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: 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.1017Test
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.1017Test
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.1017Test
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.1017Test

مصطلحات 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

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a16204b9f49adc2c5756ec98124bd5bTest
https://hdl.handle.net/1871/41666Test

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/ddv472Test
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/ddv472Test

مصطلحات 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

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff4904a1e110859cb47db18f25f9c7c0Test
https://pubmed.ncbi.nlm.nih.gov/26604143Test

المؤلفون: Kelly S. Benke, Craig E. Pennell, Xiangjun Xiao, Fleur P. Velders, Raymond K. Walters, Catharina E. M. van Beijsterveldt, Andrew J. O. Whitehouse, Dorret I. Boomsma, Vincent W. V. Jaddoe, Michel G. Nivard, Lyle J. Palmer, Irene Pappa, Maria M. Groen-Blokhuis, Henning Tiemeier, Paul Scheet, Erik A. Ehli, Gareth E. Davies, Gitta H. Lubke, Christel M. Middeldorp, James J. Hudziak, Fernando Rivadeneira, Frank C. Verhulst

المساهمون: Child and Adolescent Psychiatry / Psychology, Erasmus MC other, Internal Medicine, Psychiatry, Biological Psychology, Neuroscience Campus Amsterdam - Neurobiology of Mental Health, Clinical Child and Family Studies, APH - Mental Health, EMGO+ - Mental Health, EMGO - Mental health

المصدر: Journal of the American Academy of Child and Adolescent Psychiatry, 53(6), 667-676. Elsevier Ltd.
Early Genetics and Lifecourse Epidemiology Consortium 2014, ' A genome-wide association meta-analysis of preschool internalizing problems ', Journal of the American Academy of Child and Adolescent Psychiatry, vol. 53, no. 6, pp. 667-676.e7 . https://doi.org/10.1016/j.jaac.2013.12.028Test
Journal of the American Academy of Child and Adolescent Psychiatry, 53(6), 667-676.e7. Elsevier Limited
Benke, K S, Nivard, M G, Velders, F P, Walters, R K, Pappa, I, Scheet, P, Xiao, X, Ehli, E A, Palmer, L J, Whitehouse, A J O, Verhulst, F C, Jaddoe, V W, Rivadeneira, F, Blokhuis, M M, van Beijsterveldt, C E M, Davies, G E, Hudziak, J J, Lubke, G H, Boomsma, D I, Pennell, C E, Tiemeier, H & Middeldorp, C M 2014, ' A Genome-wide Association Meta-analysis of Preschool Internalizing Problems ', Journal of the American Academy of Child and Adolescent Psychiatry, vol. 53, no. 6, pp. 667-676 . https://doi.org/10.1016/j.jaac.2013.12.028Test
Journal of the American Academy of Child & Adolescent Psychiatry
Journal of the American Academy of Child and Adolescent Psychiatry, 53(6), 667-676. Elsevier Limited

مصطلحات موضوعية: Netherlands Twin Register (NTR), Male, Child Behavior Disorders/genetics, Single-nucleotide polymorphism, Genome-wide association study, CBCL, Child Behavior Disorders, Polymorphism, Single Nucleotide, Cohort Studies, Genome-Wide Association Study/statistics & numerical data, Developmental and Educational Psychology, Humans, Registries, Polymorphism, Child Behavior Checklist, Child, Preschool, Genetics, INT, Registries/statistics & numerical data, Explained variation, Polymorphism, Single Nucleotide/genetics, Genetic architecture, Psychiatry and Mental health, Proprotein Convertase 2, Meta-analysis, Child, Preschool, Female, Psychology, Proprotein Convertase 2/genetics, Single Nucleotide/genetics, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0bd805fb8f2d83e79c857dd8567ca72Test
https://pure.eur.nl/en/publications/ba072489-f170-4f42-9f55-78d93cb448b0Test

المؤلفون: Maria M. Groen-Blokhuis, Catharina E. M. van Beijsterveldt, Dorret I. Boomsma, Gareth E. Davies, Christel M. Middeldorp, Xiangjun Xiao, James J. Hudziak, Erik A. Ehli, Neale Bm, Paul Scheet, Kees-Jan Kan, Abdel Abdellaoui, Jouke-Jan Hottenga

