The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Conrad C. Weihl

Department of Neurology

Washington University School of Medicine

Saint Louis

MO 63110

USA

[email]@*.wustl.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Neurology, Washington University School of Medicine, Saint Louis, MO 63110, USA. 2006 - 2011
  • Department of Neurology and Hope Center for Neurological Disorders, Washington University School of Medicine, 660 S. Euclid Avenue, Saint Louis, USA. 2011

References

  1. Valosin containing protein associated fronto-temporal lobar degeneration: clinical presentation, pathologic features and pathogenesis. Weihl, C.C. Curr. Alzheimer. Res (2011) [Pubmed]
  2. Novel GNE mutations in two phenotypically distinct HIBM2 patients. Weihl, C.C., Miller, S.E., Zaidman, C.M., Pestronk, A., Baloh, R.H., Al-Lozi, M. Neuromuscul. Disord. (2011) [Pubmed]
  3. Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia. Weihl, C.C., Pestronk, A., Kimonis, V.E. Neuromuscul. Disord. (2009) [Pubmed]
  4. TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia. Weihl, C.C., Temiz, P., Miller, S.E., Watts, G., Smith, C., Forman, M., Hanson, P.I., Kimonis, V., Pestronk, A. J. Neurol. Neurosurg. Psychiatr. (2008) [Pubmed]
  5. Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice. Weihl, C.C., Miller, S.E., Hanson, P.I., Pestronk, A. Hum. Mol. Genet. (2007) [Pubmed]
  6. Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation. Weihl, C.C., Dalal, S., Pestronk, A., Hanson, P.I. Hum. Mol. Genet. (2006) [Pubmed]
 
WikiGenes - Universities