Summaries from completed ICPGC projects are made available here.

1. Wilson, Y.A., Smithers-Sheedy, H., Ostojic, K., et al., Common data elements to standardized genomics studies in cerebral palsy. Dev Med Child Neuro. Online ahead of print (DOI: 10.1111/dmcn.15245)
2. Jin, S.C., Lewis, S.A., Bakhtiari, S. et al. Mutations disrupting neuritogenesis genes confer risk for cerebral palsy. Nature Genetics 52, 1046–1056 (2020). https://doi.org/10.1038/s41588-020-0695-1
3. Pham, R., Mol, B.W., Gecz, J., MacLennan, A.H., MacLennan, S.C., Corbett, M.A., van Eyk, C.L., Webber, D.L., Palmer, L.J. and Berry, J.G., 2020. Definition and diagnosis of cerebral palsy in genetic studies: a systematic review. Developmental Medicine & Child Neurology, 62(9), pp.1024-1030. https://doi.org/10.1111/dmcn.14585
4. van Eyk, C.L., Corbett, M.A., Frank, M.S.B., Webber, D.L., Newman, M., Berry, J.G., Harper, K., Haines, B.P., McMichael, G., Woenig, J.A., MacLennan, A.H. and J.Gecz., 2019. Targeted resequencing identifies genes with recurrent variation in cerebral palsy. Genomic Medicine, 4(1), pp.1-11.  https://doi.org/10.1038/s41525-019-0101-z
5. MacLennan AH, Lewis S, Moreno-De-Luca A, et al. Genetic or Other Causation Should Not Change the Clinical Diagnosis of Cerebral Palsy. Journal of Child Neurology. 2019; 34(8):472-476. doi: 10.1177/0883073819840449.
6. MacLennan AH, Kruer MC, Baynam G, Moreno-De-Luca A, Wilson YA, Zhu C, Wintle RF, Gecz J; members of the International Cerebral Palsy Genomics Consortium. Cerebral palsy and genomics: an international consortium. Developmental Medicine & Child Neurology. 2018; 60(2):209-210. doi: 10.1111/dmcn.13643.