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1. Full Text Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu
by Leitsalu, Liis and Haller, Toomas and Esko, Tonu and Tammesoo, Mari-Liis and Alavere, Helene and Snieder, Harold and Perola, Markus and Ng, Pauline C and Maegi, Reedik and Milani, Lili and Fischer, Krista and Metspalu, Anes
International journal of epidemiology, ISSN 0300-5771, 08/2015, Volume 44, Issue 4, pp. 1137 - 1147
PERSONALITY | PROVIDES INSIGHTS | METAANALYSIS | VARIANTS | SUSCEPTIBILITY LOCI | GENETIC ARCHITECTURE | WIDE ASSOCIATION | IDENTIFICATION | TRAITS | ASSOCIATION ANALYSES IDENTIFY | Life Sciences & Biomedicine | Public, Environmental & Occupational Health | Science & Technology | Life Style | Public Health | Humans | International Classification of Diseases - standards | Middle Aged | Biological Specimen Banks - trends | Male | Genome, Human - genetics | Young Adult | Adolescent | Aged, 80 and over | Adult | Female | Aged | Cohort Studies | Databases, Factual | Estonia | Index Medicus
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2. Full Text Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index
by Yang, Jian and Bakshi, Anew and Zhu, Zhihong and Hemani, Gibran and Vinkhuyzen, Anna A. E and Lee, Sang Hong and Robinson, Matthew R and Perry, John R. B and Nolte, Ilja M and van Vliet-Ostaptchouk, Jana V and Snieder, Harold and Esko, Tonu and Milani, Lili and Maegi, Reedik and Metspalu, Anes and Hamsten, Anders and Magnusson, Patrik K. E and Pedersen, Nancy L and Ingelsson, Erik and Soranzo, Nicole and Keller, Matthew C and Wray, Naomi R and Goddard, Michael E and Visscher, Peter M and LifeLines Cohort Study and The LifeLines Cohort Study
Nature genetics, ISSN 1061-4036, 10/2015, Volume 47, Issue 10, pp. 1114 - 1120
COMMON SNPS | ARCHITECTURE | LOCI | COMPLEX DISEASES | TRAIT | PROPORTION | GENOME-WIDE ASSOCIATION | GENOTYPE-IMPUTATION | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Body Mass Index | Genetic Variation | Genome, Human | Humans | Body Height - genetics | Heritability | Genetic aspects | Single nucleotide polymorphisms | Identification and classification | Genetic screening | Innovations | Index Medicus | Medicin och hälsovetenskap
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3. Full Text Detection and replication of epistasis influencing transcription in humans
by Hemani, Gibran and Shakhbazov, Konstantin and Westra, Harm-Jan and Esko, Tonu and Henders, Anjali K and McRae, Allan F and Yang, Jian and Gibson, Greg and Martin, Nicholas G and Metspalu, Anes and Franke, Lude and Montgomery, Grant W and Visscher, Peter M and Powell, Joseph E
Nature (London), ISSN 0028-0836, 04/2014, Volume 508, Issue 7495, pp. 249 - 253
GENETIC-VARIATION | EVOLUTION | DISEASES | VARIANTS | WIDE ASSOCIATION | SELECTION | PROTEINS | GENOME | DISCOVERY | COMPLEX TRAIT | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Reproducibility of Results | Genetic Association Studies | Gene Expression Regulation - genetics | Humans | Male | Epistasis, Genetic - genetics | Gene Expression Profiling | Europe - ethnology | Linkage Disequilibrium | Pedigree | Polymorphism, Single Nucleotide - genetics | Female | Transcription, Genetic - genetics | Quantitative Trait Loci | Cohort Studies | Physiological aspects | Genetic aspects | Research | Genetic transcription | Genetic polymorphisms | Genetic epistasis | Genotype & phenotype | Hypotheses | Gene expression | Expected values | Polymorphism | Index Medicus
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4. Full Text Systematic identification of trans eQTLs as putative drivers of known disease associations
