Editorial Board Membership of Management and Business Journals: A Social Network Analysis Study of the Financial Times 40 von Burgess, Thomas F., Shaw, Nicola E.

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Mapping the operations and supply chain management field: a journal governance perspective von Burgess, Thomas F, Grimshaw, Paul, Huaccho Huatuco, Luisa, Shaw, Nicola E

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Cross-cohort gut microbiome associations with immune checkpoint inhibitor response in advanced melanoma von Lee, Karla A., Thomas, Andrew Maltez, Bolte, Laura A., Björk, Johannes R., de Ruijter, Laura Kist, Armanini, Federica, Asnicar, Francesco, Blanco-Miguez, Aitor, Board, Ruth, Calbet-Llopart, Neus, Derosa, Lisa, Dhomen, Nathalie, Brooks, Kelly, Harland, Mark, Harries, Mark, Leeming, Emily R., Lorigan, Paul, Manghi, Paolo, Marais, Richard, Newton-Bishop, Julia, Nezi, Luigi, Pinto, Federica, Potrony, Miriam, Puig, Susana, Serra-Bellver, Patricio, Shaw, Heather M., Tamburini, Sabrina, Valpione, Sara, Vijay, Amrita, Waldron, Levi, Zitvogel, Laurence, Zolfo, Moreno, de Vries, Elisabeth G. E., Nathan, Paul, Fehrmann, Rudolf S. N., Bataille, Véronique, Hospers, Geke A. P., Spector, Tim D., Weersma, Rinse K., Segata, Nicola

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Biodiversity redistribution under climate change: Impacts on ecosystems and human well-being von Pecl, Gretta T., Araújo, Miguel B., Bell, Johann D., Blanchard, Julia, Bonebrake, Timothy C., Chen, I-Ching, Clark, Timothy D., Colwell, Robert K., Danielsen, Finn, Evengård, Birgitta, Falconi, Lorena, Ferrier, Simon, Frusher, Stewart, Garcia, Raquel A., Griffis, Roger B., Hobday, Alistair J., Janion-Scheepers, Charlene, Jarzyna, Marta A., Jennings, Sarah, Lenoir, Jonathan, Linnetved, Hlif I., Martin, Victoria Y., McCormack, Phillipa C., McDonald, Jan, Mitchell, Nicola J., Mustonen, Tero, Pandolfi, John M., Pettorelli, Nathalie, Popova, Ekaterina, Robinson, Sharon A., Scheffers, Brett R., Shaw, Justine D., Sorte, Cascade J. B., Strugnell, Jan M., Sunday, Jennifer M., Tuanmu, Mao-Ning, Vergés, Adriana, Villanueva, Cecilia, Wernberg, Thomas, Wapstra, Erik, Williams, Stephen E.

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The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder von Smith, Bradley N, Newhouse, Stephen, Shatunov, Aleksey, Vance, Caroline, Topp, Simon, Johnson, Lauren, Miller, Jack, Lee, Younbok, Troakes, Claire, Scott, Kirsten M, Jones, Ashley, Gray, Ian, Wright, Jamie, Hortobágyi, Tibor, Al-Sarraj, Safa, Rogelj, Boris, Powell, John, Lupton, Michelle, Lovestone, Simon, Sapp, Peter C, Weber, Markus, Nestor, Peter J, Schelhaas, Helenius J, Asbroek, Anneloor Alm Ten, Silani, Vincenzo, Gellera, Cinzia, Taroni, Franco, Ticozzi, Nicola, Van den Berg, Leonard, Veldink, Jan, Van Damme, Phillip, Robberecht, Wim, Shaw, Pamela J, Kirby, Janine, Pall, Hardev, Morrison, Karen E, Morris, Alex, de Belleroche, Jacqueline, Vianney de Jong, J M B, Baas, Frank, Andersen, Peter M, Landers, John, Brown, Jr, Robert H, Weale, Michael E, Al-Chalabi, Ammar, Shaw, Christopher E

