Review Article: Genetics of Alzheimer Disease von Bekris, Lynn M., Yu, Chang-En, Bird, Thomas D., Tsuang, Debby W.

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Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study von Greenwood, Tiffany A, Lazzeroni, Laura C, Maihofer, Adam X, Swerdlow, Neal R, Calkins, Monica E, Freedman, Robert, Green, Michael F, Light, Gregory A, Nievergelt, Caroline M, Nuechterlein, Keith H, Radant, Allen D, Siever, Larry J, Silverman, Jeremy M, Stone, William S, Sugar, Catherine A, Tsuang, Debby W, Tsuang, Ming T, Turetsky, Bruce I, Gur, Ruben C, Gur, Raquel E, Braff, David L

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Anticholinergic Medication Burden–Associated Cognitive Impairment in Schizophrenia von Joshi, Yash B, Thomas, Michael L, Braff, David L, Green, Michael F, Gur, Ruben C, Gur, Raquel E, Nuechterlein, Keith H, Stone, William S, Greenwood, Tiffany A, Lazzeroni, Laura C, MacDonald, Laura R, Molina, Juan L, Nungaray, John A, Radant, Allen D, Silverman, Jeremy M, Sprock, Joyce, Sugar, Catherine A, Tsuang, Debby W, Tsuang, Ming T, Turetsky, Bruce I, Swerdlow, Neal R, Light, Gregory A

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Genetics of Alzheimer disease von Bekris, Lynn M, Yu, Chang-En, Bird, Thomas D, Tsuang, Debby W

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Validation of mismatch negativity and P3a for use in multi-site studies of schizophrenia: Characterization of demographic, clinical, cognitive, and functional correlates in COGS-2 von Light, Gregory A, Swerdlow, Neal R, Thomas, Michael L, Calkins, Monica E, Green, Michael F, Greenwood, Tiffany A, Gur, Raquel E, Gur, Ruben C, Lazzeroni, Laura C, Nuechterlein, Keith H, Pela, Marlena, Radant, Allen D, Seidman, Larry J, Sharp, Richard F, Siever, Larry J, Silverman, Jeremy M, Sprock, Joyce, Stone, William S, Sugar, Catherine A, Tsuang, Debby W, Tsuang, Ming T, Braff, David L, Turetsky, Bruce I

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Deficient prepulse inhibition in schizophrenia in a multi-site cohort: Internal replication and extension von Swerdlow, Neal R., Light, Gregory A., Thomas, Michael L., Sprock, Joyce, Calkins, Monica E., Green, Michael F., Greenwood, Tiffany A., Gur, Raquel E., Gur, Ruben C., Lazzeroni, Laura C., Nuechterlein, Keith H., Radant, Allen D., Seidman, Larry J., Siever, Larry J., Silverman, Jeremy M., Stone, William S., Sugar, Catherine A., Tsuang, Debby W., Tsuang, Ming T., Turetsky, Bruce I., Braff, David L.

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Detection of probable dementia cases in undiagnosed patients using structured and unstructured electronic health records von Shao, Yijun, Zeng, Qing T, Chen, Kathryn K, Shutes-David, Andrew, Thielke, Stephen M, Tsuang, Debby W

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Support for the N -Methyl-D-Aspartate Receptor Hypofunction Hypothesis of Schizophrenia From Exome Sequencing in Multiplex Families von Timms, Andrew E, Dorschner, Michael O, Wechsler, Jeremy, Choi, Kyu Yeong, Kirkwood, Robert, Girirajan, Santhosh, Baker, Carl, Eichler, Evan E, Korvatska, Olena, Roche, Katherine W, Horwitz, Marshall S, Tsuang, Debby W

