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Items: 1 to 20 of 67

1.
A Futility Study of Minocycline in Huntington’s Disease
The Huntington Study Group DOMINO Investigators
Mov Disord. Author manuscript; available in PMC 2022 Jan 30.
Published in final edited form as: Mov Disord. 2010 Oct 15; 25(13): 2219–2224. doi: 10.1002/mds.23236
PMCID:
PMC8801051
AbstractArticlePDF–260K
2.
Artificial miRNAs Reduce Human Mutant Huntingtin Throughout the Striatum in a Transgenic Sheep Model of Huntington's Disease
Edith L. Pfister, Natalie DiNardo, Erica Mondo, Florie Borel, Faith Conroy, Cara Fraser, Gwladys Gernoux, Xin Han, Danjing Hu, Emily Johnson, Lori Kennington, PengPeng Liu, Suzanne J. Reid, Ellen Sapp, Petr Vodicka, Tim Kuchel, A. Jennifer Morton, David Howland, Richard Moser, Miguel Sena-Esteves, Guangping Gao, Christian Mueller, Marian DiFiglia, Neil Aronin
Hum Gene Ther. 2018 Jun 1; 29(6): 663–673. Published online 2018 Jun 1. doi: 10.1089/hum.2017.199
PMCID:
PMC6909722
AbstractArticlePDF–517K
3.
A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes
Marc Ciosi, Alastair Maxwell, Sarah A. Cumming, Davina J. Hensman Moss, Asma M. Alshammari, Michael D. Flower, Alexandra Durr, Blair R. Leavitt, Raymund A.C. Roos, the TRACK-HD team, the Enroll-HD team, Peter Holmans, Lesley Jones, Douglas R. Langbehn, Seung Kwak, Sarah J. Tabrizi, Darren G. Monckton
EBioMedicine. 2019 Oct; 48: 568–580. Published online 2019 Oct 10. doi: 10.1016/j.ebiom.2019.09.020
PMCID:
PMC6838430
AbstractArticlePDF–2.1M
4.
CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset
Genetic Modifiers of Huntington’s Disease (GeM-HD) Consortium
Cell. 2019 Aug 8; 178(4): 887–900.e14. doi: 10.1016/j.cell.2019.06.036
PMCID:
PMC6700281
AbstractArticle
5.
Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease
Galen E.B. Wright, Jennifer A. Collins, Chris Kay, Cassandra McDonald, Egor Dolzhenko, Qingwen Xia, Kristina Bečanović, Britt I. Drögemöller, Alicia Semaka, Charlotte M. Nguyen, Brett Trost, Fiona Richards, Emilia K. Bijlsma, Ferdinando Squitieri, Colin J.D. Ross, Stephen W. Scherer, Michael A. Eberle, Ryan K.C. Yuen, Michael R. Hayden
Am J Hum Genet. 2019 Jun 6; 104(6): 1116–1126. Published online 2019 May 16. doi: 10.1016/j.ajhg.2019.04.007
PMCID:
PMC6556907
AbstractArticlePDF–1.3M
6.
Neurofilament light protein in blood predicts regional atrophy in Huntington disease
Eileanoir B. Johnson, Lauren M. Byrne, Sarah Gregory, Filipe B. Rodrigues, Kaj Blennow, Alexandra Durr, Blair R. Leavitt, Raymund A. Roos, Henrik Zetterberg, Sarah J. Tabrizi, Rachael I. Scahill, Edward J. Wild, for the TRACK-HD Study Group
Neurology. 2018 Feb 20; 90(8): e717–e723. doi: 10.1212/WNL.0000000000005005
PMCID:
PMC5818166
AbstractArticlePDF–985K
7.
Basal ganglia atrophy in prodromal Huntington’s disease is detectable over one year using automated segmentation
DS Adnan Majid, Adam R Aron, Wesley Thompson, Sarah Sheldon, Samar Hamza, Diederick Stoffers, Dominic Holland, Jody Goldstein, Jody Corey-Bloom, Anders M Dale
Mov Disord. Author manuscript; available in PMC 2017 Sep 27.
Published in final edited form as: Mov Disord. 2011 Dec; 26(14): 2544–2551. Published online 2011 Sep 19. doi: 10.1002/mds.23912
PMCID:
PMC5615846
AbstractArticlePDF–419K
8.
