Items where Subject is "diseases & disorders > mental disorders"

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Number of items at this level: 157.

A

Aberg, K., Adkins, D. E., Bukszár, J., Webb, B. T., Caroff, S. N., Miller, D. D., Sebat, J., Stroup, S., Fanous, A. H., Vladimirov, V. I., McClay, J. L., Lieberman, J. A., Sullivan, P. F., van den Oord, E. J. C. G. (2010) Genomewide Association Study of Movement-Related Adverse Antipsychotic Effects. Biological Psychiatry, 67 (3). pp. 279-282.

Akil, H., Brenner, S., Kandel, E., Kendler, K. S., King, M. C., Scolnick, E., Watson, J. D., Zoghbi, H. Y. (2010) The future of psychiatric research: Genomes and neural circuits. Science, 327 (5973). pp. 1580-1581.

Aznar, S., Klein, A. B., Santini, M. A., Knudsen, G. M., Henn, F., Gass, P., Vollmayr, B. (2010) Aging and depression vulnerability interaction results in decreased serotonin innervation associated with reduced BDNF levels in hippocampus of rats bred for learned helplessness. Synapse, 64 (7). pp. 561-5. ISSN 0887-4476

B

Badner, J. A., Koller, D., Foroud, T., Edenberg, H., Nurnberger, J. I., Zandi, P. P., Willour, V. L., McMahon, F. J., Potash, J. B., Hamshere, M., Grozeva, D., Green, E., Kirov, G., Jones, I., Jones, L., Craddock, N., Morris, D., Segurado, R., Gill, M., Sadovnick, D., Remick, R., Keck, P., Kelsoe, J., Ayub, M., MacLean, A., Blackwood, D., Liu, C. Y., Gershon, E. S., McMahon, W., Lyon, G. J., Robinson, R., Ross, J., Byerley, W. (2012) Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms. Molecular Psychiatry, 17 (8). pp. 818-826. ISSN 1476-5578

Bolduc, F. V., Bell, K. G., Rosenfelt, C., Cox, H., Tully, T. (2010) Fragile x mental retardation 1 and filamin a interact genetically in Drosophila long-term memory. Front Neural Circuits, 3. p. 22. ISSN 1662-5110 (Electronic) 1662-5110 (Linking)

Bolduc, F. V., Shevell, M. I. (2005) Corrected head circumference centiles as a possible predictor of developmental performance in high-risk neonatal intensive care unit survivors. Dev Med Child Neurol, 47 (11). pp. 766-70. ISSN 0012-1622 (Print)

Brennand, K. J., Simone, A., Jou, J., Gelboin-Burkhart, C., Tran, N., Sangar, S., Li, Y., Mu, Y., Chen, G., Yu, D., McCarthy, S. E., Sebat, J., Gage, F. H. (2011) Modelling schizophrenia using human induced pluripotent stem cells. Nature, 473 (7346). 221 - 225. ISSN 00280836 (ISSN)

C

Carvalho, C. M. B., Brennand, K., Yuan, B., Sebat, J., Malhotra, D., McCarthy, S., Rudolph, U., Levy, D., Lupski, J. R. (2015) Mosaicism May underlie Pleiotropic Psychiatric Phenotypes. Schizophrenia Bulletin, 41. S198-S199. ISSN 0586-76141745-1701

Chen, Y. C., Carter, H., Parla, J., Kramer, M., Goes, F. S., Pirooznia, M., Zandi, P. P., McCombie, W. R., Potash, J. B., Karchin, R. (2013) A Hybrid Likelihood Model for Sequence-Based Disease Association Studies. PLoS Genetics, 9 (1). ISSN 15537390 (ISSN)

Cheng, R., Juo, S. H., Loth, J. E., Nee, J., Iossifov, I., Blumenthal, R., Sharpe, L., Kanyas, K., Lerer, B., Lilliston, B., Smith, M., Trautman, K., Gilliam, T. C., Endicott, J., Baron, M. (2006) Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder. Mol Psychiatry, 11 (3). pp. 252-60. ISSN 1359-4184 (Print)1359-4184 (Linking)

