Andres Metspalu
#32,068
Most Influential Person Now
Estonian geneticist
Andres Metspalu's AcademicInfluence.com Rankings
Andres Metspalubiology Degrees
Biology
#966
World Rank
#1679
Historical Rank
Genetics
#205
World Rank
#249
Historical Rank
Download Badge
Biology
Andres Metspalu's Degrees
- PhD Genetics University of Tartu
- Doctorate Medicine University of Tartu
Why Is Andres Metspalu Influential?
(Suggest an Edit or Addition)According to Wikipedia, Andres Metspalu is an Estonian geneticist and member of the Estonian Academy of Sciences. Biography Metspalu was born on 11 March 1951 in Lääne-Viru County. In 1969 he graduated from the Rakke High School. In 1976 he graduated from the University of Tartu, Faculty of Medicine, as a physician. In 1979 he obtained a Ph.D. in Molecular Biology from the Institute of Molecular Genetics at the National Academy of Sciences of Ukraine in Kiev. His thesis was on the structure and function of the Eukaryotic ribosome.
Andres Metspalu's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) (6445)
- Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults (2017) (3677)
- Trends in adult body-mass index in 200 countries from 1975 to 2014: a pooled analysis of 1698 population-based measurement studies with 19·2 million participants (2016) (3648)
- Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
- Discovery and Refinement of Loci Associated with Lipid Levels (2013) (2475)
- Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
- Hundreds of variants clustered in genomic loci and biological pathways affect human height (2010) (1961)
- Genetics of rheumatoid arthritis contributes to biology and drug discovery (2013) (1877)
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) (1839)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (2018) (1816)
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
- Systematic identification of trans eQTLs as putative drivers of known disease associations (2013) (1593)
- A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) (1567)
- Worldwide trends in blood pressure from 1975 to 2015: a pooled analysis of 1479 population-based measurement studies with 19·1 million participants (2017) (1563)
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) (1507)
- Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals (2018) (1401)
- Analysis of shared heritability in common disorders of the brain (2016) (1385)
- New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
- Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
- A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) (1125)
- Genome-wide association study identifies 74 loci associated with educational attainment (2016) (1114)
- Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (1028)
- Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
- The genetic architecture of type 2 diabetes (2016) (927)
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2018) (914)
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
- A century of trends in adult human height (2016) (861)
- GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) (803)
- Common variants associated with plasma triglycerides and risk for coronary artery disease (2013) (767)
- Identification of seven loci affecting mean telomere length and their association with disease (2013) (761)
- Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) (758)
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) (736)
- Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries (2018) (735)
- Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (2019) (724)
- Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans (2015) (724)
- Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior (2010) (688)
- Genome-wide association analyses identify 18 new loci associated with serum urate concentrations (2012) (678)
- Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index (2015) (666)
- Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (659)
- Worldwide trends in hypertension prevalence and progress in treatment and control from 1990 to 2019: a pooled analysis of 1201 population-representative studies with 104 million participants (2021) (585)
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
- Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses (2016) (563)
- Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity (2012) (555)
- Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci (2016) (549)
- An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) (547)
- A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. (2009) (532)
- The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
- Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche (2014) (511)
- Rare and low-frequency coding variants alter human adult height (2016) (511)
- Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes. (1998) (490)
- Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies (2010) (477)
- Association analyses based on false discovery rate implicate new loci for coronary artery disease (2017) (476)
- Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA (2016) (471)
- Mapping the human genetic architecture of COVID-19 (2021) (455)
- Common Variants in KCNN3 are Associated with Lone Atrial Fibrillation (2010) (454)
- The transcriptional landscape of age in human peripheral blood (2015) (450)
- Genetic Structure of Europeans: A View from the North–East (2009) (437)
- Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus (2011) (428)
- Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (2017) (428)
- Exome-wide association study of plasma lipids in >300,000 individuals (2017) (428)
- Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure (2011) (424)
- A first-generation linkage disequilibrium map of human chromosome 22 (2002) (424)
- New gene functions in megakaryopoiesis and platelet formation (2011) (423)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (421)
- The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studies (2014) (419)
- Erratum: Detection and interpretation of shared genetic influences on 42 human traits (2016) (417)
- FTO genotype is associated with phenotypic variability of body mass index (2012) (407)
- Identification of fifteen new psoriasis susceptibility loci highlights the role of innate immunity (2012) (397)
- High carrier frequency of the 35delG deafness mutation in European populations (2000) (397)
- A structural variation reference for medical and population genetics (2020) (394)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study (2012) (382)
- Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (2013) (379)
- Meta-analysis of genome-wide association studies for personality (2012) (369)
- Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits (2013) (365)
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) (361)
- Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk (2017) (359)
- Seventy-five genetic loci influencing the human red blood cell (2012) (357)
- Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci (2015) (349)
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) (348)
- The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals (2016) (347)
- Minisequencing: a specific tool for DNA analysis and diagnostics on oligonucleotide arrays. (1997) (333)
- A recent bottleneck of Y chromosome diversity coincides with a global change in culture (2015) (329)
- Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2014) (322)
- Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa (2019) (314)
- Sequence variants at CHRNB 3 – CHRNA 6 and CYP 2 A 6 affect smoking behavior (2010) (312)
- Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. (2016) (309)
- Genomic analyses inform on migration events during the peopling of Eurasia (2016) (309)
- Large-scale genomic analyses link reproductive ageing to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair (2015) (308)
- Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci. (2012) (301)
- Rising rural body-mass index is the main driver of the global obesity epidemic in adults (2019) (300)
- The impact of low-frequency and rare variants on lipid levels (2015) (300)
- Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders (2013) (299)
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) (294)
- Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation (2015) (285)
- A genome-wide association study of anorexia nervosa (2014) (284)
- Biomarker Profiling by Nuclear Magnetic Resonance Spectroscopy for the Prediction of All-Cause Mortality: An Observational Study of 17,345 Persons (2014) (284)
- Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci (2016) (283)
- Design of a peptide-based vector, PepFect6, for efficient delivery of siRNA in cell culture and systemically in vivo (2011) (282)
- Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder. (2015) (281)
- A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium (2011) (278)
- Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism (2015) (276)
- Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu. (2015) (273)
- Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (2011) (270)
- Correction: Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (2015) (268)
- Human Disease-Associated Genetic Variation Impacts Large Intergenic Non-Coding RNA Expression (2013) (266)
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) (252)
- Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) (250)
- Signatures of negative selection in the genetic architecture of human complex traits (2018) (243)
- A novel highly-penetrant form of obesity due to microdeletions on chromosome 16p11.2 (2009) (239)
- Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age (2014) (238)
- Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension (2016) (234)
- Systems medicine and integrated care to combat chronic noncommunicable diseases (2011) (230)
- Improved polygenic prediction by Bayesian multiple regression on summary statistics (2019) (224)
- Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption (2014) (224)
- Population genetic differentiation of height and body mass index across Europe (2015) (224)
- Genetically determined height and coronary artery disease. (2015) (220)
- Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants (2016) (219)
- Arrayed primer extension: solid-phase four-color DNA resequencing and mutation detection technology. (2000) (213)
- Meta‐analysis of microRNA expression in lung cancer (2013) (211)
- Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease (2017) (204)
- The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis (2013) (199)
- Genetic evidence of assortative mating in humans (2017) (199)
- Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls (2012) (196)
- Detection and replication of epistasis influencing transcription in humans (2014) (193)
- A metabolic view on menopause and ageing (2014) (184)
- Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels (2019) (183)
- Global implementation of genomic medicine: We are not alone (2015) (183)
- Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function (2012) (180)
- Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function (2017) (180)
- Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels (2015) (179)
- Dominance genetic variation contributes little to the missing heritability for human complex traits. (2015) (175)
- Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities. (2016) (174)
- Mutation detection by solid phase primer extension (1996) (173)
- A 5S rRNA/L5 complex is a precursor to ribosome assembly in mammalian cells (1988) (170)
- Human microRNAs miR-22, miR-138-2, miR-148a, and miR-488 Are Associated with Panic Disorder and Regulate Several Anxiety Candidate Genes and Related Pathways (2011) (170)
- Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (2014) (170)
- Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci (2015) (167)
- Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium (2015) (164)
- Structure and expression of the genes coding for human alpha 1‐acid glycoprotein. (1987) (157)
- Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis (2017) (156)
- Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study (2018) (156)
- Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies (2010) (154)
- Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (153)
- The Trans-Ancestral Genomic Architecture of Glycemic Traits (2020) (151)
- Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways (2012) (150)
- Meta-analyses identify 13 novel loci associated with age at menopause and highlights DNA repair and immune pathways (2011) (149)
- Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits (2017) (149)
- Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error (2018) (147)
- Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals. (2010) (147)
- Toward a roadmap in global biobanking for health (2012) (146)
- Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances (2018) (144)
- Directional dominance on stature and cognition in diverse human populations (2015) (144)
- Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. (2013) (143)
- A KATP channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila (2011) (141)
- A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individuals (2019) (139)
- Height and body-mass index trajectories of school-aged children and adolescents from 1985 to 2019 in 200 countries and territories: a pooled analysis of 2181 population-based studies with 65 million participants (2020) (138)
- Linkage disequilibrium patterns and tagSNP transferability among European populations. (2005) (138)
- A variant in MCF2L is associated with osteoarthritis. (2011) (137)
- Association of branched-chain amino acids and other circulating metabolites with risk of incident dementia and Alzheimer’s disease: A prospective study in eight cohorts (2018) (134)
- Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium (2016) (134)
- A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip (2013) (132)
- Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study (2010) (131)
- Hidden heritability due to heterogeneity across seven populations (2017) (128)
- Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel (2017) (128)
- Adiposity as a cause of cardiovascular disease: a Mendelian randomization study. (2015) (128)
- Complementary seminovaginal microbiome in couples. (2015) (128)
- Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation (2020) (125)
- Identification of miR‐374a as a prognostic marker for survival in patients with early‐stage nonsmall cell lung cancer (2011) (122)
- Copy number variations and cognitive phenotypes in unselected populations. (2015) (122)
- Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney (2017) (121)
- Genome-wide meta-analysis of Psoriatic Arthritis Identifies Susceptibility Locus at REL (2011) (120)
- Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course. (2013) (120)
- Structural forms of the human amylase locus and their relationships to SNPs, haplotypes, and obesity (2015) (118)
- Application of non-HDL cholesterol for population-based cardiovascular risk stratification: results from the Multinational Cardiovascular Risk Consortium (2019) (118)
- Personalized early detection and prevention of breast cancer: ENVISION consensus statement (2020) (117)
- Assessment of Osteoarthritis Candidate Genes in a Meta-Analysis of Nine Genome-Wide Association Studies (2014) (117)
- Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity (2017) (117)
- Genetic variants linked to education predict longevity (2016) (116)
- Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores (2016) (116)
- Chronotype and sleep duration: The influence of season of assessment (2014) (115)
- Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of Item Response Theory (2014) (113)
- Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness (2017) (113)
- Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies (2018) (113)
- The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data (2011) (111)
- The Genetic Architecture of Gene Expression in Peripheral Blood. (2017) (110)
- Age-related profiling of DNA methylation in CD8+ T cells reveals changes in immune response and transcriptional regulator genes (2015) (109)
- A Meta-analysis of Gene Expression Signatures of Blood Pressure and Hypertension (2015) (108)
- Reconstructing the Population History of European Romani from Genome-wide Data (2012) (108)
- Genetic correlation between amyotrophic lateral sclerosis and schizophrenia (2017) (107)
- Cell Specific eQTL Analysis without Sorting Cells (2014) (105)
- Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking (2011) (105)
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
- Effects of Metformin on Metabolite Profiles and LDL Cholesterol in Patients With Type 2 Diabetes (2015) (103)
- Personality traits and eating habits in a large sample of Estonians. (2012) (102)
- Evaluating the arrayed primer extension resequencing assay of TP53 tumor suppressor gene (2002) (102)
- The role of COX-2 and Nrf2/ARE in anti-inflammation and antioxidative stress: Aging and anti-aging. (2011) (102)
- Genotype–covariate interaction effects and the heritability of adult body mass index (2017) (102)
- Genetic associations of 115 polymorphisms with cancers of the upper aerodigestive tract across 10 European countries: the ARCAGE project. (2009) (100)
- An Evaluation of the Performance of Tag SNPs Derived from HapMap in a Caucasian Population (2006) (100)
- A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. (2018) (100)
- Comprehensive catalog of European biobanks (2011) (99)
- A genome-wide association study of early menopause and the combined impact of identified variants (2013) (99)
- The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls (2018) (99)
- 52 Genetic Loci Influencing Myocardial Mass. (2016) (98)
- Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (2015) (98)
- Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error (2016) (98)
- 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function (2017) (95)
- Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (93)
- Gene Expression Profiles of Non-Small Cell Lung Cancer: Survival Prediction and New Biomarkers (2011) (92)
- Association study of 90 candidate gene polymorphisms in panic disorder (2005) (92)
- Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
- Leukocyte telomere length associates with prospective mortality independent of immune-related parameters and known genetic markers (2014) (92)
- Oral health, dental care and mouthwash associated with upper aerodigestive tract cancer risk in Europe: the ARCAGE study. (2014) (90)
- Transcript expression-aware annotation improves rare variant interpretation (2020) (89)
- An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype (2017) (89)
- Dating the Origin of the CCR 5D 32 AIDS-Resistance Allele by the Coalescence of Haplotypes (2007) (88)
- Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation (2020) (88)
- Pathogenic implications for autoimmune mechanisms derived by comparative eQTL analysis of CD4+ versus CD8+ T cells (2017) (87)
- Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium (2017) (87)
- The Genetic Architecture of Gene Expression in Peripheral Blood. (2017) (87)
- Evaluating drug targets through human loss-of-function genetic variation (2019) (86)
- BBMRI-ERIC as a resource for pharmaceutical and life science industries: the development of biobank-based Expert Centres (2014) (81)
- Evidence of Inbreeding Depression on Human Height (2012) (81)
- Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals. (2016) (81)
- Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals (2022) (80)
- Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium (2016) (80)
- Ultra-rare disruptive and damaging mutations influence educational attainment in the general population (2016) (79)
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) (78)
- Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. (2019) (77)
- Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium (2012) (75)
- A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smoking. (2016) (75)
- Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length (2020) (74)
- Simultaneous Multigene Mutation Detection in Patients With Sensorineural Hearing Loss Through a Novel Diagnostic Microarray: A New Approach for Newborn Screening Follow-up (2006) (74)
- Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (2019) (72)
- Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci (2019) (72)
- Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation (2015) (72)
- Replication and meta-analysis of TMEM132D gene variants in panic disorder (2012) (71)
- MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate. (2010) (71)
- Ontogeny, distribution and potential roles of 5-hydroxymethylcytosine in human liver function (2013) (71)
- Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity (2012) (70)
- Allelic estrogen receptor 1 (ESR1) gene variants predict the outcome of ovarian stimulation in in vitro fertilization. (2007) (70)
- Contributions of mean and shape of blood pressure distribution to worldwide trends and variations in raised blood pressure: a pooled analysis of 1018 population-based measurement studies with 88.6 million participants (2018) (70)
- The effect of LRRK2 loss-of-function variants in humans (2020) (69)
- Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index (2014) (69)
- Unravelling Genetic Data by Arrayed Primer Extension (2000) (68)
- Associations of autozygosity with a broad range of human phenotypes (2019) (68)
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2017) (68)
- Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. (2012) (67)
- The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition (2016) (67)
- Epigenetic profiling in CD4+ and CD8+ T cells from Graves' disease patients reveals changes in genes associated with T cell receptor signaling. (2016) (67)
- A common 16p11.2 inversion underlies the joint susceptibility to asthma and obesity. (2014) (66)
- Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (65)
- Polymorphisms in ESR1, ESR2 and HSD17B1 genes are associated with fertility status in endometriosis (2011) (65)
- A saturated map of common genetic variants associated with human height (2022) (65)
- Methylation Markers of Early-Stage Non-Small Cell Lung Cancer (2012) (65)
- Genome-wide association study identifies 48 common genetic variants associated with handedness (2019) (65)
- Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits. (2016) (64)
- The DOT1L rs12982744 polymorphism is associated with osteoarthritis of the hip with genome-wide statistical significance in males (2013) (64)
- De Novo SCN8A Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy, Multiple Congenital Anomalies, and Movement Disorders (2014) (64)
- Serotonin transporter promoter region polymorphisms do not influence treatment response to escitalopram in patients with major depression (2009) (63)
- Reliable Detection of β-Thalassemia and G6PD Mutations by a DNA Microarray (2002) (63)
- Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes (2016) (63)
- Age- and Sex-Specific Causal Effects of Adiposity on Cardiovascular Risk Factors (2015) (62)
- Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations (2018) (61)
- Leveraging European infrastructures to access 1 million human genomes by 2022 (2019) (60)
- A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts (2020) (60)
- An epigenome-wide association study meta-analysis of educational attainment (2017) (60)
- Another Explanation for Apparent Epistasis (2014) (59)
- Sex- and age-interacting eQTLs in human complex diseases. (2014) (59)
- A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape (2016) (59)
- Alcohol-related cancers and genetic susceptibility in Europe: the ARCAGE project: study samples and data collection (2009) (58)
- Genome-wide genetic homogeneity between sexes and populations for human height and body mass index. (2015) (58)
- Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2020) (58)
- Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. (2013) (57)
- Cerebral small vessel disease genomics and its implications across the lifespan (2020) (56)
- Haplotype sharing provides insights into fine-scale population history and disease in Finland (2017) (56)
- Genetic influence on social outcomes during and after the Soviet era in Estonia (2018) (56)
- A Missense Mutation in DUSP6 is Associated with Class III Malocclusion (2013) (56)
- The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects (2015) (55)
- 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) (55)
- Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (2013) (55)
- CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits (2017) (52)
- Sequence variation in nuclear ribosomal small subunit, internal transcribed spacer and large subunit regions of Rhizophagus irregularis and Gigaspora margarita is high and isolate‐dependent (2016) (50)
- Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases. (2016) (50)
- The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe (2002) (50)
- Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta (2014) (49)
- The prevalence of metabolic syndrome and metabolically healthy obesity in Europe (2014) (48)
- Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration (2019) (47)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depressive disorder (2017) (47)
- Selection for Genetic Variation Inducing Pro-Inflammatory Responses under Adverse Environmental Conditions in a Ghanaian Population (2009) (47)
- In-solution hybrid capture of bisulfite-converted DNA for targeted bisulfite sequencing of 174 ADME genes (2013) (46)
- Within-Trait Heterogeneity in Age Group Differences in Personality Domains and Facets: Implications for the Development and Coherence of Personality Traits (2015) (46)
- Polymorphisms in wolframin (WFS1) gene are possibly related to increased risk for mood disorders. (2005) (46)
- Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women. (2016) (45)
- Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use (2019) (45)
- Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium. (2012) (44)
- SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. (2017) (44)
- DNA mismatch repair gene MSH6 implicated in determining age at natural menopause (2013) (44)
- Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate. (2011) (44)
- Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation (2007) (43)
- Genotyping microarray for the detection of more than 200 CFTR mutations in ethnically diverse populations. (2005) (43)
- A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk (2017) (43)
- Polymorphisms in MMP-2 and MMP-9 promoter regions are associated with endometriosis. (2010) (42)
- Mapping the Genetic Architecture of Gene Regulation in Whole Blood (2014) (41)
