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1. Full Text City Sculpture Project (1972) and Nicholas Monro's King Kong
by Wood, Jon
The sculpture journal, ISSN 1366-2724, 01/2017, Volume 26, Issue 3, pp. 373 - 376
Art | Arts & Humanities | Art commissions | Sculpture | Cities and towns | United Kingdom | City planning | History | Civic improvement | Art exhibits | Commissioned works | Public art | 20th century | Motion picture directors & producers | British culture | Art history | Cities | Monro, Nicholas
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2. Full Text Rare and low-frequency coding variants alter human adult height
by Marouli, Eirini and Graff, Mariaelisa and Medina-Gomez, Carolina and Lo, Ken Sin and Wood, Anew R and Kjaer, Troels R and Fine, Rebecca S and Lu, Yingchang and Schurmann, Claudia and Highland, Heather M and Rüeger, Sina and Thorleifsson, Gudmar and Justice, Anne E and Lamparter, David and Stirrups, Kathleen E and Turcot, Valérie and Young, Kristin L and Winkler, Thomas W and Esko, Tõnu and Karaderi, Tugce and Locke, Adam E and Masca, Nicholas G. D and Ng, Maggie C. Y and Mudgal, Poorva and Rivas, Manuel A and Vedantam, Sailaja and Mahajan, Anubha and Guo, Xiuqing and Abecasis, Goncalo and Aben, Katja K and Adair, Linda S and Alam, Dewan S and Albrecht, Eva and Allin, Kristine H and Allison, Matthew and Amouyel, Philippe and Appel, Emil V and Arveiler, Dominique and Asselbergs, Folkert W and Auer, Paul L and Balkau, Beverley and Banas, Bernhard and Bang, Lia E and Benn, Marianne and Bergmann, Sven and Bielak, Lawrence F and Blüher, Matthias and Boeing, Heiner and Boerwinkle, Eric and Böger, Carsten A and Bonnycastle, Lori L and Bork-Jensen, Jette and Bots, Michiel L and Bottinger, Erwin P and Bowden, Donald W and Brandslund, Ivan and Breen, Gerome and Brilliant, Murray H and Broer, Linda and Burt, Amber A and Butterworth, Adam S and Carey, David J and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Yii-Der Ida and Chowdhury, Rajiv and Christensen, Cramer and Chu, Auey Y and Cocca, Massimiliano and Collins, Francis S and Cook, James P and Corley, Janie and Galbany, Jordi Corominas and Cox, Amanda J and Cuellar-Partida, Gabriel and Danesh, John and Davies, Gail and de Bakker, Paul I. W and de Borst, Gert J and de Denus, Simon and de Groot, Mark C. H and de Mutsert, Renée and Deary, Ian J and Dedoussis, George and Demerath, Ellen W and den Hollander, Anneke I and Dennis, Joe G and Di Angelantonio, Emanuele and nos, Fotios and Du, Mengmeng and Dunning, Alison M and Easton, Douglas F and Ebeling, Tapani and Edwards, Todd L and Ellinor, Patrick T and Elliott, Paul and Evangelou, Evangelos and Farmaki, Aliki-Eleni and Faul, Jessica D and ... and EPIC-CVD Consortium and GoT2D Genes Consortium and MAGIC Investigators and Global Lipids Genetics Consortium and EPIC-InterAct Consortium and ReproGen Consortium and ExomeBP Consortium and CHD Exome Consortium and T2D-Genes Consortium and CHD Exome+ Consortium and The EPIC-InterAct Consortium
Nature (London), ISSN 0028-0836, 2017, Volume 542, Issue 7640, pp. 186 - 190
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Cell Adhesion Molecules - genetics | Gene Frequency - genetics | Humans | Glycoproteins - metabolism | Male | Intercellular Signaling Peptides and Proteins - metabolism | Hedgehog Proteins - genetics | Proteolysis | NADPH Oxidases - genetics | Adult | Female | Interleukin-11 Receptor alpha Subunit - genetics | Somatomedins - metabolism | Glycosaminoglycans - biosynthesis | Glycoproteins - genetics | Multifactorial Inheritance - genetics | Procollagen N-Endopeptidase - genetics | Intercellular Signaling Peptides and Proteins - genetics | Interferon Regulatory Factors - genetics | Proteoglycans - biosynthesis | NADPH Oxidase 4 | Body Height - genetics | Genome, Human - genetics | Phenotype | Receptors, Androgen - genetics | Alleles | Genetic Variation - genetics | Pregnancy-Associated Plasma Protein-A - metabolism | ADAMTS Proteins - genetics | Stature | Genetic aspects | Observations | Genetic variation | Studies | Datasets | Disease | Genes | 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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3. Full Text Genome-wide associations for birth weight and correlations with adult disease
