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Publications by Philip Seibler

MtDNA Deletions Discriminate Affected From Unaffected LRRK2 Mutation Carriers

Annals of Neurology

English

The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci

Frontiers in Neurology

English

Related publications

Mitochondrial DNA Copy Number in Affected and Unaffected LHON Mutation Carriers

BMC Research Notes

Molecular Biology

English

Expanding Our Understanding of mtDNA Deletions

Cell Metabolism

Molecular Biology

English

Retinal Function and Neural Conduction Along the Visual Pathways in Affected and Unaffected Carriers With Leber's Hereditary Optic Neuropathy

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

Sensory Systems

English

Pupil Response Biomarkers Distinguish Amyloid Precursor Protein Mutation Carriers From Non-Carriers

Current Alzheimer Research

English

Clinical Heterogeneity of the LRRK2 G2019S Mutation

Archives of Neurology

English

Mutation in an mtDNA Protein-Coding Gene

Journal of Child Neurology

English

21-Hydroxylase Deficiency Families With HLA Identical Affected and Unaffected Sibs.

Journal of Medical Genetics

English

LRRK2 G2019S Mutation Attenuates Microglial Motility by Inhibiting Focal Adhesion Kinase

Nature Communications

Molecular Biology

English

Modulation of mtDNA Copy Number Ameliorates the Pathological Consequences of a Heteroplasmic mtDNA Mutation in the Mouse

Science advances

Multidisciplinary

English