Buysse, Karen
Ghent University Hospital
2 papers on CoChat
Most cited papers
- Verified
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes
Mefford, H. C., Sharp, A. J., Baker, C., Itsara, A., Jiang, Z., Buysse, K., Huang, S., Maloney, V. K., Crolla, J. A., Baralle, D., et al. (2008) · New England Journal of Medicine
Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms
Cited by 804
- Verified
Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies
Mefford, H. C., Muhle, H., Ostertag, P., von Spiczak, S., Buysse, K., Baker, C., Franke, A., Malafosse, A., Genton, P., Thomas, P., et al. (2010) · PLoS Genetics
Genomic variations and chromosomal abnormalitiesEpilepsy research and treatment
Cited by 474
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