BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

628 related articles for article (PubMed ID: 30144538)

  • 41. A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
    van der Lee SJ; Conway OJ; Jansen I; Carrasquillo MM; Kleineidam L; van den Akker E; Hernández I; van Eijk KR; Stringa N; Chen JA; Zettergren A; Andlauer TFM; Diez-Fairen M; Simon-Sanchez J; Lleó A; Zetterberg H; Nygaard M; Blauwendraat C; Savage JE; Mengel-From J; Moreno-Grau S; Wagner M; Fortea J; Keogh MJ; Blennow K; Skoog I; Friese MA; Pletnikova O; Zulaica M; Lage C; de Rojas I; Riedel-Heller S; Illán-Gala I; Wei W; Jeune B; Orellana A; Then Bergh F; Wang X; Hulsman M; Beker N; Tesi N; Morris CM; Indakoetxea B; Collij LE; Scherer M; Morenas-Rodríguez E; Ironside JW; van Berckel BNM; Alcolea D; Wiendl H; Strickland SL; Pastor P; Rodríguez Rodríguez E; ; ; ; ; ; ; Boeve BF; Petersen RC; Ferman TJ; van Gerpen JA; Reinders MJT; Uitti RJ; Tárraga L; Maier W; Dols-Icardo O; Kawalia A; Dalmasso MC; Boada M; Zettl UK; van Schoor NM; Beekman M; Allen M; Masliah E; de Munain AL; Pantelyat A; Wszolek ZK; Ross OA; Dickson DW; Graff-Radford NR; Knopman D; Rademakers R; Lemstra AW; Pijnenburg YAL; Scheltens P; Gasser T; Chinnery PF; Hemmer B; Huisman MA; Troncoso J; Moreno F; Nohr EA; Sørensen TIA; Heutink P; Sánchez-Juan P; Posthuma D; ; Clarimón J; Christensen K; Ertekin-Taner N; Scholz SW; Ramirez A; Ruiz A; Slagboom E; van der Flier WM; Holstege H
    Acta Neuropathol; 2019 Aug; 138(2):237-250. PubMed ID: 31131421
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Association of GCH1 and MIR4697, but not SIPA1L2 and VPS13C polymorphisms, with Parkinson's disease in Taiwan.
    Chen CM; Chen YC; Chiang MC; Fung HC; Chang KH; Lee-Chen GJ; Wu YR
    Neurobiol Aging; 2016 Mar; 39():221.e1-5. PubMed ID: 26804608
    [TBL] [Abstract][Full Text] [Related]  

  • 43. rs3851179 Polymorphism at 5' to the PICALM Gene is Associated with Alzheimer and Parkinson Diseases in Brazilian Population.
    Santos-Rebouças CB; Gonçalves AP; Dos Santos JM; Abdala BB; Motta LB; Laks J; de Borges MB; de Rosso ALZ; Pereira JS; Nicaretta DH; Pimentel MMG
    Neuromolecular Med; 2017 Sep; 19(2-3):293-299. PubMed ID: 28567584
    [TBL] [Abstract][Full Text] [Related]  

  • 44. COQ2 variants in Parkinson's disease and multiple system atrophy.
    Mikasa M; Kanai K; Li Y; Yoshino H; Mogushi K; Hayashida A; Ikeda A; Kawajiri S; Okuma Y; Kashihara K; Sato T; Kondo H; Funayama M; Nishioka K; Hattori N
    J Neural Transm (Vienna); 2018 Jun; 125(6):937-944. PubMed ID: 29644397
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Common variant in PTK2B is associated with late-onset Alzheimer's disease: A replication study and meta-analyses.
    Li YQ; Tan MS; Wang HF; Tan CC; Zhang W; Zheng ZJ; Kong LL; Wang ZX; Tan L; Jiang T; Tan L; Yu JT
    Neurosci Lett; 2016 May; 621():83-87. PubMed ID: 27080426
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Contribution of Five Functional Loci of Dopamine Metabolism-Related Genes to Parkinson's Disease and Multiple System Atrophy in a Chinese Population.
    Chen Y; Ou R; Zhang L; Gu X; Yuan X; Wei QQ; Cao B; Zhao B; Wu Y; Shang H
    Front Neurosci; 2020; 14():889. PubMed ID: 33013295
    [No Abstract]   [Full Text] [Related]  

