M. Farrer

Neurology · 2003–2013

A researcher in the Science corpus: 11 papers; trusts 3 researchers and is trusted by 1 researcher here, as inferred from the citation graph.

Subfields

• Neurology — 52 citations into it; #983 of 1,455 by trust here, #76 by citations
• Cellular and Molecular Neuroscience — 24 citations into it; #2,179 of 2,998 by trust here, #265 by citations
• Physiology — 18 citations into it

Whom M. Farrer trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Susan Lindquist
2. M. Feany

Who trusts M. Farrer overall

1. Dennis W. Dickson
2. Nicole Exner
3. Jose A. Obeso
4. T. Dawson
5. A. Lutz
6. S. Lesage
7. M. Egeblad

Papers from M. Farrer's perspective

Ordered by how strongly the researchers M. Farrer trusts endorse each paper. Same corpus, a different order for every researcher.

1. A Drosophila model of Parkinson's disease (Nature)
2. The Sydney multicenter study of Parkinson's disease: The inevitability of dementia at 20 years (Movement Disorders)
3. Parkinson’s Disease Patient-Derived Induced Pluripotent Stem Cells Free of Viral Reprogramming Factors (Cell)
4. The parkinson's complex: Parkinsonism is just the tip of the iceberg (Annals of Neurology)
5. Tau Suppression in a Neurodegenerative Mouse Model Improves Memory Function (Science)
6. [Parkinson's disease]. (La Revue du praticien)
7. Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease. (Brain : a journal of neurology)
8. Description of Parkinson's Disease as a Clinical Syndrome (Annals of the New York Academy of Sciences)
9. Genetics of Parkinson disease: paradigm shifts and future prospects (Nature reviews genetics)
10. Staging of brain pathology related to sporadic Parkinson's disease. (Neurobiology of Aging)

Their papers

• Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. (2004) — 3,061 citations
• Alpha‐synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease (2013) — 646 citations
• VPS35 mutations in Parkinson disease. (2011) — 896 citations
• Missing pieces in the Parkinson's disease puzzle (2010) — 765 citations
• Multi-center analysis of glucocerebrosidase mutations in Parkinson disease (2009) — 1,060 citations
• Genetics of Parkinson disease: paradigm shifts and future prospects (2006) — 716 citations
• Alpha-synuclein locus duplication as a cause of familial Parkinson's disease. (2004) — 984 citations
• Comparison of kindreds with parkinsonism and α‐synuclein genomic multiplications (2004) — 637 citations
• α-synuclein locus duplication as a cause of familial Parkinson's disease (2004) — 1,732 citations
• alpha-Synuclein locus triplication causes Parkinson's disease. (2003) — 2,110 citations
• α-Synuclein Locus Triplication Causes Parkinson's Disease (2003) — 3,975 citations