571 related articles for article (PubMed ID: 34873335)
1. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
van Rheenen W; van der Spek RAA; Bakker MK; van Vugt JJFA; Hop PJ; Zwamborn RAJ; de Klein N; Westra HJ; Bakker OB; Deelen P; Shireby G; Hannon E; Moisse M; Baird D; Restuadi R; Dolzhenko E; Dekker AM; Gawor K; Westeneng HJ; Tazelaar GHP; van Eijk KR; Kooyman M; Byrne RP; Doherty M; Heverin M; Al Khleifat A; Iacoangeli A; Shatunov A; Ticozzi N; Cooper-Knock J; Smith BN; Gromicho M; Chandran S; Pal S; Morrison KE; Shaw PJ; Hardy J; Orrell RW; Sendtner M; Meyer T; Başak N; van der Kooi AJ; Ratti A; Fogh I; Gellera C; Lauria G; Corti S; Cereda C; Sproviero D; D'Alfonso S; Sorarù G; Siciliano G; Filosto M; Padovani A; Chiò A; Calvo A; Moglia C; Brunetti M; Canosa A; Grassano M; Beghi E; Pupillo E; Logroscino G; Nefussy B; Osmanovic A; Nordin A; Lerner Y; Zabari M; Gotkine M; Baloh RH; Bell S; Vourc'h P; Corcia P; Couratier P; Millecamps S; Meininger V; Salachas F; Mora Pardina JS; Assialioui A; Rojas-García R; Dion PA; Ross JP; Ludolph AC; Weishaupt JH; Brenner D; Freischmidt A; Bensimon G; Brice A; Durr A; Payan CAM; Saker-Delye S; Wood NW; Topp S; Rademakers R; Tittmann L; Lieb W; Franke A; Ripke S; Braun A; Kraft J; Whiteman DC; Olsen CM; Uitterlinden AG; Hofman A; Rietschel M; Cichon S; Nöthen MM; Amouyel P; ; ; ; ; Traynor BJ; Singleton AB; Mitne Neto M; Cauchi RJ; Ophoff RA; Wiedau-Pazos M; Lomen-Hoerth C; van Deerlin VM; Grosskreutz J; Roediger A; Gaur N; Jörk A; Barthel T; Theele E; Ilse B; Stubendorff B; Witte OW; Steinbach R; Hübner CA; Graff C; Brylev L; Fominykh V; Demeshonok V; Ataulina A; Rogelj B; Koritnik B; Zidar J; Ravnik-Glavač M; Glavač D; Stević Z; Drory V; Povedano M; Blair IP; Kiernan MC; Benyamin B; Henderson RD; Furlong S; Mathers S; McCombe PA; Needham M; Ngo ST; Nicholson GA; Pamphlett R; Rowe DB; Steyn FJ; Williams KL; Mather KA; Sachdev PS; Henders AK; Wallace L; de Carvalho M; Pinto S; Petri S; Weber M; Rouleau GA; Silani V; Curtis CJ; Breen G; Glass JD; Brown RH; Landers JE; Shaw CE; Andersen PM; Groen EJN; van Es MA; Pasterkamp RJ; Fan D; Garton FC; McRae AF; Davey Smith G; Gaunt TR; Eberle MA; Mill J; McLaughlin RL; Hardiman O; Kenna KP; Wray NR; Tsai E; Runz H; Franke L; Al-Chalabi A; Van Damme P; van den Berg LH; Veldink JH
Nat Genet; 2021 Dec; 53(12):1636-1648. PubMed ID: 34873335
[TBL] [Abstract][Full Text] [Related]
2. A Genome-wide Expression Association Analysis Identifies Genes and Pathways Associated with Amyotrophic Lateral Sclerosis.
Du Y; Wen Y; Guo X; Hao J; Wang W; He A; Fan Q; Li P; Liu L; Liang X; Zhang F
Cell Mol Neurobiol; 2018 Apr; 38(3):635-639. PubMed ID: 28639078
[TBL] [Abstract][Full Text] [Related]
3. Shared genetic risk loci between Alzheimer's disease and related dementias, Parkinson's disease, and amyotrophic lateral sclerosis.
Wainberg M; Andrews SJ; Tripathy SJ
Alzheimers Res Ther; 2023 Jun; 15(1):113. PubMed ID: 37328865
[TBL] [Abstract][Full Text] [Related]
4. Type 2 Diabetes Mellitus and Amyotrophic Lateral Sclerosis: Genetic Overlap, Causality, and Mediation.
Chen H; Zhang J; Wang T; Zhang S; Lai Q; Huang S; Zeng P
J Clin Endocrinol Metab; 2021 Oct; 106(11):e4497-e4508. PubMed ID: 34171091
[TBL] [Abstract][Full Text] [Related]
5. Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.
Diekstra FP; Saris CG; van Rheenen W; Franke L; Jansen RC; van Es MA; van Vught PW; Blauw HM; Groen EJ; Horvath S; Estrada K; Rivadeneira F; Hofman A; Uitterlinden AG; Robberecht W; Andersen PM; Melki J; Meininger V; Hardiman O; Landers JE; Brown RH; Shatunov A; Shaw CE; Leigh PN; Al-Chalabi A; Ophoff RA; van den Berg LH; Veldink JH
PLoS One; 2012; 7(4):e35333. PubMed ID: 22509407
[TBL] [Abstract][Full Text] [Related]
6. Genome-wide genetic links between amyotrophic lateral sclerosis and autoimmune diseases.
Li CY; Yang TM; Ou RW; Wei QQ; Shang HF
BMC Med; 2021 Feb; 19(1):27. PubMed ID: 33541344
[TBL] [Abstract][Full Text] [Related]
