Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia von Hysi, Pirro G., Choquet, Hélène, Khawaja, Anthony P., Wojciechowski, Robert, Tedja, Milly S., Yin, Jie, Simcoe, Mark J., Patasova, Karina, Mahroo, Omar A., Thai, Khanh K., Cumberland, Phillippa M., Melles, Ronald B., Verhoeven, Virginie J. M., Vitart, Veronique, Segre, Ayellet, Stone, Richard A., Wareham, Nick, Hewitt, Alex W., Mackey, David A., Klaver, Caroline C. W., MacGregor, Stuart, Khaw, Peng T., Foster, Paul J., Guggenheim, Jeremy A., Rahi, Jugnoo S., Jorgenson, Eric, Hammond, Christopher J.

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Inhaler competence in asthma: Common errors, barriers to use and recommended solutions von Price, D, Bosnic-Anticevich, S, Briggs, A, Chrystyn, H, Rand, C, Scheuch, G, Bousquet, J

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Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error von Fan, Qiao, Verhoeven, Virginie J. M., Wojciechowski, Robert, Barathi, Veluchamy A., Hysi, Pirro G., Guggenheim, Jeremy A., Höhn, René, Vitart, Veronique, Khawaja, Anthony P., Yamashiro, Kenji, Hosseini, S Mohsen, Lehtimäki, Terho, Lu, Yi, Haller, Toomas, Xie, Jing, Delcourt, Cécile, Pirastu, Mario, Wedenoja, Juho, Gharahkhani, Puya, Venturini, Cristina, Miyake, Masahiro, Hewitt, Alex W., Guo, Xiaobo, Mazur, Johanna, Huffman, Jenifer E., Williams, Katie M., Polasek, Ozren, Campbell, Harry, Rudan, Igor, Vatavuk, Zoran, Wilson, James F., Joshi, Peter K., McMahon, George, St Pourcain, Beate, Evans, David M., Simpson, Claire L., Schwantes-An, Tae-Hwi, Igo, Robert P., Mirshahi, Alireza, Bellenguez, Céline, Blettner, Maria, Raitakari, Olli, Kähönen, Mika, Seppälä, Ilkka, Zeller, Tanja, Meitinger, Thomas, Ried, Janina S., Gieger, Christian, Portas, Laura, van Leeuwen, Elisabeth M., Amin, Najaf, Uitterlinden, André G., Rivadeneira, Fernando, Hofman, Albert, Vingerling, Johannes R., Wang, Ya Xing, Wang, Xu, Tai-Hui Boh, Eileen, Ikram, M. Kamran, Sabanayagam, Charumathi, Gupta, Preeti, Tan, Vincent, Zhou, Lei, Ho, Candice E. H., Lim, Wan’e, Beuerman, Roger W., Siantar, Rosalynn, Tai, E-Shyong, Vithana, Eranga, Mihailov, Evelin, Khor, Chiea-Chuen, Hayward, Caroline, Luben, Robert N., Foster, Paul J., Klein, Barbara E. K., Klein, Ronald, Wong, Hoi-Suen, Metspalu, Andres, Aung, Tin, Young, Terri L., He, Mingguang, Pärssinen, Olavi, van Duijn, Cornelia M., Jin Wang, Jie, Williams, Cathy, Jonas, Jost B., Teo, Yik-Ying, Mackey, David A., Oexle, Konrad, Yoshimura, Nagahisa, Paterson, Andrew D., Pfeiffer, Norbert, Wong, Tien-Yin, Baird, Paul N., Stambolian, Dwight, Wilson, Joan E. Bailey, Cheng, Ching-Yu, Hammond, Christopher J., Klaver, Caroline C. W., Saw, Seang-Mei

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Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel von Angelucci, Emanuele, Matthes-Martin, Susanne, Baronciani, Donatella, Bernaudin, Françoise, Bonanomi, Sonia, Cappellini, Maria Domenica, Dalle, Jean-Hugues, Di Bartolomeo, Paolo, de Heredia, Cristina Díaz, Dickerhoff, Roswitha, Giardini, Claudio, Gluckman, Eliane, Hussein, Ayad Achmed, Kamani, Naynesh, Minkov, Milen, Locatelli, Franco, Rocha, Vanderson, Sedlacek, Petr, Smiers, Frans, Thuret, Isabelle, Yaniv, Isaac, Cavazzana, Marina, Peters, Christina

