<style face="normal" font="default" size="100%">Association of structural variation with cardiometabolic traits in Finns.</style>

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<style face="normal" font="default" size="100%">Association of structural variation with cardiometabolic traits in Finns.</style>

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<style face="normal" font="default" size="100%">Efficient phasing and imputation of low-coverage sequencing data using large reference panels.</style>

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<style face="normal" font="default" size="100%">Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project.</style>

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<style face="normal" font="default" size="100%">Germline mutation in : a heterogeneous, multi-systemic developmental disorder characterized by transcriptional dysregulation.</style>

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<style face="normal" font="default" size="100%">Haplotype-resolved diverse human genomes and integrated analysis of structural variation.</style>

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<style face="normal" font="default" size="100%">Identification of Required Host Factors for SARS-CoV-2 Infection in Human Cells.</style>

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<style face="normal" font="default" size="100%">Optimized sample selection for cost-efficient long-read population sequencing.</style>

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<style face="normal" font="default" size="100%">Phylogenetic history of patrilineages rare in northern and eastern Europe from large-scale re-sequencing of human Y-chromosomes.</style>

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<style face="normal" font="default" size="100%">SVEP1 is a human coronary artery disease locus that promotes atherosclerosis.</style>

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<style face="normal" font="default" size="100%">Transethnic Transferability of a Genome-Wide Polygenic Score for Coronary Artery Disease.</style>

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<style face="normal" font="default" size="100%">Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease.</style>

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<style face="normal" font="default" size="100%">Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy.</style>

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<style face="normal" font="default" size="100%">Cell type-specific genetic regulation of gene expression across human tissues.</style>

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<style face="normal" font="default" size="100%">Combining Imaging and Genetics to Predict Recurrence of Anticoagulation-Associated Intracerebral Hemorrhage.</style>

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<style face="normal" font="default" size="100%">Copy number variants and fixed duplications among 198 rhesus macaques (Macaca mulatta).</style>

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<style face="normal" font="default" size="100%">Determinants of telomere length across human tissues.</style>

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<style face="normal" font="default" size="100%">Development and validation of the VISAGE AmpliSeq basic tool to predict appearance and ancestry from DNA.</style>

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<style face="normal" font="default" size="100%">Genetic diagnoses in epilepsy: The impact of dynamic exome analysis in a pediatric cohort.</style>

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<style face="normal" font="default" size="100%">Genetics of schizophrenia in the South African Xhosa.</style>

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<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>

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<style face="normal" font="default" size="100%">Genome-Wide Polygenic Score, Clinical Risk Factors, and Long-Term Trajectories of Coronary Artery Disease.</style>

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<style face="normal" font="default" size="100%">Heterozygous Gene Deficiency and Risk of Coronary Artery Disease.</style>

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<style face="normal" font="default" size="100%">The impact of sex on gene expression across human tissues.</style>

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<style face="normal" font="default" size="100%">Inherited causes of clonal haematopoiesis in 97,691 whole genomes.</style>

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<style face="normal" font="default" size="100%">Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.</style>

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<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>

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<style face="normal" font="default" size="100%">Major Impacts of Widespread Structural Variation on Gene Expression and Crop Improvement in Tomato.</style>

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<style face="normal" font="default" size="100%">Mapping and characterization of structural variation in 17,795 human genomes.</style>

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<style face="normal" font="default" size="100%">The Parkinson's Disease Genome-Wide Association Study Locus Browser.</style>

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<style face="normal" font="default" size="100%">Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases.</style>

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<style face="normal" font="default" size="100%">RNA Identification of PRIME Cells Predicting Rheumatoid Arthritis Flares.</style>

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<style face="normal" font="default" size="100%">Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data.</style>

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<style face="normal" font="default" size="100%">A structural variation reference for medical and population genetics.</style>

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<style face="normal" font="default" size="100%">Transcriptomic signatures across human tissues identify functional rare genetic variation.</style>

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<style face="normal" font="default" size="100%">Type 2 and interferon inflammation regulate SARS-CoV-2 entry factor expression in the airway epithelium.</style>

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<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>

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<style face="normal" font="default" size="100%">Validation of a Genome-Wide Polygenic Score for Coronary Artery Disease in South Asians.</style>

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<style face="normal" font="default" size="100%">A variant-centric perspective on geographic patterns of human allele frequency variation.</style>

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<style face="normal" font="default" size="100%">Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging.</style>

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<style face="normal" font="default" size="100%">Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome.</style>

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<style face="normal" font="default" size="100%">Bi-allelic GOT2 Mutations Cause a Treatable Malate-Aspartate Shuttle-Related Encephalopathy.</style>

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<style face="normal" font="default" size="100%">Drug-Resistant Juvenile Myoclonic Epilepsy: Misdiagnosis of Progressive Myoclonus Epilepsy.</style>

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<style face="normal" font="default" size="100%">Identification and Validation of Hematoma Volume Cutoffs in Spontaneous, Supratentorial Deep Intracerebral Hemorrhage.</style>

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<style face="normal" font="default" size="100%">Insights into genetics, human biology and disease gleaned from family based genomic studies.</style>

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<style face="normal" font="default" size="100%">MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement.</style>

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<style face="normal" font="default" size="100%">Novel homozygous ENPP1 mutation causes generalized arterial calcifications of infancy, thrombocytopenia, and cardiovascular and central nervous system syndrome.</style>

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<style face="normal" font="default" size="100%">The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy.</style>

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<style face="normal" font="default" size="100%">RaGOO: fast and accurate reference-guided scaffolding of draft genomes.</style>

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<style face="normal" font="default" size="100%">Redefining the Etiologic Landscape of Cerebellar Malformations.</style>

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<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>

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<style face="normal" font="default" size="100%">Accurate detection of complex structural variations using single-molecule sequencing.</style>

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<style face="normal" font="default" size="100%">Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease.</style>

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<style face="normal" font="default" size="100%">Cardioembolic Stroke Risk and Recovery After Anticoagulation-Related Intracerebral Hemorrhage.</style>

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<style face="normal" font="default" size="100%">Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers.</style>

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<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>

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<style face="normal" font="default" size="100%">Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.</style>

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<style face="normal" font="default" size="100%">Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.</style>

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<style face="normal" font="default" size="100%">Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk.</style>

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<style face="normal" font="default" size="100%">Whole-Genome Sequencing of Pharmacogenetic Drug Response in Racially Diverse Children with Asthma.</style>

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<style face="normal" font="default" size="100%">ANGPTL3 Deficiency and Protection Against Coronary Artery Disease.</style>

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<style face="normal" font="default" size="100%">Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans.</style>

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<style face="normal" font="default" size="100%">Genomic Patterns of De Novo Mutation in Simplex Autism.</style>

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<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>

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<style face="normal" font="default" size="100%">Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits.</style>

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<style face="normal" font="default" size="100%">Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation.</style>

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<style face="normal" font="default" size="100%">Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms.</style>

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<style face="normal" font="default" size="100%">Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease.</style>

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<style face="normal" font="default" size="100%">Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.</style>