Brain injury, endothelial injury and inflammatory markers are elevated and express sex-specific alterations after COVID-19 von Savarraj, Jude, Park, Eun S., Colpo, Gabriela D., Hinds, Sarah N., Morales, Diego, Ahnstedt, Hilda, Paz, Atzhiry S., Assing, Andres, Liu, Fudong, Juneja, Shivanki, Kim, Eunhee, Cho, Sung-Min, Gusdon, Aaron M., Dash, Pramod, McCullough, Louise D., Choi, H. Alex

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Pain and Other Neurological Symptoms Are Present at 3 Months After Hospitalization in COVID-19 Patients von Savarraj, Jude P J, Burkett, Angela B, Hinds, Sarah N, Paz, Atzhiry S, Assing, Andres, Juneja, Shivanki, Colpo, Gabriela D, Torres, Luis F, Cho, Sung-Min, Gusdon, Aaron M, McCullough, Louise D, Choi, H Alex

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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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Genetic determinants of daytime napping and effects on cardiometabolic health von Dashti, Hassan S., Daghlas, Iyas, Lane, Jacqueline M., Huang, Yunru, Udler, Miriam S., Wang, Heming, Ollila, Hanna M., Jones, Samuel E., Kim, Jaegil, Wood, Andrew R., Weedon, Michael N., Aslibekyan, Stella, Garaulet, Marta, Saxena, Richa

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Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition von Warrier, V, Grasby, K L, Uzefovsky, F, Toro, R, Smith, P, Chakrabarti, B, Khadake, J, Mawbey-Adamson, E, Litterman, N, Hottenga, J-J, Lubke, G, Boomsma, D I, Martin, N G, Hatemi, P K, Medland, S E, Hinds, D A, Bourgeron, T, Baron-Cohen, S

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Research Priorities in Pediatric Palliative Care von Baker, Justin N., MD, Levine, Deena R., MD, Hinds, Pamela S., PhD, RN, FAAN, Weaver, Meaghann S., MD, Cunningham, Melody J., MD, Johnson, Liza, MD, Anghelescu, Doralina, MD, Mandrell, Belinda, PhD, Gibson, Deborah V., MA, Jones, Barbara, MSW, Wolfe, Joanne, MD, Feudtner, Chris, MD, PhD, MPH, Friebert, Sarah, MD, Carter, Brian, MD, Kane, Javier R., MD

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Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals von Okbay, Aysu, Wu, Yeda, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Nehzati, Seyed Moeen, Sidorenko, Julia, Kweon, Hyeokmoon, Goldman, Grant, Gjorgjieva, Tamara, Jiang, Yunxuan, Hicks, Barry, Tian, Chao, Hinds, David A., Ahlskog, Rafael, Magnusson, Patrik K. E., Oskarsson, Sven, Hayward, Caroline, Campbell, Archie, Porteous, David J., Freese, Jeremy, Herd, Pamela, Watson, Chelsea, Jala, Jonathan, Conley, Dalton, Koellinger, Philipp D., Johannesson, Magnus, Laibson, David, Meyer, Michelle N., Lee, James J., Kong, Augustine, Yengo, Loic, Cesarini, David, Turley, Patrick, Visscher, Peter M., Beauchamp, Jonathan P., Benjamin, Daniel J., Young, Alexander I.

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Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology von Ferreira, Manuel A, Vonk, Judith M, Baurecht, Hansjörg, Marenholz, Ingo, Tian, Chao, Hoffman, Joshua D, Helmer, Quinta, Tillander, Annika, Ullemar, Vilhelmina, van Dongen, Jenny, Lu, Yi, Rüschendorf, Franz, Esparza-Gordillo, Jorge, Medway, Chris W, Mountjoy, Edward, Burrows, Kimberley, Hummel, Oliver, Grosche, Sarah, Brumpton, Ben M, Witte, John S, Hottenga, Jouke-Jan, Willemsen, Gonneke, Zheng, Jie, Rodríguez, Elke, Hotze, Melanie, Franke, Andre, Revez, Joana A, Beesley, Jonathan, Matheson, Melanie C, Dharmage, Shyamali C, Bain, Lisa M, Fritsche, Lars G, Gabrielsen, Maiken E, Balliu, Brunilda, Nielsen, Jonas B, Zhou, Wei, Hveem, Kristian, Langhammer, Arnulf, Holmen, Oddgeir L, Løset, Mari, Abecasis, Gonçalo R, Willer, Cristen J, Arnold, Andreas, Homuth, Georg, Schmidt, Carsten O, Thompson, Philip J, Martin, Nicholas G, Duffy, David L, Novak, Natalija, Schulz, Holger, Karrasch, Stefan, Gieger, Christian, Strauch, Konstantin, Melles, Ronald B, Hinds, David A, Hübner, Norbert, Weidinger, Stephan, Magnusson, Patrik K E, Jansen, Rick, Jorgenson, Eric, Lee, Young-Ae, Boomsma, Dorret I, Almqvist, Catarina, Karlsson, Robert, Koppelman, Gerard H, Paternoster, Lavinia

