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)
 

Editor

Share

Personal info

View

Links

Table of contents

About

Terms

 

Peter T. Clayton

Biochemistry

Endocrinology and Metabolism Unit

Institute of Child Health

University College London

U.K

[email]@ich.ucl.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Biochemistry, Endocrinology and Metabolism Unit, Institute of Child Health, University College London, U.K. 2001 - 2006
  • Department of Metabolic Medicine, Great Ormond Street Hospital for Children, WC1N 1EH, London, UK. 2003
  • London Centre for Paediatric Endocrinology and Metabolism, Biochemistry, Endocrinology and Metabolism Unit, Institute of Child Health, United Kingdom. 2001
  • Institute of Child Health, University College London, UK. 1998

References

  1. B6-responsive disorders: a model of vitamin dependency. Clayton, P.T. J. Inherit. Metab. Dis. (2006) [Pubmed]
  2. Neonatal epileptic encephalopathy. Clayton, P.T., Surtees, R.A., DeVile, C., Hyland, K., Heales, S.J. Lancet (2003) [Pubmed]
  3. Inborn errors presenting with liver dysfunction. Clayton, P.T. Semin. Neonatol (2002) [Pubmed]
  4. Mutations in the sterol 27-hydroxylase gene (CYP27A) cause hepatitis of infancy as well as cerebrotendinous xanthomatosis. Clayton, P.T., Verrips, A., Sistermans, E., Mann, A., Mieli-Vergani, G., Wevers, R. J. Inherit. Metab. Dis. (2002) [Pubmed]
  5. Clinical consequences of defects in peroxisomal beta-oxidation. Clayton, P.T. Biochem. Soc. Trans. (2001) [Pubmed]
  6. Applications of mass spectrometry in the study of inborn errors of metabolism. Clayton, P.T. J. Inherit. Metab. Dis. (2001) [Pubmed]
  7. Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion. Clayton, P.T., Eaton, S., Aynsley-Green, A., Edginton, M., Hussain, K., Krywawych, S., Datta, V., Malingre, H.E., Berger, R., van den Berg, I.E. J. Clin. Invest. (2001) [Pubmed]
  8. Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry. Clayton, P.T., Doig, M., Ghafari, S., Meaney, C., Taylor, C., Leonard, J.V., Morris, M., Johnson, A.W. Arch. Dis. Child. (1998) [Pubmed]
 
WikiGenes - Universities