Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease von Chaudhury, Sultan, Patel, Tulsi, Barber, Imelda S., Guetta-Baranes, Tamar, Brookes, Keeley J., Chappell, Sally, Turton, James, Guerreiro, Rita, Bras, Jose, Hernandez, Dena, Singleton, Andrew, Hardy, John, Mann, David, Passmore, Peter, Craig, David, Johnston, Janet, McGuinness, Bernadette, Todd, Stephen, Heun, Reinhard, Kölsch, Heike, Kehoe, Patrick G., Vardy, Emma R.L.C., Hooper, Nigel M., Pickering-Brown, Stuart, Snowden, Julie, Richardson, Anna, Jones, Matthew, Neary, David, Harris, Jennifer, Lowe, James, Smith, A. David, Wilcock, Gordon, Warden, Donald, Holmes, Clive, Morgan, Kevin

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Mutation Analysis of Sporadic Early-Onset Alzheimer’s Disease using the NeuroX Array von Barber, Imelda S, Braae, Anne, Clement, Naomi, Patel, Tulsi, Guetta-Baranes, Tamar, Brookes, Keeley, Medway, Christopher, Chappell, Sally, Guerreiro, Rita, Bras, Jose, Hernandez, Dena, Singleton, Andrew, Hardy, John, Mann, David M, Passmore, Peter, Craig, David, Johnston, Janet, McGuinness, Bernadette, Todd, Stephen, Heun, Reinhard, Kölsch, Heike, Kehoe, Patrick G, Vardy, Emma R.L.C, Hooper, Nigel M, Pickering-Brown, Stuart, Snowden, Julie, Richardson, Anna, Jones, Matthew, Neary, David, Harris, Jennifer, Lowe, James, Smith, A. David, Wilcock, Gordon, Warden, Donald, Holmes, Clive, Morgan, Kevin

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A plasma protein classifier for predicting amyloid burden for preclinical Alzheimer's disease von Ashton, Nicholas J, Nevado-Holgado, Alejo J, Barber, Imelda S, Lynham, Steven, Gupta, Veer, Chatterjee, Pratishtha, Goozee, Kathryn, Hone, Eugene, Pedrini, Steve, Blennow, Kaj, Schöll, Michael, Zetterberg, Henrik, Ellis, Kathryn A, Bush, Ashley I, Rowe, Christopher C, Villemagne, Victor L, Ames, David, Masters, Colin L, Aarsland, Dag, Powell, John, Lovestone, Simon, Martins, Ralph, Hye, Abdul

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Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's disease von Barber, Imelda S, García-Cárdenas, Jennyfer M, Sakdapanichkul, Chidchanok, Deacon, Christopher, Zapata Erazo, Gabriela, Guerreiro, Rita, Bras, Jose, Hernandez, Dena, Singleton, Andrew, Guetta-Baranes, Tamar, Braae, Anne, Clement, Naomi, Patel, Tulsi, Brookes, Keeley, Medway, Christopher, Chappell, Sally, Mann, David M, Morgan, Kevin

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Methylation Profiling RIN3 and MEF2C Identifies Epigenetic Marks Associated with Sporadic Early Onset Alzheimer's Disease von Boden, Kirsty A, Barber, Imelda S, Clement, Naomi, Patel, Tulsi, Guetta-Baranes, Tamar, Brookes, Keeley J, Chappell, Sally, Craigon, Jim, Chapman, Natalie H, Morgan, Kevin, Seymour, Graham B, Bottley, Andrew

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Proteomic analysis of Parkinson’s disease patient cohorts show similarities in mechanism to Alzheimer’s disease von Winchester, Laura M., Lawton, Michael, Barber, Imelda S., Evetts, Samuel, Ryan, Brent, Wade‐Martins, Richard, Ben‐Shlomo, Yoav, Hu, Michele, Grosset, Donald G., Nevado‐Holgado, Alejo J., Lovestone, Simon

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Prion-like α-synuclein pathology in the brain of infants with Krabbe disease von Hatton, Christopher, Ghanem, Simona S, Koss, David J, Abdi, Ilham Y, Gibbons, Elizabeth, Guerreiro, Rita, Bras, Jose, Walker, Lauren, Gelpi, Ellen, Heywood, Wendy, Outeiro, Tiago F, Attems, Johannes, McFarland, Robert, Forsyth, Rob, El-Agnaf, Omar M, Erskine, Daniel

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A PARKINSON’S DISEASE PROTEIN BIOMARKER PANEL USING THE SOMAMER ASSAY AND MACHINE LEARNING von Barber, Imelda S., Nevado-Holgado, Alejo J., Lovestone, Simon

