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1. Full Text Genome-wide association study identifies 74 loci associated with educational attainment
by Okbay, Aysu and Beauchamp, Jonathan and Fontana, M.A and Lee, James J and Pers, Tune and Rietveld, C.A and Turley, Patrick and Chen, G.-B and Emilsson, Valur and Meddens, S.F.W and Oskarsson, S and Pickrell, J.K and Thom, K and Timshel, P and Vlaming, Ronald and Abdellaoui, Abdel and Ahluwalia, Tarunveer Singh and Bacelis, Jonas and Baumbach, Clemens and Bjornsdottir, G and Brandsma, Johan and Pina Concas, M and Derringer, J and Furlotte, N.A and Galesloot, Tessel and Girotto, S and Gupta, R and Hall, Leanne M and Harris, Sarah and Hofer, E and Horikoshi, M and Huffman, Jennifer E and Kaasik, K and Kalafati, Ioanna-Panagiota and Karlsson, Robert and Kong, Augustine and Lahti, Jari and Lee, Sven and Deleeuw, C and Lind, Penelope and Lindgren, K.-O and Liu, T and Mangino, Massimo and Marten, Jonathan and Mihailov, Evelin and Miller, Mike and Most, Peter and Oldmeadow, Christopher and Payton, Antony and Pervjakova, Natalia and Peyrot, Wouter and Qian, Y and Raitakari, Olli and Rueedi, R and Salvi, E and Schmidt, B and Schraut, K.E and Shi, J and Smith, Albert Vernon and Poot, Raymond and St Pourcain, Beate and Teumer, Alexander and Thorleifsson, Gudmar and Verweij, Niek and Vuckovic, gana and Wellmann, J and Westra, Harm-Jan and Yang, J and Zhao, W and Zhu, Z and Alizadeh, Behrooz and Amin, Najaf and Bakshi, A and Baumeister, Sebastian and Biino, G and Bønnelykke, Klaus and Boyle, Patricia and Campbell, Harry and Cappuccio, F.P and Davies, Gail and Neve, Jan-Emmanuel and Deloukas, Panagiotis and Demuth, Ilja and Ding, J and Eibich, P and Eisele, L and Eklund, Niina and Evans, David and Faul, Jessica D and Feitosa, Mary Furlan and Forstner, Aneas and Gandin, Ilaria and Gunnarsson, B and Halldorsson, Bjarni and Harris, Tamara and Holliday, Elizabeth and Heath, Anew C and Hocking, L.J and Homuth, Georg and Horan, Mike and ... and LifeLines Cohort Study and Humanistisk-samhällsvetenskapliga vetenskapsområdet and Uppsala universitet and Statsvetenskapliga institutionen and Samhällsvetenskapliga fakulteten
Nature: international weekly journal of science, ISSN 0028-0836, 05/2016, Volume 533, Issue 7604, pp. 539 - 542
textabstractEducational attainment is strongly influenced by social and other environmental factors, but genetic factors are estimated to account for at least... 
ACHIEVEMENT | TRAITS | MULTIDISCIPLINARY SCIENCES | HERITABILITY | Genome-Wide Association Study | Gene Expression Regulation - genetics | Humans | Molecular Sequence Annotation | Computational Biology | Fetus - metabolism | United Kingdom | Cognition | Educational Status | Bipolar Disorder - genetics | Gene-Environment Interaction | Brain - metabolism | Schizophrenia - genetics | Polymorphism, Single Nucleotide - genetics | Alzheimer Disease - genetics | Quantitative trait loci | Academic achievement | Genome-wide association studies | Genetic aspects | Observations | Studies | Genomes | Gene expression | Genes | Educational attainment | Meta-analysis | Index Medicus | Quantitative Finance | Samhällsvetenskap | Biological Sciences | Social Sciences | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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2. Full Text Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
by Okbay, Aysu and Baselmans, B.M.L and Neve, Jan-Emmanuel and Turley, Patrick and Nivard, Michel and Fontana, M.A and Meddens, S.F.W and Linnér, R.K and Rietveld, C.A and Derringer, J and Gratten, Jacob and Lee, James J and Liu, J.Z and Vlaming, Ronald and SAhluwalia, T and Buchwald, J and Cavadino, Alana and Frazier-Wood, Alexis C and Furlotte, N.A and Garfield, V and Geisel, M.H and Gonzalez, Juan R and Haitjema, S and Karlsson, Robert and Der Laan, S.W and Ladwig, Karl-Heinz and Lahti, Jari and Lee, Sven and Lind, Penelope and Liu, T and Matteson, L and Mihailov, Evelin and Miller, Mike and CMinica, C and MNolte, I and Mook-Kanamori, Dennis and Most, Peter and Oldmeadow, Christopher and Qian, Yong and Raitakari, Olli and Rawal, R and Realo, A and Rueedi, R and Schmidt, B and Smith, Albert Vernon and Stergiakouli, Evangelia and Tanaka, Toshiko and Taylor, Kent and Wedenoja, J and Wellmann, J and Westra, Harm-Jan and MWillems, S and Zhao, W and Study, LifeLines Cohort and