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Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders von Eijsbouts, Chris, Zheng, Tenghao, Kennedy, Nicholas A., Bonfiglio, Ferdinando, Anderson, Carl A., Moutsianas, Loukas, Holliday, Joanne, Shi, Jingchunzi, Shringarpure, Suyash, Voda, Alexandru-Ioan, Farrugia, Gianrico, Franke, Andre, Hübenthal, Matthias, Abecasis, Gonçalo, Zawistowski, Matthew, Skogholt, Anne Heidi, Ness-Jensen, Eivind, Hveem, Kristian, Esko, Tõnu, Teder-Laving, Maris, Zhernakova, Alexandra, Camilleri, Michael, Boeckxstaens, Guy, Whorwell, Peter J., Spiller, Robin, McVean, Gil, D’Amato, Mauro, Jostins, Luke, Parkes, Miles

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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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Author Correction: 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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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease von Nalls, Mike A, Pankratz, Nathan, Lill, Christina M, Do, Chuong B, Hernandez, Dena G, Saad, Mohamad, DeStefano, Anita L, Kara, Eleanna, Bras, Jose, Sharma, Manu, Schulte, Claudia, Keller, Margaux F, Arepalli, Sampath, Letson, Christopher, Edsall, Connor, Stefansson, Hreinn, Liu, Xinmin, Pliner, Hannah, Lee, Joseph H, Cheng, Rong, Ikram, M Arfan, Ioannidis, John P A, Hadjigeorgiou, Georgios M, Bis, Joshua C, Martinez, Maria, Perlmutter, Joel S, Goate, Alison, Marder, Karen, Fiske, Brian, Sutherland, Margaret, Xiromerisiou, Georgia, Myers, Richard H, Clark, Lorraine N, Stefansson, Kari, Hardy, John A, Heutink, Peter, Chen, Honglei, Wood, Nicholas W, Houlden, Henry, Payami, Haydeh, Brice, Alexis, Scott, William K, Gasser, Thomas, Bertram, Lars, Eriksson, Nicholas, Foroud, Tatiana, Singleton, Andrew B

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Resource profile and user guide of the Polygenic Index Repository von Becker, Joel, Burik, Casper A. P., Goldman, Grant, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Belsky, Daniel W., Karlsson Linnér, Richard, Ahlskog, Rafael, Kleinman, Aaron, Hinds, David A., Caspi, Avshalom, Corcoran, David L., Moffitt, Terrie E., Poulton, Richie, Sugden, Karen, Williams, Benjamin S., Harris, Kathleen Mullan, Steptoe, Andrew, Ajnakina, Olesya, Milani, Lili, Esko, Tõnu, Iacono, William G., McGue, Matt, Magnusson, Patrik K. E., Mallard, Travis T., Harden, K. Paige, Tucker-Drob, Elliot M., Herd, Pamela, Freese, Jeremy, Young, Alexander, Beauchamp, Jonathan P., Koellinger, Philipp D., Oskarsson, Sven, Johannesson, Magnus, Visscher, Peter M., Meyer, Michelle N., Laibson, David, Cesarini, David, Benjamin, Daniel J., Turley, Patrick, Okbay, Aysu

