Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer’s disease von Kumar, Atul, Shoai, Maryam, Palmqvist, Sebastian, Stomrud, Erik, Hardy, John, Mattsson-Carlgren, Niklas, Hansson, Oskar

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Genome‐Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease von Tan, Manuela M.X., Lawton, Michael A., Jabbari, Edwin, Reynolds, Regina H., Iwaki, Hirotaka, Blauwendraat, Cornelis, Kanavou, Sofia, Pollard, Miriam I., Hubbard, Leon, Malek, Naveed, Grosset, Katherine A., Marrinan, Sarah L., Bajaj, Nin, Barker, Roger A., Burn, David J., Bresner, Catherine, Foltynie, Thomas, Wood, Nicholas W., Williams‐Gray, Caroline H., Hardy, John, Nalls, Michael A., Singleton, Andrew B., Williams, Nigel M., Ben‐Shlomo, Yoav, Hu, Michele T.M., Grosset, Donald G., Shoai, Maryam, Morris, Huw R.

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A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK von Morgan, Sarah, Shatunov, Aleksey, Sproviero, William, Jones, Ashley R, Shoai, Maryam, Hughes, Deborah, Al Khleifat, Ahmad, Malaspina, Andrea, Morrison, Karen E, Shaw, Pamela J, Shaw, Christopher E, Sidle, Katie, Orrell, Richard W, Fratta, Pietro, Hardy, John, Pittman, Alan, Al-Chalabi, Ammar

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What does heritability of Alzheimer's disease represent? von Baker, Emily, Leonenko, Ganna, Schmidt, Karl Michael, Hill, Matthew, Myers, Amanda J, Shoai, Maryam, de Rojas, Itziar, Tesi, Niccoló, Holstege, Henne, van der Flier, Wiesje M, Pijnenburg, Yolande A L, Ruiz, Agustin, Hardy, John, van der Lee, Sven, Escott-Price, Valentina

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Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosis von Morgan, Sarah, Shoai, Maryam, Fratta, Pietro, Sidle, Katie, Orrell, Richard, Sweeney, Mary G, Shatunov, Aleksey, Sproviero, William, Jones, Ashley, Al-Chalabi, Ammar, Malaspina, Andrea, Houlden, Henry, Hardy, John, Pittman, Alan

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Local genetic correlations exist among neurodegenerative and neuropsychiatric diseases von Reynolds, Regina H., Wagen, Aaron Z., Lona-Durazo, Frida, Scholz, Sonja W., Shoai, Maryam, Hardy, John, Gagliano Taliun, Sarah A., Ryten, Mina

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Author Correction: Local genetic correlations exist among neurodegenerative and neuropsychiatric diseases von Reynolds, Regina H., Wagen, Aaron Z., Lona-Durazo, Frida, Scholz, Sonja W., Shoai, Maryam, Hardy, John, Gagliano Taliun, Sarah A., Ryten, Mina

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Genetic meta-analysis of levodopa induced dyskinesia in Parkinson’s disease von Martinez-Carrasco, Alejandro, Real, Raquel, Lawton, Michael, Iwaki, Hirotaka, Tan, Manuela M. X., Wu, Lesley, Williams, Nigel M., Carroll, Camille, Hu, Michele T. M., Grosset, Donald G., Hardy, John, Ryten, Mina, Foltynie, Tom, Ben-Shlomo, Yoav, Shoai, Maryam, Morris, Huw R.

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Genome-wide determinants of mortality and motor progression in Parkinson’s disease von Tan, Manuela M. X., Lawton, Michael A., Pollard, Miriam I., Brown, Emmeline, Real, Raquel, Carrasco, Alejandro Martinez, Bekadar, Samir, Jabbari, Edwin, Reynolds, Regina H., Iwaki, Hirotaka, Blauwendraat, Cornelis, Kanavou, Sofia, Hubbard, Leon, Malek, Naveed, Grosset, Katherine A., Bajaj, Nin, Barker, Roger A., Burn, David J., Bresner, Catherine, Foltynie, Thomas, Wood, Nicholas W., Williams-Gray, Caroline H., Andreassen, Ole A., Toft, Mathias, Elbaz, Alexis, Artaud, Fanny, Brice, Alexis, Corvol, Jean-Christophe, Aasly, Jan, Farrer, Matthew J., Nalls, Michael A., Singleton, Andrew B., Williams, Nigel M., Ben-Shlomo, Yoav, Hardy, John, Hu, Michele T. M., Grosset, Donald G., Shoai, Maryam, Pihlstrøm, Lasse, Morris, Huw R.

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Genetic and polygenic risk score analysis for Alzheimer's disease in the Chinese population von Zhou, Xiaopu, Chen, Yu, Ip, Fanny C. F., Lai, Nicole C. H., Li, Yolanda Y. T., Jiang, Yuanbing, Zhong, Huan, Chen, Yuewen, Zhang, Yulin, Ma, Shuangshuang, Lo, Ronnie M. N., Cheung, Kit, Tong, Estella P. S., Ko, Ho, Shoai, Maryam, Mok, Kin Y., Hardy, John, Mok, Vincent C. T., Kwok, Timothy C. Y., Fu, Amy K. Y., Ip, Nancy Y.