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Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis von Rutherford, Nicola J, Zhang, Yong-Jie, Baker, Matt, Gass, Jennifer M, Finch, Nicole A, Xu, Ya-Fei, Stewart, Heather, Kelley, Brendan J, Kuntz, Karen, Crook, Richard J P, Sreedharan, Jemeen, Vance, Caroline, Sorenson, Eric, Lippa, Carol, Bigio, Eileen H, Geschwind, Daniel H, Knopman, David S, Mitsumoto, Hiroshi, Petersen, Ronald C, Cashman, Neil R, Hutton, Mike, Shaw, Christopher E, Boylan, Kevin B, Boeve, Bradley, Graff-Radford, Neill R, Wszolek, Zbigniew K, Caselli, Richard J, Dickson, Dennis W, Mackenzie, Ian R, Petrucelli, Leonard, Rademakers, Rosa

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Associations Between Fruit Intake and Risk of Diabetes in the AusDiab Cohort von Bondonno, Nicola P, Davey, Raymond J, Murray, Kevin, Radavelli-Bagatini, Simone, Bondonno, Catherine P, Blekkenhorst, Lauren C, Sim, Marc, Magliano, Dianna J, Daly, Robin M, Shaw, Jonathan E, Lewis, Joshua R, Hodgson, Jonathan M

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Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis von Zhang, Sai, Cooper-Knock, Johnathan, Weimer, Annika K., Shi, Minyi, Moll, Tobias, Marshall, Jack N.G., Harvey, Calum, Nezhad, Helia Ghahremani, Franklin, John, Souza, Cleide dos Santos, Ning, Ke, Wang, Cheng, Li, Jingjing, Dilliott, Allison A., Farhan, Sali, Elhaik, Eran, Pasniceanu, Iris, Livesey, Matthew R., Eitan, Chen, Hornstein, Eran, Kenna, Kevin P., Blair, Ian, Wray, Naomi R., Kiernan, Matthew, Mitne Neto, Miguel, Chio, Adriano, Cauchi, Ruben, Robberecht, Wim, van Damme, Philip, Corcia, Philippe, Couratier, Philippe, Hardiman, Orla, McLaughin, Russell, Gotkine, Marc, Drory, Vivian, Ticozzi, Nicola, Silani, Vincenzo, Veldink, Jan H., van den Berg, Leonard H., de Carvalho, Mamede, Mora Pardina, Jesus S., Povedano, Monica, Andersen, Peter, Weber, Markus, Başak, Nazli A., Al-Chalabi, Ammar, Shaw, Chris, Shaw, Pamela J., Morrison, Karen E., Landers, John E., Glass, Jonathan D., Veldink, Jan H., Ferraiuolo, Laura, Shaw, Pamela J., Snyder, Michael P.

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Natural variation in a homolog of Antirrhinum CENTRORADIALIS contributed to spring growth habit and environmental adaptation in cultivated barley von Comadran, Jordi, Kilian, Benjamin, Russell, Joanne, Ramsay, Luke, Stein, Nils, Ganal, Martin, Shaw, Paul, Bayer, Micha, Thomas, William, Marshall, David, Hedley, Pete, Tondelli, Alessandro, Pecchioni, Nicola, Francia, Enrico, Korzun, Viktor, Walther, Alexander, Waugh, Robbie

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Genomic diversity affects the accuracy of bacterial single-nucleotide polymorphism–calling pipelines von Bush, Stephen J, Foster, Dona, Eyre, David W, Clark, Emily L, De Maio, Nicola, Shaw, Liam P, Stoesser, Nicole, Peto, Tim E A, Crook, Derrick W, Walker, A Sarah

