Raquel Rabionet
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Cancer Genomics and Diagnostics, Genomics and Rare Diseases, Hearing, Cochlea, Tinnitus, Genetics, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → Connexin-26 mutations in sporadic and inherited sensorineural deafness(1998)642 cited
- → MicroRNA profiling of Parkinson's disease brains identifies early downregulation of miR-34b/c which modulate mitochondrial function(2011)480 cited
- → Genetic Structure of Europeans: A View from the North–East(2009)432 cited
- → Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus(1999)397 cited
- → High carrier frequency of the 35delG deafness mutation in European populations(2000)389 cited
- → Variants at APOE influence risk of deep and lobar intracerebral hemorrhage(2010)266 cited
- → MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss(2001)241 cited
- → Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene(2000)219 cited
- → Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins(2000)200 cited
- → APOE genotype and extent of bleeding and outcome in lobar intracerebral haemorrhage: a genetic association study(2011)185 cited