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1
المؤلفون: Inês Barroso, Peter D. Sly, Jose Ramon Bilbao, Nicholas J. Timpson, Johan G. Eriksson, Maria M. Groen-Blokhuis, Sijmen A. Reijneveld, Dariusz Gruszfeld, George Davey Smith, Christine Power, Eva Reischl, Mandy Vogel, Andrew T. Hattersley, Øyvind Helgeland, Niina Pitkänen, Akram Alyass, Jean-Paul Langhendries, Elina Hyppönen, Kathrin Landgraf, Loreto Santa-Marina, Frank Geller, Christopher D. Brown, Elvira Verduci, Katja Pahkala, Olli T. Raitakari, Joaquin Escribano, Torben Hansen, Hakon Hakonarson, Barbara Heude, Bridget A. Knight, Maties Torrent, Robin N Beaumont, Judith M. Vonk, Estelle Lowry, Patrick G. Holt, Harold Snieder, Carol A. Wang, Mark I. McCarthy, Christine Frithioff-Bøjsøe, Tanja G. M. Vrijkotte, Natalia Vilor-Tejedor, Lisbeth Carstensen, Catharina E. M. van Beijsterveldt, Ville Karhunen, Virpi Lindi, Marjo-Riitta Järvelin, Tarunveer S. Ahluwalia, Jordi Sunyer, Jaakko T. Leinonen, Clare S. Murray, Klaus Bønnelykke, Thorkild I. A. Sørensen, André G. Uitterlinden, Janine F. Felix, John A. Curtin, Mika Kähönen, Jorma Viikari, Leo-Pekka Lyytikäinen, Oluf Pedersen, Carmen Iñiguez, Harri Niinikoski, Wieland Kiess, Kim F. Michaelsen, Evie Stergiakouli, Anni Heiskala, Alessandra Chesi, Craig E. Pennell, Mohammed H Zafarmand, Peter Rzehak, Kook K Teo, Aihuali Li, Marie Standl, Veit Grote, Momoko Horikoshi, Ellen A. Nohr, Eleanor Wheeler, Rachel M. Freathy, Iryna O. Fedko, Gerard H. Koppelman, Elisabeth Widen, Jens-Christian Holm, Raimo Joro, David Meyre, Mustafa Atalay, Theresia M. Schnurr, Camilla Schmidt Morgen, Adnan Custovic, Niels Grarup, Trevor A. Mori, Terho Lehtimäki, Christian Theil Have, Angela Simpson, Mads Melbye, Bjarke Feenstra, Lawrence J. Beilin, Stefan Johansson, Ioanna Ntalla, Martine Vrijheid, Mariona Bustamante, George Dedoussis, Sylvain Sebert, Jonas Bacelis, Carolina Medina-Gomez, Elisabeth Thiering, Ken K. Ong, Eleftheria Zeggini, Berthold Koletzko, Karine Clément, Bo L. Chawes, Mette Hollensted, Babette S. Zemel, Markus Scholz, Holger Kirsten, Antje Körner, Albertine J. Oldehinkel, Barbera D. C. van Schaik, Philippe Froguel, Vincent W. V. Jaddoe, Dorret I. Boomsma, Struan F.A. Grant, Loic Yengo, Jonathan P. Bradfield, Tenna Ruest Haarmark Nielsen, Suzanne Vogelezang, Jakob Stokholm, Pål R. Njølstad, Bo Jacobsson, Marc Vaudel, Peter J. van der Most, Andreas Kühnapfel, Mads Vendelbo Lind, Timo A. Lakka, Saskia Selzam, Robert Plomin, Marie-Aline Charles, Jouke-Jan Hottenga, Kalliope Panoutsopoulou, Fernando Rivadeneira, Rebecca K. Vinding, Hans Bisgaard, I. S. Farooqi, Joachim Heinrich, Diana L. Cousminer, Ricardo Closa-Monasterolo, Claire Monnereau
المساهمون: European Commission, Epidemiology, Erasmus MC other, Pediatrics, Internal Medicine, Epidemiology and Data Science, ACS - Atherosclerosis & ischemic syndromes, APH - Aging & Later Life, APH - Global Health, APH - Health Behaviors & Chronic Diseases, APH - Personalized Medicine, ARD - Amsterdam Reproduction and Development, APH - Methodology, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, ACS - Amsterdam Cardiovascular Sciences, Public and occupational health, Erasmus University Medical Center [Rotterdam] (Erasmus MC), Children’s Hospital of Philadelphia (CHOP ), Herlev and Gentofte Hospital, Manchester Academic Health Science Centre (MAHSC), University of Manchester [Manchester], University of Kuopio, University of Copenhagen = Københavns Universitet (KU), Universität Leipzig [Leipzig], University Medical Center Groningen [Groningen] (UMCG), University of Bristol [Bristol], Université d'Oulu, The Wellcome Trust Centre for Human Genetics [Oxford], University of Oxford [Oxford], Vrije Universiteit Brussel (VUB), CIBER de Epidemiología y Salud Pública (CIBERESP), Helmholtz-Zentrum München (HZM), University of Newcastle [Australia] (UoN), Turku University Hospital (TYKS), Statens Serum Institut [Copenhagen], Sahlgrenska Academy at University of Gothenburg [Göteborg], Metabolic functional (epi)genomics and molecular mechanisms involved in type 2 diabetes and related diseases - UMR 8199 - UMR 1283 (GI3M), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Queen Mary University of London (QMUL), Norwegian Institute of Public Health [Oslo] (NIPH), King‘s College London, University of Groningen [Groningen], University of Amsterdam [Amsterdam] (UvA), Centre de Recherche Épidémiologie et Statistique Sorbonne Paris Cité (CRESS (U1153 / UMR_A_1125 / UMR_S_1153)), Conservatoire National des Arts et Métiers [CNAM] (CNAM)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), University of Cambridge [UK] (CAM), McMaster University [Hamilton, Ontario], University of Exeter, Ludwig-Maximilians-Universität München (LMU), University of the Basque Country [Bizkaia] (UPV/EHU), The Wellcome Trust Sanger Institute [Cambridge], The University of Western Australia (UWA), Nutrition et obésités: approches systémiques (nutriomics) (UMR-S 1269 INSERM - Sorbonne Université), Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), Universitat Rovira i Virgili, Imperial College London, University of Helsinki, Vrije Universiteit Amsterdam [Amsterdam] (VU), University College of London [London] (UCL), University of Bergen (UiB), University of Tampere [Finland], University of Oulu, Copenhagen University Hospital, University of Turku, University of Queensland [Brisbane], Haukeland University Hospital, Università degli Studi di Milano-Bicocca [Milano] (UNIMIB), National Institute for Health Research Biomedical Research Centre at Great Ormond Street Hospital for Children NHS Foundation Trust University College London Wellcome 090532106130098381203141212259WT206194United States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of Diabetes & Digestive & Kidney Diseases (NIDDK)U01DK105535National Institute for Health Research (NIHR)NF-SI-0617-10090Netherlands Organization for Health Research and DevelopmentTOP 40-00812-9811010American Diabetes Association1-17-PDF-077Daniel B. Burke Chair for Diabetes Research United States Department of Health & Human ServicesNational Institutes of Health (NIH) - USAR01 HD058886Agencia de Gestio D'Ajuts Universitaris de Recerca Agaur (AGAUR)2017 FI_B 00636Generalitat de Catalunya -Fons Social Europeu European Research Council Advanced Grant META-GROWTH (ERC-2012-AdG) 322605Oak Foundation Fellowship Wellcome TrustEuropean CommissionWT104150098497/Z/12/ZRoyal Society of LondonEuropean CommissionWT104150Wellcome Trust098395/Z/12/ZNatural Resources CanadaCanadian Forest ServiceCanada Research Chairs Finnish Cultural Foundation KNAW Academy Professor Award PAH/6635TARGET Danish Diabetes Academy Copenhagen Graduate School of Health and Medical Sciences Netherlands Organization for Health Research and Development (VIDI) 016.136.361European Research Council (ERC)European Commission648916European Research Council (ERC)European Commission UK Research & Innovation (UKRI)Medical Research Council UK (MRC)European CommissionMRC_MC_UU_12012/5MC_UU_00011/1National Institute for Health Research (NIHR) Botnar Foundation Bernard Wolfe Health Neuroscience Endowment European Community's Seventh Framework Programme (FP7/2007-2013) project Beta-JUDO 279153University of Bristol UK Research & Innovation (UKRI)Medical Research Council UK (MRC)MC_UU_00011/1MC_UU_00011/3French National Agency of Research, F-CRIN/FORCE, Clinicum, Johan Eriksson / Principal Investigator, Department of General Practice and Primary Health Care, Helsinki University Hospital Area, Genomics of Sex Differences, Institute for Molecular Medicine Finland, Centre of Excellence in Complex Disease Genetics, Elisabeth Ingrid Maria Widen / Principal Investigator, Genomic Discoveries and Clinical Translation, University of Copenhagen = Københavns Universitet (UCPH), Universität Leipzig, University of Oxford, Helmholtz Zentrum