- Nuclear import and nucleolar accumulation of the human ribosomal protein S7 depends on both a minimal nuclear localization sequence and an adjacent basic region. (1998) (41)
- Linking a Population Biobank with National Health Registries—The Estonian Experience (2015) (41)
- Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study (2010) (41)
- Analysis of SNP profiles in patients with major depressive disorder. (2005) (40)
- Feasibility of innovative dietary assessment in epidemiological studies using the approach of combining different assessment instruments (2011) (40)
- Polymorphic Variation in TPMT Is the Principal Determinant of TPMT Phenotype: A Meta‐Analysis of Three Genome‐Wide Association Studies (2017) (39)
- Comprehensive meta-analysis of microRNA expression using a robust rank aggregation approach. (2014) (39)
- Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate. (2010) (39)
- Development of a single tube 640-plex genotyping method for detection of nucleic acid variations on microarrays (2008) (38)
- Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2016) (37)
- Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches (2019) (37)
- Copper metabolism domain-containing 1 represses genes that promote inflammation and protects mice from colitis and colitis-associated cancer. (2014) (37)
- Association of polygenic score for major depression with response to lithium in patients with bipolar disorder (2020) (37)
- Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients (2009) (36)
- Aromatase gene (CYP19A1) variants, female infertility and ovarian stimulation outcome: a preliminary report. (2009) (36)
- Rare coding variants and X-linked loci associated with age at menarche (2015) (36)
- Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. (2016) (36)
- Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms (2016) (35)
- The Estonian Genome Project (2004) (35)
- Common variants in Mendelian kidney disease genes and their association with renal function. (2013) (35)
- A Genome-Wide Analysis of Populations from European Russia Reveals a New Pole of Genetic Diversity in Northern Europe (2013) (34)
- Interaction of 5-S RNA, 5.8-S RNA and tRNA with rat-liver ribosomal proteins. (1978) (34)
- Using ancestry-informative markers to identify fine structure across 15 populations of European origin (2014) (34)
- A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol (2011) (34)
- Locations of several novel 2'-O-methylated nucleotides in human 28S rRNA (2002) (34)
- Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. (2016) (34)
- Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity (2013) (34)
- An interaction map of circulating metabolites, immune gene networks, and their genetic regulation (2016) (33)
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) (33)
- CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing (2014) (33)
- Circulating metabolic biomarkers of renal function in diabetic and non-diabetic populations (2018) (33)
- Genetic variations in vascular endothelial growth factor but not in angiotensin I-converting enzyme genes are associated with endometriosis in Estonian women. (2010) (32)
- Ageing with elegans: a research proposal to map healthspan pathways (2016) (32)
- Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification (2019) (32)
- Variance determines self-observer agreement on the Big Five personality traits (2010) (32)
- Evaluation of the 124-plex SNP typing microarray for forensic testing. (2009) (32)
- Genome-wide meta-analysis of common variant differences between men and women (2012) (31)
- A polygenic resilience score moderates the genetic risk for schizophrenia (2019) (31)
- Heterogeneous contributions of change in population distribution of body mass index to change in obesity and underweight (2020) (30)
- A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response (2021) (30)
- Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour (2021) (29)
- Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia (2018) (29)
- Genetic variants in RBFOX3 are associated with sleep latency (2016) (29)
- Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome (2020) (29)
- A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine (2020) (29)
- Non-syndromic Tooth Agenesis Associated with a Nonsense Mutation in Ectodysplasin-A (EDA) (2013) (28)
- Whole-exome sequencing identifies a polymorphism in the BMP5 gene associated with SSRI treatment response in major depression (2013) (28)
- A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. (2019) (28)
- The effect of X-linked dosage compensation on complex trait variation (2018) (28)
- Human ribosomal protein S3a: cloning of the cDNA and primary structure of the protein. (1992) (27)
- A first update on mapping the human genetic architecture of COVID-19 (2022) (27)
- An epidemiological perspective of personalized medicine: the Estonian experience (2015) (27)
- The genetic architecture of sporadic and multiple consecutive miscarriage (2020) (27)
- Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression (2019) (27)
- Manifesto for a European Anxiety Disorders Research Network (2010) (26)
- Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (26)
- Coffin–Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene (2014) (26)
- Genome‐wide association study and meta‐analysis in Northern European populations replicate multiple colorectal cancer risk loci (2017) (26)
- Metabolites of milk intake: a metabolomic approach in UK twins with findings replicated in two European cohorts (2016) (26)
- Harmonising and linking biomedical and clinical data across disparate data archives to enable integrative cross-biobank research (2015) (26)
- Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records (2018) (26)
- DNA breaks and chromatin structural changes enhance the transcription of autoimmune regulator target genes (2017) (25)
- Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2017) (25)
- Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
- No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis (2016) (25)
- Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (2016) (25)
- Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. (2016) (25)
- Post-translational stabilization of thiopurine S-methyltransferase by S-adenosyl-L-methionine reveals regulation of TPMT*1 and *3C allozymes. (2012) (25)
- Extensive alterations of the whole-blood transcriptome are associated with body mass index: results of an mRNA profiling study involving two large population-based cohorts (2015) (25)
- Population distribution and ancestry of the cancer protective MDM2 SNP285 (rs117039649) (2014) (24)
- Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients. (2010) (24)
- An epigenome-wide association study of metabolic syndrome and its components (2020) (24)
- Genetic risk scores and family history as predictors of schizophrenia in Nordic registers (2017) (24)
- From pharmacogenetics to pharmacometabolomics: SAM modulates TPMT activity. (2014) (23)
- Demographic associations for autoantibodies in disease-free individuals of a European population (2017) (23)
- Defining the Effect of the 16 p 11 . 2 Duplication on Cognition , Behavior , andMedical Comorbidities (2015) (23)
- Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache (2020) (23)
- 16p11.2 Locus modulates response to satiety before the onset of obesity (2016) (23)
- Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions (2012) (23)
- Quality Matters: 2016 Annual Conference of the National Infrastructures for Biobanking. (2017) (23)
- FinnGen provides genetic insights from a well-phenotyped isolated population (2023) (22)
- Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (22)
- Genome-wide association study identifies 30 loci associated with bipolar disorder (2019) (22)
- Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy (2020) (22)
- Imprinted genes and imprinting control regions show predominant intermediate methylation in adult somatic tissues (2016) (21)
- Arrayed primer extension resequencing of mutations in the TP53 tumor suppressor gene: comparison with denaturing HPLC and direct sequencing. (2005) (21)
- Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events (2019) (21)
- Constraints on eQTL Fine Mapping in the Presence of Multisite Local Regulation of Gene Expression (2017) (21)
- The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects (2020) (21)
- Self-Other Agreement in Happiness and Life-Satisfaction: The Role of Personality Traits (2013) (21)
- Whole-genome expression analysis reveals genes associated with treatment response to escitalopram in major depression (2016) (21)
- Comparison of DNA extraction methods for multiplex polymerase chain reaction. (2010) (21)
- Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics (2019) (20)
- Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies (2019) (20)
- Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression (2020) (20)
