A review of pharmaceutical occurrence and pathways in the aquatic environment in the context of a changing climate and the COVID-19 pandemic von O'Flynn, Dylan, Lawler, Jenny, Yusuf, Azeez, Parle-McDermott, Anne, Harold, Denise, Mc Cloughlin, Thomas, Holland, Linda, Regan, Fiona, White, Blánaid

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A modifier of Huntington's disease onset at the MLH1 locus von Lee, Jong-Min, Chao, Michael J, Harold, Denise, Abu Elneel, Kawther, Gillis, Tammy, Holmans, Peter, Jones, Lesley, Orth, Michael, Myers, Richard H, Kwak, Seung, Wheeler, Vanessa C, MacDonald, Marcy E, Gusella, James F

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Genetic evidence for the involvement of lipid metabolism in Alzheimer's disease von Jones, Lesley, Harold, Denise, Williams, Julie

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Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia von Pagnamenta, Alistair T, Bacchelli, Elena, de Jonge, Maretha V, Mirza, Ghazala, Scerri, Thomas S, Minopoli, Fiorella, Chiocchetti, Andreas, Ludwig, Kerstin U, Hoffmann, Per, Paracchini, Silvia, Lowy, Ernesto, Harold, Denise H, Chapman, Jade A, Klauck, Sabine M, Poustka, Fritz, Houben, Renske H, Staal, Wouter G, Ophoff, Roel A, O'Donovan, Michael C, Williams, Julie, Nöthen, Markus M, Schulte-Körne, Gerd, Deloukas, Panos, Ragoussis, Jiannis, Bailey, Anthony J, Maestrini, Elena, Monaco, Anthony P

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Mito-SiPE is a sequence-independent and PCR-free mtDNA enrichment method for accurate ultra-deep mitochondrial sequencing von Walsh, Darren J., Bernard, David J., Pangilinan, Faith, Esposito, Madison, Harold, Denise, Parle-McDermott, Anne, Brody, Lawrence C.

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SNPs associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease von Cruchaga, Carlos, Kauwe, John S K, Mayo, Kevin, Spiegel, Noah, Bertelsen, Sarah, Nowotny, Petra, Shah, Aarti R, Abraham, Richard, Hollingworth, Paul, Harold, Denise, Owen, Michael M, Williams, Julie, Lovestone, Simon, Peskind, Elaine R, Li, Ge, Leverenz, James B, Galasko, Douglas, Morris, John C, Fagan, Anne M, Holtzman, David M, Goate, Alison M

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Remapping the Insulin Gene/IDDM2 Locus in Type 1 Diabetes von BARRATT, Bryan J, PAYNE, Felicity, MCCORMACK, Rose, GUJA, Cristian, IONESCU-URGOVIGTE, Constantin, UNDLIEN, Dag E, RØNNINGEN, Kjersti S, GILLESPIE, Kathleen M, TUOMILEHTO-WOLF, Eva, TUOMILEHTO, Jaakko, BENNETT, Simon T, CLAYTON, David G, LOWE, Chris E, CORDELL, Heather J, TODD, John A, HERMANN, Robert, HEALY, Barry C, HAROLD, Denise, CONCANNON, Patrick, GHARANI, Neda, MCCARTHY, Mark I, OLAVESEN, Mark G

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Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease von Lupton, Michelle K, Proitsi, Petroula, Danillidou, Makrina, Tsolaki, Magda, Hamilton, Gillian, Wroe, Richard, Pritchard, Megan, Lord, Kathryn, Martin, Belinda M, Kloszewska, Iwona, Soininen, Hilkka, Mecocci, Patrizia, Vellas, Bruno, Harold, Denise, Hollingworth, Paul, Lovestone, Simon, Powell, John F

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Characterisation and validation of insertions and deletions in 173 patient exomes von Lescai, Francesco, Bonfiglio, Silvia, Bacchelli, Chiara, Chanudet, Estelle, Waters, Aoife, Sisodiya, Sanjay M, Kasperavičiūtė, Dalia, Williams, Julie, Harold, Denise, Hardy, John, Kleta, Robert, Cirak, Sebahattin, Williams, Richard, Achermann, John C, Anderson, John, Kelsell, David, Vulliamy, Tom, Houlden, Henry, Wood, Nicholas, Sheerin, Una, Tonini, Gian Paolo, Mackay, Donna, Hussain, Khalid, Sowden, Jane, Kinsler, Veronica, Osinska, Justyna, Brooks, Tony, Hubank, Mike, Beales, Philip, Stupka, Elia

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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection von Pardiñas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Esben, Als, Thomas D., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bøcker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Pedersen, Marianne Giørtz, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Hansen, Christine Søholm, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J., O’Donovan, Michael C., Walters, James T. R.