München = German Research Center for Environmental Health, University of Newcastle [Callaghan, Australia] (UoN), Metabolic functional (epi)genomics and molecular mechanisms involved in type 2 diabetes and related diseases - UMR 8199 - UMR 1283 (EGENODIA (GI3M)), Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Conservatoire National des Arts et Métiers [CNAM] (CNAM), HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM)-HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), University of the Basque Country/Euskal Herriko Unibertsitatea (UPV/EHU), Nutrition et obésités: approches systémiques (UMR-S 1269) (Nutriomics), Helsingin yliopisto = Helsingfors universitet = University of Helsinki, Università degli Studi di Milano-Bicocca = University of Milano-Bicocca (UNIMIB), Felix, Janine F [0000-0002-9801-5774], Apollo - University of Cambridge Repository, Biological Psychology, APH - Mental Health, Felix, Janine F. [0000-0002-9801-5774], Tampere University, Tampere University Hospital Catchment Area, Department of Clinical Physiology and Nuclear Medicine, Clinical Medicine, Department of Clinical Chemistry, Groningen Research Institute for Asthma and COPD (GRIAC), Public Health Research (PHR), Life Course Epidemiology (LCE), Vogelezang, Suzanne, Bradfield, Jonathan P, Ahluwalia, Tarunveer S, Curtin, John A, Hyppönen, Elina, Felix, JF, Early Growth Genetics Consortium
المصدر: PLoS Genetics, Vol 16, Iss 10, p e1008718 (2020)
PLoS Genetics
Addi. Archivo Digital para la Docencia y la Investigación
instname
Vogelezang, S, Bradfield, J P, Ahluwalia, T S, Curtin, J A, Grarup, N, Schnurr, T M, Hansen, T, Michaelsen, K F, Pedersen, O B, Stokholm, J, Lind, M V, Frithioff-Bøjsøe, C, Holm, J-C, Felix, J F & Early Growth Genetics Consortium 2020, ' Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits ', P L o S Genetics, vol. 16, no. 10, e1008718 . https://doi.org/10.1371/journal.pgen.1008718
Vogelezang, S, Bradfield, J P, Ahluwalia, T S, Curtin, J A, Lakka, T A, Grarup, N, Scholz, M, van der Most, P J, Monnereau, C, Stergiakouli, E, Heiskala, A, Horikoshi, M, Fedko, I O, Vilor-Tejedor, N, Cousminer, D L, Standl, M, Wang, C A, Viikari, J, Geller, F, Íñiguez, C, Pitkänen, N, Chesi, A, Bacelis, J, Yengo, L, Torrent, M, Ntalla, I, Helgeland, Ø, Selzam, S, Vonk, J M, Zafarmand, M H, Heude, B, Farooqi, I S, Alyass, A, Beaumont, R N, Have, C T, Rzehak, P, Bilbao, J R, Schnurr, T M, Barroso, I, Bønnelykke, K, Beilin, L J, Carstensen, L, Charles, M A, Chawes, B, Clément, K, Closa-Monasterolo, R, Custovic, A, Hansen, T, Morgen, C S, Nohr, E A & Early Growth Genetics Consortium 2020, ' Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits ', PLOS Genetics, vol. 16, no. 10, e1008718 . https://doi.org/10.1371/journal.pgen.1008718
PLOS Genetics
PLoS Genetics (online), 16(10):e1008718. Public Library of Science
PLoS genetics, 16(10):e1008718. Public Library of Science
PLoS Genetics, Public Library of Science, 2020, 16 (10), pp.e1008718. ⟨10.1371/journal.pgen.1008718⟩
e1008718
PLOS GENETICS
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Fedko, I O, Groen-Blokhuis, M, Hottenga, J-J, Van Beijsterveldt, C E M, Vrijkotte, T G M, Boomsma, D I & Early Growth Genetics (EGG) Consortium 2020, ' Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits ', PLoS Genetics, vol. 16, no. 10, e1008718, pp. 1-26 . https://doi.org/10.1371/journal.pgen.1008718
PLoS Genetics, 2020, 16 (10), pp.e1008718. ⟨10.1371/journal.pgen.1008718⟩
PLoS Genetics, 16(10):e1008718, 1-26. Public Library of Science
Addi: Archivo Digital para la Docencia y la Investigación
Universidad del País Vasco
r-FISABIO. Repositorio Institucional de Producción Científica
Curtin, J, Murray, C & et al. 2020, ' Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits ', PL o S Genetics . https://doi.org/10.1371/journal.pgen.1008718
PLoS genetics, 16(10):e1008718. PUBLIC LIBRARY SCIENCE
PLoS Genet. 16:e1008718 (2020)مصطلحات موضوعية: Male, Genetic-variation, Nedd4 Ubiquitin Protein Ligases, Pooled Analysis, Blood Pressure, 0302 clinical medicine, Human genetics, Mendelian Randomization, Young adult, Child, health care economics and organizations, Body mass index, Adiposity, Genetics & Heredity, 0303 health sciences, Statistics, 1184 Genetics, developmental biology, physiology, Genomics, adulto, 3. Good health, Cardiovascular Diseases, Child, Preschool, Physical Sciences, Menarche, genetic-variation, presión sanguínea, Monosaccharide Transport Proteins, Genetic loci, education, enfermedades cardiovasculares, Prostate-specific Antigen, Genetic correlation, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Diabetes Mellitus, Genetics, Humans, prostate-specific antigen, Statistical Methods, Molecular Biology, Ecology, Evolution, Behavior and Systematics, childhood, 0604 Genetics, [SDV.GEN]Life Sciences [q-bio]/Genetics, Science & Technology, Early Growth Genetics Consortium, Biology and Life Sciences, Computational Biology, nutritional and metabolic diseases, Single nucleotide polymorphisms, Mendelian Randomization Analysis, Biological Tissue, Diabetes Mellitus, Type 2, estudio de asociación genómica completa, genetic factors, mendelian randomization, análisis de la aleatorización mendeliana, proteínas de transporte de monosacáridos, 030217 neurology & neurosurgery, Mathematics, Demography, Developmental Biology, Cardiovascular Risk, Cancer Research, obesity, Physiology, humanos, adolescente, Overweight, QH426-470, Genome-wide association studies, Waist–hip ratio, Mathematical and Statistical Techniques, Medicine and Health Sciences, body mass index (BMI), Genetics of disease, Genetics (clinical), 2. Zero hunger, adiposity, Metaanalysis, Physiological Parameters, Connective Tissue, Female, medicine.symptom, Anatomy, pooled analysis, Life Sciences & Biomedicine, Research Article, Adult, cardiovascular risk, Adolescent, Birth weight, menarquia, Adipose tissue, Biology, 3121 Internal medicine, Research and Analysis Methods, medicine, overweight, Genetic Predisposition to Disease, Obesity, 030304 developmental biology, Waist-Hip Ratio, índice de masa corporal, Body Weight, Cardiometabolic Risk Factors, predisposición genética a la enfermedad, Heritability, Genome Analysis, young-adults, Genome-wide Association, índice cintura-cadera, Young-adults, genome-wide association, Genome-Wide Association Study
وصف الملف: application/pdf; text/xml; application/zip; fulltext
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المؤلفون: Nicholas J. Timpson, Michel G. Nivard, Craig E. Pennell, Harold Snieder, Gareth E. Davies, Christel M. Middeldorp, Fernando Rivadeneira, Ilkka Seppälä, Carla M. T. Tiesler, Susan M. Ring, Marie Standl, James J. Hudziak, Kelly S. Benke, Viara R. Mileva-Seitz, Fleur P. Velders, George Davey Smith, Christine Power, Alina Rodriguez, John P. Kemp, René Veenstra, Beate St Pourcain, Harald Grallert, Liisa Keltikangas-Järvinen, Maria M. Groen-Blokhuis, Elina Hyppönen, Irene Pappa, David M. Evans, Marian J. Bakermans-Kranenburg, Joachim Heinrich, Marie-Claude Geoffroy, Christian Hakulinen, Albertine J. Oldehinkel, Dorret I. Boomsma, Elisabeth Thiering, Paul Scheet, George McMahon, Ilja M. Nolte, Henning Tiemeier, Alana Cavadino, Ehsan Motazedi, Terho Lehtimäki, Olli T. Raitakari, Andrew J. O. Whitehouse
المساهمون: Life Course Epidemiology (LCE), Sociology/ICS, Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE), Biological Psychology, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, EMGO+ - Mental Health, Child and Adolescent Psychiatry / Psychology, Erasmus MC other, Epidemiology, Internal Medicine, Psychiatry, Pappa, Irene, St, Pourcain Beate, Benke, Kelly, Cavadino, Alana, Hypponen, Elina, Tiemeier, Henning
المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 171(5), 562-572. Wiley
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 171(5), 562-572. Wiley-Liss Inc.
