Molecular biology of Huntington's disease

"It's being part of the big picture, even though you're a tiny jigsaw piece"-motivations and expectations of individuals participating in the Enroll-HD observational study.

Journal of community genetics·2020

Apathy predicts rate of cognitive decline over 24 months in premanifest Huntington's disease.

Psychological medicine·2020

Progression of motor subtypes in Huntington's disease: a 6-year follow-up study.

Journal of neurology·2016

A Method for Analyzing Videotaped Genetic Counseling Sessions.

Journal of genetic counseling·2015

Magnetization transfer imaging in premanifest and manifest huntington disease: a 2-year follow-up.

AJNR. American journal of neuroradiology·2012

Magnetization transfer imaging in premanifest and manifest Huntington disease.

AJNR. American journal of neuroradiology·2012

DNA-based immunization.

Molecular and cell biology of human diseases series·1995

Molecular biology of schizophrenia.

Molecular and cell biology of human diseases series·1994

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Research (Washington, D.C.)·2026

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Clinical case reports·2026

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Journal of human genetics·2026

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

Nature genetics·2026

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Psychiatric genetics·2026

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Frontiers in genetics·2026

Related Experiment Videos

Molecular biology of Huntington's disease

Related Concept Videos

"It's being part of the big picture, even though you're a tiny jigsaw piece"-motivations and expectations of individuals participating in the Enroll-HD observational study.

Apathy predicts rate of cognitive decline over 24 months in premanifest Huntington's disease.

Progression of motor subtypes in Huntington's disease: a 6-year follow-up study.

A Method for Analyzing Videotaped Genetic Counseling Sessions.

Magnetization transfer imaging in premanifest and manifest huntington disease: a 2-year follow-up.

Magnetization transfer imaging in premanifest and manifest Huntington disease.

DNA-based immunization.

Molecular biology of schizophrenia.

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Related Experiment Videos

Molecular biology of Huntington's disease

Related Concept Videos

Related Articles