Christine Klein
Physiology · 2006–2018
A researcher in the Science corpus: 6 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Physiology — 12 citations into it
Whom Christine Klein trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Christine Klein's perspective
Ordered by how strongly the researchers Christine Klein trusts endorse each paper. Same corpus, a different order for every researcher.
- The new mutation, E46K, of α‐synuclein causes parkinson and Lewy body dementia (Annals of Neurology)
- A Hydrophobic Stretch of 12 Amino Acid Residues in the Middle of α-Synuclein Is Essential for Filament Assembly* (Journal of Biological Chemistry)
- Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin (Nature)
- Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
- Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1 (Science)
- The Sydney multicenter study of Parkinson's disease: The inevitability of dementia at 20 years (Movement Disorders)
- Pimavanserin for patients with Parkinson's disease psychosis: a randomised, placebo-controlled phase 3 trial. (The Lancet)
- Impaired Degradation of Mutant α-Synuclein by Chaperone-Mediated Autophagy (Science)
- α-synuclein locus duplication as a cause of familial Parkinson's disease
- Gaucher’s Disease Glucocerebrosidase and -synuclein form a bidirectional pathogenic loop in synucleinopathies (Cell)
Their papers
- Parkin and PINK1 mitigate STING-induced inflammation (2018) — 1,155 citations
- LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. (2006) — 707 citations
- Past, Present, and Future of Parkinson’s Disease: A Special Essay on the 200th Anniversary of the Shaking Palsy (2017) — 734 citations
- Phenomenology and classification of dystonia: a consensus update (2013) — 2,078 citations
- Genetics of Parkinson's disease. (2012) — 866 citations
- Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study (2008) — 1,476 citations