Reedik Mägi

Genetics · 2007–2023

A researcher in the Science corpus: 28 papers; trusts 25 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 550 citations into it
• Molecular Biology — 355 citations into it
• Plant Science — 15 citations into it

Whom Reedik Mägi trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Michael Olivier
2. C. Carlson
3. Sharon R. Browning
4. Mark Lipsey
5. Kui Zhang
6. Shaun Purcell
7. Jonathan Marchini
8. Mark J. Daly
9. H. Ellegren
10. M. Eberle

Who trusts Reedik Mägi overall

1. Priit Kilgas
2. P. Kivistik
3. M. Jõesaar
4. T. Suvi
5. R. Rannap
6. Lea Hallik
7. T. Remmel
8. Radi Tegova
9. M. Starast
10. Lauri Saag

Papers from Reedik Mägi's perspective

Ordered by how strongly the researchers Reedik Mägi trusts endorse each paper. Same corpus, a different order for every researcher.

1. High-resolution haplotype structure in the human genome (Nature Genetics)
2. The Structure of Haplotype Blocks in the Human Genome (Science)
3. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex (Nature Genetics)
4. Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 (Science)
5. Linkage disequilibrium in the human genome (Nature)
6. Haplotype tagging for the identification of common disease genes (Nature Genetics)
7. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)
8. A global reference for human genetic variation
9. A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline (Nature)
10. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Their papers

• Upper Palaeolithic Siberian genome reveals dual ancestry of Native Americans (2013) — 859 citations
• The genetic architecture of type 2 diabetes (2016) — 1,066 citations
• Multiple New Loci Associated with Kidney Function and Chronic Kidney Disease: The CKDGen consortium (2010) — 799 citations
• Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) — 412 citations
• Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) — 1,485 citations
• FinnGen provides genetic insights from a well-phenotyped isolated population (2023) — 3,553 citations
• Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) — 1,654 citations
• Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
• A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) — 744 citations
• Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations
• Gene discovery and polygenic prediction from a 1.1-million-person GWAS of educational attainment (2018) — 2,165 citations
• Genetic evidence of assortative mating in humans (2017) — 288 citations
• An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) — 677 citations
• Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) — 401 citations
• Ultra-rare disruptive and damaging mutations influence educational attainment in the general population (2016) — 97 citations
• Genome-wide association study identifies 74 loci associated with educational attainment (2016) — 1,288 citations
• Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index (2015) — 781 citations
• Dominance genetic variation contributes little to the missing heritability for human complex traits. (2015) — 200 citations
• Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank (2015) — 386 citations
• Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) — 1,017 citations