- Phenylalanine Hydroxylase Gene Mutation R408W Is Present on 84% of Estonian Phenylketonuria Chromosomes (1996) (20)
- Direct-to-consumer genetic testing for health-related purposes in the European Union (2012) (19)
- Human N-benzoyl-L-tyrosyl-p-aminobenzoic acid hydrolase (human meprin): genomic structure of the alpha and beta subunits. (2000) (19)
- Sequence Variants and the Risk of Head and Neck Cancer: Pooled Analysis in the INHANCE Consortium (2011) (19)
- The Role of the Five–factor Personality Traits in General Self–rated Health (2016) (19)
- Thiopurine S-methyltransferase (TPMT) pharmacogenetics: three new mutations and haplotype analysis in the Estonian population (2008) (19)
- Occupational irritants and asthma: an Estonian cross-sectional study of 34 000 adults (2014) (19)
- A Variant in MCF 2 L Is Associated with Osteoarthritis (19)
- Estonian Genome Project - before the take-off and take-off (2002) (19)
- Association study of sporadic Parkinson's disease genetic risk factors in patients from Russia by APEX technology (2006) (19)
- Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions (2017) (19)
- Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank (2019) (18)
- Genetic diversity fuels gene discovery for tobacco and alcohol use (2022) (18)
- Location of single-stranded and double-stranded regions in rat liver ribosomal 5S RNA and 5.8S RNA. (1981) (18)
- Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error (2020) (18)
- Metagenes Associated with Survival in Non-Small Cell Lung Cancer (2011) (18)
- Reliable detection of beta-thalassemia and G6PD mutations by a DNA microarray. (2002) (18)
- The ternary complex consisting of rat liver ribosomal 5 S RNA, 5.8 S RNA and protein L5 (1980) (18)
- Correction: Corrigendum: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (2017) (18)
- Androgen receptor gene haplotype is associated with male infertility. (2008) (18)
- Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (17)
- High-density genotyping and linkage disequilibrium in the human genome using chromosome 22 as a model. (2002) (17)
- History of the diagnosis of a sexually transmitted disease is linked to normal variation in personality traits. (2012) (17)
- Longevity candidate genes and their association with personality traits in the elderly (2012) (16)
- Meta-analysis identifies loci affecting levels of the potential osteoarthritis biomarkers sCOMP and uCTX-II with genome wide significance (2014) (16)
- Development of the phenylketonuria screening programme in Estonia (1998) (16)
- Differences in local population history at the finest level: the case of the Estonian population (2020) (16)
- Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts (2017) (16)
- The human ribosomal protein S7-encoding gene: isolation, structure and localization in 2p25. (1995) (16)
- [The Estonian Genome Project in the context of European genome research]. (2004) (16)
- Distribution of CFTR gene mutations in cystic fibrosis patients from Estonia (2000) (16)
- Roadmap for a precision-medicine initiative in the Nordic region (2019) (16)
- Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta (2015) (15)
- Model-based assessment of replicability for genome-wide association meta-analysis (2021) (15)
- Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation (2019) (15)
- Signatures of negative selection in the genetic architecture of human complex traits (2017) (14)
- The human ribosomal protein S6 gene: isolation, primary structure and location in chromosome 9. (1992) (14)
- Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participants. (2016) (14)
- Erratum: Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2017) (14)
- Peripheral gene expression profiling of CCK‐4‐induced panic in healthy subjects (2008) (14)
- Development and validation of two SCORE-based cardiovascular risk prediction models for Eastern Europe: a multicohort study (2020) (14)
- Copy Number Variations and Cognitive Phenotypes in Unselected Populations (2015) (14)
- Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention (2022) (14)
- Subsequent Event Risk in Individuals With Established Coronary Heart Disease (2019) (14)
- Genetic analysis of over one million people identifies 535 novel loci for blood pressure (2017) (14)
- Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant. (2019) (13)
- Autosomal genetic control of human gene expression does not differ across the sexes (2016) (13)
- Arrayed primer extension reaction for genotyping on oligonucleotide microarray. (2008) (13)
- A human cDNA encoding the homologue of NADH: ubiquinone oxidoreductase subunit B13. (1997) (13)
- Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants (2020) (13)
- Integrating untargeted metabolomics, genetically informed causal inference, and pathway enrichment to define the obesity metabolome (2019) (13)
- Mega-analysis of 31,396 individuals from 6 countries uncovers strong gene-environment interaction for human fertility (2016) (13)
- The individual and global impact of copy-number variants on complex human traits (2022) (13)
- Analysis of polymorphisms in the SRD5A2 gene and semen parameters in Estonian men. (2010) (13)
- Genome-wide association study identifies five risk loci for pernicious anemia (2021) (12)
- Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood (2018) (12)
- A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia. (2011) (12)
- BRCA1 mutations in women with familial or early-onset breast cancer and BRCA2 mutations in familial cancer in Estonia (2010) (12)
- A novel snoRNA (U73) is encoded within the introns of the human and mouse ribosomal protein S3a genes. (1998) (12)
- Advantages of genotype imputation with ethnically matched reference panel for rare variant association analyses (2019) (12)
- A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma. (2011) (11)
- Optimization of candidate-gene SNP-genotyping by flexible oligonucleotide microarrays; analyzing variations in immune regulator genes of hay-fever samples (2007) (11)
- Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood (2017) (11)
- A high-resolution HLA reference panel capturing global population diversity enables multi-ethnic fine-mapping in HIV host response (2020) (11)
- Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia. (2015) (11)
- Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chain (2001) (11)
- PAIRUP-MS: Pathway analysis and imputation to relate unknowns in profiles from mass spectrometry-based metabolite data (2017) (11)
- Elevated incidence of chromosomally chaotic embryos among frozen-thawed preimplantation embryos. (2004) (11)
- Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium (2012) (10)
- Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche DTU Orbit (05/11/2017) (2014) (10)
- Genomic organization of the human complex I 13-kDa subunit gene NDUFA5 (1999) (10)
- Manifesto for an international digital mental health network (2019) (10)
- Haplotype Phasing and Inheritance of Copy Number Variants in Nuclear Families (2015) (10)
- Viva Europa, a Land of Excellence in Research and Innovation for Health and Wellbeing (2017) (10)
- Propelling Healthcare with Advanced Therapy Medicinal Products: A Policy Discussion (2020) (10)
- U82, a novel snoRNA identified from the fifth intron of human and mouse nucleolin gene. (1999) (9)
- DNA resequencing, mutation detection and gene expression analysis by oligonucleotide microchips (1999) (9)
- The relationship between the Five-Factor Model personality traits and peptic ulcer disease in a large population-based adult sample. (2015) (9)
- Giving and Withholding of Information following Genomic Screening: Challenges Identified in a Study of Primary Care Physicians in Estonia (2012) (9)
- Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (9)
- Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci (2020) (9)
- De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion (2016) (9)
- Is the adiposity‐associated FTO gene variant related to all‐cause mortality independent of adiposity? Meta‐analysis of data from 169,551 Caucasian adults (2015) (9)
- Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure (2021) (9)
- Unique spectrum of SPAST variants in Estonian HSP patients: presence of benign missense changes but lack of exonic rearrangements (2010) (9)
- Gene expression profiling and genome-wide association studies of non-small cell lung cancer (2011) (9)
- An RNA stem-loop structure involved in the packaging of bovine leukemia virus genomic RNA in vivo. (1995) (9)
- Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus (2020) (9)
- Hemani et al. reply (2014) (8)
- Isolation and characterization of the mouse ribosomal protein S7 gene (1998) (8)
- Genome-wide association analyses in > 119,000 individuals identifies thirteen morningness and two sleep duration loci (2016) (8)
- A bovine papillomavirus-1 based vector restores the function of the low-density lipoprotein receptor in the receptor-deficient CHO-ldlA7 cell line (2002) (8)
- Generation Scotland (2015) (8)