Choe, L., D'Ascenzo, M., Relkin, N. R., Pappin, D., Ross, P., Williamson, B., Guertin, S., Pribil, P., Lee, K. H. (2007) 8-plex quantitation of changes in cerebrospinal fluid protein expression in subjects undergoing intravenous immunoglobulin treatment for Alzheimer's disease. Proteomics, 7 (20). pp. 3651-60. ISSN 1615-9853 (Print)1615-9853 (Linking)

Chourbaji, S., Hellweg, R., Brandis, D., Zorner, B., Zacher, C., Lang, U. E., Henn, F. A., Hortnagl, H., Gass, P. (2004) Mice with reduced brain-derived neurotrophic factor expression show decreased choline acetyltransferase activity, but regular brain monoamine levels and unaltered emotional behavior. Brain Res Mol Brain Res, 121 (1-2). pp. 28-36. ISSN 0169-328X (Print)0169-328X (Linking)

Colla, M., Ende, G., Bohrer, M., Deuschle, M., Kronenberg, G., Henn, F., Heuser, I. (2003) MR spectroscopy in Alzheimer's disease: gender differences in probabilistic learning capacity. Neurobiology of Aging, 24 (4). pp. 545-52. ISSN 0197-4580 (Print)0197-4580 (Linking)

Curley, A. A., Eggan, S. M., Lazarus, M. S., Huang, Z. J., Volk, D. W., Lewis, D. A. (2013) Role of glutamic acid decarboxylase 67 in regulating cortical parvalbumin and GABA membrane transporter 1 expression: Implications for schizophrenia. Neurobiology of Disease, 50 (1). pp. 179-186. ISSN 0969-9961

D

Delevich, K., Abi-Dargham, A., Hall, J., Sawa, A. (2016) Studying schizophrenia in the post-genomic era: perspectives from the 2016 summer Banbury Workshop at Cold Spring Harbor Laboratory. Mol Psychiatry. ISSN 1476-5578 (Electronic)1359-4184 (Linking)

Deutsch, C. K., Malhotra, D., Krause, V., McCarthy, S. E., Krastoshevsky, O., Coleman, M., Francis, R. W., Bodkin, J. A., Boling, L., Cole, J., Gibbs, A., Johnson, F., Lerbinger, J., Mendell, N. R., Sebat, J., Levy, D. L. (2009) Rare Gene Copy Number Variations Are Associated with Specific Endophenotypes in Schizophrenia. Schizophrenia Bulletin, 35 (Suppl.). p. 117. ISSN 0586-7614

Dressing, H., Henn, F. A., Gass, P. (2002) Stalking behavior - an overview of the problem and a case report of male-to-male stalking during delusional disorder. Psychopathology, 35 (5). pp. 313-8. ISSN 0254-4962 (Print)0254-4962 (Linking)

E

Eisch, A. J., Cameron, H. A., Encinas, J. M., Meltzer, L. A., Ming, G. L., Overstreet-Wadiche, L. S. (2008) Adult neurogenesis, mental health, and mental illness: hope or hype? J Neurosci, 28 (46). pp. 11785-91.

Elia, J., Glessner, J. T., Wang, K., Takahashi, N., Shtir, C. J., Hadley, D., Sleiman, P. M. A., Zhang, H., Kim, C. E., Robison, R., Lyon, G. J., Flory, J. H., Bradfield, J. P., Imielinski, M., Hou, C., Frackelton, E. C., Chiavacci, R. M., Sakurai, T., Rabin, C., Middleton, F. A., Thomas, K. A., Garris, M., Mentch, F., Freitag, C. M., Steinhausen, H. C., Todorov, A. A., Reif, A., Rothenberger, A., Franke, B., Mick, E. O., Roeyers, H., Buitelaar, J., Lesch, K. P., Banaschewski, T., Ebstein, R. P., Mulas, F., Oades, R. D., Sergeant, J., Sonuga-Barke, E., Renner, T. J., Romanos, M., Romanos, J., Warnke, A., Walitza, S., Meyer, J., Pálmason, H., Seitz, C., Loo, S. K., Smalley, S. L., Biederman, J., Kent, L., Asherson, P., Anney, R. J. L., Gaynor, J. W., Shaw, P., Devoto, M., White, P. S., Grant, S. F. A., Buxbaum, J. D., Rapoport, J. L., Williams, N. M., Nelson, S. F., Faraone, S. V., Hakonarson, H. (2012) Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nature Genetics, 44 (1). pp. 78-84. ISSN 1061-4036

