Pseudotumors and High-Grade Aseptic Lymphocyte-Dominated Vasculitis-Associated Lesions Around Total Knee Replacements Identified at Aseptic Revision Surgery: Findings of a Large-Sc... von Kurmis, Andrew P., Herman, Amir, McIntyre, Adam R., Masri, Bassam A., Garbuz, Donald S.

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Unit Sales Trends of Hip Arthroplasty Procedures Performed in Ontario in 2020 von McIntyre, Adam R., Somerville, Lyndsay E., MacDonald, Steven J., Naudie, Douglas D.R.

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Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically von Wang, Jian, Dron, Jacqueline S, Ban, Matthew R, Robinson, John F, McIntyre, Adam D, Alazzam, Maher, Zhao, Pei Jun, Dilliott, Allison A, Cao, Henian, Huff, Murray W, Rhainds, David, Low-Kam, Cécile, Dubé, Marie-Pierre, Lettre, Guillaume, Tardif, Jean-Claude, Hegele, Robert A

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Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias von Dron, Jacqueline S, Wang, Jian, McIntyre, Adam D, Iacocca, Michael A, Robinson, John F, Ban, Matthew R, Cao, Henian, Hegele, Robert A

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Development and Validation of a Multivariable Prediction Model for Postoperative Intensive Care Unit Stay in a Broad Surgical Population von Rozeboom, Paul D, Henderson, William G, Dyas, Adam R, Bronsert, Michael R, Colborn, Kathryn L, Lambert-Kerzner, Anne, Hammermeister, Karl E, McIntyre, Robert C, Meguid, Robert A

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Social vulnerability is associated with increased morbidity following colorectal surgery von Carmichael, Heather, Dyas, Adam R., Bronsert, Michael R., Stearns, Dorothy, Birnbaum, Elisa H., McIntyre, Robert C., Meguid, Robert A., Velopulos, Catherine G.

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Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways von Jansen, Philip R., Watanabe, Kyoko, Stringer, Sven, Skene, Nathan, Bryois, Julien, Hammerschlag, Anke R., de Leeuw, Christiaan A., Benjamins, Jeroen S., Muñoz-Manchado, Ana B., Nagel, Mats, Savage, Jeanne E., Tiemeier, Henning, White, Tonya, Tung, Joyce Y., Hinds, David A., Vacic, Vladimir, Wang, Xin, Sullivan, Patrick F., van der Sluis, Sophie, Polderman, Tinca J. C., Smit, August B., Hjerling-Leffler, Jens, Van Someren, Eus J. W., Posthuma, Danielle

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Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways von Nagel, Mats, Jansen, Philip R., Stringer, Sven, Watanabe, Kyoko, de Leeuw, Christiaan A., Bryois, Julien, Savage, Jeanne E., Hammerschlag, Anke R., Skene, Nathan G., Muñoz-Manchado, Ana B., White, Tonya, Tiemeier, Henning, Linnarsson, Sten, Hjerling-Leffler, Jens, Polderman, Tinca J. C., Sullivan, Patrick F., van der Sluis, Sophie, Posthuma, Danielle

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Defective KIM-1 phagocytosis does not predispose to acute graft dysfunction after kidney transplantation in humans von Suri, Rita S., Lee, Ji Yun, Ban, Matthew R., Shrum, Bradly, Tutunea-Fatan, Elena, Ismail, Ola Z., Leckie, Steven, McIntyre, Adam, Xu, Qingyong, Lee, Seung Ho, de Chickera, Sonali, Hegele, Robert A., Gunaratnam, Lakshman

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Development and validation of a prediction model for conversion of outpatient to inpatient surgery von Dyas, Adam R., Henderson, William G., Madsen, Helen J., Bronsert, Michael R., Colborn, Kathryn L., Lambert-Kerzner, Anne, McIntyre, Robert C., Meguid, Robert A.

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Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis von Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.

