| 1 | Distinct Genetic Risk Profile in Aortic Stenosis Compared With Coronary Artery Disease | 11.2 | 3 | Citations (PDF) |
| 2 | A large-scale genome-wide association study on female genital tract polyps highlights role of DNA repair, cell proliferation, and cell growth | 1.0 | 4 | Citations (PDF) |
| 3 | GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets | 13.7 | 35 | Citations (PDF) |
| 4 | Atlas of genetic and phenotypic associations across 42 female reproductive health diagnoses | 33.0 | 11 | Citations (PDF) |
| 5 | Bi-allelic MED16 variants cause a MEDopathy with intellectual disability, motor delay, and craniofacial, cardiac, and limb malformations | 6.5 | 3 | Citations (PDF) |
| 6 | The Estonian Biobank’s journey from biobanking to personalized medicine | 13.7 | 32 | Citations (PDF) |
| 7 | Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum | 25.2 | 9 | Citations (PDF) |
| 8 | Genome-wide analyses identify 30 loci associated with obsessive–compulsive disorder | 25.2 | 27 | Citations (PDF) |
| 9 | Pleiotropic and sex-specific genetic mechanisms of circulating metabolic markers | 13.7 | 3 | Citations (PDF) |
| 10 | Transcriptome analysis reveals involvement of thiopurine S-methyltransferase in oxidation-reduction processes | 4.3 | 1 | Citations (PDF) |
| 11 | Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes | 25.2 | 66 | Citations (PDF) |
| 12 | Rare copy-number variants as modulators of common disease susceptibility | 9.6 | 41 | Citations (PDF) |
| 13 | Genetic drivers of heterogeneity in type 2 diabetes pathophysiology | 37.9 | 383 | Citations (PDF) |
| 14 | Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry | 3.3 | 19 | Citations (PDF) |
| 15 | Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy | 25.2 | 19 | Citations (PDF) |
| 16 | Genetic determinants of plasma protein levels in the Estonian population | 3.4 | 7 | Citations (PDF) |
| 17 | Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits | 25.2 | 142 | Citations (PDF) |
| 18 | Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction | 25.2 | 40 | Citations (PDF) |
| 19 | Genetic drivers and cellular selection of female mosaic X chromosome loss | 37.9 | 32 | Citations (PDF) |
| 20 | SMIM1 absence is associated with reduced energy expenditure and excess weightMed, 2024, 5, 1083-1095.e6 | 7.0 | 5 | Citations (PDF) |
| 21 | Distinct genetic liability profiles define clinically relevant patient strata across common diseases | 13.7 | 6 | Citations (PDF) |
| 22 | Characterising the genetic architecture of changes in adiposity during adulthood using electronic health records | 13.7 | 11 | Citations (PDF) |
| 23 | Uncovering the shared genetic components of thyroid disorders and reproductive health | 4.0 | 5 | Citations (PDF) |
| 24 | A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disorders | 13.7 | 7 | Citations (PDF) |
| 25 | Genetic architecture reconciles linkage and association studies of complex traits | 25.2 | 10 | Citations (PDF) |
| 26 | High SHBG and Low Bioavailable Testosterone are Strongly Causally Associated with Increased Forearm Fracture Risk in Women: An MR Study Leveraging Novel Female-Specific Data | 2.8 | 0 | Citations (PDF) |
| 27 | Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations | 13.7 | 6 | Citations (PDF) |
| 28 | Use of Estonian Biobank data and participant recall to improve Wilson’s disease management | 3.0 | 1 | Citations (PDF) |
| 29 | Long-range regulatory effects of Neandertal DNA in modern humans | 4.2 | 6 | Citations (PDF) |
| 30 | Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure | 13.7 | 9 | Citations (PDF) |
| 31 | Rare variant analyses across multiethnic cohorts identify novel genes for refractive error | 4.4 | 7 | Citations (PDF) |
| 32 | FinnGen provides genetic insights from a well-phenotyped isolated population | 37.9 | 3,207 | Citations (PDF) |
| 33 | Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity | 6.0 | 25 | Citations (PDF) |
| 34 | Migraine, inflammatory bowel disease and celiac disease: A Mendelian randomization study | 3.0 | 10 | Citations (PDF) |
| 35 | 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 | 9.7 | 22 | Citations (PDF) |
| 36 | Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus | 9.1 | 38 | Citations (PDF) |
| 37 | Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris | 3.0 | 24 | Citations (PDF) |
| 38 | Genome-wide association study of obstructive sleep apnoea in the Million Veteran Program uncovers genetic heterogeneity by sex | 9.7 | 48 | Citations (PDF) |
| 39 | Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia | 3.6 | 10 | Citations (PDF) |
| 40 | Nationwide health, socio-economic and genetic predictors of COVID-19 vaccination status in Finland | 9.1 | 35 | Citations (PDF) |
| 41 | Dissecting the genetic heterogeneity of gastric cancer | 9.7 | 25 | Citations (PDF) |
| 42 | Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH | 7.6 | 10 | Citations (PDF) |
| 43 | Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions | 6.8 | 28 | Citations (PDF) |
| 44 | Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets | 23.6 | 609 | Citations (PDF) |
| 45 | European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation | 13.7 | 95 | Citations (PDF) |
| 46 | HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases | 4.4 | 22 | Citations (PDF) |
| 47 | Inferring compound heterozygosity from large-scale exome sequencing data | 25.2 | 27 | Citations (PDF) |
| 48 | A genomic mutational constraint map using variation in 76,156 human genomes | 37.9 | 1,024 | Citations (PDF) |
| 49 | Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders | 5.4 | 119 | Citations (PDF) |
| 50 | <i>Cis</i>-epistasis at the <i>LPA</i> locus and risk of cardiovascular diseases | 5.5 | 25 | Citations (PDF) |
| 51 | Identifying the Common Genetic Basis of Antidepressant Response | 2.7 | 107 | Citations (PDF) |
| 52 | Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors | 5.4 | 221 | Citations (PDF) |
| 53 | Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia | 12.4 | 92 | Citations (PDF) |
| 54 | Recessive variants in
<i>COL25A1</i>
gene as novel cause of arthrogryposis multiplex congenita with ocular congenital cranial dysinnervation disorder | 4.5 | 19 | Citations (PDF) |
| 55 | Impact of the pre-examination phase on multicenter metabolomic studies | 4.7 | 28 | Citations (PDF) |
| 56 | Elucidating the relationship between migraine risk and brain structure using genetic dataBrain, 2022, 145, 3214-3224 | 8.4 | 30 | Citations (PDF) |
| 57 | Gut metagenome associations with extensive digital health data in a volunteer-based Estonian microbiome cohort | 13.7 | 56 | Citations (PDF) |
| 58 | Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals | 25.2 | 536 | Citations (PDF) |
| 59 | Spectrum and frequency of CHEK2 variants in breast cancer affected and general population in the Baltic states region, initial results and literature review | 1.6 | 10 | Citations (PDF) |
| 60 | Whole-genome sequencing reveals host factors underlying critical COVID-19 | 37.9 | 298 | Citations (PDF) |
| 61 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia | 37.9 | 2,335 | Citations (PDF) |
| 62 | The individual and global impact of copy-number variants on complex human traits | 6.5 | 79 | Citations (PDF) |
| 63 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation | 25.2 | 616 | Citations (PDF) |