Pappa, I, St Pourcain, B, Benke, K, Cavadino, A, Hakulinen, C, Nivard, M G, Nolte, I M, Tiesler, C M T, Bakermans-Kranenburg, M J, Davies, G E, Evans, D M, Geoffroy, M-C, Grallert, H, Groen-Blokhuis, M M, Hudziak, J J, Kemp, J P, Keltikangas-Järvinen, L, McMahon, G, Mileva-Seitz, V R, Motazedi, E, Power, C, Raitakari, O T, Ring, S M, Rivadeneira, F, Rodriguez, A, Scheet, P A, Seppälä, I, Snieder, H, Standl, M, Thiering, E, Timpson, N J, Veenstra, R, Velders, F P, Whitehouse, A J O, Smith, G D, Heinrich, J, Hypponen, E, Lehtimäki, T, Middeldorp, C M, Oldehinkel, A J, Pennell, C E, Boomsma, D I & Tiemeier, H 2016, ' A genome-wide approach to children's aggressive behavior: The EAGLE consortium ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 171, no. 5, pp. 562-572 . https://doi.org/10.1002/ajmg.b.32333
American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 171(5), 562-572. Wiley-Liss Inc.مصطلحات موضوعية: 0301 basic medicine, Male, Netherlands Twin Register (NTR), Receptors, Vasopressin, Poison control, Vasopressin/genetics, Genetics, Behavioral/methods, 0302 clinical medicine, Surveys and Questionnaires, Receptors, Psychology, Early childhood, genome-wide complex trait analysis (GCTA), Child, Genetics (clinical), education.field_of_study, HERITABILITY, Genetic Predisposition to Disease/genetics, aggression, Public Health, Global Health, Social Medicine and Epidemiology, ASSOCIATION, Polymorphism, Single Nucleotide/genetics, Justice and Strong Institutions, Aggression, Psychiatry and Mental health, Conduct disorder, DUTCH TWINS, ADOLESCENCE, Meta-analysis, Female, medicine.symptom, Single Nucleotide/genetics, Clinical psychology, SDG 16 - Peace, Adolescent, Population, Aggression/physiology, Single-nucleotide polymorphism, Genetics, Behavioral, Biology, Polymorphism, Single Nucleotide, GENETIC ARCHITECTURE, 03 medical and health sciences, Cellular and Molecular Neuroscience, medicine, Genetics, Humans, Genetic Predisposition to Disease, Polymorphism, EARLY-CHILDHOOD, education, Receptors, Vasopressin/genetics, Genetic Association Studies, childhood, Behavioral/methods, Behavior, Psykologi, STABILITY, ta1184, SDG 16 - Peace, Justice and Strong Institutions, Genetic Variation, ADULTS, medicine.disease, Genetic architecture, population-based, meta-analysis, Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi, Genetic Association Studies/methods, 030104 developmental biology, TISSUE, CONDUCT DISORDER, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: application/pdf
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المؤلفون: Sang Hong Lee, Danielle Posthuma, Debbie A Lawlor, Michael B. Miller, Igor Rudan, Jürgen Wellmann, François Bastardot, Lawrence F. Bielak, Anu Realo, William G. Iacono, Lude Franke, Matthew Kowgier, Marika Kaakinen, Helena Schmidt, Jorma Viikari, Jennifer A. Smith, David R. Van Wagoner, Elizabeth G. Holliday, Veronique Vitart, Robert F. Krueger, Pamela A. F. Madden, Jan Emmanuel De, Andrew Heath, David Cesarini, Najaf Amin, Dale R. Nyholt, Juliette Harris, Nicholas J. Timpson, George Dedoussis, Stefania Bandinelli, W. Hoffmann, Albert V. Smith, Beate St Pourcain, Stavroula Kanoni, Martin F. Elderson, Maria Dimitriou, Jouke-Jan Hottenga, Min A. Jhun, Daniel S. Evans, Marjo-Riitta Järvelin, Lei Yu, Krista Fischer, Jae Hoon Sul, Jennifer R. Harris, Brenda W.J.H. Penninx, Antti-Pekka Sarin, Ida Surakka, Arpana Agrawal, Bo Jacobsson, Klaus Berger, Matt McGue, Christopher F. Chabris, Marisa Loitfelder, Veikko Salomaa, David Schlessinger, Mina K. Chung, Erik A. Ehli, Kati Kristiansson, Eva Albrecht, Niina Eklund, Aarno Palotie, Sarah E. Medland, Reinhold E. Schmidt, Kurt Lohman, Luigi Ferrucci, Osorio Meirelles, Ivana Kolcic, Vilmundur Gudnason, Nicholas G. Martin, Tomi E. Mäkinen, Robert M. Kirkpatrick, Thomas Illig, Peter M. Visscher, Håkon K. Gjessing, Sebastian E. Baumeister, Carla A. Ibrahim-Verbaas, Per Hall, Elisabeth Widen, Panos Deloukas, Ronny Myhre, Michelle N. Meyer, Jonathan P. Beauchamp, Caroline Hayward, Eveline L. de Zeeuw, Penelope A. Lind, Erik Ingelsson, Ian J. Deary, George Davey-Smith, Dalton Conley, Peter Lichtner, Cornelia M. van Duijn, Samuli Ripatti, Dena G. Hernandez, Albert Hofman, George McMahon, Thais S. Rizzi, Wei Zhao, Patrick K.E. Magnusson, Jingmei Li, Mariza de Andrade, Ben A. Oostra, Abdel Abdellaoui, Andres Metspalu, Patricia A. Peyser, Jessica D. Faul, David C. Liewald, Christina Holzapfel, Lydia Quaye, John Barnard, Meike Bartels, Christian Gieger, John P. Rice, Christiaan de Leeuw, Patricia A. Boyle, Nicholas D. Hastie, David R. Weir, Adriaan Hofman, Astanand Jugessur, Tamara B. Harris, Catharina E. M. van Beijsterveldt, Gail Davies, H.-Erich Wichmann, Lynn Cherkas, Polasek Ozren Polasek, Harm-Jan Westra, Yongmei Liu, Jari Lahti, Matthijs J. H. M. van der Loos, Rodney J. Scott, Gérard Waeber, Peter Vollenweider, Behrooz Z. Alizadeh, Frank J. A. van Rooij, Susan M. Ring, Judith M. Vonk, Lyle J. Palmer, Alexander Teumer, John M. Starr, Antonio Terracciano, Sara Hägg, Erkki Vartiainen, David Laibson, Eco J. C. de Geus, Mika Kähönen, Marco Masala, Peng Lin, Nicolas W. Martin, André G. Uitterlinden, Dorret I. Boomsma, Harry Campbell, Sutapa Mukherjee, Konstantin Shakhbazov, Henning Tiemeier, Zó Ltan Kutalik, Grant W. Montgomery, Eva Reinmaa, Aldo Rustichini, Wouter J. Peyrot, David M. Evans, Martin Preisig, Cornelius A. Rietveld, T.J. Glasner, J Kaprio, John Attia, Pedro Marques Vidal, Sharon L.R. Kardia, Peter K. Joshi, Toshiko Tanaka, Rauli Svento, Magnus Johannesson, Terho Lethimäki, Jüri Allik, Philip L. De Jager, Antti Latvala, Marja-Liisa Nuotio, Juha Karjalainen, Henry Völzke, Roy Thurik, Rolf Holle, Kelly S. Benke, Christopher Oldmeadow, Esko Toñu Esko, Johan G. Eriksson, Alan F. Wright, Francesco Cucca, Ute Bültmann, Olli T. Raitakari, Melissa E. Garcia, Patrick J. F. Groenen, Maria M. Groen-Blokhuis, Gonneke Willemsen, Jian Yang, Lili Milani, Fernando Rivadeneira, David A. Bennett, Gudny Eiriksdottir, Katri Räikkönen, Harold Snieder, Laura J. Bierut, James J. Hudziak, James F. Wilson, Rudolf S N Fehrmann, Jaime Derringer, Gareth E. Davies, K. Petrovic, Markus Perola, Lenore J. Launer, Daniel J. Benjamin, Paul Lichtenstein, Philipp Koellinger, Andreas Mielck, Jeffrey A. Boatman, Henrik Grönberg
المساهمون: Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Public Health Research (PHR), Damage and Repair in Cancer Development and Cancer Treatment (DARE), Guided Treatment in Optimal Selected Cancer Patients (GUTS), Stem Cell Aging Leukemia and Lymphoma (SALL), Life Course Epidemiology (LCE), Groningen Research Institute for Asthma and COPD (GRIAC), EMGO+ - Mental Health, Biological Psychology, Methods and Techniques, Child and Adolescent Psychiatry / Psychology, Ophthalmology, Epidemiology
المصدر: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 165(6), 510-520. Wiley
de Zeeuw, E L, van Beijsterveldt, C E M, Glasner, T J, Bartels, M, Ehli, E A, Davies, G E, Hudziak, J J, Rietveld, C A, Blokhuis, M M, Hottenga, J J, de Geus, E J C & Boomsma, D I 2014, ' Polygenic scores associated with educational attainment in adults predict educational achievement and ADHD symptoms in children ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 165, no. 6, pp. 510-520 . https://doi.org/10.1002/ajmg.b.32254
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 165(6), 510-520. Wiley-Liss Inc.
American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 165(6), 510-520. Wiley-Liss Inc.