- The blood metabolome of incident kidney cancer: A case–control study nested within the MetKid consortium (2021) (8)
- Neonatal screening for the cystic fibrosis main mutation ΔF508 in Estonia (1998) (8)
- Propelling Health Care into the Twenties (2020) (8)
- DNA arrays: methods and applications: report on HUGO Meeting, Tartu, Estonia, 23–26 May, 1999 (2000) (8)
- Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits : (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x) (2018) (8)
- Erratum: Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis (American Journal of Human Genetics (2016) 99(2) (481–488)(S0002929716302208)(10.1016/j.ajhg.2016.06.016)) (2016) (8)
- Are Methylenetetrahydrofolate Reductase (MTHFR) Gene Polymorphisms C677T and A1298C Associated with Higher Risk of Pediatric Migraine in Boys and Girls (2014) (8)
- Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss (2022) (7)
- Immobilized eukaryotic 5.8 S RNA binds escherichia coli and rat liver ribosomal proteins (1979) (7)
- Cumulative Small Effect Genetic Markers and the Risk of Colorectal Cancer in Poland, Estonia, Lithuania, and Latvia (2015) (7)
- Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity (2017) (7)
- Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium (2019) (7)
- Phantom epistasis between unlinked loci (2021) (7)
- Metabolomic Fingerprints in Large Population Cohorts: Impact of Preanalytical Heterogeneity. (2021) (7)
- Correction: A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium (2011) (7)
- Genome-wide association study identifies new locus associated with OCD (2021) (7)
- Cis-epistasis at the LPA locus and risk of cardiovascular diseases (2021) (7)
- Identifying pathways modulating sleep duration: from genomics to transcriptomics (2017) (7)
- Analysis of Allele and Haplotype Diversity Across 25 Genomic Regions in Three Eastern European Populations (2009) (7)
- A linkage disequilibrium map of chromosome 22 (2002) (6)
- Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation. (2019) (6)
- Arrayed primer extension on in situ synthesized 5'-->3' oligonucleotides in microchannels. (2008) (6)
- Publisher Correction: Personalized early detection and prevention of breast cancer: ENVISION consensus statement (2020) (6)
- Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (Proceedings of the National Academy Sciences of the United States of America (2011) 108, 17, (7119-7124)) (2011) (6)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (6)
- New aspects of the eukaryotic ribosomal subunit interaction (1979) (6)
- Severe CF manifestation with anaemia and failure to thrive in a 394delTT homozygous patient. (2004) (6)
- Genome-wide Screen of Otosclerosis in Population Biobanks: 18 Loci and Shared Heritability with Skeletal Structure (2020) (6)
- Gene Expression-Based Approaches in Differentiation of Metastases and Second Primary Tumour (2010) (6)
- MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies (2017) (6)
- Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal hernia (2016) (5)
- ROS1 Asp2213Asn polymorphism is not associated with coronary artery disease in a Greek case-control study (2009) (5)
- Mutation 985A>G in the MCAD gene shows low incidence in Estonian population (2000) (5)
- Molecular diagnosis of Down syndrome using quantitative APEX‐2 microarrays (2010) (5)
- Primer Design for Large-Scale Multiplex PCR and Arrayed Primer Extension (2013) (5)
- Lynch syndrome mutations shared by the Baltic States and Poland (2014) (5)
- Human basonuclin 2 up-regulates a cascade set of interferon-stimulated genes with anti-cancerous properties in a lung cancer model (2017) (5)
- Erratum to “Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies” [Alzheimer’s & Dementia 2018;14:707-22.] (2019) (5)
- A re-examination of proximodistal patterning during vertebrate limb development (5)
- Structural characterization of the mouse ribosomal protein S6-encoding gene. (1996) (5)
- GENETIC ANALYSIS OF OVER ONE MILLION PEOPLE IDENTIFIES 535 NOVEL LOCI ASSOCIATED WITH BLOOD PRESSURE AND RISK OF CARDIOVASCULAR DISEASE (2018) (5)
- Stratification of Type 2 Diabetes by Age of Diagnosis in the UK Biobank Reveals Subgroup-Specific Genetic Associations and Causal Risk Profiles (2021) (5)
- Impact of the pre-examination phase on multicenter metabolomic studies. (2022) (4)
- Genome-Wide Association Scan of Serum Urea in European Populations Identifies Two Novel Loci (2019) (4)
- Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals (2022) (4)
- Estimating the performance of three cardiovascular disease risk scores: the Estonian Biobank cohort study (2019) (4)
- Genetic variants of inducible costimulator are associated with allergic asthma susceptibility. (2015) (4)
- Gut metagenome associations with extensive digital health data in a volunteer-based Estonian microbiome cohort (2021) (4)
- Meta-analysis of genome-wide association results in > 10.000 individuals for the big five personality traits (2009) (4)
- Exome analysis in an Estonian multiplex family with neural tube defects—a case report (2017) (4)
- Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients (2021) (4)
- Novel applications of SNP array data in the analysis of the genetic structure of Europeans and in genetic association studies (2012) (4)
- Neonatal screening for the cystic fibrosis main mutation delta F508 in Estonia. (1998) (4)
- Author Correction: Leveraging European infrastructures to access 1 million human genomes by 2022 (2019) (4)
- Manhattan Harvester and Cropper: a system for GWAS peak detection (2019) (4)
- Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2018) (4)
- COVID-19 and beyond: a call for action and audacious solidarity to all the citizens and nations, it is humanity’s fight (2020) (4)
- Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2017) (4)
- Abstracts from the 50th European Society of Human Genetics Conference: Posters (2018) (4)
- Genome-wide association study identifies 48 common genetic variants associated with handedness (2020) (4)
- 356 COMMON VARIANTS IN SKELETAL DYSPLASIA GENES ARE ASSOCIATED WITH OSTEOARTHRITIS (2011) (4)
- ePerMed - Rise of scientific excellence and collaboration for implementing personalised medicine in Estonia - H2020 (2018) (3)
- Investigating gene expression profile of non-small cell lung cancer (2011) (3)
- Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation (2018) (3)
- Supplementary Material 6 (2014) (3)
- Data Related to Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) (3)
- 83 ANALYSIS OF CANDIDATE OSTEOARTHRITIS GENES IN A META-ANALYSIS OF 8 GENOME-WIDE ASSOCIATION STUDIES (2011) (3)
- Correction for Schumann et al., Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (2011) (3)
- Supplementary Material 5 (2014) (3)
- A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank (2020) (3)
- The incidence and characterization of phenylketonuric patients in Estonia (1996) (3)
- Supplementary Material 7 (2014) (3)
- The human ribosomal protein S6 gene: isolation, primary structure and location in chromosome 9. (1993) (3)
- Advances in Genomic Discovery and Implications for Personalized Prevention and Medicine: Estonia as Example (2021) (3)
- A dinucleotide repeat polymorphism at the ribosomal protein S6 (RPS6) gene. (1993) (3)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (3)
- An epigenome-wide association study of educational attainment (n = 10,767) (2017) (3)
- Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans (2021) (3)
- Supplementary Material 3 (2015) (3)
- Constraints on eQTL fine mapping in the presence of multi-site local regulation of gene expression (2016) (3)
- Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure (2020) (3)
- Arrayed Primer Extension Microarrays for Molecular Diagnostics (2010) (3)
- Ancient Haplotypes at the 15q24.2 Microdeletion Region Are Linked to Brain Expression of MAN2C1 and Children's Intelligence (2016) (3)
- Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility (2016) (2)
- Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
- 5 S RNA and 5.8 S RNA build up eukaryotic subribosomal domains active in tRNA binding (1981) (2)
- Interethnic analyses of blood pressure loci in populations of East Asian and European descent (2018) (2)
- Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney (2017) (2)
- Spectrum and frequency of CHEK2 variants in breast cancer affected and general population in the Baltic states region, initial results and literature review. (2022) (2)
- Neandertal introgression partitions the genetic landscape of neuropsychiatric disorders and associated behavioral phenotypes (2022) (2)
- Improved Imputation Accuracy of Rare and Low-Frequency Genetic Variants Using Population-Specific High-Coverage Whole-Genome Sequencing Data Based Imputation Reference Panel (2016) (2)
- Genome-wide study identifies association between HLA-B*55:01 and penicillin allergy (2020) (2)
- Genome-wide analysis of nuclear magnetic resonance metabolites revealed parent-of-origin effect on triglycerides in medium very low-density lipoprotein in PTPRD gene. (2018) (2)
