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Author: Robert A Scott

  • Most recently observed institution: Glaxosmithkline, Gunnels Wood Road, Stevenage, Hertfordshire, SG1 2NY, UK.

Rankings

  • All-time downloads: 34,389 (rank: 798 out of 336,715)
  • Categories:
    • genetics: 16,984 (rank: 505 out of 32,498)
    • genomics: 17,405 (rank: 457 out of 36,985)

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Preprints

Whole exome sequencing and characterization of coding variation in 49,960 individuals in the UK Biobank

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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries

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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank

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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

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A Comprehensive Reanalysis Of Publicly Available GWAS Datasets Reveals An X Chromosome Rare Regulatory Variant Associated With High Risk For Type 2 Diabetes.

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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

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Cross-platform genetic discovery of small molecule products of metabolism and application to clinical outcomes

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Causal Analyses, Statistical Efficiency And Phenotypic Precision Through Recall-By-Genotype Study Design

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A robust example of collider bias in a genetic association study

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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Genome-wide scan and fine-mapping of rare nonsynonymous associations implicates intracellular lipolysis genes in fat distribution and cardio-metabolic risk

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

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Regional fat depot masses are influenced by protein-coding gene variants

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