citing works

Targeting Inflammatory-Mitochondrial Response in Major Depression: Current Evidence and Further Challenges

Visentin, A. P. V., Colombo, R., Scotton, E., Fracasso, D. S., Rosa, A. R., Branco, C. S., & Salvador, M. M. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/2972968 · Cited by 77 · see citing works

Metabolomics and neuroanatomical evaluation of post-mortem changes in the hippocampus

González-Riaño, C., Tapia‐González, S., Garcı́a, A., Muñoz, A., DeFelipe, J., & Barbas, C. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1375-5 · Cited by 76 · see citing works

Hippocampal subfield volumes in major depressive disorder and bipolar disorder

Han, K.-M., Kim, A., Kang, W., Kang, Y., Kang, J., Won, E., Tae, W.-S., & Ham, B.-J. (2019) · European Psychiatry · doi:10.1016/j.eurpsy.2019.01.016 · Cited by 68 · see citing works

Oxidative stress and brain morphology in individuals with depression, anxiety and healthy controls

van Velzen, L. S., Wijdeveld, M., Black, C. N., van Tol, M., van der Wee, N. J. A., Veltman, D. J., Penninx, B. W. J. H., & Schmaal, L. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.02.017 · Cited by 64 · see citing works

Severity of anxiety– but not depression– is associated with oxidative stress in Major Depressive Disorder

Steenkamp, L. R., Hough, C. M., Reus, V. I., Jain, F. A., Epel, E. S., James, S. J., Morford, A. E., Mellon, S. H., Wolkowitz, O. M., & Lindqvist, D. (2017) · Journal of Affective Disorders · doi:10.1016/j.jad.2017.04.042 · Cited by 62 · see citing works

Structural differences in hippocampal subfields among schizophrenia patients, major depressive disorder patients, and healthy subjects

Ota, M., Sato, N., Hidese, S., Teraishi, T., Maikusa, N., Matsuda, H., Hattori, K., & Kunugi, H. (2016) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2016.11.002 · Cited by 59 · see citing works

Effects of cortisol on hippocampal subfields volumes and memory performance in healthy control subjects and patients with major depressive disorder

Travis, S. G., Coupland, N. J., Hegadoren, K., Silverstone, P. H., Huang, Y., Carter, R., Fujiwara, E., Seres, P., & Malykhin, N. V. (2016) · Journal of Affective Disorders · doi:10.1016/j.jad.2016.04.049 · Cited by 57 · see citing works

Peripheral telomere length and hippocampal volume in adolescents with major depressive disorder

Henje Blom, E., Han, L. K. M., Connolly, C. G., Ho, T. C., Lin, J., LeWinn, K. Z., Simmons, A. N., Sacchet, M. D., Mobayed, N., Luna, M. E., et al. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.172 · Cited by 51 · see citing works

Role of primary aging hallmarks in Alzheimer´s disease

Zhao, J., & Huai, J. (2022) · Theranostics · doi:10.7150/thno.79535 · Cited by 53 · see citing works

On the Neurobiological Role of Oxidative Stress in Alcohol-Induced Impulsive, Aggressive and Suicidal Behavior

Tobore, T. O. (2019) · Substance Use & Misuse · doi:10.1080/10826084.2019.1645179 · Cited by 50 · see citing works

Molecular correlates of mitochondrial dysfunctions in major depression: Evidence from clinical and rodent studies

Rappeneau, V., Wilmes, L., & Touma, C. (2020) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2020.103555 · Cited by 46 · see citing works

Depressive disorders: Processes leading to neurogeneration and potential novel treatments

Brown, G. M., McIntyre, R. S., Rosenblat, J. D., & Hardeland, R. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.04.023 · Cited by 44 · see citing works

Posttraumatic Stress Disorder and Depression Symptom Severities Are Differentially Associated With Hippocampal Subfield Volume Loss in Combat Veterans

Averill, C. L., Satodiya, R. M., Scott, J. C., Wrocklage, K. M., Schweinsburg, B. C., Averill, L. A., Akiki, T. J., Amoroso, T., Southwick, S. M., Krystal, J. H., et al. (2017) · Chronic Stress · doi:10.1177/2470547017744538 · Cited by 34 · see citing works

Altered hippocampal subfield volumes in major depressive disorder with and without anhedonia

Wu, C., Jia, L., Mu, Q., Fang, Z., Hamoudi, H. J. A. S., Huang, M., Hu, S., Zhang, P., Xu, Y., & Lu, S. (2023) · BMC Psychiatry · doi:10.1186/s12888-023-05001-6 · Cited by 29 · see citing works

Elevating the level of hypoxia inducible factor may be a new potential target for the treatment of depression

Kang, I., Kondo, D. G., Kim, J., Lyoo, I. K., Yurgelun-Todd, D. A., Hwang, J., & Renshaw, P. F. (2020) · Medical Hypotheses · doi:10.1016/j.mehy.2020.110398 · Cited by 30 · see citing works

Volume and shape analysis of the Hippocampus and amygdala in veterans with traumatic brain injury and posttraumatic stress disorder

Bae, S., Sheth, C. S., Legarreta, M. D., McGlade, E., Lyoo, I. K., & Yurgelun-Todd, D. A. (2019) · Brain Imaging and Behavior · doi:10.1007/s11682-019-00127-2 · Cited by 27 · see citing works

Improvement in indices of cellular protection after psychological treatment for social anxiety disorder.

