Improving the Quality of Auscultation for Individuals with Cachexia von Chartier, Lucas B., Bonnycastle, Michael J.

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Systematic detection and multidisciplinary care of delirium in older medical inpatients: a randomized trial von Cole, Martin G, McCusker, Jane, Bellavance, Francois, Primeau, Francois J, Bailey, Robert F, Bonnycastle, Michael J, Laplante, Johanne

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Partial and No Recovery from Delirium in Older Hospitalized Adults: Frequency and Baseline Risk Factors von Cole, Martin G., Bailey, Robert, Bonnycastle, Michael, McCusker, Jane, Fung, Shek, Ciampi, Antonio, Belzile, Eric, Bai, Chun

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Partial and no recovery from delirium after hospital discharge predict increased adverse events von Cole, Martin G, McCusker, Jane, Bailey, Robert, Bonnycastle, Michael, Fung, Shek, Ciampi, Antonio, Belzile, Eric

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Frequency of full, partial and no recovery from subsyndromal deliriumin older hospital inpatients von Cole, Martin G., Bailey, Robert, Bonnycastle, Michael, McCusker, Jane, Fung, Shek, Ciampi, Antonio, Belzile, Eric

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Response to Alici von Cole, Martin G., Bailey, Robert, Bonnycastle, Michael, McCusker, Jane, Fung, Shek, Ciampi, Antonio, Belzile, Eric, Bai, Chun

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Beseiged von Haasz, Maya, Bonnycastle, Michael, Dylewski, Joe, Opatrny, Lucie

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Screening for Geriatric Problems in the Emergency Department: Reliability and Validity von McCusker, Jane, Bellavance, François, Cardin, Sylvie, Trepanier, Sylvain

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BUILDING A LEARNING EXPERIENCE: THE IMPLEMENTATION OF A CLERKSHIP IN GERIATRIC MEDICINE von Duque, Gustavo, Bonnycastle, Michael, Nazerali, Najmi, Bailey, Robert, Ferrier, Catherine, Heilpern, Paul, Gold, Susan

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SARS-CoV-2 infection induces beta cell transdifferentiation von Tang, Xuming, Uhl, Skyler, Zhang, Tuo, Xue, Dongxiang, Li, Bo, Vandana, J. Jeya, Acklin, Joshua A., Bonnycastle, Lori L., Narisu, Narisu, Erdos, Michael R., Bram, Yaron, Chandar, Vasuretha, Chong, Angie Chi Nok, Lacko, Lauretta A., Min, Zaw, Lim, Jean K., Borczuk, Alain C., Xiang, Jenny, Naji, Ali, Collins, Francis S., Evans, Todd, Liu, Chengyang, tenOever, Benjamin R., Schwartz, Robert E., Chen, Shuibing

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Presynaptic dysfunction in neurodevelopmental disorders: Insights from the synaptic vesicle life cycle von Bonnycastle, Katherine, Davenport, Elizabeth C., Cousin, Michael A.

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A genomic mutational constraint map using variation in 76,156 human genomes von Chen, Siwei, Francioli, Laurent C., Goodrich, Julia K., Collins, Ryan L., Kanai, Masahiro, Wang, Qingbo, Alföldi, Jessica, Watts, Nicholas A., Vittal, Christopher, Gauthier, Laura D., Poterba, Timothy, Wilson, Michael W., Tarasova, Yekaterina, Phu, William, Grant, Riley, Yohannes, Mary T., Koenig, Zan, Farjoun, Yossi, Banks, Eric, Donnelly, Stacey, Gabriel, Stacey, Gupta, Namrata, Ferriera, Steven, Tolonen, Charlotte, Novod, Sam, Bergelson, Louis, Roazen, David, Ruano-Rubio, Valentin, Covarrubias, Miguel, Llanwarne, Christopher, Petrillo, Nikelle, Wade, Gordon, Jeandet, Thibault, Munshi, Ruchi, Tibbetts, Kathleen, O’Donnell-Luria, Anne, Solomonson, Matthew, Seed, Cotton, Martin, Alicia R., Talkowski, Michael E., Rehm, Heidi L., Daly, Mark J., Tiao, Grace, Neale, Benjamin M., MacArthur, Daniel G., Karczewski, Konrad J.

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The genetic regulatory signature of type 2 diabetes in human skeletal muscle von Scott, Laura J., Erdos, Michael R., Huyghe, Jeroen R., Welch, Ryan P., Beck, Andrew T., Wolford, Brooke N., Chines, Peter S., Didion, John P., Narisu, Narisu, Stringham, Heather M., Taylor, D. Leland, Jackson, Anne U., Vadlamudi, Swarooparani, Bonnycastle, Lori L., Kinnunen, Leena, Saramies, Jouko, Sundvall, Jouko, Albanus, Ricardo D'Oliveira, Kiseleva, Anna, Hensley, John, Crawford, Gregory E., Jiang, Hui, Wen, Xiaoquan, Watanabe, Richard M., Lakka, Timo A., Mohlke, Karen L., Laakso, Markku, Tuomilehto, Jaakko, Koistinen, Heikki A., Boehnke, Michael, Collins, Francis S., Parker, Stephen C. J.

