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Author: John Danesh

  • ORCiD: http://orcid.org/0000-0003-1158-6791
  • Most recently observed institution: MRC/BHF Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge CB1 8RN, UK.

Rankings

  • All-time downloads: 56,744 (rank: 629 out of 380,214)
  • Categories:
    • epidemiology: 600 (rank: 2,680 (tie) out of 9,542)
    • genetics: 23,119 (rank: 248 out of 35,084)
    • genomics: 33,025 (rank: 226 out of 40,563)

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Preprints

Analysis of protein-coding genetic variation in 60,706 humans

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Consequences Of Natural Perturbations In The Human Plasma Proteome

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Genomic risk prediction of coronary artery disease in nearly 500,000 adults: implications for early screening and primary prevention

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

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

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A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

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

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Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations

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

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Genomic evaluation of circulating proteins for drug target characterisation and precision medicine

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Learning polygenic scores for human blood cell traits

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Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases

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

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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

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Genetic effects on promoter usage are highly context-specific and contribute to complex traits

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Use of polygenic risk scores and other molecular markers to enhance cardiovascular risk prediction: Prospective cohort study and modelling analysis

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Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

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Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke

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Metabolomic consequences of genetic inhibition of PCSK9 compared with statin treatment

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

genetics more details view paper
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Genetic Analyses of Blood Cell Structure for Biological and Pharmacological Inference

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Interleukin-6 Receptor Signalling and Abdominal Aortic Aneurysm Growth Rates

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Lipoprotein Signatures of Cholesteryl Ester Transfer Protein and HMG-CoA Reductase Inhibition

genetics more details view paper
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Heterozygous ATP-binding Cassette Transporter G5 Gene Deficiency and Risk of Coronary Artery Disease

genetics more details view paper
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The influence of rare variants in circulating metabolic biomarkers

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