A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers by Farias, Fabiana H.G, Zeng, Rong, Johnson, Gary S, Wininger, Fred A, Taylor, Jeremy F, Schnabel, Robert D, McKay, Stephanie D, Sanders, Douglas N, Lohi, Hannes, Seppälä, Eija H, Wade, Claire M, Lindblad-Toh, Kerstin, O'Brien, Dennis P, Katz, Martin L

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A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund by Sanders, Douglas N., Farias, Fabiana H., Johnson, Gary S., Chiang, Vivian, Cook, James R., O’Brien, Dennis P., Hofmann, Sandra L., Lu, Jui-Yun, Katz, Martin L.

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Export of the siderophore enterobactin in Escherichia coli: involvement of a 43 kDa membrane exporter by Furrer, Jason L., Sanders, Douglas N., Hook‐Barnard, India G., McIntosh, Mark A.

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A Missense Mutation in Canine CLN6 in an Australian Shepherd with Neuronal Ceroid Lipofuscinosis by Farias, Fabiana H., Zeng, Rong, Katz, Martin L., O'Brien, Dennis P., Johnson, Gary S., Khan, Shahnawaz, Sanders, Douglas N.

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An ADAMTS17 splice donor site mutation in dogs with primary lens luxation by Farias, Fabiana H G, Johnson, Gary S, Taylor, Jeremy F, Giuliano, Elizabeth, Katz, Martin L, Sanders, Douglas N, Schnabel, Robert D, McKay, Stephanie D, Khan, Shahnawaz, Gharahkhani, Puya, O'Leary, Caroline A, Pettitt, Louise, Forman, Oliver P, Boursnell, Mike, McLaughlin, Bryan, Ahonen, Saija, Lohi, Hannes, Hernandez-Merino, Elena, Gould, David J, Sargan, David R, Mellersh, Cathryn

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GM2 gangliosidosis associated with a HEXA missense mutation in Japanese Chin dogs: A potential model for Tay Sachs disease by Sanders, Douglas N., Zeng, Rong, Wenger, David A., Johnson, Gary S., Johnson, Gayle C., Decker, Jared E., Katz, Martin L., Platt, Simon R., O'Brien, Dennis P.

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Sulfatide accumulation begins as early as four months of age in ARSA knockout mice by Stanek, Lisa M., Matstis, Bryan, Wu, Leslie C., Sanders, Douglas N., Richman, Laura K., Matzner, Ulrich

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RPE65 gene mutation prevents development of autofluorescence in retinal pigment epithelial phagosomes by Katz, Martin L., Wendt, Kristy D., Sanders, Douglas N.

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Retinal Capillary Basement Membrane Thickening in a Porcine Model of Diabetes Mellitus by Hainsworth, Dean P., Katz, Martin L., Sanders, Deja A., Sanders, Douglas N., Wright, Ethan J., Sturek, Michael

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A reversal learning task detects cognitive deficits in a Dachshund model of late‐infantile neuronal ceroid lipofuscinosis by Sanders, D. N., Kanazono, S., Wininger, F. A., Whiting, R. E. H., Flournoy, C. A., Coates, J. R., Castaner, L. J., O'Brien, D. P., Katz, M. L.

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Autism gene variant causes hyperserotonemia, serotonin receptor hypersensitivity, social impairment and repetitive behavior by Veenstra-VanderWeele, Jeremy, Muller, Christopher L, Iwamoto, Hideki, Sauer, Jennifer E, Owens, W. Anthony, Shah, Charisma R, Cohen, Jordan, Mannangatti, Padmanabhan, Jessen, Tammy, Thompson, Brent J, Ye, Ran, Kerr, Travis M, Carneiro, Ana M, Crawley, Jacqueline N, Sanders-Bush, Elaine, McMahon, Douglas G, Ramamoorthy, Sammanda, Daws, Lynette C, Sutcliffe, James S, Blakely, Randy D

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A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder by Duan, Jubao, Shi, Jianxin, Fiorentino, Alessia, Leites, Catherine, Chen, Xiangning, Moy, Winton, Chen, Jingchun, Alexandrov, Boian S., Usheva, Anny, He, Deli, Freda, Jessica, O’Brien, Niamh L., Gejman, Pablo V., Sanders, Alan R., Duan, Jubao, Levinson, Douglas F., Shi, Jianxin, Buccola, Nancy G., Mowry, Bryan J., Freedman, Robert, Olincy, Ann, Amin, Farooq, Black, Donald W., Silverman, Jeremy M., Byerley, William F., Svrakic, Dragan M., Cloninger, C. Robert, Pato, Michele T., Sobell, Janet L., Medeiros, Helena, Abbott, Colony, Skar, Brooke, Buckley, Peter F., Bromet, Evelyn J., Escamilla, Michael A., Fanous, Ayman H., Lehrer, Douglas S., Macciardi, Fabio, Malaspina, Dolores, McCarroll, Steve A., Marder, Stephen R., Moran, Jennifer, Morley, Christopher P., Nicolini, Humberto, Perkins, Diana O., Purcell, Shaun M., Rapaport, Mark H., Sklar, Pamela, Smoller, Jordan W., Knowles, James A., Pato, Carlos N., McQuillin, Andrew, Sanders, Alan R., Gershon, Elliot S., DeLisi, Lynn E., Bishop, Alan R., Gurling, Hugh M.D., Pato, Michele T., Levinson, Douglas F., Kendler, Kenneth S., Pato, Carlos N., Gejman, Pablo V.