| 64 | Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss | 6.5 | 65 | Citations (PDF) |
| 65 | Cochlear nerve deficiency in <scp><i>SOX11</i></scp>‐related <scp>Coffin‐Siris</scp> syndrome | 1.6 | 7 | Citations (PDF) |
| 66 | Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse | 13.7 | 31 | Citations (PDF) |
| 67 | Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals | 4.4 | 31 | Citations (PDF) |
| 68 | Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome | 7.8 | 19 | Citations (PDF) |
| 69 | Do Biobank Recall Studies Matter? Long-Term Follow-Up of Research Participants With Familial Hypercholesterolemia | 2.3 | 8 | Citations (PDF) |
| 70 | Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical Setting | 2.3 | 11 | Citations (PDF) |
| 71 | Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis | 4.4 | 15 | Citations (PDF) |
| 72 | Genetic and modifiable risk factors combine multiplicatively in common disease | 2.8 | 19 | Citations (PDF) |
| 73 | A cross-disorder dosage sensitivity map of the human genomeCell, 2022, 185, 3041-3055.e25 | 33.7 | 313 | Citations (PDF) |
| 74 | Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention | 25.2 | 196 | Citations (PDF) |
| 75 | Stroke genetics informs drug discovery and risk prediction across ancestries | 37.9 | 489 | Citations (PDF) |
| 76 | Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank | 3.0 | 16 | Citations (PDF) |
| 77 | Neandertal introgression partitions the genetic landscape of neuropsychiatric disorders and associated behavioral phenotypes | 5.2 | 19 | Citations (PDF) |
| 78 | ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma | 4.4 | 20 | Citations (PDF) |
| 79 | A saturated map of common genetic variants associated with human height | 37.9 | 687 | Citations (PDF) |
| 80 | Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study | 6.6 | 32 | Citations (PDF) |
| 81 | Prioritizing autoimmunity risk variants for functional analyses by fine-mapping mutations under natural selection | 13.7 | 12 | Citations (PDF) |
| 82 | Effectiveness and feasibility of cardiovascular disease personalized prevention on high polygenic risk score subjects: a randomized controlled pilot study | 2.5 | 20 | Citations (PDF) |
| 83 | Genetic diversity fuels gene discovery for tobacco and alcohol use | 37.9 | 410 | Citations (PDF) |
| 84 | Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies | 2.6 | 54 | Citations (PDF) |
| 85 | Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability | 13.7 | 132 | Citations (PDF) |
| 86 | Model-based assessment of replicability for genome-wide association meta-analysis | 13.7 | 36 | Citations (PDF) |
| 87 | Novel variants in TUBA1A cause congenital fibrosis of the extraocular muscles with or without malformations of cortical brain development | 3.0 | 25 | Citations (PDF) |
| 88 | Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure | 7.8 | 22 | Citations (PDF) |
| 89 | Advances in Genomic Discovery and Implications for Personalized Prevention and Medicine: Estonia as Example | 2.4 | 14 | Citations (PDF) |
| 90 | The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects | 6.5 | 62 | Citations (PDF) |
| 91 | A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts | 5.4 | 182 | Citations (PDF) |
| 92 | Stratification of Type 2 Diabetes by Age of Diagnosis in the UK Biobank Reveals Subgroup-Specific Genetic Associations and Causal Risk Profiles | 4.2 | 29 | Citations (PDF) |
| 93 | The trans-ancestral genomic architecture of glycemic traits | 25.2 | 650 | Citations (PDF) |
| 94 | Genome-wide association study identifies five risk loci for pernicious anemia | 13.7 | 52 | Citations (PDF) |
| 95 | Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia | 6.1 | 47 | Citations (PDF) |
| 96 | Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients | 2.2 | 7 | Citations (PDF) |
| 97 | Mapping the human genetic architecture of COVID-19 | 37.9 | 871 | Citations (PDF) |
| 98 | Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour | 9.1 | 140 | Citations (PDF) |
| 99 | Genetic insights into biological mechanisms governing human ovarian ageing | 37.9 | 343 | Citations (PDF) |
| 100 | Metabolomic Fingerprints in Large Population Cohorts: Impact of Preanalytical Heterogeneity | 1.1 | 13 | Citations (PDF) |
| 101 | Phantom epistasis between unlinked loci | 37.9 | 32 | Citations (PDF) |
| 102 | The blood metabolome of incident kidney cancer: A case–control study nested within the MetKid consortium | 8.1 | 35 | Citations (PDF) |
| 103 | Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation | 25.2 | 436 | Citations (PDF) |
| 104 | The Genetic Architecture of Depression in Individuals of East Asian Ancestry | 12.4 | 169 | Citations (PDF) |
| 105 | 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 | 62.3 | 2,827 | Citations (PDF) |
| 106 | Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome | 13.7 | 111 | Citations (PDF) |
| 107 | A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response | 25.2 | 153 | Citations (PDF) |
| 108 | Mendelian Randomization Identifies the Potential Causal Impact of Dietary Patterns on Circulating Blood Metabolites | 2.3 | 10 | Citations (PDF) |
| 109 | SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues | 6.3 | 37 | Citations (PDF) |
| 110 | Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression | 5.4 | 34 | Citations (PDF) |
| 111 | The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls | 5.4 | 191 | Citations (PDF) |
| 112 | Development and validation of two SCORE-based cardiovascular risk prediction models for Eastern Europe: a multicohort study | 2.2 | 24 | Citations (PDF) |
| 113 | The genetic architecture of sporadic and multiple consecutive miscarriage | 13.7 | 97 | Citations (PDF) |
| 114 | Differences in local population history at the finest level: the case of the Estonian population | 3.0 | 40 | Citations (PDF) |
| 115 | Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus | 2.9 | 10 | Citations (PDF) |
| 116 | An epigenome-wide association study of metabolic syndrome and its components | 3.4 | 40 | Citations (PDF) |
| 117 | Cerebral small vessel disease genomics and its implications across the lifespan | 13.7 | 179 | Citations (PDF) |
| 118 | Habitual sleep disturbances and migraine: a Mendelian randomization study | 3.8 | 36 | Citations (PDF) |
| 119 | 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 | 62.3 | 343 | Citations (PDF) |
| 120 | Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci | 7.8 | 23 | Citations (PDF) |
| 121 | A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank | 13.7 | 112 | Citations (PDF) |
| 122 | Evaluating drug targets through human loss-of-function genetic variation | 37.9 | 167 | Citations (PDF) |
| 123 | The mutational constraint spectrum quantified from variation in 141,456 humans | 37.9 | 8,804 | Citations (PDF) |
| 124 | Integrating untargeted metabolomics, genetically informed causal inference, and pathway enrichment to define the obesity metabolome | 3.0 | 26 | Citations (PDF) |
| 125 | Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals | 13.7 | 151 | Citations (PDF) |
| 126 | Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes | 13.7 | 125 | Citations (PDF) |
| 127 | A structural variation reference for medical and population genetics | 37.9 | 921 | Citations (PDF) |
