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Author: Braxton D Mitchell

Rankings

  • All-time downloads: 30,648 (rank: 6,122 )
  • Categories:
    • bioinformatics: 32 (rank: 44,457 (tie) )
    • epidemiology: 146 (rank: 30,946 (tie) )
    • genetic and genomic medicine: 3,803 (rank: 861 )
    • genetics: 19,694 (rank: 670 )
    • genomics: 4,985 (rank: 5,175 (tie) )
    • hematology: 698 (rank: 487 (tie) )
    • neuroscience: 1,290 (rank: 20,561 (tie) )

Downloads per author, site-wide

Preprints

Recovery of trait heritability from whole genome sequence data

genetics more details view paper
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    • Site-wide: 696
    • In genetics: 15
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    • Site-wide: 1,534
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Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

genomics more details view paper
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    • Site-wide: 4,719
    • In genomics: 488
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    • Site-wide: 10,255
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A trans-ancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.

genetic and genomic medicine more details view paper
  • Downloaded 2,015 times
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    • Site-wide: 8,809
    • In genetic and genomic medicine: 39
  • Year to date:
    • Site-wide: 1,308
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    • Site-wide: 636

Population sequencing data reveal a compendium of mutational processes in human germline

genetics more details view paper
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    • Site-wide: 14,628
    • In genetics: 668
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Genome-wide Meta-analysis of 158,000 Individuals of European Ancestry Identifies Three Loci Associated with Chronic Back Pain

genomics more details view paper
  • Downloaded 988 times
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    • Site-wide: 25,294
    • In genomics: 2,346
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    • Site-wide: 128,704
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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

genetics more details view paper
  • Downloaded 861 times
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    • Site-wide: 30,806
    • In genetics: 1,416
  • Year to date:
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Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies

genetics more details view paper
  • Downloaded 858 times
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    • Site-wide: 30,945
    • In genetics: 1,420
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    • Site-wide: 125,838
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    • Site-wide: 114,215

Do Candidate Genes Affect the Brain's White Matter Microstructure? Large-Scale Evaluation of 6,165 Diffusion MRI Scans

neuroscience more details view paper
  • Downloaded 858 times
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    • In neuroscience: 4,023
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De novo mutations across 1,465 diverse genomes reveal novel mutational insights and reductions in the Amish founder population.

genetics more details view paper
  • Downloaded 724 times
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    • Site-wide: 39,219
    • In genetics: 1,766
  • Year to date:
    • Site-wide: 102,167
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    • Site-wide: None

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

hematology more details view paper
  • Downloaded 698 times
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    • Site-wide: 41,182
    • In hematology: 34
  • Year to date:
    • Site-wide: 8,778
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Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

genetics more details view paper
  • Downloaded 615 times
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    • Site-wide: 48,478
    • In genetics: 2,164
  • Year to date:
    • Site-wide: 93,851
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Genome Sequencing Unveils a New Regulatory Landscape of Platelet Reactivity

genomics more details view paper
  • Downloaded 601 times
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    • Site-wide: 49,892
    • In genomics: 3,841
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    • Site-wide: 53,493
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Genetic and functional evidence relates a missense variant in B4GALT1 to lower LDL-C and fibrinogen

genetics more details view paper
  • Downloaded 547 times
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    • Site-wide: 56,018
    • In genetics: 2,475
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    • Site-wide: 49,966
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    • Site-wide: 116,683

A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

genetics more details view paper
  • Downloaded 499 times
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    • Site-wide: 62,408
    • In genetics: 2,758
  • Year to date:
    • Site-wide: 23,513
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    • Site-wide: 43,323

Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes: Trans-Omics for Precision Medicine (TOPMed) Program

genetic and genomic medicine more details view paper
  • Downloaded 460 times
  • Download rankings, all-time:
    • Site-wide: 68,186
    • In genetic and genomic medicine: 281
  • Year to date:
    • Site-wide: 24,951
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    • Site-wide: 42,238

