<style face="normal" font="default" size="100%">Accurate, scalable cohort variant calls using DeepVariant and GLnexus.</style>

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<style face="normal" font="default" size="100%">Accurate, scalable cohort variant calls using DeepVariant and GLnexus.</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%">Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese.</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%">SVEP1 is a human coronary artery disease locus that promotes atherosclerosis.</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%">dbMTS: A comprehensive database of putative human microRNA target site SNVs and their functional predictions.</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%">Next Generation Sequencing of 134 Children with Autism Spectrum Disorder and Regression.</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%">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%">Biallelic and De Novo Variants in DONSON Reveal a Clinical Spectrum of Cell Cycle-opathies with Microcephaly, Dwarfism and Skeletal Abnormalities.</style>

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<style face="normal" font="default" size="100%">Capitalizing on Insights from Human Genetics to Identify Novel Therapeutic Targets for Coronary Artery Disease.</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%">Genetic architecture of laterality defects revealed by whole exome sequencing.</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%">Cell type-specific CLIP reveals that NOVA regulates cytoskeleton interactions in motoneurons.</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%">Genetic variants in microRNA genes and targets associated with cardiovascular disease risk factors in the African-American population.</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%">Genome-wide profiling of heritable and de novo STR variations.</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>