Genome-wide association study of susceptibility to hospitalised respiratory infections von Williams, Alexander T., Shrine, Nick, Naghra-van Gijzel, Hardeep, Betts, Joanna C., Hessel, Edith M., John, Catherine, Packer, Richard, Reeve, Nicola F., Yeo, Astrid J., Abner, Erik, Åsvold, Bjørn Olav, Auvinen, Juha, Bartz, Traci M., Bradford, Yuki, Brumpton, Ben, Campbell, Archie, Cho, Michael H., Chu, Su, Crosslin, David R., Feng, QiPing, Esko, Tõnu, Gharib, Sina A., Hayward, Caroline, Hebbring, Scott, Hveem, Kristian, Jarvelin, Marjo-Riitta, Jarvik, Gail P., Landis, Sarah H., Larson, Eric B., Liu, Jiangyuan, Loos, Ruth J.F., Luo, Yuan, Moscati, Arden, Mullerova, Hana, Namjou, Bahram, Porteous, David J., Quint, Jennifer K., Ritchie, Marylyn D., Sliz, Eeva, Stanaway, Ian B., Thomas, Laurent, Wilson, James F., Hall, Ian P., Wain, Louise V., Michalovich, David, Tobin, Martin D.

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Genome-wide association study of susceptibility to hospitalised respiratory infections von Williams, Alexander T, Shrine, Nick, Naghra-van Gijzel, Hardeep, Betts, Joanna C, Chen, Jing, Hessel, Edith M, John, Catherine, Packer, Richard, Reeve, Nicola F, Yeo, Astrid J, Abner, Erik, Åsvold, Bjørn Olav, Auvinen, Juha, Bartz, Traci M, Bradford, Yuki, Brumpton, Ben, Campbell, Archie, Cho, Michael H, Chu, Su, Crosslin, David R, Feng, QiPing, Esko, Tõnu, Gharib, Sina A, Hayward, Caroline, Hebbring, Scott, Hveem, Kristian, Järvelin, Marjo-Riitta, Jarvik, Gail P, Landis, Sarah H, Larson, Eric B, Liu, Jiangyuan, Loos, Ruth J F, Luo, Yuan, Moscati, Arden, Mullerova, Hana, Namjou, Bahram, Porteous, David J, Quint, Jennifer K, Ritchie, Marylyn D, Sliz, Eeva, Stanaway, Ian B, Thomas, Laurent, Wilson, James F, Hall, Ian P, Wain, Louise V, Michalovich, David, Tobin, Martin D

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Williams_et_al_extended_data von Williams, Alexander, Shrine, Nick, Naghra-van Gijzel, Hardeep, Betts, Joanna, Chen, Jing, Hessel, Edith, John, Catherine, Packer, Richard, Reeve, Nicola, Yeo, Astrid, Abner, Erik, Åsvold, Bjørn Olav, Auvinen, Juha, Bartz, Traci, Bradford, Yuki, Brumpton, Ben, Campbell, Archie, Cho, Michael, Chu, Su, Crosslin, David, Feng, QiPing, Esko, Tõnu, Gharib, Sina, Hayward, Caroline, Hebbring, Scott, Hveem, Kristian, Jarvelin, Marjo-Riitta, Jarvik, Gail, Landis, Sarah, Larson, Eric, Liu, Jiangyuan, Loos, Ruth, luo, yuan, Moscati, Arden, Mullerova, Hana, Namjou, Bahram, Porteous, David, Quint, Jennifer, Regeneron Genomics Center, Ritchie, Marylyn, Sliz, Eeva, Stanaway, Ian, Thomas, Laurent, Wilson, James, Hall, Ian, Wain, Louise, Michalovich, David, Tobin, Martin

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WilliamsAT_prePMID_HRI.tsv.gz von Williams, Alexander, Shrine, Nick, Naghra-van Gijzel, Hardeep, Betts, Joanna, Hessel, Edith, John, Catherine, Packer, Richard, Reeve, Nicola, Yeo, Astrid, Abner, Erik, Åsvold, Bjørn Olav, Auvinen, Juha, Bartz, Traci, Bradford, Yuki, Brumpton, Ben, Campbell, Archie, Cho, Michael, Chu, Su, Crosslin, David, Feng, QiPing, Esko, Tõnu, Gharib, Sina, Hayward, Caroline, Hebbring, Scott, Hveem, Kristian, Jarvelin, Marjo-Riitta, Jarvik, Gail, Landis, Sarah, Larson, Eric, Liu, Jiangyuan, Loos, Ruth, luo, yuan, Moscati, Arden, Mullerova, Hana, Namjou, Bahram, Porteous, David, Quint, Jennifer, Regeneron Genomics Center, Ritchie, Marylyn, Sliz, Eeva, Stanaway, Ian, Thomas, Laurent, Wilson, James, Hall, Ian, Wain, Louise, Michalovich, David, Tobin, Martin

