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Modification of Huntington's disease by short tandem repeats.
Hong EP, Ramos EM, Aziz NA, Massey TH, McAllister B, Lobanov S, Jones L, Holmans P, Kwak S, Orth M, Ciosi M, Lomeikaite V, Monckton DG, Long JD, Lucente D, Wheeler VC, Gillis T, MacDonald ME, Sequeiros J, Gusella JF, Lee JM. Hong EP, et al. Among authors: long jd. Brain Commun. 2024 Jan 23;6(2):fcae016. doi: 10.1093/braincomms/fcae016. eCollection 2024. Brain Commun. 2024. PMID: 38449714 Free PMC article.
8OHdG as a marker for Huntington disease progression.
Long JD, Matson WR, Juhl AR, Leavitt BR, Paulsen JS; PREDICT-HD Investigators and Coordinators of the Huntington Study Group. Long JD, et al. Neurobiol Dis. 2012 Jun;46(3):625-34. doi: 10.1016/j.nbd.2012.02.012. Epub 2012 Mar 5. Neurobiol Dis. 2012. PMID: 22414782 Free PMC article.
Cognitive domains that predict time to diagnosis in prodromal Huntington disease.
Harrington DL, Smith MM, Zhang Y, Carlozzi NE, Paulsen JS; PREDICT-HD Investigators of the Huntington Study Group. Harrington DL, et al. J Neurol Neurosurg Psychiatry. 2012 Jun;83(6):612-9. doi: 10.1136/jnnp-2011-301732. Epub 2012 Mar 26. J Neurol Neurosurg Psychiatry. 2012. PMID: 22451099 Free PMC article.
Identification of extreme motor phenotypes in Huntington's disease.
Braisch U, Hay B, Muche R, Rothenbacher D, Landwehrmeyer GB, Long JD, Orth M; REGISTRY Investigators of the European Huntington's Disease Network and COHORT Investigators of the Huntington Study Group. Braisch U, et al. Among authors: long jd. Am J Med Genet B Neuropsychiatr Genet. 2017 Apr;174(3):283-294. doi: 10.1002/ajmg.b.32514. Epub 2016 Nov 21. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 27868347
Testing a longitudinal compensation model in premanifest Huntington's disease.
Gregory S, Long JD, Klöppel S, Razi A, Scheller E, Minkova L, Johnson EB, Durr A, Roos RAC, Leavitt BR, Mills JA, Stout JC, Scahill RI, Tabrizi SJ, Rees G; Track-On investigators. Gregory S, et al. Among authors: long jd. Brain. 2018 Jul 1;141(7):2156-2166. doi: 10.1093/brain/awy122. Brain. 2018. PMID: 29788038 Free PMC article.
Identification of symbol digit modality test score extremes in Huntington's disease.
Braisch U, Muche R, Rothenbacher D, Landwehrmeyer GB, Long JD, Orth M; REGISTRY Investigators of the European Huntington's Disease Network and COHORT Investigators of the Huntington Study Group. Braisch U, et al. Among authors: long jd. Am J Med Genet B Neuropsychiatr Genet. 2019 Apr;180(3):232-245. doi: 10.1002/ajmg.b.32719. Epub 2019 Feb 20. Am J Med Genet B Neuropsychiatr Genet. 2019. PMID: 30788902
483 results