| 128 | Transcript expression-aware annotation improves rare variant interpretation | 37.9 | 182 | Citations (PDF) |
| 129 | The effect of LRRK2 loss-of-function variants in humans | 33.0 | 105 | Citations (PDF) |
| 130 | Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness | 4.2 | 97 | Citations (PDF) |
| 131 | Personalized early detection and prevention of breast cancer: ENVISION consensus statement | 70.8 | 331 | Citations (PDF) |
| 132 | Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error | 4.4 | 35 | Citations (PDF) |
| 133 | Association of polygenic score for major depression with response to lithium in patients with bipolar disorder | 7.8 | 72 | Citations (PDF) |
| 134 | A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine | 13.7 | 78 | Citations (PDF) |
| 135 | Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length | 6.5 | 162 | Citations (PDF) |
| 136 | Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank | 7.8 | 178 | Citations (PDF) |
| 137 | Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease | 25.2 | 343 | Citations (PDF) |
| 138 | Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache | 4.9 | 46 | Citations (PDF) |
| 139 | Genome-wide association study identifies 48 common genetic variants associated with handedness | 9.1 | 126 | Citations (PDF) |
| 140 | Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants | 3.0 | 36 | Citations (PDF) |
| 141 | Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy | 6.5 | 54 | Citations (PDF) |
| 142 | Identification of ALK in ThinnessCell, 2020, 181, 1246-1262.e22 | 33.7 | 103 | Citations (PDF) |
| 143 | COVID-19 and beyond: a call for action and audacious solidarity to all the citizens and nations, it is humanity’s fight | 0.5 | 3 | Citations (PDF) |
| 144 | Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant | 1.6 | 17 | Citations (PDF) |
| 145 | A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individuals | 13.7 | 295 | Citations (PDF) |
| 146 | Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium | 3.4 | 17 | Citations (PDF) |
| 147 | Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa | 25.2 | 987 | Citations (PDF) |
| 148 | The effect of X-linked dosage compensation on complex trait variation | 13.7 | 66 | Citations (PDF) |
| 149 | Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression | 7.8 | 131 | Citations (PDF) |
| 150 | Associations of autozygosity with a broad range of human phenotypes | 13.7 | 117 | Citations (PDF) |
| 151 | Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration | 13.7 | 82 | Citations (PDF) |
| 152 | Leveraging European infrastructures to access 1 million human genomes by 2022 | 47.0 | 83 | Citations (PDF) |
| 153 | Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels | 25.2 | 363 | Citations (PDF) |
| 154 | Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions | 3.3 | 110 | Citations (PDF) |
| 155 | Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity | 13.7 | 84 | Citations (PDF) |
| 156 | Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation | 4.2 | 31 | Citations (PDF) |
| 157 | A catalog of genetic loci associated with kidney function from analyses of a million individuals | 25.2 | 796 | Citations (PDF) |
| 158 | Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics | 2.5 | 25 | Citations (PDF) |
| 159 | Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns | 13.7 | 126 | Citations (PDF) |
| 160 | Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification | 2.9 | 48 | Citations (PDF) |
| 161 | Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches | 5.4 | 61 | Citations (PDF) |
| 162 | Subsequent Event Risk in Individuals With Established Coronary Heart Disease | 2.9 | 19 | Citations (PDF) |
| 163 | Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events | 2.9 | 30 | Citations (PDF) |
| 164 | Genome-wide association study identifies 30 loci associated with bipolar disorder | 25.2 | 1,478 | Citations (PDF) |
| 165 | Genetic Overlap Between Alzheimer’s Disease and Bipolar Disorder Implicates the MARK2 and VAC14 Genes | 2.7 | 56 | Citations (PDF) |
| 166 | A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure | 2.9 | 44 | Citations (PDF) |
| 167 | Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids | 25.2 | 133 | Citations (PDF) |
| 168 | Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia | 1.5 | 4 | Citations (PDF) |
| 169 | Improved polygenic prediction by Bayesian multiple regression on summary statistics | 13.7 | 473 | Citations (PDF) |
| 170 | Application of non-HDL cholesterol for population-based cardiovascular risk stratification: results from the Multinational Cardiovascular Risk Consortium | 62.3 | 247 | Citations (PDF) |
| 171 | Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric DisordersCell, 2019, 179, 1469-1482.e11 | 33.7 | 1,304 | Citations (PDF) |
| 172 | Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank | 1.2 | 18 | Citations (PDF) |
| 173 | Estimating the performance of three cardiovascular disease risk scores: the Estonian Biobank cohort study | 2.9 | 7 | Citations (PDF) |
| 174 | PAIRUP-MS: Pathway analysis and imputation to relate unknowns in profiles from mass spectrometry-based metabolite data | 3.1 | 20 | Citations (PDF) |
| 175 | Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection | 2.3 | 180 | Citations (PDF) |
| 176 | Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use | 25.2 | 1,819 | Citations (PDF) |
| 177 | Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use | 5.4 | 84 | Citations (PDF) |
| 178 | Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia | 4.2 | 47 | Citations (PDF) |
| 179 | Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci | 7.8 | 107 | Citations (PDF) |
| 180 | Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders | 7.8 | 46 | Citations (PDF) |
| 181 | Signatures of negative selection in the genetic architecture of human complex traits | 25.2 | 402 | Citations (PDF) |
| 182 | Genetic influence on social outcomes during and after the Soviet era in Estonia | 9.1 | 104 | Citations (PDF) |
| 183 | Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes | 25.2 | 429 | Citations (PDF) |
| 184 | A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure | 6.5 | 156 | Citations (PDF) |
| 185 | Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression | 25.2 | 2,886 | Citations (PDF) |
| 186 | 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 | 4.9 | 76 | Citations (PDF) |
| 187 | Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland | 6.5 | 67 | Citations (PDF) |
| 188 | Genome‐wide association study and meta‐analysis in Northern European populations replicate multiple colorectal cancer risk loci | 4.3 | 30 | Citations (PDF) |
| 189 | Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium | 5.4 | 112 | Citations (PDF) |
| 190 | Interethnic analyses of blood pressure loci in populations of East Asian and European descent | 13.7 | 108 | Citations (PDF) |
| 191 | Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps | 25.2 | 1,673 | Citations (PDF) |
| 192 | Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations | 8.1 | 103 | Citations (PDF) |
| 193 | Circulating metabolic biomarkers of renal function in diabetic and non-diabetic populations | 3.4 | 54 | Citations (PDF) |
| 194 | Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder | 4.4 | 20 | Citations (PDF) |
