BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 36130218)

  • 1. Spanish HTT gene study reveals haplotype and allelic diversity with possible implications for germline expansion dynamics in Huntington disease.
    Ruiz de Sabando A; Urrutia Lafuente E; Galbete A; Ciosi M; García Amigot F; García Solaesa V; ; Monckton DG; Ramos-Arroyo MA
    Hum Mol Genet; 2023 Mar; 32(6):897-906. PubMed ID: 36130218
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Investigation of intermediate CAG alleles of the HTT in the general population of Rio de Janeiro, Brazil, in comparison with a sample of Huntington disease-affected families.
    Apolinário TA; da Silva IDS; Agostinho LA; Paiva CLA
    Mol Genet Genomic Med; 2020 Apr; 8(4):e1181. PubMed ID: 32067426
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Comprehensive Haplotype-Targeting Strategy for Allele-Specific HTT Suppression in Huntington Disease.
    Kay C; Collins JA; Caron NS; Agostinho LA; Findlay-Black H; Casal L; Sumathipala D; Dissanayake VHW; Cornejo-Olivas M; Baine F; Krause A; Greenberg JL; Paiva CLA; Squitieri F; Hayden MR
    Am J Hum Genet; 2019 Dec; 105(6):1112-1125. PubMed ID: 31708117
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Loss of CAA interruption and intergenerational CAG instability in Chinese patients with Huntington's disease.
    Bao YF; Li XY; Dong Y; Wu ZY
    J Mol Med (Berl); 2023 Jul; 101(7):869-876. PubMed ID: 37231148
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin America.
    Kay C; Tirado-Hurtado I; Cornejo-Olivas M; Collins JA; Wright G; Inca-Martinez M; Veliz-Otani D; Ketelaar ME; Slama RA; Ross CJ; Mazzetti P; Hayden MR
    Eur J Hum Genet; 2017 Feb; 25(3):332-340. PubMed ID: 28000697
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypes.
    Baine FK; Kay C; Ketelaar ME; Collins JA; Semaka A; Doty CN; Krause A; Greenberg LJ; Hayden MR
    Eur J Hum Genet; 2013 Oct; 21(10):1120-7. PubMed ID: 23463025
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Tracing the mutated HTT and haplotype of the African ancestor who spread Huntington disease into the Middle East.
    Squitieri F; Mazza T; Maffi S; De Luca A; AlSalmi Q; AlHarasi S; Collins JA; Kay C; Baine-Savanhu F; Landwhermeyer BG; Sabatini U; Hayden MR
    Genet Med; 2020 Nov; 22(11):1903-1908. PubMed ID: 32661355
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease.
    Ramos EM; Gillis T; Mysore JS; Lee JM; Gögele M; D'Elia Y; Pichler I; Sequeiros J; Pramstaller PP; Gusella JF; MacDonald ME; Alonso I
    Am J Med Genet B Neuropsychiatr Genet; 2015 Mar; 168B(2):135-43. PubMed ID: 25656686
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Distribution of the
    Apolinário TA; Rodrigues DC; Lemos MB; Antão Paiva CL; Agostinho LA
    Clin Med Res; 2020 Dec; 18(4):145-152. PubMed ID: 32878904
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Haplotype analysis encompassing HTT gene in Chinese patients with Huntington's disease.
    Li XY; Li HL; Dong Y; Gao B; Cheng HR; Ni W; Gan SR; Liu ZJ; Burgunder JM; Wu ZY
    Eur J Neurol; 2020 Feb; 27(2):273-279. PubMed ID: 31444920
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Huntingtin Haplotypes Provide Prioritized Target Panels for Allele-specific Silencing in Huntington Disease Patients of European Ancestry.
    Kay C; Collins JA; Skotte NH; Southwell AL; Warby SC; Caron NS; Doty CN; Nguyen B; Griguoli A; Ross CJ; Squitieri F; Hayden MR
    Mol Ther; 2015 Nov; 23(11):1759-1771. PubMed ID: 26201449
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population.
    Kay C; Collins JA; Wright GEB; Baine F; Miedzybrodzka Z; Aminkeng F; Semaka AJ; McDonald C; Davidson M; Madore SJ; Gordon ES; Gerry NP; Cornejo-Olivas M; Squitieri F; Tishkoff S; Greenberg JL; Krause A; Hayden MR
    Am J Med Genet B Neuropsychiatr Genet; 2018 Apr; 177(3):346-357. PubMed ID: 29460498
    [TBL] [Abstract][Full Text] [Related]  

  • 13. High frequency of intermediate alleles on Huntington disease-associated haplotypes in British Columbia's general population.
    Semaka A; Kay C; Doty CN; Collins JA; Tam N; Hayden MR
    Am J Med Genet B Neuropsychiatr Genet; 2013 Dec; 162B(8):864-71. PubMed ID: 24038799
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The CAG repeat at the Huntington disease gene in the Portuguese population: insights into its dynamics and to the origin of the mutation.
    Costa MDC; Magalhães P; Guimarães L; Maciel P; Sequeiros J; Sousa A
    J Hum Genet; 2006; 51(3):189-195. PubMed ID: 16372132
    [TBL] [Abstract][Full Text] [Related]  

  • 15. HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia.
    Warby SC; Visscher H; Collins JA; Doty CN; Carter C; Butland SL; Hayden AR; Kanazawa I; Ross CJ; Hayden MR
    Eur J Hum Genet; 2011 May; 19(5):561-6. PubMed ID: 21248742
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sequence-Level Analysis of the Major European Huntington Disease Haplotype.
    Lee JM; Kim KH; Shin A; Chao MJ; Abu Elneel K; Gillis T; Mysore JS; Kaye JA; Zahed H; Kratter IH; Daub AC; Finkbeiner S; Li H; Roach JC; Goodman N; Hood L; Myers RH; MacDonald ME; Gusella JF
    Am J Hum Genet; 2015 Sep; 97(3):435-44. PubMed ID: 26320893
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes.
    Ciosi M; Maxwell A; Cumming SA; Hensman Moss DJ; Alshammari AM; Flower MD; Durr A; Leavitt BR; Roos RAC; ; ; Holmans P; Jones L; Langbehn DR; Kwak S; Tabrizi SJ; Monckton DG
    EBioMedicine; 2019 Oct; 48():568-580. PubMed ID: 31607598
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.
    García-Planells J; Burguera JA; Solís P; Millán JM; Ginestar D; Palau F; Espinós C
    Hum Mutat; 2005 May; 25(5):453-9. PubMed ID: 15832309
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Incidence of Huntington disease in a northeastern Spanish region: a 13-year retrospective study at tertiary care centre.
    Sienes Bailo P; Lahoz R; Sánchez Marín JP; Izquierdo Álvarez S
    BMC Med Genet; 2020 Nov; 21(1):233. PubMed ID: 33228555
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population.
    Ma M; Yang Y; Shang H; Su D; Zhang H; Ma Y; Liu Y; Tao D; Zhang S
    J Neurol Sci; 2010 Nov; 298(1-2):57-60. PubMed ID: 20864123
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.