Gastrointestinal Health Questionnaire for Rett Syndrome: Tool Development von Motil, Kathleen J., Khan, Nabeel, Coon, Jennifer L., Barrish, Judy O., Suter, Bernhard, Pehlivan, Davut, Schultz, Rebecca J., Glaze, Daniel G.

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Gastrointestinal Health Questionnaire for Rett Syndrome von Motil, Kathleen J., Khan, Nabeel, Coon, Jennifer L., Barrish, Judy O., Suter, Bernhard, Pehlivan, Davut, Schultz, Rebecca J., Glaze, Daniel G.

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Documenting Microcomputer Systems von Coon, Jennifer L.

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Proteomic and phosphoproteomic comparison of human ES and iPS cells von Phanstiel, Douglas H, Brumbaugh, Justin, Wenger, Craig D, Tian, Shulan, Probasco, Mitchell D, Bailey, Derek J, Swaney, Danielle L, Tervo, Mark A, Bolin, Jennifer M, Ruotti, Victor, Stewart, Ron, Thomson, James A, Coon, Joshua J

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Directed Evolution Reveals Unexpected Epistatic Interactions That Alter Metabolic Regulation and Enable Anaerobic Xylose Use by Saccharomyces cerevisiae von Sato, Trey K, Tremaine, Mary, Parreiras, Lucas S, Hebert, Alexander S, Myers, Kevin S, Higbee, Alan J, Sardi, Maria, McIlwain, Sean J, Ong, Irene M, Breuer, Rebecca J, Avanasi Narasimhan, Ragothaman, McGee, Mick A, Dickinson, Quinn, La Reau, Alex, Xie, Dan, Tian, Mingyuan, Reed, Jennifer L, Zhang, Yaoping, Coon, Joshua J, Hittinger, Chris Todd, Gasch, Audrey P, Landick, Robert

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A survey of genetic human cortical gene expression von Myers, Amanda J, Gibbs, J Raphael, Webster, Jennifer A, Rohrer, Kristen, Zhao, Alice, Marlowe, Lauren, Kaleem, Mona, Leung, Doris, Bryden, Leslie, Nath, Priti, Zismann, Victoria L, Joshipura, Keta, Huentelman, Matthew J, Hu-Lince, Diane, Coon, Keith D, Craig, David W, Pearson, John V, Holmans, Peter, Heward, Christopher B, Reiman, Eric M, Stephan, Dietrich, Hardy, John

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Increased Synthesis of MCL-1 Protein Underlies Initial Survival of EGFR -Mutant Lung Cancer to EGFR Inhibitors and Provides a Novel Drug Target von Song, Kyung-A, Hosono, Yasuyuki, Turner, Crystal, Jacob, Sheeba, Lochmann, Timothy L, Murakami, Yoshiko, Patel, Neha U, Ham, Jungoh, Hu, Bin, Powell, Krista M, Coon, Colin M, Windle, Brad E, Oya, Yuko, Koblinski, Jennifer E, Harada, Hisashi, Leverson, Joel D, Souers, Andrew J, Hata, Aaron N, Boikos, Sosipatros, Yatabe, Yasushi, Ebi, Hiromichi, Faber, Anthony C

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Genetic Control of Human Brain Transcript Expression in Alzheimer Disease von Webster, Jennifer A., Gibbs, J. Raphael, Clarke, Jennifer, Ray, Monika, Zhang, Weixiong, Holmans, Peter, Rohrer, Kristen, Zhao, Alice, Marlowe, Lauren, Kaleem, Mona, McCorquodale, Donald S., Cuello, Cindy, Leung, Doris, Bryden, Leslie, Nath, Priti, Zismann, Victoria L., Joshipura, Keta, Huentelman, Matthew J., Hu-Lince, Diane, Coon, Keith D., Craig, David W., Pearson, John V., Heward, Christopher B., Reiman, Eric M., Stephan, Dietrich, Hardy, John, Myers, Amanda J.

