The Emerging Link Between Autoimmune Disorders and Neuropsychiatric Disease

Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies

Dalmau, J., Gleichman, A. J., Hughes, E. G., Rossi, J. E., Peng, X., Lai, M., Dessain, S. K., Rosenfeld, M. R., Balice-Gordon, R., & Lynch, D. R. (2008) · The Lancet Neurology · doi:10.1016/s1474-4422(08)70224-2 · Cited by 3,488

Paraneoplastic anti– N ‐methyl‐ D ‐aspartate receptor encephalitis associated with ovarian teratoma

Dalmau, J., Tüzün, E., Wu, H., Masjuan, J., Rossi, J. E., Voloschin, A., Baehring, J. M., Shimazaki, H., Koide, R., King, D., et al. (2007) · Annals of Neurology · doi:10.1002/ana.21050 · Cited by 2,492

Neuroligins and neurexins link synaptic function to cognitive disease

Südhof, T. C. (2008) · Nature · doi:10.1038/nature07456 · Cited by 1,849

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Glessner, J. T., Wang, K., Cai, G., Korvatska, O., Kim, C. E., Wood, S., Zhang, H., Estes, A., Brune, C. W., Bradfield, J. P., et al. (2009) · Nature · doi:10.1038/nature07953 · Cited by 1,421

Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan’s syndrome and acquired neuromyotonia

Irani, S. R., Alexander, S. K., Waters, P. J., Kleopa, K. A., Pettingill, P., Zuliani, L., Peles, E., Buckley, C. J., Lang, B., & Vincent, A. C. (2010) · Brain · doi:10.1093/brain/awq213 · Cited by 1,374

Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series

Lai, M., Huijbers, M. G. M., Lancaster, E., Graus, F., Bataller, L., Balice‐Gordon, R. J., Cowell, J. K., & Dalmau, J. O. (2010) · The Lancet Neurology · doi:10.1016/s1474-4422(10)70137-x · Cited by 1,363

NMDA receptor trafficking in synaptic plasticity and neuropsychiatric disorders

Lau, C. G., & Zukin, R. S. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2153 · Cited by 1,159

Cellular and synaptic mechanisms of anti-NMDA receptor encephalitis

Hughes, E. G., Peng, X., Gleichman, A. J., Lai, M., Zhou, L., Tsou, R., Parsons, T. D., Lynch, D. R., Dalmau, J., & Balice-Gordon, R. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.0167-10.2010 · Cited by 1,143

Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis in children and adolescents

Florance, N. R., Davis, R. L., Lam, C., Szperka, C., Zhou, L., Ahmad, S., Campen, C. J., Moss, H., Peter, N., Gleichman, A. J., et al. (2009) · Annals of Neurology · doi:10.1002/ana.21756 · Cited by 1,090

Potassium channel antibody‐associated encephalopathy: a potentially immunotherapy‐responsive form of limbic encephalitis

Vincent, A. C., Buckley, C. J., Schott, J. M., Baker, I., Dewar, B., Detert, N., Clover, L. M., Parkinson, A., Bien, C. G., Omer, S., et al. (2004) · Brain · doi:10.1093/brain/awh077 · Cited by 1,032

Treatment and prognostic factors for long-term outcome in patients with anti-NMDA receptor encephalitis: an observational cohort study

Titulaer, M. J., McCracken, L., Gabilondo, I., Armangué, T., Glaser, C., Iizuka, T., Honig, L. S., Benseler, S. M., Kawachi, I., Martinez-Hernandez, E., et al. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(12)70310-1 · Cited by 3,165

Suicide and suicide risk

Turecki, G., Brent, D. A., Gunnell, D., O’Connor, R. C., Oquendo, M. A., Pirkis, J., & Stanley, B. H. (2019) · Nature Reviews Disease Primers · doi:10.1038/s41572-019-0121-0 · Cited by 1,074

Neuroinflammation and psychiatric illness

Najjar, S., Pearlman, D. M., Alper, K., Najjar, A., & Devinsky, O. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-43 · Cited by 733

Autoimmune encephalopathies

Leypoldt, F., Armangué, T., & Dalmau, J. O. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12553 · Cited by 424

Hallucinations: A Systematic Review of Points of Similarity and Difference Across Diagnostic Classes

Waters, F., & Fernyhough, C. (2016) · Schizophrenia Bulletin · doi:10.1093/schbul/sbw132 · Cited by 351

