Commercial chicken breeds exhibit highly divergent patterns of linkage disequilibrium von Pengelly, R J, Gheyas, A A, Kuo, R, Mossotto, E, Seaby, E G, Burt, D W, Ennis, S, Collins, A

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Treatment of multisystem inflammatory syndrome in children von McArdle, A J, Vito, O, Patel, H, Seaby, E G, Shah, P, Wilson, C, Broderick, C, Nijman, R, Tremoulet, A H, Munblit, D, Ulloa-Gutierrez, R, Carter, M J, De, T, Hoggart, C, Whittaker, E, Herberg, J A, Kaforou, M, Cunnington, A J, Levin, M, Hoste, Levi, Haerynck, Filomeen, Consortium, BATS

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Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney disease von Gast, Christine, Marinaki, Anthony, Arenas-Hernandez, Monica, Campbell, Sara, Seaby, Eleanor G, Pengelly, Reuben J, Gale, Daniel P, Connor, Thomas M, Bunyan, David J, Hodaňová, Kateřina, Živná, Martina, Kmoch, Stanislav, Ennis, Sarah, Venkat-Raman, G

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Treatment of Multisystem Inflammatory Syndrome in Children: Understanding Differences in Results of Comparative Effectiveness Studies von Melgar, Michael, Seaby, Eleanor G., McArdle, Andrew J., Young, Cameron C., Campbell, Angela P., Murray, Nancy L., Patel, Manish M., Levin, Michael, Randolph, Adrienne G., Son, Mary Beth F.

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Treatment of multisystem inflammatory syndrome in children von McArdle, AJ, Vito, O, Patel, H, Seaby, EG, Shah, P, Wilson, C, Broderick, C, Nijman, R, Tremoulet, AH, Munblit, D, Ulloa-Gutierrez, R, Carter, MJ, De, T, Hoggart, C, Whittaker, E, Herberg, JA, Kaforou, M, Cunnington, AJ, Levin, M

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Transcript expression-aware annotation improves rare variant interpretation von Cummings, BB, Karczewski, KJ, Kosmicki, JA, Seaby, EG, Watts, NA, Singer-Berk, M, Mudge, JM, Karjalainen, J, Satterstrom, FK, O'Donnell-Luria, AH, Poterba, T, Seed, C, Solomonson, M, Alföldi, J, Genome Aggregation Database Production Team, Genome Aggregation Database Consortium, Daly, MJ, MacArthur, DG

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Identification of novel locus associated with coronary artery aneurysms and validation of loci for susceptibility to Kawasaki disease von Hoggart, C, Shimizu, C, Galassini, R, Wright, VJ, Shailes, H, Bellos, E, Herberg, JA, Pollard, AJ, O'Connor, D, Choi, SW, Seaby, EG, Menikou, S, Hibberd, M, Sallah, N, Burgner, D, Brogan, P, Patel, H, Kim, J, Tremoulet, AH, Salo, E, Van Stijn, D, Kuijpers, T, Burns, JC, Levin, M

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Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans von Karczewski, KJ, Francioli, LC, Tiao, G, Cummings, BB, Alfoldi, J, Wang, Q, Collins, RL, Laricchia, KM, Ganna, A, Birnbaum, DP, Gauthier, LD, Brand, H, Solomonson, M, Watts, NA, Rhodes, D, Singer-Berk, M, England, EM, Seaby, EG, Kosmicki, JA, Walters, RK, Tashman, K, Farjoun, Y, Banks, E, Poterba, T, Wang, A, Seed, C, Whiffin, N, Chong, JX, Samocha, KE, Pierce-Hoffman, E, Zappala, Z, O'Donnell-Luria, AH, Minikel, EV, Weisburd, B, Lek, M, Ware, JS, Vittal, C, Armean, IM, Bergelson, L, Cibulskis, K, Connolly, KM, Covarrubias, M, Donnelly, S, Ferriera, S, Gabriel, S, Gentry, J, Gupta, N, Jeandet, T, Kaplan, D, Llanwarne, C, Munshi, R, Novod, S, Petrillo, N, Roazen, D, Ruano-Rubio, V, Saltzman, A, Schleicher, M, Soto, J, Tibbetts, K, Tolonen, C, Wade, G, Talkowski, ME, Aggregation, G, Neale, BM, Daly, MJ, MacArthur, DG

