Growth Hormone-Like Activity in Hypophysectomized Rats Implanted with Spirometra Mansonoides Spargana von Steelman, Sanford L., Morgan, Evan R., Cuccaro, Anthony J., Glitzer, Monroe S.

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Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways von O'Dushlaine, C., Rossin, L., Lee P., H., Duncan, L., Parikshak N., N., Newhouse, S., Ripke, S., Neale B., M., Purcell S., M., Posthuma, D., Nurnberger J., I., Lee S., H., Faraone S., V., Perlis R., H., Mowry B., J., Thapar, A., Goddard M., E., Witte J., S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen O., A., Anjorin, A., Anney, R., Anttila, V., Arking D., E., Asherson, P., Azevedo M., H., Backlund, L., Badner J., A., Bailey A., J., Banaschewski, T., Barchas J., D., Barnes M., R., Barrett T., B., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen S., E., Berrettini, W., Betancur, Catalina, Bettecken, T., Biederman, J., Binder E., B., Black D., W., Blackwood D., H., Bloss C., S., Boehnke, M., Boomsma D., I., Breuer, R., Bruggeman, R., Cormican, P., Buccola N., G., Buitelaar J., K., Bunney W., E., Buxbaum J., D., Byerley W., F., Byrne E., M., Caesar, S., Cahn, W., Cantor R., M., Casas, M., Chakravarti, A., Chambert, K., Choudhury, K., Cichon, S., Mattheisen, M., Cloninger C., R., Collier D., A., Cook E., H., Coon, H., Cormand, B., Corvin, A., Coryell W., H., Craig D., W., Craig I., W., Crosbie, J., Cuccaro M., L., Curtis, D., Czamara, D., Datta, S., Dawson, G., Day, R., de Geus E., J., Degenhardt, F., Djurovic, S., Donohoe G., J., Doyle A., E., Duan, J., Dudbridge, F., Duketis, E., Ebstein R., P., Edenberg H., J., Elia, J., Ennis, S., Etain, B., Fanous, F.

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Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways von GRISWOLD, Anthony J, DEQIONG MA, WRIGHT, Harry H, ABRAMSON, Ruth K, WILLIAMS, Scott M, MENON, Ramkumar, MARTIN, Eden R, HAINES, Jonathan L, GILBERT, John R, CUCCARO, Michael L, PERICAK-VANCE, Margaret A, CUKIER, Holly N, NATIONS, Laura D, SCHMIDT, Mike A, CHUNG, Ren-Hua, JAWORSKI, James M, SALYAKINA, Daria, KONIDARI, Loanna, WHITEHEAD, Patrice L

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A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism von Hussman, John P, Chung, Ren-Hua, Griswold, Anthony J, Jaworski, James M, Salyakina, Daria, Ma, Deqiong, Konidari, Ioanna, Whitehead, Patrice L, Vance, Jeffery M, Martin, Eden R, Cuccaro, Michael L, Gilbert, John R, Haines, Jonathan L, Pericak-Vance, Margaret A

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A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer's Disease in African Ancestry von Rajabli, Farid, Beecham, Gary W, Hendrie, Hugh C, Baiyewu, Olusegun, Ogunniyi, Adesola, Gao, Sujuan, Kushch, Nicholas A, Lipkin-Vasquez, Marina, Hamilton-Nelson, Kara L, Young, Juan I, Dykxhoorn, Derek M, Nuytemans, Karen, Kunkle, Brian W, Wang, Liyong, Jin, Fulai, Liu, Xiaoxiao, Feliciano-Astacio, Briseida E, Schellenberg, Gerard D, Dalgard, Clifton L, Griswold, Anthony J, Byrd, Goldie S, Reitz, Christiane, Cuccaro, Michael L, Haines, Jonathan L, Pericak-Vance, Margaret A, Vance, Jeffery M

