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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 A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness
by O'Connell, Jared and Gurdasani, Deepti and Delaneau, Olivier and Pirastu, Nicola and Ulivi, Sheila and Cocca, Massimiliano and Traglia, Michela and Huang, Jie and Huffman, Jennifer E and Rudan, Igor and McQuillan, Ruth and Fraser, Ross M and Campbell, Harry and Polasek, Ozren and Asiki, Gershim and Ekoru, Kenneth and Hayward, Caroline and Wright, Alan F and Vitart, Veronique and Navarro, Pau and Zagury, Jean-Francois and Wilson, James F and Toniolo, Daniela and Gasparini, Paolo and Soranzo, Nicole and Sandhu, Manjinder S and Marchini, Jonathan
PLoS Genetics, ISSN 1553-7390, 2014, Volume 10, Issue 4, pp. e1004234 - e1004234
Many existing cohorts contain a range of relatedness between genotyped individuals, either by design or by chance. Haplotype estimation in such cohorts is a... 
IDENTITY | POPULATION | RECOMBINATION | GENOTYPE IMPUTATION | RECONSTRUCTION | SEQUENCE | GENETICS & HEREDITY | LINKAGE ANALYSIS | INFERENCE | DESCENT | GENOME-WIDE ASSOCIATION | Haplotypes - genetics | Phenotype | Pedigree | Chromosome Mapping - methods | Humans | Recombination, Genetic - genetics | Family | Genotype | Cohort Effect | Models, Genetic | Genetic research | Research | Gene expression | Index Medicus | Studies | Haplotypes | Population | Parents & parenting | Statistical methods | Genetic recombination
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3. Full Text Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks
by Peloso, Gina M and Auer, Paul L and Bis, Joshua C and Voorman, Arend and Morrison, Alanna C and Stitziel, Nathan O and Brody, Jennifer A and Khetarpal, Sumeet A and Crosby, Jacy R and Fornage, Myriam and Isaacs, Aaron and Jakobsdottir, Johanna and Feitosa, Mary F and Davies, Gail and Huffman, Jennifer E and Manichaikul, Ani and Davis, Brian and Lohman, Kurt and Joon, Aron Y and Smith, Albert V and Grove, Megan L and Zanoni, Paolo and Redon, Valeska and Demissie, Serkalem and Lawson, Kim and Peters, Ulrike and Carlson, Christopher and Jackson, Rebecca D and Ryckman, Kelli K and Mackey, Rachel H and Robinson, Jennifer G and Siscovick, David S and Schreiner, Pamela J and Mychaleckyj, Josyf C and Pankow, James S and Hofman, Albert and Uitterlinden, Andre G and Harris, Tamara B and Taylor, Herman A and Taylor, Kent D and Stafford, Jeanette M and Reynolds, Lindsay M and Marioni, Riccardo E and Dehghan, Abbas and Franco, Oscar H and Patel, Aniruddh P and Lu, Yingchang and Hindy, George and Gottesman, Omri and Bottinger, Erwin P and Melander, Olle and Orho-Melander, Marju and Loos, Ruth J.F and Duga, Stefano and Merlini, Piera Angelica and Farrall, Martin and Goel, Anuj and Asselta, Rosanna and Girelli, Domenico and Martinelli, Nicola and Shah, Svati H and Kraus, William E and Li, Mingyao and Rader, Daniel J and Reilly, Muredach P and McPherson, Ruth and Watkins, Hugh and Ardissino, Diego and Zhang, Qunyuan and Wang, Judy and Tsai, Michael Y and Correa, Adolfo and Griswold, Michael E and Lange, Leslie A and Starr, John M and Rudan, Igor and Eiriksdottir, Gudny and Launer, Lenore J and Ordovas, Jose M and Levy, Daniel and Chen, Y.-D. Ida and Reiner, Alexander P and Hayward, Caroline and Polasek, Ozren and Deary, Ian J and Borecki, Ingrid B and Liu, Yongmei and Gudnason, Vilmundur and Wilson, James G and van Duijn, Cornelia M and Kooperberg, Charles and Rich, Stephen S and Psaty, Bruce M and Rotter, Jerome I and O’Donnell, Christopher J and Rice, Kenneth and Boerwinkle, Eric and Kathiresan, Sekar and Cupples, L. Adrienne and NHLBI GO Exome Sequencing Project and Diabetes - Cardiovascular Disease and Diabetes - kardiovaskulär sjukdom and Kardiovaskulär forskning - hypertoni and Cardiovascular Research - Hypertension and Lund University and EpiHealth: Epidemiology for Health and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
The American Journal of Human Genetics, ISSN 0002-9297, 02/2014, Volume 94, Issue 2, pp. 223 - 232
Low-frequency coding DNA sequence variants in the proprotein convertase subtilisin/kexin type 9 gene ( ) lower plasma low-density lipoprotein cholesterol... 