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Common polygenic variation enhances risk prediction for Alzheimer's disease von Escott-Price, Valentina, Sims, Rebecca, Bannister, Christian, Harold, Denise, Vronskaya, Maria, Majounie, Elisa, Badarinarayan, Nandini, Morgan, Kevin, Passmore, Peter, Holmes, Clive, Powell, John, Brayne, Carol, Gill, Michael, Mead, Simon, Goate, Alison, Cruchaga, Carlos, Lambert, Jean-Charles, van Duijn, Cornelia, Maier, Wolfgang, Ramirez, Alfredo, Holmans, Peter, Jones, Lesley, Hardy, John, Seshadri, Sudha, Schellenberg, Gerard D, Amouyel, Philippe, Williams, Julie

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Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease von Lee, Jong-Min, Wheeler, Vanessa C., Chao, Michael J., Vonsattel, Jean Paul G., Pinto, Ricardo Mouro, Lucente, Diane, Abu-Elneel, Kawther, Ramos, Eliana Marisa, Mysore, Jayalakshmi Srinidhi, Gillis, Tammy, MacDonald, Marcy E., Gusella, James F., Harold, Denise, Stone, Timothy C., Escott-Price, Valentina, Han, Jun, Vedernikov, Alexey, Holmans, Peter, Jones, Lesley, Kwak, Seung, Mahmoudi, Mithra, Orth, Michael, Landwehrmeyer, G. Bernhard, Paulsen, Jane S., Dorsey, E. Ray, Shoulson, Ira, Myers, Richard H.

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Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease von Lambert, Jean-Charles, Ibrahim-Verbaas, Carla A, Naj, Adam C, Sims, Rebecca, Bellenguez, Céline, DeStefano, Anita L, Bis, Joshua C, Grenier-Boley, Benjamin, Russo, Giancarlo, Thornton-Wells, Tricia A, Chouraki, Vincent, Zelenika, Diana, Vardarajan, Badri N, Lin, Chiao-Feng, Gerrish, Amy, Schmidt, Helena, Pasquier, Florence, Hollingworth, Paul, Ramirez, Alfredo, Fitzpatrick, Annette L, Buxbaum, Joseph D, Crane, Paul K, Gudnason, Vilmundur, Cruchaga, Carlos, Craig, David, Amin, Najaf, De Jager, Philip L, Deramecourt, Vincent, Johnston, Janet A, Letenneur, Luc, Morón, Francisco J, Kamboh, M Ilyas, Keller, Lina, Barberger-Gateau, Pascale, McGuinness, Bernadette, Larson, Eric B, Green, Robert, Dufouil, Carole, Wallon, David, Love, Seth, St George-Hyslop, Peter, Clarimon, Jordi, Lleo, Alberto, Tsuang, Debby W, Yu, Lei, Bossù, Paola, Proitsi, Petroula, Sorbi, Sandro, Hardy, John, Naranjo, Maria Candida Deniz, Clarke, Robert, Brayne, Carol, Galimberti, Daniela, Mancuso, Michelangelo, Matthews, Fiona, Hampel, Harald, Pilotto, Alberto, Panza, Francesco, Caffarra, Paolo, Gilbert, John R, Mayhaus, Manuel, Lannfelt, Lars, Pichler, Sabrina, Carrasquillo, Minerva M, Alvarez, Victoria, Valladares, Otto, Younkin, Steven G, Coto, Eliecer, Razquin, Cristina, Pastor, Pau, Mateo, Ignacio, O'Donovan, Michael C, Cantwell, Laura B, Blacker, Deborah, Mosley, Thomas H, Bennett, David A, Harris, Tamara B, Holmes, Clive, Passmore, Peter, Montine, Thomas J, Bettens, Karolien, Rotter, Jerome I, Brice, Alexis, Morgan, Kevin, Lunetta, Kathryn L, Kauwe, John S K, Boerwinkle, Eric, Hiltunen, Mikko, Rujescu, Dan, Mayeux, Richard, Hofman, Albert, Graff, Caroline, Psaty, Bruce M, Farrer, Lindsay A, van Duijn, Cornelia M, Van Broeckhoven, Christine, Moskvina, Valentina, Seshadri, Sudha, Williams, Julie, Amouyel, Philippe

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P4‐098: Genome‐wide association study of Alzheimer's disease with depressive symptoms von Harold, Denise

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Genome-wide association study of Alzheimer's disease with depressive symptoms von Harold, Denise

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TREM2 Variants in Alzheimer's Disease von Guerreiro, Rita, Wojtas, Aleksandra, Bras, Jose, Carrasquillo, Minerva, Rogaeva, Ekaterina, Majounie, Elisa, Cruchaga, Carlos, Sassi, Celeste, Kauwe, John S.K, Younkin, Steven, Hazrati, Lilinaz, Collinge, John, Pocock, Jennifer, Lashley, Tammaryn, Williams, Julie, Lambert, Jean-Charles, Amouyel, Philippe, Goate, Alison, Rademakers, Rosa, Morgan, Kevin, Powell, John, St. George-Hyslop, Peter, Singleton, Andrew, Hardy, John

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Can Studies of Neuroinflammation in a TSPO Genetic Subgroup (HAB or MAB) Be Applied to the Entire AD Cohort? von Fan, Zhen, Harold, Denise, Pasqualetti, Giuseppe, Williams, Julie, Brooks, David J, Edison, Paul

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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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S1‐03‐01: New susceptibility genes identified for Alzheimer's disease: Progress from the GERAD (genetic and environmental risk in Alzheimer's disease) consortium von Harold, Denise

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New susceptibility genes identified for Alzheimer's disease: Progress from the GERAD (genetic and environmental risk in Alzheimer's disease) consortium von Harold, Denise

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