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Genome-wide association analysis and admixture mapping in a Puerto Rican cohort supports an Alzheimer disease risk locus on chromosome 12 von Akgun, Bilcag, Feliciano-Astacio, Briseida E, Hamilton-Nelson, Kara L, Scott, Kyle, Rivero, Joe, Adams, Larry D, Sanchez, Jose J, Valladares, Glenies S, Tejada, Sergio, Bussies, Parker L, Silva-Vergara, Concepcion, Rodriguez, Vanessa C, Mena, Pedro R, Celis, Katrina, Whitehead, Patrice G, Prough, Michael, Kosanovic, Christina, Van Booven, Derek J, Schmidt, Michael A, Acosta, Heriberto, Griswold, Anthony J, Dalgard, Clifton L, McInerney, Katalina F, Beecham, Gary W, Cuccaro, Michael L, Vance, Jeffery M, Pericak-Vance, Margaret A, Rajabli, Farid

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An Alzheimer’s disease risk variant in TTC3 modifies the actin cytoskeleton organization and the PI3K-Akt signaling pathway in iPSC-derived forebrain neurons von Cukier, Holly N., Duarte, Carolina L., Laverde-Paz, Mayra J., Simon, Shaina A., Van Booven, Derek J., Miyares, Amanda T., Whitehead, Patrice L., Hamilton-Nelson, Kara L., Adams, Larry D., Carney, Regina M., Cuccaro, Michael L., Vance, Jeffery M., Pericak-Vance, Margaret A., Griswold, Anthony J., Dykxhoorn, Derek M.

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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders von Weiner, Daniel J, Wigdor, Emilie M, Ripke, Stephan, Walters, Raymond K, Kosmicki, Jack A, Grove, Jakob, Samocha, Kaitlin E, Goldstein, Jacqueline I, Okbay, Aysu, Bybjerg-Grauholm, Jonas, Werge, Thomas, Hougaard, David M, Taylor, Jacob, Skuse, David, Devlin, Bernie, Anney, Richard, Sanders, Stephan J, Bishop, Somer, Mortensen, Preben Bo, Børglum, Anders D, Smith, George Davey, Daly, Mark J, Robinson, Elise B

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Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis von Kozol, Robert A, Cukier, Holly N, Zou, Bing, Mayo, Vera, De Rubeis, Silvia, Cai, Guiqing, Griswold, Anthony J, Whitehead, Patrice L, Haines, Jonathan L, Gilbert, John R, Cuccaro, Michael L, Martin, Eden R, Baker, James D, Buxbaum, Joseph D, Pericak-Vance, Margaret A, Dallman, Julia E

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Functional impact of global rare copy number variation in autism spectrum disorders von Gillberg, Christopher, Kolevzon, Alexander, Nelson, Stanley F, Sansom, Katherine, Casallo, Guillermo, Miller, Judith, Brennan, Sean, Leboyer, Marion, Bacchelli, Elena, Delorme, Richard, Fombonne, Eric, Hallmayer, Joachim, Green, Jonathan, Pickles, Andrew, Heron, Elizabeth A, Salt, Jeff, Battaglia, Agatino, Klauck, Sabine M, McDougle, Christopher J, Mahoney, William, Noor, Abdul, Cytrynbaum, Cheryl, Sato, Daisuke, Almeida, Joana, Korvatska, Olena, Dawson, Geraldine, Bierut, Laura J, Coon, Hilary, Rickaby, Jessica, Freitag, Christine M, Roeder, Kathryn, Bader, Gary D, Wijsman, Ellen M, Vincent, John B, Hakonarson, Hakon, Segurado, Ricardo, Paton, Tara, Roge, Bernadette, Ennis, Sean, Kim, Cecilia, Monaco, Anthony P, Paterson, Andrew D, Crossett, Andrew, McGrath, Jane, Carson, Andrew R, Le Couteur, Ann, Cook, Edwin H, Chung, Brian H.Y, Cuccaro, Michael L, Van Engeland, Herman, Conroy, Judith, Holt, Richard, Strawbridge, Christina, Kustanovich, Vlad, Migita, Ohsuke, Stoppioni, Vera, Igliozzi, Roberta, Poustka, Fritz, Stein, Olaf, Posey, David J, Sheffield, Val C, Duque, Frederico, Parrini, Barbara, Berney, Tom, Hus, Vanessa, Baird, Gillian, Duketis, Eftichia, Soorya, Latha, Corsello, Christina, Drmic, Irene, Sousa, Inês, Abrahams, Brett S, Thomson, Susanne, Lajonchere, Clara M, Tsiantis, John, Pinto, Dalila, Green, Andrew, Hughes, Gillian, Mantoulan, Carine, Betancur, Catalina, Volkmar, Fred, Poustka, Annemarie, Shah, Naisha, Bryson, Susan E, Munson, Jeff, Tancredi, Raffaella, Nygren, Gudrun, Wittemeyer, Kerstin, Merikangas, Alison, Oliveira, Guiomar, Farrar, Penny, Maestrini, Elena, Liu, Xiao-Qing, Gallagher, Louise, McConachie, Helen, Zurawiecki, Danielle, Schellenberg, Gerard D, Glessner, Joseph T, Lord, Catherine, Piven, Joseph