The CREST-E study of creatine for Huntington disease: A randomized controlled trial
Steven M. Hersch, Giovanni Schifitto, David Oakes, Amy-Lee Bredlau, Catherine M. Meyers, Richard Nahin, Herminia Diana Rosas, For the Huntington Study Group CREST-E Investigators and Coordinators
Neurology. 2017 Aug 8; 89(6): 594–601. doi: 10.1212/WNL.0000000000004209
PMCID:
PMC5562960
AbstractArticlePDF–415K
9.
Neurofilament light protein in blood as a potential biomarker of neurodegeneration in Huntington's disease: a retrospective cohort analysis
Lauren M Byrne, Filipe B Rodrigues, Kaj Blennow, Alexandra Durr, Blair R Leavitt, Raymund A C Roos, Rachael I Scahill, Sarah J Tabrizi, Henrik Zetterberg, Douglas Langbehn, Edward J Wild
Lancet Neurol. 2017 Aug; 16(8): 601–609. doi: 10.1016/S1474-4422(17)30124-2
Correction in:
Lancet Neurol. 2017 Sep; 16(9): 683.
PMCID:
PMC5507767
AbstractArticle
10.
Longitudinal Psychiatric Symptoms Progress in Prodromal Huntington Disease: a Decade of Data
Eric A. Epping, Ji-In Kim, David Craufurd, Thomas M. Brashers-Krug, Karen E. Anderson, Elizabeth McCusker, Jolene Luther, Jeffrey D. Long, Jane S. Paulsen, the PREDICT-HD Investigators and Coordinators of the Huntington Study Group
Am J Psychiatry. Author manuscript; available in PMC 2017 Jun 9.
Published in final edited form as: Am J Psychiatry. 2016 Feb 1; 173(2): 184–192. Published online 2015 Oct 16. doi: 10.1176/appi.ajp.2015.14121551
PMCID:
PMC5465431
AbstractArticlePDF–502K
11.
The expanded CAG repeat in the huntingtin gene as target for therapeutic RNA modulation throughout the HD mouse brain
Nicole A. Datson, Anchel González-Barriga, Eleni Kourkouta, Rudie Weij, Jeroen van de Giessen, Susan Mulders, Outi Kontkanen, Taneli Heikkinen, Kimmo Lehtimäki, Judith C. T. van Deutekom
PLoS One. 2017; 12(2): e0171127. Published online 2017 Feb 9. doi: 10.1371/journal.pone.0171127
PMCID:
PMC5300196
AbstractArticlePDF–5.1M
12.
A randomized, double-blind, placebo-controlled trial of coenzyme Q10 in Huntington disease
Andrew McGarry, Michael McDermott, Karl Kieburtz, Elisabeth A. de Blieck, Flint Beal, Karen Marder, Christopher Ross, Ira Shoulson, Peter Gilbert, William M. Mallonee, Mark Guttman, Joanne Wojcieszek, Rajeev Kumar, Mark S. LeDoux, Mary Jenkins, H. Diana Rosas, Martha Nance, Kevin Biglan, Peter Como, Richard M. Dubinsky, Kathleen M. Shannon, Padraig O'Suilleabhain, Kelvin Chou, Francis Walker, Wayne Martin, Vicki L. Wheelock, Elizabeth McCusker, Joseph Jankovic, Carlos Singer, Juan Sanchez-Ramos, Burton Scott, Oksana Suchowersky, Stewart A. Factor, Donald S. Higgins, Jr, Eric Molho, Fredy Revilla, John N. Caviness, Joseph H. Friedman, Joel S. Perlmutter, Andrew Feigin, Karen Anderson, Ramon Rodriguez, Nikolaus R. McFarland, Russell L. Margolis, Eric S. Farbman, Lynn A. Raymond, Valerie Suski, Sandra Kostyk, Amy Colcher, Lauren Seeberger, Eric Epping, Sherali Esmail, Nancy Diaz, Wai Lun Alan Fung, Alan Diamond, Samuel Frank, Philip Hanna, Neal Hermanowicz, Leon S. Dure, Merit Cudkowicz, For the Huntington Study Group 2CARE Investigators and Coordinators
Neurology. 2017 Jan 10; 88(2): 152–159. doi: 10.1212/WNL.0000000000003478
PMCID:
PMC5224719
AbstractArticlePDF–346K
13.
