These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

361 related articles for article (PubMed ID: 33981200)

  • 1. Gene4PD: A Comprehensive Genetic Database of Parkinson's Disease.
    Li B; Zhao G; Zhou Q; Xie Y; Wang Z; Fang Z; Lu B; Qin L; Zhao Y; Zhang R; Jiang L; Pan H; He Y; Wang X; Luo T; Zhang Y; Wang Y; Chen Q; Liu Z; Guo J; Tang B; Li J
    Front Neurosci; 2021; 15():679568. PubMed ID: 33981200
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterizing the Expression Patterns of Parkinson's Disease Associated Genes.
    Li B; Zhao G; Li K; Wang Z; Fang Z; Wang X; Luo T; Zhang Y; Wang Y; Chen Q; Huang Y; Dong L; Guo J; Tang B; Li J
    Front Neurosci; 2021; 15():629156. PubMed ID: 33867917
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Association Between Lysosomal Storage Disorder Genes and Parkinson's Disease: A Large Cohort Study in Chinese Mainland Population.
    Zhao YW; Pan HX; Liu Z; Wang Y; Zeng Q; Fang ZH; Luo TF; Xu K; Wang Z; Zhou X; He R; Li B; Zhao G; Xu Q; Sun QY; Yan XX; Tan JQ; Li JC; Guo JF; Tang BS
    Front Aging Neurosci; 2021; 13():749109. PubMed ID: 34867278
    [No Abstract]   [Full Text] [Related]  

  • 4. Variable Effects of PD-Risk Associated SNPs and Variants in Parkinsonism-Associated Genes on Disease Phenotype in a Community-Based Cohort.
    Markopoulou K; Chase BA; Premkumar AP; Schoneburg B; Kartha N; Wei J; Yu H; Epshteyn A; Garduno L; Pham A; Vazquez R; Frigerio R; Maraganore D
    Front Neurol; 2021; 12():662278. PubMed ID: 33935957
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic Analysis of Six Transmembrane Protein Family Genes in Parkinson's Disease in a Large Chinese Cohort.
    Zhao Y; Zhang K; Pan H; Wang Y; Zhou X; Xiang Y; Xu Q; Sun Q; Tan J; Yan X; Li J; Guo J; Tang B; Liu Z
    Front Aging Neurosci; 2022; 14():889057. PubMed ID: 35860667
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease.
    Benitez BA; Davis AA; Jin SC; Ibanez L; Ortega-Cubero S; Pastor P; Choi J; Cooper B; Perlmutter JS; Cruchaga C
    Mol Neurodegener; 2016 Apr; 11():29. PubMed ID: 27094865
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease.
    Hopfner F; Mueller SH; Szymczak S; Junge O; Tittmann L; May S; Lohmann K; Grallert H; Lieb W; Strauch K; Müller-Nurasyid M; Berger K; Schormair B; Winkelmann J; Mollenhauer B; Trenkwalder C; Maetzler W; Berg D; Kasten M; Klein C; Höglinger GU; Gasser T; Deuschl G; Franke A; Krawczak M; Dempfle A; Kuhlenbäumer G
    Mov Disord; 2020 Jul; 35(7):1245-1248. PubMed ID: 32267580
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials.
    Illés A; Csabán D; Grosz Z; Balicza P; Gézsi A; Molnár V; Bencsik R; Gál A; Klivényi P; Molnar MJ
    Front Genet; 2019; 10():1061. PubMed ID: 31737044
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comprehensive assessment of genetic sequence variants in the antioxidant 'master regulator' NRF2 in idiopathic Parkinson's disease.
    Todorovic M; Newman JR; Shan J; Bentley S; Wood SA; Silburn PA; Mellick GD
    PLoS One; 2015; 10(5):e0128030. PubMed ID: 26010367
    [TBL] [Abstract][Full Text] [Related]  