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The Surveillance Error Grid von Klonoff, David C., Lias, Courtney, Vigersky, Robert, Clarke, William, Parkes, Joan Lee, Sacks, David B., Kirkman, M. Sue, Kovatchev, Boris, Aurand, Lisa, Benson, Carol, Bernhardt, Patricia, Blonde, Lawrence, Breton, Mark, Buckingham, Bruce, Cariski, Alan, Colburn, Scott, Flacke, Frank, Harrison, Bern, Herman, Carol, Hinzmann, Rolf, Johnson-Lyles, Denise, Karinka, Shridhara Alva, Landree, Leslie, Lebinger, Tessa, Lee, Scott, Mastrototaro, John, Peyser, Tom, Phillips, Stephen, Pinkos, Arleen, Price, David, Scott, Steve, Serrano, Katherine, Simmons, David

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Coronavirus disease 2019 in patients with inborn errors of immunity: An international study von Meyts, Isabelle, Bucciol, Giorgia, Quinti, Isabella, Neven, Bénédicte, Fischer, Alain, Seoane, Elena, Lopez-Granados, Eduardo, Gianelli, Carla, Robles-Marhuenda, Angel, Jeandel, Pierre-Yves, Paillard, Catherine, Sankaran, Vijay G., Demirdag, Yesim Yilmaz, Lougaris, Vassilios, Aiuti, Alessandro, Plebani, Alessandro, Milito, Cinzia, Dalm, Virgil ASH, Guevara-Hoyer, Kissy, Sánchez-Ramón, Silvia, Bezrodnik, Liliana, Barzaghi, Federica, Gonzalez-Granado, Luis Ignacio, Hayman, Grant R., Uzel, Gulbu, Mendonça, Leonardo Oliveira, Agostini, Carlo, Spadaro, Giuseppe, Badolato, Raffaele, Soresina, Annarosa, Vermeulen, François, Bosteels, Cedric, Lambrecht, Bart N., Keller, Michael, Mustillo, Peter J., Abraham, Roshini S., Gupta, Sudhir, Ozen, Ahmet, Karakoc-Aydiner, Elif, Baris, Safa, Freeman, Alexandra F., Yamazaki-Nakashimada, Marco, Scheffler-Mendoza, Selma, Espinosa-Padilla, Sara, Gennery, Andrew R., Jolles, Stephen, Espinosa, Yazmin, Poli, M. Cecilia, Fieschi, Claire, Hauck, Fabian, Cunningham-Rundles, Charlotte, Mahlaoui, Nizar, Warnatz, Klaus, Sullivan, Kathleen E., Tangye, Stuart G.

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Epidemiologic analyses with error-prone exposures: review of current practice and recommendations von Shaw, Pamela A., Deffner, Veronika, Keogh, Ruth H., Tooze, Janet A., Dodd, Kevin W., Küchenhoff, Helmut, Kipnis, Victor, Freedman, Laurence S.

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Hematopoietic cell transplantation in chronic granulomatous disease: a study of 712 children and adults von Chiesa, Robert, Wang, Junfeng, Blok, Henric-Jan, Hazelaar, Sheree, Neven, Benedicte, Moshous, Despina, Schulz, Ansgar, Hoenig, Manfred, Hauck, Fabian, Al Seraihy, Amal, Gozdzik, Jolanta, Ljungman, Per, Lindemans, Caroline A., Fernandes, Juliana F., Kalwak, Krzysztof, Strahm, Brigitte, Schanz, Urs, Sedlacek, Petr, Sykora, Karl-Walter, Aksoylar, Serap, Locatelli, Franco, Stepensky, Polina, Wynn, Robert, Lum, Su Han, Zecca, Marco, Porta, Fulvio, Taskinen, Mervi, Gibson, Brenda, Matthes, Susanne, Karakukcu, Musa, Hauri-Hohl, Mathias, Veys, Paul, Gennery, Andrew R., Lucchini, Giovanna, Felber, Matthias, Albert, Michael H., Balashov, Dmitry, Lankester, Arjan, Güngör, Tayfun, Slatter, Mary A.