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Mitochondrial encephalopathy with lactic-acidosis and stroke-like episodes syndrome presenting as progressive supranuclear palsy von Hass, Reece M., Whitwell, Jennifer L., Coon, Elizabeth A., Josephs, Keith A., Ali, Farwa

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F-box protein FBXL2 targets cyclin D2 for ubiquitination and degradation to inhibit leukemic cell proliferation von Chen, Bill B., Glasser, Jennifer R., Coon, Tiffany A., Zou, Chunbin, Miller, Hannah L., Fenton, Moon, McDyer, John F., Boyiadzis, Michael, Mallampalli, Rama K.

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Valosin-containing protein (VCP)–Adaptor Interactions are Exceptionally Dynamic and Subject to Differential Modulation by a VCP Inhibitor von Xue, Liang, Blythe, Emily E., Freiberger, Elyse C., Mamrosh, Jennifer L., Hebert, Alexander S., Reitsma, Justin M., Hess, Sonja, Coon, Joshua J., Deshaies, Raymond J.

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Robotic-arm assisted lateral unicompartmental knee arthroplasty: 5-Year outcomes & survivorship von Gaudiani, Michael A, Samuel, Linsen T, Diana, John N, DeBattista, Jennifer L, Coon, Thomas M, Moore, Ryan E, Kamath, Atul F

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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders von Tucker-Drob, Elliot M., Yu, Dongmei, Ge, Tian, Derks, Eske M., Keski-Rahkonen, Anna, Kirov, George, Asherson, Philip, Baldursson, Gísli, Bybjerg-Grauholm, Jonas, Churchhouse, Claire, Crosbie, Jennifer, Demontis, Ditte, Grove, Jakob, Martin, Joanna, McGough, James J., Pedersen, Carsten B., Poulsen, Jesper B., Rothenberger, Aribert, Schachar, Russell, Turley, Patrick, Arking, Dan E., Collins, Ryan L., Coon, Hilary, Delorme, Richard, Hope, Sigrun, Nyegaard, Mette, Pinto, Dalila, Qvist, Per, Talkowski, Michael E., Albani, Diego, Alda, Martin, Bass, Nicholas, Bauer, Michael, Cichon, Sven, Clarke, Toni-Kim, Czerski, Piotr M., Fischer, Sascha B., Frank, Josef, Goes, Fernando S., Holland, Dominic, Jones, Lisa A., Joachim, Oedegaard Ketil, Maaser, Anna, Malt, Ulrik F., McMahon, Francis J., Montgomery, Grant W., Myers, Richard M., Nöthen, Markus M., Perry, Amy, Vieta, Eduard, Aschauer, Harald, Bencko, Vladimir, Burghardt, Roland, Carlberg, Laura, Guo, Yiran, Klump, Kelly L., Le Hellard, Stephanie, Monteleone, Alessio Maria, Seitz, Jochen, Treasure, Janet, Wade, Tracey D., Wichmann, H-Erich, Woodside, D. Blake, Grabe, Hans J., Horn, Carsten, Penninx, Brenda WJH, Schulte, Eva C., Smith, Daniel J., Alexander, Madeline, Begemann, Martin, Campion, Dominique, Ehrenreich, Hannelore, Murphy, Kieran C., Riley, Brien, Sham, Pak C., van Os, Jim, Weiser, Mark, Brown, Lawrence W., Cheon, Keun-Ah, Denys, Damiaan, Gilbert, Donald L., Grados, Marco A., Ibanez-Gomez, Laura, King, Robert A., Leventhal, Bennett L., Okun, Michael S., Piras, Federica, Robertson, Mary, Samuels, Jack F., Spalletta, Gianfranco, Stein, Dan J., Stewart, S Evelyn, Storch, Eric A., Stranger, Barbara, Tübing, Jennifer, Visscher, Frank, Wagner, Michael, Santangelo, Susan L., Thornton, Laura M., Neale, Benjamin M.