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Genetic architecture of RNA editing regulation in Alzheimer’s disease across diverse ancestral populations von Gardner, Olivia K, Van Booven, Derek, Wang, Lily, Gu, Tianjie, Hofmann, Natalia K, Whitehead, Patrice L, Nuytemans, Karen, Hamilton-Nelson, Kara L, Adams, Larry D, Starks, Takiyah D, Cuccaro, Michael L, Martin, Eden R, Vance, Jeffery M, Bush, William S, Byrd, Goldie S, Haines, Jonathan L, Beecham, Gary W, Pericak-Vance, Margaret A, Griswold, Anthony J

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RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathways von Gardner, Olivia K, Wang, Lily, Van Booven, Derek, Whitehead, Patrice L, Hamilton-Nelson, Kara L, Adams, Larry D, Starks, Takiyah D, Hofmann, Natalia K, Vance, Jeffery M, Cuccaro, Michael L, Martin, Eden R, Byrd, Goldie S, Haines, Jonathan L, Bush, William S, Beecham, Gary W, Pericak-Vance, Margaret A, Griswold, Anthony J

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Linkage of Alzheimer disease families with Puerto Rican ancestry identifies a chromosome 9 locus von Rajabli, Farid, Feliciano-Astacio, Briseida E., Cukier, Holly N., Wang, Liyong, Griswold, Anthony J., Hamilton-Nelson, Kara L., Adams, Larry D., Rodriguez, Vanessa C., Mena, Pedro R., Tejada, Sergio, Celis, Katrina, Whitehead, Patrice L., Van Booven, Derek J., Hofmann, Natalia K., Bussies, Parker L., Prough, Michael, Chinea, Angel, Feliciano, Nereida I., Vardarajan, Badri N., Reitz, Christiane, Lee, Joseph H., Prince, Martin J., Jimenez, Ivonne Z., Mayeux, Richard P., Acosta, Heriberto, Dalgard, Clifton L., Haines, Jonathan L., Vance, Jeffery M., Cuccaro, Michael L., Beecham, Gary W., Pericak-Vance, Margaret A.

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Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorder von Griswold, Anthony J., Van Booven, Derek, Cuccaro, Michael L., Haines, Jonathan L., Gilbert, John R., Pericak-Vance, Margaret A.

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Admixture mapping identifies novel Alzheimer's disease risk regions in African Americans von Rajabli, Farid, Tosto, Giuseppe, Hamilton‐Nelson, Kara L., Kunkle, Brian W., Vardarajan, Badri N., Naj, Adam, Whitehead, Patrice G., Gardner, Olivia K., Bush, William S., Sariya, Sanjeev, Mayeux, Richard P., Farrer, Lindsay A., Cuccaro, Michael L., Vance, Jeffrey M., Griswold, Anthony J., Schellenberg, Gerard D., Haines, Jonathan L., Byrd, Goldie S., Reitz, Christiane, Beecham, Gary W., Pericak‐Vance, Margaret A., Martin, Eden R.

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ATAC‐seq on iPSC derived astrocytes to assess chromatin accessibility differences between African and European local ancestry von Celis, Katrina, Oron, Oded, Griswold, Anthony J., Rajabli, Farid, Trittipo, Jack, Feliciano‐Astacio, Briseida E, Cuccaro, Michael L., Pericak‐Vance, Margaret A., Dykxhoorn, Derek M., Young, Juan, Vance, Jeffery M.

