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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 65,351 bioRxiv papers from 289,483 authors.

Author: James F Wilson

  • Most recently observed institution: MRC Human Genetics Unit, Institute of Genetic and Molecular Medicine, University of Edinburgh, Western General Hospital

Rankings

  • All-time downloads: 51,182 (rank: 271 out of 289,484)
  • Categories:
    • biochemistry: 333 (rank: 5,527 (tie) out of 11,210)
    • epidemiology: 115 (rank: 8,552 (tie) out of 9,549)
    • genetics: 44,669 (rank: 68 out of 28,760)
    • genomics: 6,065 (rank: 1,981 out of 32,918)

Downloads per author, site-wide

Preprints

The genetic structure of the world's first farmers

genetics more details view paper
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A reference panel of 64,976 haplotypes for genotype imputation

genetics more details view paper
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Beyond power: Multivariate discovery, replication, and interpretation of pleiotropic loci using summary association statistics

genetics more details view paper
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Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

genetics more details view paper
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Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

genetics more details view paper
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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

genetics more details view paper
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Genomic underpinnings of lifespan allow prediction and reveal basis in modern risks

genomics more details view paper
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Genome-wide association analyses in >119,000 individuals identifies thirteen morningness and two sleep duration loci

genetics more details view paper
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New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries

genomics more details view paper
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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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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

genetics more details view paper
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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

genetics more details view paper
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Narrow-sense heritability estimation of complex traits using identity-by-descent information.

genetics more details view paper
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Proteome-by-phenome Mendelian Randomisation detects 38 proteins with causal roles in human diseases and traits

genomics more details view paper
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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

genomics more details view paper
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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
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Discovering patterns of pleiotropy in genome-wide association studies

genetics more details view paper
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Novel Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk Of Coronary Artery Disease

genomics more details view paper
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Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

genetics more details view paper
  • Downloaded 363 times
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    • In genetics: 1,869 out of 3,698
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Global variability of the human IgG glycome

biochemistry more details view paper
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Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions

genomics more details view paper
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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

genetics more details view paper
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    • In genetics: 2,191 out of 3,698
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Using genetics to disentangle the complex relationship between food choices and health status

genetics more details view paper
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    • In genetics: 2,489 out of 3,698
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Associations of ‘Relative corticosterone deficiency’ with genetic variation in CYP17A1 and metabolic syndrome features

epidemiology more details view paper
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