On the public citation graph
Homer1a-dependent recovery from depression-like behavior by photic stimulation in mice
0 signed · 60 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s002130050456openalex-snapshot
Validity, reliability and utility of the chronic mild stress model of depression: a 10-year review and evaluation
inferredcites →https://doi.org/10.1016/0031-9384(89)90261-8openalex-snapshot
Learned immobility explains the behavior of rats in the forced swimming test
inferredcites →https://doi.org/10.1016/0278-5846(90)90073-popenalex-snapshot
Neurobehavioral studies of forced swimming: The role of learning and memory in the forced swim test
inferredcites →https://doi.org/10.1016/j.bbr.2014.10.009openalex-snapshot
Evidence for the involvement of extinction-associated inhibitory learning in the forced swimming test
inferredcites →https://doi.org/10.1016/j.biopsych.2007.01.018openalex-snapshot
Efficacy and Safety of Transcranial Magnetic Stimulation in the Acute Treatment of Major Depression: A Multisite Randomized Controlled Trial
inferredcites →https://doi.org/10.1016/j.biopsych.2010.05.038openalex-snapshot
Genome-Wide Association-, Replication-, and Neuroimaging Study Implicates HOMER1 in the Etiology of Major Depression
inferredcites →https://doi.org/10.1016/j.brainres.2015.02.008openalex-snapshot
Homer1a disruption increases vulnerability to predictable subtle stress normally sub-threshold for behavioral changes
inferredcites →https://doi.org/10.1016/j.conb.2006.05.002openalex-snapshot
Homer proteins: implications for neuropsychiatric disorders
inferredcites →https://doi.org/10.1016/j.expneurol.2009.03.038openalex-snapshot
Treatment of depression with transcranial direct current stimulation (tDCS): A Review
inferredcites →https://doi.org/10.1016/j.mppsy.2009.01.002openalex-snapshot
Electroconvulsive therapy
inferredcites →https://doi.org/10.1016/j.neures.2009.01.014openalex-snapshot
Neurophysiological mechanisms of electroconvulsive therapy for depression
inferredcites →https://doi.org/10.1016/j.neuron.2005.02.014openalex-snapshot
Deep brain stimulation for treatment-resistant depression.
inferredcites →https://doi.org/10.1016/j.neuron.2010.11.008openalex-snapshot
Homeostatic Scaling Requires Group I mGluR Activation Mediated by Homer1a
inferredcites →https://doi.org/10.1016/j.neuropharm.2014.12.033openalex-snapshot
Cognitive recovery by chronic activation of the large-conductance calcium-activated potassium channel in a mouse model of Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.physbeh.2014.10.005openalex-snapshot
Fear conditioning suppresses large-conductance calcium-activated potassium channels in lateral amygdala neurons
inferredcites →https://doi.org/10.1016/s0014-5793(97)00775-8openalex-snapshot
vesl, a gene encoding VASP/Ena family related protein, is upregulated during seizure, long‐term potentiation and synaptogenesis1
inferredcites →https://doi.org/10.1016/s0022-3956(01)00023-1openalex-snapshot
Transcranial magnetic stimulation as a therapeutic tool in psychiatry: what do we know about the neurobiological mechanisms?
inferredcites →https://doi.org/10.1016/s0165-0327(98)00005-6openalex-snapshot
Light treatment for nonseasonal depression: speed, efficacy, and combined treatment1Presented at American Psychiatric Association Symposium 54, San Diego, California, May 20, 1997. Supported by AG12364, HL55983, ES08930, and the Sam and Rose Stein Institute for Research on Aging.1
inferredcites →https://doi.org/10.1016/s0197-2456(03)00112-0openalex-snapshot
Sequenced treatment alternatives to relieve depression (STAR*D): rationale and design
inferredcites →https://doi.org/10.1038/266730a0openalex-snapshot
Depression: a new animal model sensitive to antidepressant treatments
inferredcites →https://doi.org/10.1038/386284a0openalex-snapshot
Homer: a protein that selectively binds metabotropic glutamate receptors
inferredcites →https://doi.org/10.1038/ncpneuro0530openalex-snapshot
Technology Insight: noninvasive brain stimulation in neurology—perspectives on the therapeutic potential of rTMS and tDCS
inferredcites →https://doi.org/10.1038/nn.2647openalex-snapshot
Animal models of neuropsychiatric disorders
inferredcites →https://doi.org/10.1038/sj.npp.1301082openalex-snapshot
VNS Therapy in Treatment-Resistant Depression: Clinical Evidence and Putative Neurobiological Mechanisms
inferredcites →https://doi.org/10.1046/j.1365-2826.2003.00986.xopenalex-snapshot
Genetic Selection For Coping Style Predicts Stressor Susceptibility
inferredcites →https://doi.org/10.1073/pnas.0710131104openalex-snapshot
Homer1a is a core brain molecular correlate of sleep loss
inferredcites →https://doi.org/10.1080/10401230701675222openalex-snapshot
Treatment Resistant Depression— Advances in Somatic Therapies
inferredcites →https://doi.org/10.1097/00000441-196712000-00052openalex-snapshot
Comprehensive Textbook of Psychiatry
inferredcites →https://doi.org/10.1097/00124509-200403000-00004openalex-snapshot
Efficacy of ECT in Depression: A Meta-Analytic Review
inferredcites →https://doi.org/10.1111/j.1460-9568.2005.04165.xopenalex-snapshot
Essential roles of Homer‐1a in homeostatic regulation of pyramidal cell excitability: a possible link to clinical benefits of electroconvulsive shock
inferredcites →https://doi.org/10.1139/jpn.0428openalex-snapshot
