Author: Reedik Mägi

ORCiD: http://orcid.org/0000-0002-2964-6011
Most recently observed institution: Estonian Genome Center, University of Tartu, Tartu, Estonia, Institute of Molecular and Cell Biology, University of Tartu

Rankings

All-time downloads: 36,023 (rank: 3,310 out of 510,946)
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- developmental biology: 495 (rank: 7,677 (tie) out of 17,427)
- epidemiology: 927 (rank: 7,447 (tie) out of 23,897)
- genetic and genomic medicine: 196 (rank: 4,739 (tie) out of 6,821)
- genetics: 25,969 (rank: 225 out of 38,712)
- genomics: 7,500 (rank: 2,441 out of 45,704)
- pharmacology and toxicology: 936 (rank: 936 (tie) out of 6,657)

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Preprints

Genome-wide association analysis of lifetime cannabis use (N=184,765) identifies new risk loci, genetic overlap with mental health, and a causal influence of schizophrenia on cannabis use

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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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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

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

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

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

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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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Lifelong genetically lowered sclerostin and risk of cardiovascular disease.

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The genetic architecture of sporadic and recurrent miscarriage

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Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions

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Causal relationships between obesity and the leading causes of death in women and men

epidemiology more details view paper

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GWAS identifies novel risk locus for erectile dysfunction and implicates hypothalamic neurobiology and diabetes in etiology

genomics more details view paper

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Personalized Risk Prediction for Type 2 Diabetes: the Potential of Genetic Risk Scores

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Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

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Endometrial receptivity revisited: endometrial transcriptome adjusted for tissue cellular heterogeneity

genomics more details view paper

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GWAS meta-analysis highlights the hypothalamic-pituitary-gonadal axis (HPG axis) in the genetic regulation of menstrual cycle length

genetics more details view paper

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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Advantages of genotype imputation with ethnically matched reference panel for rare variant association analyses

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Genome-wide study identifies association between HLA-B*55:01 and penicillin allergy

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The complement system supports normal postnatal development and gonadal function in both sexes

developmental biology more details view paper

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Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile

genomics more details view paper

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Polygenic prediction of breast cancer: comparison of genetic predictors and implications for screening

genetics more details view paper

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Analytical strategies to include the X-chromosome in variance heterogeneity analyses: evidence for trait-specific polygenic variance structure

genetics more details view paper

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Leveraging biobank-scale rare and common variant analyses to identify ASPHD1 as the main driver of reproductive traits in the 16p11.2 locus

genomics more details view paper

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Genetics of fasting indices of glucose homeostasis using GWIS unravels tight relationships with inflammatory markers

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Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health

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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

genomics more details view paper

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Genome-wide association study identifies five risk loci for pernicious anemia and implicates the role of HLA-DR15 haplotype

genetic and genomic medicine more details view paper

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Genome-wide Screen of Otosclerosis in Population Biobanks: 18 Loci and Shared Heritability with Skeletal Structure

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