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Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts by Zhang, Xianglong, Abdellaoui, Abdel, Rucker, James, de Jong, Simone, Potash, James B., Weissman, Myrna M., Shi, Jianxin, Knowles, James A., Pato, Carlos, Pato, Michele, Sobell, Janet, Smit, Johannes H., Hottenga, Jouke-Jan, de Geus, Eco J.C., Lewis, Cathryn M., Buttenschøn, Henriette N., Craddock, Nick, Jones, Ian, Jones, Lisa, McGuffin, Peter, Mors, Ole, Owen, Michael J., Preisig, Martin, Rietschel, Marcella, Rice, John P., Rivera, Margarita, Uher, Rudolf, Gejman, Pablo V., Sanders, Alan R., Boomsma, Dorret, Penninx, Brenda W.J.H., Breen, Gerome, Levinson, Douglas F.

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Aging changes in protective balance and startle responses to sudden drop perturbations by Sanders, Ozell, Hsiao, Hao Yuan, Savin, Douglas N, Creath, Robert A, Rogers, Mark W

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Safety and immunogenicity of ChAdOx1 nCoV-19 vaccine administered in a prime-boost regimen in young and old adults (COV002): a single-blind, randomised, controlled, phase 2/3 trial by Folegatti, Pedro M, Bibi, Sagida, Chappell, Harry, Fedosyuk, Sofiya, Gbesemete, Diane, Kelly, Elizabeth J, Makinson, Rebecca, Rawlinson, Thomas, Ross-Russell, Amy L, Saich, Stephen, Smith, Catherine C, Tarrant, Richard, Thomas, Kelly M, Warren, Sarah C, Lambe, Teresa, Adams, Kelly, Ali, Aabidah, Allen, Lauren, Baker, Natalie, Barrett, Kelly, Bellamy, Duncan, Berg, Adam, Beveridge, Amy, Bewley, Kevin, Bijker, Else M., Boland, Elena, Bormans, Daan, Bower, Thomas, Boyd, Amy, Brenner, Tanja, Buttigieg, Karen R., Cao, Michelangelo, Chapman, David, Chelysheva, Irina, Cifuentes, Liliana, Collins, Sarah, Conlon, Christopher P., Davis, Judith, Dong, Tao, Drake, Jonathan, Fisher, Richard, Garlant, Harriet, Gavrila, Madita, Gibbons, Felicity, Gill, Hardeep, Hart, Thomas C., Hartnell, Birgit, Haskell, Louise, Hawkins, Sophia, Hermosin Herrera, Macarena, Hill, David, Hill, Jennifer, Howes, Jessica, Jackson, Susan, Joshi, Amar, Kelly, Dearbhla M., King, Lloyd D.W., Knott, Daniel, Lee, Kim Y.N., Leung, Stephanie, Liu, Shuchang, Loew, Lisa, Madhavan, Meera, Marius, Phedra, Marshall, Julia L., Martin, Jane, Moore, Maria, Morris, Susan J., O'Reilly, Peter John, Owino, Nelly, Patel, Bhumika, Patrick-Smith, Maia, Perring, James, Phillips, Daniel J., Poulton, Ian, Presland, Laura, Pulido, David, Rajapaska, Durga, Ramos Lopez, Fernando, Rollier, Christine S., Romani, Rossana, Sedik, Cynthia, Seddiqi, Samiullah, Segireddy, Rameswara R., Sharpe, Hannah R., Silva-Reyes, Laura, Smith, David J., Smith, Daniel C., Smith, Nicholas, Stockley, David, Summerton, Eloise, Szigeti, Anna, Taylor, Ursula, Tonks, Susan, Tree, Julian A., Truby, Adam, Varughese, Rachel, Woodyer, Mark, Worth, Andrew T., Yao, Xin Li

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Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease by Eissman, Jaclyn M, Dumitrescu, Logan, Mahoney, Emily R, Smith, Alexandra N, Mukherjee, Shubhabrata, Lee, Michael L, Scollard, Phoebe, Choi, Seo Eun, Bush, William S, Engelman, Corinne D, Lu, Qiongshi, Fardo, David W, Trittschuh, Emily H, Mez, Jesse, Kaczorowski, Catherine C, Hernandez Saucedo, Hector, Widaman, Keith F, Buckley, Rachel F, Properzi, Michael J, Mormino, Elizabeth C, Yang, Hyun Sik, Harrison, Theresa M, Hedden, Trey, Nho, Kwangsik, Andrews, Shea J, Tommet, Douglas, Hadad, Niran, Sanders, R Elizabeth, Ruderfer, Douglas M, Gifford, Katherine A, Zhong, Xiaoyuan, Raghavan, Neha S, Vardarajan, Badri N, Pericak-Vance, Margaret A, Farrer, Lindsay A, Wang, Li San, Cruchaga, Carlos, Schellenberg, Gerard D, Cox, Nancy J, Haines, Jonathan L, Keene, C Dirk, Saykin, Andrew J, Larson, Eric B, Sperling, Reisa A, Mayeux, Richard, Cuccaro, Michael L, Bennett, David A, Schneider, Julie A, Crane, Paul K, Jefferson, Angela L, Hohman, Timothy J

