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

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John Christodoulou

Program in Genetics and Genomic Biology

Research Institute

Hospital for Sick Children

University of Toronto

Canada

[email]@chw.edu.au

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Affiliations

Program in Genetics and Genomic Biology, Research Institute, Hospital for Sick Children, University of Toronto, Canada. 2006
Western Sydney Genetics Program, Children's Hospital at Westmead, Sydney, Australia. 2003 - 2004

References

Deletion hotspot in the argininosuccinate lyase gene: association with topoisomerase II and DNA polymerase alpha sites. Christodoulou, J., Craig, H.J., Walker, D.C., Weaving, L.S., Pearson, C.E., McInnes, R.R. Hum. Mutat. (2006) [Pubmed]
Perimortem laboratory investigation of genetic metabolic disorders. Christodoulou, J., Wilcken, B. Semin. Neonatol (2004) [Pubmed]
RettBASE: The IRSA MECP2 variation database-a new mutation database in evolution. Christodoulou, J., Grimm, A., Maher, T., Bennetts, B. Hum. Mutat. (2003) [Pubmed]
MECP2 and beyond: phenotype-genotype correlations in Rett syndrome. Christodoulou, J., Weaving, L.S. J. Child Neurol. (2003) [Pubmed]