Transcranial magnetic stimulation (TMS) of the human frontal cortex: implications for repetitive TMS treatment of depression
inferredcites →https://doi.org/10.1176/ajp.2007.164.1.73openalex-snapshot
A Randomized, Controlled Trial With 6-Month Follow-Up of Repetitive Transcranial Magnetic Stimulation and Electroconvulsive Therapy for Severe Depression
inferredcites →https://doi.org/10.1186/1756-6606-2-7openalex-snapshot
Requirement of the immediate early gene vesl-1S/homer-1a for fear memory formation
inferredcites →https://doi.org/10.1186/1756-6606-5-2openalex-snapshot
Understanding the physiological roles of the neuronal calcium sensor proteins
inferredcites →https://doi.org/10.1523/jneurosci.1542-11.2011openalex-snapshot
Increase in Cortical Pyramidal Cell Excitability Accompanies Depression-Like Behavior in Mice: A Transcranial Magnetic Stimulation Study
inferredcites →https://doi.org/10.1523/jneurosci.3308-11.2012openalex-snapshot
Epigenetic Modulation of Homer1a Transcription Regulation in Amygdala and Hippocampus with Pavlovian Fear Conditioning
inferredcites →https://doi.org/10.1523/jneurosci.3764-05.2005openalex-snapshot
Distinct Roles for Different Homer1 Isoforms in Behaviors and Associated Prefrontal Cortex Function
inferredcites →https://doi.org/10.1523/jneurosci.5377-03.2004openalex-snapshot
Electroconvulsive Seizures Regulate Gene Expression of Distinct Neurotrophic Signaling Pathways
inferredcites →https://doi.org/10.1523/jneurosci.6752-10.2011openalex-snapshot
Suppression of a Neocortical Potassium Channel Activity by Intracellular Amyloid-β and Its Rescue with Homer1a
inferredcites →https://doi.org/10.1615/critrevneurobiol.v15.i2.30openalex-snapshot
Rodent Models of Depression: Reexamining Validity Without Anthropomorphic Inference
inferredcites →https://doi.org/10.4088/jcp.v69n0208openalex-snapshot
Transcranial Magnetic Stimulation in the Treatment of Major Depressive Disorder
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4757666openalex-extracted
Targeting a Visual Circuit Rescues Mood Deficit in Intractable Depression Model
inferred← citeshttps://doi.org/10.1002/alz.70337openalex-snapshot
The neurobiological foundation of effective repetitive transcranial magnetic brain stimulation in Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.bbalip.2019.05.010openalex-snapshot
24S-hydroxycholesterol alters activity of large-conductance Ca2+-dependent K+ (slo1 BK) channel through intercalation into plasma membrane
inferred← citeshttps://doi.org/10.1016/j.ibror.2017.05.001openalex-snapshot
Impaired retention of depression-like behavior in a mouse model of Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2019.08.019openalex-snapshot
Translating preclinical findings in clinically relevant new antipsychotic targets: focus on the glutamatergic postsynaptic density. Implications for treatment resistant schizophrenia
inferred← citeshttps://doi.org/10.1016/j.neulet.2019.134383openalex-snapshot
Layer-specific modulation of pyramidal cell excitability by electroconvulsive shock
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2020.03.031openalex-snapshot
Homer1a Undergoes Bimodal Transcriptional Regulation by CREB and the Circadian Clock
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2017.10.011openalex-snapshot
A Homer 1 gene variant influences brain structure and function, lithium effects on white matter, and antidepressant response in bipolar disorder: A multimodal genetic imaging study
inferred← citeshttps://doi.org/10.1101/2020.07.31.230201openalex-snapshot
Astroglia in lateral habenula is essential for antidepressant efficacy of light
inferred← citeshttps://doi.org/10.1134/s0006297921060018openalex-snapshot
The Role of Stress-Induced Changes of Homer1 Expression in Stress Susceptibility
inferred← citeshttps://doi.org/10.1159/000500267openalex-snapshot
Regulation and Function of Activity-Dependent Homer in Synaptic Plasticity
inferred← citeshttps://doi.org/10.1515/hsz-2015-0267openalex-snapshot
Signaling pathways regulating Homer1a expression: implications for antidepressant therapy
inferred← citeshttps://doi.org/10.1523/jneurosci.0026-21.2021openalex-snapshot
The Complex Formed by Group I Metabotropic Glutamate Receptor (mGluR) and Homer1a Plays a Central Role in Metaplasticity and Homeostatic Synaptic Scaling
inferred← citeshttps://doi.org/10.31857/s0320972521060014openalex-snapshot
Роль изменений экспрессии Homer1 в чувствительности к стрессу
inferred← citeshttps://doi.org/10.3389/fnins.2023.1109735openalex-snapshot
Low frequency repetitive transcranial magnetic stimulation promotes plasticity of the visual cortex in adult amblyopic rats
inferred← citeshttps://doi.org/10.3389/fphar.2025.1592909openalex-snapshot
Lateral habenula astroglia modulate the potentiating antidepressant-like effects of bright light stimulation in intractable depression
inferred← citeshttps://doi.org/10.70675/7468b6d3zbf12z4888z88afzc63efcc91723openalex-snapshot
Potentialisation de la réponse antidépressive par la lumière : étude préclinique
inferred← citeshttps://doi.org/10.70675/d20c8f2azc2f7z48a8z9545z80352abaf664openalex-snapshot
Rôle des connexines 43 astrocytaires : une étude fonctionnelle dans un modèle murin de dépression basé sur le stress chronique
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.