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Author: Laura M. Raffield

Rankings

  • All-time downloads: 14,412 (rank: 18,150 )
  • Categories:
    • bioinformatics: 374 (rank: 36,094 (tie) )
    • genetic and genomic medicine: 5,934 (rank: 333 )
    • genetics: 6,144 (rank: 3,528 (tie) )
    • hematology: 866 (rank: 521 (tie) )
    • nephrology: 301 (rank: 1,086 (tie) )
    • psychiatry and clinical psychology: 793 (rank: 2,266 (tie) )

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Preprints

The Polygenic and Monogenic Basis of Blood Traits and Diseases

genetic and genomic medicine more details view paper
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    • In genetic and genomic medicine: 44
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    • Site-wide: 45,277
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Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

genetic and genomic medicine more details view paper
  • Downloaded 1,891 times
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    • Site-wide: 11,293
    • In genetic and genomic medicine: 51
  • Year to date:
    • Site-wide: 2,937
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    • Site-wide: 7,200

The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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  • Downloaded 1,202 times
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    • Site-wide: 22,424
    • In genetics: 965
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A Fully-Adjusted Two-Stage Procedure for Rank Normalization in Genetic Association Studies

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    • Site-wide: 28,650
    • In genetics: 1,236
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Genetic analysis of mitochondrial DNA copy number and associated traits identifies loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation, and reveals a causal association of mitochondrial function with mortality

genetics more details view paper
  • Downloaded 922 times
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    • Site-wide: 33,344
    • In genetics: 1,435
  • Year to date:
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    • Site-wide: 11,282

Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program

hematology more details view paper
  • Downloaded 866 times
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    • Site-wide: 36,488
    • In hematology: 34
  • Year to date:
    • Site-wide: 60,924
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    • Site-wide: 25,471

Clonal hematopoiesis is driven by aberrant activation of TCL1A

genetics more details view paper
  • Downloaded 855 times
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    • Site-wide: 37,177
    • In genetics: 1,599
  • Year to date:
    • Site-wide: 374
  • Since beginning of last month:
    • Site-wide: 419

Common genetic risk variants identified in the SPARK cohort implicate DDHD2 as a novel autism risk gene

psychiatry and clinical psychology more details view paper
  • Downloaded 793 times
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    • Site-wide: 41,484
    • In psychiatry and clinical psychology: 161
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    • Site-wide: 39,504

Polygenic Risk Prediction using Gradient Boosted Trees Captures Non-Linear Genetic Effects and Allele Interactions in Complex Phenotypes

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  • Downloaded 607 times
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    • Site-wide: 59,781
    • In genetic and genomic medicine: 300
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    • Site-wide: 7,380
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    • Site-wide: 10,475

Bidirectional Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of intermediate potential

genetic and genomic medicine more details view paper
  • Downloaded 518 times
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    • Site-wide: 72,597
    • In genetic and genomic medicine: 368
  • Year to date:
    • Site-wide: 22,502
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    • Site-wide: 28,715

From GWAS Variant to Function: a Study of ~148,000 Variants for Blood Cell Traits.

genetics more details view paper
  • Downloaded 439 times
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    • Site-wide: 87,249
    • In genetics: 3,597
  • Year to date:
    • Site-wide: 57,460
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    • Site-wide: 77,049

Whole Genome Sequence Association Analysis of Fasting Glucose and Fasting Insulin Levels in Diverse Cohorts from the NHLBI TOPMed Program

genetic and genomic medicine more details view paper
  • Downloaded 383 times
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    • Site-wide: 99,262
    • In genetic and genomic medicine: 543
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    • Site-wide: 30,029
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    • Site-wide: 76,678

CUE: CpG impUtation Ensemble for DNA Methylation Levels Across the Human Methylation450 (HM450) and EPIC (HM850) BeadChip Platforms

bioinformatics more details view paper
  • Downloaded 374 times
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    • Site-wide: 101,467
    • In bioinformatics: 8,667
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  • Since beginning of last month:
    • Site-wide: 133,490

A large-scale transcriptome-wide association study (TWAS) of ten blood cell phenotypes reveals complexities of TWAS fine-mapping

genetics more details view paper
  • Downloaded 372 times
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    • Site-wide: 102,045
    • In genetics: 4,165
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    • Site-wide: 38,561
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    • Site-wide: 48,379

Analyses of Biomarker Traits in Diverse UK Biobank Participants Identify Associations Missed by European-centric Analysis Strategies

genetics more details view paper
  • Downloaded 370 times
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    • Site-wide: 102,317
    • In genetics: 4,193
  • Year to date:
    • Site-wide: None
  • Since beginning of last month:
    • Site-wide: 107,853

Assay-related Differences in SuPAR Levels: Implications for Measurement and Data Interpretation

nephrology more details view paper
  • Downloaded 301 times
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    • Site-wide: 120,109
    • In nephrology: 105
  • Year to date:
    • Site-wide: 57,469
  • Since beginning of last month:
    • Site-wide: 36,713

eSCAN: Scan Regulatory Regions for Aggregate Association Testing using Whole Genome Sequencing Data

genetics more details view paper
  • Downloaded 264 times
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    • Site-wide: 130,057
    • In genetics: 5,167
  • Year to date:
    • Site-wide: 42,771
  • Since beginning of last month:
    • Site-wide: 92,710

Super interactive promoters provide insight into cell type-specific regulatory networks in blood lineage cell types

genetics more details view paper
  • Downloaded 263 times
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    • Site-wide: 130,342
    • In genetics: 5,172
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Presence and Transmission of Mitochondrial Heteroplasmic Mutations in Human Populations of European and African Ancestry

genetics more details view paper
  • Downloaded 228 times
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    • In genetics: 5,491
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Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits.

genetics more details view paper
  • Downloaded 208 times
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    • Site-wide: 144,763
    • In genetics: 5,638
  • Year to date:
    • Site-wide: 67,954
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Genetic Underpinnings of Regional Adiposity Distribution in African Americans: Assessments from the Jackson Heart Study

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  • Downloaded 197 times
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    • Site-wide: 147,557
    • In genetic and genomic medicine: 923
  • Year to date:
    • Site-wide: 87,439
  • Since beginning of last month:
    • Site-wide: 112,824

Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program

genetic and genomic medicine more details view paper
  • Downloaded 173 times
  • Download rankings, all-time:
    • Site-wide: 153,106
    • In genetic and genomic medicine: 984
  • Year to date:
    • Site-wide: 1,268
  • Since beginning of last month:
    • Site-wide: 4,378

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