7. Genome-wide analyses identify NEAT1 as genetic modifier of age at onset of amyotrophic lateral sclerosis.
Li C; Wei Q; Hou Y; Lin J; Ou R; Zhang L; Jiang Q; Xiao Y; Liu K; Chen X; Yang T; Song W; Zhao B; Wu Y; Shang H
Mol Neurodegener; 2023 Oct; 18(1):77. PubMed ID: 37872557
[TBL] [Abstract][Full Text] [Related]
8. Abnormal Brain Protein Abundance and Cross-tissue mRNA Expression in Amyotrophic Lateral Sclerosis.
Ma Y; Jia T; Qin F; He Y; Han F; Zhang C
Mol Neurobiol; 2024 Jan; 61(1):510-518. PubMed ID: 37639066
[TBL] [Abstract][Full Text] [Related]
9. Shared Genetics and Comorbid Genes of Amyotrophic Lateral Sclerosis and Parkinson's Disease.
Tian Y; Ma G; Li H; Zeng Y; Zhou S; Wang X; Shan S; Xu Y; Xiong J; Cheng G
Mov Disord; 2023 Oct; 38(10):1813-1821. PubMed ID: 37534731
[TBL] [Abstract][Full Text] [Related]
10. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1.
Restuadi R; Steyn FJ; Kabashi E; Ngo ST; Cheng FF; Nabais MF; Thompson MJ; Qi T; Wu Y; Henders AK; Wallace L; Bye CR; Turner BJ; Ziser L; Mathers S; McCombe PA; Needham M; Schultz D; Kiernan MC; van Rheenen W; van den Berg LH; Veldink JH; Ophoff R; Gusev A; Zaitlen N; McRae AF; Henderson RD; Wray NR; Giacomotto J; Garton FC
Genome Med; 2022 Jan; 14(1):7. PubMed ID: 35042540
[TBL] [Abstract][Full Text] [Related]
11. Genetic variation in targets of lipid-lowering drugs and amyotrophic lateral sclerosis risk: a Mendelian randomization study.
Li Z; Tian M; Jia H; Li X; Liu Q; Zhou X; Li R; Dong H; Liu Y
Amyotroph Lateral Scler Frontotemporal Degener; 2024 Feb; 25(1-2):197-206. PubMed ID: 37688479
[TBL] [Abstract][Full Text] [Related]
12. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis.
Bandres-Ciga S; Noyce AJ; Hemani G; Nicolas A; Calvo A; Mora G; ; ; Tienari PJ; Stone DJ; Nalls MA; Singleton AB; Chiò A; Traynor BJ
Ann Neurol; 2019 Apr; 85(4):470-481. PubMed ID: 30723964
[TBL] [Abstract][Full Text] [Related]
13. Single-cell RNA-seq analysis of the brainstem of mutant SOD1 mice reveals perturbed cell types and pathways of amyotrophic lateral sclerosis.
Liu W; Venugopal S; Majid S; Ahn IS; Diamante G; Hong J; Yang X; Chandler SH
Neurobiol Dis; 2020 Jul; 141():104877. PubMed ID: 32360664
[TBL] [Abstract][Full Text] [Related]
14. Investigating Casual Associations Among Gut Microbiota, Metabolites, and Neurodegenerative Diseases: A Mendelian Randomization Study.
Ning J; Huang SY; Chen SD; Zhang YR; Huang YY; Yu JT
J Alzheimers Dis; 2022; 87(1):211-222. PubMed ID: 35275534
[TBL] [Abstract][Full Text] [Related]
15. Shared genetic links between amyotrophic lateral sclerosis and obesity-related traits: a genome-wide association study.
Li C; Ou R; Wei Q; Shang H
Neurobiol Aging; 2021 Jun; 102():211.e1-211.e9. PubMed ID: 33640203
[TBL] [Abstract][Full Text] [Related]
16. NEK1 and STMN2 short tandem repeat lengths are not associated with Australian amyotrophic lateral sclerosis risk.
Grima N; Henden L; Fearnley LG; Rowe DB; D'Silva S; Pamphlett R; Adams L; Kiernan MC; Mazumder S; Timmins HC; Zoing M; Bahlo M; Blair IP; Williams KL
Neurobiol Aging; 2022 Aug; 116():92-95. PubMed ID: 35613520
[TBL] [Abstract][Full Text] [Related]
17. Bidirectional Mendelian randomization to explore the causal relationships between Sleep traits, Parkinson's disease and Amyotrophic lateral sclerosis.
Di H; Zhu Y; Xia W; Meng X; Zhang M; Xu M; Feng J; Tian Q; He Y; Cao S; Lu Z
Sleep Med; 2022 Aug; 96():42-49. PubMed ID: 35594779
[TBL] [Abstract][Full Text] [Related]
18. Causal effects of blood lipids on amyotrophic lateral sclerosis: a Mendelian randomization study.
Zeng P; Zhou X
Hum Mol Genet; 2019 Feb; 28(4):688-697. PubMed ID: 30445611
[TBL] [Abstract][Full Text] [Related]
19. Identifying novel genes for amyotrophic lateral sclerosis by integrating human brain proteomes with genome-wide association data.
Gu XJ; Su WM; Dou M; Jiang Z; Duan QQ; Wang H; Ren YL; Cao B; Wang Y; Chen YP
J Neurol; 2023 Aug; 270(8):4013-4023. PubMed ID: 37148340
[TBL] [Abstract][Full Text] [Related]
20. Inflammation and Brain Structure in Alzheimer's Disease and Other Neurodegenerative Disorders: a Mendelian Randomization Study.
Liu WS; Zhang YR; Ge YJ; Wang HF; Cheng W; Yu JT
Mol Neurobiol; 2024 Mar; 61(3):1593-1604. PubMed ID: 37736795
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