by Horikoshi, Momoko and Beaumont, R.N and Day, Felix and Warrington, Nicole and Kooijman, Marjolein and Fernandez-Tajes, Juan and Feenstra, Bjarke and Van Zuydam, Natalie R and Gaulton, Kyle and Grarup, Niels and Bradfield, Jonathan and Strachan, David and Li-Gao, R and Ahluwalia, Tarunveer Singh and Kreiner, E and Rueedi, R and Lyytikäinen, Leo-Pekka and Cousminer, Diana and Wu, Ying and Thiering, Elisabeth and Wang, Carol A and Have, Christian T and Hottenga, Jouke Jan and Vilor-Tejedor, Natàlia and Joshi, Peter and Boh, E.T.H and Ntalla, Ioanna and Pitkanen, Niina and Mahajan, Anubha and Leeuwen, Elisa and Joro, Raimo and Lagou, Vasiliki and Nodzenski, Michael and Diver, L.A and Zondervan, Krina and Bustamante, Mariona and Marques-Vidal, Peo and Mercader, Josep and Bennett, Amanda and Rahmioglu, Nilufer and Nyholt, Dale and Ma, R.C.W and Tam, C.H.T and Tam, W.H and Ganesh, Santhi and Rooij, Frank and Jones, Samuel E and Loh, Po-Ru and Ruth, Katherine S and Tuke, M.A and Tyrrell, A.W.R and Wood, Anew and Yaghootkar, Hanieh and Scholtens, Denise M and Paternoster, Lavinia and Prokopenko, Inga and Kovacs, Peter and Atalay, Mustafa and Willems, Sara and Panoutsopoulou, K and Wang, Xu and Carstensen, Lisbeth and Geller, Frank and Schraut, K.E and Murcia, Mario and Beijsterveldt, Toos and Willemsen, Gonneke and Appel, E.V.R and Fonvig, C.E and Trier, C and Tiesler, C.M.T and Standl, Eberhard and Kutalik, Zoltán and Bonàs-Guarch, Silvia and Hougaard, David and Sánchez, F and Torrents, David and Waage, Johannes and Hollegaard, Mads V and Haan, Hugoline and Rosendaal, Frits and Medina-Gomez, C and Ring, Susan and Hemani, G and Mcmahon, George and Robertson, Neil and Groves, Christopher and Langenberg, Claudia and Luan, Jian'An and Scott, Robert and Zhao, Jing Hua and Mentch, Frank and MacKenzie, S.M and Reynolds, Rebecca and Lowe, William and Tönjes, Anke and Stumvoll, Michael and Lindi, Virpi and Lakka, Timo and Duijn, Cornelia and ... and EGG Consortium and CHARGE Consortium Hematology Worki and CHARGE Consortium Hematology Working Group and Early Growth Genetics (EGG) Consortium
Nature (London), ISSN 0028-0836, 01/2016, Volume 538, Issue 7624, pp. 248 - 252
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Blood Pressure - genetics | Anthropometry | Diabetes Mellitus, Type 2 - genetics | Humans | Fetus - metabolism | Genetic Loci - genetics | Male | Aging - genetics | Glycogen - biosynthesis | Adult | Female | Genetic Predisposition to Disease | Genome-Wide Association Study | Datasets as Topic | Signal Transduction | Chromatin Assembly and Disassembly | Genotype | Birth Weight - genetics | Genomic Imprinting - genetics | Insulin - metabolism | Phenotype | Coronary Artery Disease - genetics | Glucose - metabolism | Genetic Variation - genetics | Cohort Studies | Genome-wide association studies | Birth size | Metabolic diseases | Genetic aspects | Birth weight | Cardiovascular diseases | Health aspects | Risk factors | Studies | Genomes | Disease | Correlation analysis | Index Medicus
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4. Full Text Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
by Nalls, Mike A and Pankratz, Nathan and Lill, Christina M and Do, Chuong B and Hernandez, Dena G and Saad, Mohamad and DeStefano, Anita L and Kara, Eleanna and Bras, Jose and Sharma, Manu and Schulte, Claudia and Keller, Margaux F and Arepalli, Sampath and Letson, Christopher and Edsall, Connor and Stefansson, Hreinn and Liu, Xinmin and Pliner, Hannah and Lee, Joseph H and Cheng, Rong and Ikram, M. Arfan and Ioannidis, John P. A and Hadjigeorgiou, Georgios M and Bis, Joshua C and Martinez, Maria and Perlmutter, Joel S and Goate, Alison and Marder, Karen and Fiske, Brian and Sutherland, Margaret and Xiromerisiou, Georgia and Myers, Richard H and Clark, Lorraine N and Stefansson, Kari and Hardy, John A and Heutink, Peter and Chen, Honglei and Wood, Nicholas W and Houlden, Henry and Payami, Haydeh and Brice, Alexis and Scott, William K and Gasser, Thomas and Bertram, Lars and Eriksson, Nicholas and Foroud, Tatiana and Singleton, Anew B and GenePD and IPDG and Ashkenazi Jewish Dataset Investiga and 23AndMe and NABEC and HIHG and Greek Parkinson's Dis Consortium and GParkinson's Study Grp PSG Parkins and NGRC and Alzheimer Genetic Analysis Gr and CHARGE and UKBEC and Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) and Hussman Institute of Human Genomics (HIHG) and 23andMe and Greek Parkinson's Disease Consortium and International Parkinson's Disease Genomics Consortium (IPDGC) and Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE) and United Kingdom Brain Expression Consortium (UKBEC) and NeuroGenetics Research Consortium (NGRC) and Ashkenazi Jewish Dataset Investigator and North American Brain Expression Consortium (NABEC) and Alzheimer Genetic Analysis Group and The Ashkenazi Jewish Dataset Investigator