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LRP10 in α-synucleinopathies von Kia, Demis A, Sabir, Marya S, Ahmed, Sarah, Bandres-Ciga, Sara, Noyce, Alastair J, Kaiyrzhanov, Rauan, Middlehurst, Ben, Tan, Manuela, Plun-Favreau, Helene, Holmans, Peter, Hardy, John, Trabzuni, Daniah, Quinn, John, Kinghorn, Kerri J., Billingsley, Kimberley, Wood, Nicholas W, Guerreiro, Rita, Lovering, Ruth, R'Bibo, Lea, Rizig, Mie, Ryten, Mina, Escott-Price, Valentina, Chelban, Viorica, Foltynie, Thomas, Williams, Nigel, Danjou, Fabrice, Lesage, Suzanne, Corvol, Jean-Christophe, Schulte, Claudia, Simón-Sánchez, Javier, Heutink, Peter, Rizzu, Patrizia, Sharma, Manu, Nicolas, Aude, Cookson, Mark R, Bandres-Ciga, Sara, Craig, David W., Faghri, Faraz, Shulman, Joshua M., Iwaki, Hirotaka, Leonard, Hampton L., Nalls, Mike A., Lubbe, Steven, Finkbeiner, Steven, Lungu, Codrin, Singleton, Andrew B, Reed, Xylena, Alcalay, Roy N., Gan-Or, Ziv, Rouleau, Guy A., van Hilten, Jacobus J, Marinus, Johan, Adarmes-Gómez, Astrid D., Barrero, Francisco J., Bergareche Yarza, Jesús A., Bernal-Bernal, Inmaculada, Blazquez, Marta, Botía, Juan A., Boungiorno, María Teresa, Cámara, Ana, Carrillo, Fátima, Carrión-Claro, Mario, Cerdan, Debora, Clarimón, Jordi, Diez-Farien, Monica, Dols-Icardo, Oriol, Duarte, Jacinto, Escamilla-Sevilla, Francisco, Feliz, Cici, Fernández, Manel, Garcia, Ciara, García-Ruiz, Pedro, Gómez-Garre, Pilar, Gonzalez-Aramburu, Isabel, Infante, Jon, Kulisevsky, Jaime, Labrador-Espinosa, Miguel A., López de Munain Arregui, Adolfo, Macias, Daniel, Marín, Juan, Marti, Maria Jose, Martínez- Castrillo, Juan Carlos, Menéndez González, Manuel, Mondragon Rezola, Elisabet, Muñoz, Esteban, Pagonabarraga, Javier, Pastor, Pau, Ruiz-Martínez, Javier, Ruz, Clara, Sierra, María, Suarez-Sanmartin, Esther, Tabernero, Cesar, Tejera-Parrado, Cristina, Tolosa, Eduard, Valldeoriola, Francesc, Pihlstrom, Lasse, Toft, Mathias, Koks, Sulev, Taba, Pille, Hassin-Baer, Sharon

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Screening Exon 16 and 17 of the Amyloid Precursor Protein Gene in Sporadic Early-Onset Alzheimer’s Disease (sEOAD) von Barber, Imelda S., García-Cárdenas, Jennyfer M., Sakdapanichkul, Chidchanok, Deacon, Christopher, Erazo, Gabriela Zapata, Guerreiro, Rita, Bras, Jose, Hernandez, Dena, Singleton, Andrew, Guetta-Baranes, Tamar, Braae, Anne, Clement, Naomi, Patel, Tulsi, Brookes, Keeley, Medway, Christopher, Chappell, Sally, Mann, David M., Morgan, Kevin

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Complement receptor 1 gene (CR1) intragenic duplication and risk of Alzheimer’s disease von Kucukkilic, Ezgi, Brookes, Keeley, Barber, Imelda, Guetta-Baranes, Tamar, Morgan, Kevin, Hollox, Edward J.

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Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease von Cruchaga, Carlos, Karch, Celeste M., Jin, Sheng Chih, Benitez, Bruno A., Cai, Yefei, Guerreiro, Rita, Harari, Oscar, Norton, Joanne, Budde, John, Bertelsen, Sarah, Jeng, Amanda T., Cooper, Breanna, Skorupa, Tara, Carrell, David, Levitch, Denise, Hsu, Simon, Choi, Jiyoon, Ryten, Mina, Sassi, Celeste, Bras, Jose, Gibbs, J. Raphael, Hernandez, Dena G., Lupton, Michelle K., Powell, John, Forabosco, Paola, Ridge, Perry G., Corcoran, Christopher D., Tschanz, JoAnn T., Norton, Maria C., Munger, Ronald G., Schmutz, Cameron, Leary, Maegan, Demirci, F. Yesim, Bamne, Mikhil N., Wang, Xingbin, Lopez, Oscar L., Ganguli, Mary, Medway, Christopher, Turton, James, Lord, Jenny, Braae, Anne, Barber, Imelda, Brown, Kristelle, Pastor, Pau, Lorenzo-Betancor, Oswaldo, Brkanac, Zoran, Scott, Erick, Topol, Eric, Morgan, Kevin, Rogaeva, Ekaterina, Singleton, Andrew B., Hardy, John, Kamboh, M. Ilyas, St George-Hyslop, Peter, Cairns, Nigel, Morris, John C., Kauwe, John S. K., Goate, Alison M.