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Prevalence of Amblyopia in School-Aged Children and Variations by Age, Gender, and Ethnicity in a Multi-Country Refractive Error Study von Xiao, Ou, MD, Morgan, Ian G., PhD, Ellwein, Leon B., PhD, He, Mingguang, MD, PhD

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Genetically low vitamin D concentrations and myopic refractive error: a Mendelian randomization study von Cuellar-Partida, Gabriel, Williams, Katie M, Yazar, Seyhan, Guggenheim, Jeremy A, Hewitt, Alex W, Williams, Cathy, Wang, Jie Jin, Kho, Pik-Fang, Saw, Seang Mei, Cheng, Ching-Yu, Wong, Tien Yin, Aung, Tin, Young, Terri L, Tideman, J Willem L, Jonas, Jost B, Mitchell, Paul, Wojciechowski, Robert, Stambolian, Dwight, Hysi, Pirro, Hammond, Christopher J, Mackey, David A, Lucas, Robyn M, MacGregor, Stuart

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APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans von Tkatchenko, Andrei V, Tkatchenko, Tatiana V, Guggenheim, Jeremy A, Verhoeven, Virginie J M, Hysi, Pirro G, Wojciechowski, Robert, Singh, Pawan Kumar, Kumar, Ashok, Thinakaran, Gopal, Williams, Cathy

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Reduced-intensity conditioning and HLA-matched haemopoietic stem-cell transplantation in patients with chronic granulomatous disease: a prospective multicentre study von Güngör, Tayfun, Dr, Teira, Pierre, MD, Slatter, Mary, MBChB, Stussi, Georg, MD, Stepensky, Polina, MD, Moshous, Despina, MD, Vermont, Clementien, MD, Ahmad, Imran, MD, Shaw, Peter J, FRACP, da Cunha, José Marcos Telles, MD, Schlegel, Paul G, MD, Hough, Rachel, MD, Fasth, Anders, Prof, Kentouche, Karim, MD, Gruhn, Bernd, MD, Fernandes, Juliana F, MD, Lachance, Silvy, FRCP, Bredius, Robbert, MD, Resnick, Igor B, MD, Belohradsky, Bernd H, Prof, Gennery, Andrew, MD, Fischer, Alain, Prof, Gaspar, H Bobby, Prof, Schanz, Urs, MD, Seger, Reinhard, MD, Rentsch, Katharina, PhD, Veys, Paul, FRCP, Haddad, Elie, MD, Albert, Michael H, MD, Hassan, Moustapha, Prof

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Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia von Tideman, J. Willem L, Pärssinen, Olavi, Haarman, Annechien E. G, Khawaja, Anthony P, Wedenoja, Juho, Williams, Katie M, Biino, Ginevra, Ding, Xiaohu, Kähönen, Mika, Lehtimäki, Terho, Raitakari, Olli T, Cheng, Ching-Yu, Jonas, Jost B, Young, Terri L, Bailey-Wilson, Joan E, Rahi, Jugnoo, Williams, Cathy, He, Mingguang, Mackey, David A, Guggenheim, Jeremy A

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DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients von Aydin, Susanne E., Kilic, Sara Sebnem, Aytekin, Caner, Kumar, Ashish, Porras, Oscar, Kainulainen, Leena, Kostyuchenko, Larysa, Genel, Ferah, Kütükcüler, Necil, Karaca, Neslihan, Gonzalez-Granado, Luis, Abbott, Jordan, Al-Zahrani, Daifulah, Rezaei, Nima, Baz, Zeina, Thiel, Jens, Ehl, Stephan, Marodi, László, Orange, Jordan S., Sawalle-Belohradsky, Julie, Keles, Sevgi, Holland, Steven M., Sanal, Özden, Ayvaz, Deniz C., Tezcan, Ilhan, Al-Mousa, Hamoud, Alsum, Zobaida, Hawwari, Abbas, Metin, Ayse, Matthes-Martin, Susanne, Hönig, Manfred, Schulz, Ansgar, Picard, Capucine, Barlogis, Vincent, Gennery, Andrew, Ifversen, Marianne, van Montfrans, Joris, Kuijpers, Taco, Bredius, Robbert, Dückers, Gregor, Al-Herz, Waleed, Pai, Sung-Yun, Geha, Raif, Notheis, Gundula, Schwarze, Carl-Philipp, Tavil, Betül, Azik, Fatih, Bienemann, Kirsten, Grimbacher, Bodo, Heinz, Valerie, Gaspar, H. Bobby, Aydin, Roland, Hagl, Beate, Gathmann, Benjamin, Belohradsky, Bernd H., Ochs, Hans D., Chatila, Talal, Renner, Ellen D., Su, Helen, Freeman, Alexandra F., Engelhardt, Karin, Albert, Michael H.

