Export 23 results:Autore [ Titolo] Tipo Anno
Filtri: Autore è Girotto, Giorgia [Clear All Filters]
Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar. Hum Hered 2015;79(1):14-9..
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss. Eur J Hum Genet 2019;27(1):70-79..
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Hypertension 2017;.
The p.Cys169Tyr variant of connexin 26 is not a polymorphism. Hum Mol Genet 2015;24(9):2641-8..
Pharmacogenetics driving personalized medicine: analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations. J Transl Med 2016;14:22..
PSIP1/LEDGF: a new gene likely involved in sensorineural progressive hearing loss. Sci Rep 2015;5:18568..
Rare and low-frequency coding variants alter human adult height. Nature 2017;542(7640):186-190..
Salt-inducible kinase 3, SIK3, is a new gene associated with hearing. Hum Mol Genet 2014;23(23):6407-18..