  • 10. SZDB: A Database for Schizophrenia Genetic Research.
    Wu Y; Yao YG; Luo XJ
    Schizophr Bull; 2017 Mar; 43(2):459-471. PubMed ID: 27451428
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Construction of Parkinson's disease marker-based weighted protein-protein interaction network for prioritization of co-expressed genes.
    George G; Valiya Parambath S; Lokappa SB; Varkey J
    Gene; 2019 May; 697():67-77. PubMed ID: 30776463
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identifying the Association Between Alzheimer's Disease and Parkinson's Disease Using Genome-Wide Association Studies and Protein-Protein Interaction Network.
    Liu G; Bao X; Jiang Y; Liao M; Jiang Q; Feng R; Zhang L; Ma G; Chen Z; Wang G; Wang R; Zhao B; Li K
    Mol Neurobiol; 2015 Dec; 52(3):1629-1636. PubMed ID: 25370933
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci.
    Germer EL; Imhoff S; Vilariño-Güell C; Kasten M; Seibler P; Brüggemann N; ; Klein C; Trinh J
    Front Neurol; 2019; 10():1284. PubMed ID: 31920912
    [No Abstract]   [Full Text] [Related]  

  • 14. The genetic landscape of Parkinson's disease.
    Lunati A; Lesage S; Brice A
    Rev Neurol (Paris); 2018 Nov; 174(9):628-643. PubMed ID: 30245141
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Whole-Exome Sequencing in Familial Parkinson Disease.
    Farlow JL; Robak LA; Hetrick K; Bowling K; Boerwinkle E; Coban-Akdemir ZH; Gambin T; Gibbs RA; Gu S; Jain P; Jankovic J; Jhangiani S; Kaw K; Lai D; Lin H; Ling H; Liu Y; Lupski JR; Muzny D; Porter P; Pugh E; White J; Doheny K; Myers RM; Shulman JM; Foroud T
    JAMA Neurol; 2016 Jan; 73(1):68-75. PubMed ID: 26595808
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic risk factors in Finnish patients with Parkinson's disease.
    Ylönen S; Siitonen A; Nalls MA; Ylikotila P; Autere J; Eerola-Rautio J; Gibbs R; Hiltunen M; Tienari PJ; Soininen H; Singleton AB; Majamaa K
    Parkinsonism Relat Disord; 2017 Dec; 45():39-43. PubMed ID: 29029963
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A genetic analysis of a Spanish population with early onset Parkinson's disease.
    Cristina TP; Pablo M; Teresa PM; Lydia VD; Irene AR; Araceli AC; Inmaculada BB; Marta BT; Dolores BR; José CM; Rocío GR; José GP; Ismael HF; Silvia J; Labrador MA; Lydia LM; Carlos MJ; Posada IJ; Ana RS; Cristina RH; Javier DV; Gómez-Garre P
    PLoS One; 2020; 15(9):e0238098. PubMed ID: 32870915
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gene4HL: An Integrated Genetic Database for Hearing Loss.
    Huang S; Zhao G; Wu J; Li K; Wang Q; Fu Y; Zhang H; Bi Q; Li X; Wang W; Guo C; Zhang D; Wu L; Li X; Xu H; Han M; Wang X; Lei C; Qiu X; Li Y; Li J; Dai P; Yuan Y
    Front Genet; 2021; 12():773009. PubMed ID: 34733322
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Assessment of risk factor variants of LRRK2, MAPT, SNCA and TCEANC2 genes in Hungarian sporadic Parkinson's disease patients.
    Boros FA; Török R; Vágvölgyi-Sümegi E; Pesei ZG; Klivényi P; Vécsei L
    Neurosci Lett; 2019 Jul; 706():140-145. PubMed ID: 31085292
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease.
    Gaare JJ; Nido GS; Sztromwasser P; Knappskog PM; Dahl O; Lund-Johansen M; Maple-Grødem J; Alves G; Tysnes OB; Johansson S; Haugarvoll K; Tzoulis C
    Mov Disord; 2018 Oct; 33(10):1591-1600. PubMed ID: 30256453
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.