PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses von Purcell, Shaun, Neale, Benjamin, Todd-Brown, Kathe, Thomas, Lori, Ferreira, Manuel A.R., Bender, David, Maller, Julian, Sklar, Pamela, de Bakker, Paul I.W., Daly, Mark J., Sham, Pak C.

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A multivariate test of association von Ferreira, Manuel A. R., Purcell, Shaun M.

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Association between Microdeletion and Microduplication at 16p11.2 and Autism von Weiss, Lauren A, Shen, Yiping, Korn, Joshua M, Arking, Dan E, Miller, David T, Fossdal, Ragnheidur, Saemundsen, Evald, Stefansson, Hreinn, Stefansson, Kari, Ferreira, Manuel A.R, Green, Todd, Platt, Orah S, Ruderfer, Douglas M, Walsh, Christopher A, Altshuler, David, Chakravarti, Aravinda, Tanzi, Rudolph E, Santangelo, Susan L, Gusella, James F, Sklar, Pamela, Wu, Bai-Lin, Daly, Mark J

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Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct von Ferreira, Manuel A.R., Mathur, Riddhima, Vonk, Judith M., Szwajda, Agnieszka, Brumpton, Ben, Granell, Raquel, Brew, Bronwyn K., Ullemar, Vilhelmina, Lu, Yi, Jiang, Yunxuan, Magnusson, Patrik K.E., Karlsson, Robert, Hinds, David A., Paternoster, Lavinia, Koppelman, Gerard H., Almqvist, Catarina

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Gene Ontology Analysis of GWA Study Data Sets Provides Insights into the Biology of Bipolar Disorder von Holmans, Peter, Green, Elaine K., Pahwa, Jaspreet Singh, Ferreira, Manuel A.R., Purcell, Shaun M., Sklar, Pamela, Owen, Michael J., O'Donovan, Michael C., Craddock, Nick

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Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings von Visscher, Peter M, Medland, Sarah E, Ferreira, Manuel A R, Morley, Katherine I, Zhu, Gu, Cornes, Belinda K, Montgomery, Grant W, Martin, Nicholas G

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Practical aspects of imputation-driven meta-analysis of genome-wide association studies von de Bakker, Paul I.W., Ferreira, Manuel A.R., Jia, Xiaoming, Neale, Benjamin M., Raychaudhuri, Soumya, Voight, Benjamin F.

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Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype von Ferreira, Manuel A.R., PhD, Matheson, Melanie C., PhD, Tang, Clara S., PhD, Granell, Raquel, PhD, Ang, Wei, PhD, Hui, Jennie, PhD, Kiefer, Amy K., PhD, Duffy, David L., PhD, Baltic, Svetlana, PhD, Danoy, Patrick, PhD, Bui, Minh, PhD, Price, Loren, PhD, Sly, Peter D., FRACP, Eriksson, Nicholas, PhD, Madden, Pamela A., PhD, Abramson, Michael J., PhD, Holt, Patrick G., FAA, Heath, Andrew C., DPhil, Hunter, Michael, PhD, Musk, Bill, FRACP, Robertson, Colin F., FRACP, Le Souëf, Peter, FRACP, Montgomery, Grant W., PhD, Henderson, A. John, MD, Tung, Joyce Y., PhD, Dharmage, Shyamali C., PhD, Brown, Matthew A., FRACP, James, Alan, FRACP, Thompson, Philip J., FRACP, Pennell, Craig, PhD, Martin, Nicholas G., PhD, Evans, David M., PhD, Hinds, David A., PhD, Hopper, John L., PhD

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Exome sequencing and analysis of 454,787 UK Biobank participants von Backman, Joshua D., Li, Alexander H., Marcketta, Anthony, Sun, Dylan, Mbatchou, Joelle, Kessler, Michael D., Benner, Christian, Liu, Daren, Locke, Adam E., Balasubramanian, Suganthi, Yadav, Ashish, Banerjee, Nilanjana, Gillies, Christopher E., Damask, Amy, Liu, Simon, Bai, Xiaodong, Hawes, Alicia, Maxwell, Evan, Gurski, Lauren, Watanabe, Kyoko, Kosmicki, Jack A., Rajagopal, Veera, Mighty, Jason, Jones, Marcus, Mitnaul, Lyndon, Stahl, Eli, Coppola, Giovanni, Jorgenson, Eric, Habegger, Lukas, Salerno, William J., Shuldiner, Alan R., Lotta, Luca A., Overton, John D., Cantor, Michael N., Reid, Jeffrey G., Yancopoulos, George, Kang, Hyun M., Marchini, Jonathan, Baras, Aris, Abecasis, Gonçalo R., Ferreira, Manuel A. R.