| 195 | Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits | 25.2 | 1,300 | Citations (PDF) |
| 196 | Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error | 25.2 | 324 | Citations (PDF) |
| 197 | Age at first birth in women is genetically associated with increased risk of schizophrenia | 3.4 | 20 | Citations (PDF) |
| 198 | Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals | 25.2 | 2,406 | Citations (PDF) |
| 199 | Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes | 13.7 | 770 | Citations (PDF) |
| 200 | Analysis of shared heritability in common disorders of the brain | 36.2 | 1,340 | Citations (PDF) |
| 201 | Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries | 13.7 | 105 | Citations (PDF) |
| 202 | Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 SubphenotypesCell, 2018, 173, 1705-1715.e16 | 33.7 | 755 | Citations (PDF) |
| 203 | Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood | 13.7 | 408 | Citations (PDF) |
| 204 | Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries | 2.3 | 114 | Citations (PDF) |
| 205 | Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records | 3.0 | 40 | Citations (PDF) |
| 206 | Genetic evidence of assortative mating in humans | 9.1 | 308 | Citations (PDF) |
| 207 | Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk | 25.2 | 573 | Citations (PDF) |
| 208 | Rare and low-frequency coding variants alter human adult height | 37.9 | 612 | Citations (PDF) |
| 209 | DNA breaks and chromatin structural changes enhance the transcription of autoimmune regulator target genes | 2.2 | 63 | Citations (PDF) |
| 210 | Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease | 2.3 | 243 | Citations (PDF) |
| 211 | Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel | 3.0 | 247 | Citations (PDF) |
| 212 | Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk | 25.2 | 514 | Citations (PDF) |
| 213 | Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa | 8.8 | 512 | Citations (PDF) |
| 214 | Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits | 13.7 | 198 | Citations (PDF) |
| 215 | 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function | 3.4 | 108 | Citations (PDF) |
| 216 | A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling | 3.4 | 30 | Citations (PDF) |
| 217 | Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants | 13.7 | 333 | Citations (PDF) |
| 218 | An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans | 4.2 | 717 | Citations (PDF) |
| 219 | A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk | 4.2 | 51 | Citations (PDF) |
| 220 | Genetic correlation between amyotrophic lateral sclerosis and schizophrenia | 13.7 | 140 | Citations (PDF) |
| 221 | SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function | 0.4 | 44 | Citations (PDF) |
| 222 | Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms | 7.5 | 45 | Citations (PDF) |
| 223 | An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype | 5.4 | 91 | Citations (PDF) |
| 224 | The Genetic Architecture of Gene Expression in Peripheral Blood | 6.5 | 224 | Citations (PDF) |
| 225 | Exome-wide association study of plasma lipids in >300,000 individuals | 25.2 | 543 | Citations (PDF) |
| 226 | CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits | 13.7 | 85 | Citations (PDF) |
| 227 | 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 | 62.3 | 6,316 | Citations (PDF) |
| 228 | Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity | 13.7 | 163 | Citations (PDF) |
| 229 | Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis | 17.9 | 237 | Citations (PDF) |
| 230 | Hidden heritability due to heterogeneity across seven populations | 9.1 | 158 | Citations (PDF) |
| 231 | Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood | 13.7 | 25 | Citations (PDF) |
| 232 | Exome analysis in an Estonian multiplex family with neural tube defects—a case report | 0.9 | 7 | Citations (PDF) |
| 233 | Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney | 6.6 | 143 | Citations (PDF) |
| 234 | Association analyses based on false discovery rate implicate new loci for coronary artery disease | 25.2 | 679 | Citations (PDF) |
| 235 | Constraints on eQTL Fine Mapping in the Presence of Multisite Local Regulation of Gene Expression | 1.9 | 27 | Citations (PDF) |
| 236 | Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes | 3.4 | 63 | Citations (PDF) |
| 237 | Genotype–covariate interaction effects and the heritability of adult body mass index | 25.2 | 159 | Citations (PDF) |
| 238 | Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness | 13.7 | 192 | Citations (PDF) |
| 239 | Identifying pathways modulating sleep duration: from genomics to transcriptomics | 3.4 | 10 | Citations (PDF) |
| 240 | Human basonuclin 2 up-regulates a cascade set of interferon-stimulated genes with anti-cancerous properties in a lung cancer model | 5.3 | 11 | Citations (PDF) |
| 241 | Worldwide trends in blood pressure from 1975 to 2015: a pooled analysis of 1479 population-based measurement studies with 19·1 million participants | 62.3 | 2,027 | Citations (PDF) |
| 242 | Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores | 4.2 | 145 | Citations (PDF) |
| 243 | Sequence data and association statistics from 12,940 type 2 diabetes cases and controls | 5.7 | 36 | Citations (PDF) |
| 244 | Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts | 2.3 | 20 | Citations (PDF) |
| 245 | Pathogenic implications for autoimmune mechanisms derived by comparative eQTL analysis of CD4+ versus CD8+ T cells | 3.2 | 129 | Citations (PDF) |
| 246 | An interaction map of circulating metabolites, immune gene networks, and their genetic regulation | 8.1 | 56 | Citations (PDF) |
| 247 | Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults | 3.2 | 181 | Citations (PDF) |
| 248 | Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions | 3.2 | 30 | Citations (PDF) |
| 249 | MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies | 2.3 | 9 | Citations (PDF) |
| 250 | The genetic architecture of type 2 diabetes | 37.9 | 1,051 | Citations (PDF) |
| 251 | Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits | 6.5 | 66 | Citations (PDF) |
| 252 | Sequence variation in nuclear ribosomal small subunit, internal transcribed spacer and large subunit regions of <i>Rhizophagus irregularis</i> and <i>Gigaspora margarita</i> is high and isolate‐dependent | 3.7 | 72 | Citations (PDF) |
| 253 | Coding Variation in<i>ANGPTL4,</i><i>LPL,</i>and<i>SVEP1</i>and the Risk of Coronary Disease | 34.6 | 481 | Citations (PDF) |
| 254 | Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses | 25.2 | 1,005 | Citations (PDF) |
| 255 | Genetic variants in RBFOX3 are associated with sleep latency | 3.0 | 33 | Citations (PDF) |
| 256 | Imprinted Genes and Imprinting Control Regions Show Predominant Intermediate Methylation in Adult Somatic Tissues | 2.2 | 46 | Citations (PDF) |
| 257 | Genome-wide association study identifies 74 loci associated with educational attainment | 37.9 | 1,361 | Citations (PDF) |
| 258 | Whole-genome expression analysis reveals genes associated with treatment response to escitalopram in major depression | 1.0 | 26 | Citations (PDF) |
| 259 | Ultra-rare disruptive and damaging mutations influence educational attainment in the general population | 17.0 | 108 | Citations (PDF) |
