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: 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.32254Test
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 Genetics

مصطلحات 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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f535ea43e1b4d360bda43b76def5e7fTest
https://doi.org/10.1002/ajmg.b.32254Test

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: 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: 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.3424Test
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.3424Test
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.3424Test
Nature Genetics, 47(12), 1449-+. Nature Publishing Group

مصطلحات 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

وصف الملف: application/pdf; text

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffaf379dca827e2cb3391d8b5a2c1ae9Test
https://research.vumc.nl/en/publications/d354d61b-393a-4249-90bc-0be5aeaa1fd3Test

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: Lot M. Geels, Gareth E. Davies, Christel M. Middeldorp, Catharina E. M. van Beijsterveldt, Jacqueline M. Vink, Maria M. Groen-Blokhuis, Patricia E. Huizenga, Dorret I. Boomsma, Kelly A. Nelson, Meike Bartels

المساهمون: Biological Psychology, Neuroscience Campus Amsterdam - Anxiety & Depression, EMGO+ - Lifestyle, Overweight and Diabetes

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B(8), 1009-1012. Wiley-Liss Inc.
Geels, L M, Groen-Blokhuis, M M, van Beijsterveldt, C E M, Vink, J M, Middeldorp, C M, Bartels, M, Nelson, K A, Huizenga, P E, Davies, G E & Boomsma, D I 2012, ' Maternal prenatal smoking and offspring emotional problems: No moderating effect of maternal or child 5-HTTLPR genotype ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 159B, no. 8, pp. 1009-1012 . https://doi.org/10.1002/ajmg.b.32110Test

مصطلحات موضوعية: Male, Netherlands Twin Register (NTR), Offspring, Mothers, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Pregnancy, Genotype, Medicine, Humans, Genetic Predisposition to Disease, Affective Symptoms, Genetics (clinical), Serotonin transporter, Depression (differential diagnoses), 030304 developmental biology, Serotonin Plasma Membrane Transport Proteins, 0303 health sciences, Fetus, biology, business.industry, Confounding, Smoking, medicine.disease, 030227 psychiatry, Psychiatry and Mental health, 5-HTTLPR, Prenatal Exposure Delayed Effects, biology.protein, Female, business, Clinical psychology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9b894bf5a61bdb2b15f3d83b7237794Test

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