DENSITY-LIPOPROTEIN CHOLESTEROL | FACTOR ACETYLHYDROLASES | PROTEIN | LDL | GENETICS & HEREDITY | PCSK9 | PLATELET-ACTIVATING-FACTOR | TRAITS | Genetic Code | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Humans | Middle Aged | Male | Genetic Variation | 1-Alkyl-2-acetylglycerophosphocholine Esterase - genetics | Adult | Cholesterol, LDL - blood | Female | Subtilisins - metabolism | African Continental Ancestry Group - genetics | Coronary Disease - blood | European Continental Ancestry Group - genetics | Genetic Association Studies | Gene Frequency | Mice, Inbred C57BL | Linear Models | Cholesterol, HDL - genetics | Sequence Analysis, DNA | 1-Alkyl-2-acetylglycerophosphocholine Esterase - metabolism | Cholesterol, LDL - genetics | Phenotype | Animals | Coronary Disease - genetics | Alleles | Triglycerides - blood | Cholesterol, HDL - blood | Subtilisins - genetics | Aged | Mice | Cohort Studies | Genetic code | Genetic variation | Physiological aspects | Genetic research | Genetic aspects | Research | Coronary heart disease | Population genetics | Lipids | Cardiovascular disease | Low density lipoprotein | Risk assessment | Deoxyribonucleic acid--DNA | Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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4. Full Text Comparative performance of four methods for high-throughput glycosylation analysis of immunoglobulin G in genetic and epidemiological research
by Huffman, J.E and Pučić-Baković, M and Klarić, L and Hennig, R and Selman, M.H and Vučković, F and Novokmet, M and Krištić, J and Borowiak, M and Muth, T and Polašek, O and Razdorov, G and Gornik, O and Plomp, R and Theodoratou, E and Wright, A.F and Rudan, I and Hayward, C and Campbell, H and Deelder, A.M and Reichl, U and Aulchenko, Y.S and Rapp, E and Wuhrer, M and Lauc, G
Molecular and Cellular Proteomics, ISSN 1535-9476, 2014, Volume 13, Issue 6, pp. 1598 - 1610
The biological and clinical relevance of glycosylation is becoming increasingly recognized, leading to a growing interest in large-scale clinical and... 
