<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>

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<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>

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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%">Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium.</style>

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<style face="normal" font="default" size="100%">Genetic Predictor to Identify Individuals With High Lipoprotein(a) Concentrations.</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%">Towards population-scale long-read sequencing.</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%">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%">Community-based recruitment and exome sequencing indicates high diagnostic yield in adults with intellectual disability.</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%">Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.</style>

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<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>

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<style face="normal" font="default" size="100%">Forensic evaluation of the Asia Pacific ancestry-informative MAPlex assay.</style>

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

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<style face="normal" font="default" size="100%">A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.</style>

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<style face="normal" font="default" size="100%">Next Generation Sequencing of 134 Children with Autism Spectrum Disorder and Regression.</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%">RNA Identification of PRIME Cells Predicting Rheumatoid Arthritis Flares.</style>

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<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>

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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%">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%">Ancestral Admixture Is the Main Determinant of Global Biodiversity in Fission Yeast.</style>

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<style face="normal" font="default" size="100%">Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel.</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%">Differential NOVA2-Mediated Splicing in Excitatory and Inhibitory Neurons Regulates Cortical Development and Cerebellar Function.</style>

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<style face="normal" font="default" size="100%">EphrinB2-EphB4-RASA1 Signaling in Human Cerebrovascular Development and Disease.</style>

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<style face="normal" font="default" size="100%">Evaluation of the detection of GBA missense mutations and other variants using the Oxford Nanopore MinION.</style>

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<style face="normal" font="default" size="100%">Genetic architecture of laterality defects revealed by whole exome sequencing.</style>

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<style face="normal" font="default" size="100%">Genetic regulatory variation in populations informs transcriptome analysis in rare disease.</style>

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<style face="normal" font="default" size="100%">Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes.</style>

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<style face="normal" font="default" size="100%">Genome-wide patterns of transposon proliferation in an evolutionary young hybrid fish.</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%">Monogenic causes of chronic kidney disease in adults.</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%">Pathogenic Abnormal Splicing Due to Intronic Deletions that Induce Biophysical Space Constraint for Spliceosome Assembly.</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%">Structural variant calling: the long and the short of it.</style>

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<style face="normal" font="default" size="100%">svtools: population-scale analysis of structural variation.</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%">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%">Cell type-specific CLIP reveals that NOVA regulates cytoskeleton interactions in motoneurons.</style>

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<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>

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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%">Differential 3' Processing of Specific Transcripts Expands Regulatory and Protein Diversity Across Neuronal Cell Types.</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%">cTag-PAPERCLIP Reveals Alternative Polyadenylation Promotes Cell-Type Specific Protein Diversity and Shifts Araf Isoforms with Microglia Activation.</style>

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<style face="normal" font="default" size="100%">Exome sequencing reveals novel genetic loci influencing obesity-related traits in Hispanic children.</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%">The impact of structural variation on human gene expression.</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>