Ende, G., Braus, D. F., Walter, S., Henn, F. A. (2001) Lower concentration of thalamic n-acetylaspartate in patients with schizophrenia: a replication study. Am J Psychiatry, 158 (8). pp. 1314-6. ISSN 0002-953X (Print)0002-953X (Linking)

Ende, G., Braus, D. F., Walter, S., Weber-Fahr, W., Henn, F. A. (2003) Multiregional 1H-MRSI of the hippocampus, thalamus, and basal ganglia in schizophrenia. European Archives of Psychiatry and Clinical Neuroscience, 253 (1). pp. 9-15. ISSN 0940-1334 (Print)0940-1334 (Linking)

Ende, G., Braus, D. F., Walter, S., Weber-Fahr, W., Soher, B., Maudsley, A. A., Henn, F. A. (2000) Effects of age, medication, and illness duration on the N-acetyl aspartate signal of the anterior cingulate region in schizophrenia. Schizophr Res, 41 (3). pp. 389-95. ISSN 0920-9964 (Print)

Ende, G., Demirakca, T., Walter, S., Wokrina, T., Sartorius, A., Wildgruber, D., Henn, F. A. (2007) Subcortical and medial temporal MR-detectable metabolite abnormalities in unipolar major depression. Eur Arch Psychiatry Clin Neurosci, 257 (1). pp. 36-9. ISSN 0940-1334 (Print)0940-1334 (Linking)

Ende, G., Hubrich, P., Walter, S., Weber-Fahr, W., Kammerer, N., Braus, D. F., Henn, F. A. (2005) Further evidence for altered cerebellar neuronal integrity in schizophrenia. Am J Psychiatry, 162 (4). pp. 790-2. ISSN 0002-953X (Print)0002-953X (Linking)

F

Fendt, M., Lex, A., Falkai, P., Henn, F. A., Schmitt, A. (2008) Behavioural alterations in rats following neonatal hypoxia and effects of clozapine: implications for schizophrenia. Pharmacopsychiatry, 41 (4). pp. 138-45. ISSN 0176-3679 (Print)0176-3679 (Linking)

Fillit, H. M., Butler, R. N., O'Connell, A. W., Albert, M. S., Birren, J. E., Cotman, C. W., Greenough, W. T., Gold, P. E., Kramer, A. F., Kuller, L. H., Perls, T. T., Sahagan, B. G., Tully, T. (2002) Achieving and maintaining cognitive vitality with aging. Mayo Clinic Proceedings, 77 (7). pp. 681-696. ISSN 0025-6196

Forgeard, M. J. C., Haigh, E. A. P., Beck, A. T., Davidson, R. J., Henn, F. A., Maier, S. F., Mayberg, H. S., Seligman, M. E. P. (2011) Beyond depression: Toward a process-based approach to research, diagnosis, and treatment. Clinical Psychology: Science and Practice, 18 (4). pp. 275-299. ISSN 09695893 (ISSN)

Friddle, C., Koskela, R., Ranade, K., Hebert, J., Cargill, M., Clark, C. D., McInnis, M., Simpson, S., McMahon, F., Stine, O. C., Meyers, D., Xu, J. F., MacKinnon, D., Swift-Scanlan, T., Jamison, K., Folstein, S., Daly, M., Kruglyak, L., Marr, T., DePaulo, J. R., Botstein, D. (2000) Full-genome scan for linkage in 50 families segregating the bipolar affective disease phenotype. American Journal of Human Genetics, 66 (1). pp. 205-215. ISSN 0002-9297

G

Gass, P., Reichardt, H. M., Strekalova, T., Henn, F., Tronche, F. (2001) Mice with targeted mutations of glucocorticoid and mineralocorticoid receptors: models for depression and anxiety? Physiol Behav, 73 (5). pp. 811-25. ISSN 0031-9384 (Print)0031-9384 (Linking)