RHEUMATOID-ARTHRITIS | OLIGOSACCHARIDES | STRUCTURAL-CHANGES | N-GLYCANS | BIOCHEMICAL RESEARCH METHODS | IGG | GLYCOMICS | GLYCOPEPTIDES | MASS-SPECTROMETRY | GENOME-WIDE ASSOCIATION | Electrophoresis, Capillary | Immunoglobulin G - genetics | Polysaccharides - isolation & purification | Humans | Polysaccharides - genetics | Chromatography, Liquid | Hydrophobic and Hydrophilic Interactions | Adult | Glycosylation | Mass Spectrometry - methods | High-Throughput Screening Assays - methods | Polymorphism, Genetic | Index Medicus | Technological Innovation and Resources
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5. Full Text Genomics meets glycomics-the first gwas study of human N-glycome identifies HNF1A as a master regulator of plasma protein fucosylation
by Lauc, Gordan and Essafi, Abdelkader and Huffman, Jennifer E and Hayward, Caroline and Knežević, Ana and Kattla, Jayesh J and Polašek, Ozren and Gornik, Olga and Vitart, Veronique and Abrahams, Jodie L and Pučić, Maja and Novokmet, Mislav and Redžić, Irma and Campbell, Susan and Wild, Sarah H and Borovečki, Fran and Wang, Wei and Kolčić, Ivana and Zgaga, Lina and Gyllensten, Ulf and Wilson, James F and Wright, Alan F and Hastie, Nicholas D and Campbell, Harry and Rudd, Pauline M and Rudan, Igor
PLoS Genetics, ISSN 1553-7390, 2010, Volume 6, Issue 12, pp. 1 - 14
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6. Full Text Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
by Warren, Helen R and Evangelou, Evangelos and Cabrera, Claudia P and Gao, He and Ren, Meixia and Mifsud, Borbala and Ntalla, Ioanna and Surenan, Praveen and Liu, Chunyu and Cook, James P and Kraja, Aldi T and nos, Fotios and Loh, Marie and Verweij, Niek and Marten, Jonathan and Karaman, Ibrahim and Lepe, Marcelo P. Segura and O'Reilly, Paul F and Knight, Joanne and Snieder, Harold and Kato, Norihiro and He, Jiang and Tai, E. Shyong and Said, M. Abdullah and Porteous, David and Alver, Maris and Poulter, Neil and Farrall, Martin and Gansevoort, Ron T and Padmanabhan, Sandosh and Magi, Reedik and Stanton, Alice and Connell, John and Bakker, Stephan J. L and Metspalu, Anes and Shields, Denis C and Thom, Simon and Brown, Morris and Sever, Peter and Esko, Tonu and Hayward, Caroline and van der Harst, Pim and Saleheen, Danish and Chowdhury, Rajiv and Chambers, John C and Chasman, Daniel I and Chakravarti, Aravinda and Newton-Cheh, Christopher and Lindgren, Cecilia M and Levy, Daniel and Kooner, Jaspal S and Keavney, Bernard and Tomaszewski, Maciej and Samani, Nilesh J and Howson, Joanna M. M and Tobin, Martin D and Munroe, Patricia B and Ehret, Georg B and Wain, Louise V and Barnes, Michael R and Tzoulaki, Joanna and Caulfield, Mark J and Elliott, Paul and Vaez, Ahmad and Jansen, Rick and Joehanes, Roby and van der Most, Peter J and Erzurumluoglu, A. Mesut and O'Reilly, Paul and Rose, Lynda M and Verwoert, Germaine C and Hottenga, Jouke-Jan and Strawbridge, Rona J and Arking, Dan E and Hwang, Shih-Jen and Guo, Xiuqing and Kutalik, Zoltan and Trompet, Stella and Shrine, Nick and Teumer, Alexander and Ried, Janina S and Bis, Joshua C and Smith, Albert V and Amin, Najaf and Nolte, Ilja M and Lyytikainen, Leo-Pekka and Mahajan, Anubha and Wareham, Nicholas J and Hofer, Edith and Joshi, Peter K and Kristiansson, Kati and Traglia, Michela and Havulinna, Aki S and Goel, Anuj and Nalls, Mike A and Sober, Siim and Vuckovic, gana and Luan, Jian'an and del Greco, Fabiola M and Ayers, Kristin L and ... and CHARGE BP Exome Consortium and UK Biobank CardioMetab Consortium and GoT2D Genes Consortium and Understanding Soc Sci Grp and Lifelines Cohort Study and Int Consortium Blood Pressure ICBP and BIOS Consortium and ExomeBP Consortium and CHD Exome Consortium and T2D-GENES Consortium and iGEN-BP Consortium and International Consortium of Blood Pressure (ICBP) 1000G Analyses and Understanding Society Scientific group and CHD Exome+ Consortium and Cohorts for Heart and Ageing Research in Genome Epidemiology (CHARGE) BP Exome Consortium and International Genomics of Blood Pressure (iGEN-BP) Consortium and UK Biobank CardioMetabolic Consortium BP working group and GoT2DGenes Consortium and The CHD Exome+ Consortium and The International Consortium of Blood Pressure (ICBP) 1000G Analyses and The International Genomics of Blood Pressure (iGEN-BP) Consortium and The UK Biobank CardioMetabolic Consortium BP working group and The Cohorts for Heart and Ageing Research in Genome Epidemiology (CHARGE) BP Exome Consortium and The GoT2DGenes Consortium and The ExomeBP Consortium and The T2D-GENES Consortium and Stockholms universitet and Numerisk analys och datalogi (NADA) and Naturvetenskapliga fakulteten
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 3, pp. 403 - 415
Elevated blood pressure is the leading heritable risk factor for cardiovascular disease worldwide. We report genetic association of blood pressure (systolic,... 
