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Page 1
Oral and gut microbiome profiles in people with early idiopathic Parkinson's disease.
Stagaman K, Kmiecik MJ, Wetzel M, Aslibekyan S, Sonmez TF, Fontanillas P; 23andMe Research Team; Tung J, Holmes MV, Walk ST, Houser MC, Norcliffe-Kaufmann L. Stagaman K, et al. Commun Med (Lond). 2024 Oct 23;4(1):209. doi: 10.1038/s43856-024-00630-8. Commun Med (Lond). 2024. PMID: 39443634 Free PMC article.
Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders.
Strom NI, Halvorsen MW, Grove J, Ásbjörnsdóttir B, Luðvígsson P, Thorarensen Ó, de Schipper E, Bäckmann J, Andrén P, Tian C; PGC TS Working Group; 23andMe Research Team; Als TD, Nissen JB, Meier SM, Bybjerg-Grauholm J, Hougaard DM, Werge T, Børglum AD, Hinds DA, Rück C, Mataix-Cols D, Stefánsson H, Stefansson K, Crowley JJ, Mattheisen M. Strom NI, et al. Among authors: hinds da. Biol Psychiatry. 2024 Oct 9:S0006-3223(24)01648-2. doi: 10.1016/j.biopsych.2024.07.025. Online ahead of print. Biol Psychiatry. 2024. PMID: 39389409 Free article.
Genetic neurodevelopmental clustering and dyslexia.
Ciulkinyte A, Mountford HS, Fontanillas P; 23andMe Research Team; Bates TC, Martin NG, Fisher SE, Luciano M. Ciulkinyte A, et al. Mol Psychiatry. 2024 Jul 15. doi: 10.1038/s41380-024-02649-8. Online ahead of print. Mol Psychiatry. 2024. PMID: 39009701
Genome-wide association studies of coffee intake in UK/US participants of European ancestry uncover cohort-specific genetic associations.
Thorpe HHA, Fontanillas P, Pham BK, Meredith JJ, Jennings MV, Courchesne-Krak NS, Vilar-Ribó L, Bianchi SB, Mutz J; 23andMe Research Team; Elson SL, Khokhar JY, Abdellaoui A, Davis LK, Palmer AA, Sanchez-Roige S. Thorpe HHA, et al. Neuropsychopharmacology. 2024 Sep;49(10):1609-1618. doi: 10.1038/s41386-024-01870-x. Epub 2024 Jun 11. Neuropsychopharmacology. 2024. PMID: 38858598
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction.
Schormair B, Zhao C, Bell S, Didriksen M, Nawaz MS, Schandra N, Stefani A, Högl B, Dauvilliers Y, Bachmann CG, Kemlink D, Sonka K, Paulus W, Trenkwalder C, Oertel WH, Hornyak M, Teder-Laving M, Metspalu A, Hadjigeorgiou GM, Polo O, Fietze I, Ross OA, Wszolek ZK, Ibrahim A, Bergmann M, Kittke V, Harrer P, Dowsett J, Chenini S, Ostrowski SR, Sørensen E, Erikstrup C, Pedersen OB, Topholm Bruun M, Nielsen KR, Butterworth AS, Soranzo N, Ouwehand WH, Roberts DJ, Danesh J, Burchell B, Furlotte NA, Nandakumar P; 23andMe Research Team; D.E.S.I.R. study group; Earley CJ, Ondo WG, Xiong L, Desautels A, Perola M, Vodicka P, Dina C, Stoll M, Franke A, Lieb W, Stewart AFR, Shah SH, Gieger C, Peters A, Rye DB, Rouleau GA, Berger K, Stefansson H, Ullum H, Stefansson K, Hinds DA, Di Angelantonio E, Oexle K, Winkelmann J. Schormair B, et al. Among authors: hinds da. Nat Genet. 2024 Jun;56(6):1090-1099. doi: 10.1038/s41588-024-01763-1. Epub 2024 Jun 5. Nat Genet. 2024. PMID: 38839884 Free PMC article.
330 results