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The mutational constraint spectrum quantified from variation in 141,456 humans (vol 581, pg 434, 2020) von Gudmundsson, S, Karczewski, KJ, Francioli, LC, Tiao, G, Cummings, BB, Alfoldi, J, Wang, Q, Collins, RL, Laricchia, KM, Ganna, A, Birnbaum, DP, Gauthier, LD, Brand, H, Solomonson, M, Watts, NA, Rhodes, D, Singer-Berk, M, England, EM, Seaby, EG, Kosmicki, JA, Walters, RK, Tashman, K, Farjoun, Y, Banks, E, Poterba, T, Wang, A, Seed, C, Whiffin, N, Chong, JX, Samocha, KE, Pierce-Hoffman, E, Zappala, Z, O'Donnell-Luria, AH, Minikel, EV, Weisburd, B, Lek, M, Ware, JS, Vittal, C, Armean, IM, Bergelson, L, Cibulskis, K, Connolly, KM, Covarrubias, M, Donnelly, S, Ferriera, S, Gabriel, S, Gentry, J, Gupta, N, Jeandet, T, Kaplan, D, Llanwarne, C, Munshi, R, Novod, S, Petrillo, N, Roazen, D, Ruano-Rubio, V, Saltzman, A, Schleicher, M, Soto, J, Tibbetts, K, Tolonen, C, Wade, G, Talkowski, ME, Neale, BM, Daly, MJ, MacArthur, DG

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The mutational constraint spectrum quantified from variation in 141,456 humans von Karczewski, KJ, Francioli, LC, Tiao, G, Cummings, BB, Alföldi, J, Wang, Q, Collins, RL, Laricchia, KM, Ganna, A, Birnbaum, DP, Gauthier, LD, Brand, H, Solomonson, M, Watts, NA, Rhodes, D, Singer-Berk, M, England, EM, Seaby, EG, Kosmicki, JA, Walters, RK, Tashman, K, Farjoun, Y, Banks, E, Poterba, T, Wang, A, Seed, C, Whiffin, N, Chong, JX, Samocha, KE, Pierce-Hoffman, E, Zappala, Z, O’Donnell-Luria, AH, Vallabh Minikel, E, Weisburd, B, Lek, M, Ware, JS, Vittal, C, Armean, IM, Bergelson, L, Cibulskis, K, Connolly, JM, Covarrubias, M, Donnelly, S, Ferriera, S, Gabriel, S, Gentry, J, Gupta, N, Jeandet, T, Kaplan, D, Llanwarne, C, Munshi, J, Novod, S, Petrillo, N, Roazen, D, Ruano-Rubio, V, Saltzman, A, Schleicher, M, Soto, J, Tibbetts, K, Tolonen, C, Wade, G, Talkowski, ME, Genome Aggregation Database (gnomAD) Consortium, Neale, BM, Daly, MJ, MacArthur, DG

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Genome-wide association studies in infectious diseases von Seaby, EG, Wright, VJ, Levin, M

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Treatment of Multisystem Inflammatory Syndrome in Children von McArdle, AJ, Vito, O, Patel, H, Seaby, EG, Shah, P, Wilson, C, Broderick, C, Nijman, R, Tremoulet, AH, Munblit, D, Ulloa-Gutierrez, R, Carter, MJ, De, T, Hoggart, C, Whittaker, E, Herberg, JA, Kaforou, M, Cunnington, AJ, Levin, M

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Rare pathogenic variants in WNK3 cause X-linked intellectual disability von Küry, S, Zhang, J, Besnard, T, Caro-Llopis, A, Zeng, X, Robert, SM, Josiah, SS, Kiziltug, E, Denommé-Pichon, AS, Cogné, B, Kundishora, AJ, Hao, LT, Li, H, Stevenson, RE, Louie, RJ, Deb, W, Torti, E, Vignard, V, McWalter, K, Raymond, FL, Rajabi, F, Ranza, E, Grozeva, D, Coury, SA, Blanc, X, Brischoux-Boucher, E, Keren, B, Õunap, K, Reinson, K, Ilves, P, Wentzensen, IM, Barr, EE, Guihard, SH, Charles, P, Seaby, EG, Monaghan, KG, Rio, M, van Bever, Y, van Slegtenhorst, M, Chung, WK, Wilson, A, Quinquis, D, Bréhéret, F, Retterer, K, Lindenbaum, P, Scalais, E, Rhodes, L, Stouffs, K, Pereira, EM, Berger, SM, Milla, SS, Jaykumar, AB, Cobb, MH, Panchagnula, S, Duy, PQ, Vincent, M, Mercier, S, Gilbert-Dussardier, B, Le Guillou, X, Audebert-Bellanger, S, Odent, S, Schmitt, S, Boisseau, P, Bonneau, D, Toutain, A, Colin, E, Pasquier, L, Redon, R, Bouman, A, Rosenfeld, JA, Friez, MJ, Pérez-Peña, H, Akhtar Rizvi, SR, Haider, S, Antonarakis, SE, Schwartz, CE, Martínez, F, Bézieau, S, Kahle, KT, Isidor, B

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Identification of novel locus associated with coronary artery aneurysms and validation of loci for susceptibility to Kawasaki disease von Hoggart, C, Shimizu, C, Galassini, R, Wright, VJ, Shailes, H, Bellos, E, Herberg, JA, Pollard, AJ, O'Connor, D, Choi, SW, Seaby, EG, Menikou, S, Hibberd, M, Sallah, N, Burgner, D, Brogan, P, Patel, H, Kim, J, Tremoulet, AH, Salo, E, van Stijn, D, Kuijpers, T, Burns, JC, Levin, M, International Kawasaki Disease Genetics Consortium, UK Kawasaki Disease Genetics Consortium, EUCLIDS Consortium