METAANALYSIS | INHIBITION | GENE | NEUROTROPHIC FACTOR | GENETICS & HEREDITY | KEY ROLE | COMMON | NOX4 | ENDOTHELIAL-CELL | HYPERTENSION | CORONARY-ARTERY-DISEASE | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Blood Pressure - genetics | Humans | Middle Aged | Risk Factors | Genetic Loci - genetics | Male | Cardiovascular Diseases - genetics | Polymorphism, Single Nucleotide - genetics | Adult | Female | Hypertension - genetics | Genome-Wide Association Study - methods | Genotype | Genetic aspects | Single nucleotide polymorphisms | Cardiovascular diseases | Health aspects | Risk factors | Hypertension | Studies | Consortia | Medical research | Genealogy | Biomedical research | Councils | Cardiovascular disease | Genomes | Gene expression | Research centers | Meta-analysis | 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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7. Full Text Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers
by Lauc, G and Huffman, J.E and Pucic, M and Zgaga, L and Adamczyk, B and Muzinic, A and Novokmet, M and Polasek, O and Gornik, O and Kristic, J and Keser, T and Vitart, V and Scheijen, B and Uh, H.W and Molokhia, M and Patrick, A.L and McKeigue, P and Kolcic, I and Lukic, I.K and Swann, O and Leeuwen, F.N. van and Ruhaak, L.R and Houwing-Duistermaat, J.J and Slagboom, P.E and Beekman, M and Craen, A.J. de and Deelder, A.M and Zeng, Q and Wang, W and Hastie, N.D and Gyllensten, U and Wilson, J.F and Wuhrer, M and Wright, A.F and Rudd, P.M and Hayward, C and Aulchenko, Y and Campbell, H and Rudan, I and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Genomik and Uppsala universitet
PLOS Genetics, ISSN 1553-7390, 2013, Volume 9, Issue 1, pp. e1003225 - e1003225
Glycosylation of immunoglobulin G (IgG) influences IgG effector function by modulating binding to Fc receptors. To identify genetic loci associated with IgG... 