American Journal of Medical Genetics Part B: Neuropsychiatric Geneticsمصطلحات موضوعية: Netherlands Twin Register (NTR), Multifactorial Inheritance, genetic association, genotype, Academic achievement, Educational achievement, single nucleotide polymorphism, genetic variability, Genetics (clinical), Netherlands, child, article, symptom, academic achievement, Psychiatry and Mental health, priority journal, achievement test, Regression Analysis, Psychology, SDG 4 - Quality Education, Clinical psychology, Adult, phenotype, effect size, attention deficit disorder, gene frequency, educational status, Cellular and Molecular Neuroscience, reading, study skills, mental disorders, Genetics, medicine, Humans, ADHD, Attention deficit hyperactivity disorder, Achievement test, controlled study, human, Association (psychology), Genetic association, attention disturbance, language, School performance, medicine.disease, arithmetic, major clinical study, Polygenic scores, Educational attainment, gene linkage disequilibrium, Attention Deficit Disorder with Hyperactivity, Study skills
وصف الملف: application/pdf
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المؤلفون: James J. Hudziak, Catharina E. M. van Beijsterveldt, Eco J. C. de Geus, Charlotte Huppertz, Gareth E. Davies, Conor V. Dolan, Meike Bartels, Maria M. Groen-Blokhuis, Gonneke Willemsen, Xiangjun Xiao, Marleen H. M. de Moor, Jouke-Jan Hottenga, Erik A. Ehli, A. Abdellaoui, Paul Scheet, Dorret I. Boomsma
المساهمون: Biological Psychology, Clinical Child and Family Studies, EMGO+ - Lifestyle, Overweight and Diabetes, Epidemiology, Child and Adolescent Psychiatry / Psychology
المصدر: Huppertz, C, Bartels, M, Blokhuis, M M, Dolan, C V, de Moor, M H M, Abdellaoui, A, van Beijsterveldt, C E M, Ehli, E A, Hottenga, J J, Willemsen, G, Xiao, X, Scheet, P, Davies, G E, Boomsma, D I, Hudziak, J J & de Geus, E J C 2014, ' The Dopaminergic Reward System and Leisure Time Exercise Behavior: A Candidate Allele Study ', Biomed research international, vol. 2014, 591717 . https://doi.org/10.1155/2014/591717
BioMed Research International, Vol 2014 (2014)
Biomed research international, 2014:591717. Hindawi Publishing Corporation
BioMed Research International, 2014. Hindawi Publishing Corporation
BioMed Research Internationalمصطلحات موضوعية: Adult, Male, Netherlands Twin Register (NTR), Adolescent, Genotype, Article Subject, Dopamine, Health Behavior, lcsh:Medicine, Single-nucleotide polymorphism, Minisatellite Repeats, Biology, Polymorphism, Single Nucleotide, General Biochemistry, Genetics and Molecular Biology, Receptors, Dopamine, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Reward, Genetic variation, Humans, Computer Simulation, Registries, Allele, Child, Exercise, Life Style, Alleles, Netherlands, 030304 developmental biology, Genetic association, Genetics, 0303 health sciences, General Immunology and Microbiology, lcsh:R, Genetic Variation, General Medicine, Middle Aged, Heritability, Twin study, Variable number tandem repeat, Phenotype, Female, Algorithms, 030217 neurology & neurosurgery, Research Article, rs4680
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المؤلفون: Dorret I. Boomsma, Erik A. Ehli, Xiangjun Xiao, James J. Hudziak, Meike Bartels, Catharina E. M. van Beijsterveldt, Eco J. C. de Geus, Maria M. Groen-Blokhuis, Gareth E. Davies, Robert R. Althoff, Christel M. Middeldorp, Paul Scheet, Sanja Franić
المساهمون: Biological Psychology, Neuroscience Campus Amsterdam - Neurobiology of Mental Health, Neuroscience Campus Amsterdam - Brain Mechanisms in Health & Disease, Child Psychiatry
المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 162(5), 457-465. Wiley-Liss Inc.
American journal of medical genetics. Part B, Neuropsychiatric genetics, 162(5), 457-465. Wiley-Liss Inc.
Groen-Blokhuis, M M, Franic, S, van Beijsterveldt, C E M, de Geus, E J C, Bartels, M, Davies, G E, Ehli, E A, Xiao, X, Scheet, P, Althoff, R R, Hudziak, J J, Middeldorp, C M & Boomsma, D I 2013, ' A prospective study of the effects of breastfeeding and FADS2 polymorphisms on cognition and hyperactivity/attention problems ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 162, no. 5, pp. 457-465 . https://doi.org/10.1002/ajmg.b.32175
American Journal of Medical Genetics Part B: Neuropsychiatric Geneticsمصطلحات موضوعية: Adult, Fatty Acid Desaturases, Netherlands Twin Register (NTR), FADS2, Breastfeeding, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Structural equation modeling, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, SDG 3 - Good Health and Well-being, Humans, Medicine, Prospective Studies, 030212 general & internal medicine, Cognitive skill, Prospective cohort study, Genetics (clinical), business.industry, Infant, Newborn, Infant, Cognition, Educational attainment, Psychiatry and Mental health, Breast Feeding, Attention Deficit Disorder with Hyperactivity, Twin Studies as Topic, Female, Cognition Disorders, business, 030217 neurology & neurosurgery, Clinical psychology
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المؤلفون: Diane J. Lamb, Catharina E. M. van Beijsterveldt, Dorret I. Boomsma, Paul Scheet, James J. Hudziak, Eco J. C. de Geus, Jacob F. Orlebeke, Nienke M. Schutte, Michel G. Nivard, Cyrina Brouwer, Erik A. Ehli, T.J. Glasner, T.M. Stroet, Suzanne C. Swagerman, Conor V. Dolan, Dustin Nowotny, Kees-Jan Kan, Sanja Franić, Dirk J.A. Smit, Gareth E. Davies, Eveline L. de Zeeuw, Meike Bartels, Charlotte Huppertz, Christel M. Middeldorp, Jouke-Jan Hottenga, Maria M. Groen-Blokhuis, Michelle Van Fulpen
المساهمون: Neuroscience Campus Amsterdam - Neurobiology of Mental Health, EMGO+ - Mental Health, Biological Psychology, Methods and Techniques
المصدر: Twin Research and Human Genetics, 16(1), 252-267. Australian Academic Press
Twin Research and Human Genetics
van Beijsterveldt, C E M, Groen-Blokhuis, M M, Franic, S, Hudziak, J J, Lamb, D J, Huppertz, C, de Zeeuw, E L, Nivard, M G, Schutte, N M, Swagerman, S C, Glasner, T J, van Fulpen, M J, Brouwer, C D, Stroet, T M, Nowotny, D, Ehli, E A, Davies, G E, Scheet, P, Orlebeke, J F, Kan, K J, Smit, D J A, Dolan, C V, Middeldorp, C M, de Geus, E J C, Bartels, M & Boomsma, D I 2013, ' The Young Netherlands Twin Register (YNTR): Longitudinal Twin and Family Studies in Over 70,000 Children ', Twin Research and Human Genetics, vol. 16, no. 1, pp. 252-267 . https://doi.org/10.1017/thg.2012.118مصطلحات موضوعية: Male, Gerontology, Netherlands Twin Register (NTR), Adolescent, Twins, Neuropsychological Tests, 03 medical and health sciences, 0302 clinical medicine, SDG 3 - Good Health and Well-being, Pregnancy, Surveys and Questionnaires, Diseases in Twins, Humans, Medicine, Family, Longitudinal Studies, Registries, Child, Genetics (clinical), Netherlands, 030304 developmental biology, 0303 health sciences, Data collection, business.industry, Mental Disorders, Neuropsychology, Infant, Obstetrics and Gynecology, medicine.disease, Twin study, Zygosity, Child, Preschool, Pediatrics, Perinatology and Child Health, Female, business, Twins Early Development Study, 030217 neurology & neurosurgery, Record linkage, Psychopathology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::252e503b2541d286b19e7cb9daa119b2
https://doi.org/10.1017/thg.2012.118 -
