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The Lancet Psychiatry

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Oncogene

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Evidence That Paternal Expression of the ε-Sarcoglycan Gene Accounts for Reduced Penetrance in Myoclonus-Dystonia

B. Müller, Katja Hedrich, Norman Kock, +12

The American Journal of Human Genetics

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Clinical Spectrum of Homozygous and Heterozygous PINK1 Mutations in a Large German Family With Parkinson Disease

Katja Hedrich, Johann Hagenah, Ana Djarmati, +14

Archives of Neurology

PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism

Christine Klein, Ana Djarmati, Katja Hedrich, +14

European Journal of Human Genetics

Early-onset ParkinsonismDj-1 MutationsMendelian DisorderNeurological DisorderParkinson Disease +6

Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patients

Aleksandar Raković, Anne Grünewald, Philip Seibler, +4

Human Molecular Genetics

MitophagyParkinson Disease PatientsGeneticsPathologyNeurochemical Biomarkers +15

<i>Parkin</i> gene alterations in hepatocellular carcinoma

Fang Wang, Stacy R. Denison, Jinping Lai, +7

Genes Chromosomes and Cancer

Differential effects of PINK1 nonsense and missense mutations on mitochondrial function and morphology

Anne Grünewald, Matthew E. Gegg, Jan‐Willem Taanman, +4

Experimental Neurology

Effects of genetic variations in the dystonia protein torsinA: identification of polymorphism at residue 216 as protein modifier

Norman Kock, Teresa V. Naismith, Heather Boston, +4

Human Molecular Genetics

ε‐sarcoglycan mutations found in combination with other dystonia gene mutations

Christine Klein, Liu Liu, Dana Doheny, +17

Annals of Neurology