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Toward a fine-scale population health monitoring system von Belbin, Gillian M., Cullina, Sinead, Wenric, Stephane, Soper, Emily R., Glicksberg, Benjamin S., Torre, Denis, Moscati, Arden, Wojcik, Genevieve L., Shemirani, Ruhollah, Beckmann, Noam D., Cohain, Ariella, Sorokin, Elena P., Park, Danny S., Ambite, Jose-Luis, Ellis, Steve, Auton, Adam, Bottinger, Erwin P., Cho, Judy H., Loos, Ruth J.F., Abul-Husn, Noura S., Zaitlen, Noah A., Gignoux, Christopher R., Kenny, Eimear E.

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Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank von Abul-Husn, Noura S, Soper, Emily R, Odgis, Jacqueline A, Cullina, Sinead, Bobo, Dean, Moscati, Arden, Rodriguez, Jessica E, Loos, Ruth J F, Cho, Judy H, Belbin, Gillian M, Suckiel, Sabrina A, Kenny, Eimear E

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Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis von Ghouse, Jonas, Sveinbjörnsson, Gardar, Vujkovic, Marijana, Seidelin, Anne-Sofie, Gellert-Kristensen, Helene, Ahlberg, Gustav, Tragante, Vinicius, Rand, Søren A., Brancale, Joseph, Vilarinho, Silvia, Lundegaard, Pia Rengtved, Sørensen, Erik, Erikstrup, Christian, Bruun, Mie Topholm, Jensen, Bitten Aagaard, Brunak, Søren, Banasik, Karina, Ullum, Henrik, Verweij, Niek, Lotta, Luca, Baras, Aris, Mirshahi, Tooraj, Carey, David J., Kaplan, David E., Lynch, Julie, Morgan, Timothy, Schwantes-An, Tae-Hwi, Dochtermann, Daniel R., Pyarajan, Saiju, Tsao, Philip S., Laisk, Triin, Mägi, Reedik, Kozlitina, Julia, Tybjærg-Hansen, Anne, Jones, David, Knowlton, Kirk U., Nadauld, Lincoln, Ferkingstad, Egil, Björnsson, Einar S., Ulfarsson, Magnus O., Sturluson, Árni, Sulem, Patrick, Pedersen, Ole B., Ostrowski, Sisse R., Gudbjartsson, Daniel F., Stefansson, Kari, Olesen, Morten Salling, Chang, Kyong-Mi, Holm, Hilma, Bundgaard, Henning, Stender, Stefan

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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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Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target von Roychowdhury, Tanmoy, Klarin, Derek, Levin, Michael G., Spin, Joshua M., Rhee, Yae Hyun, Deng, Alicia, Headley, Colwyn A., Tsao, Noah L., Gellatly, Corry, Zuber, Verena, Shen, Fred, Hornsby, Whitney E., Laursen, Ina Holst, Verma, Shefali S., Locke, Adam E., Einarsson, Gudmundur, Thorleifsson, Gudmar, Graham, Sarah E., Dikilitas, Ozan, Pattee, Jack W., Judy, Renae L., Pauls-Verges, Ferran, Nielsen, Jonas B., Wolford, Brooke N., Brumpton, Ben M., Dilmé, Jaume, Peypoch, Olga, Juscafresa, Laura Calsina, Edwards, Todd L., Li, Dadong, Banasik, Karina, Brunak, Søren, Jacobsen, Rikke L., Garcia-Barrio, Minerva T., Zhang, Jifeng, Rasmussen, Lars M., Lee, Regent, Handa, Ashok, Wanhainen, Anders, Mani, Kevin, Lindholt, Jes S., Obel, Lasse M., Strauss, Ewa, Oszkinis, Grzegorz, Nelson, Christopher P., Saxby, Katie L., van Herwaarden, Joost A., van der Laan, Sander W., van Setten, Jessica, Camacho, Mercedes, Davis, Frank M., Wasikowski, Rachael, Tsoi, Lam C., Gudjonsson, Johann E., Eliason, Jonathan L., Coleman, Dawn M., Henke, Peter K., Ganesh, Santhi K., Chen, Y. Eugene, Guan, Weihua, Pankow, James S., Pankratz, Nathan, Pedersen, Ole B., Erikstrup, Christian, Tang, Weihong, Hveem, Kristian, Gudbjartsson, Daniel, Gretarsdottir, Solveig, Thorsteinsdottir, Unnur, Holm, Hilma, Stefansson, Kari, Ferreira, Manuel A., Baras, Aris, Kullo, Iftikhar J., Ritchie, Marylyn D., Christensen, Alex H., Iversen, Kasper K., Eldrup, Nikolaj, Sillesen, Henrik, Ostrowski, Sisse R., Bundgaard, Henning, Ullum, Henrik, Burgess, Stephen, Gill, Dipender, Gallagher, Katherine, Sabater-Lleal, Maria, Surakka, Ida, Jones, Gregory T., Bown, Matthew J., Tsao, Philip S., Willer, Cristen J., Damrauer, Scott M.

