Reducing Infusion Clinic Wait Times Using Quality Improvement von Plourde, Collin L, Varnado, William T, Gleaton, Barbara J, Das, Devika G

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Impact of COVID-19 on Hematology-Oncology Trainees: A Quantitative and Qualitative Assessment von Durani, Urshila, Major, Ajay, Velazquez, Ana I, May, Jori, Nelson, Marquita, Zheng, Ze, Hall, Anurekha G, Alam, Sara Taveras, Reynolds, Robby, Thompson, J Colton, Kumbamu, Ashok, Das, Devika G, Murphy, Martina C, Henry, Elizabeth, Lee, Alfred Ian, Marshall, Ariela L, Wun, Ted, Weeks, Lachelle Dawn

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Impact of COVID-19 on Hematology-Oncology Fellowship Programs: A Quantitative and Qualitative Survey Assessment of Fellowship Program Directors von Velazquez, Ana I, Durani, Urshila, Weeks, Lachelle D, Major, Ajay, Reynolds, Robby, Kumbamu, Ashok, Das, Devika G, Murphy, Martina C, Henry, Elizabeth, Lee, Alfred I, Marshall, Ariela L

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Evaluation of Real-World Patient Volume for a Low Risk Pulmonary Embolism Outpatient Clinic at a Large, Public Medical Center von Ye, Star, Griffin, Russell, Hearld, Kristine, Barlow, Brett R, Bodine, Charles, Patel, Rishi R, Pywell, Cameron, Das, Devika G., May, Jori E.

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The Impact of COVID-19 on Hematology-Oncology Fellowship Programs: Program Director Perspectives von Velazquez Manana, Ana I., Durani, Urshila, Reynolds, Robby, Kumbamu, Ashok, Das, Devika G., Murphy, Martina C., Henry, Elizabeth, Lee, Alfred Ian, Marshall, Ariela L.

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Measuring the Impact of COVID-19 on Hematology-Oncology Trainees: A Quantitative and Qualitative Assessment von Durani, Urshila, Velazquez Manana, Ana I., May, Jori, Nelson, Marquita, Zheng, Ze, Gollapudi, Anurekha, Taveras Alam, Sara, Reynolds, Robby, Thompson, John Colton, Kumbamu, Ashok, Das, Devika G., Murphy, Martina C., Henry, Elizabeth, Lee, Alfred Ian, Marshall, Ariela L., Wun, Ted, Weeks, Lachelle

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A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease von Wightman, Douglas P., Jansen, Iris E., Savage, Jeanne E., Shadrin, Alexey A., Bahrami, Shahram, Holland, Dominic, Rongve, Arvid, Børte, Sigrid, Winsvold, Bendik S., Drange, Ole Kristian, Martinsen, Amy E., Skogholt, Anne Heidi, Willer, Cristen, Bråthen, Geir, Bosnes, Ingunn, Nielsen, Jonas Bille, Fritsche, Lars G., Thomas, Laurent F., Pedersen, Linda M., Gabrielsen, Maiken E., Johnsen, Marianne Bakke, Meisingset, Tore Wergeland, Zhou, Wei, Proitsi, Petroula, Hodges, Angela, Dobson, Richard, Velayudhan, Latha, Heilbron, Karl, Auton, Adam, Sealock, Julia M., Davis, Lea K., Pedersen, Nancy L., Reynolds, Chandra A., Karlsson, Ida K., Magnusson, Sigurdur, Stefansson, Hreinn, Thordardottir, Steinunn, Jonsson, Palmi V., Snaedal, Jon, Zettergren, Anna, Skoog, Ingmar, Kern, Silke, Waern, Margda, Zetterberg, Henrik, Blennow, Kaj, Stordal, Eystein, Hveem, Kristian, Zwart, John-Anker, Athanasiu, Lavinia, Selnes, Per, Saltvedt, Ingvild, Sando, Sigrid B., Ulstein, Ingun, Djurovic, Srdjan, Fladby, Tormod, Aarsland, Dag, Selbæk, Geir, Ripke, Stephan, Stefansson, Kari, Andreassen, Ole A., Posthuma, Danielle

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NCOA5 deficiency promotes a unique liver protumorigenic microenvironment through p21WAF1/CIP1 overexpression, which is reversed by metformin von Williams, Mark, Liu, Xinhui, Zhang, Yueqi, Reske, Jake, Bahal, Devika, Gohl, Trevor G., Hollern, Daniel, Ensink, Elliot, Kiupel, Matti, Luo, Rongcheng, Das, Rupali, Xiao, Hua

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Discovery of 42 genome-wide significant loci associated with dyslexia von Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Pourcain, Beate St, Francks, Clyde, Marioni, Riccardo E., Zhao, Jingjing, Paracchini, Silvia, Talcott, Joel B., Monaco, Anthony P., Stein, John F., Gruen, Jeffrey R., Olson, Richard K., Willcutt, Erik G., DeFries, John C., Pennington, Bruce F., Smith, Shelley D., Wright, Margaret J., Martin, Nicholas G., Auton, Adam, Bates, Timothy C., Fisher, Simon E., Luciano, Michelle