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Safety and Efficacy of NVX-CoV2373 Covid-19 Vaccine von Heath, Paul T, Galiza, Eva P, Baxter, David N, Boffito, Marta, Browne, Duncan, Burns, Fiona, Chadwick, David R, Clark, Rebecca, Cosgrove, Catherine, Galloway, James, Goodman, Anna L, Heer, Amardeep, Higham, Andrew, Iyengar, Shalini, Jamal, Arham, Jeanes, Christopher, Kalra, Philip A, Kyriakidou, Christina, McAuley, Daniel F, Meyrick, Agnieszka, Minassian, Angela M, Minton, Jane, Moore, Patrick, Munsoor, Imrozia, Nicholls, Helen, Osanlou, Orod, Packham, Jonathan, Pretswell, Carol H, San Francisco Ramos, Alberto, Saralaya, Dinesh, Sheridan, Ray P, Smith, Richard, Soiza, Roy L, Swift, Pauline A, Thomson, Emma C, Turner, Jeremy, Viljoen, Marianne E, Albert, Gary, Cho, Iksung, Dubovsky, Filip, Glenn, Greg, Rivers, Joy, Robertson, Andreana, Smith, Kathy, Toback, Seth

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The impact of age on genetic testing decisions in amyotrophic lateral sclerosis von Mehta, Puja R, Iacoangeli, Alfredo, Opie-Martin, Sarah, van Vugt, Joke J F A, Al Khleifat, Ahmad, Bredin, Andrea, Ossher, Lynn, Andersen, Peter M, Hardiman, Orla, Mehta, Arpan R, Fratta, Pietro, Talbot, Kevin, Al-Chalabi, Ammar

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Monitoring of childhood ALL using BCR-ABL1 genomic breakpoints identifies a subgroup with CML-like biology von Hovorkova, Lenka, Zaliova, Marketa, Venn, Nicola C., Bleckmann, Kirsten, Trkova, Marie, Potuckova, Eliska, Vaskova, Martina, Linhartova, Jana, Machova Polakova, Katerina, Fronkova, Eva, Muskovic, Walter, Giles, Jodie E., Shaw, Peter J., Cario, Gunnar, Sutton, Rosemary, Stary, Jan, Trka, Jan, Zuna, Jan

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A single risk assessment for the most common diseases of ageing, developed and validated on 10 cohort studies von Huque, Md Hamidul, Kootar, Scherazad, Kiely, Kim M, Anderson, Craig S, van Boxtel, Martin, Brodaty, Henry, Sachdev, Perminder S, Carlson, Michelle, Fitzpatrick, Annette L, Whitmer, Rachel A, Kivipelto, Miia, Jorm, Louisa, Köhler, Sebastian, Lautenschlager, Nicola T, Lopez, Oscar L, Shaw, Jonathan E, Matthews, Fiona E, Peters, Ruth, Anstey, Kaarin J

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The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration von Opie-Martin, Sarah, Iacoangeli, Alfredo, Topp, Simon D., Abel, Olubunmi, Mayl, Keith, Mehta, Puja R., Shatunov, Aleksey, Fogh, Isabella, Bowles, Harry, Limbachiya, Naomi, Spargo, Thomas P., Al-Khleifat, Ahmad, Williams, Kelly L., Jockel-Balsarotti, Jennifer, Bali, Taha, Self, Wade, Henden, Lyndal, Nicholson, Garth A., Ticozzi, Nicola, McKenna-Yasek, Diane, Tang, Lu, Shaw, Pamela J., Chio, Adriano, Ludolph, Albert, Weishaupt, Jochen H., Landers, John E., Glass, Jonathan D., Mora, Jesus S., Robberecht, Wim, Damme, Philip Van, McLaughlin, Russell, Hardiman, Orla, van den Berg, Leonard, Veldink, Jan H., Corcia, Phillippe, Stevic, Zorica, Siddique, Nailah, Silani, Vincenzo, Blair, Ian P., Fan, Dong-sheng, Esselin, Florence, de la Cruz, Elisa, Camu, William, Basak, Nazli A., Siddique, Teepu, Miller, Timothy, Brown, Robert H., Al-Chalabi, Ammar, Shaw, Christopher E.

