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6. Interrupting sequence variants and age of onset in Huntington's disease: clinical implications and emerging therapies. Wright GEB; Black HF; Collins JA; Gall-Duncan T; Caron NS; Pearson CE; Hayden MR Lancet Neurol; 2020 Nov; 19(11):930-939. PubMed ID: 33098802 [TBL] [Abstract][Full Text] [Related]
7. The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease. Metzger S; Bauer P; Tomiuk J; Laccone F; Didonato S; Gellera C; Soliveri P; Lange HW; Weirich-Schwaiger H; Wenning GK; Melegh B; Havasi V; Balikó L; Wieczorek S; Arning L; Zaremba J; Sulek A; Hoffman-Zacharska D; Basak AN; Ersoy N; Zidovska J; Kebrdlova V; Pandolfo M; Ribaï P; Kadasi L; Kvasnicova M; Weber BH; Kreuz F; Dose M; Stuhrmann M; Riess O Neurogenetics; 2006 Mar; 7(1):27-30. PubMed ID: 16369839 [TBL] [Abstract][Full Text] [Related]
8. Genetic modifiers of Mendelian disease: Huntington's disease and the trinucleotide repeat disorders. Holmans PA; Massey TH; Jones L Hum Mol Genet; 2017 Oct; 26(R2):R83-R90. PubMed ID: 28977442 [TBL] [Abstract][Full Text] [Related]
9. Genetic modifiers of Huntington's disease. Gusella JF; MacDonald ME; Lee JM Mov Disord; 2014 Sep; 29(11):1359-65. PubMed ID: 25154728 [TBL] [Abstract][Full Text] [Related]
10. Association Analysis of Chromosome X to Identify Genetic Modifiers of Huntington's Disease. Hong EP; Chao MJ; Massey T; McAllister B; Lobanov S; Jones L; Holmans P; Kwak S; Orth M; Ciosi M; Monckton DG; Long JD; Lucente D; Wheeler VC; MacDonald ME; Gusella JF; Lee JM J Huntingtons Dis; 2021; 10(3):367-375. PubMed ID: 34180418 [TBL] [Abstract][Full Text] [Related]
11. Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease. Metzger S; Bauer P; Tomiuk J; Laccone F; Didonato S; Gellera C; Mariotti C; Lange HW; Weirich-Schwaiger H; Wenning GK; Seppi K; Melegh B; Havasi V; Balikó L; Wieczorek S; Zaremba J; Hoffman-Zacharska D; Sulek A; Basak AN; Soydan E; Zidovska J; Kebrdlova V; Pandolfo M; Ribaï P; Kadasi L; Kvasnicova M; Weber BH; Kreuz F; Dose M; Stuhrmann M; Riess O Hum Genet; 2006 Sep; 120(2):285-92. PubMed ID: 16847693 [TBL] [Abstract][Full Text] [Related]
12. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study. Moss DJH; Pardiñas AF; Langbehn D; Lo K; Leavitt BR; Roos R; Durr A; Mead S; ; ; Holmans P; Jones L; Tabrizi SJ Lancet Neurol; 2017 Sep; 16(9):701-711. PubMed ID: 28642124 [TBL] [Abstract][Full Text] [Related]
13. Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease. Metzger S; Rong J; Nguyen HP; Cape A; Tomiuk J; Soehn AS; Propping P; Freudenberg-Hua Y; Freudenberg J; Tong L; Li SH; Li XJ; Riess O Hum Mol Genet; 2008 Apr; 17(8):1137-46. PubMed ID: 18192679 [TBL] [Abstract][Full Text] [Related]
14. Genetic Modification of Huntington Disease Acts Early in the Prediagnosis Phase. Long JD; Lee JM; Aylward EH; Gillis T; Mysore JS; Abu Elneel K; Chao MJ; Paulsen JS; MacDonald ME; Gusella JF Am J Hum Genet; 2018 Sep; 103(3):349-357. PubMed ID: 30122542 [TBL] [Abstract][Full Text] [Related]
15. Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease. Masuda N; Goto J; Murayama N; Watanabe M; Kondo I; Kanazawa I J Med Genet; 1995 Sep; 32(9):701-5. PubMed ID: 8544189 [TBL] [Abstract][Full Text] [Related]
16. The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease. Klempíř J; Zidovská J; Stochl J; Ing VK; Uhrová T; Roth J Mov Disord; 2011 Jan; 26(1):125-9. PubMed ID: 21322024 [TBL] [Abstract][Full Text] [Related]
17. Chromosome substitution strain assessment of a Huntington's disease modifier locus. Ramos EM; Kovalenko M; Guide JR; St Claire J; Gillis T; Mysore JS; Sequeiros J; Wheeler VC; Alonso I; MacDonald ME Mamm Genome; 2015 Apr; 26(3-4):119-30. PubMed ID: 25645993 [TBL] [Abstract][Full Text] [Related]
18. Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis. Fusilli C; Migliore S; Mazza T; Consoli F; De Luca A; Barbagallo G; Ciammola A; Gatto EM; Cesarini M; Etcheverry JL; Parisi V; Al-Oraimi M; Al-Harrasi S; Al-Salmi Q; Marano M; Vonsattel JG; Sabatini U; Landwehrmeyer GB; Squitieri F Lancet Neurol; 2018 Nov; 17(11):986-993. PubMed ID: 30243861 [TBL] [Abstract][Full Text] [Related]
19. Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds. Andresen JM; Gayán J; Cherny SS; Brocklebank D; Alkorta-Aranburu G; Addis EA; ; Cardon LR; Housman DE; Wexler NS J Med Genet; 2007 Jan; 44(1):44-50. PubMed ID: 17018562 [TBL] [Abstract][Full Text] [Related]
20. A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington's Disease Symptoms. Chheda P; Chanekar M; Salunkhe Y; Dama T; Pais A; Pande S; Bendre R; Shah N Mol Diagn Ther; 2018 Jun; 22(3):353-359. PubMed ID: 29619771 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]