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Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error von Tedja, Milly S., Wojciechowski, Robert, Hysi, Pirro G., Eriksson, Nicholas, Furlotte, Nicholas A., Verhoeven, Virginie J. M., Iglesias, Adriana I., Meester-Smoor, Magda A., Tompson, Stuart W., Fan, Qiao, Khawaja, Anthony P., Cheng, Ching-Yu, Höhn, René, Yamashiro, Kenji, Wenocur, Adam, Grazal, Clare, Haller, Toomas, Metspalu, Andres, Wedenoja, Juho, Jonas, Jost B., Wang, Ya Xing, Xie, Jing, Mitchell, Paul, Foster, Paul J., Klein, Barbara E. K., Klein, Ronald, Paterson, Andrew D., Hosseini, S. Mohsen, Shah, Rupal L., Williams, Cathy, Teo, Yik Ying, Tham, Yih Chung, Gupta, Preeti, Zhao, Wanting, Shi, Yuan, Saw, Woei-Yuh, Tai, E-Shyong, Sim, Xue Ling, Huffman, Jennifer E., Polašek, Ozren, Hayward, Caroline, Bencic, Goran, Rudan, Igor, Wilson, James F., Joshi, Peter K., Tsujikawa, Akitaka, Matsuda, Fumihiko, Whisenhunt, Kristina N., Zeller, Tanja, van der Spek, Peter J., Haak, Roxanna, Meijers-Heijboer, Hanne, van Leeuwen, Elisabeth M., Iyengar, Sudha K., Lass, Jonathan H., Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, André G., Vingerling, Johannes R., Lehtimäki, Terho, Raitakari, Olli T., Biino, Ginevra, Concas, Maria Pina, Schwantes-An, Tae-Hwi, Igo, Robert P., Cuellar-Partida, Gabriel, Martin, Nicholas G., Craig, Jamie E., Gharahkhani, Puya, Williams, Katie M., Nag, Abhishek, Rahi, Jugnoo S., Cumberland, Phillippa M., Delcourt, Cécile, Bellenguez, Céline, Ried, Janina S., Bergen, Arthur A., Meitinger, Thomas, Gieger, Christian, Wong, Tien Yin, Hewitt, Alex W., Mackey, David A., Simpson, Claire L., Pfeiffer, Norbert, Pärssinen, Olavi, Baird, Paul N., Vitart, Veronique, Amin, Najaf, van Duijn, Cornelia M., Bailey-Wilson, Joan E., Young, Terri L., Saw, Seang-Mei, Stambolian, Dwight, MacGregor, Stuart, Guggenheim, Jeremy A., Tung, Joyce Y., Hammond, Christopher J., Klaver, Caroline C. W.

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Microarrays Reveal that Each of the Ten Dominant Lineages of Staphylococcus aureus Has a Unique Combination of Surface-Associated and Regulatory Genes von Lindsay, Jodi A, Moore, Catrin E, Day, Nicholas P, Peacock, Sharon J, Witney, Adam A, Stabler, Richard A, Husain, Sarah E, Butcher, Philip D, Hinds, Jason

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Inclusion of a core patient-reported outcomes battery in adolescent and young adult cancer clinical trials von Roth, Michael E, Parsons, Susan K, Ganz, Patricia A, Wagner, Lynne I, Hinds, Pamela S, Alexander, Sarah, Bingen, Kristin, Bober, Sharon L, Brackett, Julienne, Cella, David, Henry, N Lynn, Indelicato, Daniel J, Johnson, Rebecca H, Miller, Tamara P, Rosenberg, Shoshana M, Schmitz, Kathryn H, Thanarajasingam, Gita, Reeve, Bryce B, Salsman, John M

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Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries von Gharahkhani, Puya, Jorgenson, Eric, Hysi, Pirro, Khawaja, Anthony P., Pendergrass, Sarah, Han, Xikun, Ong, Jue Sheng, Hewitt, Alex W., Segrè, Ayellet V., Rouhana, John M., Hamel, Andrew R., Igo, Robert P., Choquet, Helene, Qassim, Ayub, Josyula, Navya S., Cooke Bailey, Jessica N., Bonnemaijer, Pieter W. M., Iglesias, Adriana, Siggs, Owen M., Young, Terri L., Vitart, Veronique, Thiadens, Alberta A. H. J., Karjalainen, Juha, Uebe, Steffen, Melles, Ronald B., Nair, K. Saidas, Luben, Robert, Simcoe, Mark, Amersinghe, Nishani, Cree, Angela J., Hohn, Rene, Poplawski, Alicia, Chen, Li Jia, Rong, Shi-Song, Aung, Tin, Vithana, Eranga Nishanthie, Tamiya, Gen, Shiga, Yukihiro, Yamamoto, Masayuki, Nakazawa, Toru, Currant, Hannah, Birney, Ewan, Wang, Xin, Auton, Adam, Lupton, Michelle K., Martin, Nicholas G., Ashaye, Adeyinka, Olawoye, Olusola, Williams, Susan E., Akafo, Stephen, Ramsay, Michele, Hashimoto, Kazuki, Kamatani, Yoichiro, Akiyama, Masato, Momozawa, Yukihide, Foster, Paul J., Khaw, Peng T., Morgan, James E., Strouthidis, Nicholas G., Kraft, Peter, Kang, Jae H., Pang, Chi Pui, Pasutto, Francesca, Mitchell, Paul, Lotery, Andrew J., Palotie, Aarno, van Duijn, Cornelia, Haines, Jonathan L., Hammond, Chris, Pasquale, Louis R., Klaver, Caroline C. W., Hauser, Michael, Khor, Chiea Chuen, Mackey, David A., Kubo, Michiaki, Cheng, Ching-Yu, Craig, Jamie E., MacGregor, Stuart, Wiggs, Janey L.