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10-MDP Based Dental Adhesives: Adhesive Interface Characterization and Adhesive Stability-A Systematic Review von Carrilho, Eunice, Cardoso, Miguel, Marques Ferreira, Manuel, Marto, Carlos Miguel, Paula, Anabela, Coelho, Ana Sofia

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Connecting Circuits for Supraspinal Control of Locomotion von Ferreira-Pinto, Manuel J., Ruder, Ludwig, Capelli, Paolo, Arber, Silvia

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Exome-wide evaluation of rare coding variants using electronic health records identifies new gene–phenotype associations von Park, Joseph, Lucas, Anastasia M., Zhang, Xinyuan, Chaudhary, Kumardeep, Cho, Judy H., Nadkarni, Girish, Dobbyn, Amanda, Chittoor, Geetha, Josyula, Navya S., Katz, Nathan, Breeyear, Joseph H., Ahmadmehrabi, Shadi, Drivas, Theodore G., Chavali, Venkata R. M., Fasolino, Maria, Sawada, Hisashi, Daugherty, Alan, Li, Yanming, Zhang, Chen, Bradford, Yuki, Weaver, JoEllen, Verma, Anurag, Judy, Renae L., Kember, Rachel L., Overton, John D., Reid, Jeffrey G., Ferreira, Manuel A. R., Li, Alexander H., Baras, Aris, LeMaire, Scott A., Shen, Ying H., Naji, Ali, Kaestner, Klaus H., Vahedi, Golnaz, Edwards, Todd L., Chen, Jinbo, Damrauer, Scott M., Justice, Anne E., Do, Ron, Ritchie, Marylyn D., Rader, Daniel J.

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Common and rare variant associations with clonal haematopoiesis phenotypes von Kessler, Michael D., Damask, Amy, O’Keeffe, Sean, Banerjee, Nilanjana, Li, Dadong, Watanabe, Kyoko, Marketta, Anthony, Van Meter, Michael, Semrau, Stefan, Horowitz, Julie, Tang, Jing, Kosmicki, Jack A., Rajagopal, Veera M., Zou, Yuxin, Houvras, Yariv, Ghosh, Arkopravo, Gillies, Christopher, Mbatchou, Joelle, White, Ryan R., Verweij, Niek, Bovijn, Jonas, Parikshak, Neelroop N., LeBlanc, Michelle G., Jones, Marcus, Glass, David J., Lotta, Luca A., Cantor, Michael N., Atwal, Gurinder S., Locke, Adam E., Ferreira, Manuel A. R., Deering, Raquel, Paulding, Charles, Shuldiner, Alan R., Thurston, Gavin, Ferrando, Adolfo A., Salerno, Will, Reid, Jeffrey G., Overton, John D., Marchini, Jonathan, Kang, Hyun M., Baras, Aris, Abecasis, Gonçalo R., Jorgenson, Eric

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Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease von Horowitz, Julie E., Kosmicki, Jack A., Damask, Amy, Sharma, Deepika, Roberts, Genevieve H. L., Justice, Anne E., Banerjee, Nilanjana, Coignet, Marie V., Yadav, Ashish, Leader, Joseph B., Marcketta, Anthony, Park, Danny S., Lanche, Rouel, Maxwell, Evan, Knight, Spencer C., Bai, Xiaodong, Guturu, Harendra, Sun, Dylan, Baltzell, Asher, Kury, Fabricio S. P., Backman, Joshua D., Girshick, Ahna R., O’Dushlaine, Colm, McCurdy, Shannon R., Partha, Raghavendran, Mansfield, Adam J., Turissini, David A., Li, Alexander H., Zhang, Miao, Mbatchou, Joelle, Watanabe, Kyoko, Gurski, Lauren, McCarthy, Shane E., Kang, Hyun M., Dobbyn, Lee, Stahl, Eli, Verma, Anurag, Sirugo, Giorgio, Ritchie, Marylyn D., Jones, Marcus, Balasubramanian, Suganthi, Siminovitch, Katherine, Salerno, William J., Shuldiner, Alan R., Rader, Daniel J., Mirshahi, Tooraj, Locke, Adam E., Marchini, Jonathan, Overton, John D., Carey, David J., Habegger, Lukas, Cantor, Michael N., Rand, Kristin A., Hong, Eurie L., Reid, Jeffrey G., Ball, Catherine A., Baras, Aris, Abecasis, Gonçalo R., Ferreira, Manuel A. R.

