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1. Crossroads of American sculpture
: David Smith, George Rickey, John Chamberlain, Robert Indiana, William T. Wiley, Bruce Nauman
by Day, Holliday T and Ashton, Dore and Vigna, Lena, 1973 and Indianapolis Museum of Art and New Orleans Museum of Art
2000, ISBN 9780936260723, 252
Sculpture, American
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2. 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, Ginevra 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 | Quantitative Finance | Samhällsvetenskap | Biological Sciences | Social Sciences | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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3. 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 | MULTIDISCIPLINARY SCIENCES | LOCI | 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 | Medical and Health Sciences | Medicin och hälsovetenskap
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4. Full Text Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
by Lee, J.J and Wedow, R and Okbay, A and Kong, E and Maghzian, O and Zacher, M and Galesloot, T.E and Kiemeney, L.A.L.M and Franke, B and Benjamin, D.J and Cesarini, D 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, 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 | Humans | Middle Aged | Male | Educational Status | Multifactorial Inheritance | Phenotype | Aged, 80 and over | Adult | Female | Aged | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Cohort Studies | 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 | 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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5. Full Text Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
by Davies, Gail and Lam, M and Harris, Sarah and Trampush, J.W and Luciano, Michelle and Hill, W.D and Hagenaars, Saskia and Ritchie, S.J and Marioni, Riccardo and Fawns-Ritchie, C and Liewald, D.C.M and Okely, J.A and Ahola-Olli, A.V and Barnes, C.L.K and Bertram, Lars and Bis, Joshua and Burdick, K.E and Christoforou, Anea and Derosse, P and Djurovic, Srdjan and Espeseth, Thomas and Giakoumaki, S and Giddaluru, Sudheer and Gustavson, D.E and Hayward, Caroline and Hofer, Edith and Ikram, Arfan and Karlsson, Robert and Knowles, E and Lahti, Jari and Leber, Isabelle and Li, S and Mather, R and Melle, Ingrid and Morris, D and Oldmeadow, Christopher and Palviainen, T and Payton, Antony and Pazoki, Raha and Petrovic, Katja and Reynolds, C and Sargurupremraj, M and Scholz, Markus and Smith, Jennifer A and Smith, Albert and Terzikhan, Natalie and Thalamuthu, Anbupalam and Trompet, Stella and Lee, Sven and Ware, Erin B and Windham, B Gwen and Wright, M.J and Yang, J and Yu, J and Ames, David and Amin, Najaf and Amouyel, Philippe and Aneassen, Ole and Armstrong, Nicola J and Assareh, A.A and Attia, John and Attix, D and Avramopoulos, D and Bennett, David and Böhmer, Marcel and Boyle, P.A and Brodaty, Henry and Campbell, Harry and Cannon, T.D and Cirulli, E.T and Congdon, E and Conley, E.D and Corley, J and Cox, Simon R and Dale, Anders and Dehghan, Abbas and Dick, D and Dickinson, D and Hagen, Knut and Evangelou, Evangelos and Faul, Jessica D and Ford, Ian and Freimer, N.A and Gao, H and Giegling, Ina and Gillespie, N.A and Gordon, Scott D and Gottesman, Rebecca and Griswold, Michael and Gudnason, V and Harris, Tamara and Hartmann, Annette M and Hatzimanolis, A and Heiss, Gerardo and Holliday, Elizabeth and Joshi, Peter and Kähönen, Mika and Kardia, S.L.R and Karlsson, I and Kleineidam, L and ...
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2098 - 16
textabstractGeneral cognitive function is a prominent and relatively stable human trait that is associated with many important life outcomes. We combine... 
