Author details

Full Name

Andres Metspalu

Affiliation

ORCID

Career Start Year

1978

Papers

457

H Index

118

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37480624	Corrigendum to "Dissecting the genetic heterogeneity of gastric cancer".	EBioMedicine	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
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
37794016	European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation.	Nat Commun	2023
37632466	Global Effect of Modifiable Risk Factors on Cardiovascular Disease and Mortality.	N Engl J Med	2023
37865284	Transcriptome analysis reveals involvement of thiopurine S-methyltransferase in oxidation-reduction processes.		2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	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
37209533	Dissecting the genetic heterogeneity of gastric cancer.	EBioMedicine	2023
37076744	Correction: Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris.		2023
36922633	Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris.		2023
35066155	Impact of the pre-examination phase on multicenter metabolomic studies.	N Biotechnol	2022
35396580	Mapping genomic loci implicates genes and synaptic biology in schizophrenia.	Nature	2022
36353106	Editorial: Can population health be personalized? Estonia and Finland as examples.	Frontiers in Genetics	2022
35697829	Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.	Commun Biol	2022
35938029	Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical Setting.	Frontiers in Genetics	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
35928446	Do Biobank Recall Studies Matter? Long-Term Follow-Up of Research Participants With Familial Hypercholesterolemia.	Frontiers in Genetics	2022
36778137	Global priorities for large-scale biomarker-based prospective cohorts.	Cell Genom	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
36600884	Effectiveness and feasibility of cardiovascular disease personalized prevention on high polygenic risk score subjects: a randomized controlled pilot study.		2022
33878186	Cis-epistasis at the LPA locus and risk of cardiovascular diseases.	Cardiovasc Res	2022
35314380	Spectrum and frequency of CHEK2 variants in breast cancer affected and general population in the Baltic states region, initial results and literature review.	Eur J Med Genet	2022
35169130	Gut metagenome associations with extensive digital health data in a volunteer-based Estonian microbiome cohort.	Nature Communications	2022
34543281	The blood metabolome of incident kidney cancer: A case-control study nested within the MetKid consortium.	PLoS Med	2021
32064741	Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.	Addict Biol	2021
31712720	Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression.	Mol Psychiatry	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
33740458	The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects.	Am J Hum Genet	2021
34223627	Metabolomic Fingerprints in Large Population Cohorts: Impact of Preanalytical Heterogeneity.	Clin Chem	2021
33946982	Advances in Genomic Discovery and Implications for Personalized Prevention and Medicine: Estonia as Example.	J Pers Med	2021
34101054	Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients.	Clinical Rheumatology	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
33230308	Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants.	European Journal of Human Genetics	2021
33402679	Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
34790224	Mendelian Randomization Identifies the Potential Causal Impact of Dietary Patterns on Circulating Blood Metabolites.	Frontiers in Genetics	2021
34561431	Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome.	Nat Commun	2021
34611364	A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response.	Nat Genet	2021
34493871	Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation.	Nat Genet	2021
34381240	Retraction Note: Detection and replication of epistasis influencing transcription in humans.	Nature	2021
34381229	Phantom epistasis between unlinked loci.	Nature	2021
30617275	Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci.	Mol Psychiatry	2020
32467615	Integrating untargeted metabolomics, genetically informed causal inference, and pathway enrichment to define the obesity metabolome.	Int J Obes (Lond)	2020
33987187	Propelling Healthcare with Advanced Therapy Medicinal Products: A Policy Discussion.		2020
32712624	Differences in local population history at the finest level: the case of the Estonian population.	European Journal of Human Genetics	2020