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Plasma proteomic associations with genetics and health in the UK Biobank von Sun, Benjamin B., Chiou, Joshua, Traylor, Matthew, Benner, Christian, Hsu, Yi-Hsiang, Richardson, Tom G., Surendran, Praveen, Mahajan, Anubha, Robins, Chloe, Vasquez-Grinnell, Steven G., Hou, Liping, Kvikstad, Erika M., Burren, Oliver S., Davitte, Jonathan, Ferber, Kyle L., Gillies, Christopher E., Hedman, Åsa K., Hu, Sile, Lin, Tinchi, Mikkilineni, Rajesh, Pendergrass, Rion K., Pickering, Corran, Prins, Bram, Baird, Denis, Chen, Chia-Yen, Ward, Lucas D., Deaton, Aimee M., Welsh, Samantha, Willis, Carissa M., Lehner, Nick, Arnold, Matthias, Wörheide, Maria A., Suhre, Karsten, Kastenmüller, Gabi, Sethi, Anurag, Cule, Madeleine, Raj, Anil, Burkitt-Gray, Lucy, Melamud, Eugene, Black, Mary Helen, Fauman, Eric B., Howson, Joanna M. M., Kang, Hyun Min, McCarthy, Mark I., Nioi, Paul, Petrovski, Slavé, Scott, Robert A., Smith, Erin N., Szalma, Sándor, Waterworth, Dawn M., Mitnaul, Lyndon J., Szustakowski, Joseph D., Gibson, Bradford W., Miller, Melissa R., Whelan, Christopher D.

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Derivation and Validation of Genome-Wide Polygenic Score for Ischemic Heart Failure von Paranjpe, Ishan, Tsao, Noah L, De Freitas, Jessica K, Judy, Renae, Chaudhary, Kumardeep, Forrest, Iain S, Jaladanki, Suraj K, Paranjpe, Manish, Sharma, Pranav, Glicksberg, Benjamin S, Narula, Jagat, Do, Ron, Damrauer, Scott M, Nadkarni, Girish N

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Germline Exome Sequencing for Men with Testicular Germ Cell Tumor Reveals Coding Defects in Chromosomal Segregation and Protein-targeting Genes von Pyle, Louise C., Kim, Jung, Bradfield, Jonathan, Damrauer, Scott M., D'Andrea, Kurt, Einhorn, Lawrence H., Godse, Rama, Hakonarson, Hakon, Kanetsky, Peter A., Kember, Rachel L., Jacobs, Linda A., Maxwell, Kara N., Rader, Daniel J., Vaughn, David J., Weathers, Benita, Wubbenhorst, Bradley, Regeneron Genetics Center Research Team, Cancer Genomics Research Laboratory, Greene, Mark H., Nathanson, Katherine L., Stewart, Douglas R.

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High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease von Tcheandjieu, Catherine, Xiao, Ke, Tejeda, Helio, Lynch, Julie A., Ruotsalainen, Sanni, Bellomo, Tiffany, Palnati, Madhuri, Judy, Renae, Klarin, Derek, Kember, Rachel L., Verma, Shefali, Palotie, Aarno, Daly, Mark, Ritchie, Marylyn, Rader, Daniel J., Rivas, Manuel A., Assimes, Themistocles, Tsao, Philip, Damrauer, Scott, Priest, James R.

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