ICPGC News + Activities

Scientific Publications

  1. Jin, S.C., Lewis, S.A., Bakhtiari, S. et al. Mutations disrupting neuritogenesis genes confer risk for cerebral palsyNature Genetics 521046–1056 (2020). https://doi.org/10.1038/s41588-020-0695-1
  2. 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 reviewDevelopmental Medicine & Child Neurology62(9), pp.1024-1030. https://doi.org/10.1111/dmcn.14585
  3. 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. and MacLennan, A.H., 2019. Targeted resequencing identifies genes with recurrent variation in cerebral palsy. Genomic Medicine4(1), pp.1-11. https://doi.org/10.1038/s41525-019-0101-z
  4. 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.
  5. 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 ConsortiumCerebral palsy and genomics: an international consortiumDevelopmental Medicine & Child Neurology. 2018; 60(2):209-210. doi: 10.1111/dmcn.13643.

ICPGC Meetings

2019 Meeting

The next ICPGC meeting will be held in Anaheim, California, USA on the 17th-18th September  2019, hosted by The American Academy of Cerebral Palsy and Developmental Medicine.

For more information and registration details, please visit: https://www.aacpdm.org/meetings/2019/attendee/registration

2018 Meeting

The next ICPGC meeting will be held in the Henan Province, China in April 2018, hosted by The Third Affiliated Hospital of Zhengzhou University and Fudan University.

For more information and registration details, please visit: https://icpgc2018.medmeeting.org/en

2017 Meeting

The inaugural ICPGC meeting was held at Umbrae House in Adelaide, South Australia in March 2017. The meeting was hosted by the Australian Collaborative Cerebral Palsy Research Group, under the leadership of Emeritus Professor Alastair MacLennan and Jozef Gecz. The meeting was sponsored by the Cerebral Palsy Alliance and brought together researchers from all over Australia, China, Canada, Sweden, Turkey, Spain and the United States of America to establish a collaborative research network and discuss the development on an online database dedicated to CP genomics.

ICPGC Research Opportunities

Phenotype Working Group

Develop information models used to describe the clinical phenotype of individuals with CP for use in genomic medicine.

CONTACT: info@icpgc.org

Bioinformatics Working Group

Develop statistical models, pipeline standards, and bioinformatics tools to help the consortium achieve its goals.

CONTACT: info@icpgc.org

CP Commons Working Group

Assist with the direction and development of the CP Commons data management and analysis platform

CONTACT: info@icpgc.org

Functional Validation Working Group

Streamlining functional validation workflows for molecular or biological assay.

CONTACT: info@icpgc.org