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Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene von Cooper-Knock, Johnathan, Zhang, Sai, Kenna, Kevin P., Moll, Tobias, Franklin, John P., Allen, Samantha, Nezhad, Helia Ghahremani, Iacoangeli, Alfredo, Yacovzada, Nancy Y., Eitan, Chen, Hornstein, Eran, Elhaik, Eran, Celadova, Petra, Bose, Daniel, Farhan, Sali, Fishilevich, Simon, Lancet, Doron, Morrison, Karen E., Shaw, Christopher E., Al-Chalabi, Ammar, Blair, Ian, Wray, Naomi, Kiernan, Matthew, Neto, Miguel Mitne, Chio, Adriano, Cauchi, Ruben, Robberecht, Wim, van Damme, Philip, Corcia, Phillippe, Couratier, Phillipe, Hardiman, Orla, McLaughlin, Russel, Gotkine, Marc, Drory, Vivan, Ticozzi, Nicola, Silani, Vincenzo, Veldink, Jan, van den Berg, Leonard, de Carvalho, Mamede, Pardina, Jesus Mora, Povedano, Monica, Andersen, Peter, Wber, Markus, Başak, Nazli, Al-Chalabi, Ammar, Shaw, Christopher, Shaw, Pamela, Morrison, Karen, Landers, John, Glass, Jonathan, Veldink, Jan H., Kirby, Janine, Snyder, Michael P., Shaw, Pamela J.

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Evidence for 28 genetic disorders discovered by combining healthcare and research data von Kaplanis, Joanna, Samocha, Kaitlin E., Wiel, Laurens, Zhang, Zhancheng, Arvai, Kevin J., Eberhardt, Ruth Y., Gallone, Giuseppe, Lelieveld, Stefan H., Martin, Hilary C., McRae, Jeremy F., Short, Patrick J., Torene, Rebecca I., de Boer, Elke, Danecek, Petr, Gardner, Eugene J., Huang, Ni, Lord, Jenny, Martincorena, Iñigo, Pfundt, Rolph, Reijnders, Margot R. F., Yeung, Alison, Yntema, Helger G., Vissers, Lisenka E. L. M., Juusola, Jane, Wright, Caroline F., Brunner, Han G., Firth, Helen V., FitzPatrick, David R., Barrett, Jeffrey C., Hurles, Matthew E., Gilissen, Christian, Retterer, Kyle

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Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS von Smith, Bradley N., Ticozzi, Nicola, Fallini, Claudia, Gkazi, Athina Soragia, Topp, Simon, Kenna, Kevin P., Scotter, Emma L., Kost, Jason, Keagle, Pamela, Miller, Jack W., Calini, Daniela, Vance, Caroline, Danielson, Eric W., Troakes, Claire, Tiloca, Cinzia, Al-Sarraj, Safa, Lewis, Elizabeth A., King, Andrew, Colombrita, Claudia, Pensato, Viviana, Castellotti, Barbara, de Belleroche, Jacqueline, Baas, Frank, ten Asbroek, Anneloor LMA, Sapp, Peter C., McKenna-Yasek, Diane, McLaughlin, Russell L., Polak, Meraida, Asress, Seneshaw, Esteban-Pérez, Jesús, Muñoz-Blanco, José Luis, Simpson, Michael, D’Alfonso, Sandra, Mazzini, Letizia, Comi, Giacomo P., Del Bo, Roberto, Ceroni, Mauro, Gagliardi, Stella, Querin, Giorgia, Bertolin, Cinzia, van Rheenen, Wouter, Diekstra, Frank P., Lauria, Giuseppe, Duga, Stefano, Corti, Stefania, Cereda, Cristina, Corrado, Lucia, Sorarù, Gianni, Morrison, Karen E., Williams, Kelly L., Nicholson, Garth A., Blair, Ian P., Dion, Patrick A., Leblond, Claire S., Rouleau, Guy A., Hardiman, Orla, Veldink, Jan H., van den Berg, Leonard H., Al-Chalabi, Ammar, Pall, Hardev, Shaw, Pamela J., Turner, Martin R., Talbot, Kevin, Taroni, Franco, García-Redondo, Alberto, Wu, Zheyang, Glass, Jonathan D., Gellera, Cinzia, Ratti, Antonia, Brown, Robert H., Silani, Vincenzo, Shaw, Christopher E., Landers, John E.