- Genes, technology and public dialogue in Tartu, Estonia. (2002) (2)
- The genetic architecture of sporadic and recurrent miscarriage (2019) (2)
- Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (2)
- Mendelian Randomization Identifies the Potential Causal Impact of Dietary Patterns on Circulating Blood Metabolites (2020) (2)
- Correction: Genetic Structure of Europeans: A View from the North–East (2010) (2)
- Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error (2020) (1)
- Large scale trans-ethnic meta-analyses identify novel rare and common variants associated with blood pressure and hypertension (2016) (1)
- Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome (2022) (1)
- CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing (2014) (1)
- Multi-ancestry meta-analysis of host genetic susceptibility to tuberculosis identifies shared genetic architecture (2022) (1)
- Supplementary Material 4 (2015) (1)
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
- Supplementary Material 9 (2013) (1)
- Discovery and Refinement Supplementary (2015) (1)
- An interaction map of circulating metabolites, immune gene networks, and their genetic regulation (2017) (1)
- Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population (2023) (1)
- Supplementary Material 15 (2013) (1)
- ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma (2022) (1)
- Polygenic prediction of breast cancer: comparison of genetic predictors and implications for screening (2018) (1)
- Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes (2017) (1)
- Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (1)
- Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (1)
- Physical activity and sedentary behavior; mechanistic insights and role in disease prevention (2021) (1)
- Genetic influence on educational attainment and occupational status during and after the Soviet era in Estonia (2016) (1)
- Causal Effects of Adiposity on Cardiovascular Risk Factors (2015) (1)
- Human N-benzoyl-L-tyrosyl-p-aminobenzoic acid hydrolase (human meprin) : genomic structure of the α and β subunits (1)
- Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure (2023) (1)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
- University of Groningen A Genome-Wide Screen for Interactions Reveals a New Locus on 4 p 15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol (2011) (1)
- Autosomal genetic control of human gene expression does not differ across the sexes (2016) (1)
- Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2021) (1)
- Corrigendum: Rare coding variants and X-linked loci associated with age at menarche (2015) (1)
- Feitosa, M. F., & Levy, D. (2018). Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K (2018) (1)
- Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus (2020) (1)
- Ontogeny, distribution and potential roles of 5-hydroxymethylcytosine in human liver function (2013) (1)
- The role of adiposity in cardiometabolic traits (2013) (1)
- Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2021) (1)
- From Biobanking to Precision Medicine (2016) (1)
- Transcript expression-aware annotation improves rare variant interpretation (2020) (1)
- Global priorities for large-scale biomarker-based prospective cohorts (2022) (1)
- Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse (2022) (1)
- 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 (2019) (1)
- Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (2020) (1)
- Abstracts from the 52nd European Society of Human Genetics (ESHG) Conference: Oral Presentations (2019) (0)
- MARI NELIS Genetic structure of the Estonian population and genetic distance from other populations of European descent (2010) (0)
- Effectiveness and feasibility of cardiovascular disease personalized prevention on high polygenic risk score subjects: a randomized controlled pilot study (2022) (0)
- COVID-19 and Beyond: A Call for Action and Audacious Solidarity to All the Citizens and Nations, It Is Humanity’s Fight (2020) (0)
- Evaluating drug targets through human loss-of-function genetic variation (2020) (0)
- CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits (2017) (0)
- Author Correction: Evaluating drug targets through human loss-of-function genetic variation (2021) (0)
- Abstract: P868 A PROSTACYCLIN SYNTHASE (PTGIS) GENE POLYMORPHISM INCREASES RISK OF CORONARY ARTERY DISEASE (CAD) (2009) (0)
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) (0)
- Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (0)
- 621 GENETIC PREDISPOSITION AND ADHERENCE TO THE MEDITERRANEAN DIET IN CORONARY ARTERY DISEASE (2011) (0)
- Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (0)
- Access sequence analysis of nucleic acids by primer extension in parallel. (1994) (0)
- Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation. (2019) (0)
- Extensive alterations of the whole-blood transcriptome are associated with body mass index: results of an mRNA profiling study involving two large population-based cohorts (2015) (0)
- Publisher Correction: Identification of 371 genetic variants for age at first sex and birth linked to externalising behavior (2021) (0)
- Possible association of serotonin 1B receptor and cholecystolkinin 1 receptor gene polymorphisms in bipolar and unipolar affective disorder cases in Estonia (2002) (0)
- Circulating metabolic biomarkers of renal function in diabetic and non-diabetic populations (2018) (0)
- Correction: Methylation Markers of Early-Stage Non-Small Cell Lung Cancer (2017) (0)
- Hidden heritability due to heterogeneity across seven populations (2017) (0)
- OP-EHEA200570 1..9 (2020) (0)
- ResearchBRCA 1 mutations in women with familial or early-onset breast cancer and BRCA 2 mutations in familial cancer in Estonia (2015) (0)
- Universal and flexible DNA microarray approach: arrayed primer extension (1999) (0)
- Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response (2021) (0)
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2020) (0)
- Rare variant analyses across multiethnic cohorts identify novel genes for refractive error (2021) (0)
- Author Correction: Transcript expression-aware annotation improves rare variant interpretation (2021) (0)
- Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium (2015) (0)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (2018) (0)
- A structural variation reference for medical and population genetics (2020) (0)
- ESF Workshop on SNPs analysis , tools and applications 28-29 November , 2003 (2003) (0)
- FUNCTIONAL ACTIVITIES OF 5S RNA- AND 5.8S RNA-PROTEIN COMPLEXES IN EUKARYOTIC TRANSLATION (1981) (0)
- MS471 FIBRINOGEN BETA VARIANTS CONFER PROTECTION AGAINST CORONARY ARTERY DISEASE IN A GREEK CASE–CONTROL STUDY (2010) (0)
- Insights from the largest genetic study of sporadic and recurrent miscarriage (2019) (0)
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2018) (0)
- Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals (2018) (0)
- Peer Review Status: Peer reviewed Citation for item: (2012) (0)
- Abstract A06: Associations of prediagnostic metabolomic profiles with colorectal cancer risk—a collaborative reanalysis within the COnsortium of METabolomic Studies (COMETS) (2020) (0)
- Abstract 19854: Whole Genome Sequences and Plasma Lipids in 2,255 Participants (2016) (0)
- Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease (2020) (0)
- Gene-nutrition interactions that modify the risk of upper aero-digestive tract cancer. Screening results of a European multi-center case-control study (2010) (0)
- P460: Electroencephalography and clinical findings in a SCN8A epileptic encephalopathy: a case report (2014) (0)
- Meta-analysis identi fi es loci affecting levels of the potential osteoarthritis biomarkers sCOMP and uCTX-II with genome wide signi fi cance (2014) (0)
- Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years (2017) (0)
- Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications (2023) (0)
- Molecular diagnostics of Down syndrome using quantitative apex microarrays (2008) (0)
- Human basonuclin 2 up-regulates a cascade set of interferon-stimulated genes with anti-cancerous properties in a lung cancer model (2017) (0)
- A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine (2020) (0)
- Short sequence-paper A human cDNA encoding the homologue of NADH:ubiquinone oxidoreductase subunit B13 1 (1997) (0)
- Survey of Estonian Primary Care Physicians (2015) (0)
- Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta (2015) (0)
- Age at first birth in women is genetically associated with increased risk of schizophrenia (2018) (0)
- Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling (2017) (0)
- Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (0)
- Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical Setting (2022) (0)
- New insights into the biological role of COMMD 1 Bartuzi , Paulina (2014) (0)
- Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes (2018) (0)
