Gilfillan, Gregor D.
Oslo University Hospital · Norwegian Sequencing Centre
3 papers on CoChatORCID 0000-0001-8116-0134
Most cited papers
- Verified
Endogenous RNAs modulate microRNA sorting to exosomes and transfer to acceptor cells.
Squadrito, M. L., Baer, C., Burdet, F., Maderna, C., Gilfillan, G. D., Lyle, R., Ibberson, M., & De Palma, M. (2014) · Cell Reports
Extracellular vesicles in diseaseMicroRNA in disease regulation
Cited by 604
- Verified
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome
Gilfillan, G. D., Selmer, K. K., Roxrud, I., Smith, R., Kyllerman, M., Eiklid, K., Kroken, M., Mattingsdal, M., Egeland, T., Stenmark, H., et al. (2008) · The American Journal of Human Genetics
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 232
- Verified
Genome-wide Ancestry Patterns in Rapanui Suggest Pre-European Admixture with Native Americans
Moreno-Mayar, J. V., Rasmussen, S., Seguin-Orlando, A., Rasmussen, M., Liang, M., Flåm, S. T., Lie, B. A., Gilfillan, G. D., Nielsen, R., Thorsby, E., et al. (2014) · Current Biology
Forensic and Genetic ResearchPacific and Southeast Asian Studies
Cited by 74
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