Anti-NMDA Receptor Encephalitis Antibody Binding Is Dependent on Amino Acid Identity of a Small Region within the GluN1 Amino Terminal Domain

Gleichman, A. J., Spruce, L. A., Dalmau, J. O., Seeholzer, S. H., & Lynch, D. R. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0064-12.2012 · Cited by 292

Immune aging, dysmetabolism, and inflammation in neurological diseases

Deleidi, M., Jäggle, M., & Rubino, G. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00172 · Cited by 260

Red Flags: Clinical Signs for Identifying Autoimmune Encephalitis in Psychiatric Patients

Herken, J., & Prüß, H. (2017) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2017.00025 · Cited by 255

Anti-NMDA Receptor Encephalitis in Psychiatry

Kayser, M. S., & Dalmau, J. O. (2011) · Current Psychiatry Reviews · doi:10.2174/157340011797183184 · Cited by 185

Neuroleptic intolerance in patients with anti-NMDAR encephalitis

Lejuste, F., Thomas, L., Picard, G., Desestret, V., Ducray, F., Rogemond, V., Psimaras, D., Antoine, J.-C. G., Delattre, J., Groc, L., et al. (2016) · Neurology Neuroimmunology & Neuroinflammation · doi:10.1212/nxi.0000000000000280 · Cited by 182

Translating Glutamate: From Pathophysiology to Treatment

Javitt, D. C., Schoepp, D., Kalivas, P. W., Volkow, N. D., Zarate, C., Merchant, K., Bear, M. F., Umbricht, D., Hajos, M., Potter, W. Z., et al. (2011) · Science Translational Medicine · doi:10.1126/scitranslmed.3002804 · Cited by 168

Neuropathology of suicide: Recent findings and future directions

Lutz, P.-E., Mechawar, N., & Turecki, G. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.141 · Cited by 158

Major channels involved in neuropsychiatric disorders and therapeutic perspectives

Imbrici, P., Camerino, D. C., & Tricarico, D. (2013) · Frontiers in Genetics · doi:10.3389/fgene.2013.00076 · Cited by 151

Th17 Pathway-Mediated Immunopathogenesis of Schizophrenia: Mechanisms and Implications

Debnath, M., & Berk, M. (2014) · Schizophrenia Bulletin · doi:10.1093/schbul/sbu049 · Cited by 131

Blood–brain barrier: emerging trends on transport models and new-age strategies for therapeutics intervention against neurological disorders

Alajangi, H. K., Kaur, M., Sharma, A., Rana, S., Thakur, S., Chatterjee, M., Singla, N., Jaiswal, P. K., Singh, G., & Barnwal, R. P. (2022) · Molecular Brain · doi:10.1186/s13041-022-00937-4 · Cited by 137

Neuropsychiatric systemic lupus erythematosus and cognitive dysfunction: The MRL-lpr mouse strain as a model

Jeltsch‐David, H., & Muller, S. (2014) · Autoimmunity Reviews · doi:10.1016/j.autrev.2014.08.015 · Cited by 111

Neuroimmunomodulation in Major Depressive Disorder: Focus on Caspase 1, Inducible Nitric Oxide Synthase, and Interferon-Gamma

Inserra, A., Mastronardi, C. A., Rogers, G. B., Licinio, J., & Wong, M. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1359-3 · Cited by 99

Immune dysregulation and autoimmunity in bipolar disorder: Synthesis of the evidence and its clinical application

Rege, S., & Hodgkinson, S. J. (2013) · Australian & New Zealand Journal of Psychiatry · doi:10.1177/0004867413499077 · Cited by 90

Diagnosing and treating depression in epilepsy

Elger, C. E., Johnston, S. A., & Hoppe, C. (2016) · Seizure · doi:10.1016/j.seizure.2016.10.018 · Cited by 89

A clinical approach to new-onset psychosis associated with immune dysregulation: the concept of autoimmune psychosis

Najjar, S., Steiner, J. H., Najjar, A., & Bechter, K. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1067-y · Cited by 88

Postoperative neurocognitive disorders

Olotu, C. (2019) · Current Opinion in Anaesthesiology · doi:10.1097/aco.0000000000000812 · Cited by 79

Inflammation and depression but where does the inflammation come from?

