Drupal-Biblio17<style face="normal" font="default" size="100%">Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Rare and low-frequency coding variants alter human adult height.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide association study identifies 74 loci associated with educational attainment.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Pharmacogenetics driving personalized medicine: analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Directional dominance on stature and cognition in diverse human populations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The p.Cys169Tyr variant of connexin 26 is not a polymorphism.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">PSIP1/LEDGF: a new gene likely involved in sensorineural progressive hearing loss.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Consanguinity and hereditary hearing loss in Qatar.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Expression and replication studies to identify new candidate genes involved in normal hearing function.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic landscape of populations along the Silk Road: admixture and migration patterns.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Salt-inducible kinase 3, SIK3, is a new gene associated with hearing.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Evidence of inbreeding depression on human height.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways.</style>