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 9, pp. 989 - +
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Humans | Risk Factors | Genotype | Polymorphism, Single Nucleotide | Genetic Loci | Parkinson Disease - genetics | Genome-Wide Association Study - methods | Case-Control Studies | Genome-wide association studies | Parkinson's disease | Genetic aspects | Single nucleotide polymorphisms | Identification and classification | Methods | Risk factors | Studies | Genealogy | Parkinsons disease | Quality control | DNA methylation | Statistical methods | Genomes | Health risk assessment | Meta-analysis | Index Medicus
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5. 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
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | 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 | Medicin och hälsovetenskap
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6. Full Text Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus
by Su, Zhan and Gay, Laura J and Strange, Amy and Palles, Claire and Band, Gavin and Whiteman, David C and Lescai, Francesco and Langford, Cordelia and Nanji, Manoj and Edkins, Sarah and van der Winkel, Anouk and Levine, David and Sasieni, Peter and Bellenguez, Céline and Howarth, Kimberley and Freeman, Colin and Trudgill, Nigel and Tucker, Art T and Pirinen, Matti and Peppelenbosch, Maikel P and van der Laan, Luc J. W and Kuipers, Ernst J and nth, Joost P. H and Peters, Wilbert H and Reynolds, John V and Kelleher, Dermot P and McManus, Ross and Grabsch, Heike and Prenen, Hans and Bisschops, Raf and Krishnadath, Kausila and Siersema, Peter D and van Baal, Jantine W. P. M and Middleton, Mark and Petty, Russell and Gillies, Richard and Burch, Nicola and Bhandari, Pradeep and Paterson, Stuart and Edwards, Cathryn and Penman, Ian and Vaidya, Kishor and Ang, Yeng and Murray, Iain and Patel, Praful and Ye, Weimin and Mullins, Paul and Wu, Anna H and Bird, Nigel C and Dallal, Helen and Shaheen, Nicholas J and Murray, Liam J and Koss, Konrad and Bernstein, Leslie and Romero, Yvonne and Hardie, Laura J and Zhang, Rui and Winter, Helen and Corley, Douglas A and Panter, Simon and Risch, Harvey A and Reid, Brian J and Sargeant, Ian and Gammon, Marilie D and Smart, Howard and Dhar, Anjan and McMurtry, Hugh and Ali, Haythem and Liu, Geoffrey and Casson, Alan G and Chow, Wong-Ho and Rutter, Matt and Tawil, Ashref and Morris, Danielle and Nwokolo, Chuka and Isaacs, Peter and Rodgers, Colin and Ragunath, Krish and MacDonald, Chris and Haigh, Chris and Monk, David and Davies, Gareth and Wajed, Saj and Johnston, David and Gibbons, Michael and Cullen, Sue and Church, Nicholas and Langley, Ruth and Griffin, Michael and Alderson, Derek and Deloukas, Panos and Hunt, Sarah E and Gray, Emma and nov, Serge and Potter, Simon C and Tashakkori-Ghanbaria, Avazeh and Anderson, Mark and Brooks, Claire and Blackwell, Jenefer M and Bramon, Elvira and ... and Wellcome Trust Case Control Consor and Esophageal Adenocarcinoma Genetics and Wellcome Trust Case Control Consortium 2 and Esophageal Adenocarcinoma Genetics Consortium and The Wellcome Trust Case Control Consortium 2 and The Esophageal Adenocarcinoma Genetics Consortium
Nature genetics, ISSN 1061-4036, 2012, Volume 44, Issue 10, pp. 1131 - +
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Gastroenterology. Liver. Pancreas. Abdomen | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Other diseases. Semiology | Esophagus | Genetic Predisposition to Disease | Genome-Wide Association Study | Major Histocompatibility Complex | Gene Frequency | Humans | Middle Aged | Male | Genetic Loci | Case-Control Studies | Linkage Disequilibrium | Chromosomes, Human, Pair 16 | Adult | Female | Aged | Models, Genetic | Polymorphism, Single Nucleotide | Barrett Esophagus - genetics | Major histocompatibility complex | Genetic variation | Barrett's esophagus | Physiological aspects | Genetic aspects | Research | Risk factors | Studies | Medical research | Throat | Cancer | Index Medicus | Genome-wide association (GWA) study | Esophageal adenocarcinoma (EAC) | Single nucleotide polymorphisms (SNPs) | Barrett’s Esophagus | Gastro-esophageal reflux disease (GERD) | Medicin och hälsovetenskap
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