Summary and recommendations from the Australasian guidelines for the management of pancreatic exocrine insufficiency von Smith, Ross C, Smith, Sarah F, Wilson, Jeremy, Pearce, Callum, Wray, Nick, Vo, Ruth, Chen, John, Ooi, Chee Y, Oliver, Mark, Katz, Tamarah, Turner, Richard, Nikfarjam, Mehrdad, Rayner, Christopher, Horowitz, Michael, Holtmann, Gerald, Talley, Nick, Windsor, John, Pirola, Ron, Neale, Rachel

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The promise and potential of Queensland's 'Human Rights Act' for Indigenous peoples: Interpreting the 'environmental right' von Nick Wray-Jones, Justine Bell-James

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The promise and potential of Queensland's human rights act for Indigenous peoples: Interpreting the 'environmental right' von Nick Wray-Jones, Justine Bell-James

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W11. GENOME-WIDE ANALYSIS OF THE ANXIETY DISORDER SPECTRUM von Kuile, Abigail ter, Davies, Molly, Purves, Kirstin, Coleman, Jonathan, Hübel, Christopher, Kalsi, Gursharan, Mundy, Jessica, Skelton, Megan, Morneau-Vaillancourt, Genevieve, Zvrskovec, Johan, Breen, Gerome, Eley, Thalia

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Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis von Loh, Po-Ru, Bhatia, Gaurav, Gusev, Alexander, Finucane, Hilary K, Bulik-Sullivan, Brendan K, Pollack, Samuela J, de Candia, Teresa R, Lee, Sang Hong, Wray, Naomi R, Kendler, Kenneth S, O'Donovan, Michael C, Neale, Benjamin M, Patterson, Nick, Price, Alkes L

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Familial Alzheimer’s disease patient-derived neurons reveal distinct mutation-specific effects on amyloid beta von Arber, Charles, Toombs, Jamie, Lovejoy, Christopher, Ryan, Natalie S., Paterson, Ross W., Willumsen, Nanet, Gkanatsiou, Eleni, Portelius, Erik, Blennow, Kaj, Heslegrave, Amanda, Schott, Jonathan M., Hardy, John, Lashley, Tammaryn, Fox, Nick C., Zetterberg, Henrik, Wray, Selina

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Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis von Lee, S Hong, Harold, Denise, Nyholt, Dale R, Goddard, Michael E, Zondervan, Krina T, Williams, Julie, Montgomery, Grant W, Wray, Naomi R, Visscher, Peter M

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Familial Alzheimer’s Disease Mutations in PSEN1 Lead to Premature Human Stem Cell Neurogenesis von Arber, Charles, Lovejoy, Christopher, Harris, Lachlan, Willumsen, Nanet, Alatza, Argyro, Casey, Jackie M., Lines, Georgie, Kerins, Caoimhe, Mueller, Anika K., Zetterberg, Henrik, Hardy, John, Ryan, Natalie S., Fox, Nick C., Lashley, Tammaryn, Wray, Selina

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder von Purcell, Shaun M, Wray, Naomi R, Stone, Jennifer L, Visscher, Peter M, O'Donovan, Michael C, Sullivan, Patrick F, Sklar, Pamela

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Pathogenic VCP Mutations Induce Mitochondrial Uncoupling and Reduced ATP Levels von Bartolome, Fernando, Wu, Hsiu-Chuan, Burchell, Victoria S., Preza, Elisavet, Wray, Selina, Mahoney, Colin J., Fox, Nick C., Calvo, Andrea, Canosa, Antonio, Moglia, Cristina, Mandrioli, Jessica, Chiò, Adriano, Orrell, Richard W., Houlden, Henry, Hardy, John, Abramov, Andrey Y., Plun-Favreau, Helene

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Knockdown of Amyloid Precursor Protein: Biological Consequences and Clinical Opportunities von Gabriele, Rebecca M C, Abel, Emily, Fox, Nick C, Wray, Selina, Arber, Charles