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Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent by de Candia, Teresa R., Lee, S. Hong, Yang, Jian, Browning, Brian L., Gejman, Pablo V., Levinson, Douglas F., Mowry, Bryan J., Hewitt, John K., Goddard, Michael E., O’Donovan, Michael C., Purcell, Shaun M., Posthuma, Danielle, Visscher, Peter M., Wray, Naomi R., Keller, Matthew C.

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Proteogenomic Landscape of Breast Cancer Tumorigenesis and Targeted Therapy by Krug, Karsten, Jaehnig, Eric J., Satpathy, Shankha, Blumenberg, Lili, Karpova, Alla, Anurag, Meenakshi, Miles, George, Mertins, Philipp, Geffen, Yifat, Tang, Lauren C., Heiman, David I., Cao, Song, Maruvka, Yosef E., Lei, Jonathan T., Huang, Chen, Kothadia, Ramani B., Colaprico, Antonio, Birger, Chet, Wang, Jarey, Dou, Yongchao, Wen, Bo, Shi, Zhiao, Liao, Yuxing, Wiznerowicz, Maciej, Wyczalkowski, Matthew A., Chen, Xi Steven, Kennedy, Jacob J., Paulovich, Amanda G., Thiagarajan, Mathangi, Kinsinger, Christopher R., Hiltke, Tara, Boja, Emily S., Mesri, Mehdi, Robles, Ana I., Rodriguez, Henry, Westbrook, Thomas F., Ding, Li, Getz, Gad, Clauser, Karl R., Fenyö, David, Ruggles, Kelly V., Zhang, Bing, Mani, D.R., Carr, Steven A., Ellis, Matthew J., Gillette, Michael A., Avanessian, Shayan C., Cai, Shuang, Chan, Daniel, Chen, Xian, Edwards, Nathan J., Hoofnagle, Andrew N., Kane, M. Harry, Ketchum, Karen A., Kuhn, Eric, Levine, Douglas A., Li, Shunqiang, Liebler, Daniel C., Liu, Tao, Luo, Jingqin, Madhavan, Subha, Maher, Chris, McDermott, Jason E., McGarvey, Peter B., Oberti, Mauricio, Pandey, Akhilesh, Payne, Samuel H., Ransohoff, David F., Rivers, Robert C., Rodland, Karin D., Rudnick, Paul, Sanders, Melinda E., Shaw, Kenna M., Shih, Ie-Ming, Slebos, Robbert J.C., Smith, Richard D., Snyder, Michael, Stein, Stephen E., Tabb, David L., Thangudu, Ratna R., Thomas, Stefani, Wang, Yue, White, Forest M., Whiteaker, Jeffrey R., Whiteley, Gordon A., Zhang, Hui, Zhang, Zhen, Zhao, Yingming, Zhu, Heng, Zimmerman, Lisa J.

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Proteogenomics connects somatic mutations to signalling in breast cancer by Mertins, Philipp, Mani, D R, Ruggles, Kelly V, Gillette, Michael A, Clauser, Karl R, Wang, Pei, Wang, Xianlong, Qiao, Jana W, Cao, Song, Petralia, Francesca, Kawaler, Emily, Mundt, Filip, Krug, Karsten, Tu, Zhidong, Lei, Jonathan T, Gatza, Michael L, Wilkerson, Matthew, Perou, Charles M, Yellapantula, Venkata, Huang, Kuan-lin, Lin, Chenwei, McLellan, Michael D, Yan, Ping, Davies, Sherri R, Townsend, R Reid, Skates, Steven J, Wang, Jing, Zhang, Bing, Kinsinger, Christopher R, Mesri, Mehdi, Rodriguez, Henry, Ding, Li, Paulovich, Amanda G, Fenyö, David, Ellis, Matthew J, Carr, Steven A

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Polycomb repressor complex 2 suppresses interferon-responsive MHC-II expression in melanoma cells and is associated with anti-PD-1 resistance by James, Jamaal L, Taylor, Brandie C, Axelrod, Margaret L, Sun, Xiaopeng, Guerin, Lindsey N, Gonzalez-Ericsson, Paula I, Wang, Yu, Sanchez, Violeta, Fahey, Catherine C, Sanders, Melinda E, Xu, Yaomin, Hodges, Emily, Johnson, Douglas B, Balko, Justin M

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