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 Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.</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%">A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.</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%">A reference panel of 64,976 haplotypes for genotype imputation.</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%">Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Rare coding variants and X-linked loci associated with age at menarche.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis.</style>