  • 47. HLA-DRA/HLA-DRB5 polymorphism affects risk of sporadic ALS and survival in a southwest Chinese cohort.
    Yang X; Zheng J; Tian S; Chen Y; An R; Zhao Q; Xu Y
    J Neurol Sci; 2017 Feb; 373():124-128. PubMed ID: 28131168
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Mutation Screening of TFG in α-Synucleinopathy and Amyotrophic Lateral Sclerosis.
    Li C; Lin J; Gu X; Hou Y; Liu K; Jiang Q; Ou R; Wei Q; Chen X; Song W; Zhao B; Wu Y; Chen Y; Shang H
    Mov Disord; 2022 Aug; 37(8):1756-1761. PubMed ID: 35642252
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Hospital-treated infections in early- and mid-life and risk of Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis: A nationwide nested case-control study in Sweden.
    Sun J; Ludvigsson JF; Ingre C; Piehl F; Wirdefeldt K; Zagai U; Ye W; Fang F
    PLoS Med; 2022 Sep; 19(9):e1004092. PubMed ID: 36107840
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Alzheimer's, Parkinson's Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement.
    Garofalo M; Pandini C; Bordoni M; Pansarasa O; Rey F; Costa A; Minafra B; Diamanti L; Zucca S; Carelli S; Cereda C; Gagliardi S
    Int J Mol Sci; 2020 Dec; 21(24):. PubMed ID: 33327559
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Association of three candidate genetic variants in ACMSD/TMEM163, GPNMB and BCKDK /STX1B with sporadic Parkinson's disease in Han Chinese.
    Wang L; Li NN; Lu ZJ; Li JY; Peng JX; Duan LR; Peng R
    Neurosci Lett; 2019 Jun; 703():45-48. PubMed ID: 30880162
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk.
    Moskvina V; Harold D; Russo G; Vedernikov A; Sharma M; Saad M; Holmans P; Bras JM; Bettella F; Keller MF; Nicolaou N; Simón-Sánchez J; Gibbs JR; Schulte C; Durr A; Guerreiro R; Hernandez D; Brice A; Stefánsson H; Majamaa K; Gasser T; Heutink P; Wood N; Martinez M; Singleton AB; Nalls MA; Hardy J; Owen MJ; O'Donovan MC; Williams J; Morris HR; Williams NM;
    JAMA Neurol; 2013 Oct; 70(10):1268-76. PubMed ID: 23921447
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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]  

  • 54. No association between 5 new GWAS-linked loci in Parkinson's disease and multiple system atrophy in a Chinese population.
    Chen Y; Cao B; Gu X; Ou R; Wei Q; Liu H; Zhang L; Yuan X; Song W; Zhao B; Wu Y; Yuan L; Cheng J; Shang H
    Neurobiol Aging; 2018 Jul; 67():202.e7-202.e8. PubMed ID: 29691093
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.
    van Blitterswijk M; Blokhuis A; van Es MA; van Vught PW; Rowicka PA; Schelhaas HJ; van der Kooi AJ; de Visser M; Veldink JH; van den Berg LH
    Neurobiol Aging; 2012 Aug; 33(8):1845.e1-3. PubMed ID: 22330174
    [TBL] [Abstract][Full Text] [Related]  

  • 56. TREM2 Variants and Neurodegenerative Diseases: A Systematic Review and Meta-Analysis.
    Zhou SL; Tan CC; Hou XH; Cao XP; Tan L; Yu JT
    J Alzheimers Dis; 2019; 68(3):1171-1184. PubMed ID: 30883352
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Causal relationship between immune cells and neurodegenerative diseases: a two-sample Mendelian randomisation study.
    Tang C; Lei X; Ding Y; Yang S; Ma Y; He D
    Front Immunol; 2024; 15():1339649. PubMed ID: 38348026
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Association of VEGF gene polymorphisms with sporadic Parkinson's disease in Chinese Han population.
    Wu Y; Zhang Y; Han X; Li X; Xue L; Xie A
    Neurol Sci; 2016 Dec; 37(12):1923-1929. PubMed ID: 27481110
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population.
    Chen X; Huang R; Chen Y; Zheng Z; Chen K; Song W; Zhao B; Yang Y; Yuan L; Shang H
    Neurol Sci; 2014 Jul; 35(7):1089-95. PubMed ID: 24493373
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Mutational analysis of TARDBP in neurodegenerative diseases.
    Ticozzi N; LeClerc AL; van Blitterswijk M; Keagle P; McKenna-Yasek DM; Sapp PC; Silani V; Wills AM; Brown RH; Landers JE
    Neurobiol Aging; 2011 Nov; 32(11):2096-9. PubMed ID: 20031275
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 32.