White Matter Hyperintensity Quantification in Large-Scale Clinical Acute Ischemic Stroke Cohorts - The MRI-GENIE Study

neuroscience more details view paper
  • Downloaded 432 times
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    • Site-wide: 72,760
    • In neuroscience: 10,746
  • Year to date:
    • Site-wide: 105,281
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    • Site-wide: 32,447

Impact of rare and common genetic variants on diabetes diagnosis by hemoglobin A1c in multi-ancestry cohorts: The Trans-Omics for Precision Medicine Program.

genetics more details view paper
  • Downloaded 412 times
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    • Site-wide: 76,338
    • In genetics: 3,328
  • Year to date:
    • Site-wide: 107,097
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    • Site-wide: 104,140

Genetics of Unexplained Sudden Cardiac Death in Adult Caucasian and African American Individuals Living in the State of Maryland

genetic and genomic medicine more details view paper
  • Downloaded 410 times
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    • Site-wide: 76,603
    • In genetic and genomic medicine: 333
  • Year to date:
    • Site-wide: 66,775
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The Subtype Specificity of Genetic Loci Associated with Stroke in 16,664 cases and 32,792 controls

genetics more details view paper
  • Downloaded 406 times
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    • Site-wide: 77,442
    • In genetics: 3,369
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    • Site-wide: 136,701
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Bidirectional Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of intermediate potential

genetic and genomic medicine more details view paper
  • Downloaded 327 times
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    • Site-wide: 93,329
    • In genetic and genomic medicine: 422
  • Year to date:
    • Site-wide: 17,095
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    • Site-wide: 66,892

A genome-wide association study identifies that the GDF5 and COL27A1 genes are associated with knee pain in UK Biobank (N = 171, 516)

genetics more details view paper
  • Downloaded 315 times
  • Download rankings, all-time:
    • Site-wide: 96,053
    • In genetics: 4,128
  • Year to date:
    • Site-wide: 119,413
  • Since beginning of last month:
    • Site-wide: 33,548

Rare variant enriched identity-by-descent enables the detection of distant relatedness and older divergence between populations

genomics more details view paper
  • Downloaded 302 times
  • Download rankings, all-time:
    • Site-wide: 98,974
    • In genomics: 6,010
  • Year to date:
    • Site-wide: 106,020
  • Since beginning of last month:
    • Site-wide: 126,028

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 290 times
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    • Site-wide: 101,910
    • In genetic and genomic medicine: 488
  • Year to date:
    • Site-wide: 20,205
  • Since beginning of last month:
    • Site-wide: 52,507

Monogenic and Polygenic Contributions to QTc Prolongation in the Population

genetic and genomic medicine more details view paper
  • Downloaded 244 times
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    • Site-wide: 112,985
    • In genetic and genomic medicine: 580
  • Year to date:
    • Site-wide: 25,464
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    • Site-wide: 18,753

Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke

genetics more details view paper
  • Downloaded 198 times
  • Download rankings, all-time:
    • Site-wide: 124,497
    • In genetics: 5,137
  • Year to date:
    • Site-wide: 153,181
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    • Site-wide: 116,547

Parkinson's disease-related motor and non-motor symptoms are not more prevalent in the Lancaster Amish

epidemiology more details view paper
  • Downloaded 146 times
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    • Site-wide: 136,660
    • In epidemiology: 5,675
  • Year to date:
    • Site-wide: 126,921
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    • Site-wide: None

Endophenotype Effect Sizes Provide Evidence Supporting Variant Pathogenicity in Monogenic Disease Susceptibility Genes

genetic and genomic medicine more details view paper
  • Downloaded 57 times
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    • Site-wide: 151,562
    • In genetic and genomic medicine: 907
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    • Site-wide: 105,651
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An Omics Analysis Search and Information System (OASIS) for Enabling Biological Discovery in the Old Order Amish

bioinformatics more details view paper
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    • Site-wide: 153,105
    • In bioinformatics: 11,527
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