Drupal-Biblio17<style face="normal" font="default" size="100%">Association of Genetic Variation With Cirrhosis: A Multi-Trait Genome-Wide Association and Gene-Environment Interaction Study.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic Predictor to Identify Individuals With High Lipoprotein(a) Concentrations.</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%">Cell type-specific genetic regulation of gene expression across human tissues.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A common variant in PNPLA3 is associated with age at diagnosis of NAFLD in patients from a multi-ethnic biobank.</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%">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%">Heterozygous Gene Deficiency and Risk of Coronary Artery Disease.</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%">Lung Function in African American Children with Asthma Is Associated with Novel Regulatory Variants of the KIT Ligand and Gene-By-Air-Pollution Interaction.</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%">Neurophysiological and Genetic Findings in Patients With Juvenile Myoclonic Epilepsy.</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%">The Parkinson's Disease Genome-Wide Association Study Locus Browser.</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%">Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data.</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%">Transcriptomic signatures across human tissues identify functional rare genetic variation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Type 2 and interferon inflammation regulate SARS-CoV-2 entry factor expression in the airway epithelium.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Type 2 and interferon inflammation strongly regulate SARS-CoV-2 related gene expression in the airway epithelium.</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%">A variant-centric perspective on geographic patterns of human allele frequency variation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ancestral Admixture Is the Main Determinant of Global Biodiversity in Fission Yeast.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic architecture of laterality defects revealed by whole exome sequencing.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide patterns of transposon proliferation in an evolutionary young hybrid fish.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Insights into genetics, human biology and disease gleaned from family based genomic studies.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mendelian Gene Discovery: Fast and Furious with No End in Sight.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Monogenic causes of chronic kidney disease in adults.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Redefining the Etiologic Landscape of Cerebellar Malformations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Accurate detection of complex structural variations using single-molecule sequencing.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Whole-Genome Sequencing of Pharmacogenetic Drug Response in Racially Diverse Children with Asthma.</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%">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>