S. Barber

Neurology · 2010

A researcher in the Science corpus: 1 paper; trusts 6 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

Whom S. Barber trusts overall

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

  1. Christopher A. Ross
  2. M. Beal
  3. M. Schröder
  4. A. A. Starkov
  5. Michelle A. Poirier
  6. K. Bedard
  7. D. Cleveland
  8. L. Bruijn
  9. P. Cox

Papers from S. Barber's perspective

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

  1. TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis (Science)
  2. Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6 (Science)
  3. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. (Biochemical and Biophysical Research Communications - BBRC)
  4. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis (Nature Genetics)
  5. Protofibrils, pores, fibrils, and neurodegeneration: separating the responsible protein aggregates from the innocent bystanders. (Annual Review of Neuroscience)
  6. Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis (Science)
  7. Mutated Human SOD1 Causes Dysfunction of Oxidative Phosphorylation in Mitochondria of Transgenic Mice* (Journal of Biological Chemistry)
  8. A role for motoneuron subtype–selective ER stress in disease manifestations of FALS mice (Nature Neuroscience)
  9. Formation of high molecular weight complexes of mutant Cu, Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis. (Proceedings of the National Academy of Sciences of the United States of America)
  10. Unraveling the mechanisms involved in motor neuron degeneration in ALS. (Annual Review of Neuroscience)

Their papers