DEPENDENT CELLULAR CYTOTOXICITY | RHEUMATOID-ARTHRITIS | STEM-CELLS | METAANALYSIS | ULCERATIVE-COLITIS | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | COLITIS-RISK LOCI | SITE-SPECIFIC GLYCOSYLATION | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Genome-Wide Association Study | Immunoglobulin G - blood | Glycosyltransferases - blood | Humans | Multiple Sclerosis - genetics | Genetic Pleiotropy | Glycosylation | Mice, Knockout | Autoimmune Diseases - genetics | Animals | Immunoglobulin G - genetics | Hematologic Neoplasms - genetics | Mice | Glycosyltransferases - genetics | Autoimmune Diseases - metabolism | Hematologic Neoplasms - metabolism | Quantitative genetics | Immunoglobulin G | Physiological aspects | Genetic aspects | Research | Autoimmune diseases | Health aspects | High performance liquid chromatography | Methods | Lupus | Proteins | Medical research | Gene loci | Immune system | Index Medicus | Naturvetenskap | Natural Sciences
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8. Full Text Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
by Berndt, Sonja I and Gustafsson, Stefan and Mägi, Reedik and Ganna, Anea and Wheeler, Eleanor and Feitosa, Mary F and Justice, Anne E and Monda, Keri L and Croteau-Chonka, Damien C and Day, Felix R and Esko, Tõnu and Fall, Tove and Ferreira, Teresa and Gentilini, Davide and Jackson, Anne U and Luan, Jian'an and Randall, Joshua C and Vedantam, Sailaja and Willer, Cristen J and Winkler, Thomas W and Wood, Anew R and Workalemahu, Tsegaselassie and Hu, Yi-Juan and Lee, Sang Hong and Liang, Liming and Lin, Dan-Yu and Min, Josine L and Neale, Benjamin M and Thorleifsson, Gudmar and Yang, Jian and Albrecht, Eva and Amin, Najaf and Bragg-Gresham, Jennifer L and Cadby, Gemma and den Heijer, Martin and Eklund, Niina and Fischer, Krista and Goel, Anuj and Hottenga, Jouke-Jan and Huffman, Jennifer E and Jarick, Ivonne and Johansson, Asa and Johnson, Toby and Kanoni, Stavroula and Kleber, Marcus E and König, Inke R and Kristiansson, Kati and Kutalik, Zoltán and Lamina, Claudia and Lecoeur, Cecile and Li, Guo and Mangino, Massimo and McArdle, Wendy L and Medina-Gomez, Carolina and Müller-Nurasyid, Martina and Ngwa, Julius S and Nolte, Ilja M and Paternoster, Lavinia and Pechlivanis, Sonali and Perola, Markus and Peters, Marjolein J and Preuss, Michael and Rose, Lynda M and Shi, Jianxin and Shungin, Dmitry and Smith, Albert Vernon and Strawbridge, Rona J and Surakka, Ida and Teumer, Alexander and Trip, Mieke D and Tyrer, Jonathan and van Vliet-Ostaptchouk, Jana V and Vandenput, Liesbeth and Waite, Lindsay L and Zhao, Jing Hua and Absher, Devin and Asselbergs, Folkert W and Atalay, Mustafa and Attwood, Antony P and Balmforth, Anthony J and Basart, Hanneke and Beilby, John and Bonnycastle, Lori L and Brambilla, Paolo and Bruinenberg, Marcel and Campbell, Harry and Chasman, Daniel I and Chines, Peter S and Collins, Francis S and Connell, John M and Cookson, William O and de Faire, Ulf and de Vegt, Femmie and dei, Mariano and Dimitriou, Maria and Edkins, Sarah and Estrada, Karol and Evans, David M and Farrall, Martin and Ferrario, Marco M and ... and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet and Medicin
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 5, pp. 501 - 512
Approaches exploiting trait distribution extremes may be used to identify loci associated with common traits, but it is unknown whether these loci are... 
EXTREME OBESITY | COMMON VARIANTS | POPULATION | GENETICS & HEREDITY | EARLY-ONSET | BODY-MASS INDEX | MISSING HERITABILITY | CONFER RISK | SORTILIN | ASSOCIATION | EXPRESSION | Body Mass Index | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Meta-Analysis as Topic | Anthropometry | Humans | Genotype | Obesity - genetics | Body Height - genetics | Case-Control Studies | Phenotype | Polymorphism, Single Nucleotide - genetics | Quantitative Trait Loci | Waist-Hip Ratio | Quantitative trait loci | Physiological aspects | Body mass index | Genetic aspects | Research | Obesity | Medical research | Biomedical research | Architecture | Gene loci | Genomes | Diabetes | Charitable foundations | Cancer | Index Medicus | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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9. 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