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

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

المصدر: Groen-Blokhuis, M M, Middeldorp, C M, van Beijsterveldt, C E M & Boomsma, D I 2011, ' Crying Without a Cause and Being Easily Upset in Two-Year-Olds: Heritability and Predictive Power of Behavioral Problems ', Twin Research and Human Genetics, vol. 14, no. 5, pp. 393-400 . https://doi.org/10.1375/twin.14.5.393Test
Twin research and human genetics, 14(5), 393-400. Cambridge University Press
Twin Research and Human Genetics, 14(5), 393-400. Australian Academic Press

مصطلحات موضوعية: Male, Netherlands Twin Register (NTR), media_common.quotation_subject, Mothers, Child Behavior Disorders, Crying, Environment, Structural equation modeling, Developmental psychology, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Pregnancy, medicine, Diseases in Twins, Twins, Dizygotic, Personality, Humans, 0501 psychology and cognitive sciences, Child, Life Style, Genetics (clinical), 030304 developmental biology, media_common, Netherlands, 0303 health sciences, 05 social sciences, Obstetrics and Gynecology, Twins, Monozygotic, Heritability, Explained variation, Neuroticism, Twin study, Child, Preschool, Pediatrics, Perinatology and Child Health, Temperament, Female, medicine.symptom, Psychology, 050104 developmental & child psychology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a053ec19de3d0e6e45c837978d53c46Test
https://research.vu.nl/en/publications/b2aa18b8-d1fe-41d6-9608-1ad14a2abab5Test

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: Diana L Cousminer, Diane J Berry, Nicholas J Timpson, Wei Ang, Elisabeth Thiering, Enda Byrne, H Rob Taal, Ville Huikari, Jonathan P Bradfield, Marjan Kerkhof, Maria M Groen-blokhuis, Eskil Kreiner-møller, Claus Holst, Jaakko T Leinonen, John R B Perry, Ida Surakka, Olli Pietiläinen, Johannes Kettunen, Terho Lehtimäki, Jorma S Viikari, Mika Kähönen, Nicole M Warrington, Stephen J Lye, Lyle J Palmer, Carla M T Tiesler, Claudia Flexeder, Grant W Montgomery, Sarah E Medl, Albert Hofman, Jaakko Kaprio, Thorkild I A Sørensen, Ferran Ballester, Hans Bisgaard, Dorret I Boomsma, Struan F A Grant, Vincent W V Jaddoe, Nicholas G Martin, Joachim Heinrich, Craig E Pennell, Olli Raitakari, Johan G Eriksson, George Davey Smith, Marjo-riitta Järvelin, Mark I Mccarthy, Samuli Ripatti

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://keppel.qimr.edu.au/contents/p/staff/Cousminer_hmg.EPUB27Feb_OSI.pdfTest.

وصف الملف: application/pdf

العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.667.4757Test; http://keppel.qimr.edu.au/contents/p/staff/Cousminer_hmg.EPUB27Feb_OSI.pdfTest

الإتاحة: http://keppel.qimr.edu.au/contents/p/staff/Cousminer_hmg.EPUB27Feb_OSI.pdfTest