Gershon, E. S., Kelsoe, J. R., Kendler, K. S., Watson, J. D. (2001) A scientific opportunity. Science, 294 (5544). p. 957. ISSN 0036-8075

Girirajan, S., Mendoza-Londono, R., Vlangos, C. N., Dupuis, L., Nowak, N. J., Bunyan, D. J., Hatchwell, E., Elsea, S. H. (2007) Smith-Magenis syndrome and Moyamoya disease in a patient with del(17)(p11.2p13.1). American Journal of Medical Genetics Part A, 143A (9). pp. 999-1008. ISSN 1552-4825

Girirajan, S., Rosenfeld, J. A., Cooper, G. M., Antonacci, F., Siswara, P., Itsara, A., Vives, L., Walsh, T., McCarthy, S. E., Baker, C., Mefford, H. C., Kidd, J. M., Browning, S. R., Browning, B. L., Dickel, D. E., Levy, D. L., Ballif, B. C., Platky, K., Farber, D. M., Gowans, G. C., Wetherbee, J. J., Asamoah, A., Weaver, D. D., Mark, P. R., Dickerson, J., Garg, B. P., Ellingwood, S. A., Smith, R., Banks, V. C., Smith, W., McDonald, M. T., Hoo, J. J., French, B. N., Hudson, C., Johnson, J. P., Ozmore, J. R., Moeschler, J. B., Surti, U., Escobar, L. F., El-Khechen, D., Gorski, J. L., Kussmann, J., Salbert, B., Lacassie, Y., Biser, A., McDonald-McGinn, D. M., Zackai, E. H., Deardorff, M. A., Shaikh, T. H., Haan, E., Friend, K. L., Fichera, M., Romano, C., Gécz, J., DeLisi, L. E., Sebat, J., King, M. C., Shaffer, L. G., Eichler, E. E. (2010) A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. Nature Genetics.

Goes, F. S., Pirooznia, M., Parla, J. S., Kramer, M., Ghiban, E., Mavruk, S., Chen, Y. C., Monson, E. T., Willour, V. L., Karchin, R., Flickinger, M., Locke, A. E., Levy, S. E., Scott, L. J., Boehnke, M., Stahl, E., Moran, J. L., Hultman, C. M., Landen, M., Purcell, S. M., Sklar, P., Zandi, P. P., McCombie, W. R., Potash, J. B. (2016) Exome Sequencing of Familial Bipolar Disorder. JAMA Psychiatry, 73 (6). pp. 590-597. ISSN 2168-6238 (Electronic)2168-622X (Linking)

Guha, S., Rees, E., Darvasi, A., Ivanov, D., Ikeda, M., Bergen, S. E., Magnusson, P. K., Cormican, P., Morris, D., Gill, M., Cichon, S., Rosenfeld, J. A., Lee, A., Gregersen, P. K., Kane, J. M., Malhotra, A. K., Rietschel, M., Nothen, M. M., Degenhardt, F., Priebe, L., Breuer, R., Strohmaier, J., Ruderfer, D. M., Moran, J. L., Chambert, K. D., Sanders, A. R., Shi, J. X., Kendler, K., Riley, B., O'Neill, T., Walsh, D., Malhotra, D., Corvin, A., Purcell, S., Sklar, P., Iwata, N., Hultman, C. M., Sullivan, P. F., Sebat, J., McCarthy, S., Gejman, P. V., Levinson, D. F., Owen, M. J., O'Donovan, M. C., Lencz, T., Kirov, G. (2013) Implication of a Rare Deletion at Distal 16p11.2 in Schizophrenia. Jama Psychiatry, 70 (3). pp. 253-260. ISSN 2168-622X

H

Henn, F. A. (2012) Circuits, Cells, and Synapses: Toward a New Target for Deep Brain Stimulation in Depression. Neuropsychopharmacology, 37 (1). pp. 307-308. ISSN 0893-133X

Henn, F. A. (2013) Deep Brain Stimulation of the Lateral Habenula in Treatment Resistant Depression. Biological Psychiatry, 73 (9). 231S-231S. ISSN 0006-3223