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Amalgamated Reference Data for Size‐Adjusted Bone Densitometry Measurements in 3598 Children and Young Adults—the ALPHABET Study von Crabtree, Nicola J, Shaw, Nicholas J, Bishop, Nicholas J, Adams, Judith E, Mughal, M Zulf, Arundel, Paul, Fewtrell, Mary S, Ahmed, S Faisal, Treadgold, Laura A, Högler, Wolfgang, Bebbington, Natalie A, Ward, Kate A

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Reactogenicity and immunogenicity after a late second dose or a third dose of ChAdOx1 nCoV-19 in the UK: a substudy of two randomised controlled trials (COV001 and COV002) von Aboagye, Jeremy, Aley, Parvinder K, Angus, Brian, Belij-Rammerstorfer, Sandra, Bittaye, Mustapha, Davies, Sophie, Dejnirattisai, Wanwisa, Ewer, Katie J, Folegatti, Pedro M, Fowler, Jamie, Hill, Adrian V S, Kerridge, Simon, Mujadidi, Yama F, Plested, Emma, Robinson, Hannah, Sheehan, Emma, Smith, Holly, Woods, Danielle, Screaton, Gavin, Gilbert, Sarah C, Lambe, Teresa, Adlou, Syed, Aley, Robert, Ali, Aabidah, Baker, Phillip, Barrett, Jordan R., Beadon, Kirsten, Beckley, Rebecca, Bellamy, Duncan, Beveridge, Amy, Blackwell, Luke, Bridges-Webb, Alice, Brown, Charlie, Collins, Andrea M., Crocker, Wendy E.M., Davies, Hannah, Davies, Judith, Demissie, Tesfaye, Di Maso, Claudio, Dinesh, Tanya, Donnellan, Francesca R., Drake-Brockman, Rachael, Duncan, Christopher J.A., Emary, Katherine R.W., Ferreira, Daniela, Finn, Adam, Francis, Emma, Fuskova, Michelle, Galiza, Eva, Green, Christopher A., Harrison, Daisy, Hawkins, Sophia, Heath, Paul T., Horsington, Bryn, Jones, Elizabeth, Kasanyinga, Mwila, Kerr, David, Kinch, Jasmin, Koleva, Stanislava, Kwok, Jonathan, Lawrie, Alison M., Li, Grace, Libri, Vincenzo, Lopez Ramon, Raquel, Makinson, Rebecca, Mazur, Olga, McGregor, Alastair C., Muller, Jilly, Mweu, Philomena, Noristani, Rabiullah, Polo Peralta Alvarez, Marco, Platt, Abigail, Pollock, Katrina M., Poulton, Ian, Provstgaard-Morys, Samuel, Pulido-Gomez, David, Rajan, Matthew, Ramos Lopez, Fernando, Roberts, Hannah, Rudiansyah, Indra, Sanders, Katherine, Saunders, Jack E., Seddiqi, Samiullah, Shaw, Robert, Silva-Reyes, Laura, Smith, Andrew, Spencer, Alexandra J., Stuart, Arabella S.V., Sutherland, Rebecca, Tang, Karly, Thomas, Tonia M., Thomson, Emma C., Török, Estée M., Toshner, Mark, Turnbull, Iain, Vichos, Iason, Whelan, Conor, Williams, Christopher J.A., Wright, Daniel, Yao, Andy

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