| 260 | A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape | 13.7 | 90 | Citations (PDF) |
| 261 | Genomic analyses inform on migration events during the peopling of Eurasia | 37.9 | 414 | Citations (PDF) |
| 262 | 52 Genetic Loci Influencing Myocardial Mass | 2.3 | 132 | Citations (PDF) |
| 263 | Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension | 25.2 | 298 | Citations (PDF) |
| 264 | The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals | 25.2 | 410 | Citations (PDF) |
| 265 | No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis | 3.4 | 30 | Citations (PDF) |
| 266 | Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error | 13.7 | 128 | Citations (PDF) |
| 267 | Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA | 13.7 | 745 | Citations (PDF) |
| 268 | Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium | 3.4 | 93 | Citations (PDF) |
| 269 | The Role of the Five–factor Personality Traits in General Self–rated Health | 2.9 | 27 | Citations (PDF) |
| 270 | Genome-wide analysis identifies 12 loci influencing human reproductive behavior | 25.2 | 323 | Citations (PDF) |
| 271 | Genetic variants linked to education predict longevity | 7.5 | 125 | Citations (PDF) |
| 272 | Autosomal genetic control of human gene expression does not differ across the sexes | 8.1 | 17 | Citations (PDF) |
| 273 | Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participants | 1.3 | 15 | Citations (PDF) |
| 274 | Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine | 25.2 | 632 | Citations (PDF) |
| 275 | Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals | 6.5 | 90 | Citations (PDF) |
| 276 | Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases | 6.5 | 58 | Citations (PDF) |
| 277 | The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition | 5.4 | 89 | Citations (PDF) |
| 278 | De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion | 0.7 | 9 | Citations (PDF) |
| 279 | Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease | 36.2 | 506 | Citations (PDF) |
| 280 | Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women | 12.4 | 59 | Citations (PDF) |
| 281 | Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function | 13.7 | 493 | Citations (PDF) |
| 282 | Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci | 25.2 | 728 | Citations (PDF) |
| 283 | Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities | 12.4 | 239 | Citations (PDF) |
| 284 | Epigenetic profiling in CD4+ and CD8+ T cells from Graves' disease patients reveals changes in genes associated with T cell receptor signaling | 6.6 | 108 | Citations (PDF) |
| 285 | Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index | 7.8 | 70 | Citations (PDF) |
| 286 | Metabolites of milk intake: a metabolomic approach in UK twins with findings replicated in two European cohorts | 3.4 | 32 | Citations (PDF) |
| 287 | Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects | 25.2 | 1,026 | Citations (PDF) |
| 288 | Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci | 3.2 | 374 | Citations (PDF) |
| 289 | Ancient Haplotypes at the 15q24.2 Microdeletion Region Are Linked to Brain Expression of MAN2C1 and Children's Intelligence | 2.3 | 3 | Citations (PDF) |
| 290 | 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 | 1.7 | 45 | Citations (PDF) |
| 291 | Age-related profiling of DNA methylation in CD8+ T cells reveals changes in immune response and transcriptional regulator genes | 3.4 | 179 | Citations (PDF) |
| 292 | The relationship between the Five‐Factor Model personality traits and peptic ulcer disease in a large population‐based adult sample | 2.0 | 12 | Citations (PDF) |
| 293 | Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair | 0.5 | 0 | Citations (PDF) |
| 294 | Linking a Population Biobank with National Health Registries—The Estonian Experience | 2.4 | 64 | Citations (PDF) |
| 295 | Haplotype Phasing and Inheritance of Copy Number Variants in Nuclear Families | 2.3 | 9 | Citations (PDF) |
| 296 | The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study | 3.2 | 393 | Citations (PDF) |
| 297 | Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation | 3.2 | 84 | Citations (PDF) |
| 298 | Adiposity as a cause of cardiovascular disease: a Mendelian randomization study | 4.9 | 136 | Citations (PDF) |
| 299 | Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder | 12.4 | 320 | Citations (PDF) |
| 300 | Copy Number Variations and Cognitive Phenotypes in Unselected Populations | 16.6 | 173 | Citations (PDF) |
| 301 | Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci | 13.7 | 174 | Citations (PDF) |
| 302 | Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels | 13.7 | 209 | Citations (PDF) |
| 303 | Rare coding variants and X-linked loci associated with age at menarche | 13.7 | 39 | Citations (PDF) |
| 304 | Genetic variants of inducible costimulator are associated with allergic asthma susceptibility | 6.1 | 4 | Citations (PDF) |
| 305 | New genetic loci link adipose and insulin biology to body fat distribution | 37.9 | 1,561 | Citations (PDF) |
| 306 | Genetic studies of body mass index yield new insights for obesity biology | 37.9 | 4,431 | Citations (PDF) |
| 307 | Dominance Genetic Variation Contributes Little to the Missing Heritability for Human Complex Traits | 6.5 | 217 | Citations (PDF) |
| 308 | Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu | 4.9 | 444 | Citations (PDF) |
| 309 | Age- and Sex-Specific Causal Effects of Adiposity on Cardiovascular Risk Factors | 4.2 | 71 | Citations (PDF) |
| 310 | Cell Specific eQTL Analysis without Sorting Cells | 3.2 | 129 | Citations (PDF) |
| 311 | Directional dominance on stature and cognition in diverse human populations | 37.9 | 198 | Citations (PDF) |
| 312 | Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity | 25.2 | 138 | Citations (PDF) |
| 313 | A Meta-analysis of Gene Expression Signatures of Blood Pressure and Hypertension | 3.2 | 125 | Citations (PDF) |
| 314 | The impact of low-frequency and rare variants on lipid levels | 25.2 | 347 | Citations (PDF) |
| 315 | A recent bottleneck of Y chromosome diversity coincides with a global change in culture | 4.6 | 423 | Citations (PDF) |
| 316 | Genetically Determined Height and Coronary Artery Disease | 34.6 | 244 | Citations (PDF) |
| 317 | Complementary seminovaginal microbiome in couples | 3.0 | 210 | Citations (PDF) |
| 318 | Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores | 6.5 | 1,332 | Citations (PDF) |
| 319 | Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair | 25.2 | 417 | Citations (PDF) |
| 320 | Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia | 2.8 | 16 | Citations (PDF) |
| 321 | Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation | 25.2 | 335 | Citations (PDF) |
| 322 | Genome-wide genetic homogeneity between sexes and populations for human height and body mass index | 2.9 | 75 | Citations (PDF) |
| 323 | The transcriptional landscape of age in human peripheral blood | 13.7 | 686 | Citations (PDF) |
| 324 | Effects of Metformin on Metabolite Profiles and LDL Cholesterol in Patients With Type 2 Diabetes | 6.2 | 118 | Citations (PDF) |
| 325 | Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index | 25.2 | 809 | Citations (PDF) |
| 326 | Population genetic differentiation of height and body mass index across Europe | 25.2 | 243 | Citations (PDF) |