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Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans von Medland, Sarah E., Nyholt, Dale R., Painter, Jodie N., McEvoy, Brian P., McRae, Allan F., Zhu, Gu, Gordon, Scott D., Ferreira, Manuel A.R., Wright, Margaret J., Henders, Anjali K., Campbell, Megan J., Duffy, David L., Hansell, Narelle K., Macgregor, Stuart, Slutske, Wendy S., Heath, Andrew C., Montgomery, Grant W., Martin, Nicholas G.

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Chordoma: current concepts, management, and future directions von Walcott, Brian P, Dr, Nahed, Brian V, MD, Mohyeldin, Ahmed, MD, Coumans, Jean-Valery, MD, Kahle, Kristopher T, MD, Ferreira, Manuel J, MD

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Computationally efficient whole-genome regression for quantitative and binary traits von Mbatchou, Joelle, Barnard, Leland, Backman, Joshua, Marcketta, Anthony, Kosmicki, Jack A., Ziyatdinov, Andrey, Benner, Christian, O’Dushlaine, Colm, Barber, Mathew, Boutkov, Boris, Habegger, Lukas, Ferreira, Manuel, Baras, Aris, Reid, Jeffrey, Abecasis, Goncalo, Maxwell, Evan, Marchini, Jonathan

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Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity von Akbari, Parsa, Gilani, Ankit, Sosina, Olukayode, Kosmicki, Jack A, Khrimian, Lori, Fang, Yi-Ya, Persaud, Trikaldarshi, Garcia, Victor, Sun, Dylan, Li, Alexander, Mbatchou, Joelle, Locke, Adam E, Benner, Christian, Verweij, Niek, Lin, Nan, Hossain, Sakib, Agostinucci, Kevin, Pascale, Jonathan V, Dirice, Ercument, Dunn, Michael, Kraus, William E, Shah, Svati H, Chen, Yii-Der I, Rotter, Jerome I, Rader, Daniel J, Melander, Olle, Still, Christopher D, Mirshahi, Tooraj, Carey, David J, Berumen-Campos, Jaime, Kuri-Morales, Pablo, Alegre-Díaz, Jesus, Torres, Jason M, Emberson, Jonathan R, Collins, Rory, Balasubramanian, Suganthi, Hawes, Alicia, Jones, Marcus, Zambrowicz, Brian, Murphy, Andrew J, Paulding, Charles, Coppola, Giovanni, Overton, John D, Reid, Jeffrey G, Shuldiner, Alan R, Cantor, Michael, Kang, Hyun M, Abecasis, Goncalo R, Karalis, Katia, Economides, Aris N, Marchini, Jonathan, Yancopoulos, George D, Sleeman, Mark W, Altarejos, Judith, Della Gatta, Giusy, Tapia-Conyer, Roberto, Schwartzman, Michal L, Baras, Aris, Ferreira, Manuel A R, Lotta, Luca A

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Integration of management systems: towards a sustained success and development of organizations von Rebelo, Manuel Ferreira, Santos, Gilberto, Silva, Rui

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Common variants in TMPRSS6 are associated with iron status and erythrocyte volume von Benyamin, Beben, Ferreira, Manuel A R, Willemsen, Gonneke, Gordon, Scott, Middelberg, Rita P S, McEvoy, Brian P, Hottenga, Jouke-Jan, Henders, Anjali K, Campbell, Megan J, Wallace, Leanne, Frazer, Ian H, Heath, Andrew C, de Geus, Eco J C, Nyholt, Dale R, Visscher, Peter M, Penninx, Brenda W, Boomsma, Dorret I, Martin, Nicholas G, Montgomery, Grant W, Whitfield, John B

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