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.1008718Test
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.1008718Test
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.1008718Test
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.1008718Test
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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f7e3e9c63ac8faa6aa819187732da43Test
https://doi.org/10.1371/journal.pgen.1008718Test

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.32333Test
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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29cb6c186dc4295c1834d7ff83288ce0Test
https://research.vu.nl/en/publications/d9fa8984-7732-494c-8511-a553b0e3cef4Test

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/10.1155/2014/591717Test
BioMed Research International, Vol 2014 (2014)
Biomed research international, 2014:591717. Hindawi Publishing Corporation
BioMed Research International, 2014. Hindawi Publishing Corporation
BioMed Research International

مصطلحات 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

وصف الملف: text/xhtml

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89775fcca68e457df71083440c246ddaTest
https://doi.org/10.1155/2014/591717Test

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.32175Test
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

مصطلحات 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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2961f71e6947ace036c4cd562d40808Test
https://doi.org/10.1002/ajmg.b.32175Test

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.2012.118Test

مصطلحات 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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::252e503b2541d286b19e7cb9daa119b2Test
https://doi.org/10.1017/thg.2012.118Test

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.2245Test
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.2245Test
Nature genetics 44(5), 539-544 (2012). doi:10.1038/ng.2245

مصطلحات 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

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62d6054f0dfc1871406dd0e078ab45e5Test

المؤلفون: Dorret I. Boomsma, Maria M. Groen-Blokhuis, Christel M. Middeldorp, Catharina E. M. van Beijsterveldt

المساهمون: Biological Psychology, Neuroscience Campus Amsterdam - Attention & Cognition, EMGO+ - Mental Health, Child Psychiatry

المصدر: Journal of the American Academy of Child and Adolescent Psychiatry, 50(12), 1247-1254. Elsevier Limited
Journal of the American Academy of Child and Adolescent Psychiatry, 50(12), 1247-54.e2. Elsevier Limited
Groen-Blokhuis, M M, Middeldorp, C M, van Beijsterveldt, C E M & Boomsma, D I 2011, ' Evidence for a causal association of low birth weight and attention problems ', Journal of the American Academy of Child and Adolescent Psychiatry, vol. 50, no. 12, pp. 1247-1254 . https://doi.org/10.1016/j.jaac.2011.09.007Test

مصطلحات موضوعية: Netherlands Twin Register (NTR), Pediatrics, medicine.medical_specialty, Birth weight, Gestational age, Physiology, medicine.disease, 030227 psychiatry, Correlation, 03 medical and health sciences, Psychiatry and Mental health, Low birth weight, 0302 clinical medicine, Attention Problems, Causal association, Developmental and Educational Psychology, medicine, Etiology, Attention deficit hyperactivity disorder, medicine.symptom, Psychology, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bb374a642033ba575a56132b846abddTest
https://doi.org/10.1016/j.jaac.2011.09.007Test