Amin, Najaf and Bakshi, A and Boyle, Patricia and Cherney, S and Cox, S.R and Davies, Gail and Davis, Oliver S and Ding, Jun and Direk, Nese and Eibich, P and Emeny, Rebecca and Fatemifar, G and Faul, J.D and Ferrucci, Luigi and Forstner, Aneas and Gieger, Christian and Gupta, R and Harris, Tamara B and Harris, Juliette and Holliday, Elizabeth and Hottenga, Jouke Jan and Jager, Philip and Kaakinen, Marika and Kajantie, Eero and Karhunen, V and Kolcic, Ivana and Kumari, Meena and Launer, Lenore and Franke, Lude and Li-Gao, R and Koini, M and Loukola, Anu and Marques-Vidal, P and Montgomery, Grant and Mosing, Miriam and Paternoster, Lavinia and Pattie, Alison and Petrovic, Katja and Pulkki-R'back, L and Quaye, Lydia and R'ikkönen, K and Rudan, Igor and Scott, Rodney and Smith, Jennifer A and Sutin, A.R and Trzaskowski, M and ... and LifeLines Cohort Study
Nature Genetics, ISSN 1061-4036, 06/2016, Volume 48, Issue 6, pp. 624 - 633
textabstractVery few genetic variants have been associated with depression and neuroticism, likely because of limitations on sample size in previous studies.... 
PERSONALITY | COMMON VARIANTS | HUMAN HEIGHT | METAANALYSIS | DISEASE | GENETICS & HEREDITY | RISK | MAJOR DEPRESSION | HAPPINESS | HERITABILITY | RESOURCE | Neuroticism | Genome-Wide Association Study | Phenotype | Humans | Bayes Theorem | Anxiety Disorders - genetics | Polymorphism, Single Nucleotide | Depression - genetics | Genome-wide association studies | Genetic variation | Depression, Mental | Genetic aspects | Identification and classification | Methods | Risk factors | Studies | Psychological aspects | Consortia | Social sciences | Quality control | Personality | Genomes | Behavior | Mental depression | Statistics | Epidemiology | Meta-analysis | Index Medicus | Quantitative Finance
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3. Full Text Genome-wide meta-analysis identifies new susceptibility loci for migraine
by Anttila, Verneri and Winsvold, Bendik S and Gormley, Padhraig and Kurth, Tobias and Bettella, Francesco and McMahon, George and Kallela, Mikko and Malik, Rainer and de Vries, Boukje and Terwindt, Gisela and Medland, Sarah E and Todt, Unda and McArdle, Wendy L and Quaye, Lydia and Koiranen, Markku and Ikram, M. Arfan and Lehtimaki, Terho and Stam, Anine H and Ligthart, Lannie and Wedenoja, Juho and Dunham, Ian and Neale, Benjamin M and Palta, Priit and Hamalainen, Eija and Schuerks, Markus and Rose, Lynda M and Buring, Julie E and Ridker, Paul M and Steinberg, Stacy and Stefansson, Hreinn and Jakobsson, Finnbogi and Lawlor, Debbie A and Evans, David M and Ring, Susan M and Farkkila, Markus and Artto, Ville and Kaunisto, Mari A and Freilinger, Tobias and Schoenen, Jean and Frants, Rune R and Pelzer, Nadine and Weller, Claudia M and Zielman, Ronald and Heath, Anew C and Madden, Pamela A. F and Montgomery, Grant W and Martin, Nicholas G and Borck, Guntram and Goebel, Hartmut and Heinze, Axel and Heinze-Kuhn, Katja and Williams, Frances M. K and Hartikainen, Anna-Liisa and Pouta, Anneli and van den Ende, Joyce and Uitterlinden, Ane G and Hofman, Albert and Amin, Najaf and Hottenga, Jouke-Jan and Vink, Jacqueline M and Heikkila, Kauko and Alexander, Michael and Muller-Myhsok, Bertram and Schreiber, Stefan and Meitinger, Thomas and Wichmann, Heinz Erich and Aromaa, Arpo and Eriksson, Johan G and Traynor, Bryan J and Trabzuni, Daniah and Rossin, Elizabeth and Lage, Kasper and Jacobs, Suzanne B. R and Gibbs, J. Raphael and Birney, Ewan and Kaprio, Jaakko and Penninx, Brenda W and Boomsma, Dorret I and van Duijn, Cornelia and Raitakari, Olli and Jarvelin, Marjo-Riitta and Zwart, John-Anker and Cherkas, Lynn and Strachan, David P and Kubisch, Christian and Ferrari, Michel D and van den Maagdenberg, Arn M. J. M and Dichgans, Martin and Wessman, Maija and Smith, George Davey and Stefansson, Kari and Daly, Mark J and Nyholt, Dale R and Chasman, Daniel I and Palotie, Aarno and UK Brain Expression Consortium and Int Headache Genetics Consortium and North Amer Brain Expression and North American Brain Expression Consortium and the International Headache Genetics Consortium
Nature Genetics, ISSN 1061-4036, 08/2013, Volume 45, Issue 8, pp. 912 - U255
Migraine is the most common brain disorder, affecting approximately 14% of the adult population, but its molecular mechanisms are poorly understood. We report... 