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المؤلفون: Julie A. Marsh, Meike W. Vernooij, Nicholas J. Timpson, Linda S. Adair, Maksim Struchalin, Kelly S. Benke, Alex P. Zijdenbos, Wiro J. Niessen, Dexter Hadley, André Scherag, Niina Siitonen, Johannes Hedebrand, Helena Schmidt, Iona Y. Millwood, Emily Oken, David S. Knopman, James F. Wilson, H. Rob Taal, Henri A. Vrooman, Karen L. Mohlke, Myriam Fornage, Vilmundur Gudnason, Leslie A. Lange, Sigurdur Sigurdsson, Maria M. Groen-Blokhuis, Diane J. Catellier, Stefan Ropele, Seang Mei Saw, Sylvain Sebert, Alexa S. Beiser, Lyle J. Palmer, Claudia Flexeder, Paul Elliott, George Davey Smith, John W. Holloway, Michel G. Nivard, Mike A. Nalls, Albert V. Smith, Cyrus Cooper, E Zeggini, Terho Lehtimäki, Struan F.A. Grant, Virpi Lindi, Romy Gaillard, B. Gwen Windham, Dennis O. Mook-Kanamori, Claus Holst, Timo A. Lakka, Stéphanie Debette, Liang Kee Goh, Ewan R. Pearson, Tamara B. Harris, Momoko Horikoshi, Jeffrey C. Murray, Mirna Kirin, M. Arfan Ikram, George V. Dedoussis, Anita L. DeStefano, Clifford R. Jack, Alex Lewin, Reedik Maggi, Vincent W. V. Jaddoe, Haukur Gudnason, Hakon Hakonarson, Thomas H. Mosley, Alina Rodriguez, Sudha Seshadri, William M. Meeks, Philip A. Wolf, Gonneke Willemsen, B. Valcarcel, Anke Hinney, Eric A.P. Steegers, Lenore J. Launer, Elina Hyppönen, Lachlan J. M. Coin, Elisabeth Thiering, Mustafa Atalay, W. T. Longstreth, Thorkild I. A. Sørensen, André G. Uitterlinden, Christel M. Middeldorp, Matthew W. Gillman, Ken K. Ong, Oliver S. P. Davis, Monique M.B. Breteler, Wei Ang, Ulla Sovio, Tuomas O. Kilpeläinen, Ioanna Ntalla, Marjo-Riitta Järvelin, Aad van der Lugt, Cornelia M. van Duijn, Cecilia M. Lindgren, Rany M. Salem, Laura H. Coker, Craig E. Pennell, Fernando Rivadeneira, Thomas S. Price, Charles DeCarli, Dorret I. Boomsma, Ellen Aagaard Nohr, Diane Berry, Rhoda Au, Yik Y. Teo, Ville Huikari, Jouke-Jan Hottenga, Matthew Kowgier, Joachim Heinrich, Nienke E. Bergen, Beate St Pourcain, Reinhold Schmidt, C Power, Kalliope Panoutsopoulou, Olli T. Raitakari, Albert Hofman, Mark I. McCarthy, Joel N. Hirschhorn, Olli Simell, Claire M. A. Haworth, Mark A. van Buchem, Anna-Liisa Hartikainen, Berthold Hocher, Debbie A Lawlor, Jennifer Pararajasingham, Toos C. E. M. van Beijsterveldt, David P. Strachan, Hanna Maaria Lakka, Timothy M. Frayling
المساهمون: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Early Growth Genetics (EGG) Consortium, Ikram, M Afran, Fornage, Myriam, Smith, Albert V, Seshadri, Sudha, Hypponen, Elina Tuulikki, Wilson, James F, Biological Psychology, Radiology & Nuclear Medicine, Epidemiology, Erasmus MC other, Internal Medicine, Obstetrics & Gynecology, Public Health, Medical Oncology
المصدر: Nature Genetics
Nature Genetics, 44(5), 539
Ikram, M A, Fornage, M, Smith, A V, Seshadri, S, Schmidt, R, Debette, S, Vrooman, H A, Sigurdsson, S, Ropele, S, Taal, H R, Mook-Kanamori, D O, Coker, L H, Longstreth, W T, Niessen, W J, DeStefano, A L, Beiser, A, Zijdenbos, A P, Struchalin, M, Jack, C R, Rivadeneira, F, Uitterlinden, A G, Knopman, D S, Hartikainen, A-L, Pennell, C E, Thiering, E, Steegers, E A P, Hakonarson, H, Heinrich, J, Palmer, L J, Jarvelin, M-R, McCarthy, M I, Grant, S F A, St Pourcain, B, Timpson, N J, Smith, G D, Sovio, U, Nalls, M A, Au, R, Hofman, A, Gudnason, H, van der Lugt, A, Harris, T B, Meeks, W M, Vernooij, M W, van Buchem, M A, Catellier, D, Jaddoe, V W V, Gudnason, V & Windham, B G & Wilson, J F 2012, ' Common variants at 6q22 and 17q21 are associated with intracranial volume ', Nature Genetics, vol. 44, no. 5, pp. 539-+ . https://doi.org/10.1038/ng.2245
Nature Genetics, 44(5), 539-544. Nature Publishing Group
Nature Genetics; Vol 44
Nature Genetics, 44(5), 539-+. Nature Publishing Group
Arfan Ikram, M, Fornage, M, Smith, A V, Seshadri, S, Schmidt, R, Debette, S, Vrooman, H A, Sigurdsson, S, Ropele, S, Taal, H R, Mook-Kanamori, D O, Coker, L H, Longstreth, J W T, Niessen, W J, DeStefano, A L, Beiser, A, Zijdenbos, A P, Struchalin, M, Jack, C R, Rivadeneira, F, Uitterlinden, A G, Knopman, D S, Hartikainen, A-L, Pennell, C E, Thiering, E, Steegers, E A P, Hakonarson, H, Heinrich, J, Palmer, L J, Jarvelin, M-R, McCarthy, M I, Grant, S F A, St Pourcain, B, Timpson, N J, Smith, G D, Sovio, U, van Beijsterveldt, C E M, Groen-Blokhuis, M M, Hottenga, J J, Middeldorp, C M, Nivard, M G, Willemsen, G, Boomsma, D I, Nalls, M A, Au, R, Hofman, A, Gudnason, H, van der Lugt, A, Harris, T B, Meeks, W M, Vernooij, M W, van Buchem, M A, Catellier, D, Jaddoe, V W V, Gudnason, V, Windham, B G, Wolf, P A, van Duijn, C M, Mosley, T H, Schmidt, H, Launer, L J, Breteler, M M B & DeCarli, C S 2012, ' Common variants at 6q22 and 17q21 are associated with intracranial volume ', Nature Genetics, vol. 44, no. 5, pp. 539-544 . https://doi.org/10.1038/ng.2245
Nature genetics 44(5), 539-544 (2012). doi:10.1038/ng.2245مصطلحات موضوعية: Netherlands Twin Register (NTR), Genetic Markers, Male, medicine.medical_specialty, Medizin, Locus (genetics), Genome-wide association study, physiopathology [Brain], Biology, Bioinformatics, Polymorphism, Single Nucleotide, Article, genetics [Chromosomes, Human, Pair 17], 03 medical and health sciences, 0302 clinical medicine, ddc:570, Intracranial volume, Internal medicine, medicine, Genetics, Humans, 030304 developmental biology, Aged, Aged, 80 and over, 0303 health sciences, Haplotype, Chromosome, Brain, Infant, genetics [Chromosomes, Human, Pair 6], Microdeletion syndrome, ta3121, physiopathology [Head], Endocrinology, Genetic marker, Genetic Loci, Brain size, genetics [Polymorphism, Single Nucleotide], Institut für Ernährungswissenschaft, Chromosomes, Human, Pair 6, Female, Head, 030217 neurology & neurosurgery, Chromosomes, Human, Pair 17, Genome-Wide Association Study
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المؤلفون: Norman Klopp, Chih-Mei Chen, Erik Melén, Dirkje S. Postma, Klaus Bønnelykke, Gerard H. Koppelman, Ivan Curjuric, Massimo Mangino, Nicholas J. Timpson, Alexandra I. F. Blakemore, Stephen B. Montgomery, Marjo-Riitta Järvelin, Anneli Pouta, Dorret I. Boomsma, Melanie C. Matheson, Albert Hofman, Matthias Wjst, Hans Bisgaard, Natalija Novak, Deborah Jarvis, Grant W. Montgomery, Frank Geller, Beate St Pourcain, Craig E. Pennell, Manuel A. R. Ferreira, Andre Franke, Alexessander Couto Alves, Frank D. Mentch, Vincent W. V. Jaddoe, Marie Standl, Nicole M. Warrington, Jouke-Jan Hottenga, Jessica L. Buxton, Peter N. Le Souëf, Bjarke Feenstra, Peter D. Sly, Bo L. Chawes, Martina Mueller-Nurasyid, Angela Simpson, Philip J. Thompson, Jacob P. Thyssen, Patrick G. Holt, Eskil Kreiner-Møller, David L. Duffy, Thomas Illig, Johan C. de Jongste, Bo Jacobsson, Joachim Heinrich, Mads Melbye, Wenche Nystad, H-Erich Wichmann, Medea Imboden, Wendy L. McArdle, Carla M. T. Tiesler, Susan M. Ring, Jeff Murray, Lavinia Paternoster, Torkil Menné, Marjan Kerkhof, John Henderson, Ronny Myhre, Lyle J. Palmer, George Davey Smith, Eva Albrecht, Pamela A. F. Madden, Marika Kaakinen, Hansjoerg Baurecht, Nicole Probst-Hensch, Cecilia Kim, Cornelia M. van Duijin, Panos Deloukas, Patrick M. A. Sleiman, Christian Gieger, John A. Curtin, Adnan Custovic, Daniel Glass, Cilla Söderhäll, Annika Sääf, Elke Rodriguez, Nicholas G. Martin, Stephan Weidinger, Tim D. Spector, Adaikalavan Ramasamy, John P. Kemp, Heather A. Boyd, Elisabeth Thiering, David P. Strachan, Anna-Liisa Hartikainen, Hakon Hakonarson, Allan Linneberg, Ralf J. P. van der Valk, Pirro G. Hysi, David M. Evans, Rain Jögi, Ellen A. Nohr, Liesbeth Duijts, Katharina Heim, Veronique Bataille, Fernando Rivadeneira, Maria M. Groen-Blokhuis, Andrew C. Heath, David Ellinghaus, Michael E. March, Holger Prokisch, Regina Foelster-Holst, André G. Uitterlinden, Emmanouil T. Dermitzakis, Juha Pekkanen, Henriette A. Smit
المساهمون: Medical Research Council (MRC), Dermitzakis, Emmanouil, Montgomery, Stephen, Biological Psychology, EMGO+ - Mental Health, Pediatrics, Surgery, Internal Medicine, Epidemiology, Erasmus MC other, Public Health, Groningen Research Institute of Pharmacy, Faculteit Medische Wetenschappen/UMCG, Groningen Research Institute for Asthma and COPD (GRIAC)