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Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation von BONNYCASTLE, Lori L, CHINES, Peter S, NARISU, Narisu, GOLDFEDER, Rachel L, STITZEL, Michael L, SIMIN LU, BOEHNKE, Michael, URANO, Fumihiko, COLLINS, Francis S, LAAKSO, Markku, HARA, Takashi, HUYGHE, Jeroen R, SWIFT, Amy J, HEIKINHEIMO, Pirkko, MAHADEVAN, Jana, PELTONEN, Sirkku, HUOPIO, Hanna, NUUTILA, Pirjo

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Mitochondrial Calcium Uptake Modulates Synaptic Vesicle Endocytosis in Central Nerve Terminals von Marland, Jamie Roslin Keynes, Hasel, Philip, Bonnycastle, Katherine, Cousin, Michael Alan

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Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci von Service, Susan K, Teslovich, Tanya M, Fuchsberger, Christian, Ramensky, Vasily, Yajnik, Pranav, Koboldt, Daniel C, Larson, David E, Zhang, Qunyuan, Lin, Ling, Welch, Ryan, Ding, Li, McLellan, Michael D, O'Laughlin, Michele, Fronick, Catrina, Fulton, Lucinda L, Magrini, Vincent, Swift, Amy, Elliott, Paul, Jarvelin, Marjo-Riitta, Kaakinen, Marika, McCarthy, Mark I, Peltonen, Leena, Pouta, Anneli, Bonnycastle, Lori L, Collins, Francis S, Narisu, Narisu, Stringham, Heather M, Tuomilehto, Jaakko, Ripatti, Samuli, Fulton, Robert S, Sabatti, Chiara, Wilson, Richard K, Boehnke, Michael, Freimer, Nelson B

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Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci von Yin, Xianyong, Chan, Lap Sum, Bose, Debraj, Jackson, Anne U., VandeHaar, Peter, Locke, Adam E., Fuchsberger, Christian, Stringham, Heather M., Welch, Ryan, Yu, Ketian, Fernandes Silva, Lilian, Service, Susan K., Zhang, Daiwei, Hector, Emily C., Young, Erica, Ganel, Liron, Das, Indraniel, Abel, Haley, Erdos, Michael R., Bonnycastle, Lori L., Kuusisto, Johanna, Stitziel, Nathan O., Hall, Ira M., Wagner, Gregory R., Kang, Jian, Morrison, Jean, Burant, Charles F., Collins, Francis S., Ripatti, Samuli, Palotie, Aarno, Freimer, Nelson B., Mohlke, Karen L., Scott, Laura J., Wen, Xiaoquan, Fauman, Eric B., Laakso, Markku, Boehnke, Michael

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Association of 18 Confirmed Susceptibility Loci for Type 2 Diabetes With Indices of Insulin Release, Proinsulin Conversion, and Insulin Sensitivity in 5,327 Nondiabetic Finnish Men von Stancáková, Alena, Kuulasmaa, Teemu, Paananen, Jussi, Jackson, Anne U, Bonnycastle, Lori L, Collins, Francis S, Boehnke, Michael, Kuusisto, Johanna, Laakso, Markku

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The mutational constraint spectrum quantified from variation in 141,456 humans von Karczewski, Konrad J., Francioli, Laurent C., Tiao, Grace, Cummings, Beryl B., Alföldi, Jessica, Wang, Qingbo, Collins, Ryan L., Laricchia, Kristen M., Ganna, Andrea, Birnbaum, Daniel P., Gauthier, Laura D., Brand, Harrison, Solomonson, Matthew, Watts, Nicholas A., Rhodes, Daniel, Singer-Berk, Moriel, England, Eleina M., Seaby, Eleanor G., Kosmicki, Jack A., Walters, Raymond K., Tashman, Katherine, Farjoun, Yossi, Banks, Eric, Poterba, Timothy, Wang, Arcturus, Seed, Cotton, Whiffin, Nicola, Chong, Jessica X., Samocha, Kaitlin E., Pierce-Hoffman, Emma, Zappala, Zachary, O’Donnell-Luria, Anne H., Minikel, Eric Vallabh, Weisburd, Ben, Lek, Monkol, Ware, James S., Vittal, Christopher, Armean, Irina M., Bergelson, Louis, Cibulskis, Kristian, Connolly, Kristen M., Covarrubias, Miguel, Donnelly, Stacey, Ferriera, Steven, Gabriel, Stacey, Gentry, Jeff, Gupta, Namrata, Jeandet, Thibault, Kaplan, Diane, Llanwarne, Christopher, Munshi, Ruchi, Novod, Sam, Petrillo, Nikelle, Roazen, David, Ruano-Rubio, Valentin, Saltzman, Andrea, Schleicher, Molly, Soto, Jose, Tibbetts, Kathleen, Tolonen, Charlotte, Wade, Gordon, Talkowski, Michael E., Neale, Benjamin M., Daly, Mark J., MacArthur, Daniel G.

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Modeling islet enhancers using deep learning identifies candidate causal variants at loci associated with T2D and glycemic traits von Hudaiberdiev, Sanjarbek, Taylor, D Leland, Song, Wei, Narisu, Narisu, Bhuiyan, Redwan M, Taylor, Henry J, Tang, Xuming, Yan, Tingfen, Swift, Amy J, Bonnycastle, Lori L, Consortium, Diamante, Chen, Shuibing, Stitzel, Michael L, Erdos, Michael R, Ovcharenko, Ivan, Collins, Francis S

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