POPULATION | HUMAN-DISEASE | PROTEIN | NEURITE OUTGROWTH | GENETICS & HEREDITY | DOWN-REGULATION | TRANSFORMING-GROWTH-FACTOR | PROTEOLYSIS | ASSOCIATION | EXPRESSION | FAMILY | Genetic Predisposition to Disease | Genome-Wide Association Study | Frontal Lobe - metabolism | Migraine Disorders - genetics | Cerebellum - metabolism | Humans | Computational Biology | Polymorphism, Single Nucleotide | Genetic Loci | Quantitative Trait Loci | Genetic susceptibility | Genetic variation | Migraine | Physiological aspects | Genetic aspects | Research | Risk factors | Studies | Proteins | Signal transduction | Headaches | Population | Genomes | Meta-analysis | Index Medicus
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4. Full Text Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
by Gormley, A.M and Stefansson, Hreinn and Winsvold, Bendik and Palta, Priit and Esko, Tõnu and Pers, Tune and Farh, Kai-How and Cuenca-Leon, E and Muona, M and Furlotte, N.A and Kurth, Karl and Ingason, Anes and Mcmahon, George and Ligthart, Lannie and Terwindt, Gisela and Todt, Unda and Müller-Myhsok, Bertram and Ran, C and Gordon, S.G and Stam, Anine and Steinberg, Stacy and Göbel, Hartmut and Koiranen, Markku and Quaye, Lydia and Adams, H.H.H and Lehtimäki, Terho and Sarin, A.-P and Wedenoja, J and Hinds, David A and Buring, J.E and Schürks, Markus and Ridker, Paul and Hrafnsdottir, M.G and Ring, Susan and Hottenga, Jouke Jan and Penninx, Brenda and Färkkilä, Markus and Artto, Ville and Hämäläinen, Eija and Lucae, Susanne and Malik, Rainer and Heath, Anew C and Madden, Pamela and Martin, Nicholas and Montgomery, Grant and Kurki, M.I and Kals, Mart and Mägi, Reedik and Pärn, K and Hamalainen, Eija and Huang, H and Byrnes, A.E and Franke, Lude and Huang, Jian and Stergiakouli, Evangelia and Lee, Phil and Sandor, C and Webber, C and Cader, Z and Müller-Myhsok, B and Schreiber, Stefan and Meitinger, Thomas and Hagen, Knut and Salomaa, Veikko and Heikkilä, Kauko and Loehrer, Elizabeth and Uitterlinden, Ané and Hofman, A and Duijn, Cornelia and Cherkas, Lynn and Pedersen, L.M and Stubhaug, A and Nielsen, C.S and Männikkö, M and Mihailov, Evelin and Milani, Lili and Esserlind, A.-L and Christensen, A.F and Hansen, T.F and Werge, Thomas and Kaprio, Jaakko and Aromaa, Arpo and Raitakari, Olli and Ikram, Arfan and Ikram, Kamran and Jarvelin, Marjo-Riitta and Metspalu, Anes and Kubisch, Christian and Strachan, David and Ferrari, Michel and Belin, A.C and Wessman, Maija and Maagdenberg, Arn and Zwart, John-Anker and Boomsma, Dorret and Smith, G.D and Stefansson, K and Eriksson, Nicholas and Daly, Mark and Neale, Benjamin and ... and Int Headache Genetics Consortium and International Headache Genetics Consortium
Nature Genetics, ISSN 1061-4036, 08/2016, Volume 48, Issue 8, pp. 856 - 866
textabstractMigraine is a debilitating neurological disorder affecting around one in seven people worldwide, but its molecular mechanisms remain poorly... 
