BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 35812739)

  • 1. Causal Inference of Genetic Variants and Genes in Amyotrophic Lateral Sclerosis.
    Pan S; Liu X; Liu T; Zhao Z; Dai Y; Wang YY; Jia P; Liu F
    Front Genet; 2022; 13():917142. PubMed ID: 35812739
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Multiple-Tissue Integrative Transcriptome-Wide Association Studies Discovered New Genes Associated With Amyotrophic Lateral Sclerosis.
    Xiao L; Yuan Z; Jin S; Wang T; Huang S; Zeng P
    Front Genet; 2020; 11():587243. PubMed ID: 33329728
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of multiple novel susceptibility genes associated with autoimmune thyroid disease.
    Liu X; Miao Y; Liu C; Lu W; Feng Q; Zhang Q
    Front Immunol; 2023; 14():1161311. PubMed ID: 37197658
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Identifying Candidate Genes Associated with Sporadic Amyotrophic Lateral Sclerosis via Integrative Analysis of Transcriptome-Wide Association Study and Messenger RNA Expression Profile.
    Li P; Cheng S; Wen Y; Cheng B; Liu L; Wu X; Ao X; Huang Z; Liao C; Li S; Zhang F; Zhang Z
    Cell Mol Neurobiol; 2023 Jan; 43(1):327-338. PubMed ID: 35038056
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. An Integrative Transcriptome-Wide Analysis of Amyotrophic Lateral Sclerosis for the Identification of Potential Genetic Markers and Drug Candidates.
    Park S; Kim D; Song J; Joo JWJ
    Int J Mol Sci; 2021 Mar; 22(6):. PubMed ID: 33809961
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genome-wide association analysis reveals potential genetic correlation and causality between circulating inflammatory proteins and amyotrophic lateral sclerosis.
    Shen J; Gu X; Xiao C; Yan H; Feng Y; Li X
    Aging (Albany NY); 2024 May; 16():. PubMed ID: 38819224
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Evidence based on Mendelian randomization and colocalization analysis strengthens causal relationships between structural changes in specific brain regions and risk of amyotrophic lateral sclerosis.
    Shi J; Wang Z; Yi M; Xie S; Zhang X; Tao D; Liu Y; Yang Y
    Front Neurosci; 2024; 18():1333782. PubMed ID: 38505770
    [TBL] [Abstract][Full Text] [Related]  

  • 14.
    Iacoangeli A; Fogh I; Selvackadunco S; Topp SD; Shatunov A; van Rheenen W; Al-Khleifat A; Opie-Martin S; Ratti A; Calvo A; ; Van Damme P; Robberecht W; Chio A; Dobson RJ; Hardiman O; Shaw CE; van den Berg LH; Andersen PM; Smith BN; Silani V; Veldink JH; Breen G; Troakes C; Al-Chalabi A; Jones AR
    Brain Commun; 2021; 3(4):fcab236. PubMed ID: 34708205
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Causal association of type 2 diabetes with amyotrophic lateral sclerosis: new evidence from Mendelian randomization using GWAS summary statistics.
    Zeng P; Wang T; Zheng J; Zhou X
    BMC Med; 2019 Dec; 17(1):225. PubMed ID: 31796040
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Physical exercise is a risk factor for amyotrophic lateral sclerosis: Convergent evidence from Mendelian randomisation, transcriptomics and risk genotypes.
    Julian TH; Glascow N; Barry ADF; Moll T; Harvey C; Klimentidis YC; Newell M; Zhang S; Snyder MP; Cooper-Knock J; Shaw PJ
    EBioMedicine; 2021 Jun; 68():103397. PubMed ID: 34051439
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Exploring Potential Causal Genes for Uterine Leiomyomas: A Summary Data-Based Mendelian Randomization and FUMA Analysis.
    Dai Y; Liu X; Zhu Y; Mao S; Yang J; Zhu L
    Front Genet; 2022; 13():890007. PubMed ID: 35903355
    [No Abstract]   [Full Text] [Related]  

  • 20. From GWAS to Gene: Transcriptome-Wide Association Studies and Other Methods to Functionally Understand GWAS Discoveries.
    Li B; Ritchie MD
    Front Genet; 2021; 12():713230. PubMed ID: 34659337
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.