Henn, F. A. (2011) Dopamine: A Marker of Psychosis and Final Common Driver of Schizophrenia Psychosis. American Journal of Psychiatry, 168 (12). pp. 1239-1240. ISSN 0002-953X

Henn, F. A. (1995) The NMDA receptor as a site for psychopathology. Primary or secondary role? Archives of General Psychiatry, 52 (12). 1008-10; discussion 1019. ISSN 0003-990X (Print)0003-990X (Linking)

Henn, F. A. (2008) Pharmacogenetic studies of depression. Biol Psychiatry, 63 (12). pp. 1101-2. ISSN 1873-2402 (Electronic)0006-3223 (Linking)

Henn, F. A., Herjanic, M., Vanderpearl, R. H. (1977) Forensic psychiatry: anatomy of a service. Comprehensive psychiatry, 18 (4). pp. 337-45. ISSN 0010-440X (Print)0010-440x

Henn, F. A., Li, B., Piriz, J., Sartorius, A., Mirrone, M. M., Malinow, R. (2010) The l. habenula, a key to understanding depression. Neuroscience Research, 68 (Supple). e17-e17.

Henn, F. A., Vollmayr, B. (2004) Basic pathophysiological mechanisms in depression: what are they and how might they affect the course of the illness? Pharmacopsychiatry, 37 Sup. S152-6. ISSN 0176-3679 (Print)0176-3679 (Linking)

Henn, F. A., Vollmayr, B. (2004) Neurogenesis and depression: etiology or epiphenomenon? Biol Psychiatry, 56 (3). pp. 146-50. ISSN 0006-3223 (Print)0006-3223 (Linking)

Henn, F. A., Vollmayr, B. (2005) Stress models of depression: forming genetically vulnerable strains. Neurosci Biobehav Rev, 29 (4-5). pp. 799-804. ISSN 0149-7634 (Print)0149-7634 (Linking)

Herjanic, M., Henn, F. A., Vanderpearl, R. H. (1977) Forensic psychiatry: female offenders. American journal of psychiatry, 134 (5). pp. 556-8. ISSN 0002-953X (Print)0002-953x

Hirschtritt, M. E., Darrow, S. M., Illmann, C., Osiecki, L., Grados, M., Sandor, P., Dion, Y., King, R. A., Pauls, D. L., Budman, C. L., Cath, D. C., Greenberg, E., Lyon, G. J., Yu, D., McGrath, L. M., McMahon, W. M., Lee, P. C., Delucchi, K. L., Scharf, J. M., Mathews, C. A. (2016) Social disinhibition is a heritable subphenotype of tics in Tourette syndrome. Neurology, 87 (5). pp. 497-504. ISSN 0028-3878

Hirschtritt, M. E., Lee, P. C., Pauls, D. L., Dion, Y., Grados, M. A., Illmann, C., King, R. A., Sandor, P., McMahon, W. M., Lyon, G. J., Cath, D. C., Kurlan, R., Robertson, M. M., Osiecki, L., Scharf, J. M., Mathews, C. A. (2015) Lifetime Prevalence, Age of Risk, and Genetic Relationships of Comorbid Psychiatric Disorders in Tourette Syndrome. JAMA Psychiatry, 72 (4). p. 325. ISSN 2168-622x

Hirschtritt, Matthew, Darrow, Sabrina M., Illmann, Cornelia, Osiecki, Lisa, Grados, Marco, Sandor, Paul, Dion, Yves, King, Robert A., Pauls, David, Budman, Cathy L., Cath, Danielle C., Greenberg, Erica, Lyon, Gholson J., Yu, Dongmei, McGrath, Lauren M., McMahon, William M., Lee, Paul C., Delucchi, Kevin L., Scharf, Jeremiah M., Mathews, Carol A. (2017) 896 - Genetic and Phenotypic Overlap of Specific Obsessive-Compulsive Subtypes with Tourette Syndrome. Biological Psychiatry, 81 (10, Su). S361-S362. ISSN 0006-3223

I

Iijima-Ando, K., Hearn, S. A., Shenton, C., Gatt, A., Zhao, L., Iijima, K. (2009) Mitochondrial mislocalization underlies Ab42-induced neuronal dysfunction in a drosophila model of alzheimer's disease. PLoS ONE, 4 (12). pp. 1-13.

