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Author: Patrick Sulem

Rankings

  • All-time downloads: 16,211 (rank: 4,399 (tie) out of 423,760)
  • Categories:
    • bioinformatics: 559 (rank: 18,789 (tie) out of 35,792)
    • genetics: 12,602 (rank: 997 out of 37,727)
    • genomics: 3,050 (rank: 6,734 (tie) out of 44,207)

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Preprints

Long read sequencing of 1,817 Icelanders provides insight into the role of structural variants in human disease

genetics more details view paper
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    • In genetics: 100 out of 4,991
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    • Site-wide: 1,647 out of 100,173
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    • Site-wide: None out of 100,173

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

genetics more details view paper
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    • In genetics: 129 out of 4,991
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    • Site-wide: 12,571 out of 100,173
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    • Site-wide: None out of 100,173

Estimating heritability without environmental bias

genetics more details view paper
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    • In genetics: 212 out of 4,991
  • Year to date:
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    • Site-wide: None out of 100,173

Recurrence of de novo mutations in families

genomics more details view paper
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    • In genomics: 736 out of 6,213
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Genetic predisposition to mosaic Y chromosome loss in blood is associated with genomic instability in other tissues and susceptibility to non-haematological cancers

genetics more details view paper
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    • In genetics: 578 out of 4,991
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    • Site-wide: 33,162 out of 100,173
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    • Site-wide: None out of 100,173

Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

genomics more details view paper
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    • In genomics: 1,391 out of 6,213
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CCR5-del32 is not deleterious in the homozygous state in humans

genetics more details view paper
  • Downloaded 597 times
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    • In genetics: 1,643 out of 4,991
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PopDel identifies medium-size deletions jointly in tens of thousands of genomes

bioinformatics more details view paper
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    • Site-wide: 5,396 out of 100,173

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

genetics more details view paper
  • Downloaded 539 times
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    • Site-wide: 30,838 out of 100,173
    • In genetics: 1,830 out of 4,991
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    • Site-wide: 24,567 out of 100,173
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A rare missense mutation in MYH6 confers high risk of coarctation of the aorta

genetics more details view paper
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    • In genetics: 2,143 out of 4,991
  • Year to date:
    • Site-wide: 83,052 out of 100,173
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    • Site-wide: None out of 100,173

Mutations in RPL3L and MYZAP increase risk of atrial fibrillation

genetics more details view paper
  • Downloaded 406 times
  • Download rankings, all-time:
    • Site-wide: 43,070 out of 100,173
    • In genetics: 2,466 out of 4,991
  • Year to date:
    • Site-wide: 82,137 out of 100,173
  • Since beginning of last month:
    • Site-wide: None out of 100,173

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