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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 62,666 bioRxiv papers from 278,077 authors.

Author: Michael Boehnke

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  • All-time downloads: 66,591 (rank: 174 out of 278,077)
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    • bioinformatics: 2,110 (rank: 3,474 (tie) out of 24,398)
    • genetics: 28,592 (rank: 135 out of 27,703)
    • genomics: 35,889 (rank: 143 out of 31,942)

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Preprints

A powerful subset-based gene-set analysis method identifies novel associations and improves interpretation in UK Biobank

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Analysis of protein-coding genetic variation in 60,706 humans

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Genomewide association study identifies 30 loci associated with bipolar disorder

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A reference panel of 64,976 haplotypes for genotype imputation

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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Genome-wide association study of 1 million people identifies 111 loci for atrial fibrillation

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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Clustering of Type 2 Diabetes Genetic Loci by Multi-Trait Associations Identifies Disease Mechanisms and Subtypes

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Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

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Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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emeraLD: Rapid Linkage Disequilibrium Estimation with Massive Data Sets

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Association Analysis and Meta-Analysis of Multi-allelic Variants for Large Scale Sequence Data

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Exome sequencing identifies high-impact trait-associated alleles enriched in Finns

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Narrow-sense heritability estimation of complex traits using identity-by-descent information.

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Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders

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Influence of genetic variants on gene expression in human pancreatic islets – implications for type 2 diabetes

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Identification of type 2 diabetes loci in 433,540 East Asian individuals

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Multi-SKAT: General framework to test multiple phenotype associations of rare variants

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Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

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Imputation aware tag SNP selection to improve power for multi-ethnic association studies

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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Sequencing and Imputation in GWAS: Cost-Effective Strategies to Increase Power and Genomic Coverage Across Diverse Populations

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Exome chip meta-analysis elucidates the genetic architecture of rare coding variants in smoking and drinking behavior

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Interactions between genetic variation and cellular environment in skeletal muscle gene expression

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Complement component 4 genes contribute sex-specific vulnerability in diverse illnesses

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Integrating Comprehensive Functional Annotations to Boost Power and Accuracy in Gene-Based Association Analysis

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Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

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Subset-Based Analysis using Gene-Environment Interactions for Discovery of Genetic Associations across Multiple Studies or Phenotypes

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Proper Conditional Analysis in the Presence of Missing Data Identified Novel Independently Associated Low Frequency Variants in Nicotine Dependence Genes

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