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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 03, 2024
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An exploration of the genetics of the mutant Huntingtin (mHtt) gene in a cohort of patients with chorea from different ethnic groups in sub-Saharan Africa.
Mendi J Muthinja et al. Ann Hum Genet 2024
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What Is Huntington Disease?
R Marcus, JAMA, August 21, 2023
A pilot evaluation of an 8-week mindfulness-based stress reduction program for people with pre-symptomatic Huntington's disease.
Sarah Velissaris et al. J Community Genet 2023
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Genetic screening for Huntington disease phenocopies in Sweden: A tertiary center case series focused on short tandem repeat (STR) disorders.
Martin Paucar et al. J Neurol Sci 2023 451120707
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Ethical Considerations in Clinical Trials for Rare Genetic Diseases: The Case of Huntington's Disease.
Adys Mendizabal et al. Am J Bioeth 2023 23(7) 94-96
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Intrapersonal and Interpersonal Disengagement Coping: Associations with Emotions of Youth At-Risk for Huntington's Disease.
Kelly H Watson et al. J Huntingtons Dis 2023
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Pharmacogenetics in the Treatment of Huntington’s Disease: Review and Future Perspectives
XG Gonzalez et al, J Pers Med, February 22, 2023
The Nuclear Envelope in Ageing and Progeria.
Fragoso-Luna Adrián et al. Sub-cellular biochemistry 2023 10253-75
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Health related quality of life, service utilization and costs for patients with Huntington's disease in Norway.
van Walsem Marleen R et al. BMC health services research 2022 22(1) 1527
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Identification of psychoeducation needs and an intervention response for pre-symptomatic Huntington's disease.
Gluyas Cathy et al. Journal of community genetics 2022 1-9
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The Vasopressin 1a Receptor Antagonist SRX246 Reduces Aggressive Behavior in Huntington’s Disease
HT Mailbach et al, J Pers Medicine, September 22, 2022
PAM-altering SNP-based allele-specific CRISPR-Cas9 therapeutic strategies for Huntington's disease.
Shin Jun Wan et al. Molecular therapy. Methods & clinical development 2022 26547-561
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Clinical and molecular findings of intermediate allele carriers in the HTT gene from the Mexican Mestizo population.
Ramírez-García Miguel Ángel et al. Neuro-degenerative diseases 2022
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Pepinemab antibody blockade of SEMA4D in early Huntington's disease: a randomized, placebo-controlled, phase 2 trial.
Feigin Andrew et al. Nature medicine 2022
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Canadian healthcare capacity gaps for disease-modifying treatment in Huntington's disease: a survey of current practice and modelling of future needs.
Bénard Angèle et al. BMJ open 2022 12(6) e062740
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Searching for Answers: Information-Seeking by Young People At-Risk for Huntington's Disease.
Chase Colby L et al. Journal of Huntington's disease 2022
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Predicting clinical scores in Huntington's disease: a lightweight speech test.
Riad Rachid et al. Journal of neurology 2022
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Predicting Severity of Huntington's Disease With Wearable Sensors.
Scheid Brittany H et al. Frontiers in digital health 2022 4874208
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Haplotype-specific insertion-deletion variations for allele-specific targeting in Huntington's disease.
Shin Jun Wan et al. Molecular therapy. Methods & clinical development 2022 2584-95
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Clinical and Genetic Aspects of Huntington's Disease in the Malian Population.
Bocoum Abdoulaye et al. Journal of Huntington's disease 2022
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Advance Directive Documentation in a Huntington's Disease Clinic: A Retrospective Chart Review.
Cooper Christa S et al. Tremor and other hyperkinetic movements (New York, N.Y.) 2022 124
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A Machine-Learning Derived Huntington's Disease Progression Model: Insights for Clinical Trial Design.
Mohan Amrita et al. Movement disorders : official journal of the Movement Disorder Society 2021
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A MDS Evidence-Based Review on Treatments for Huntington's Disease.
Ferreira Joaquim J et al. Movement disorders : official journal of the Movement Disorder Society 2021
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Health services utilization of Chinese patients with Huntington's disease: a cross-sectional study.
Ke Huiyi et al. BMC health services research 2021 21(1) 806
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Huntington's disease: Nearly four decades of human molecular genetics.
Gusella James F et al. Human molecular genetics 2021
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Failure of genetic therapies for Huntington’s devastates community- Hopes were high for drugs designed to lower levels of a mutant protein, but development has stalled.
D Kwon, Nature News, May 5, 2021
Genetic counseling and testing practices for late-onset neurodegenerative disease: a systematic review.
Crook Ashley et al. Journal of neurology 2021
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DNA methylation study of Huntington's disease and motor progression in patients and in animal models.
Lu Ake T et al. Nature communications 2020 11(1) 4529
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Mutant huntingtin and neurofilament light have distinct longitudinal dynamics in Huntington’s disease
FB Rodrigues et al, Science Trans Med, December 6, 2020
Informing about genetic risk in families with Huntington disease: comparison of attitudes across two decades.
Pierron Lucie et al. European journal of human genetics : EJHG 2020 Dec
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 03, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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