Halaris, A. E. (2019) · Current Opinion in Psychiatry · doi:10.1097/yco.0000000000000531 · Cited by 76

Differentiating Psychosomatic, Somatopsychic, Multisystem Illnesses and Medical Uncertainty

Bransfield, R. C., & Friedman, K. J. (2019) · Healthcare · doi:10.3390/healthcare7040114 · Cited by 75

Autoimmune encephalitis in psychiatric institutions: current perspectives

Bost, C., Pascual, O., & Honnorat, J. (2016) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s82380 · Cited by 73

Establishing a Pediatric Acute-Onset Neuropsychiatric Syndrome Clinic: Baseline Clinical Features of the Pediatric Acute-Onset Neuropsychiatric Syndrome Cohort at Karolinska Institutet

Gromark, C., Harris, R. A., Wickström, R., Horne, A., Silverberg-Mörse, M., Serlachius, E., & Mataix‐Cols, D. (2019) · Journal of Child and Adolescent Psychopharmacology · doi:10.1089/cap.2018.0127 · Cited by 68

Autoantibody-associated psychiatric syndromes: a systematic literature review resulting in 145 cases

Endres, D., Maier, V., Leypoldt, F., Wandinger, K., Lennox, B., Pollak, T. A., Nickel, K., Maier, S. J., Feige, B., Domschke, K., et al. (2020) · Psychological Medicine · doi:10.1017/s0033291720002895 · Cited by 59

Dysfunction in the coagulation system and schizophrenia

Hoirisch-Clapauch, S., Amaral, O. B., Mezzasalma, M. A., Panizzutti, R., & Nardi, A. E. (2016) · Translational Psychiatry · doi:10.1038/tp.2015.204 · Cited by 57

Chronic cerebral lipocalin 2 exposure elicits hippocampal neuronal dysfunction and cognitive impairment

Olson, B. G., Zhu, X., Norgard, M. A., Diba, P., Levasseur, P. R., Buenafe, A. C., Huisman, C., Burfeind, K. G., Michaelis, K. A., Kong, G., et al. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.07.002 · Cited by 56

Prevalences of autoimmune diseases in schizophrenia, bipolar I and II disorder, and controls

Cremaschi, L., Kardell, M., Johansson, V., Isgren, A., Sellgren, C. M., Altamura, A. C., Hultman, C. M., & Landén, M. (2017) · Psychiatry Research · doi:10.1016/j.psychres.2017.09.071 · Cited by 52

The TRIPS (Toll-like receptors in immuno-inflammatory pathogenesis) Hypothesis: a novel postulate to understand schizophrenia

Venkatasubramanian, G., & Debnath, M. (2013) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2013.04.001 · Cited by 56

Depression, mitochondrial bioenergetics, and electroconvulsive therapy: a new approach towards personalized medicine in psychiatric treatment - a short review and current perspective

Karabatsiakis, A., & Schönfeldt‐Lecuona, C. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-00901-7 · Cited by 53

Autoimmune encephalitis: a potentially treatable cause of mental disorder

Rickards, H. E., Jacob, S., Lennox, B., & Nicholson, T. R. (2014) · Advances in Psychiatric Treatment · doi:10.1192/apt.bp.113.011304 · Cited by 49

Depressive Syndromes in Autoimmune Disorders of the Nervous System: Prevalence, Etiology, and Influence

Liu, Y., & Tang, X.-Q. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00451 · Cited by 39

Serum Interferon-Gamma Level Is Associated with Drug-Naïve Major Depressive Disorder

Daria, S., Proma, M. A., Shahriar, M., Islam, S. M. A., Bhuiyan, M. A., & Islam, M. R. (2020) · SAGE Open Medicine · doi:10.1177/2050312120974169 · Cited by 46

A Critical Review of Pro-Cognitive Drug Targets in Psychosis: Convergence on Myelination and Inflammation

Kroken, R. A., Løberg, E., Drønen, T., Grüner, R., Hugdahl, K., Kompus, K., Skrede, S., & Johnsen, E. (2014) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2014.00011 · Cited by 49

Autoimmune encephalitis and psychiatric disorders

Honnorat, J., & Plazat, L.-O. (2018) · Revue Neurologique · doi:10.1016/j.neurol.2017.11.004 · Cited by 43

Autoimmunity in psychiatry

Davison, K. (2012) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.111.104471 · Cited by 43

Neuropsychiatric Autoimmune Encephalitis without VGKC-Complex, NMDAR, and GAD Autoantibodies

Najjar, S., Pearlman, D. M., Devinsky, O., Najjar, A., Nadkarni, S. S., Butler, T., & Zagzag, D. (2013) · Cognitive and Behavioral Neurology · doi:10.1097/wnn.0b013e31828b6531 · Cited by 41

