Drupal-Biblio17<style face="normal" font="default" size="100%">Association of structural variation with cardiometabolic traits in Finns.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Haplotype-resolved diverse human genomes and integrated analysis of structural variation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Association of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Combining Imaging and Genetics to Predict Recurrence of Anticoagulation-Associated Intracerebral Hemorrhage.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Community-based recruitment and exome sequencing indicates high diagnostic yield in adults with intellectual disability.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Copy number variants and fixed duplications among 198 rhesus macaques (Macaca mulatta).</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic diagnoses in epilepsy: The impact of dynamic exome analysis in a pediatric cohort.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetics of schizophrenia in the South African Xhosa.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-Wide Polygenic Score, Clinical Risk Factors, and Long-Term Trajectories of Coronary Artery Disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The GTEx Consortium atlas of genetic regulatory effects across human tissues.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The impact of sex on gene expression across human tissues.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Inherited causes of clonal haematopoiesis in 97,691 whole genomes.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mapping and characterization of structural variation in 17,795 human genomes.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Next Generation Sequencing of 134 Children with Autism Spectrum Disorder and Regression.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary Statistics.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">RNA Identification of PRIME Cells Predicting Rheumatoid Arthritis Flares.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Serum sphingolipids and incident diabetes in a US population with high diabetes burden: the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A structural variation reference for medical and population genetics.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Titin Truncating Variants in Adults Without Known Congestive Heart Failure.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Validation of a Genome-Wide Polygenic Score for Coronary Artery Disease in South Asians.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic variants in microRNA genes and targets associated with cardiovascular disease risk factors in the African-American population.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">ANGPTL3 Deficiency and Protection Against Coronary Artery Disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">cTag-PAPERCLIP Reveals Alternative Polyadenylation Promotes Cell-Type Specific Protein Diversity and Shifts Araf Isoforms with Microglia Activation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic effects on gene expression across human tissues.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genomic Patterns of De Novo Mutation in Simplex Autism.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Polygenic Risk Score Identifies Subgroup With Higher Burden of Atherosclerosis and Greater Relative Benefit From Statin Therapy in the Primary Prevention Setting.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.</style>