SYSTEMATIC ANALYSIS | MYOCARDIAL-INFARCTION | GENOTYPE IMPUTATION | GENETICS & HEREDITY | GENE-EXPRESSION | SMOOTH-MUSCLE-CELLS | FAMILIAL HEMIPLEGIC MIGRAINE | RECEPTOR-RELATED PROTEIN-1 | SINGLE-NUCLEOTIDE POLYMORPHISMS | SPREADING DEPRESSION | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Genome-Wide Association Study | Migraine Disorders - genetics | Genetic Markers - genetics | Genomics | Humans | Genetic Loci - genetics | Polymorphism, Single Nucleotide - genetics | Vascular Diseases - genetics | Muscle, Smooth - metabolism | Case-Control Studies | Quantitative trait loci | Genome-wide association studies | Migraine | Genetic aspects | Gene expression | Identification and classification | Health aspects | Risk factors | Methods | Studies | Confidence intervals | Consortia | Headaches | Gene loci | Genomes | Meta-analysis | Index Medicus
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5. Full Text GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment
by Cornelius A. Rietveld and Sarah E. Medland and Jaime Derringer and Jian Yang and Tõnu Esko and Nicolas W. Martin and Harm-Jan Westra and Konstantin Shakhbazov and Abdel Abdellaoui and Arpana Agrawal and Eva Albrecht and Behrooz Z. Alizadeh and Najaf Amin and John Barnard and Sebastian E. Baumeister and Kelly S. Benke and Lawrence F. Bielak and Jeffrey A. Boatman and Patricia A. Boyle and Gail Davies and Christiaan de Leeuw and Niina Eklund and Daniel S. Evans and Rudolf Ferhmann and Krista Fischer and Christian Gieger and Håkon K. Gjessing and Sara Hägg and Jennifer R. Harris and Caroline Hayward and Christina Holzapfel and Carla A. Ibrahim-Verbaas and Erik Ingelsson and Bo Jacobsson and Peter K. Joshi and Astanand Jugessur and Marika Kaakinen and Stavroula Kanoni and Juha Karjalainen and Ivana Kolcic and Kati Kristiansson and Zoltán Kutalik and Jari Lahti and Sang H. Lee and Peng Lin and Penelope A. Lind and Yongmei Liu and Kurt Lohman and Marisa Loitfelder and George McMahon and Pedro Marques Vidal and Osorio Meirelles and Lili Milani and Ronny Myhre and Marja-Liisa Nuotio and Christopher J. Oldmeadow and Katja E. Petrovic and Wouter J. Peyrot and Ozren Polašek and Lydia Quaye and Eva Reinmaa and John P. Rice and Thais S. Rizzi and Helena Schmidt and Reinhold Schmidt and Albert V. Smith and Jennifer A. Smith and Toshiko Tanaka and Antonio Terracciano and Matthijs J. H. M. van der Loos and Veronique Vitart and Henry Völzke and Jürgen Wellmann and Lei Yu and Wei Zhao and Jüri Allik and John R. Attia and Stefania Bandinelli and François Bastardot and Jonathan Beauchamp and David A. Bennett and Klaus Berger and Laura J. Bierut and Dorret I. Boomsma and Ute Bültmann and Harry Campbell and Christopher F. Chabris and Lynn Cherkas and Mina K. Chung and Francesco Cueca and Mariza de Andrade and Philip L. De Jager and Jan-Emmanuel De Neve and Ian J. Deary and George V. Dedoussis and Panos Deloukas and Maria Dimitriou and Guðný Eiríksdóttir and Martin F. Elderson and Johan G. Eriksson and ... and LifeLines Cohort Study and The LifeLines Cohort Study and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Institutionen för medicinska vetenskaper
Science, ISSN 0036-8075, 6/2013, Volume 340, Issue 6139, pp. 1467 - 1471
A genome-wide association study (GWAS) of educational attainment was conducted in a discovery sample of 101,069 individuals and a replication sample of 25,490.... 