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Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants von Griswold, Anthony J, Dueker, Nicole D, Van Booven, Derek, Rantus, Joseph A, Jaworski, James M, Slifer, Susan H, Schmidt, Michael A, Hulme, William, Konidari, Ioanna, Whitehead, Patrice L, Cuccaro, Michael L, Martin, Eden R, Haines, Jonathan L, Gilbert, John R, Hussman, John P, Pericak-Vance, Margaret A

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Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder von Moser, Gerhard, Agartz, Ingrid, Andreassen, Ole A., Anjorin, Adebayo, Bass, Nicholas, Bergen, Sarah E., Betancur, Catalina, Black, Donald W., Bloss, Cinnamon S., Buxbaum, Joseph D., Cantor, Rita M., Cormand, Bru, Coryell, William H., Craig, Ian W., Crosbie, Jennifer, Djurovic, Srdjan, Ebstein, Richard P., Etain, Bruno, Faraone, Stephen V., Farmer, Anne E., Ferrier, I. Nicol, Fombonne, Eric, Frank, Josef, Franke, Barbara, Freitag, Christine M., Friedl, Marion, Gershon, Elliot S., Gill, Michael, Gordon, Scott D., Green, Elaine K., De Haan, Lieuwe, Haines, Jonathan L., Hakonarson, Hakon, Hallmayer, Joachim, Hamilton, Steven P., Hamshere, Marian L., Hoogendijk, Witte J., Hottenga, Jouke-Jan, Hus, Vanessa, Jamain, Stéphane, Jones, Lisa, Kenny, Elaine, Krabbendam, Lydia, Kuntsi, Jonna, Landén, Mikael, Lesch, Klaus-Peter, Lichtenstein, Paul, Lieberman, Jeffrey A., Linszen, Don H., Loo, Sandra K., Lowe, Jennifer K., Lucae, Susanne, Magnusson, Patrik K.E., Mahon, Pamela B., Martin, Christa L., McGhee, Kevin A., McGuffin, Peter, McInnis, Melvin G., McIntosh, Andrew, McLean, Alan W., McMahon, William M., Meier, Sandra, Meng, Fan, Meyer, Jobst, Middeldorp, Christel M., Miranda, Ana, Montgomery, Grant W., Mühleisen, Thomas W., Neale, Benjamin M., Nyholt, Dale R., O’Donovan, Michael C., Olsen, Line, Penninx, Brenda W., Pergadia, Michele L., Pericak-Vance, Margaret A., Perlis, Roy H., Posthuma, Danielle, Rasmussen, Henrik B., Reif, Andreas, Ribasés, Marta, Rice, John P., Rossin, Lizzy, Sanders, Stephan J., Schachar, Russell, Schellenberg, Gerard D., Schumacher, Johannes, Scott, Laura J., Smalley, Susan L., Smit, Johannes H., Szelinger, Szabocls, Thapar, Anita, Thirumalai, Srinivasa, Treutlein, Jens, Visscher, Peter M., Willemsen, Gonneke, Young, Allan H., Zammit, Stanley, Zitman, Frans G., Potash, James B., Shi, Jianxin

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A Genome‐wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1 von Ma, Deqiong, Salyakina, Daria, Jaworski, James M., Konidari, Ioanna, Whitehead, Patrice L., Andersen, Ashley N., Hoffman, Joshua D., Slifer, Susan H., Hedges, Dale J., Cukier, Holly N., Griswold, Anthony J., McCauley, Jacob L., Beecham, Gary W., Wright, Harry H., Abramson, Ruth K., Martin, Eden R., Hussman, John P., Gilbert, John R., Cuccaro, Michael L., Haines, Jonathan L., Pericak‐Vance, Margaret A.

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Expression quantitative trait loci (eQTL) analysis in a diverse Alzheimer disease cohort reveals ancestry‐specific regulatory architectures von Griswold, Anthony J., Gardner, Olivia K., Feliciano‐Astacio, Briseida E., Van Booven, Derek, Hamilton‐Nelson, Kara L., Whitehead, Patrice L., Adams, Larry D., Starks, Takiyah D., Acosta, Heriberto, Cuccaro, Michael L., Vance, Jeffery M., Byrd, Goldie S., Haines, Jonathan L., Bush, William S., Beecham, Gary W., Pericak‐Vance, Margaret A.

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