The Role of Inflammation in the Pathophysiology of Depression and Suicidal Behavior

Serafini, G., Costanza, A., Aguglia, A., Amerio, A., Trabucco, A., Escelsior, A., Sher, L., & Amore, M. (2022) · Medical Clinics of North America · doi:10.1016/j.mcna.2022.09.001 · Cited by 48

Autoimmunity, neuroinflammation, pathogen load: A decisive crosstalk in neuropsychiatric SLE

Jeltsch‐David, H., & Muller, S. (2016) · Journal of Autoimmunity · doi:10.1016/j.jaut.2016.04.005 · Cited by 40

Sex Steroids, Adult Neurogenesis, and Inflammation in CNS Homeostasis, Degeneration, and Repair

Larson, T. A. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00205 · Cited by 39

Anti‐GAPDH Autoantibodies as a Pathogenic Determinant and Potential Biomarker of Neuropsychiatric Diseases

Delunardo, F., Soldati, D., Bellisario, V., Berry, A., Camerini, S., Crescenzi, M., Alessandri, C., Conti, F., Ceccarelli, F., Francia, A., et al. (2016) · Arthritis & Rheumatology · doi:10.1002/art.39750 · Cited by 35

Brain profiling in murine colitis and human epilepsy reveals neutrophils and TNFα as mediators of neuronal hyperexcitability

Barnes, S. E., Zera, K. A., Ivison, G. T., Buckwalter, M. S., & Engleman, E. G. (2021) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02262-4 · Cited by 33

The link between thyroid autoimmunity, depression and bipolar disorder

Jucevičiūtė, N., Žilaitienė, B., Aniulienė, R., & Vanagienė, V. (2019) · Open Medicine · doi:10.1515/med-2019-0008 · Cited by 30

The Role of IgLON Cell Adhesion Molecules in Neurodegenerative Diseases

Salluzzo, M., Vianello, C., Abdullatef, S., Rimondini, R., Piccoli, G., & Carboni, L. (2023) · Genes · doi:10.3390/genes14101886 · Cited by 29

Evaluation and Management of Autoimmune Encephalitis

Mooneyham, G. C., Gallentine, W. B., & Mater, H. V. (2017) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/j.chc.2017.08.011 · Cited by 26

Psychiatric emergencies (part III): psychiatric symptoms resulting from organic diseases.

Testa, A. C., Giannuzzi, R., Daini, S., Bernardini, L., Petrongolo, L., & Silveri, N. G. (2013) · PubMed · Cited by 25

Neuropsychiatric Features of a Cohort of Patients with Systemic Lupus Erythematosus

Moraes‐Fontes, M. F., Lúcio, I., Santos, C. M. P., Campos, M. M., Riso, N., & Riscado, M. V. (2012) · ISRN Rheumatology · doi:10.5402/2012/989218 · Cited by 23

Clinical characterization of autoimmune encephalitis and psychosis

Hao, Q., Wang, D., Guo, L., & Zhang, B. (2016) · Comprehensive Psychiatry · doi:10.1016/j.comppsych.2016.12.006 · Cited by 23

Anti-AMPA-Receptor Encephalitis Presenting as a Rapid-Cycling Bipolar Disorder in a Young Woman with Turner Syndrome

Quaranta, G., Maremmani, A. G. I., & Perugi, G. (2015) · Case Reports in Psychiatry · doi:10.1155/2015/273192 · Cited by 21

TNFAIP3 Reduction-of-Function Drives Female Infertility and CNS Inflammation

Zammit, N. W., McDowell, J., Warren, J. A., Muskovic, W., Gamble, J., Shi, Y., Kaczorowski, D. C., Chan, C., Powell, J. E., Ormandy, C. J., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.811525 · Cited by 21

Anti-neuropeptide Y plasma immunoglobulins in relation to mood and appetite in depressive disorder

Garcia, F. D., Coquerel, Q., do-Rego, J.-C., Cravezic, A., Bôle‐Feysot, C., Kiive, E., Déchelotte, P., Harro, J., & Fetissov, S. O. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.01.015 · Cited by 20

Glutamatergic autoencephalitides: an emerging field

Panzer, J. A., Gleichman, A. J., & Lynch, D. R. (2014) · Journal of Neural Transmission · doi:10.1007/s00702-013-1152-4 · Cited by 21

