Awareness of family health history in a predominantly young adult population by Madhavan, Sarina, Bullis, Emily, Myers, Rachel, Zhou, Chris J, Cai, Elise M, Sharma, Anu, Bhatia, Shreya, Orlando, Lori A, Haga, Susanne B

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Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects by Krohn, Lynne, Heilbron, Karl, Blauwendraat, Cornelis, Reynolds, Regina H., Yu, Eric, Senkevich, Konstantin, Rudakou, Uladzislau, Estiar, Mehrdad A., Gustavsson, Emil K., Brolin, Kajsa, Ruskey, Jennifer A., Freeman, Kathryn, Asayesh, Farnaz, Chia, Ruth, Arnulf, Isabelle, Hu, Michele T. M., Montplaisir, Jacques Y., Gagnon, Jean-François, Desautels, Alex, Dauvilliers, Yves, Gigli, Gian Luigi, Valente, Mariarosaria, Janes, Francesco, Bernardini, Andrea, Högl, Birgit, Stefani, Ambra, Ibrahim, Abubaker, Šonka, Karel, Kemlink, David, Oertel, Wolfgang, Janzen, Annette, Plazzi, Giuseppe, Biscarini, Francesco, Antelmi, Elena, Figorilli, Michela, Puligheddu, Monica, Mollenhauer, Brit, Trenkwalder, Claudia, Sixel-Döring, Friederike, Cochen De Cock, Valérie, Monaca, Christelle Charley, Heidbreder, Anna, Ferini-Strambi, Luigi, Dijkstra, Femke, Viaene, Mineke, Abril, Beatriz, Boeve, Bradley F., Scholz, Sonja W., Ryten, Mina, Bandres-Ciga, Sara, Noyce, Alastair, Cannon, Paul, Pihlstrøm, Lasse, Nalls, Mike A., Singleton, Andrew B., Rouleau, Guy A., Postuma, Ronald B., Gan-Or, Ziv

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A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma by Seviiri, Mathias, Law, Matthew H., Ong, Jue-Sheng, Gharahkhani, Puya, Fontanillas, Pierre, Olsen, Catherine M., Whiteman, David C., MacGregor, Stuart

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Discovery of genomic loci associated with sleep apnea risk through multi-trait GWAS analysis with snoring by Campos, Adrian I, Ingold, Nathan, Huang, Yunru, Mitchell, Brittany L, Kho, Pik-Fang, Han, Xikun, García-Marín, Luis M, Ong, Jue-Sheng, Law, Matthew H, Yokoyama, Jennifer S, Martin, Nicholas G, Dong, Xianjun, Cuellar-Partida, Gabriel, MacGregor, Stuart, Aslibekyan, Stella, Rentería, Miguel E

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The genetic legacy of African Americans from Catoctin Furnace by Harney, Éadaoin, Micheletti, Steven, Bruwelheide, Karin S, Freyman, William A, Bryc, Katarzyna, Akbari, Ali, Jewett, Ethan, Comer, Elizabeth, Gates, Jr, Henry Louis, Heywood, Linda, Thornton, John, Curry, Roslyn, Esselmann, Samantha Ancona, Barca, Kathryn G, Sedig, Jakob, Sirak, Kendra, Olalde, Iñigo, Adamski, Nicole, Bernardos, Rebecca, Broomandkhoshbacht, Nasreen, Ferry, Matthew, Qiu, Lijun, Stewardson, Kristin, Workman, J Noah, Zalzala, Fatma, Mallick, Shop, Micco, Adam, Mah, Matthew, Zhang, Zhao, Rohland, Nadin, Mountain, Joanna L, Owsley, Douglas W, Reich, David