| 327 | A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease | 25.2 | 2,461 | Citations (PDF) |
| 328 | Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci | 25.2 | 408 | Citations (PDF) |
| 329 | Harmonising and linking biomedical and clinical data across disparate data archives to enable integrative cross-biobank research | 3.0 | 31 | Citations (PDF) |
| 330 | Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium | 1.3 | 207 | Citations (PDF) |
| 331 | Within-Trait Heterogeneity in Age Group Differences in Personality Domains and Facets: Implications for the Development and Coherence of Personality Traits | 2.3 | 43 | Citations (PDF) |
| 332 | Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans | 2.3 | 71 | Citations (PDF) |
| 333 | Mapping the Genetic Architecture of Gene Regulation in Whole Blood | 2.3 | 32 | Citations (PDF) |
| 334 | <i>De Novo</i><i>SCN8A</i> Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy, Multiple Congenital Anomalies, and Movement Disorders | 1.6 | 63 | Citations (PDF) |
| 335 | From Pharmacogenetics to Pharmacometabolomics: SAM Modulates TPMT Activity | 1.5 | 24 | Citations (PDF) |
| 336 | Meta-analysis identifies loci affecting levels of the potential osteoarthritis biomarkers sCOMP and uCTX-II with genome wide significance | 3.8 | 22 | Citations (PDF) |
| 337 | Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index | 3.2 | 85 | Citations (PDF) |
| 338 | Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population | 3.2 | 387 | Citations (PDF) |
| 339 | Assessment of Osteoarthritis Candidate Genes in a Meta‐Analysis of Nine Genome‐Wide Association Studies | 6.2 | 116 | Citations (PDF) |
| 340 | A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip | 6.9 | 113 | Citations (PDF) |
| 341 | Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta | 3.0 | 80 | Citations (PDF) |
| 342 | Occupational irritants and asthma: an Estonian cross-sectional study of 34 000 adults | 8.7 | 25 | Citations (PDF) |
| 343 | Leukocyte telomere length associates with prospective mortality independent of immune-related parameters and known genetic markers | 4.9 | 99 | Citations (PDF) |
| 344 | DNA mismatch repair gene MSH6 implicated in determining age at natural menopause | 2.9 | 65 | Citations (PDF) |
| 345 | Biomarker Profiling by Nuclear Magnetic Resonance Spectroscopy for the Prediction of All-Cause Mortality: An Observational Study of 17,345 Persons | 8.1 | 342 | Citations (PDF) |
| 346 | Copper Metabolism Domain-Containing 1 Represses Genes That Promote Inflammation and Protects Mice From Colitis and Colitis-Associated Cancer | 0.9 | 41 | Citations (PDF) |
| 347 | The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studies | 2.9 | 519 | Citations (PDF) |
| 348 | A Common 16p11.2 Inversion Underlies the Joint Susceptibility to Asthma and Obesity | 6.5 | 70 | Citations (PDF) |
| 349 | Chronotype and sleep duration: The influence of season of assessment | 1.9 | 139 | Citations (PDF) |
| 350 | Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis | 13.7 | 244 | Citations (PDF) |
| 351 | Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases | 6.5 | 627 | Citations (PDF) |
| 352 | A metabolic view on menopause and ageing | 13.7 | 249 | Citations (PDF) |
| 353 | Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche | 37.9 | 620 | Citations (PDF) |
| 354 | Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age | 2.9 | 257 | Citations (PDF) |
| 355 | Defining the role of common variation in the genomic and biological architecture of adult human height | 25.2 | 1,965 | Citations (PDF) |
| 356 | Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of Item Response Theory | 1.3 | 115 | Citations (PDF) |
| 357 | Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility | 25.2 | 1,030 | Citations (PDF) |
| 358 | Sex- and age-interacting eQTLs in human complex diseases | 2.9 | 78 | Citations (PDF) |
| 359 | Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer | 25.2 | 423 | Citations (PDF) |
| 360 | Oral health, dental care and mouthwash associated with upper aerodigestive tract cancer risk in Europe: The ARCAGE study | 2.4 | 109 | Citations (PDF) |
| 361 | BBMRI-ERIC as a resource for pharmaceutical and life science industries: the development of biobank-based Expert Centres | 3.0 | 79 | Citations (PDF) |
| 362 | Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption | 7.8 | 266 | Citations (PDF) |
| 363 | Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics | 6.5 | 65 | Citations (PDF) |
| 364 | Discovery and refinement of loci associated with lipid levels | 25.2 | 2,993 | Citations (PDF) |
| 365 | Common variants associated with plasma triglycerides and risk for coronary artery disease | 25.2 | 833 | Citations (PDF) |
| 366 | Systematic identification of trans eQTLs as putative drivers of known disease associations | 25.2 | 1,672 | Citations (PDF) |
| 367 | Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error | 6.5 | 154 | Citations (PDF) |
| 368 | Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function | 0.4 | 35 | Citations (PDF) |
| 369 | Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia | 25.2 | 439 | Citations (PDF) |
| 370 | Identification of seven loci affecting mean telomere length and their association with disease | 25.2 | 901 | Citations (PDF) |
| 371 | Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture | 25.2 | 645 | Citations (PDF) |
| 372 | Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders | 25.2 | 308 | Citations (PDF) |
| 373 | Meta‐analysis of microRNA expression in lung cancer | 4.3 | 200 | Citations (PDF) |
| 374 | Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course | 2.9 | 126 | Citations (PDF) |
| 375 | The <i>DOT1L</i> rs12982744 polymorphism is associated with osteoarthritis of the hip with genome-wide statistical significance in males | 6.9 | 54 | Citations (PDF) |
| 376 | Human Disease-Associated Genetic Variation Impacts Large Intergenic Non-Coding RNA Expression | 3.2 | 264 | Citations (PDF) |
| 377 | Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits | 3.2 | 416 | Citations (PDF) |
| 378 | The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis | 8.1 | 192 | Citations (PDF) |
| 379 | A genome-wide association study of early menopause and the combined impact of identified variants | 2.9 | 119 | Citations (PDF) |
| 380 | Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent | 3.3 | 57 | Citations (PDF) |
| 381 | In-solution hybrid capture of bisulfite-converted DNA for targeted bisulfite sequencing of 174 ADME genes | 15.5 | 43 | Citations (PDF) |
| 382 | Whole-exome sequencing identifies a polymorphism in the BMP5 gene associated with SSRI treatment response in major depression | 4.8 | 32 | Citations (PDF) |
| 383 | Genetics of rheumatoid arthritis contributes to biology and drug discovery | 37.9 | 2,269 | Citations (PDF) |
| 384 | Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity | 2.3 | 36 | Citations (PDF) |
| 385 | A Genome-Wide Analysis of Populations from European Russia Reveals a New Pole of Genetic Diversity in Northern Europe | 2.3 | 38 | Citations (PDF) |
| 386 | Personality traits and eating habits in a large sample of Estonians. | 1.6 | 110 | Citations (PDF) |
| 387 | Evidence of Inbreeding Depression on Human Height | 3.2 | 93 | Citations (PDF) |