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Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network von Gulsuner, Suleyman, Walsh, Tom, Watts, Amanda C., Lee, Ming K., Thornton, Anne M., Casadei, Silvia, Rippey, Caitlin, Shahin, Hashem, Braff, David, Cadenhead, Kristin S., Calkins, Monica E., Dobie, Dorcas J., Freedman, Robert, Green, Michael, Greenwood, Tiffany, Gur, Raquel E., Gur, Ruben C., Lazzeroni, Laura, Light, Gregory, Nuechterlein, Keith, Olincy, Ann, Radant, Al, Ray, Amrita, Schork, Nik, Seidman, Larry J., Siever, Larry, Silverman, Jeremy, Stone, William S., Sugar, Catherine, Swerdlow, Neal, Tsuang, Debby, Tsuang, Ming, Turetsky, Bruce, Aduroja, Tolulope, Allen, Trina, Bradford, L. Diane, Calkins, Monica E., Devlin, Bernie, Edwards, Neil B., Ganguli, Rohan, Go, Rodney C.P., Gur, Raquel E., Gur, Ruben C., Kwentus, Joseph, Lahti, Adrienne C., Lyons, Paul, Mathos, Kim, May, Roberta, McLeod-Bryant, Steve, McEvoy, Joseph P., Montgomery-Barefield, Laura, Nimgaonkar, Vishwajit L., O’Jile, Judith, Santos, Al, Savage, Robert M., Swanson, Charles L., Wilson, William, Nimgaonkar, Vishwajit L., Go, Rodney C.P., Savage, Robert M., Swerdlow, Neal R., Gur, Raquel E., Braff, David L., King, Mary-Claire, McClellan, Jon M.

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Criteria for Psychosis in Major and Mild Neurocognitive Disorders: International Psychogeriatric Association (IPA) Consensus Clinical and Research Definition von Cummings, Jeffrey, Pinto, Luiz Cortez, Cruz, Manuel, Fischer, Corinne E., Gerritsen, Debby L., Grossberg, George T., Hwang, Tzung-Jeng, Ismail, Zahinoor, Jeste, Dilip V., Koopmans, Raymond, Lanctot, Krista L., Mateos, Raimundo, Peschin, Susan, Sampaio, Cristina, Tsuang, Debby, Wang, Huali, Zhong, Kate, Bain, Lisa J., Sano, Mary

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The effects of age and sex on cognitive impairment in schizophrenia: Findings from the Consortium on the Genetics of Schizophrenia (COGS) study von Lee, Junghee, Green, Michael F., Nuechterlein, Keith H., Swerdlow, Neal R., Greenwood, Tiffany A., Hellemann, Gerhard S., Lazzeroni, Laura C., Light, Gregory A., Radant, Allen D., Seidman, Larry J., Siever, Larry J., Silverman, Jeremy M., Sprock, Joyce, Stone, William S., Sugar, Catherine A., Tsuang, Debby W., Tsuang, Ming T., Turetsky, Bruce I., Gur, Ruben C., Gur, Raquel E., Braff, David L.

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Sensitivity of Schizophrenia Endophenotype Biomarkers to Anticholinergic Medication Burden von Joshi, Yash B, Molina, Juan L, Braff, David L, Green, Michael F, Gur, Ruben C, Gur, Raquel E, Nuechterlein, Keith H, Stone, William S, Greenwood, Tiffany A, Lazzeroni, Laura C, Radant, Allen D, Silverman, Jeremy M, Sprock, Joyce, Sugar, Catherine A, Tsuang, Debby W, Tsuang, Ming T, Turetsky, Bruce I, Swerdlow, Neal R, Light, Gregory A

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Deficient prepulse inhibition in schizophrenia detected by the multi-site COGS von Swerdlow, Neal R, Light, Gregory A, Sprock, Joyce, Calkins, Monica E, Green, Michael F, Greenwood, Tiffany A, Gur, Raquel E, Gur, Ruben C, Lazzeroni, Laura C, Nuechterlein, Keith H, Radant, Allen D, Ray, Amrita, Seidman, Larry J, Siever, Larry J, Silverman, Jeremy M, Stone, William S, Sugar, Catherine A, Tsuang, Debby W, Tsuang, Ming T, Turetsky, Bruce I, Braff, David L