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Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney disease von Gast, C, Marinaki, A, Arenas-Hernandez, M, Campbell, S, Seaby, EG, Pengelly, RJ, Gale, DP, Connor, TM, Bunyan, DJ, Hodaňová, K, Živná, M, Kmoch, S, Ennis, S, Venkat-Raman, G

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Impaired expression of metallothioneins contributes to allergen-induced inflammation in patients with atopic dermatitis von Sirvent, Sofia, Vallejo, Andres F., Corden, Emma, Teo, Ying, Davies, James, Clayton, Kalum, Seaby, Eleanor G., Lai, Chester, Ennis, Sarah, Alyami, Rfeef, Douilhet, Gemma, Dean, Lareb S. N., Loxham, Matthew, Horswill, Sarah, Healy, Eugene, Roberts, Graham, Hall, Nigel J., Friedmann, Peter S., Singh, Harinder, Bennett, Clare L., Ardern-Jones, Michael R, Polak, Marta E.

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The mutational constraint spectrum quantified from variation in 141,456 humans von Karczewski, Konrad J., Francioli, Laurent C., Tiao, Grace, Cummings, Beryl B., Alföldi, Jessica, Wang, Qingbo, Collins, Ryan L., Laricchia, Kristen M., Ganna, Andrea, Birnbaum, Daniel P., Gauthier, Laura D., Brand, Harrison, Solomonson, Matthew, Watts, Nicholas A., Rhodes, Daniel, Singer-Berk, Moriel, England, Eleina M., Seaby, Eleanor G., Kosmicki, Jack A., Walters, Raymond K., Tashman, Katherine, Farjoun, Yossi, Banks, Eric, Poterba, Timothy, Wang, Arcturus, Seed, Cotton, Whiffin, Nicola, Chong, Jessica X., Samocha, Kaitlin E., Pierce-Hoffman, Emma, Zappala, Zachary, O’Donnell-Luria, Anne H., Minikel, Eric Vallabh, Weisburd, Ben, Lek, Monkol, Ware, James S., Vittal, Christopher, Armean, Irina M., Bergelson, Louis, Cibulskis, Kristian, Connolly, Kristen M., Covarrubias, Miguel, Donnelly, Stacey, Ferriera, Steven, Gabriel, Stacey, Gentry, Jeff, Gupta, Namrata, Jeandet, Thibault, Kaplan, Diane, Llanwarne, Christopher, Munshi, Ruchi, Novod, Sam, Petrillo, Nikelle, Roazen, David, Ruano-Rubio, Valentin, Saltzman, Andrea, Schleicher, Molly, Soto, Jose, Tibbetts, Kathleen, Tolonen, Charlotte, Wade, Gordon, Talkowski, Michael E., Neale, Benjamin M., Daly, Mark J., MacArthur, Daniel G.

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A genomic mutational constraint map using variation in 76,156 human genomes von Chen, Siwei, Francioli, Laurent C., Goodrich, Julia K., Collins, Ryan L., Kanai, Masahiro, Wang, Qingbo, Alföldi, Jessica, Watts, Nicholas A., Vittal, Christopher, Gauthier, Laura D., Poterba, Timothy, Wilson, Michael W., Tarasova, Yekaterina, Phu, William, Grant, Riley, Yohannes, Mary T., Koenig, Zan, Farjoun, Yossi, Banks, Eric, Donnelly, Stacey, Gabriel, Stacey, Gupta, Namrata, Ferriera, Steven, Tolonen, Charlotte, Novod, Sam, Bergelson, Louis, Roazen, David, Ruano-Rubio, Valentin, Covarrubias, Miguel, Llanwarne, Christopher, Petrillo, Nikelle, Wade, Gordon, Jeandet, Thibault, Munshi, Ruchi, Tibbetts, Kathleen, O’Donnell-Luria, Anne, Solomonson, Matthew, Seed, Cotton, Martin, Alicia R., Talkowski, Michael E., Rehm, Heidi L., Daly, Mark J., Tiao, Grace, Neale, Benjamin M., MacArthur, Daniel G., Karczewski, Konrad J.

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Treatment of Multisystem Inflammatory Syndrome in Children von McArdle, Andrew J, Vito, Ortensia, Patel, Harsita, Seaby, Eleanor G, Shah, Priyen, Wilson, Clare, Broderick, Claire, Nijman, Ruud, Tremoulet, Adriana H, Munblit, Daniel, Ulloa-Gutierrez, Rolando, Carter, Michael J, De, Tisham, Hoggart, Clive, Whittaker, Elizabeth, Herberg, Jethro A, Kaforou, Myrsini, Cunnington, Aubrey J, Levin, Michael

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Structure and Thermodynamics of Lipid Bilayers on Polyethylene Glycol Cushions: Fact and Fiction of PEG Cushioned Membranes von Watkins, Erik B, El-khouri, Rita J, Miller, Chad E, Seaby, Brian G, Majewski, Jaroslaw, Marques, Carlos M, Kuhl, Tonya L

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