المصدر: Paternoster, L, Standl, M, Chen, C-M, Ramasamy, A, Bønnelykke, K, Duijts, L, Ferreira, M A, Alves, A C, Thyssen, J P, Albrecht, E, Baurecht, H, Feenstra, B, Sleiman, P M A, Hysi, P, Warrington, N M, Curjuric, I, Myhre, R, Curtin, J A, Groen-Blokhuis, M M, Kerkhof, M, Sääf, A, Franke, A, Ellinghaus, D, Fölster-Holst, R, Dermitzakis, E, Montgomery, S B, Prokisch, H, Heim, K, Hartikainen, A-L, Pouta, A, Pekkanen, J, Blakemore, A I F, Buxton, J L, Kaakinen, M, Duffy, D L, Madden, P A, Heath, A C, Montgomery, G W, Thompson, P J, Matheson, M C, Le Souëf, P, Pourcain, B S, Smith, G D, Henderson, J, Kemp, J P, Timpson, N J, Deloukas, P, Ring, S M, Wichmann, H-E, Nøhr, E A & Australian Asthma Genetics Consortium (AAGC) 2011, ' Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis ', Nature Genetics, vol. 44, no. 2, pp. 187-192 . https://doi.org/10.1038/ng.1017
Nature Genetics
Nature Genetics; Vol 44
Paternoster, L, Standl, M, Chen, C-M, Ramasamy, A, Bønnelykke, K, Duijts, L, Ferreira, M A, Alves, A C, Thyssen, J P, Albrecht, E, Baurecht, H, Feenstra, B, Sleiman, P M A, Hysi, P, Warrington, N M, Curjuric, I, Myhre, R, Curtin, J A, Groen-Blokhuis, M M, Kerkhof, M, Sääf, A, Franke, A, Ellinghaus, D, Fölster-Holst, R, Dermitzakis, E, Montgomery, S B, Prokisch, H, Heim, K, Hartikainen, A-L, Pouta, A, Pekkanen, J, Blakemore, A I F, Buxton, J L, Kaakinen, M, Duffy, D L, Madden, P A, Heath, A C, Montgomery, G W, Thompson, P J, Matheson, M C, Le Souëf, P, Pourcain, B S, Smith, G D, Henderson, J, Kemp, J P, Timpson, N J, Deloukas, P, Ring, S M, Nøhr, E A, Jacobsson, B & Australian Asthma Genetics Consortium (AAGC) 2011, ' Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis ', Nature Genetics, vol. 44, no. 2, pp. 187-192 . https://doi.org/10.1038/ng.1017
Nature Genetics, Vol. 44, No 2 (2012) pp. 187-92
Nature genetics
Nature Genetics, 44(2), 187-192. Nature Publishing Group
Paternoster, L, Standl, M, Chen, C-M, Ramasamy, A, Bonnelykke, K, Duijts, L, Ferreira, M A, Alves, A C, Thyssen, J P, Albrecht, E, Baurecht, H, Feenstra, B, Sleiman, P M A, Hysi, P, Warrington, N M, Curjuric, I, Myhre, R, Curtin, J A, Groen-Blokhuis, M M, Kerkhof, M, Saaf, A, Franke, A, Ellinghaus, D, Foelster-Holst, R, Dermitzakis, E, Montgomery, S B, Prokisch, H, Heim, K, Hartikainen, A-L, Pouta, A, Pekkanen, J, Blakemore, A I F, Buxton, J L, Kaakinen, M, Duffy, D L, Madden, P A, Heath, A C, Montgomery, G W, Thompson, P J, Matheson, M C, Le Souef, P, St Pourcain, B, Smith, G D, Henderson, J, Kemp, J P, Timpson, N J, Deloukas, P, Ring, S M, Wichmann, H-E, Mueller-Nurasyid, M, Novak, N, Klopp, N, Rodriguez, E, McArdle, W, Linneberg, A, Menne, T, Nohr, E A, Hofman, A, Uitterlinden, A G, van Duijin, C M, Rivadeneira, F, de Jongste, J C, van der Valk, R J P, Wjst, M, Jogi, R, Geller, F, Boyd, H A, Murray, J C, Kim, C, Mentch, F, March, M, Mangino, M, Spector, T D, Bataille, V, Pennell, C E, Holt, P G, Sly, P, Tiesler, C M T, Thiering, E, Illig, T, Imboden, M, Nystad, W, Simpson, A, Hottenga, J-J, Postma, D, Koppelman, G H, Smit, H A, Soderhall, C, Chawes, B, Kreiner-Moller, E, Bisgaard, H, Melen, E, Boomsma, D I, Custovic, A, Jacobsson, B, Probst-Hensch, N M, Palmer, L J, Glass, D, Hakonarson, H, Melbye, M, Jarvis, D L, Jaddoe, V W V, Gieger, C, Strachan, D P, Martin, N G, Jarvelin, M-R, Heinrich, J, Evans, D M & Weidinger, S 2012, ' Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis ', Nature Genetics, vol. 44, no. 2, pp. 187-192 . https://doi.org/10.1038/ng.1017
Paternoster, L, Standl, M, Chen, C M, Ramasamy, A, Bønnelykke, K, Duijts, L, Ferreira, M A, Couto Alves, A, Thyssen, J P, Albrecht, E, Baurecht, H, Feenstra, B, Sleiman, P M A, Hysi, P, Warrington, N M, Curjuric, I, Myhre, R, Curtin, J A, Groen-Blokhuis, M M, Kerkhof, M, Sääf, A, Franke, A, Ellinghaus, D, Fölster-Holst, R, Dermitzakis, E, Montgomery, S B, Prokisch, H, Heim, K, Hartikainen, A-L, Pouta, A, Pekkanen, J, Blakemore, A I F, Buxton, J L, Kaakinen, M, Duffy, DL, Madden, P A F, Heath, A C, Montgomery, G W, Thompson, P J, Matheson, M C, Le Souëf, P, St Pourcain, B, Davey Smith, G, Henderson, J, Kemp, J P, Timpson, N J, Deloukas, P, Ring, S M, Wichmann, H-E, Müller-Nurasyid, M, Novak, N, Klopp, N, Rodríguez, E, McArdle, W, Linneberg, A, Menné, T, Nohr, E A, Hofman, A, Uitterlinden, A G, van Duijn, C M, Rivadeneira, F, de Jongste, J C, van der Valk, R J P, Wjst, M, Jogi, R, Geller, F, Boyd, H A, Murray, J C, Kim, C, Mentch, F, March, M, Mangino, M, Spector, T D, Bataille, V, Pennell, C E, Holt, P G, Sly, P, Tiesler, C M T, Hottenga, J J, Boomsma, D I, Hakonarson, H, Melbye, M, Ljarvis, D, Jaddoe, V W V, Gieger, C, Strachan, D P, Martin, N G, Jarvelin, M-R, Heinrich, J, Evans, D M & Weidinger, S 2012, ' Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis ', Nature Genetics, vol. 44, no. 2, pp. 187-192 . https://doi.org/10.1038/ng.1017مصطلحات موضوعية: Male, Genetics of Overweight Young Adults (GOYA) Consortium, Netherlands Twin Register (NTR), Epidemiology, Cell Differentiation/genetics Chromosomes, Human, Pair 11/genetics Chromosomes, Human, Pair 20/genetics Chromosomes, Human, Pair 5 Cytokines/genetics DNA-Binding Proteins/genetics Dermatitis, Atopic/*genetics/immunology Epidermis/immunology Female *Genetic Loci Genetic Predisposition to Disease *Genome-Wide Association Study Humans Intermediate Filament Proteins/genetics Kinesin/genetics Male Polymorphism, Single Nucleotide Risk Transcription Factors/genetics, Chromosomes, Human, Pair 20, Kinesins, Genome-wide association study, Filaggrin Proteins, VARIANTS, Chromosomes, Human, Pair 11/genetics, medicine.disease_cause, Genome-wide association studies, DISEASE, 030207 dermatology & venereal diseases, 0302 clinical medicine, Intermediate Filament Proteins, Epidermis/immunology, ddc:576.5, GENETICS & HEREDITY, Genetics, 0303 health sciences, education.field_of_study, PSORIASIS, Cytokines/genetics, Cell Differentiation, Kinesin, 11 Medical And Health Sciences, Atopic dermatitis, 3. Good health, DNA-Binding Proteins, DIFFERENTIATION, Chromosomes, Human, Pair 5, Cytokines, Female, Dermatitis, Atopic/genetics/immunology, Life Sciences & Biomedicine, Kinesin/genetics, Filaggrin, EXPRESSION, Risk, Cell Differentiation/genetics, Population, Transcription Factors/genetics, Single-nucleotide polymorphism, Locus (genetics), Biology, Polymorphism, Single Nucleotide, Australian Asthma Genetics Consortium (AAGC), Article, MECHANISMS, Dermatitis, Atopic, 03 medical and health sciences, SDG 3 - Good Health and Well-being, medicine, FILAGGRIN, Humans, SPERMATOGENESIS, Genetic Predisposition to Disease, EArly Genetics & Lifecourse Epidemiology (EAGLE) Consortium, education, 030304 developmental biology, Science & Technology, Chromosomes, Human, Pair 11, Odds ratio, 06 Biological Sciences, Immune dysregulation, medicine.disease, Chromosomes, Human, Pair 20/genetics, Genetic Loci, Intermediate Filament Proteins/genetics, Immunology, ASTHMA, Epidermis, CELLULAR MOTILITY, DNA-Binding Proteins/genetics, Genome-Wide Association Study, Transcription Factors, Developmental Biology
