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

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Merlin G. Butler

Children's Mercy Hospitals and Clinics and University of Missouri-Kansas City School of Medicine

Kansas City

Missouri 64108

USA

[email]@cmh.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Children's Mercy Hospitals and Clinics and University of Missouri-Kansas City School of Medicine, Kansas City, Missouri 64108, USA. 2000 - 2008
  • Children's Mercy Hospitals and Clinics, Kansas City, Missouri 64108, USA. 2000

References

  1. Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndrome. Butler, M.G., Fischer, W., Kibiryeva, N., Bittel, D.C. Am. J. Med. Genet. A (2008) [Pubmed]
  2. Plasma obestatin and ghrelin levels in subjects with Prader-Willi syndrome. Butler, M.G., Bittel, D.C. Am. J. Med. Genet. A (2007) [Pubmed]
  3. Energy expenditure and physical activity in Prader-Willi syndrome: comparison with obese subjects. Butler, M.G., Theodoro, M.F., Bittel, D.C., Donnelly, J.E. Am. J. Med. Genet. A (2007) [Pubmed]
  4. X-chromosome inactivation patterns in females with Prader-Willi syndrome. Butler, M.G., Theodoro, M.F., Bittel, D.C., Kuipers, P.J., Driscoll, D.J., Talebizadeh, Z. Am. J. Med. Genet. A (2007) [Pubmed]
  5. Thyroid function studies in Prader-Willi syndrome. Butler, M.G., Theodoro, M., Skouse, J.D. Am. J. Med. Genet. A (2007) [Pubmed]
  6. Management of obesity in Prader-Willi syndrome. Butler, M.G. Nature Clinical Practice. Endocrinology & Metabolism (2006) [Pubmed]
  7. Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations. Butler, M.G., Dasouki, M.J., Zhou, X.P., Talebizadeh, Z., Brown, M., Takahashi, T.N., Miles, J.H., Wang, C.H., Stratton, R., Pilarski, R., Eng, C. J. Med. Genet. (2005) [Pubmed]
  8. Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy. Butler, M.G., Bittel, D.C., Kibiryeva, N., Talebizadeh, Z., Thompson, T. Pediatrics (2004) [Pubmed]
  9. Plasma peptide YY and ghrelin levels in infants and children with Prader-Willi syndrome. Butler, M.G., Bittel, D.C., Talebizadeh, Z. J. Pediatr. Endocrinol. Metab. (2004) [Pubmed]
  10. Coenzyme Q10 levels in Prader-Willi syndrome: comparison with obese and non-obese subjects. Butler, M.G., Dasouki, M., Bittel, D., Hunter, S., Naini, A., DiMauro, S. Am. J. Med. Genet. A (2003) [Pubmed]
  11. Imprinting disorders: non-Mendelian mechanisms affecting growth. Butler, M.G. J. Pediatr. Endocrinol. Metab. (2002) [Pubmed]
  12. Decreased bone mineral density in Prader-Willi syndrome: comparison with obese subjects. Butler, M.G., Haber, L., Mernaugh, R., Carlson, M.G., Price, R., Feurer, I.D. Am. J. Med. Genet. (2001) [Pubmed]
  13. Specific genetic diseases at risk for sedation/anesthesia complications. Butler, M.G., Hayes, B.G., Hathaway, M.M., Begleiter, M.L. Anesth. Analg. (2000) [Pubmed]
  14. Plasma cholecystokinin levels in Prader-Willi syndrome and obese subjects. Butler, M.G., Carlson, M.G., Schmidt, D.E., Feurer, I.D., Thompson, T. Am. J. Med. Genet. (2000) [Pubmed]
 
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