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: 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: 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: Hilleke E. Hulshoff Pol, Eco J. C. de Geus, Nicholas G. Martin, Gareth E. Davies, Abdel Abdellaoui, Sanja Franić, Conor V. Dolan, James J. Hudziak, Xiangjun Xiao, Jouke-Jan Hottenga, Erik A. Ehli, Paul Scheet, Maria M. Groen-Blokhuis, Suzanne C. Swagerman, Catherina E. M. van Beijsterveldt, Mathijs Kattenberg, Sophie van der Sluis, René Pool, Hans-Hilger Ropers, Meike Bartels, Narelle K. Hansell, Dorret I. Boomsma

المساهمون: Biological Psychology, Complex Trait Genetics, Faculty of Behavioural and Movement Sciences, Neuroscience Campus Amsterdam - Neurobiology of Mental Health, Neuroscience Campus Amsterdam - Brain Mechanisms in Health & Disease, EMGO+ - Mental Health, Human genetics, NCA - Brain mechanisms in health and disease, NCA - Neurobiology of mental health, EMGO - Mental health

المصدر: Franic, S, Blokhuis, M M, Dolan, C V, Kattenberg, V M, Pool, R, Xiao, X, Scheet, P, Ehli, E A, Davies, G E, van der Sluis, S, Abdellaoui, A, Hansell, N K, Martin, N G, Hudziak, J J, van Beijsterveldt, C E M, Swagerman, S C, Hulshoff Pol, H E, de Geus, E J C, Bartels, M, Ropers, H-H, Hottenga, J J & Boomsma, D I 2015, ' Intelligence: shared genetic basis between Mendelian disorders and a polygenic trait ', European Journal of Human Genetics, vol. 23, no. 10, pp. 1378-1383 . https://doi.org/10.1038/ejhg.2015.3Test
European Journal of Human Genetics, 23(10), 1378-1383. Nature Publishing Group
European journal of human genetics
European Journal of Human Genetics, 23(10), 1378. Nature Publishing Group

مصطلحات موضوعية: Netherlands Twin Register (NTR), Adult, Male, Multifactorial Inheritance, Adolescent, Intelligence, Quantitative Trait Loci, Biology, Quantitative trait locus, Research Support, Polymorphism, Single Nucleotide, Article, N.I.H, symbols.namesake, Quantitative Trait, Quantitative Trait, Heritable, Research Support, N.I.H., Extramural, Genetics, medicine, Journal Article, SNP, Humans, Genetic variability, Genetic Testing, Polymorphism, Preschool, Non-U.S. Gov't, Child, Heritable, Genetics (clinical), Genetic testing, Genome, medicine.diagnostic_test, Genome, Human, Research Support, Non-U.S. Gov't, Extramural, Infant, Single Nucleotide, Phenotype, Human genetics, Child, Preschool, Mendelian inheritance, symbols, Female, Human

وصف الملف: image/pdf; application/pdf; application/msword

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8414f7568cdd937bfe6667bcdf08e483Test
https://pubmed.ncbi.nlm.nih.gov/25712083Test

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: 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

المؤلفون: Maria M. Groen-Blokhuis

المصدر: Twin Research and Human Genetics. 16:1126-1126

مصطلحات موضوعية: Gerontology, Psychoanalysis, media_common.quotation_subject, Pediatrics, Perinatology and Child Health, Obstetrics and Gynecology, Boundary (topology), Temperament, Sociology, Genetics (clinical), media_common

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::e2b4c2c6aa3cef7682d56efdcd3c731eTest
https://doi.org/10.1017/thg.2013.78Test

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

المصدر: Twin Research and Human Genetics. 16:650-650

مصطلحات موضوعية: Crying, Pediatrics, Perinatology and Child Health, Predictive power, medicine, Obstetrics and Gynecology, Easily upset, Heritability, medicine.symptom, Psychology, Twin study, Genetics (clinical), Human genetics, Developmental psychology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::4ab57eb3c4da437f038d8f02cd11240eTest
https://doi.org/10.1017/thg.2012.52Test