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Genome-wide association study of musical beat synchronization demonstrates high polygenicity von Niarchou, Maria, Gustavson, Daniel E., Sathirapongsasuti, J. Fah, Anglada-Tort, Manuel, Eising, Else, Bell, Eamonn, McArthur, Evonne, Straub, Peter, McAuley, J. Devin, Capra, John A., Ullén, Fredrik, Creanza, Nicole, Mosing, Miriam A., Hinds, David A., Davis, Lea K., Jacoby, Nori, Gordon, Reyna L.

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Genome-wide association study identifies 74 loci associated with educational attainment von Turley, Patrick, Chen, Guo-Bo, Emilsson, Valur, Meddens, S. Fleur W., Thom, Kevin, Timshel, Pascal, Bacelis, Jonas, Baumbach, Clemens, Girotto, Giorgia, Gupta, Richa, Hofer, Edith, Horikoshi, Momoko, Lind, Penelope A., Mangino, Massimo, Marten, Jonathan, Pervjakova, Natalia, Peyrot, Wouter J., Qian, Yong, Schmidt, Börge, Schraut, Katharina E., Teumer, Alexander, Westra, Harm-Jan, Alizadeh, Behrooz Z., Bakshi, Andrew, Baumeister, Sebastian E., Bønnelykke, Klaus, Boyle, Patricia A., Davies, Gail, De Neve, Jan-Emmanuel, Demuth, Ilja, Ding, Jun, Eisele, Lewin, Eklund, Niina, Faul, Jessica D., Forstner, Andreas J., Gunnarsson, Bjarni, Halldórsson, Bjarni V., Heath, Andrew C., Hocking, Lynne J., Hottenga, Jouke-Jan, de Jager, Philip L., Joshi, Peter K., Kaakinen, Marika A., Kiemeney, Lambertus A. L. M., Koskinen, Seppo, Kraja, Aldi T., Kroh, Martin, Lichtenstein, Paul, Lichtner, Peter, Liewald, David C. M., Loukola, Anu, Madden, Pamela A., Mäki-Opas, Tomi, Marioni, Riccardo E., Marques-Vidal, Pedro, Meddens, Gerardus A., Meisinger, Christa, Montgomery, Grant W., Nyholt, Dale R., Ollier, William E. R., Pedersen, Nancy L., Robino, Antonietta, Rostapshova, Olga, Sanders, Alan R., Sarin, Antti-Pekka, Terracciano, Antonio, Tobin, Martin D., Ulivi, Sheila, van Rooij, Frank J. A., Venturini, Cristina, Vinkhuyzen, Anna A. E., Vonk, Judith M., Vozzi, Diego, Ware, Erin B., Berger, Klaus, Chabris, Christopher F., Cucca, Francesco, Deary, Ian J., Dedoussis, George V., Groenen, Patrick J. F., Hinds, David A., Kaprio, Jaakko, Magnusson, Patrik K. E., Metspalu, Andres, Perola, Markus, Samani, Nilesh J., Schlessinger, David, Schmidt, Reinhold, Sørensen, Thorkild I. A., Spector, Tim D., Stefansson, Kari, Thorsteinsdottir, Unnur, Tiemeier, Henning, Weir, David R., Krueger, Robert F., Hofman, Albert, Meyer, Michelle N., Visscher, Peter M., Esko, Tõnu, Koellinger, Philipp D.

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Age-of-onset information helps identify 76 genetic variants associated with allergic disease von Ferreira, Manuel A. R., Vonk, Judith M., Baurecht, Hansjoerg, Marenholz, Ingo, Tian, Chao, Hoffman, Joshua D., Helmer, Quinta, Tillander, Annika, Ullemar, Vilhelmina, Lu, Yi, Grosche, Sarah, Rueschendorf, Franz, Granell, Raquel, Brumpton, Ben M., Fritsche, Lars G., Bhatta, Laxmi, Gabrielsen, Maiken E., Nielsen, Jonas B., Zhou, Wei, Hveem, Kristian, Langhammer, Arnulf, Holmen, Oddgeir L., Loset, Mari, Abecasis, Goncalo R., Willer, Cristen J., Emami, Nima C., Cavazos, Taylor B., Witte, John S., Szwajda, Agnieszka, Hinds, David A., Huebner, Norbert, Weidinger, Stephan, Magnusson, Patrik K. E., Jorgenson, Eric, Karlsson, Robert, Paternoster, Lavinia, Boomsma, Dorret, Almqvist, Catarina, Lee, Young-Ae, Koppelman, Gerard H.

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