J. Wuu
Neuron · 2005–2011
A researcher in the Science corpus: 3 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Whom J. Wuu trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from J. Wuu's perspective
Ordered by how strongly the researchers J. Wuu trusts endorse each paper. Same corpus, a different order for every researcher.
- Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis (Science)
- Neuropathological stageing of Alzheimer-related changes
- Regulation of Cell Survival by Secreted Proneurotrophins (Science)
- Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis (Science)
- Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein (Nature Genetics)
- Exome sequencing identifies the cause of a Mendelian disorder (Nature Genetics)
- Merlin—rapid analysis of dense genetic maps using sparse gene flow trees (Nature Genetics)
- The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. (Genome Research)
- TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis (Nature Genetics)
- TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia. (Lancet Neurology)
Their papers
- A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD (2011) — 4,318 citations
- Exome sequencing reveals VCP mutations as a cause of familial ALS (2010) — 1,260 citations
- Precursor form of brain‐derived neurotrophic factor and mature brain‐derived neurotrophic factor are decreased in the pre‐clinical stages of Alzheimer's disease (2005) — 680 citations