Unified Huntington's disease rating scale for advanced patients: Validation and follow-up study
Katia Youssov, Guillaume Dolbeau, Patrick Maison, Marie-Françoise Boissé, Laurent Cleret De Langavant, Raymund Roos, Anne-Catherine Bachoud-Lévi
Mov Disord. Author manuscript;
Published in final edited form as: Mov Disord. 2013 Oct; 28(12): 1717–1723. doi: 10.1002/mds.25654
PMCID:
PMC5071381
AbstractArticle
14.
22 Years of predictive testing for Huntington's disease: the experience of the UK Huntington's Prediction Consortium
Sheharyar S Baig, Mark Strong, Elisabeth Rosser, Nicola V Taverner, Ruth Glew, Zosia Miedzybrodzka, Angus Clarke, David Craufurd, UK Huntington's Disease Prediction Consortium, Oliver W Quarrell
Eur J Hum Genet. 2016 Oct; 24(10): 1396–1402. Published online 2016 May 11. doi: 10.1038/ejhg.2016.36
Correction in:
Eur J Hum Genet. 2016 Oct; 24(10): 1515.
Correction in:
Eur J Hum Genet. 2017 Nov; 25(11): 1290.
PMCID:
PMC5027682
AbstractArticlePDF–622K
15.
Huntington disease reduced penetrance alleles occur at high frequency in the general population
Chris Kay, Jennifer A. Collins, Zosia Miedzybrodzka, Steven J. Madore, Erynn S. Gordon, Norman Gerry, Mark Davidson, Ramy A. Slama, Michael R. Hayden
Neurology. 2016 Jul 19; 87(3): 282–288. doi: 10.1212/WNL.0000000000002858
PMCID:
PMC4955276
AbstractArticlePDF–355K
16.
Huntingtin Haplotypes Provide Prioritized Target Panels for Allele-specific Silencing in Huntington Disease Patients of European Ancestry
Chris Kay, Jennifer A Collins, Niels H Skotte, Amber L Southwell, Simon C Warby, Nicholas S Caron, Crystal N Doty, Betty Nguyen, Annamaria Griguoli, Colin J Ross, Ferdinando Squitieri, Michael R Hayden
Mol Ther. 2015 Nov; 23(11): 1759–1771. Prepublished online 2015 Jul 23. Published online 2015 Aug 25. doi: 10.1038/mt.2015.128
PMCID:
PMC4817952
AbstractArticlePDF–907K
17.
The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease
Jae Whan Keum, Aram Shin, Tammy Gillis, Jayalakshmi Srinidhi Mysore, Kawther Abu Elneel, Diane Lucente, Tiffany Hadzi, Peter Holmans, Lesley Jones, Michael Orth, Seung Kwak, Marcy E. MacDonald, James F. Gusella, Jong-Min Lee
Am J Hum Genet. 2016 Feb 4; 98(2): 287–298. Published online 2016 Feb 4. doi: 10.1016/j.ajhg.2015.12.018
PMCID:
PMC4746370
AbstractArticlePDF–1.0M
18.
Huntington Disease in Asia
Miao Xu, Zhi-Ying Wu
Chin Med J (Engl) 2015 Jul 5; 128(13): 1815–1819. doi: 10.4103/0366-6999.159359
PMCID:
PMC4733723
AbstractArticlePDF–318K
19.
Motor onset and diagnosis in Huntington disease using the diagnostic confidence level
Dawei Liu, Jeffrey D. Long, Ying Zhang, Lynn A. Raymond, Karen Marder, Anne Rosser, Elizabeth A. McCusker, James A. Mills, Jane S. Paulsen
J Neurol. Author manuscript; available in PMC 2016 Dec 1.
Published in final edited form as: J Neurol. 2015 Dec; 262(12): 2691–2698. Published online 2015 Sep 26. doi: 10.1007/s00415-015-7900-7
PMCID:
PMC4666501
AbstractArticlePDF–206K
20.
Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease
Genetic Modifiers of Huntington’s Disease (GeM-HD) Consortium
Cell. Author manuscript; available in PMC 2016 Jul 30.
Published in final edited form as: Cell. 2015 Jul 30; 162(3): 516–526. doi: 10.1016/j.cell.2015.07.003
PMCID:
PMC4524551
AbstractArticlePDF–1.2M

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