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Polygenic score prediction captures nearly all common genetic risk for Alzheimer’s disease von Escott-Price, Valentina, Shoai, Maryam, Pither, Richard, Williams, Julie, Hardy, John

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Genetic risk for alzheimer disease is distinct from genetic risk for amyloid deposition von Leonenko, Ganna, Shoai, Maryam, Bellou, Eftychia, Sims, Rebecca, Williams, Julie, Hardy, John, Escott‐Price, Valentina

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Novel screening tool for secondary headache in acute care—A pilot study von Haider, Salman, Shoai, Maryam, Shah, Runil, Turner, Chris, Bahra, Anish

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Geographical distribution of host's specific SARS-CoV-2 mutations in the early phase of the COVID-19 pandemic von Khalid, Mohammad, Murphy, David, Shoai, Maryam, George-William, Jonahunnatha Nesson, Al-ebini, Yousef

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A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene von Magusali, Naciye, Graham, Andrew C., Piers, Thomas M., Panichnantakul, Pantila, Yaman, Umran, Shoai, Maryam, Reynolds, Regina H., Botia, Juan A., Brookes, Keeley J., Guetta-Baranes, Tamar, Bellou, Eftychia, Bayram, Sevinc, Sokolova, Dimitra, Ryten, Mina, Frigerio, Carlo Sala, Escott-Price, Valentina, Morgan, Kevin, Pocock, Jennifer M., Hardy, John, Salih, Dervis A.

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Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis von Johnson, Janel O, Pioro, Erik P, Boehringer, Ashley, Chia, Ruth, Feit, Howard, Renton, Alan E, Pliner, Hannah A, Abramzon, Yevgeniya, Marangi, Giuseppe, Winborn, Brett J, Gibbs, J Raphael, Nalls, Michael A, Morgan, Sarah, Shoai, Maryam, Hardy, John, Pittman, Alan, Orrell, Richard W, Malaspina, Andrea, Sidle, Katie C, Fratta, Pietro, Harms, Matthew B, Baloh, Robert H, Pestronk, Alan, Weihl, Conrad C, Rogaeva, Ekaterina, Zinman, Lorne, Drory, Vivian E, Borghero, Giuseppe, Mora, Gabriele, Calvo, Andrea, Rothstein, Jeffrey D, Drepper, Carsten, Sendtner, Michael, Singleton, Andrew B, Taylor, J Paul, Cookson, Mark R, Restagno, Gabriella, Sabatelli, Mario, Bowser, Robert, Chiò, Adriano, Traynor, Bryan J

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Assessing clinical progression measures in Alzheimer's disease trials: A systematic review and meta-analysis von McLaughlin, Jonathan, Scotton, William J, Ryan, Natalie S, Hardy, John A, Shoai, Maryam

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Genetic analysis suggests high misassignment rates in clinical Alzheimer's cases and controls von Escott-Price, Valentina, Baker, Emily, Shoai, Maryam, Leonenko, Ganna, Myers, Amanda J., Huentelman, Matt, Hardy, John

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Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study von Jabbari, Edwin, Koga, Shunsuke, Valentino, Rebecca R, Reynolds, Regina H, Ferrari, Raffaele, Tan, Manuela M X, Rowe, James B, Dalgard, Clifton L, Scholz, Sonja W, Dickson, Dennis W, Warner, Thomas T, Revesz, Tamas, Höglinger, Günter U, Ross, Owen A, Ryten, Mina, Hardy, John, Shoai, Maryam, Morris, Huw R, Mok, Kin Y., Murphy, David P., Al-Sarraj, Safa, Troakes, Claire, Gentleman, Steve M., Allinson, Kieren S.J., Jaunmuktane, Zane, Holton, Janice L., Lees, Andrew J., Morris, Christopher M., Compta, Yaroslau, Gelpi, Ellen, van Swieten, John C., Rajput, Alex, Ferguson, Leslie, Cookson, Mark R., Gibbs, J. Raphael, Blauwendraat, Cornelis, Ding, Jinhui, Chia, Ruth, Traynor, Bryan J., Pantelyat, Alexander, Viollet, Coralie, Pletnikova, Olga, Troncoso, Juan C., Rosenthal, Liana S., Boxer, Adam L., Respondek, Gesine, Arzberger, Thomas, Roeber, Sigrun, Giese, Armin, Burn, David J., Pavese, Nicola, Gerhard, Alexander, Kobylecki, Christopher, Leigh, P. Nigel, Church, Alistair, T.M. Hu, Michele

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Association between the LRP1B and APOE loci and the development of Parkinson’s disease dementia von Real, Raquel, Martinez-Carrasco, Alejandro, Reynolds, Regina H, Lawton, Michael A, Tan, Manuela M X, Shoai, Maryam, Corvol, Jean-Christophe, Ryten, Mina, Bresner, Catherine, Hubbard, Leon, Brice, Alexis, Lesage, Suzanne, Faouzi, Johann, Elbaz, Alexis, Artaud, Fanny, Williams, Nigel, Hu, Michele T M, Ben-Shlomo, Yoav, Grosset, Donald G, Hardy, John, Morris, Huw R

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