by Westra, Harm-Jan and Peters, Marjolein J and Esko, Tonu and Yaghootkar, Hanieh and Schurmann, Claudia and Kettunen, Johannes and Christiansen, Mark W and Fairfax, Benjamin P and Schramm, Katharina and Powell, Joseph E and Zhernakova, Alexana and Zhernakova, Daria V and Veldink, Jan H and Van den Berg, Leonard H and Karjalainen, Juha and Withoff, Sebo and Uitterlinden, Ane G and Hofman, Albert and Rivadeneira, Fernando and t Hoen, Peter A. C and Reinmaa, Eva and Fischer, Krista and Nelis, Mari and Milani, Lili and Melzer, David and Ferrucci, Luigi and Singleton, Anew B and Hernandez, Dena G and Nalls, Michael A and Homuth, Georg and Nauck, Matthias and Radke, Doerte and Voelker, Uwe and Perola, Markus and Salomaa, Veikko and Brody, Jennifer and Suchy-Dicey, Astrid and Gharib, Sina A and Enquobahrie, Daniel A and Lumley, Thomas and Montgomery, Grant W and Makino, Seiko and Prokisch, Holger and Herder, Christian and Roden, Michael and Grallert, Harald and Meitinger, Thomas and Strauch, Konstantin and Li, Yang and Jansen, Ritsert C and Visscher, Peter M and Knight, Julian C and Psaty, Bruce M and Ripatti, Samuli and Teumer, Alexander and Frayling, Timothy M and Metspalu, Anes and van Meurs, Joyce B. J and Franke, Lude and Hoen, Peter A.C. ’t
Nature genetics, ISSN 1061-4036, 10/2013, Volume 45, Issue 10, pp. 1238 - 1243
POPULATION | INTERFERON | MYOCARDIAL-INFARCTION | VARIANTS | GENE-EXPRESSION | SUSCEPTIBILITY LOCI | LUPUS-ERYTHEMATOSUS | RISK | GENOME-WIDE ASSOCIATION | BLOOD | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Diabetes Mellitus, Type 1 - genetics | Genetic Predisposition to Disease | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Humans | Lupus Erythematosus, Systemic - genetics | Quantitative trait loci | Genetic aspects | Systemic lupus erythematosus | Single nucleotide polymorphisms | Research | Identification and classification | Studies | Genomes | Disease | Gene expression | Binding sites | Meta-analysis | Index Medicus
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5. Full Text Signatures of negative selection in the genetic architecture of human complex traits
by Zeng, Jian and De Vlaming, Ronald and Wu, Yang and Robinson, Matthew R and Lloyd-Jones, Luke R and Yengo, Loic and Yap, Chloe X and Xue, Angli and Sidorenko, Julia and McRae, Allan F and Powell, Joseph E and Montgomery, Grant W and Metspalu, Anes and Esko, Tonu and Gibson, Greg and Wray, Naomi R and Visscher, Peter M and Yang, Jian
Nature genetics, ISSN 1061-4036, 04/2018, Volume 50, Issue 5, pp. 746 - 753
Genetics | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Multifactorial Inheritance - genetics | Gene Frequency - genetics | Phenotype | Quantitative Trait, Heritable | Humans | Bayes Theorem | Polymorphism, Single Nucleotide - genetics | Genotype | Linear Models | Models, Genetic | Genome-Wide Association Study - methods | Selection, Genetic - genetics | Type 2 diabetes | Analysis | Genomics | Genetic aspects | Models | Genomes | Single nucleotide polymorphisms | Natural selection | Parameter estimation | Computer simulation | Architecture | Anthropometry | Phenotypic variations | Negative selection | Single-nucleotide polymorphism | Gene expression | Consortia | Genetic variance | Genotype & phenotype | Gene frequency | Alleles | Evolution | Heritability | Mutation | Signatures | Bayesian analysis | Methods | Polymorphism | Index Medicus
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6. Full Text Chronotype and sleep duration: The influence of season of assessment
by Allebrandt, Karla V and Teder-Laving, Maris and Kantermann, Thomas and Peters, Annette and Campbell, Harry and Rudan, Igor and Wilson, James F and Metspalu, Andres and Roenneberg, Till
Chronobiology international, ISSN 0742-0528, 6/2014, Volume 31, Issue 5, pp. 731 - 740
sleep duration | social jetlag | Chronotype | DST | photoperiod | seasonality | Social jetlag | Photoperiod | Sleep duration | Seasonality | Biology | Physiology | Life Sciences & Biomedicine - Other Topics | Life Sciences & Biomedicine | Science & Technology | Adaptation, Physiological | Age Factors | Cross-Sectional Studies | Europe | Humans | Middle Aged | Male | Young Adult | Phenotype | Time Factors | Wakefulness | Light | Sex Factors | Adult | Female | Seasons | Circadian Rhythm - radiation effects | Sleep - radiation effects | Index Medicus
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7. Full Text Dominance Genetic Variation Contributes Little to the Missing Heritability for Human Complex Traits