Iossifov, I., Ronemus, M., Levy, D., Wang, Z. H., Hakker, I., Rosenbaum, J., Yamrom, B., Lee, Y. H., Narzisi, G., Leotta, A., Kendall, J., Grabowska, E., Ma, B. C., Marks, S., Rodgers, L., Stepansky, A., Troge, J., Andrews, P., Bekritsky, M., Pradhan, K., Ghiban, E., Kramer, M., Parla, J., Demeter, R., Fulton, L. L., Fulton, R. S., Magrini, V. J., Ye, K., Darnell, J. C., Darnell, R. B., Mardis, E. R., Wilson, R. K., Schatz, M. C., McCombie, W. R., Wigler, M. (2012) De Novo Gene Disruptions in Children on the Autistic Spectrum. Neuron, 74 (2). pp. 285-299. ISSN 0896-6273

K

Kim, Y., Pradhan, K., Fitzgerald, G., Umadevi Venkataraju, K, Osten, P. (2013) Serial two-photon tomography-based whole-brain activity mapping in cntnap2 ko mouse model of autism. In: Neuroscience 2013, Nov 9th-13th 2013, San Diego, CA.

Kopf, D., Westphal, S., Luley, C. W., Ritter, S., Gilles, M., Weber-Hamann, B., Lederbogen, F., Lehnert, H., Henn, F. A., Heuser, I., Deuschle, M. (2004) Lipid metabolism and insulin resistance in depressed patients: significance of weight, hypercortisolism, and antidepressant treatment. J Clin Psychopharmacol, 24 (5). pp. 527-31. ISSN 0271-0749 (Print)0271-0749 (Linking)

Kusenda, M., Sebat, J. (2008) The role of rare structural variants in the genetics of autism spectrum disorders. Cytogenet Genome Res, 123 (1--4). pp. 36-43. ISSN 1424-8581 (Print)1424-859X (Electronic)

L

Lederbogen, F., Hermann, D., Hewer, W., Henn, F. A. (2001) Thyroid function test abnormalities in newly admitted psychiatric patients residing in an iodine-deficient area: patterns and clinical significance. Acta Psychiatr Scand, 104 (4). pp. 305-10. ISSN 0001-690X (Print)0001-690X (Linking)

Lee, I. S., Carvalho, C. M., Douvaras, P., Ho, S. M., Hartley, B. J., Zuccherato, L. W., Ladran, I. G., Siegel, A. J., McCarthy, S., Malhotra, D., Sebat, J., Rapoport, J., Fossati, V., Lupski, J. R., Levy, D. L., Brennand, K. J. (2015) Characterization of molecular and cellular phenotypes associated with a heterozygous deletion using patient-derived hiPSC neural cells. NPJ Schizophr, 1. ISSN 2334-265X (Print)2334-265X (Linking)

Levy, D., Coleman, M., Godfrey, L., Sebat, J., Ongur, D., Kaufman, M. J., McCarthy, S., Malhotra, D., Lewandowski, K., Javitt, D., Waldstreicher, E., Vuckovic, A., Visscher, T., Kirchhoff, C., Coyle, J. T., Suckow, R., Rudolph, U., Bodkin, J. (2015) Successful Targeted Treatment of a Medically Actionable Mutation in Psychotic Disorders. Schizophrenia Bulletin, 41. S207-S207. ISSN 0586-7614

Li, B. (2011) SYNAPTIC AND CIRCUITRY MECHANISMS UNDERLYING COGNITIVE ABERRATIONS IN MICE DEFICIENT IN GENES LINKED TO SCHIZOPHRENIA. Schizophrenia Bulletin, 37. p. 37. ISSN 1745-1701

Li, B. (2012) Talk from Bo Li at the Cold Spring Harbor Laboratory In-House Symposium (2012). [Video] (Unpublished)

Li, B., Devidze, N., Barengolts, D., Prostak, N., Sphicas, E., Apicella, A. J., Malinow, R., Emamian, E. S. (2009) NMDA Receptor Phosphorylation at a Site Affected in Schizophrenia Controls Synaptic and Behavioral Plasticity. J Neurosci, 29 (38). pp. 11965-11972.

