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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Heritability Enrichment Implicates Microglia in Parkinson's Disease Pathogenesis von Andersen, Maren Stolp, Bandres‐Ciga, Sara, Reynolds, Regina H., Hardy, John, Ryten, Mina, Krohn, Lynne, Gan‐Or, Ziv, Holtman, Inge R., Pihlstrøm, Lasse

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ggtranscript: an R package for the visualization and interpretation of transcript isoforms using ggplot2 von Gustavsson, Emil K, Zhang, David, Reynolds, Regina H, Garcia-Ruiz, Sonia, Ryten, Mina

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Analysis of subcellular RNA fractions demonstrates significant genetic regulation of gene expression in human brain post-transcriptionally von D’Sa, Karishma, Guelfi, Sebastian, Vandrovcova, Jana, Reynolds, Regina H., Zhang, David, Hardy, John, Botía, Juan A., Weale, Michael E., Taliun, Sarah A. Gagliano, Small, Kerrin S., Ryten, Mina

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The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases von Chen, Zhongbo, Reynolds, Regina H., Pardiñas, Antonio F., Gagliano Taliun, Sarah A., van Rheenen, Wouter, Lin, Kuang, Shatunov, Aleksey, Gustavsson, Emil K., Fogh, Isabella, Jones, Ashley R., Robberecht, Wim, Corcia, Philippe, Chiò, Adriano, Shaw, Pamela J., Morrison, Karen E., Veldink, Jan H., van den Berg, Leonard H., Shaw, Christopher E., Powell, John F., Silani, Vincenzo, Hardy, John A., Houlden, Henry, Owen, Michael J., Turner, Martin R., Ryten, Mina, Al-Chalabi, Ammar

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Regional genetic correlations highlight relationships between neurodegenerative disease loci and the immune system von Lona-Durazo, Frida, Reynolds, Regina H., Scholz, Sonja W., Ryten, Mina, Gagliano Taliun, Sarah A.

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CoExp: A Web Tool for the Exploitation of Co-expression Networks von Garcia-Ruiz, Sonia, Gil-Martinez, Ana L., Cisterna, Alejandro, Jurado-Ruiz, Federico, Reynolds, Regina H., Cookson, Mark R., Hardy, John, Ryten, Mina, Botia, Juan A.

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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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Mitochondrial-nuclear cross-talk in the human brain is modulated by cell type and perturbed in neurodegenerative disease von Fairbrother-Browne, Aine, Ali, Aminah T., Reynolds, Regina H., Garcia-Ruiz, Sonia, Zhang, David, Chen, Zhongbo, Ryten, Mina, Hodgkinson, Alan

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Dementia risk in Parkinson’s disease is associated with interhemispheric connectivity loss and determined by regional gene expression von Zarkali, Angeliki, McColgan, Peter, Ryten, Mina, Reynolds, Regina H., Leyland, Louise-Ann, Lees, Andrew J., Rees, Geraint, Weil, Rimona S.

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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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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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Cross-platform transcriptional profiling identifies common and distinct molecular pathologies in Lewy body diseases von Feleke, Rahel, Reynolds, Regina H., Smith, Amy M., Tilley, Bension, Taliun, Sarah A. Gagliano, Hardy, John, Matthews, Paul M., Gentleman, Steve, Owen, David R., Johnson, Michael R., Srivastava, Prashant K., Ryten, Mina

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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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Informing disease modelling with brain-relevant functional genomic annotations von Reynolds, Regina H, Hardy, John, Ryten, Mina, Gagliano Taliun, Sarah A

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IntroVerse: a comprehensive database of introns across human tissues von García-Ruiz, Sonia, Gustavsson, Emil K, Zhang, David, Reynolds, Regina H, Chen, Zhongbo, Fairbrother-Browne, Aine, Gil-Martínez, Ana Luisa, Botia, Juan A, Collado-Torres, Leonardo, Ryten, Mina

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The non-specific lethal complex regulates genes and pathways genetically linked to Parkinson's disease von Hicks, Amy R, Reynolds, Regina H, O'Callaghan, Benjamin, García-Ruiz, Sonia, Gil-Martínez, Ana Luisa, Botía, Juan, Plun-Favreau, Hélène, Ryten, Mina

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Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype von Jabbari, Edwin, Woodside, John, Tan, Manuela M. X., Shoai, Maryam, Pittman, Alan, Ferrari, Raffaele, Mok, Kin Y., Zhang, David, Reynolds, Regina H., de Silva, Rohan, Grimm, Max‐Joseph, Respondek, Gesine, Müller, Ulrich, Al‐Sarraj, Safa, Gentleman, Stephen M., Lees, Andrew J., Warner, Thomas T., Hardy, John, Revesz, Tamas, Höglinger, Günter U., Holton, Janice L., Ryten, Mina, Morris, Huw R.

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Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types von Saez-Atienzar, Sara, Bandres-Ciga, Sara, Langston, Rebekah G., Kim, Jonggeol J., Choi, Shing Wan, Reynolds, Regina H., Abramzon, Yevgeniya, Dewan, Ramita, Ahmed, Sarah, Landers, John E., Chia, Ruth, Ryten, Mina, Cookson, Mark R., Nalls, Michael A., Chio, Adriano, Traynor, Bryan J.

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