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Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency von Ghosh, Sujal, Köstel Bal, Sevgi, Edwards, Emily S.J., Pillay, Bethany, Jiménez Heredia, Raúl, Erol Cipe, Funda, Rao, Geetha, Salzer, Elisabeth, Zoghi, Samaneh, Abolhassani, Hassan, Momen, Tooba, Gostick, Emma, Price, David A., Zhang, Yu, Oler, Andrew J., Gonzaga-Jauregui, Claudia, Erman, Baran, Metin, Ayse, Ilhan, Inci, Haskologlu, Sule, Islamoglu, Candan, Baskin, Kubra, Ceylaner, Serdar, Yilmaz, Ebru, Unal, Ekrem, Karakukcu, Musa, Berghuis, Dagmar, Cole, Theresa, Gupta, Aditya K., Hauck, Fabian, Kogler, Hubert, Hoepelman, Andy I.M., Baris, Safa, Karakoc-Aydiner, Elif, Ozen, Ahmet, Kager, Leo, Holzinger, Dirk, Paulussen, Michael, Krüger, Renate, Meisel, Roland, Oommen, Prasad T., Morris, Emma, Neven, Benedicte, Worth, Austen, van Montfrans, Joris, Fraaij, Pieter L.A., Choo, Sharon, Dogu, Figen, Davies, E. Graham, Burns, Siobhan, Dückers, Gregor, Becker, Ruy Perez, von Bernuth, Horst, Latour, Sylvain, Faraci, Maura, Gattorno, Marco, Su, Helen C., Pan-Hammarström, Qiang, Hammarström, Lennart, Lenardo, Michael J., Ma, Cindy S., Niehues, Tim, Aghamohammadi, Asghar, Rezaei, Nima, Ikinciogullari, Aydan, Tangye, Stuart G., Lankester, Arjan C., Boztug, Kaan

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Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium von Wong, Yee-Ling, Hysi, Pirro, Cheung, Gemmy, Tedja, Milly, Hoang, Quan V, Tompson, Stuart W J, Whisenhunt, Kristina N, Verhoeven, Virginie, Zhao, Wanting, Hess, Moritz, Wong, Chee-Wai, Kifley, Annette, Hosoda, Yoshikatsu, Haarman, Annechien E G, Hopf, Susanne, Laspas, Panagiotis, Sensaki, Sonoko, Sim, Xueling, Miyake, Masahiro, Tsujikawa, Akitaka, Lamoureux, Ecosse, Ohno-Matsui, Kyoko, Nickels, Stefan, Mitchell, Paul, Wong, Tien-Yin, Wang, Jie Jin, Hammond, Christopher J, Barathi, Veluchamy A, Cheng, Ching-Yu, Yamashiro, Kenji, Young, Terri L, Klaver, Caroline C W, Saw, Seang-Mei

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Education influences the role of genetics in myopia von Verhoeven, Virginie J. M., Buitendijk, Gabriëlle H. S., Rivadeneira, Fernando, Uitterlinden, André G., Vingerling, Johannes R., Hofman, Albert, Klaver, Caroline C. W.

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Issues in Implementing Regression Calibration Analyses von Boe, Lillian A, Shaw, Pamela A, Midthune, Douglas, Gustafson, Paul, Kipnis, Victor, Park, Eunyoung, Sotres-Alvarez, Daniela, Freedman, Laurence, of the STRATOS Initiative, on behalf of the Measurement Error and Misclassification Topic Group (TG4)

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Prediction of Juvenile-Onset Myopia von Zadnik, Karla, Sinnott, Loraine T, Cotter, Susan A, Jones-Jordan, Lisa A, Kleinstein, Robert N, Manny, Ruth E, Twelker, J. Daniel, Mutti, Donald O

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Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene von Zastrow, Diane B., Baudet, Heather, Shen, Wei, Thomas, Amanda, Si, Yue, Weaver, Meredith A., Lager, Angela M., Liu, Jixia, Mangels, Rachel, Dwight, Selina S., Wright, Matt W., Dobrowolski, Steven F., Eilbeck, Karen, Enns, Gregory M., Feigenbaum, Annette, Lichter‐Konecki, Uta, Lyon, Elaine, Pasquali, Marzia, Watson, Michael, Blau, Nenad, Steiner, Robert D., Craigen, William J., Mao, Rong

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