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Trends in Low-Value Care Among Children's Hospitals von House, Samantha A, Marin, Jennifer R, Coon, Eric R, Ralston, Shawn L, Hall, Matthew, Gruhler De Souza, Heidi, Ho, Timmy, Reyes, Mario, Schroeder, Alan R

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Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders von Pinto, Dalila, Delaby, Elsa, Merico, Daniele, Barbosa, Mafalda, Merikangas, Alison, Klei, Lambertus, Thiruvahindrapuram, Bhooma, Xu, Xiao, Ziman, Robert, Vorstman, Jacob A.S., Thompson, Ann, Regan, Regina, Pilorge, Marion, Pellecchia, Giovanna, Pagnamenta, Alistair T., Oliveira, Bárbara, Magalhaes, Tiago R., Lowe, Jennifer K., Howe, Jennifer L., Gilbert, John, Duketis, Eftichia, Dombroski, Beth A., Cuccaro, Michael, Crawford, Emily L., Correia, Catarina T., Conroy, Judith, Conceição, Inês C., Chiocchetti, Andreas G., Casey, Jillian P., Cai, Guiqing, Cabrol, Christelle, Bacchelli, Elena, Gallinger, Steven, Cotterchio, Michelle, Zwaigenbaum, Lonnie, Wittemeyer, Kerstin, Wing, Kirsty, van Engeland, Herman, Tryfon, Ana, Thomson, Susanne, Rogé, Bernadette, Roberts, Wendy, Poustka, Fritz, Mouga, Susana, Minshew, Nancy, McInnes, L. Alison, McGrew, Susan G., Lord, Catherine, Leboyer, Marion, Le Couteur, Ann S., Kolevzon, Alexander, Jiménez González, Patricia, Jacob, Suma, Holt, Richard, Guter, Stephen, Green, Jonathan, Green, Andrew, Gillberg, Christopher, Duque, Frederico, Delorme, Richard, Dawson, Geraldine, Chaste, Pauline, Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F., Bernier, Raphael, Baird, Gillian, Bailey, Anthony J., Almeida, Joana, Wijsman, Ellen M., Vieland, Veronica J., Vicente, Astrid M., Schellenberg, Gerard D., Pericak-Vance, Margaret, Paterson, Andrew D., Parr, Jeremy R., Oliveira, Guiomar, Nurnberger, John I., Monaco, Anthony P., Maestrini, Elena, Klauck, Sabine M., Hakonarson, Hakon, Haines, Jonathan L., Geschwind, Daniel H., Freitag, Christine M., Folstein, Susan E., Ennis, Sean, Coon, Hilary, Battaglia, Agatino, Szatmari, Peter, Sutcliffe, James S., Hallmayer, Joachim, Gill, Michael, Cook, Edwin H., Buxbaum, Joseph D., Devlin, Bernie, Gallagher, Louise, Betancur, Catalina, Scherer, Stephen W.

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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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Using a Multiple-Schedule Procedure to Signal the Availability of Attention: Three Demonstrations von Niedfeld, Amanda, Rapp, John T., Coon, Jodi C., Cook, Jennifer L.

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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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TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A von Brown, Anna-Leigh, Wilkins, Oscar G., Keuss, Matthew J., Hill, Sarah E., Zanovello, Matteo, Lee, Weaverly Colleen, Bampton, Alexander, Lee, Flora C. Y., Masino, Laura, Qi, Yue A., Bryce-Smith, Sam, Gatt, Ariana, Hallegger, Martina, Fagegaltier, Delphine, Phatnani, Hemali, Newcombe, Jia, Gustavsson, Emil K., Seddighi, Sahba, Reyes, Joel F., Coon, Steven L., Ramos, Daniel, Schiavo, Giampietro, Fisher, Elizabeth M. C., Raj, Towfique, Secrier, Maria, Lashley, Tammaryn, Ule, Jernej, Buratti, Emanuele, Humphrey, Jack, Ward, Michael E., Fratta, Pietro

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Identification of the Genetic Basis for Complex Disorders by Use of Pooling-Based Genomewide Single-Nucleotide–Polymorphism Association Studies von Pearson, John V., Huentelman, Matthew J., Halperin, Rebecca F., Tembe, Waibhav D., Melquist, Stacey, Homer, Nils, Brun, Marcel, Szelinger, Szabolcs, Coon, Keith D., Zismann, Victoria L., Webster, Jennifer A., Beach, Thomas, Sando, Sigrid B., Aasly, Jan O., Heun, Reinhard, Jessen, Frank, Kölsch, Heike, Tsolaki, Magdalini, Daniilidou, Makrina, Reiman, Eric M., Papassotiropoulos, Andreas, Hutton, Michael L., Stephan, Dietrich A., Craig, David W.

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