| 388 | Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function | 3.2 | 182 | Citations (PDF) |
| 389 | Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls | 2.9 | 216 | Citations (PDF) |
| 390 | Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function | 2.9 | 65 | Citations (PDF) |
| 391 | Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways | 25.2 | 803 | Citations (PDF) |
| 392 | Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium | 2.8 | 43 | Citations (PDF) |
| 393 | History of the Diagnosis of a Sexually Transmitted Disease is Linked to Normal Variation in Personality Traits | 0.5 | 16 | Citations (PDF) |
| 394 | Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study | 62.3 | 405 | Citations (PDF) |
| 395 | Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium | 2.9 | 68 | Citations (PDF) |
| 396 | Seventy-five genetic loci influencing the human red blood cell | 37.9 | 339 | Citations (PDF) |
| 397 | Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes | 25.2 | 1,863 | Citations (PDF) |
| 398 | Genome-wide meta-analysis of common variant differences between men and women | 2.9 | 38 | Citations (PDF) |
| 399 | FTO genotype is associated with phenotypic variability of body mass index | 37.9 | 426 | Citations (PDF) |
| 400 | Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity | 25.2 | 950 | Citations (PDF) |
| 401 | Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways | 25.2 | 343 | Citations (PDF) |
| 402 | Toward a roadmap in global biobanking for health | 3.0 | 151 | Citations (PDF) |
| 403 | Combined Analysis of Genome-wide Association Studies for Crohn Disease and Psoriasis Identifies Seven Shared Susceptibility Loci | 6.5 | 332 | Citations (PDF) |
| 404 | Genome-Wide Meta-Analysis of Psoriatic Arthritis Identifies Susceptibility Locus at REL | 2.3 | 109 | Citations (PDF) |
| 405 | Giving and Withholding of Information following Genomic Screening: Challenges Identified in a Study of Primary Care Physicians in Estonia | 1.7 | 7 | Citations (PDF) |
| 406 | Post-translational stabilization of thiopurine S-methyltransferase by S-adenosyl-l-methionine reveals regulation of TPMT*1 and *3C allozymes | 5.1 | 19 | Citations (PDF) |
| 407 | Longevity candidate genes and their association with personality traits in the elderly | 1.5 | 14 | Citations (PDF) |
| 408 | Self-Other Agreement in Happiness and Life-Satisfaction: The Role of Personality Traits | 2.4 | 20 | Citations (PDF) |
| 409 | Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity | 3.0 | 68 | Citations (PDF) |
| 410 | Large-scale association analysis identifies new risk loci for coronary artery disease | 25.2 | 1,557 | Citations (PDF) |
| 411 | Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions | 3.0 | 25 | Citations (PDF) |
| 412 | Genome-wide association analyses identify 18 new loci associated with serum urate concentrations | 25.2 | 776 | Citations (PDF) |
| 413 | Methylation Markers of Early-Stage Non-Small Cell Lung Cancer | 2.3 | 65 | Citations (PDF) |
| 414 | Systems medicine and integrated care to combat chronic noncommunicable diseases | 9.6 | 185 | Citations (PDF) |
| 415 | Polymorphisms in<i>ESR1</i>,<i>ESR2</i>and<i>HSD17B1</i>genes are associated with fertility status in endometriosis | 1.8 | 55 | Citations (PDF) |
| 416 | 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 | 5.4 | 176 | Citations (PDF) |
| 417 | Design of a peptide-based vector, PepFect6, for efficient delivery of siRNA in cell culture and systemically in vivo | 15.5 | 278 | Citations (PDF) |
| 418 | Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus | 37.9 | 439 | Citations (PDF) |
| 419 | New gene functions in megakaryopoiesis and platelet formation | 37.9 | 426 | Citations (PDF) |
| 420 | Comprehensive catalog of European biobanks | 29.8 | 86 | Citations (PDF) |
| 421 | A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia | 1.6 | 9 | Citations (PDF) |
| 422 | The role of COX-2 and Nrf2/ARE in anti-inflammation and antioxidative stress: Aging and anti-aging | 0.7 | 112 | Citations (PDF) |
| 423 | Sequence Variants and the Risk of Head and Neck Cancer: Pooled Analysis in the INHANCE Consortium | 2.6 | 12 | Citations (PDF) |
| 424 | A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium | 3.2 | 169 | Citations (PDF) |
| 425 | Identification of miR‐374a as a prognostic marker for survival in patients with early‐stage nonsmall cell lung cancer | 3.0 | 126 | Citations (PDF) |
| 426 | Variation in FGF1, FOXE1, and TIMP2genes is associated with nonsyndromic cleft lip with or without cleft palate | 1.9 | 43 | Citations (PDF) |
| 427 | Genome-wide association and genetic functional studies identify
<i>autism susceptibility candidate 2</i>
gene (
<i>AUTS2</i>
) in the regulation of alcohol consumption | 7.5 | 260 | Citations (PDF) |
| 428 | Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure | 25.2 | 421 | Citations (PDF) |
| 429 | A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol | 3.2 | 30 | Citations (PDF) |
| 430 | Susceptibility locus for non‐syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients | 1.7 | 21 | Citations (PDF) |
| 431 | Variance determines self-observer agreement on the Big Five personality traits | 2.3 | 26 | Citations (PDF) |
| 432 | Genetic variants in <i>COL2A1</i>, <i>COL11A2</i>, and <i>IRF6</i> contribute risk to nonsyndromic cleft palate | 1.9 | 48 | Citations (PDF) |
| 433 | Comparison of DNA extraction methods for multiplex polymerase chain reaction | 2.4 | 16 | Citations (PDF) |
| 434 | Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study | 1.8 | 27 | Citations (PDF) |
| 435 | Molecular diagnosis of Down syndrome using quantitative APEX‐2 microarrays | 2.3 | 1 | Citations (PDF) |
| 436 | <i>MTHFR</i> and <i>MSX1</i> contribute to the risk of nonsyndromic cleft lip/palate | 1.7 | 55 | Citations (PDF) |
| 437 | Hundreds of variants clustered in genomic loci and biological pathways affect human height | 37.9 | 1,875 | Citations (PDF) |
| 438 | Common variants in KCNN3 are associated with lone atrial fibrillation | 25.2 | 462 | Citations (PDF) |
| 439 | Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior | 25.2 | 672 | Citations (PDF) |
| 440 | Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution | 25.2 | 899 | Citations (PDF) |
| 441 | Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index | 25.2 | 2,774 | Citations (PDF) |
| 442 | Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies | 25.2 | 476 | Citations (PDF) |
| 443 | Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies | 4.9 | 164 | Citations (PDF) |
| 444 | Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals | 4.9 | 125 | Citations (PDF) |
| 445 | Analysis of Polymorphisms in the SRD5A2 Gene and Semen Parameters in Estonian Men | 2.1 | 10 | Citations (PDF) |
| 446 | Manifesto for a European Anxiety Disorders Research Network | 1.0 | 21 | Citations (PDF) |
| 447 | Genetic Structure of Europeans: A View from the North–East | 2.3 | 297 | Citations (PDF) |
| 448 | Selection for Genetic Variation Inducing Pro-Inflammatory Responses under Adverse Environmental Conditions in a Ghanaian Population | 2.3 | 41 | Citations (PDF) |
| 449 | ROS1 Asp2213Asn polymorphism is not associated with coronary artery disease in a Greek case-control study | 2.3 | 9 | Citations (PDF) |