Li, B., Piriz, J., Mirrione, M., Chung, C. H., Proulx, C. D., Schulz, D., Henn, F. A., Malinow, R. (2011) Synaptic potentiation onto habenula neurons in the learned helplessness model of depression. Nature, 470 (7335). 535-U125. ISSN 0028-0836

Li, K., Zhou, T., Liao, L., Yang, Z., Wong, C., Henn, F., Malinow, R., Yates Iii, J. R., Hu, H. (2013) βCaMKII in lateral habenula mediates core symptoms of depression. Science, 341 (6149). pp. 1016-1020. ISSN 00368075 (ISSN)

Lyon, G. J. (2015) Discovery and genetic characterization of new neuropsychiatric syndromes from family-based studies. In: Cold Spring Harbor Laboratory: The Biology of Genomes Meeting, Cold Spring Harbor, NY. (Unpublished)

Lyon, G. J., Coffey, B. (2008) Book Review: Attention-Deficit Hyperactivity Disorder: A Handbook for Diagnosis and Treatment, 3rd ed. Journal of Clinical Psychiatry, 69 (6). p. 1023. ISSN 1555-2101 (online)

Lyon, G. J., Coffey, B. (2008) Book Review: Treating Tourette Syndrome and Tic Disorders: A Guide for Practitioners. Journal of Child and Adolescent Psychopharmacology, 18 (4). pp. 411-412.

Lyon, G. J., Coffey, B. J. (2009) Complex tics and complex management in a case of severe Tourette's disorder (TD) in an adolescent. Journal of Child and Adolescent Psychopharmacology, 19 (4). pp. 469-74. ISSN 1557-8992 (Electronic)1044-5463 (Linking)

Lyon, G. J., Koplewicz, H. S. (2007) Schizophrenia in childhood. The Scientist, 21 (12 SUP). pp. 22-25. ISSN 08903670 (ISSN)

Lyon, Gholson J. (2013) Childhood-­onset Neuropsychiatric Disorders. In: FarGen Summit (Faroe Genome Project), Sept 19th-20th 2013, Tórshavn, The Faroe Islands. (Unpublished)

Lyon, Gholson J. (2014) Clinical Genomics of Neuropsychiatric Illnesses. In: Stony Brook University Division of Child and Adolescent Psychiatry, Seminar, Invited Speaker, January 2014, Stony Brook, NY. (Unpublished)

Lyon, Gholson J. (2013) Clinical genetics and other aspects of neuropsychiatric disorders. In: The International Behavioural and Neural Genetics Society (IBANGS), Genes, Brain & Behavior 15th Annual Meeting, May 20th-24th 2013, Leuven, Belgium. (Unpublished)

Lyon, Gholson J. (2013) Clinical genetics and other aspects of neuropsychiatric disorders. In: NGS Translate World Forum, May 28th-31st 2013, Boston, MA. (Unpublished)

Lyon, Gholson J. (2012) Clinical progress in autism genetics and treatment. In: Systems biology of autism: from basic science to therapeutic strategies , Sept 9-­12, 2012. (Unpublished)

Lyon, Gholson J. (2014) Deep Brain Stimulation, Psychiatric Genetics, and iPS cell models of disease. In: CSHL In-House Seminar Series, Jan 24th 2014, Cold Spring Harbor Laboratory . (Unpublished)

Lyon, Gholson J. (2011) Finding and Analyzing Human Genetic Variation in Neuropsychiatric Disorders. In: Faculty Recruitment Talk, Dec 2011, Cold Spring Harbor Laboratory. (Unpublished)

Lyon, Gholson J. (2013) Genetic and Biochemical Analysis of Childhood-­Onset Idiopathic Neuropsychiatric Disorders. In: Institute for Computational Biomedicine and Department of Physiology and Biophysics Seminar Series, Feb 13th 2013, Weill Cornell Medical College, New York, NY. (Unpublished)