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Targeted next-generation sequencing in monogenic dyslipidemias von Hegele, Robert A, Ban, Matthew R, Cao, Henian, McIntyre, Adam D, Robinson, John F, Wang, Jian

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Polygenic determinants in extremes of high-density lipoprotein cholesterol von Dron, Jacqueline S., Wang, Jian, Low-Kam, Cécile, Khetarpal, Sumeet A., Robinson, John F., McIntyre, Adam D., Ban, Matthew R., Cao, Henian, Rhainds, David, Dubé, Marie-Pierre, Rader, Daniel J., Lettre, Guillaume, Tardif, Jean-Claude, Hegele, Robert A.

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An atlas of genetic influences on osteoporosis in humans and mice von Morris, John A., Kemp, John P., Youlten, Scott E., Laurent, Laetitia, Logan, John G., Chai, Ryan C., Vulpescu, Nicholas A., Forgetta, Vincenzo, Kleinman, Aaron, Mohanty, Sindhu T., Sergio, C. Marcelo, Quinn, Julian, Nguyen-Yamamoto, Loan, Luco, Aimee-Lee, Vijay, Jinchu, Simon, Marie-Michelle, Pramatarova, Albena, Medina-Gomez, Carolina, Trajanoska, Katerina, Ghirardello, Elena J., Butterfield, Natalie C., Curry, Katharine F., Leitch, Victoria D., Sparkes, Penny C., Adoum, Anne-Tounsia, Mannan, Naila S., Komla-Ebri, Davide S. K., Pollard, Andrea S., Dewhurst, Hannah F., Hassall, Thomas A. D., Beltejar, Michael-John G., Adams, Douglas J., Vaillancourt, Suzanne M., Kaptoge, Stephen, Baldock, Paul, Cooper, Cyrus, Reeve, Jonathan, Ntzani, Evangelia E., Evangelou, Evangelos, Ohlsson, Claes, Karasik, David, Rivadeneira, Fernando, Kiel, Douglas P., Tobias, Jonathan H., Gregson, Celia L., Harvey, Nicholas C., Grundberg, Elin, Goltzman, David, Adams, David J., Lelliott, Christopher J., Hinds, David A., Ackert-Bicknell, Cheryl L., Hsu, Yi-Hsiang, Maurano, Matthew T., Croucher, Peter I., Williams, Graham R., Bassett, J. H. Duncan, Evans, David M., Richards, J. Brent

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Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use von Liu, Mengzhen, Jiang, Yu, Wedow, Robbee, Li, Yue, Brazel, David M., Chen, Fang, Datta, Gargi, Davila-Velderrain, Jose, Tian, Chao, Zhan, Xiaowei, Choquet, Hélène, Docherty, Anna R., Faul, Jessica D., Foerster, Johanna R., Fritsche, Lars G., Gabrielsen, Maiken Elvestad, Gordon, Scott D., Haessler, Jeffrey, Hottenga, Jouke-Jan, Huang, Hongyan, Jang, Seon-Kyeong, Jansen, Philip R., Ling, Yueh, Matoba, Nana, McMahon, George, Orrù, Valeria, Palviainen, Teemu, Pandit, Anita, Reginsson, Gunnar W., Skogholt, Anne Heidi, Smith, Jennifer A., Taylor, Amy E., Turman, Constance, Willemsen, Gonneke, Young, Hannah, Young, Kendra A., Zhao, Wei, Zhou, Wei, Bjornsdottir, Gyda, Boehnke, Michael, Boomsma, Dorret I., Chen, Chu, Cucca, Francesco, Davies, Gareth E., Eaton, Charles B., Ehringer, Marissa A., Esko, Tõnu, Fiorillo, Edoardo, Gillespie, Nathan A., Heath, Andrew C., Hokanson, John E., Hopfer, Christian J., Iacono, William G., Kamatani, Yoichiro, Kardia, Sharon L. R., Keller, Matthew C., Kellis, Manolis, Kooperberg, Charles, Kraft, Peter, Krauter, Kenneth S., Laakso, Markku, Lind, Penelope A., Loukola, Anu, Lutz, Sharon M., Madden, Pamela A. F., Martin, Nicholas G., McQueen, Matthew B., Medland, Sarah E., Mohlke, Karen L., Nielsen, Jonas B., Okada, Yukinori, Peters, Ulrike, Polderman, Tinca J. C., Rimm, Eric, Rose, Richard J., Runarsdottir, Valgerdur, Stallings, Michael C., Stefansson, Hreinn, Thai, Khanh K., Tindle, Hilary A., Tyrfingsson, Thorarinn, Wall, Tamara L., Weir, David R., Weisner, Constance, Whitfield, John B., Yin, Jie, Zuccolo, Luisa, Bierut, Laura J., Hveem, Kristian, Lee, James J., Munafò, Marcus R., Saccone, Nancy L., David, Sean P., Jorgenson, Eric, Kaprio, Jaakko, Stefansson, Kari, Thorgeirsson, Thorgeir E., Abecasis, Gonçalo, Liu, Dajiang J., Vrieze, Scott

