Author details

Full Name

Reedik MÃ¤gi

Affiliation

ORCID

Career Start Year

2002

Papers

225

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
35987817	Genetic and modifiable risk factors combine multiplicatively in common disease.	Clin Res Cardiol	2023
36192438	Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank.	European Journal of Human Genetics	2023
37945903	Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.	Nat Genet	2023
38028628	Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.	Front Genet	2023
37923823	HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases.	Commun Biol	2023
37919453	An atlas of genetic determinants of forearm fracture.	Nat Genet	2023
37794016	European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation.	Nat Commun	2023
38076931	Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events.	medRxiv	2023
37877466	Genome-wide association study meta-analysis supports association between MUC1 and ectopic pregnancy.		2023
37873414	GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets.	medRxiv	2023
36653562	FinnGen provides genetic insights from a well-phenotyped isolated population.	Nature	2023
36829046	Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.	Nature	2023
36653343	Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.	Nat Commun	2023
37012456	Genetic effects on the timing of parturition and links to fetal birth weight.	Nat Genet	2023
36929174	GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer.	Hum Mol Genet	2023
37296919	Polygenic Risk Score Predicts Modified Risk in Pathogenic Variant c.4035del and c.5266dup Carriers in Breast Cancer Patients.		2023
37503126	Understanding the genetic complexity of puberty timing across the allele frequency spectrum.	medRxiv	2023
37543033	Genetic insights into the age-specific biological mechanisms governing human ovarian aging.	Am J Hum Genet	2023
35220425	Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.	Hum Mol Genet	2022
35713579	Endometriosis and irritable bowel syndrome: similarities and differences in the spectrum of comorbidities.	Human Reproduction	2022
35591975	Genome-wide risk prediction of common diseases across ancestries in one million people.	Cell Genom	2022
35905320	Improving GWAS discovery and genomic prediction accuracy in biobank data.	Proceedings of the National Academy of Sciences of the United States of America	2022
36035246	Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations.	HGG Adv	2022
35697829	Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.	Commun Biol	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
34454985	Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis.	Journal of Allergy and Clinical Immunology	2022
35020900	Cohort Profile: COVIDMENT: COVID-19 cohorts on mental health across six nations.	Int J Epidemiol	2022
35165703	Estimation of recurrent atherosclerotic cardiovascular event risk in patients with established cardiovascular disease: the updated SMART2 algorithm.	Eur Heart J	2022
34411538	Patterns of genetic connectedness between modern and medieval Estonian genomes reveal the origins of a major ancestry component of the Finnish population.	American Journal of Human Genetics	2021
33972266	Stratification of Type 2 Diabetes by Age of Diagnosis in the UK Biobank Reveals Subgroup-Specific Genetic Associations and Causal Risk Profiles.		2021
33859359	Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.	Mol Psychiatry	2021
33958743	Phylogenetic history of patrilineages rare in northern and eastern Europe from large-scale re-sequencing of human Y-chromosomes.	European Journal of Human Genetics	2021
33740458	The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects.	Am J Hum Genet	2021
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2021
33879782	Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis.	Nat Commun	2021
33558525	Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
32989287	Genome-wide association study identifies 48 common genetic variants associated with handedness.	Nat Hum Behav	2021
33243845	Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health.	European Respiratory Journal	2021
33402679	Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
34851696	Response to comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics".	Sci Transl Med	2021
34848700	Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits.	Nat Commun	2021
33170024	Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease.	Circ Genom Precis Med	2020
32242022	Ancestry deconvolution and partial polygenic score can improve susceptibility predictions in recently admixed individuals.	Nature Communications	2020
32086293	Erratum. Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease. Diabetes 2019;68:2235-2246.	Diabetes	2020
32712624	Differences in local population history at the finest level: the case of the Estonian population.	European Journal of Human Genetics	2020
32581134	Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics.	Sci Transl Med	2020
33239672	The genetic architecture of sporadic and multiple consecutive miscarriage.	Nat Commun	2020
33230300	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2020