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Genome-wide association studies of coffee intake in UK/US participants of European ancestry uncover cohort-specific genetic associations by Thorpe, Hayley H A, Fontanillas, Pierre, Pham, Benjamin K, Meredith, John J, Jennings, Mariela V, Courchesne-Krak, Natasia S, Vilar-Ribó, Laura, Bianchi, Sevim B, Mutz, Julian, Elson, Sarah L, Khokhar, Jibran Y, Abdellaoui, Abdel, Davis, Lea K, Palmer, Abraham A, Sanchez-Roige, Sandra

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CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice by Sanchez-Roige, Sandra, Jennings, Mariela V., Thorpe, Hayley H. A., Mallari, Jazlene E., van der Werf, Lieke C., Bianchi, Sevim B., Huang, Yuye, Lee, Calvin, Mallard, Travis T., Barnes, Samuel A., Wu, Jin Yi, Barkley-Levenson, Amanda M., Boussaty, Ely C., Snethlage, Cedric E., Schafer, Danielle, Babic, Zeljana, Winters, Boyer D., Watters, Katherine E., Biederer, Thomas, Mackillop, James, Stephens, David N., Elson, Sarah L., Fontanillas, Pierre, Khokhar, Jibran Y., Young, Jared W., Palmer, Abraham A.

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Using a polygenic score in a family design to understand genetic influences on musicality by Wesseldijk, Laura W., Abdellaoui, Abdel, Gordon, Reyna L., Ullén, Fredrik, Mosing, Miriam A.

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Characterizing mood disorders in the AFFECT study: a large, longitudinal, and phenotypically rich genetic cohort in the US by Dalby, Maria, Vitezic, Morana, Plath, Niels, Hammer-Helmich, Lene, Jiang, Yunxuan, Tian, Chao, Dhamija, Devika, Wilson, Catherine H., Hinds, David, Sullivan, Patrick F., Buckholtz, Joshua W., Smoller, Jordan W.

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The genetic architecture of dog ownership: large-scale genome-wide association study in 97,552 European-ancestry individuals by Gong, Tong, Karlsson, Robert, Yao, Shuyang, Magnusson, Patrik K E, Ajnakina, Olesya, Steptoe, Andrew, Bhatta, Laxmi, Brumpton, Ben, Kumar, Ashish, Mélen, Erik, Lin, Keng-Han, Tian, Chao, Fall, Tove, Almqvist, Catarina

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A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals by Jennings, Mariela V., Martínez-Magaña, José Jaime, Courchesne-Krak, Natasia S., Cupertino, Renata B., Vilar-Ribó, Laura, Bianchi, Sevim B., Hatoum, Alexander S., Atkinson, Elizabeth G., Giusti-Rodriguez, Paola, Montalvo-Ortiz, Janitza L., Gelernter, Joel, Artigas, María Soler, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Eriksson, Nicholas, Filshtein, Teresa, Fitch, Alison, Fletez-Brant, Kipper, Fontanillas, Pierre, Freyman, Will, Granka, Julie M., Heilbron, Karl, Hernandez, Alejandro, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn, Kwong, Alan, Lin, Keng-Han, Llamas, Bianca A., Lowe, Maya, McCreight, Jey C., McIntyre, Matthew H., Micheletti, Steven J., Moreno, Meghan E., Nandakumar, Priyanka, Nguyen, Dominique T., Noblin, Elizabeth S., O'Connell, Jared, Petrakovitz, Aaron A., Poznik, G. David, Reynoso, Alexandra, Schumacher, Morgan, Shastri, Anjali J., Shelton, Janie F., Shi, Jingchunzi, Shringarpure, Suyash, Su, Qiaojuan Jane, Tat, Susana A., Tchakouté, Christophe Toukam, Tran, Vinh, Tung, Joyce Y., Wang, Xin, Wang, Wei, Weldon, Catherine H., Wilton, Peter, Wong, Corinna D., Elson, Sarah L., Edenberg, Howard J., Fontanillas, Pierre, Palmer, Abraham A., Sanchez-Roige, Sandra

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A population-specific reference panel for improved genotype imputation in African Americans by O’Connell, Jared, Yun, Taedong, Moreno, Meghan, Li, Helen, Litterman, Nadia, Kolesnikov, Alexey, Noblin, Elizabeth, Chang, Pi-Chuan, Shastri, Anjali, Dorfman, Elizabeth H., Shringarpure, Suyash, Auton, Adam, Carroll, Andrew, McLean, Cory Y.