Lyon, Gholson J. (2012) Genetics and Genome Sequencing of Childhood-Onset Neuropsychiatric Disorders. In: Department of Psychiatry and Behavioral Science Grand Rounds, Dec 18th 2012, Stony Brook University . (Unpublished)

Lyon, Gholson J. (2008) Possible varenicline-induced paranoia and irritability in a patient with major depressive disorder, borderline personality disorder, and methamphetamine abuse in remission. Journal of Clinical Psychopharmacology, 28 (6). pp. 720-721. ISSN 0271-0749

Lyon, Gholson J. (2013) Whole Genome Sequencing Analysis of a severe Idiopathic Intellectual Disability Syndrome or "limitations of theory may not be revealed when the facts are too few" - Knox 1958. In: 20th Annual Molecular Psychiatry Meeting, Feb 3rd-5th 2013, Park City, UT. (Unpublished)

Lyon, Gholson J. (2013) Whole genome sequencing, clinical interpretation, and deep brain stimulation in a severely mentally ill person. In: Wiring the Brain - Cold Spring Harbor Laboratory, July 18th-22nd 2013, Cold Spring Harbor, New York. (Unpublished)

Lyon, Gholson J. (2014) "Whole genome sequencing, clinical interpretation, and deep brain stimulation in a severely mentally ill person". In: CSHL Neuronal Circuits Meeting, April 2nd-5th 2014, Cold Spring Harbor Laboratory. (Unpublished)

Lyon, Gholson J., Abi-Dargham, Anissa, Moore, Holly, Lieberman, Jeffrey A., Javitch, Jonathan A., Sulzer, David (2011) Presynaptic regulation of dopamine transmission in schizophrenia. Schizophrenia Bulletin, 37 (1). pp. 108-117. ISSN 1745-1701

Lyon, Gholson J., Coffey, Barbara, Silva, Raul (2008) Postraumatic stress disorder and reactive attachment disorder: outcome in an adolescent. Journal of Child and Adolescent Psychopharmacology, 18 (6). pp. 641-646. ISSN 1557-8992

Lyon, Gholson J., Samar, Stephanie, Jummani, Rahil, Hirsch, Scott, Spirgel, Arie, Goldman, Rachel, Coffey, Barbara J. (2009) Aripiprazole in children and adolescents with Tourette's disorder: an open-label safety and tolerability study. Journal of Child and Adolescent Psychopharmacology, 19 (6). pp. 623-633. ISSN 1557-8992

Lyon, Gholson J., Samar, Stephanie M., Conelea, Christine, Trujillo, Marcel R., Lipinski, Christina M., Bauer, Christopher C., Brandt, Bryan C., Kemp, Joshua J., Lawrence, Zoe E., Howard, Jonathan, Castellanos, F. Xavier, Woods, Douglas, Coffey, Barbara J. (2010) Testing tic suppression: comparing the effects of dexmethylphenidate to no medication in children and adolescents with attention-deficit/hyperactivity disorder and Tourette's disorder. Journal of Child and Adolescent Psychopharmacology, 20 (4). pp. 283-289. ISSN 1557-8992

Lyon, Gholson J., Shprecher, David, Coffey, Barbara, Kurlan, Roger (2010) Tourette's Disorder. Current Treatment Options in Neurology, 12 (4). pp. 274-286. ISSN 1534-3138

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Sartorius, A., Munoz-Canales, E. M., Krumm, B., Krier, A., Andres, F. J., Bender, H. J., Henn, F. A. (2006) ECT anesthesia: the lighter the better? Pharmacopsychiatry, 39 (6). pp. 201-4. ISSN 0176-3679 (Print)0176-3679 (Linking)

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Schmitt, A., May, B., Muller, B., Jatzko, A., Petroianu, G., Braus, D. F., Henn, F. A. (2003) Effects of chronic haloperidol and clozapine treatment on AMPA and kainate receptor binding in rat brain. Pharmacopsychiatry, 36 (6). pp. 292-6. ISSN 0176-3679 (Print)0176-3679 (Linking)

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