Author: Christian Benner

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Preprints

Computationally efficient whole genome regression for quantitative and binary traits

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  • Site-wide: 848
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  • Site-wide: 891

Interrogation of human hematopoiesis at single-cell and single-variant resolution

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  • Site-wide: 3,810
  • In genetics: 159
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  • Site-wide: 53,260
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  • Site-wide: 43,665

Functionally-informed fine-mapping and polygenic localization of complex trait heritability

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  • Site-wide: 5,676
  • In genetics: 266
• Year to date:
  • Site-wide: 7,997
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An Effector Index to Predict Causal Genes at GWAS Loci

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  • Site-wide: 7,503
  • In bioinformatics: 899
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  • Site-wide: 6,953
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  • Site-wide: 13,017

Refining fine-mapping: effect sizes and regional heritability

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  • Site-wide: 11,953
  • In genetics: 580
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  • Site-wide: 33,779
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  • Site-wide: 25,682

FINEMAP: Efficient variable selection using summary data from genome-wide association studies

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  • Site-wide: 14,963
  • In genetics: 741
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  • Site-wide: 100,492
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  • Site-wide: 84,906

An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease

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  • Site-wide: 36,822
  • In genetics: 1,756
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  • Site-wide: 19,216
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biMM: Efficient estimation of genetic variances and covariances for cohorts with high-dimensional phenotype measurements

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  • Site-wide: 48,482
  • In genetics: 2,276
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Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

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  • Site-wide: 78,991
  • In genetic and genomic medicine: 279
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  • Site-wide: 14,521

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

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  • Site-wide: 86,571
  • In genomics: 5,512
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  • Site-wide: 96,742
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  • Site-wide: 116,018