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المؤلفون: Virpi Lindi, Clare S. Murray, Liming Liang, Wieland Kiess, Philippe Froguel, Tarunveer S. Ahluwalia, Hakon Hakonarson, Dorret I. Boomsma, Pitkänen Niina Pitkänen, Romy Gaillard, Mandy Geserick, John A. Curtin, Shana E. McCormack, Niinikoski Harri, Jens-Christian Holm, Vicente Gilsanz, Ville Huikari, Maties Torrent, Nicholas J. Timpson, George Dedoussis, Angela Simpson, Struan F.A. Grant, Klaus Bønnelykke, Anubha Mahajan, George McMahon, Raimo Joro, Christel M. Middeldorp, Johan G. Eriksson, Vilor-Tejedor Natalia Vilor-Tejedor, Gerard H. Koppelman, Frank Geller, Amélie Bonnefond, Hanna Maaria Lakka, Jinyan Huang, Craig E. Pennell, Johannes Waage, Jane Wardle, Torben Hansen, Olli T. Raitakari, John A. Shepherd, Lisbeth Carstensen, Andrea Kelly, Katja Pahkala, Jordi Sunyer, Claire M. A. Haworth, Per Magnus, Juan R. González, Babette S. Zemel, Mads Melbye, Steve Franks, Carla M. T. Tiesler, Roland Pfäffle, Momoko Horikoshi, Susan M. Ring, Adnan Custovic, Claudia Flexeder, Claire Monnereau, Heidi J. Kalkwarf, Janine F. Felix, Julie A. Marsh, Thorkild I. A. Sørensen, André G. Uitterlinden, Mustafa Atalay, Jouke-Jan Hottenga, Mark I. McCarthy, Joel N. Hirschhorn, Niels Grarup, Lude Franke, Diana L. Cousminer, Timo A. Lakka, Robert Plomin, Ronny Myhre, Albert Hofman, Baoshan Ma, Eskil Kreiner-Møller, Jesús Vioque, Vincent W. V. Jaddoe, Hans Bisgaard, Bjarke Feenstra, Sylvain Sebert, Evie Stergiakouli, Eleftheria Zeggini, Joachim Heinrich, Bo Jacobsson, Tune H. Pers, Dirkje S. Postma, Elina Hyppönen, Loic Yengo, Haja N. Kadarmideen, Alana Cavadino, Jonathan P. Bradfield, Elisabeth Thiering, Ralf J. P. van der Valk, George Davey Smith, Alexandra I. F. Blakemore, Christine Power, Marjo-Riitta Järvelin, Wei Ang, Ioanna Ntalla, Sharon E. Oberfield, Fernando Rivadeneira, Rebecca K. Vinding, Alexandra M. Lewin, Mika Kähönen, Verena Sengpiel, Maria M. Groen-Blokhuis, Anna-Liisa Hartikainen, Antje Körner, Oluf Pedersen, Joyce B. J. van Meurs, Alessandra Chesi, Widén Elisabeth Widén, Terho Lehtimäki, Thomas S. Price, Frank D. Mentch, Joan M. Lappe, Leo-Pekka Lyytikäinen
المساهمون: Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Groningen Research Institute for Asthma and COPD (GRIAC), Stem Cell Aging Leukemia and Lymphoma (SALL), Early Growth Genetics (EGG) Consortium, Bone Mineral Density in Childhood Study (BMDCS), Early Genetics and Lifecourse Epidemiology (EAGLE) consortium, Felix, Janine F, Bradfield, Jonathan P, Monnereau, Claire, van der Valk, Ralf JP, Hypponen, Elina, Jaddoe, Vincent WV, Biological Psychology, EMGO+ - Lifestyle, Overweight and Diabetes, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, Erasmus MC other, Epidemiology, Pediatrics, Child and Adolescent Psychiatry / Psychology, Internal Medicine, Public Health
المصدر: Hum. Mol. Genet. 25, 389-403 (2016)
Human Molecular Genetics
Human Molecular Genetics, 25(2), 389-403. Oxford University Press
Felix, J F, Bradfield, J P, Monnereau, C, van der Valk, R J P, Stergiakouli, E, Chesi, A, Gaillard, R, Feenstra, B, Thiering, E, Kreiner-Møller, E, Blokhuis, M M, Horikoshi, M, Hottenga, J J, Middeldorp, C M, Uitterlinden, A G, Plomin, R, Boomsma, D I, Heinrich, J, Melbye, M, Rivadeneira, F, Hakonarson, H, Ring, S M, Davey Smith, G, Sørensen, T I A, Timpson, N J, Grant, S F A & Jaddoe, V W V 2016, ' Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index ', Human Molecular Genetics, vol. 25, no. 2, pp. 389-403 . https://doi.org/10.1093/hmg/ddv472
Felix, J F, Bradfield, J P, Monnereau, C, Van Der Valk, R J P, Stergiakouli, E, Chesi, A, Gaillard, R, Feenstra, B, Thiering, E, Kreiner-Møller, E, Mahajan, A, Pitk??nen, N, Joro, R, Cavadino, A, Huikari, V, Franks, S, Groen-blokhuis, M M, Cousminer, D L, Marsh, J A, Lehtimäki, T, Curtin, J A, Vioque, J, Ahluwalia, T S, Myhre, R, Price, T S, Vilor-tejedor, N, Yengo, L, Grarup, N, Ntalla, I, Ang, W, Atalay, M, Bisgaard, H, Blakemore, A I, Bonnefond, A, Carstensen, L, Eriksson, J, Flexeder, C, Franke, L, Geller, F, Geserick, M, Hartikainen, A, Haworth, C M A, Hirschhorn, J N, Hofman, A, Holm, J, Horikoshi, M, Hottenga, J J, Huang, J, Kadarmideen, H N, Kähönen, M, Kiess, W, Lakka, H, Lakka, T A, Lewin, A M, Liang, L, Lyytikäinen, L, Ma, B, Magnus, P, Mccormack, S E, Mcmahon, G, Mentch, F D, Middeldorp, C M, Murray, C S, Pahkala, K, Pers, T H, Pfäffle, R, Postma, D S, Power, C, Simpson, A, Sengpiel, V, Tiesler, C M T, Torrent, M, Uitterlinden, A G, Van Meurs, J B, Vinding, R, Waage, J, Wardle, J, Zeggini, E, Zemel, B S, Dedoussis, G V, Pedersen, O, Froguel, P, Sunyer, J, Plomin, R, Jacobsson, B, Hansen, T, Gonzalez, J R, Custovic, A, Raitakari, O T, Pennell, C E, Widøn, E, Boomsma, D I, Koppelman, G H, Sebert, S, Jørvelin, M, Hyppønen, E, Mccarthy, M I, Lindi, V, Harri, N, Kørner, A, Bønnelykke, K, Heinrich, J, Melbye, M, Rivadeneira, F, Hakonarson, H, Ring, S M, Smith, G D, Sørensen, T I A, Timpson, N J, Grant, S F A & Jaddoe, V W V 2015, ' Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index ', Human Molecular Genetics, vol. 25, pp. 389-403 . https://doi.org/10.1093/hmg/ddv472مصطلحات موضوعية: 0301 basic medicine, Netherlands Twin Register (NTR), Male, ADAM23, Genome-wide association study, VARIANTS, ENVIRONMENTAL-FACTORS, Body Mass Index, Child, Genetics (clinical), 2. Zero hunger, Genetics, education.field_of_study, Association Studies Articles, General Medicine, INSIGHTS, Child, Preschool, Female, childhood obesity, EXPRESSION, Adult, Risk, Adolescent, Population, body mass index, Single-nucleotide polymorphism, Biology, ta3111, Polymorphism, Single Nucleotide, Childhood obesity, White People, 03 medical and health sciences, Young Adult, children, SDG 3 - Good Health and Well-being, medicine, Humans, Obesity, Allele, education, Molecular Biology, METAANALYSIS, Genetic association, FAT DISTRIBUTION, ta3121, medicine.disease, ta3123, GENE, 030104 developmental biology, Genetic Loci, WEIGHT, Body mass index, Genome-Wide Association Study
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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff4904a1e110859cb47db18f25f9c7c0
https://pubmed.ncbi.nlm.nih.gov/26604143 -
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المؤلفون: Supinda Bunyavanich, Mayumi Tamari, Ronny Myhre, Birgit Kalb, Benjamin A. Raby, Xuejun Zhang, Wendy L. McArdle, Daniel Glass, Gabrielle A. Lockett, Chao Tian, Adnan Custovic, Frank Geller, Albert M. Levin, Susanne Lau, Nicole Probst-Hensch, Marie Standl, Tim D. Spector, Elke Rodriguez, Badri Pahukasahasram, Craig E. Pennell, Carole Ober, Alexessander Couto Alves, George Davey Smith, Cheng-Jian Xu, James J. Yang, Nicholas G. Martin, Elisabeth Altmaier, Feng Li Xiao, Regina Foelster-Holst, Lise Lotte N. Husemoen, Atsushi Takahashi, Angela Simpson, Markus M. Noethen, Grainne M. O'Regan, Patrick M. A. Sleiman, Anja Bauerfeind, Linda E. Campbell, Jacob P. Thyssen, Caoimhe M. R. Fahy, Ingo Marenholz, André G. Uitterlinden, Jorge Esparza-Gordillo, Albert Hofman, John A. Curtin, John P. Kemp, Jie Zheng, Melanie C. Matheson, Suzanne G.M.A. Pasmans, Christian Gieger, Pirro G. Hysi, Esteban G. Burchard, Eskil Kreiner-Møller, Keith M. Godfrey, Erik Melén, Jin Li, Hans Bisgaard, Michael Kurek, X. Zheng, Min Ae Lee-Kirsch, Lavinia Paternoster, Mads Melbye, Juha Pekkanen, Natalia Vilor-Tejedor, Elisabeth Thiering, Carsten Oliver Schmidt, Anja Matanovic, W.H. Irwin McLean, Wenche Nystad, Carla M. T. Tiesler, Sheila J. Barton, Michiaki Kubo, Klaus Bønnelykke, Guy B. Marks, Stephan Weidinger, Deborah A. Meyers, David P. Strachan, Bjarke Feenstra, Wolfgang Lieb, Thomas Keil, Celeste Eng, Elisabeth Mangold, Christel M. Middeldorp, Cristina Venturini, Niels J. Elbert, Jouke-Jan Hottenga, Xian Bo Zuo, Georg Homuth, L. Keoki Williams, Sylvain Sebert, Maria Pino-Yanes, Mariona Bustamante, Scott T. Weiss, Donglei Hu, Allan Linneberg, Ashok Kumar, Ivan Curjuric, Johannes Waage, Joachim Heinrich, Philip J. Thompson, Johan C. de Jongste, Fernando Rivadeneira, Veronique Bataille, David M. Evans, Joyce Y. Tung, Bo Jacobsson, Natalija Novak, Sara J. Brown, Andre Franke, Medea Imboden, Lisbeth Carstensen, Maeve A. McAleer, Jordi Sunyer, Momoko Horikoshi, Hakon Hakonarson, Liesbeth Duijts, Juan R. González, Scott Huntsman, Xianyong Yin, Melanie Hotze, Niels Grarup, Carol A. Wang, Norbert Huebner, Tomomitsu Hirota, Rachel A. Myers, Milan Macek, Cilla Soederhaell, Maria M. Groen-Blokhuis, Herman T. den Dekker, Dorret I. Boomsma, Franz Rueschendorf, Deborah Jarvis, Alan D. Irvine, Sven Cichon, Manuel A. R. Ferreira, Janina S. Ried, Young-Ae Lee, Andreas Arnold, H. Baurecht, Gerard H. Koppelman, David A. Hinds, Colin F. Robertson, Liangdan Sun, Vincent W. V. Jaddoe, Dirkje S. Postma, Marjo-Riitta Järvelin, Annette Peters, John W. Holloway, Caroline L Relton, A. John Henderson, Jonas Bacelis