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The apolipoprotein C-III (Gln38Lys) variant associated with human hypertriglyceridemia is a gain-of-function mutation von Sundaram, Meenakshi, Curtis, Kaitlin R., Amir Alipour, Mohsen, LeBlond, Nicholas D., Margison, Kaitlyn D., Yaworski, Rebecca A., Parks, Robin J., McIntyre, Adam D., Hegele, Robert A., Fullerton, Morgan D., Yao, Zemin

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Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior von Ganna, Andrea, Verweij, Karin J. H., Nivard, Michel G., Maier, Robert, Wedow, Robbee, Busch, Alexander S., Abdellaoui, Abdel, Guo, Shengru, Sathirapongsasuti, J. Fah, Lichtenstein, Paul, Lundström, Sebastian, Långström, Niklas, Auton, Adam, Harris, Kathleen Mullan, Beecham, Gary W., Martin, Eden R., Sanders, Alan R., Perry, John R. B., Neale, Benjamin M., Zietsch, Brendan P.

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Multi-trait analysis of genome-wide association summary statistics using MTAG von Turley, Patrick, Walters, Raymond K., Maghzian, Omeed, Okbay, Aysu, Lee, James J., Fontana, Mark Alan, Nguyen-Viet, Tuan Anh, Wedow, Robbee, Zacher, Meghan, Furlotte, Nicholas A., Magnusson, Patrik, Oskarsson, Sven, Johannesson, Magnus, Visscher, Peter M., Laibson, David, Cesarini, David, Neale, Benjamin M., Benjamin, Daniel J.

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Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms von Jones, Samuel E., Lane, Jacqueline M., Wood, Andrew R., van Hees, Vincent T., Tyrrell, Jessica, Beaumont, Robin N., Jeffries, Aaron R., Dashti, Hassan S., Hillsdon, Melvyn, Ruth, Katherine S., Tuke, Marcus A., Yaghootkar, Hanieh, Sharp, Seth A., Jie, Yingjie, Thompson, William D., Harrison, Jamie W., Dawes, Amy, Byrne, Enda M., Tiemeier, Henning, Allebrandt, Karla V., Bowden, Jack, Ray, David W., Freathy, Rachel M., Murray, Anna, Mazzotti, Diego R., Gehrman, Philip R., Lawlor, Debbie A., Frayling, Timothy M., Rutter, Martin K., Hinds, David A., Saxena, Richa, Weedon, Michael N.

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Partial LPL deletions: rare copy-number variants contributing towards severe hypertriglyceridemia von Dron, Jacqueline S., Wang, Jian, McIntyre, Adam D., Cao, Henian, Robinson, John F., Duell, P. Barton, Manjoo, Priya, Feng, James, Movsesyan, Irina, Malloy, Mary J., Pullinger, Clive R., Kane, John P., Hegele, Robert A.

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