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Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease von Kim, Jonggeol Jeffrey, Vitale, Dan, Otani, Diego Véliz, Lian, Michelle Mulan, Heilbron, Karl, Iwaki, Hirotaka, Lake, Julie, Solsberg, Caroline Warly, Leonard, Hampton, Makarious, Mary B., Tan, Eng-King, Singleton, Andrew B., Bandres-Ciga, Sara, Noyce, Alastair J., Blauwendraat, Cornelis, Nalls, Mike A., Foo, Jia Nee, Mata, Ignacio

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Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects von 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 von Seviiri, Mathias, Law, Matthew H., Ong, Jue-Sheng, Gharahkhani, Puya, Fontanillas, Pierre, Olsen, Catherine M., Whiteman, David C., MacGregor, Stuart

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The genetic legacy of African Americans from Catoctin Furnace von 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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Discovery of genomic loci associated with sleep apnea risk through multi-trait GWAS analysis with snoring von 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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A new method for multiancestry polygenic prediction improves performance across diverse populations von Zhang, Haoyu, Zhan, Jianan, Jin, Jin, Zhang, Jingning, Lu, Wenxuan, Zhao, Ruzhang, Ahearn, Thomas U., Yu, Zhi, O’Connell, Jared, Jiang, Yunxuan, Chen, Tony, Okuhara, Dayne, Garcia-Closas, Montserrat, Lin, Xihong, Koelsch, Bertram L., Chatterjee, Nilanjan

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Genome-wide association studies of coffee intake in UK/US participants of European ancestry uncover cohort-specific genetic associations von 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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Prevalence of Alpha-1 Antitrypsin Deficiency, Self-Reported Behavior Change, and Health Care Engagement Among Direct-to-Consumer Recipients of a Personalized Genetic Risk Report von Ashenhurst, James R., Nhan, Hoang, Shelton, Janie F., Wu, Shirley, Tung, Joyce Y., Elson, Sarah L., Stoller, James K., Agee, Michelle, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Cameron, Briana, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Fontanillas, Pierre, Freyman, Will, Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Huber, Karen E., Jewett, Ethan M., Jiang, Yunxuan, Kleinman, Aaron, Kukar, Katelyn, Lane, Vanessa A., Lin, Keng-Han, Lowe, Maya, Luff, Marie K., McCreight, Jennifer C., McIntyre, Matthew H., McManus, Kimberly F., Micheletti, Steven J., Moreno, Meghan E., Mountain, Joanna L., Mozaffari, Sahar V., Nandakumar, Priyanka, Noblin, Elizabeth S., O’Connell, Jared, Petrakovitz, Aaron A., Poznik, G. David, Schumacher, Morgan, Shastri, Anjali J., Shelton, Janie F., Shi, Jingchunzi, Shringarpure, Suyash, Tian, Chao, Tran, Vinh, Tung, Joyce Y., Wang, Xin, Wang, Wei, Weldon, Catherine H., Wilton, Peter

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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 von 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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Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma von Liyanage, Upekha E., MacGregor, Stuart, Bishop, D. Timothy, Shi, Jianxin, An, Jiyuan, Ong, Jue Sheng, Han, Xikun, Scolyer, Richard A., Martin, Nicholas G., Medland, Sarah E., Byrne, Enda M., Green, Adèle C., Saw, Robyn P.M., Thompson, John F., Stretch, Jonathan, Spillane, Andrew, Jiang, Yunxuan, Tian, Chao, Agee, Michelle, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Cameron, Briana, Coker, Daniella, Cuellar Partida, Gabriel, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Fontanillas, Pierre, Freyman, Will, Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Huber, Karen E., Jewett, Ethan M., Kleinman, Aaron, Kukar, Katelyn, Lin, Keng-Han, Lowe, Maya, Luff, Marie K., McCreight, Jennifer C., McIntyre, Matthew H., McManus, Kimberly F., Micheletti, Steven J., Moreno, Meghan E., Mountain, Joanna L., Mozaffari, Sahar V., Nandakumar, Priyanka, Noblin, Elizabeth S., O'Connell, Jared, Petrakovitz, Aaron A., Poznik, G. David, Shastri, Anjali J., Shelton, Janie F., Shi, Jingchunzi, Shringarpure, Suyash, Tran, Vinh, Tung, Joyce Y., Wang, Xin, Wang, Wei, Weldon, Catherine H., Wilton, Peter, Gordon, Scott G., Duffy, David L., Olsen, Catherine M., Whiteman, David C., Long, Georgina V., Iles, Mark M., Landi, Maria Teresa, Law, Matthew H.

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Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia von Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Pourcain, Beate St, Francks, Clyde, Marioni, Riccardo E., Zhao, Jingjing, Paracchini, Silvia, Talcott, Joel B., Monaco, Anthony P., Stein, John F., Gruen, Jeffrey R., Olson, Richard K., Willcutt, Erik G., DeFries, John C., Pennington, Bruce F., Smith, Shelley D., Wright, Margaret J., Martin, Nicholas G., Auton, Adam, Bates, Timothy C., Fisher, Simon E., Luciano, Michelle

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