COMMON VARIANTS | METAANALYSIS | REACTION-TIME | PROCESSING SPEED | MULTIDISCIPLINARY SCIENCES | INTELLIGENCE DIFFERENCES | SCHIZOPHRENIA | DCDC2 | DISCOVERY | GENOME-WIDE ASSOCIATION | REVEALS | Multifactorial Inheritance - genetics | Genetic Predisposition to Disease | Humans | Middle Aged | Genetic Loci - genetics | Neurodegenerative Diseases - genetics | Neurodevelopmental Disorders - genetics | Reaction Time - genetics | Young Adult | Mental Disorders - genetics | Adolescent | Aged, 80 and over | Cognition - physiology | Polymorphism, Single Nucleotide - genetics | Adult | Aged | Hypertension | Brain | Cognitive ability | Genomes | Gene expression | Neurodevelopmental disorders | Loci | Consortia | Illnesses | Mathematical analysis | Reaction time | Heritability | Gene loci | Polygenic inheritance | brain cortex | Medical and Health Sciences | Medicin och hälsovetenskap | major clinical study | osteoarthritis | Article | heart infarction | Klinisk medicin | lung cancer | identification method | longevity | grip strength | angina pectoris | genetic correlation | human | major depression | Neurologi | cognition | data set | aged | brain | gene locus | Clinical Medicine | Neurology | genome | vision | genetic analysis | controlled study | response time | adolescent | nervous system disorder | adult | hypertension | gene expression
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6. Full Text DAVID HALCYON LAND (1927-2010) Obituary
by Holliday, D
PROCEEDINGS OF THE YORKSHIRE GEOLOGICAL SOCIETY, ISSN 0044-0604, 05/2013, Volume 59, pp. 219 - 219
GEOLOGY
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7. Full Text Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
by Davies, Gail and Lam, Max and Harris, Sarah E and Trampush, Joey W and Luciano, Michelle and Hill, W David and Hagenaars, Saskia P and Ritchie, Stuart J and Marioni, Riccardo E and Fawns-Ritchie, Chloe and Liewald, David C M and Okely, Judith A and Ahola-Olli, Ari V and Barnes, Catriona L K and Bertram, Lars and Bis, Joshua C and Burdick, Katherine E and Christoforou, Andrea and DeRosse, Pamela and Djurovic, Srdjan and Espeseth, Thomas and Giakoumaki, Stella and Giddaluru, Sudheer and Gustavson, Daniel E and Hayward, Caroline and Hofer, Edith and Ikram, M Arfan and Karlsson, Robert and Knowles, Emma and Lahti, Jari and Leber, Markus and Li, Shuo and Mather, Karen A and Melle, Ingrid and Morris, Derek and Oldmeadow, Christopher and Palviainen, Teemu and Payton, Antony and Pazoki, Raha and Petrovic, Katja and Reynolds, Chandra A and Sargurupremraj, Muralidharan and Scholz, Markus and Smith, Jennifer A and Smith, Albert V and Terzikhan, Natalie and Thalamuthu, Anbupalam and Trompet, Stella and van der Lee, Sven J and Ware, Erin B and Windham, B Gwen and Wright, Margaret J and Yang, Jingyun and Yu, Jin and Ames, David and Amin, Najaf and Amouyel, Philippe and Andreassen, Ole A and Armstrong, Nicola J and Assareh, Amelia A and Attia, John R and Attix, Deborah and Avramopoulos, Dimitrios and Bennett, David A and Böhmer, Anne C and Boyle, Patricia A and Brodaty, Henry and Campbell, Harry and Cannon, Tyrone D and Cirulli, Elizabeth T and Congdon, Eliza and Conley, Emily Drabant and Corley, Janie and Cox, Simon R and Dale, Anders M and Dehghan, Abbas and Dick, Danielle and Dickinson, Dwight and Eriksson, Johan G and Evangelou, Evangelos and Faul, Jessica D and Ford, Ian and Freimer, Nelson A and Gao, He and Giegling, Ina and Gillespie, Nathan A and Gordon, Scott D and Gottesman, Rebecca F and Griswold, Michael E and Gudnason, Vilmundur and Harris, Tamara B and Hartmann, Annette M and Hatzimanolis, Alex and Heiss, Gerardo and Holliday, Elizabeth G and Joshi, Peter K and Kähönen, Mika and Kardia, Sharon L R and Karlsson, Ida and Kleineidam, Luca and ...
Nature communications, ISSN 2041-1723, 05/2019, Volume 10, Issue 1, pp. 2068 - 5
Christina M. Lill, who contributed to analysis of data, was inadvertently omitted from the author list in the originally published version of this article.... 
Cognitive ability
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8. 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, Fleur and Karlsson Linner, Richard and Rietveld, Niels 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, Rajesh and Realo, Anu 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 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 | Quantitative Finance
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9. Full Text Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
by Evangelou, Evangelos and Warren, Helen R and Mosen-Ansorena, David and Mifsud, Borbala and Pazoki, Raha and Gao, He and Ntritsos, Georgios and Dimou, Niki and Cabrera, Claudia P and Karaman, Ibrahim and Ng, Fu Liang and Evangelou, Marina and Witkowska, Katarzyna and Tzanis, Evan and Hellwege, Jacklyn N and Giri, Ayush and Velez Edwards, Digna R and Sun, Yan V and Cho, Kelly and Gaziano, J Michael and Wilson, Peter W F and Tsao, Philip S and Kovesdy, Csaba P and Esko, Tonu and Mägi, Reedik and Milani, Lili and Almgren, Peter and Boutin, Thibaud and Debette, Stéphanie and Ding, Jun and Giulianini, Franco and Holliday, Elizabeth G and Jackson, Anne U and Li-Gao, Ruifang and Prins, Bram Peter and Verweij, Niek and Zhao, Jing-Hua and Borst, Martin H de and Hartman, Catharina A and Lin, Li and Nolte, Ilja M and Oldehinkel, Albertine J and Penninx, Brenda W J H and Riese, Harriëtte and Smith, Albert V and Snieder, Harold and Swertz, Morris A and Vaez, Ahmad and van der Most, Peter J and van der Harst, Pim and Million Vet Program and Million Veteran Program and the Million Veteran Program and Stockholms universitet and Matematiska institutionen and Naturvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 10/2018, Volume 50, Issue 10, pp. 1412 - +
High blood pressure is a highly heritable and modifiable risk factor for cardiovascular disease. We report the largest genetic association study of blood... 
CARDIOVASCULAR-DISEASE RISK | UK BIOBANK | METAANALYSIS | VARIANTS | RARE | HYPERALDOSTERONISM | COMMON | HEALTH