| 450 | Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients | 1.6 | 36 | Citations (PDF) |
| 451 | Aromatase gene (CYP19A1) variants, female infertility and ovarian stimulation outcome: a preliminary report | 2.7 | 31 | Citations (PDF) |
| 452 | Serotonin transporter promoter region polymorphisms do not influence treatment response to escitalopram in patients with major depression | 1.0 | 67 | Citations (PDF) |
| 453 | Evaluation of the 124-plex SNP typing microarray for forensic testing | 2.2 | 32 | Citations (PDF) |
| 454 | Alcohol-related cancers and genetic susceptibility in Europe: the ARCAGE project: study samples and data collection | 2.0 | 54 | Citations (PDF) |
| 455 | Thiopurine S-methyltransferase (TPMT) pharmacogenetics: three new mutations and haplotype analysis in the Estonian population | 2.3 | 19 | Citations (PDF) |
| 456 | Development of a single tube 640-plex genotyping method for detection of nucleic acid variations on microarrays | 15.5 | 34 | Citations (PDF) |
| 457 | Allelic estrogen receptor 1 (ESR1) gene variants predict the outcome of ovarian stimulation in in vitro fertilization | 2.9 | 73 | Citations (PDF) |
| 458 | Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation | 3.3 | 29 | Citations (PDF) |
| 459 | Analysis of SNP profiles in patients with major depressive disorder | 2.7 | 43 | Citations (PDF) |
| 460 | Association study of sporadic Parkinson's disease genetic risk factors in patients from Russia by APEX technology | 1.9 | 13 | Citations (PDF) |
| 461 | An Evaluation of the Performance of Tag SNPs Derived from HapMap in a Caucasian Population | 3.2 | 109 | Citations (PDF) |
| 462 | Simultaneous Multigene Mutation Detection in Patients With Sensorineural Hearing Loss Through a Novel Diagnostic Microarray: A New Approach for Newborn Screening Follow-up | 4.5 | 75 | Citations (PDF) |
| 463 | Association study of 90 candidate gene polymorphisms in panic disorder | 1.3 | 84 | Citations (PDF) |
| 464 | Arrayed Primer Extension Resequencing of Mutations in the TP53 Tumor Suppressor Gene: Comparison with Denaturing HPLC and Direct Sequencing | 1.1 | 16 | Citations (PDF) |
| 465 | Polymorphisms in wolframin (WFS1) gene are possibly related to increased risk for mood disorders | 2.7 | 43 | Citations (PDF) |
| 466 | Linkage Disequilibrium Patterns and tagSNP Transferability among European Populations | 6.5 | 117 | Citations (PDF) |
| 467 | Genotyping Microarray for the Detection of More Than 200 CFTR Mutations in Ethnically Diverse Populations | 2.5 | 41 | Citations (PDF) |
| 468 | Severe CF manifestation with anaemia and failure to thrive in a 394delTT homozygous patient | 0.8 | 7 | Citations (PDF) |
| 469 | The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe | 3.0 | 46 | Citations (PDF) |
| 470 | Evaluating the arrayed primer extension resequencing assay of TP53 tumor suppressor gene | 7.5 | 100 | Citations (PDF) |
| 471 | Genes, technology and public dialogue in Tartu, Estonia | 8.7 | 1 | Citations (PDF) |
| 472 | High-density genotyping and linkage disequilibrium in the human genome using chromosome 22 as a model | 5.8 | 5 | Citations (PDF) |
| 473 | Title is missing! | 4.0 | 36 | Citations (PDF) |
| 474 | A first-generation linkage disequilibrium map of human chromosome 22 | 37.9 | 382 | Citations (PDF) |
| 475 | Title is missing! 2002 | | 1 | Citations (PDF) |
| 476 | Reliable Detection of β-Thalassemia and G6PD Mutations by a DNA Microarray | 1.1 | 59 | Citations (PDF) |
| 477 | Mutation 985A>G in the MCAD gene shows low incidence in Estonian population | 4.5 | 5 | Citations (PDF) |
| 478 | High carrier frequency of the 35delG deafness mutation in European populations | 3.0 | 374 | Citations (PDF) |
| 479 | Unravelling Genetic Data by Arrayed Primer Extension | 2.3 | 52 | Citations (PDF) |
| 480 | Arrayed Primer Extension: Solid-Phase Four-Color DNA Resequencing and Mutation Detection Technology | 1.5 | 169 | Citations (PDF) |
| 481 | U82, a novel snoRNA identified from the fifth intron of human and mouse nucleolin gene | 3.4 | 5 | Citations (PDF) |
| 482 | Isolation and characterization of the mouse ribosomal protein S7 gene | 2.9 | 3 | Citations (PDF) |
| 483 | A novel snoRNA (U73) is encoded within the introns of the human and mouse ribosomal protein S3a genes | 2.3 | 13 | Citations (PDF) |
| 484 | Dating the Origin of the CCR5-Δ32 AIDS-Resistance Allele by the Coalescence of Haplotypes | 6.5 | 518 | Citations (PDF) |
| 485 | Nuclear Import and Nucleolar Accumulation of the Human Ribosomal Protein S7 Depends on both a Minimal Nuclear Localization Sequence and an Adjacent Basic Region | 2.1 | 34 | Citations (PDF) |
| 486 | Minisequencing: A Specific Tool for DNA Analysis and Diagnostics on Oligonucleotide Arrays | 4.6 | 326 | Citations (PDF) |
| 487 | Structural characterization of the mouse ribosomal protein S6-encoding gene | 2.3 | 5 | Citations (PDF) |
| 488 | Mutation detection by solid phase primer extension | 4.5 | 146 | Citations (PDF) |
| 489 | The human ribosomal protein S7-encoding gene: isolation, structure and localization in 2p25 | 2.3 | 16 | Citations (PDF) |
| 490 | Human ribosomal protein S3a: cloning of the cDNA and primary structure of the protein | 2.3 | 30 | Citations (PDF) |
| 491 | The human ribosomal protein S6 gene: isolation, primary structure and location in chromosome 9 | 2.3 | 16 | Citations (PDF) |
| 492 | 5 S RNA and 5.8 S RNA build up eukaryotic subribosomal domains active in tRNA binding | 2.7 | 2 | Citations (PDF) |
| 493 | Location of single-stranded and double-stranded regions in rat liver ribosomal 5S RNA and 5.8S RNA | 15.5 | 28 | Citations (PDF) |
| 494 | The ternary complex consisting of rat liver ribosomal 5 S RNA, 5.8 S RNA and protein L5 | 2.7 | 25 | Citations (PDF) |
| 495 | Interaction of 5-S RNA, 5.8-S RNA and tRNA with Rat-Liver Ribosomal Proteins | 0.2 | 51 | Citations (PDF) |
| 496 | A Whole-Blood Transcriptome Meta-Analysis Identifies Gene Expression Signatures of Cigarette Smoking | 2.9 | 81 | Citations (PDF) |
| 497 | Heterogeneous contributions of change in population distribution of body mass index to change in obesity and underweight | 1.6 | 64 | Citations (PDF) |
| 498 | Title is missing! 0 | | 4 | Citations (PDF) |
| 499 | Polygenic prediction of body mass index and obesity through the life course and across ancestries | 33.0 | 10 | Citations (PDF) |
| 500 | Parent-of-origin effects on complex traits in up to 236,781 individuals | 37.9 | 8 | Citations (PDF) |
| 501 | Characterization of prevalent genetic variants in the Estonian Biobank body-mass index GWAS | 13.7 | 1 | Citations (PDF) |
| 502 | Cohort Profiles: Personality Measurements at the Estonian Biobank of the Estonian Genome Center, University of Tartu | 2.0 | 1 | Citations (PDF) |
| 503 | Genome-wide association study identifies ABCG1 as a susceptibility locus for tick-borne encephalitis | 3.6 | 0 | Citations (PDF) |
| 504 | Genetic effects on migration behavior contribute to increasing spatial differentiation at trait-associated loci in Estonia | 3.6 | 1 | Citations (PDF) |
| 505 | Genome-wide association study and polygenic risk prediction of hypothyroidism | 25.2 | 0 | Citations (PDF) |
| 506 | Genome-wide meta-analyses of non-response to antidepressants provide insights into underlying molecular genetics and suggest potential pharmacotherapies | 7.8 | 0 | Citations (PDF) |