by Zhu, Zhihong and Bakshi, Andrew and Vinkhuyzen, Anna A.E and Hemani, Gibran and Lee, Sang Hong and Nolte, Ilja M and van Vliet-Ostaptchouk, Jana V and Snieder, Harold and Esko, Tonu and Milani, Lili and Mägi, Reedik and Metspalu, Andres and Hill, William G and Weir, Bruce S and Goddard, Michael E and Visscher, Peter M and Yang, Jian and The LifeLines Cohort Study and LifeLines Cohort Study
American journal of human genetics, ISSN 0002-9297, 03/2015, Volume 96, Issue 3, pp. 377 - 385
COMMON | FOUNDER POPULATION | QUANTITATIVE TRAITS | DISEASES | ASSOCIATION | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | European Continental Ancestry Group - genetics | Phenotype | Quantitative Trait, Heritable | Humans | Female | Linear Models | Male | Models, Genetic | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Evaluation Studies as Topic | Cohort Studies | Quantitative trait loci | Genetic research | Epigenetic inheritance | Research | Genetic variation | Genetics | Heredity | Personality traits | Index Medicus
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8. Full Text Genotype-covariate interaction effects and the heritability of adult body mass index
by Robinson, Matthew R and English, Geoffrey and Moser, Gerhard and Lloyd-Jones, Luke R and Triplett, Marcus A and Zhu, Zhihong and Nolte, Ilja M and van Vliet-Ostaptchouk, Jana V and Snieder, Harold and Esko, Tonu and Milani, Lili and Mägi, Reedik and Metspalu, Anes and Magnusson, Patrik K. E and Pedersen, Nancy L and Ingelsson, Erik and Johannesson, Magnus and Yang, Jian and Cesarini, David and Visscher, Peter M and LifeLines Cohort Study and The LifeLines Cohort Study
Nature genetics, ISSN 1061-4036, 08/2017, Volume 49, Issue 8, pp. 1174 - +
HUMAN HEIGHT | OBESITY | MISSING HERITABILITY | FTO GENOTYPE | GENETIC ARCHITECTURE | SEX-DIFFERENCES | EDUCATIONAL-ATTAINMENT | COMPLEX TRAITS | DAIRY-CATTLE | TWIN | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Body Mass Index | Twins - genetics | Life Style | Humans | Middle Aged | Genotype | Male | Sex Characteristics | Gene-Environment Interaction | Multifactorial Inheritance | Obesity - genetics | Young Adult | Aging - genetics | Adolescent | Bayes Theorem | Adult | Female | Aged | Polymorphism, Single Nucleotide | Obesity | Complications and side effects | Body mass index | Physiological aspects | Genetic aspects | Research | Association analysis | Likelihood ratio | Gender differences | Genomes | Single-nucleotide polymorphism | Estimates | Loci | Studies | Design | Genotype & phenotype | Body mass | Population | Gene loci | Heritability | Economic impact | Twins | Bayesian analysis | Age | Siblings | Smoking | Index Medicus | Medicin och hälsovetenskap
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9. Full Text A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individuals
by Deelen, Joris and Kettunen, J and Fischer, Krista and Spek, Ashley and Trompet, Stella and Kastenmuller, Gabi and Boyd, A and Zierer, J and Akker, Erik and Ala-Korpela, Mika and Amin, N and Demirkan, A and Ghanbari, Mohsen and Heemst, Diana and Ikram, Arfan and Klinken, Jan Bert and Mooijaart, Simon and Peters, Annette and Salomaa, Veikko and Sattar, Naveed and Spector, Timothy and Tiemeier, Henning and Verhoeven, Aswin and Waldenberger, M and Würtz, Peter and Davey Smith, G and Metspalu, Anes and Perola, Markus and Menni, Cristina and Geleijnse, J.M and nos, F and Beekman, M and Jukema, Jan Wouter and Duijn, Cornelia and Slagboom, Eline
Nature communications, ISSN 2041-1723, 08/2019, Volume 10, Issue 1, pp. 3346 - 8
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Prognosis | Follow-Up Studies | Risk Assessment | Humans | Middle Aged | Mortality | Risk Factors | Metabolome | Male | Biomarkers - blood | Metabolomics - methods | Young Adult | Adolescent | Survival Analysis | Aged, 80 and over | Adult | Female | Aged | Metabolomics | Men | Predictions | Biomarkers | Health risk assessment | Metabolism | Risk analysis | Risk factors | Index Medicus
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