- Genome-wide association study of obstructive sleep apnea in the Million Veteran Program uncovers genetic heterogeneity by sex (2022) (0)
- Do Biobank Recall Studies Matter? Long-Term Follow-Up of Research Participants With Familial Hypercholesterolemia (2022) (0)
- Molecular genetic overlap between migraine and major depressive disorder (2018) (0)
- P2-030: NSCLC gene expression study in Estonia (2007) (0)
- Genetic influence on social outcomes during and after the Soviet era in Estonia (2018) (0)
- Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels (2019) (0)
- Feasibility of innovative dietary assessment in epidemiological studies using the approach of combining different assessment instruments – Corrigendum (2011) (0)
- COVID-19 and beyond: a call for action and audacious solidarity to all the citizens and nations, it is humanity’s fight [version 1; peer review: 3 approved with reservations] (2021) (0)
- Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations (2018) (0)
- Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood (2017) (0)
- Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans (2021) (0)
- Practice Preferences for Neurosurgical Management in Spina Bifida : a survey of the American Society for Pediatric Neurosurgery (2017) (0)
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris. (2023) (0)
- Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records (2018) (0)
- Manhattan Harvester and Cropper: a system for GWAS peak detection (2019) (0)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture ofmajor depressive disorder (2018) (0)
- Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia (2018) (0)
- Detecting Lesch-Nyhan syndrome by solid phase primer extension (1994) (0)
- Abundance and distribution of hydroxymethylcytosine (5hmC) in human liver (2014) (0)
- Roadmap for a precision-medicine initiative in the Nordic region (2019) (0)
- Nature Genetics | Article (2015) (0)
- Genome-wide asociation study and meta-analysis in Northrn European populations replicate multiple colorectal cancer risk (2017) (0)
- The effect of LRRK2 loss-of-function variants in humans (2020) (0)
- POSTER VIEWING SESSION - REPRODUCTIVE (EPI) GENETICS (2011) (0)
- P.2.c.012 Serotonin transporter promoter polymorphism does not influence treatment response to escitalopram in depression (2008) (0)
- University of Groningen Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index Hoggart, (2014) (0)
- A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degeneration. (2023) (0)
- COVID-19 and beyond: a call for action and audacious solidarity to all the citizens and nations, it is humanity’s fight [version 1; peer review: awaiting peer review] (2020) (0)
- Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study (2022) (0)
- Meeting abstracts from the 10th International Conference on cGMP: Generators, Effectors and Therapeutic Implications (2023) (0)
- Investigation of the role of alcohol- metabolizing genes and DNA repair genes in the increase of levels of N2-ethylidenedeoxyguanosine (2008) (0)
- Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (0)
- Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank. (2022) (0)
- Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (0)
- Self-Other Agreement in Happiness and Life-Satisfaction: The Role of Personality Traits (2012) (0)
- A method and apparatus for imaging and analysis of biopolymer arrays (2000) (0)
- KAAREL KRJUTŠKOV Arrayed Primer Extension-2 as a multiplex PCR-based method for nucleic acid variation analysis: method and applications (2010) (0)
- GENOME-WIDE ANALYSIS IDENTIFIES SORCS3 AS A NOVEL SUSCEPTIBILITY LOCUS FOR PANIC DISORDER IN THE FINNGEN STUDY (2022) (0)
- A systematic study of hereditary pastic paraplegia in Estonia revealing new data (2010) (0)
- Imprinting landscape of human placenta as discovered by whole transcriptome RNA-sequencing and exome variant data analysis (2014) (0)
- Ageing with elegans: a research proposal to map healthspan pathways (2016) (0)
- Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns (2019) (0)
- The effect of X-linked dosage compensation on complex trait variation (2019) (0)
- Large population cohorts reveal unrecognized adult traits of the 16p11.2 CNV syndromes (2018) (0)
- [Conformational isomers of rat liver 5S ribosomal RNA]. (1978) (0)
- Functional characterization of GWAS loci associated with fracture risk (2013) (0)
- Editorial: Can population health be personalized? Estonia and Finland as examples (2022) (0)
- Author Correction: A structural variation reference for medical and population genetics (2021) (0)
- The effect of maternal sleep on epigenome of newborn (2015) (0)
- eQTLGen Consortium (2018). Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. (2018) (0)
- Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error (2018) (0)
- A Computational Linguistics Approach to the Identification of Biological Factors that Contribute to the Development and Progression of Lung Cancer (2011) (0)
- Discovery and validation of 107 blood pressure loci from UK Biobank offers novel biological insights into cardiovascular risk (2016) (0)
- Oligonucleotide Array for Mutation Analysis in Familial Breast Cancer (2002) (0)
- Identification of common genetic risk variants for autism spectrum disorder (2019) (0)
- HGV2009 meeting: bigger and better studies provide more answers and more questions (2010) (0)
- P.3.031 Association study of 90 candidategenetic polymorphisms in panic disorder: Positive findings with SNPs in serotonin, cholecystokinin and dopamine related genes (2004) (0)
- A bovine papillomavirus-1 based vector restores the function of the low-density lipoprotein receptor in the receptor-deficient CHO-ldlA7 cell line: Correction (2002) (0)
- Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2020) (0)
- Nucleic Acid Sequence Analysis BY THE WAY OF PARALLEL PRIMER EXTENSION (1994) (0)
- Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification (2019) (0)
- Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking Terracciano, A (0)
- Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa (2019) (0)
- Association analyses based on false discovery rate implicate 243 susceptibility loci for coronary artery disease (2017) (0)
- Genome-wide association and functional follow-up reveals new loci for kidney function | NOVA. The University of Newcastle's Digital Repository (2012) (0)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2020) (0)
- Correction: Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris. (2023) (0)
- Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of Item Response Theory (2014) (0)
- Bio-resources for sharing: which communities and what specific needs (2011) (0)
- Microarray analysis of gene expression in scrapie-infected neuroblastoma cells: Implication of oxidative stress (2007) (0)
- Asp 2213 Asn polymorphism is not associated with coronary artery disease in a Greek case-control study (2009) (0)
- Identifying pathways modulating sleep duration: from genomics to transcriptomics (2017) (0)
- VKučinskas-2001-2016 (2016) (0)
- 1 Subsequent Event Risk in Individuals with Established Coronary Heart Disease : Design and Rationale of the GENIUS-CHD Consortium Running title : (2019) (0)
- A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling (2017) (0)
- Author Correction: Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2021) (0)
- P202 – 2912: Methylenetetrahydrofolate reductase (MTHFR) polymorphisms A1298C and C677T as genetic risk factors for perinatal and childhood arterial ischemic stroke? (2015) (0)
- Retraction Note: Detection and replication of epistasis influencing transcription in humans (2021) (0)
- Microarrays and Single Nucleotide Polymorphism (SNP) Genotyping (2006) (0)
- P.3.05 Association and haplotype analaysis of90 single-nucleotide polymorphisms in mood disorders (2005) (0)
- Correction: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (0)
- Title Sequence variants and the risk of head and neck cancer : Pooledanalysis in the INHANCE consortium (2011) (0)
- Edinburgh Research Explorer Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index (2017) (0)
- Nordic Exome Variant Catalogue a Web Resource for Genomic Data Browsing (2018) (0)
- Genetic and modifiable risk factors combine multiplicatively in common disease (2022) (0)
- Analysis of single nucleotide polymorphisms in patients with mood disorders (2003) (0)
- Correction: Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2017) (0)
- The mutational constraint spectrum quantified from variation in 141,456 humans (2020) (0)
- Immobilisation of arrayed oligonucleotides for mutation detection by primer extension (2000) (0)
- The genetic basis of cross-phenotype correlation with bone fracture risk: the GEFOS consortium (2013) (0)
This paper list is powered by the following services:
Other Resources About Andres Metspalu
What Schools Are Affiliated With Andres Metspalu?
Andres Metspalu is affiliated with the following schools:
