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%">Chromosome-scale, haplotype-resolved assembly of human genomes.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient phasing and imputation of low-coverage sequencing data using large reference panels.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project.</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%">Haplotype-resolved diverse human genomes and integrated analysis of structural variation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Identification of Required Host Factors for SARS-CoV-2 Infection in Human Cells.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Towards population-scale long-read sequencing.</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%">Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy.</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%">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%">Determinants of telomere length across human tissues.</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%">Evaluation of the VISAGE Basic Tool for Appearance and Ancestry Prediction Using PowerSeq Chemistry on the MiSeq FGx System.</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 association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease.</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%">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%">Rapid, Paralog-Sensitive CNV Analysis of 2457 Human Genomes Using QuicK-mer2.</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%">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%">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%">What Is Familial Hypercholesterolemia, and Why Does It Matter?</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A multi-task convolutional deep neural network for variant calling in single molecule sequencing.</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%">Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms.</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%">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%">Is Coronary Atherosclerosis One Disease or Many? Setting Realistic Expectations for Precision Medicine.</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%">Exome sequencing reveals novel genetic loci influencing obesity-related traits in Hispanic children.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Fast, scalable prediction of deleterious noncoding variants from functional and population genomic data.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic association studies in cardiovascular diseases: Do we have enough power?</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%">Genetics of coronary artery disease: discovery, biology and clinical translation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide profiling of heritable and de novo STR variations.</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%">Human genetic insights into lipoproteins and risk of cardiometabolic disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The impact of structural variation on human gene expression.</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%">Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Quantifying the regulatory effect size of -acting genetic variation using allelic fold change.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">SVScore: an impact prediction tool for structural variation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Concerted Genetic Function in Blood Traits.</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>