Are (CTG)n expansions at the SCA8 locus rare polymorphisms?

Genetic variation and pesticide exposure influence blood DNA methylation signatures in females with early-stage Parkinson's disease.

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The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells.

Scientific reports·2019

The genetic landscape of Parkinson's disease.

Revue neurologique·2018

Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein.

Scientific reports·2017

Inflammatory profile discriminates clinical subtypes in LRRK2-associated Parkinson's disease.

European journal of neurology·2017

Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's disease.

Neurobiology of aging·2016

Enhancer control of promoter activity and variability via frequency modulation of clustered transcriptional bursts.

Nature genetics·2026

Pervasive interactions between exposures and polygenic risk can inform more effective clinical and behavioral interventions.

Nature genetics·2026

Multiscale analysis and functional validation of the cellular and genetic determinants of skeletal disease.

Nature genetics·2026

Graph-based pan-genome reveals structural variations associated with agronomic traits in mung bean.

Nature genetics·2026

Evolving patterns of co-mutations from tumor initiation to metastatic progression.

Nature genetics·2026

Metabolically and epigenetically reprogrammed splenic TRNP1hiCD8+ T cells exacerbate liver fibrosis.

Nature genetics·2026

The Genetics of Coronary Artery Disease: Insights from Genome-wide Association Studies.

Current cardiology reviews·2026

Establishment of the endocrine variant extractor and its clinical application in identifying a novel GATA3 mutation in HDR syndrome.

Frontiers in endocrinology·2026

Sex- and Population-Specific Formulas for Glenoid Height-Based Assessment of Glenoid Bone Loss: A Systematic Review and Meta-analysis.

Orthopaedic journal of sports medicine·2026

Root cause discovery via permutations and Cholesky decomposition.

Journal of the Royal Statistical Society. Series B, Statistical methodology·2026

In-silico analysis of Bifidobacterium bifidum strain 900791 genome in the context of the B. bifidum pangenome.

Frontiers in cellular and infection microbiology·2026

Sex Differences in Behavioral Responses to Chronic Unpredictable Mild Stress in Swiss Mice.

The European journal of neuroscience·2026

Related Experiment Videos

Are (CTG)n expansions at the SCA8 locus rare polymorphisms?

Related Concept Videos

Genetic variation and pesticide exposure influence blood DNA methylation signatures in females with early-stage Parkinson's disease.

The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells.

The genetic landscape of Parkinson's disease.

Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein.

Inflammatory profile discriminates clinical subtypes in LRRK2-associated Parkinson's disease.

Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's disease.

Enhancer control of promoter activity and variability via frequency modulation of clustered transcriptional bursts.

Pervasive interactions between exposures and polygenic risk can inform more effective clinical and behavioral interventions.

Multiscale analysis and functional validation of the cellular and genetic determinants of skeletal disease.

Graph-based pan-genome reveals structural variations associated with agronomic traits in mung bean.

Evolving patterns of co-mutations from tumor initiation to metastatic progression.

Metabolically and epigenetically reprogrammed splenic TRNP1<sup>hi</sup>CD8<sup>+</sup> T cells exacerbate liver fibrosis.

The Genetics of Coronary Artery Disease: Insights from Genome-wide Association Studies.

Establishment of the endocrine variant extractor and its clinical application in identifying a novel <i>GATA3</i> mutation in HDR syndrome.

Sex- and Population-Specific Formulas for Glenoid Height-Based Assessment of Glenoid Bone Loss: A Systematic Review and Meta-analysis.

Root cause discovery via permutations and Cholesky decomposition.

<i>In-silico</i> analysis of <i>Bifidobacterium bifidum</i> strain 900791 genome in the context of the <i>B. bifidum</i> pangenome.

Sex Differences in Behavioral Responses to Chronic Unpredictable Mild Stress in Swiss Mice.

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Are (CTG)n expansions at the SCA8 locus rare polymorphisms?

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