The Science of Neuropsychiatry: Past, Present, and Future

Arzy, S., & Danziger, S. (2014) · Journal of Neuropsychiatry · doi:10.1176/appi.neuropsych.13120371 · Cited by 21

Neuroinflammation and Neurotransmission Mechanisms Involved in Neuropsychiatric Disorders

Leite, J. A., Orellana, A. M., Kinoshita, P. F., de Mello, N. P., Scavone, C., & Kawamoto, E. M. (2017) · InTech eBooks · doi:10.5772/intechopen.69343 · Cited by 20

Association between autoimmune diseases of the nervous system and schizophrenia: A systematic review and meta-analysis of cohort studies

Cao, Y., Ji, S., Chen, Y., Zhang, X., Ding, G., & Tang, F. (2023) · Comprehensive Psychiatry · doi:10.1016/j.comppsych.2023.152370 · Cited by 22

A Novel Striated Muscle-Specific Myosin-Blocking Drug for the Study of Neuromuscular Physiology

Heredia, D. J., Schubert, D., Maligireddy, S. S., Hennig, G. W., & Gould, T. W. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00276 · Cited by 21

Neurodegeneration in systemic lupus erythematosus: layer by layer retinal study using optical coherence tomography

Dias‐Santos, A., Ferreira, J., Pinheiro, S., Cunha, J. P., Alves, M., Papoila, A. L., Moraes‐Fontes, M. F., & Proença, R. D. (2020) · International Journal of Retina and Vitreous · doi:10.1186/s40942-020-00219-y · Cited by 18

Mechanisms of Psychiatric Comorbidities in Epilepsy

Maguire, J. L. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_192 · Cited by 22

Anti-brain autoantibodies in the serum of schizophrenic patients: A case-control study

Margari, F., Petruzzelli, M. G., Mianulli, R., Toto, M., Pastore, A., Bizzaro, N., & Tampoia, M. (2013) · Psychiatry Research · doi:10.1016/j.psychres.2013.09.006 · Cited by 18

First-onset psychosis, anti-NMDAR encephalitis, schizophrenia and Consultation–Liaison psychiatry

van de Riet, E. H. C. W., & Schieveld, J. N. M. (2013) · General Hospital Psychiatry · doi:10.1016/j.genhosppsych.2013.01.014 · Cited by 17

Altered hippocampal functional connectivity in primary Sjögren syndrome: a resting-state fMRI study

Zhang, X., Zhao, L.-R., Zhou, J.-M., Su, Y.-Y., Ke, J., Cheng, Y., Li, J., & Shen, W. (2020) · Lupus · doi:10.1177/0961203320908936 · Cited by 17

An exploratory study of the damage markers NfL, GFAP, and t-Tau, in cerebrospinal fluid and other findings from a patient cohort enriched for suspected autoimmune psychiatric disease

Syk, M., Tornvind, E., Gallwitz, M., Fällmar, D., Amandusson, Å., Rothkegel, H., Danfors, T., Thulin, M., Rasmusson, A. J., Červenka, S., et al. (2024) · Translational Psychiatry · doi:10.1038/s41398-024-03021-8 · Cited by 17

Mental Disorders Among Offspring Prenatally Exposed to Systemic Glucocorticoids

Laugesen, K., Skajaa, N., Petersen, I., Andersen, M., Feldt‐Rasmussen, U., Al-Mashhadi, S. K., Stewart, P. M., Jørgensen, J. O. L., & Sørensen, H. T. (2025) · JAMA Network Open · doi:10.1001/jamanetworkopen.2024.53245 · Cited by 19

Interplay of immune modulation, adaptive response and hormesis: Suggestive of threshold for clinical manifestation of effects of ionizing radiation at low doses?

Chaurasia, R. K., Sapra, B. K., & Aswal, D. K. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.170178 · Cited by 17

Cortical Thickness and Episodic Memory Impairment in Systemic Lupus Erythematosus

Bizzo, B. C., Sanchez, T. A., Tukamoto, G., Zimmermann, N., Netto, T. M., & Gasparetto, E. L. (2016) · Journal of Neuroimaging · doi:10.1111/jon.12394 · Cited by 15

Early neuropsychiatric involvement in antiphospholipid syndrome

Lai, J.-Y., Wu, P., Chen, H., & Lee, M. (2012) · General Hospital Psychiatry · doi:10.1016/j.genhosppsych.2012.02.005 · Cited by 14

Immune mediated pediatric encephalitis – need for comprehensive evaluation and consensus guidelines