Medical research | Phenotypes | Psychology | REPORTS | Personality traits | Genetic research | Research facilities | Genetics | Epidemiology | Research universities | Educational attainment | LOCI | PREFERENCES | MULTIDISCIPLINARY SCIENCES | ENVIRONMENT | Genome-Wide Association Study | Endophenotypes | Humans | Female | Male | Cognition | Educational Status | Polymorphism, Single Nucleotide | Genetic Loci | Multifactorial Inheritance | Academic achievement | Genetic aspects | Research | Single nucleotide polymorphisms | Genetic variation | Genomics | Science education | Index Medicus | Medical and Health Sciences | Medicin och hälsovetenskap
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6. Full Text Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
by Lee, James J and Wedow, Robbee and Okbay, Aysu and Kong, Edward and Maghzian, Omeed and Zacher, Meghan and Nguyen-Viet, Tuan Anh and Bowers, Peter and Sidorenko, Julia and Karlsson Linnér, Richard and Fontana, Mark Alan and Kundu, Tushar and Lee, Chanwook and Li, Hui and Li, Ruoxi and Royer, Rebecca and Timshel, Pascal N and Walters, Raymond K and Willoughby, Emily A and Yengo, Loïc and Agee, Michelle and Alipanahi, Babak and Auton, Adam and Bell, Robert K and Bryc, Katarzyna and Elson, Sarah L and Fontanillas, Pierre and Hinds, David A and McCreight, Jennifer C and Huber, Karen E and Litterman, Nadia K and McIntyre, Matthew H and Mountain, Joanna L and Noblin, Elizabeth S and Northover, Carrie A. M and Pitts, Steven J and Sathirapongsasuti, J. Fah and Sazonova, Olga V and Shelton, Janie F and Shringarpure, Suyash and Tian, Chao and Vacic, Vladimir and Wilson, Catherine H and Okbay, Aysu and Beauchamp, Jonathan P and Fontana, Mark Alan and Lee, James J and Pers, Tune H and Rietveld, Cornelius A and Turley, Patrick and Chen, Guo-Bo and Emilsson, Valur and Meddens, S. Fleur W and Oskarsson, Sven and Pickrell, Joseph K and Thom, Kevin and Timshel, Pascal and Vlaming, Ronald de and Abdellaoui, Abdel and Ahluwalia, Tarunveer S and Bacelis, Jonas and Baumbach, Clemens and Bjornsdottir, Gyda and Brandsma, Johannes H and Concas, Maria Pina and Derringer, Jaime and Furlotte, Nicholas A and Galesloot, Tessel E and Girotto, Giorgia and Gupta, Richa and Hall, Leanne M and Harris, Sarah E and Hofer, Edith and Horikoshi, Momoko and Huffman, Jennifer E and Kaasik, Kadri and Kalafati, Ioanna P and Karlsson, Robert and Kong, Augustine and Lahti, Jari and van der Lee, Sven J and Leeuw, Christiaan de and Lind, Penelope A and Lindgren, Karl-Oskar and Liu, Tian and Mangino, Massimo and Marten, Jonathan and Mihailov, Evelin and Miller, Michael B and van der Most, Peter J and Oldmeadow, Christopher and Payton, Antony and Pervjakova, Natalia and Peyrot, Wouter J and Qian, Yong and Raitakari, Olli and Rueedi, Rico and Salvi, Erika and Schmidt, Börge and Schraut, Katharina E and ... and 23Me Res Team and Social Sci Genetic Assoc Consortiu and COGENT Cognitive Genomics Consorti and 23andMe Research Team and COGENT (Cognitive Genomics Consortium) and Social Science Genetic Association Consortium and Humanistisk-samhällsvetenskapliga vetenskapsområdet and Uppsala universitet and Statsvetenskapliga institutionen and Samhällsvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 08/2018, Volume 50, Issue 8, pp. 1112 - 1121
Here we conducted a large-scale genetic association analysis of educational attainment in a sample of approximately 1.1 million individuals and identify 1,271... 
INTELLIGENCE | HUMAN TRAITS | HUMAN BRAIN | METAANALYSIS | GWAS | STATISTICS | GENETICS & HEREDITY | POPULATIONS | LOCI | MAPPING CAUSAL VARIANTS | HERITABILITY | Cell interaction | Genome-wide association studies | Usage | Analysis | Multifactorial traits | Research | Health education | Brain | Phenotypes | Dosage compensation | Sample size | Cognitive ability | Association analysis | Genomes | Single-nucleotide polymorphism | Gene expression | Estimates | Environmental effects | Educational attainment | Meta-analysis | Consortia | Education | Genetic analysis | Heritability | Index Medicus | Basic Medicine | Medical Genetics | Medicinsk genetik | Biological Sciences | Naturvetenskap | Medical and Health Sciences | Medicin och hälsovetenskap | Biologiska vetenskaper | Medicinska och farmaceutiska grundvetenskaper | Natural Sciences
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