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The utility of P300 as a schizophrenia endophenotype and predictive biomarker: Clinical and socio-demographic modulators in COGS-2 von Turetsky, Bruce I, Dress, Erich M, Braff, David L, Calkins, Monica E, Green, Michael F, Greenwood, Tiffany A, Gur, Raquel E, Gur, Ruben C, Lazzeroni, Laura C, Nuechterlein, Keith H, Radant, Allen D, Seidman, Larry J, Siever, Larry J, Silverman, Jeremy M, Sprock, Joyce, Stone, William S, Sugar, Catherine A, Swerdlow, Neal R, Tsuang, Debby W, Tsuang, Ming T, Light, Gregory

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Evolution of a Human-Specific Tandem Repeat Associated with ALS von Course, Meredith M., Gudsnuk, Kathryn, Smukowski, Samuel N., Winston, Kosuke, Desai, Nitin, Ross, Jay P., Sulovari, Arvis, Bourassa, Cynthia V., Spiegelman, Dan, Couthouis, Julien, Yu, Chang-En, Tsuang, Debby W., Jayadev, Suman, Kay, Mark A., Gitler, Aaron D., Dupre, Nicolas, Eichler, Evan E., Dion, Patrick A., Rouleau, Guy A., Valdmanis, Paul N.

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Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases von Nakashima-Yasuda, Hanae, Uryu, Kunihiro, Robinson, John, Xie, Sharon X, Hurtig, Howard, Duda, John E, Arnold, Steven E, Siderowf, Andrew, Grossman, Murray, Leverenz, James B, Woltjer, Randy, Lopez, Oscar L, Hamilton, Ronald, Tsuang, Debby W, Galasko, Douglas, Masliah, Eliezer, Kaye, Jeffrey, Clark, Christopher M, Montine, Thomas J, Lee, Virginia M-Y, Trojanowski, John Q

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Association of CSF α-Synuclein Seeding Amplification Assay Results With Clinical Features of Possible and Probable Dementia With Lewy Bodies von Coughlin, David G, MacLeod, Karen R, Middleton, John S, Bozoki, Andrea C, Galvin, James E, Irwin, David J, Lippa, Carol F, Litvan, Irene, Lopez, Oscar L, Berman, Sarah, Tsuang, Debby W, Zabetian, Cyrus P, Honig, Lawrence S, Marder, Karen S, Fleisher, Jori E, Sabbagh, Marwan, Wint, Dylan, Taylor, Angela S, Bekris, Lynn, Leverenz, James B, Galasko, Douglas

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Mild disease course in cognitively impaired oldest old individuals with COVID‐19: A description of two cases von Tsuang, Debby W., Payne, Sarah, Jankowski, Adrienne, Shutes‐David, Andrew, Ritchey, Katherine

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Genome-Wide Linkage Analyses of 12 Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia von Greenwood, Tiffany A., Swerdlow, Neal R., Gur, Raquel E., Cadenhead, Kristin S., Calkins, Monica E., Dobie, Dorcas J., Freedman, Robert, Green, Michael F., Gur, Ruben C., Lazzeroni, Laura C., Nuechterlein, Keith H., Olincy, Ann, Radant, Allen D., Ray, Amrita, Schork, Nicholas J., Seidman, Larry J., Siever, Larry J., Silverman, Jeremy M., Stone, William S., Sugar, Catherine A., Tsuang, Debby W., Tsuang, Ming T., Turetsky, Bruce I., Light, Gregory A., Braff, David L.

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Homozygous CADPS2 Mutations Cause Neurodegenerative Disease with Lewy Body‐like Pathology in Parrots von Lorenzo‐Betancor, Oswaldo, Galosi, Livio, Bonfili, Laura, Eleuteri, Anna Maria, Cecarini, Valentina, Verin, Ranieri, Dini, Fabrizio, Attili, Anna‐Rita, Berardi, Sara, Biagini, Lucia, Robino, Patrizia, Stella, Maria Cristina, Yearout, Dora, Dorschner, Michael O., Tsuang, Debby W., Rossi, Giacomo, Zabetian, Cyrus P.

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