Månsson, K. N. T., Lindqvist, D., Yang, L. L., Svanborg, C., Isung, J., Nilsonne, G., Bergman-Nordgren, L., El Alaoui, S., Hedman-Lagerlöf, E., Kraepelien, M., et al. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0668-2 · Cited by 25 · see citing works

Plasma oxidative stress marker levels related to functional brain abnormalities in first-episode drug-naive major depressive disorder

Liu, Y., Zhang, B., Zhou, Y., Li, M., Gao, Y. H., Qin, W., Xie, Y., Liu, W., Jing, Y., & Li, J. (2024) · Psychiatry Research · doi:10.1016/j.psychres.2024.115742 · Cited by 22 · see citing works

Dentate gyrus−cornu ammonis (CA) 4 volume is decreased and associated with depressive episodes and lipid peroxidation in bipolar II disorder: Longitudinal and cross‐sectional analyses

Elvsåshagen, T., Zuzarte, P., Westlye, L. T., Bøen, E., Josefsen, D., Boye, B., Hol, P. K., Malt, U. F., Young, L. T., & Andreazza, A. C. (2016) · Bipolar Disorders · doi:10.1111/bdi.12457 · Cited by 21 · see citing works

Predicting a Potential Link to Antidepressant Effect: Neuroprotection of Zhi-zi-chi Decoction on Glutamate-induced Cytotoxicity in PC12 Cells

Zhang⋆, Y., Luo, Y., Zhang, D., Pang, B., Wen, J., & Zhou, T. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.625108 · Cited by 16 · see citing works

Psychosocial factors and hippocampal subfields: The Medea‐7T study

Twait, E. L., Blom, K., Koek, H. L., Zwartbol, M. H. T., Ghaznawi, R., Hendrikse, J., Gerritsen, L., Geerlings, M. I., & UCC SMART Study Group (2022) · Human Brain Mapping · doi:10.1002/hbm.26185 · Cited by 15 · see citing works

Sub-regional hippocampal volumes in first-episode drug-naïve major depression disorder

Liu, M.-N., Pantouw, J. G., Yang, K.-C., Hu, L.-Y., Liou, Y.-J., Lirng, J.-F., & Chou, Y.-H. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136178 · Cited by 13 · see citing works

Age-dependent brain morphometry in Major Depressive disorder

Myoraku, A., Lang, A., Taylor, C. T., Mackin, R. S., Meyerhoff, D. J., Mueller, S. G., Strigo, I. A., & Tosun, D. (2021) · NeuroImage Clinical · doi:10.1016/j.nicl.2021.102924 · Cited by 13 · see citing works

Oxidative stress and cognitive function in Chinese patients with major depressive disorder: the mediating role of depression severity

Peng, R., Sun, C., Fan, Y., Li, J., Gao, J., Sun, W.-X., Zhang, X.-B., & Tian, Q. (2025) · BMC Psychiatry · doi:10.1186/s12888-025-07478-9 · Cited by 7 · see citing works

Association between Advanced Glycation End products and brain volumes in recent onset psychosis

Wezenberg, B. N., Hagen, J. M., Sutterland, A. L., Schrantee, A., & de Haan, L. (2020) · Schizophrenia Research · doi:10.1016/j.schres.2020.09.010 · Cited by 5 · see citing works

On alcohol disinhibition and inhibition: The intricate relationship between oxidative stress and behavior

Tobore, T. O. (2020) · Aggression and Violent Behavior · doi:10.1016/j.avb.2020.101378 · Cited by 2 · see citing works

Rôle des connexines 43 astrocytaires : une étude fonctionnelle dans un modèle murin de dépression basé sur le stress chronique

Portal, B. (2019) · theses.fr (ABES) · doi:10.70675/d20c8f2azc2f7z48a8z9545z80352abaf664

Peripheral indices of oxidative stress are correlated with hippocampal volume in major depression and in controls

Wolkowitz, O. M., Mellon, S. H., Su, Y., Reus, V. I., Mackin, S. R., Burke, H. M., Rosser, R., Coetzee, J. P., Epel, E. S., Hamilton, S. P., et al. (2012) · European Journal of Psychotraumatology · doi:10.3402/ejpt.v3i0.19373

Oxidative stress and brain morphology in individuals with depression, anxiety and healthy controls

van Velzen, L. S., Wijdeveld, M., Black, C. N., van Tol, M., van der Wee, N. J. A., Veltman, D. J., Penninx, B. W. J. H., & Schmaal, L. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.02.017 · Cited by 64 · see citing works

P.1.28 Modulation of intracellular signaling patwhays by acute swim stress in rat hippocampus

Pasini, M., Fumagalli, F., Drago, F., Racagni, G., & Riva, M. A. (2008) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(08)70029-4

Dentate gyrus−cornu ammonis (CA) 4 volume is decreased and associated with depressive episodes and lipid peroxidation in bipolar II disorder: Longitudinal and cross‐sectional analyses

Elvsåshagen, T., Zuzarte, P., Westlye, L. T., Bøen, E., Josefsen, D., Boye, B., Hol, P. K., Malt, U. F., Young, L. T., & Andreazza, A. C. (2016) · Bipolar Disorders · doi:10.1111/bdi.12457 · Cited by 21 · see citing works

Oxidative stress and cognitive function in Chinese patients with major depressive disorder: the mediating role of depression severity

Peng, R., Sun, C., Fan, Y., Li, J., Gao, J., Sun, W.-X., Zhang, X.-B., & Tian, Q. (2025) · BMC Psychiatry · doi:10.1186/s12888-025-07478-9 · Cited by 7 · see citing works