المساهمون: Psychiatry, EMGO - Musculoskeletal health, NCA - Neurobiology of mental health, Groningen Research Institute for Asthma and COPD (GRIAC), Epidemiology, Pediatrics, Internal Medicine, Erasmus MC other, Dermatology, Gastroenterology & Hepatology, Child and Adolescent Psychiatry / Psychology, Public Health, Biological Psychology, EMGO+ - Musculoskeletal Health, Neuroscience Campus Amsterdam - Neurobiology of Mental Health
المصدر: Nature Genetics, 47(12), 1449-1456. Nature Publishing Group
Paternoster, L, Standl, M, Waage, J, Baurecht, H, Hotze, M, Strachan, D P, Curtin, J A, Bonnelykke, K, Tian, C, Takahashi, A, Esparza-Gordillo, J, Alves, A C, Thyssen, J P, den Dekker, H T, Ferreira, M A, Altmaier, E, Sleiman, P M A, Xiao, F L, Gonzalez, J R, Marenholz, I, Kalb, B, Pino-Yanes, M, Xu, C, Carstensen, L, Groen-Blokhuis, M M, Venturini, C, Pennell, C E, Barton, S J, Levin, A M, Curjuric, I, Bustamante, M, Kreiner-Moller, E, Lockett, G A, Bacelis, J, Bunyavanich, S, Myers, R A, Matanovic, A, Kumar, A, Tung, J Y, Hirota, T, Kubo, M, McArdle, W L, Henderson, A J, Kemp, J P, Zheng, J, Smith, G D, Rueschendorf, F, Bauerfeind, A, Lee-Kirsch, M A, Arnold, A, Homuth, G, Schmidt, C O, Mangold, E, Cichon, S, Keil, T, Rodriguez, E, Peters, A, Franke, A, Lieb, W, Novak, N, Foelster-Holst, R, Horikoshi, M, Pekkanen, J, Sebert, S, Husemoen, L L, Grarup, N, de Jongste, J C, Rivadeneira, F, Hofman, A, Jaddoe, V W V, Pasmans, S G M A, Elbert, N J, Uitterlinden, A G, Marks, G B, Thompson, P J, Matheson, M C, Robertson, C F, Ried, J S, Li, J, Zuo, X B, Zheng, X D, Yin, X Y, Sun, L D, McAleer, M A, O'Regan, G M, Fahy, C M R, Campbell, L E, Macek, M, Kurek, M, Hu, D, Eng, C, Postma, D S, Feenstra, B, Geller, F, Hottenga, J J, Middeldorp, C M, Hysi, P, Bataille, V, Spector, T, Tiesler, C M T, Thiering, E, Pahukasahasram, B, Yang, J J, Imboden, M, Huntsman, S, Vilor-Tejedor, N, Relton, C L, Myhre, R, Nystad, W, Custovic, A, Weiss, S T, Meyers, D A, Soederhaell, C, Melen, E, Ober, C, Raby, B A, Simpson, A, Jacobsson, B, Holloway, J W, Bisgaard, H, Sunyer, J, Probst-Hensch, N M, Williams, L K, Godfrey, K M, Wang, C A, Boomsma, D I, Melbye, M, Koppelman, G H, Jarvis, D, McLean, W H I, Irvine, A D, Zhang, X J, Hakonarson, H, Gieger, C, Burchard, E G, Martin, N G, Duijts, L, Linneberg, A, Jarvelin, M, Noethen, M M, Lau, S, Huebner, N, Lee, Y, Tamari, M, Hinds, D A, Glass, D, Brown, S J, Heinrich, J, Evans, D M & Weidinger, S 2015, ' Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis ', Nature Genetics, vol. 47, no. 12, pp. 1449-1456 . https://doi.org/10.1038/ng.3424
Paternoster, L, Standl, M, Waage, J, Baurecht, H, Hotze, M, Strachan, D P, Curtin, J A, Bønnelykke, K, Tian, C, Takahashi, A, Esparza-Gordillo, J, Alves, A C, Thyssen, J P, den Dekker, H T, Ferreira, M A, Altmaier, E, Sleiman, P M A, Xiao, F L, Gonzalez, J R, Marenholz, I, Kalb, B, Pino-Yanes, M, Xu, C-J, Carstensen, L, Groen-Blokhuis, M M, Venturini, C, Pennell, C E, Barton, S J, Levin, A M, Curjuric, I, Bustamante, M, Kreiner-Møller, E, Lockett, G A, Bacelis, J, Bunyavanich, S, Myers, R A, Matanovic, A, Kumar, A, Tung, J Y, Hirota, T, Kubo, M, McArdle, W L, Henderson, A J, Kemp, J P, Zheng, J, Smith, G D, Relton, C L, Duijts, L, Lee, Y-A, Evans, D M 2015, ' Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis ', Nature Genetics, vol. 47, no. 12, pp. 1449-1456 . https://doi.org/10.1038/ng.3424
Nature Genetics, 47(12), 1449-1458. Nature Publishing Group
Recercat. Dipósit de la Recerca de Catalunya
instname
Nature genetics
Paternoster, L, Standl, M, Waage, J, Baurecht, H, Hotze, M, Strachan, D P, Curtin, J A, Bønnelykke, K, Tian, C, Takahashi, A, Esparza-Gordillo, J, Alves, A C, Thyssen, J P, den Dekker, H T, Ferreira, M A, Altmaier, E, Sleiman, P M A, Xiao, F L, Gonzalez, J R, Marenholz, I, Kalb, B, Pino-Yanes, M, Xu, C-J, Carstensen, L, Groen-Blokhuis, M M, Venturini, C, Pennell, C E, Barton, S J, Levin, A M, Curjuric, I, Bustamante, M, Kreiner-Møller, E, Lockett, G A, Bacelis, J, Bunyavanich, S, Myers, R A, Matanovic, A, Kumar, A, Tung, J Y, Hirota, T, Kubo, M, McArdle, W L, Henderson, A J, Kemp, J P, Zheng, J, Smith, G D, Rüschendorf, F, Bauerfeind, A, Lee-Kirsch, M A, Arnold, A, Homuth, G, Schmidt, C O, Mangold, E, Cichon, S, Keil, T, Rodríguez, E, Peters, A, Franke, A, Lieb, W, Novak, N, Fölster-Holst, R, Horikoshi, M, Pekkanen, J, Sebert, S, Husemoen, L L, Grarup, N, de Jongste, J C, Rivadeneira, F, Hofman, A, Jaddoe, V W V, Pasmans, S G M A, Elbert, N J, Uitterlinden, A G, Marks, G B, Thompson, P J, Matheson, M C, Robertson, C F, (AAGC), A A G C, Ried, J S, Li, J, Zuo, X B, Zheng, X D, Yin, X Y, Sun, L D, McAleer, M A, O'Regan, G M, Fahy, C M R, Campbell, L E, Macek, M, Kurek, M, Hu, D, Eng, C, Postma, D S, Feenstra, B, Geller, F, Hottenga, J J, Middeldorp, C M, Hysi, P, Bataille, V, Spector, T, Tiesler, C M T, Thiering, E, Pahukasahasram, B, Yang, J J, Imboden, M, Huntsman, S, Vilor-Tejedor, N, Relton, C L, Myhre, R, Nystad, W, Custovic, A, Weiss, S T, Meyers, D A, Söderhäll, C, Melén, E, Ober, C, Raby, B A, Simpson, A, Jacobsson, B, Holloway, J W, Bisgaard, H, Sunyer, J, Probst-Hensch, N M, Williams, L K, Godfrey, K M, Wang, C A, Boomsma, D I, Melbye, M, Koppelman, G H, Jarvis, D, McLean, W H I, Irvine, A D, Zhang, X J, Hakonarson, H, Gieger, C, Burchard, E G, Martin, N G, Duijts, L, Linneberg, A, Jarvelin, M-R, Nöthen, M M, Lau, S, Hübner, N, Lee, Y-A, Tamari, M, Hinds, D A, Glass, D, Brown, S J, Heinrich, J, Evans, D M, Weidinger, S, Genetics, EA & Consortium, L E E 2015, ' Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis ', Nature Genetics, vol. 47, no. 12, pp. 1449—1456 . https://doi.org/10.1038/ng.3424
Nature Genetics, 47(12), 1449-+. Nature Publishing Groupمصطلحات موضوعية: Netherlands Twin Register (NTR), Candidate gene, T-Lymphocytes, Genome-wide association study, VARIANTS, Genome-wide association studies, EArly Genetics and Lifecourse Epidemiology (EAGLE) Eczema Consortium, Risk Factors, Ethnicity, health care economics and organizations, Genetics & Heredity, Genetics, PSORIASIS, 11 Medical And Health Sciences, Atopic dermatitis, 3. Good health, Life Sciences & Biomedicine, Dermatitis atòpica, Genetic Markers, medicine.medical_specialty, SUSCEPTIBILITY LOCI, education, Biology, Australian Asthma Genetics Consortium (AAGC), Polymorphism, Single Nucleotide, Article, Dermatitis, Atopic, GENETIC ARCHITECTURE, SDG 3 - Good Health and Well-being, Molecular genetics, medicine, Humans, FILAGGRIN, Genetic Predisposition to Disease, JAPANESE POPULATION, Genomes, METAANALYSIS, Genetic association, Science & Technology, Case-control study, Grups ètnics, INTERLEUKIN-7 RECEPTOR, 06 Biological Sciences, medicine.disease, Immunity, Innate, Genetic architecture, Genetic Loci, Genetic marker, Case-Control Studies, Immunology, ASTHMA, Genètica, Developmental Biology, Genome-Wide Association Study, INFLAMMATORY-BOWEL-DISEASE
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