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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Kevin A. Strauss

Clinic for Special Children

Strasburg

PA 17579

USA

[email]@clinicforspecialchildren.org

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Clinic for Special Children, Strasburg, PA 17579, USA. 2003 - 2010

References

  1. Classical maple syrup urine disease and brain development: principles of management and formula design. Strauss, K.A., Wardley, B., Robinson, D., Hendrickson, C., Rider, N.L., Puffenberger, E.G., Shelmer, D., Moser, A.B., Morton, D.H. Mol. Genet. Metab. (2010) [Pubmed]
  2. Cerebral haemodynamics in patients with glutaryl-coenzyme A dehydrogenase deficiency. Strauss, K.A., Donnelly, P., Wintermark, M. Brain (2010) [Pubmed]
  3. Genetics, medicine, and the Plain people. Strauss, K.A., Puffenberger, E.G. Annu. Rev. Genomics. Hum. Genet (2009) [Pubmed]
  4. Clinical application of DNA microarrays: molecular diagnosis and HLA matching of an Amish child with severe combined immune deficiency. Strauss, K.A., Puffenberger, E.G., Bunin, N., Rider, N.L., Morton, M.C., Eastman, J.T., Morton, D.H. Clin. Immunol. (2008) [Pubmed]
  5. Prevention of brain disease from severe 5,10-methylenetetrahydrofolate reductase deficiency. Strauss, K.A., Morton, D.H., Puffenberger, E.G., Hendrickson, C., Robinson, D.L., Wagner, C., Stabler, S.P., Allen, R.H., Chwatko, G., Jakubowski, H., Niculescu, M.D., Mudd, S.H. Mol. Genet. Metab. (2007) [Pubmed]
  6. Multimodal imaging of striatal degeneration in Amish patients with glutaryl-CoA dehydrogenase deficiency. Strauss, K.A., Lazovic, J., Wintermark, M., Morton, D.H. Brain (2007) [Pubmed]
  7. Management of hyperbilirubinemia and prevention of kernicterus in 20 patients with Crigler-Najjar disease. Strauss, K.A., Robinson, D.L., Vreman, H.J., Puffenberger, E.G., Hart, G., Morton, D.H. Eur. J. Pediatr. (2006) [Pubmed]
  8. Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. Strauss, K.A., Puffenberger, E.G., Huentelman, M.J., Gottlieb, S., Dobrin, S.E., Parod, J.M., Stephan, D.A., Morton, D.H. N. Engl. J. Med. (2006) [Pubmed]
  9. Glutaric aciduria type 1: a clinician's view of progress. Strauss, K.A. Brain (2005) [Pubmed]
  10. Genome-wide SNP arrays as a diagnostic tool: clinical description, genetic mapping, and molecular characterization of Salla disease in an Old Order Mennonite population. Strauss, K.A., Puffenberger, E.G., Craig, D.W., Panganiban, C.B., Lee, A.M., Hu-Lince, D., Stephan, D.A., Morton, D.H. Am. J. Med. Genet. A (2005) [Pubmed]
  11. Type I glutaric aciduria, part 1: natural history of 77 patients. Strauss, K.A., Puffenberger, E.G., Robinson, D.L., Morton, D.H. American J. Medical Genetics. C, Seminars Medical Genetics (2003) [Pubmed]
  12. Type I glutaric aciduria, part 2: a model of acute striatal necrosis. Strauss, K.A., Morton, D.H. American J. Medical Genetics. C, Seminars Medical Genetics (2003) [Pubmed]
 
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