The role of TREM2 in Alzheimer's disease and other neurodegenerative disorders von Carmona, Susana, Zahs, Kathleen, Wu, Elizabeth, Dakin, Kelly, Bras, Jose, Guerreiro, Rita

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Reply to: Genome-wide association studies of polygenic risk score-derived phenotypes may lead to inflated false positive rates von Guerreiro, Rita, Bras, Jose

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Challenge accepted: uncovering the role of rare genetic variants in Alzheimer's disease von Khani, Marzieh, Gibbons, Elizabeth, Bras, Jose, Guerreiro, Rita

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Use of next-generation sequencing and other whole-genome strategies to dissect neurological disease von Bras, Jose, Guerreiro, Rita, Hardy, John

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Genome-wide association of polygenic risk extremes for Alzheimer's disease in the UK Biobank von Gouveia, Catarina, Gibbons, Elizabeth, Dehghani, Nadia, Eapen, James, Guerreiro, Rita, Bras, Jose

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Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis von BRAS, Jose, VERLOES, Alain, SCHNEIDER, Susanne A, MOLE, Sara E, GUERREIRO, Rita J

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Microdeletion in a FAAH pseudogene identified in a patient with high anandamide concentrations and pain insensitivity von Habib, Abdella M., Okorokov, Andrei L., Hill, Matthew N., Bras, Jose T., Lee, Man-Cheung, Li, Shengnan, Gossage, Samuel J., van Drimmelen, Marie, Morena, Maria, Houlden, Henry, Ramirez, Juan D., Bennett, David L.H., Srivastava, Devjit, Cox, James J.

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Bordetella hinzii Pneumonia in Patient with SARS-CoV-2 Infection von Ben Lakhal, Hend, Cachinho, José Bras, Kalfon, Pierre, Naas, Thierry, Benseddik, Zehaira

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Genetic architecture of common non-Alzheimer’s disease dementias von Guerreiro, Rita, Gibbons, Elizabeth, Tábuas-Pereira, Miguel, Kun-Rodrigues, Celia, Santo, Gustavo C., Bras, Jose

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Correction: Challenge accepted: Uncovering the role of rare genetic variants in Alzheimer’s disease von Khani, Marzieh, Gibbons, Elizabeth, Bras, Jose, Guerreiro, Rita

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Genome-wide association study reveals genetic risk underlying Parkinson's disease von Singleton, Andrew B, Gasser, Thomas, Simón-Sánchez, Javier, Schulte, Claudia, Bras, Jose M, Sharma, Manu, Gibbs, J Raphael, Berg, Daniela, Paisan-Ruiz, Coro, Lichtner, Peter, Scholz, Sonja W, Hernandez, Dena G, Krüger, Rejko, Federoff, Monica, Klein, Christine, Goate, Alison, Perlmutter, Joel, Bonin, Michael, Nalls, Michael A, Illig, Thomas, Gieger, Christian, Houlden, Henry, Steffens, Michael, Okun, Michael S, Racette, Brad A, Cookson, Mark R, Foote, Kelly D, Fernandez, Hubert H, Traynor, Bryan J, Schreiber, Stefan, Arepalli, Sampath, Zonozi, Ryan, Gwinn, Katrina, van der Brug, Marcel, Lopez, Grisel, Chanock, Stephen J, Schatzkin, Arthur, Park, Yikyung, Hollenbeck, Albert, Gao, Jianjun, Huang, Xuemei, Wood, Nick W, Lorenz, Delia, Deuschl, Günther, Chen, Honglei, Riess, Olaf, Hardy, John A

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Mutations in ANO3 Cause Dominant Craniocervical Dystonia: Ion Channel Implicated in Pathogenesis von Charlesworth, Gavin, Plagnol, Vincent, Holmström, Kira M., Bras, Jose, Sheerin, Una-Marie, Preza, Elisavet, Rubio-Agusti, Ignacio, Ryten, Mina, Schneider, Susanne A., Stamelou, Maria, Trabzuni, Daniah, Abramov, Andrey Y., Bhatia, Kailash P., Wood, Nicholas W.

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Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease von Neumann, Juliane, Bras, Jose, Deas, Emma, O'Sullivan, Sean S., Parkkinen, Laura, Lachmann, Robin H., Li, Abi, Holton, Janice, Guerreiro, Rita, Paudel, Reema, Segarane, Badmavady, Singleton, Andrew, Lees, Andrew, Hardy, John, Houlden, Henry, Revesz, Tamas, Wood, Nicholas W.

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Homozygous TREM2 mutation in a family with atypical frontotemporal dementia von Le Ber, Isabelle, De Septenville, Anne, Guerreiro, Rita, Bras, José, Camuzat, Agnès, Caroppo, Paola, Lattante, Serena, Couarch, Philippe, Kabashi, Edor, Bouya-Ahmed, Kawtar, Dubois, Bruno, Brice, Alexis

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Coding variation in GBA explains the majority of the SYT11‐GBA Parkinson's disease GWAS locus von Blauwendraat, Cornelis, Bras, Jose M., Nalls, Mike A., Lewis, Patrick A., Hernandez, Dena G., Singleton, Andrew B.

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The age factor in Alzheimer's disease von Guerreiro, Rita, Bras, Jose

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Genotype, haplotype and copy-number variation in worldwide human populations von Rosenberg, Noah A, Singleton, Andrew B, Jakobsson, Mattias, Scholz, Sonja W, Scheet, Paul, Gibbs, J. Raphael, VanLiere, Jenna M, Fung, Hon-Chung, Szpiech, Zachary A, Degnan, James H, Wang, Kai, Guerreiro, Rita, Bras, Jose M, Schymick, Jennifer C, Hernandez, Dena G, Traynor, Bryan J, Simon-Sanchez, Javier, Matarin, Mar, Britton, Angela, van de Leemput, Joyce, Rafferty, Ian, Bucan, Maja, Cann, Howard M, Hardy, John A

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Understanding How Intelligent Process Automation Impacts Business Continuity: Mapping IEEE/2755:2020 and ISO/22301:2019 von Cascais Bras, Jose, Pereira, Ruben Filipe, Moro, Sergio, Bianchi, Isaias Scalabrin, Ribeiro, Rui

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H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations? von Erro, Roberto, Hersheson, Joshua, Ganos, Christos, Mencacci, Niccoló E., Stamelou, Maria, Batla, Amit, Thust, Stefanie Catherine, Bras, Jose M., Guerreiro, Rita J., Hardy, John, Quinn, Niall P., Houlden, Henry, Bhatia, Kailash P.

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TYROBP genetic variants in early-onset Alzheimer's disease von Pottier, Cyril, Ravenscroft, Thomas A, Brown, Patricia H, Finch, NiCole A, Baker, Matt, Parsons, Meeia, Asmann, Yan W, Ren, Yingxue, Christopher, Elizabeth, Levitch, Denise, van Blitterswijk, Marka, Cruchaga, Carlos, Campion, Dominique, Nicolas, Gaël, Richard, Anne-Claire, Guerreiro, Rita, Bras, Jose T, Zuchner, Stephan, Gonzalez, Michael A, Bu, Guojun, Younkin, Steven, Knopman, David S, Josephs, Keith A, Parisi, Joseph E, Petersen, Ronald C, Ertekin-Taner, Nilüfer, Graff-Radford, Neill R, Boeve, Bradley F, Dickson, Dennis W, Rademakers, Rosa

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