HuGE Literature Finder
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Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects. Nature communications 2022 12 13 (1): 7496. Krohn Lynne, Heilbron Karl, Blauwendraat Cornelis, Reynolds Regina H, Yu Eric, Senkevich Konstantin, Rudakou Uladzislau, Estiar Mehrdad A, Gustavsson Emil K, Brolin Kajsa, Ruskey Jennifer A, Freeman Kathryn, Asayesh Farnaz, Chia Ruth, Arnulf Isabelle, Hu Michele T M, Montplaisir Jacques Y, Gagnon Jean-François, Desautels Alex, Dauvilliers Yves, Gigli Gian Luigi, Valente Mariarosaria, Janes Francesco, Bernardini Andrea, Högl Birgit, Stefani Ambra, Ibrahim Abubaker, Šonka Karel, Kemlink David, Oertel Wolfgang, Janzen Annette, Plazzi Giuseppe, Biscarini Francesco, Antelmi Elena, Figorilli Michela, Puligheddu Monica, Mollenhauer Brit, Trenkwalder Claudia, Sixel-Döring Friederike, Cochen De Cock Valérie, Monaca Christelle Charley, Heidbreder Anna, Ferini-Strambi Luigi, Dijkstra Femke, Viaene Mineke, Abril Beatriz, Boeve Bradley F, , Scholz Sonja W, Ryten Mina, Bandres-Ciga Sara, Noyce Alastair, Cannon Paul, Pihlstrøm Lasse, Nalls Mike A, Singleton Andrew B, Rouleau Guy A, Postuma Ronald B, Gan-Or Z |
Hypomethylation of SNCA in Idiopathic REM Sleep Behavior Disorder Associated With Phenoconversion. Movement disorders : official journal of the Movement Disorder Society 2020 12 36 (4): 955-962. Li Yuan, Hao Shuwen, Zhang Hui, Mao Wei, Xue Jinhua, Zhang Yanli, Cai Yanning, Chan P |
SNCA 3'UTR genetic variants in patients with Parkinson's disease and REM sleep behavior disorder. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2017 Apr . Toffoli M, Dreussi E, Cecchin E, Valente M, Sanvilli N, Montico M, Gagno S, Garziera M, Polano M, Savarese M, Calandra-Buonaura G, Placidi F, Terzaghi M, Toffoli G, Gigli G |
Hyposmia Is Associated with RBD for PD Patients with Variants of SNCA. Frontiers in aging neuroscience 2017 9 303. Li Yuanyuan, Kang Wenyan, Zhang Linyuan, Zhou Liche, Niu Mengyue, Liu J |
TREM2 p.R47H substitution is not associated with dementia with Lewy bodies. Neurology. Genetics 2016 Aug 2 (4): e85. Walton Ronald L, Soto-Ortolaza Alexandra I, Murray Melissa E, Lorenzo-Betancor Oswaldo, Ogaki Kotaro, Heckman Michael G, Rayaprolu Sruti, Rademakers Rosa, Ertekin-Taner Nilüfer, Uitti Ryan J, van Gerpen Jay A, Wszolek Zbigniew K, Smith Glenn E, Kantarci Kejal, Lowe Val J, Parisi Joseph E, Jones David T, Savica Rodolfo, Graff-Radford Jonathan, Knopman David S, Petersen Ronald C, Graff-Radford Neill R, Ferman Tanis J, Dickson Dennis W, Boeve Bradley F, Ross Owen A, Labbé Catheri |
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