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MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups by Jin, Jin, Zhan, Jianan, Zhang, Jingning, Zhao, Ruzhang, O’Connell, Jared, Jiang, Yunxuan, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Cuellar Partida, Gabriel, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Eriksson, Nicholas, Filshtein, Teresa, Fitch, Alison, Fletez-Brant, Kipper, Fontanillas, Pierre, Freyman, Will, Granka, Julie M., Heilbron, Karl, Hernandez, Alejandro, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn, Kwong, Alan, Lin, Keng-Han, Llamas, Bianca A., Lowe, Maya, McCreight, Jey C., McIntyre, Matthew H., Micheletti, Steven J., Moreno, Meghan E., Nandakumar, Priyanka, Nguyen, Dominique T., Noblin, Elizabeth S., O’Connell, Jared, Petrakovitz, Aaron A., Poznik, G. David, Reynoso, Alexandra, Schumacher, Morgan, Shastri, Anjali J., Shelton, Janie F., Shi, Jingchunzi, Shringarpure, Suyash, Su, Qiaojuan Jane, Tat, Susana A., Tchakouté, Christophe Toukam, Tran, Vinh, Tung, Joyce Y., Wang, Xin, Wang, Wei, Weldon, Catherine H., Wilton, Peter, Wong, Corinna D., Buyske, Steven, Gignoux, Christopher, Haiman, Christopher, Kenny, Eimear E., Kooperberg, Charles, North, Kari, Koelsch, Bertram L., Wojcik, Genevieve, Zhang, Haoyu, Chatterjee, Nilanjan

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Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma by Choquet, Hélène, Jiang, Chen, Yin, Jie, Kim, Yuhree, Hoffmann, Thomas J., Jorgenson, Eric, Asgari, Maryam M.

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Analysis of rare Parkinson’s disease variants in millions of people by Pitz, Vanessa, Makarious, Mary B., Bandres-Ciga, Sara, Iwaki, Hirotaka, Singleton, Andrew B., Nalls, Mike, Heilbron, Karl, Blauwendraat, Cornelis

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Correlations in sleeping patterns and circadian preference between spouses by Richmond, Rebecca C., Howe, Laurence J., Heilbron, Karl, Jones, Samuel, Liu, Junxi, Wang, Xin, Weedon, Michael N., Rutter, Martin K., Lawlor, Deborah A., Davey Smith, George, Vetter, Céline

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FUT6 deficiency compromises basophil function by selectively abrogating their sialyl-Lewis x expression by Puan, Kia Joo, San Luis, Boris, Yusof, Nurhashikin, Kumar, Dilip, Andiappan, Anand Kumar, Lee, Wendy, Cajic, Samanta, Vuckovic, Dragana, Chan, Jing De, Döllner, Tobias, Hou, Han Wei, Jiang, Yunxuan, Tian, Chao, Rapp, Erdmann, Poidinger, Michael, Wang, De Yun, Soranzo, Nicole, Lee, Bernett, Rötzschke, Olaf

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Rat bite fever in a patient with human immunodeficiency virus by Bougioukas, Lauren, Vicks, Emily, Hale, Andrew J., Dejace, Jean, Bullis, Sean

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X + Y Scheduling in Pediatric Residency: Continuity, Handoffs, and Trainee Experience by Osborn, Rachel, Bullis, Eliza, Fenick, Ada M., Powers, Emily, Banker, Sumeet, Asnes, Andrea

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Effect on Continuity of Care and Trainee Experience of Immersion Scheduling in Pediatric Residency by Osborn, Rachel R., Bullis, Eliza, Fenick, Ada, Powers, Emily, Asnes, Andrea

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