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Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies von Bras, Jose, Guerreiro, Rita, Darwent, Lee, Parkkinen, Laura, Ansorge, Olaf, Escott-Price, Valentina, Hernandez, Dena G, Nalls, Michael A, Clark, Lorraine N, Honig, Lawrence S, Marder, Karen, Van Der Flier, Wiesje M, Lemstra, Afina, Scheltens, Philip, Rogaeva, Ekaterina, St George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Ortega-Cubero, Sara, Pastor, Pau, Ferman, Tanis J, Graff-Radford, Neill R, Ross, Owen A, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Maetzler, Walter, Berg, Daniela, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Compta, Yaroslau, Revesz, Tamas, Lees, Andrew, Cairns, Nigel, Halliday, Glenda M, Mann, David, Pickering-Brown, Stuart, Dickson, Dennis W, Singleton, Andrew, Hardy, John

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Complement receptor 1 gene von Kucukkilic, Ezgi, Brookes, Keeley, Barber, Imelda, Guetta-Baranes, Tamar, Morgan, Kevin, Hollox, Edward J

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Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases von Guerreiro, Rita, Escott-Price, Valentina, Darwent, Lee, Parkkinen, Laura, Ansorge, Olaf, Hernandez, Dena G, Nalls, Michael A, Clark, Lorraine, Honig, Lawrence, Marder, Karen, van der Flier, Wiesje, Holstege, Henne, Louwersheimer, Eva, Lemstra, Afina, Scheltens, Philip, Rogaeva, Ekaterina, St George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Ortega-Cubero, Sara, Pastor, Pau, Ferman, Tanis J, Graff-Radford, Neill R, Ross, Owen A, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Maetzler, Walter, Berg, Daniela, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Compta, Yaroslau, Revesz, Tamas, Lees, Andrew, Cairns, Nigel J, Halliday, Glenda M, Mann, David, Pickering-Brown, Stuart, Powell, John, Lunnon, Katie, Lupton, Michelle K, Dickson, Dennis, Hardy, John, Singleton, Andrew, Bras, Jose

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Missense variant in TREML2 protects against Alzheimer's disease von Benitez, Bruno A, Jin, Sheng Chih, Guerreiro, Rita, Graham, Rob, Lord, Jenny, Harold, Denise, Sims, Rebecca, Lambert, Jean-Charles, Gibbs, J. Raphael, Bras, Jose, Sassi, Celeste, Harari, Oscar, Bertelsen, Sarah, Lupton, Michelle K, Powell, John, Bellenguez, Celine, Brown, Kristelle, Medway, Christopher, Haddick, Patrick CG, van der Brug, Marcel P, Bhangale, Tushar, Ortmann, Ward, Behrens, Tim, Mayeux, Richard, Pericak-Vance, Margaret A, Farrer, Lindsay A, Schellenberg, Gerard D, Haines, Jonathan L, Turton, Jim, Braae, Anne, Barber, Imelda, Fagan, Anne M, Holtzman, David M, Morris, John C, Williams, Julie, Kauwe, John S.K, Amouyel, Philippe, Morgan, Kevin, Singleton, Andy, Hardy, John, Goate, Alison M, Cruchaga, Carlos

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Identification of a possible proteomic biomarker in Parkinson’s disease: discovery and replication in blood, brain and cerebrospinal fluid von Winchester, Laura, Barber, Imelda, Lawton, Michael, Ash, Jessica, Liu, Benjamine, Evetts, Samuel, Hopkins-Jones, Lucinda, Lewis, Suppalak, Bresner, Catherine, Malpartida, Ana Belen, Williams, Nigel, Gentlemen, Steve, Wade-Martins, Richard, Ryan, Brent, Holgado-Nevado, Alejo, Hu, Michele, Ben-Shlomo, Yoav, Grosset, Donald, Lovestone, Simon

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Evaluating pathogenic dementia variants in posterior cortical atrophy von Carrasquillo, Minerva M, Barber, Imelda, Lincoln, Sarah J, Murray, Melissa E, Camsari, Gamze Balci, Khan, Qurat ul Ain, Nguyen, Thuy, Ma, Li, Bisceglio, Gina D, Crook, Julia E, Younkin, Steven G, Dickson, Dennis W, Boeve, Bradley F, Graff-Radford, Neill R, Morgan, Kevin, Ertekin-Taner, Nilüfer

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P3‐091: Investigating SARM1 Variants in Alzheimer’s Disease Cohorts von Patel, Tulsi, Clement, Naomi S., Barber, Imelda, Braae, Anne, Brookes, Keeley J., Guetta-Baranes, Tamar, Chappell, Sally, Guerreiro, Rita, Bras, Jose T., Singleton, Andrew, Hardy, John, Morgan, Kevin

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P2‐065: Identifying Polymorphisms in The Alzheimer’s Related APP Gene Using The Oxford Nanopore Minion Sequencer von Brookes, Keeley J., Patel, Tulsi, Zapata-Erazo, Gabriela, Barber, Imelda, Braae, Anne, Guetta-Baranes, Tamar, Clement, Naomi S., Medway, Christopher, Chappell, Sally, Morgan, Kevin

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