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CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits von Macé, Aurélien, Tuke, Marcus A., Deelen, Patrick, Kristiansson, Kati, Mattsson, Hannele, Nõukas, Margit, Sapkota, Yadav, Schick, Ursula, Rüeger, Sina, McDaid, Aaron F., Porteous, David, Winkler, Thomas W., Shrine, Nick, Liu, Xueping, Ang, Wei Q., Zhang, Weihua, Feitosa, Mary F., Venturini, Cristina, van der Most, Peter J., Rosengren, Anders, Wood, Andrew R., Beaumont, Robin N., Jones, Samuel E., Ruth, Katherine S., Yaghootkar, Hanieh, Tyrrell, Jessica, Havulinna, Aki S., Boers, Harmen, Mägi, Reedik, Kriebel, Jennifer, Perola, Markus, Nieminen, Markku, Lokki, Marja-Liisa, Kähönen, Mika, Viikari, Jorma S., Geller, Frank, Lahti, Jari, Palotie, Aarno, Koponen, Päivikki, Lundqvist, Annamari, Bottinger, Erwin P., Afaq, Saima, Wojczynski, Mary K., Lenzini, Petra, Nolte, Ilja M., Sparsø, Thomas, Schupf, Nicole, Christensen, Kaare, Perls, Thomas T., Newman, Anne B., Werge, Thomas, Snieder, Harold, Spector, Timothy D., Chambers, John C., Koskinen, Seppo, Melbye, Mads, Raitakari, Olli T., Lehtimäki, Terho, Tobin, Martin D., Wain, Louise V., Sinisalo, Juha, Peters, Annette, Meitinger, Thomas, Martin, Nicholas G., Wray, Naomi R., Montgomery, Grant W., Medland, Sarah E., Swertz, Morris A., Vartiainen, Erkki, Borodulin, Katja, Männistö, Satu, Murray, Anna, Bochud, Murielle, Jacquemont, Sébastien, Rivadeneira, Fernando, Hansen, Thomas F., Oldehinkel, Albertine J., Mangino, Massimo, Province, Michael A., Deloukas, Panos, Kooner, Jaspal S., Freathy, Rachel M., Pennell, Craig, Feenstra, Bjarke, Strachan, David P., Hirschhorn, Joel, Cusi, Daniele, Hayward, Caroline, Männik, Katrin, Beckmann, Jacques S., Loos, Ruth J. F., Nyholt, Dale R., Metspalu, Andres, Eriksson, Johan G., Weedon, Michael N., Salomaa, Veikko, Franke, Lude, Reymond, Alexandre, Frayling, Timothy M., Kutalik, Zoltán

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SILK studies — capturing the turnover of proteins linked to neurodegenerative diseases von Paterson, Ross W., Gabelle, Audrey, Lucey, Brendan P., Barthélemy, Nicolas R., Leckey, Claire A., Hirtz, Christophe, Lehmann, Sylvain, Sato, Chihiro, Patterson, Bruce W., West, Tim, Yarasheski, Kevin, Rohrer, Jonathan D., Wildburger, Norelle C., Schott, Jonathan M., Karch, Celeste M., Wray, Selina, Miller, Timothy M., Elbert, Donald L., Zetterberg, Henrik, Fox, Nick C., Bateman, Randall J.

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Stem cell therapy for Alzheimer's disease: hope or hype? von Wray, Selina, Fox, Nick C

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Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness von Willems, Sara M., Wright, Daniel J., Day, Felix R., Trajanoska, Katerina, Joshi, Peter K., Morris, John A., Matteini, Amy M., Garton, Fleur C., Grarup, Niels, Oskolkov, Nikolay, Thalamuthu, Anbupalam, Mangino, Massimo, Liu, Jun, Demirkan, Ayse, Lek, Monkol, Xu, Liwen, Wang, Guan, Oldmeadow, Christopher, Gaulton, Kyle J., Lotta, Luca A., Miyamoto-Mikami, Eri, Rivas, Manuel A., White, Tom, Loh, Po-Ru, Aadahl, Mette, Amin, Najaf, Attia, John R., Austin, Krista, Benyamin, Beben, Brage, Søren, Cheng, Yu-Ching, Cięszczyk, Paweł, Derave, Wim, Eriksson, Karl-Fredrik, Eynon, Nir, Linneberg, Allan, Lucia, Alejandro, Massidda, Myosotis, Mitchell, Braxton D., Miyachi, Motohiko, Murakami, Haruka, Padmanabhan, Sandosh, Pandey, Ashutosh, Papadimitriou, Ioannis, Rajpal, Deepak K., Sale, Craig, Schnurr, Theresia M., Sessa, Francesco, Shrine, Nick, Tobin, Martin D., Varley, Ian, Wain, Louise V., Wray, Naomi R., Lindgren, Cecilia M., MacArthur, Daniel G., Waterworth, Dawn M., McCarthy, Mark I., Pedersen, Oluf, Khaw, Kay-Tee, Kiel, Douglas P., Pitsiladis, Yannis, Fuku, Noriyuki, Franks, Paul W., North, Kathryn N., van Duijn, Cornelia M., Mather, Karen A., Hansen, Torben, Hansson, Ola, Spector, Tim, Murabito, Joanne M., Richards, J. Brent, Rivadeneira, Fernando, Langenberg, Claudia, Perry, John R. B., Wareham, Nick J., Scott, Robert A.

