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Publications by Britt I. Drögemöller

Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease

American Journal of Human Genetics
Genetics
2019English

Further Investigation of the Role of ACYP2 and WFS1 Pharmacogenomic Variants in the Development of Cisplatin-Induced Ototoxicity in Testicular Cancer Patients

Clinical Cancer Research
Cancer ResearchOncology
2018English

Related publications

CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset

Cell
BiochemistryGeneticsMolecular Biology
2019English

CAG-repeat Length and the Age of Onset in Huntington Disease (HD): A Review and Validation Study of Statistical Approaches

American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics
PsychiatryMolecular NeuroscienceMental HealthGeneticsCellular
2009English

Modelling and Inference Reveal Nonlinear Length-Dependent Suppression of Somatic Instability for Small Disease Associated Alleles in Myotonic Dystrophy Type 1 and Huntington Disease

Journal of the Royal Society Interface
BiochemistryBiophysicsBiomaterialsBiotechnologyBioengineeringBiomedical Engineering
2013English

Unbiased Profiling of Isogenic Huntington Disease hPSC-Derived CNS and Peripheral Cells Reveals Strong Cell-Type Specificity of CAG Length Effects

Cell Reports
BiochemistryGeneticsMolecular Biology
2019English

Germ-Line CAG Repeat Instability Causes Extreme CAG Repeat Expansion With Infantile-Onset Spinocerebellar Ataxia Type 2

European Journal of Human Genetics
Genetics
2012English

The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease

American Journal of Human Genetics
Genetics
2016English

Late Onset Huntington Disease: Clinical and Genetic Characteristics of 34 Cases

Journal of the Neurological Sciences
Neurology
2009English

Linking SNPs to CAG Repeat Length in Huntington's Disease Patients

Nature Methods
BiochemistryBiotechnologyCell BiologyMolecular Biology
2008English

Glyceraldehyde 3-Phosphate Dehydrogenase Augments the Intercellular Transmission and Toxicity of Polyglutamine Aggregates in a Cell Model of Huntington Disease

Journal of Neurochemistry
BiochemistryMolecular NeuroscienceCellular
2016English

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