Shekunov, J., Blacker, C. J., Voort, J. L. V., Tillema, J., Croarkin, P. E., & Romanowicz, M. (2020) · BMC Neurology · doi:10.1186/s12883-020-1605-y · Cited by 14

Mild Thyrotoxicosis Leads to Brain Perfusion Changes: An Arterial Spin Labelling Study

Göbel, A., Heldmann, M., Sartorius, A., Göttlich, M., Dirk, A.-L., Brabant, G., & Münte, T. (2017) · Journal of neuroendocrinology · doi:10.1111/jne.12446 · Cited by 13

Autoimmune Encephalitides

Younger, D. S. (2019) · Neurologic Clinics · doi:10.1016/j.ncl.2019.01.015 · Cited by 13

Rare genetic diseases in India: Steps toward a nationwide mission program

Kar, A., Sundaravadivel, P., & Dalal, A. B. (2024) · Journal of Biosciences · doi:10.1007/s12038-024-00430-1 · Cited by 11

Neue serologische Marker zur Differentialdiagnose der Autoimmun-Enzephalitis/New serological markers for the differential diagnosis of autoimmune limbic encephalitis

Wandinger, K., Klingbeil, C., Gneiss, C., Waters, P. J., Dalmau, J. O., Saschenbrecker, S., Borowski, K., Deisenhammer, F., Vincent, A. C., Probst, C., et al. (2011) · Journal of Laboratory Medicine · doi:10.1515/jlm.2011.059et · Cited by 15

Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study

Li, J., Hojlo, M. A., Chennuri, S., Gujral, N., Paterson, H. L., Shefchek, K., Genetti, C. A., Cohn, E. L., Sewalk, K. C., Garvey, E. A., et al. (2021) · Journal of Medical Internet Research · doi:10.2196/21023 · Cited by 10

Posterior cortical and white matter changes on MRI in anti–AMPA receptor antibody encephalitis

Elamin, M., Lonergan, R. M., Killeen, R. P., O’Riordan, S., Tubridy, N. J., & McGuigan, C. (2015) · Neurology Neuroimmunology & Neuroinflammation · doi:10.1212/nxi.0000000000000118 · Cited by 10

Autoimmune encephalitis in the elderly: who to test and what to test for

Behrman, S., & Lennox, B. (2019) · Evidence-Based Mental Health · doi:10.1136/ebmental-2019-300110 · Cited by 10

Characteristics of emerging new autoimmune diseases after COVID ‐19 vaccination: A sub‐study by the COVAD group

Shumnalieva, R., Ravichandran, N., Hannah, J. R., Javaid, M., Darooka, N., Roy, D., Gonzalez, D. E., Velikova, T. V., Milchert, M., Kuwana, M., et al. (2024) · International Journal of Rheumatic Diseases · doi:10.1111/1756-185x.15178 · Cited by 11

Differences in Incidence and Risks of Suicide Attempt and Suicidal Drug Overdose between Patients with Epilepsy with and without Comorbid Depression

Lin, C.-Y., Harnod, T., Lin, C., Shen, W., & Kao, C. (2019) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph16224533 · Cited by 10

Onconeural Antibodies in Acute Psychiatric Inpatient Care

Sæther, S. G., Schou, M. B., Stoecker, W., Teegen, B., Borowski, K., Vaaler, A., Kondziella, D., & Reitan, S. K. (2016) · Journal of Neuropsychiatry · doi:10.1176/appi.neuropsych.16050110 · Cited by 9

Autoimmune meningitis and encephalitis in adult-onset still disease – Case report

Bożek, M., Konopko, M., Wierzba‐Bobrowicz, T., Witkowski, G., Makowicz, G., & Sienkiewicz‐Jarosz, H. (2017) · Neurologia i Neurochirurgia Polska · doi:10.1016/j.pjnns.2017.06.006 · Cited by 9

Schizophrenia Spectrum and Other Psychotic Disorders

(2022) · American Psychiatric Association Publishing eBooks · doi:10.1176/appi.books.9780890425787.x02_schizophrenia_spectrum · Cited by 12

Convulsive therapy for psychiatric disorders

Kaster, T. S., & Blumberger, D. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-18496-3.00010-0 · Cited by 7

Integrating biobehavioral information to predict mood disorder suicide risk

Jackson, N., & Jabbi, M. (2022) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2022.100495 · Cited by 7

Racial and gender-based disparities and trends in common psychiatric conditions in liver cirrhosis hospitalizations: A ten-year United States study

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