المساهمون: Biological Psychology, EMGO+ - Mental Health, Psychiatry, EMGO - Mental health

المصدر: Blokhuis, M M, Middeldorp, C M, Kan, K J, Abdellaoui, A, van Beijsterveldt, C E M, Ehli, E A, Davies, G E, Scheet, P, Xiao, X, Hudziak, J J, Hottenga, J J, Neale, B M & Boomsma, D I 2014, ' Attention-Deficit/Hyperactivity Disorder Polygenic Risk Scores Predict Attention Problems in a Population-Based Sample of Children ', Journal of the American Academy of Child and Adolescent Psychiatry, vol. 53, no. 10, pp. 1123-1129 . https://doi.org/10.1016/j.jaac.2014.06.014Test
Journal of the American Academy of Child and Adolescent Psychiatry, 53(10), 1123-1129. Elsevier Limited
Journal of the American Academy of Child & Adolescent Psychiatry

مصطلحات موضوعية: Male, Netherlands Twin Register (NTR), Multifactorial Inheritance, medicine.medical_specialty, Population, Single-nucleotide polymorphism, Impulsivity, Polymorphism, Single Nucleotide, Risk Assessment, behavioral disciplines and activities, Attention Problems, SDG 3 - Good Health and Well-being, mental disorders, Developmental and Educational Psychology, medicine, Humans, Attention deficit hyperactivity disorder, Registries, Child, education, Psychiatry, Netherlands, education.field_of_study, Explained variation, medicine.disease, 3. Good health, Psychiatry and Mental health, Attention Deficit Disorder with Hyperactivity, Child, Preschool, Cohort, Female, Polygenic risk score, medicine.symptom, Psychology, SDG 4 - Quality Education, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a847351d365512a4edbb1947c0f38465Test
https://research.vumc.nl/en/publications/3c47b69a-3a5b-43d1-9e9f-1cdd785eecf4Test

المؤلفون: Xiangjun Xiao, James J. Hudziak, Erik A. Ehli, Abdel Abdellaoui, Patricia E. Huizenga, Gareth E. Davies, Christopher I. Amos, Robert R. Althoff, Eco J. C. de Geus, Meike Bartels, Catharina E. M. van Beijsterveldt, Yueshan Hu, Dorret I. Boomsma, Kelly A. Nelson, Maria M. Groen-Blokhuis, Gonneke Willemsen, Paul Scheet, Jouke-Jan Hottenga

المساهمون: Biological Psychology, Neuroscience Campus Amsterdam - Anxiety & Depression, EMGO+ - Mental Health

المصدر: Twin Research and Human Genetics
Twin Research and Human Genetics, 15(6), 737-745. Australian Academic Press
Scheet, P, Ehli, E A, Xiao, X, van Beijsterveldt, C E M, Abdellaoui, A, Althoff, R R, Hottenga, J J, Willemsen, G, Nelson, K A, Huizenga, P E, Hu, Y, Amos, C I, Bartels, M, Groen-Blokhuis, M M, de Geus, E J C, Hudziak, J J, Davies, G E & Boomsma, D I 2012, ' Twins, Tissue, and Time: An Assessment of SNPs and CNVs ', Twin Research and Human Genetics, vol. 15, no. 6, pp. 737-745 . https://doi.org/10.1017/thg.2012.61Test

مصطلحات موضوعية: Netherlands Twin Register (NTR), Adult, Male, Adolescent, DNA Copy Number Variations, Genotype, Concordance, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Article, Specimen Handling, 03 medical and health sciences, Polymorphism (computer science), Genetic variation, SNP, Medicine, Humans, Copy-number variation, Child, Genetics (clinical), 030304 developmental biology, Oligonucleotide Array Sequence Analysis, Genetics, 0303 health sciences, business.industry, 030305 genetics & heredity, Obstetrics and Gynecology, DNA, Twins, Monozygotic, Middle Aged, Twin study, Child, Preschool, Pediatrics, Perinatology and Child Health, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff8b81b9f54a0e4b335db57f679cd0a8Test
https://pubmed.ncbi.nlm.nih.gov/23021707Test