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Whole-genome sequencing reveals host factors underlying critical COVID-19 von Kousathanas, Athanasios, Pairo-Castineira, Erola, Rawlik, Konrad, Stuckey, Alex, Odhams, Christopher A., Walker, Susan, Russell, Clark D., Malinauskas, Tomas, Wu, Yang, Millar, Jonathan, Shen, Xia, Elliott, Katherine S., Griffiths, Fiona, Oosthuyzen, Wilna, Morrice, Kirstie, Keating, Sean, Wang, Bo, Rhodes, Daniel, Klaric, Lucija, Zechner, Marie, Parkinson, Nick, Siddiq, Afshan, Goddard, Peter, Donovan, Sally, Maslove, David, Nichol, Alistair, Semple, Malcolm G., Zainy, Tala, Maleady-Crowe, Fiona, Todd, Linda, Salehi, Shahla, Knight, Julian, Elgar, Greg, Chan, Georgia, Arumugam, Prabhu, Patch, Christine, Rendon, Augusto, Bentley, David, Kingsley, Clare, Kosmicki, Jack A., Horowitz, Julie E., Baras, Aris, Abecasis, Goncalo R., Ferreira, Manuel A. R., Justice, Anne, Mirshahi, Tooraj, Oetjens, Matthew, Rader, Daniel J., Ritchie, Marylyn D., Verma, Anurag, Fowler, Tom A., Shankar-Hari, Manu, Summers, Charlotte, Hinds, Charles, Horby, Peter, Ling, Lowell, McAuley, Danny, Montgomery, Hugh, Openshaw, Peter J. M., Elliott, Paul, Walsh, Timothy, Tenesa, Albert, Fawkes, Angie, Murphy, Lee, Rowan, Kathy, Ponting, Chris P., Vitart, Veronique, Wilson, James F., Yang, Jian, Bretherick, Andrew D., Scott, Richard H., Hendry, Sara Clohisey, Moutsianas, Loukas, Law, Andy, Caulfield, Mark J., Baillie, J. Kenneth

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How To Make A Million (Mdd Cases) von Martin, Nick, Sullivan, Patrick, Wray, Naomi

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Revealing Elasmobranch Distributions in Turbid Coastal Waters: Insights From Environmental DNA and Particle Tracking von Dunn, Nick, Ward, Sophie, Barker, Joanna, Davies, Jake, Davies, Sarah, Wray, Ben, Robins, Peter, Apetroaie, Isabelle, Williams, Jake, Hopkins, Kevin, Curnick, David

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T46. ASSOCIATION BETWEEN POLYGENIC RISK FOR INDIVIDUAL DEPRESSION SYMPTOMS AND CLINICAL FEATURES OF MAJOR DEPRESSION von Thorp, Jackson, Gerring, Zachary, Byrne, Enda, Medland, Sarah, Wray, Naomi, Martin, Nick, Derks, Eske

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Developmental regulation of tau splicing is disrupted in stem cell-derived neurons from frontotemporal dementia patients with the 10 + 16 splice-site mutation in MAPT von Sposito, Teresa, Preza, Elisavet, Mahoney, Colin J, Setó-Salvia, Núria, Ryan, Natalie S, Morris, Huw R, Arber, Charles, Devine, Michael J, Houlden, Henry, Warner, Thomas T, Bushell, Trevor J, Zagnoni, Michele, Kunath, Tilo, Livesey, Frederick J, Fox, Nick C, Rossor, Martin N, Hardy, John, Wray, Selina

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