المؤلفون: Dorret I. Boomsma, Erik A. Ehli, Xiangjun Xiao, James J. Hudziak, Meike Bartels, Catharina E. M. van Beijsterveldt, Eco J. C. de Geus, Maria M. Groen-Blokhuis, Gareth E. Davies, Robert R. Althoff, Christel M. Middeldorp, Paul Scheet, Sanja Franić

المساهمون: Biological Psychology, Neuroscience Campus Amsterdam - Neurobiology of Mental Health, Neuroscience Campus Amsterdam - Brain Mechanisms in Health & Disease, Child Psychiatry

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 162(5), 457-465. Wiley-Liss Inc.
American journal of medical genetics. Part B, Neuropsychiatric genetics, 162(5), 457-465. Wiley-Liss Inc.
Groen-Blokhuis, M M, Franic, S, van Beijsterveldt, C E M, de Geus, E J C, Bartels, M, Davies, G E, Ehli, E A, Xiao, X, Scheet, P, Althoff, R R, Hudziak, J J, Middeldorp, C M & Boomsma, D I 2013, ' A prospective study of the effects of breastfeeding and FADS2 polymorphisms on cognition and hyperactivity/attention problems ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 162, no. 5, pp. 457-465 . https://doi.org/10.1002/ajmg.b.32175Test
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

مصطلحات موضوعية: Adult, Fatty Acid Desaturases, Netherlands Twin Register (NTR), FADS2, Breastfeeding, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Structural equation modeling, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, SDG 3 - Good Health and Well-being, Humans, Medicine, Prospective Studies, 030212 general & internal medicine, Cognitive skill, Prospective cohort study, Genetics (clinical), business.industry, Infant, Newborn, Infant, Cognition, Educational attainment, Psychiatry and Mental health, Breast Feeding, Attention Deficit Disorder with Hyperactivity, Twin Studies as Topic, Female, Cognition Disorders, business, 030217 neurology & neurosurgery, Clinical psychology

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

المؤلفون: Diane J. Lamb, Catharina E. M. van Beijsterveldt, Dorret I. Boomsma, Paul Scheet, James J. Hudziak, Eco J. C. de Geus, Jacob F. Orlebeke, Nienke M. Schutte, Michel G. Nivard, Cyrina Brouwer, Erik A. Ehli, T.J. Glasner, T.M. Stroet, Suzanne C. Swagerman, Conor V. Dolan, Dustin Nowotny, Kees-Jan Kan, Sanja Franić, Dirk J.A. Smit, Gareth E. Davies, Eveline L. de Zeeuw, Meike Bartels, Charlotte Huppertz, Christel M. Middeldorp, Jouke-Jan Hottenga, Maria M. Groen-Blokhuis, Michelle Van Fulpen

المساهمون: Neuroscience Campus Amsterdam - Neurobiology of Mental Health, EMGO+ - Mental Health, Biological Psychology, Methods and Techniques

المصدر: Twin Research and Human Genetics, 16(1), 252-267. Australian Academic Press
Twin Research and Human Genetics
van Beijsterveldt, C E M, Groen-Blokhuis, M M, Franic, S, Hudziak, J J, Lamb, D J, Huppertz, C, de Zeeuw, E L, Nivard, M G, Schutte, N M, Swagerman, S C, Glasner, T J, van Fulpen, M J, Brouwer, C D, Stroet, T M, Nowotny, D, Ehli, E A, Davies, G E, Scheet, P, Orlebeke, J F, Kan, K J, Smit, D J A, Dolan, C V, Middeldorp, C M, de Geus, E J C, Bartels, M & Boomsma, D I 2013, ' The Young Netherlands Twin Register (YNTR): Longitudinal Twin and Family Studies in Over 70,000 Children ', Twin Research and Human Genetics, vol. 16, no. 1, pp. 252-267 . https://doi.org/10.1017/thg.2012.118Test

مصطلحات موضوعية: Male, Gerontology, Netherlands Twin Register (NTR), Adolescent, Twins, Neuropsychological Tests, 03 medical and health sciences, 0302 clinical medicine, SDG 3 - Good Health and Well-being, Pregnancy, Surveys and Questionnaires, Diseases in Twins, Humans, Medicine, Family, Longitudinal Studies, Registries, Child, Genetics (clinical), Netherlands, 030304 developmental biology, 0303 health sciences, Data collection, business.industry, Mental Disorders, Neuropsychology, Infant, Obstetrics and Gynecology, medicine.disease, Twin study, Zygosity, Child, Preschool, Pediatrics, Perinatology and Child Health, Female, business, Twins Early Development Study, 030217 neurology & neurosurgery, Record linkage, Psychopathology

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

المؤلفون: Julie A. Marsh, Meike W. Vernooij, Nicholas J. Timpson, Linda S. Adair, Maksim Struchalin, Kelly S. Benke, Alex P. Zijdenbos, Wiro J. Niessen, Dexter Hadley, André Scherag, Niina Siitonen, Johannes Hedebrand, Helena Schmidt, Iona Y. Millwood, Emily Oken, David S. Knopman, James F. Wilson, H. Rob Taal, Henri A. Vrooman, Karen L. Mohlke, Myriam Fornage, Vilmundur Gudnason, Leslie A. Lange, Sigurdur Sigurdsson, Maria M. Groen-Blokhuis, Diane J. Catellier, Stefan Ropele, Seang Mei Saw, Sylvain Sebert, Alexa S. Beiser, Lyle J. Palmer, Claudia Flexeder, Paul Elliott, George Davey Smith, John W. Holloway, Michel G. Nivard, Mike A. Nalls, Albert V. Smith, Cyrus Cooper, E Zeggini, Terho Lehtimäki, Struan F.A. Grant, Virpi Lindi, Romy Gaillard, B. Gwen Windham, Dennis O. Mook-Kanamori, Claus Holst, Timo A. Lakka, Stéphanie Debette, Liang Kee Goh, Ewan R. Pearson, Tamara B. Harris, Momoko Horikoshi, Jeffrey C. Murray, Mirna Kirin, M. Arfan Ikram, George V. Dedoussis, Anita L. DeStefano, Clifford R. Jack, Alex Lewin, Reedik Maggi, Vincent W. V. Jaddoe, Haukur Gudnason, Hakon Hakonarson, Thomas H. Mosley, Alina Rodriguez, Sudha Seshadri, William M. Meeks, Philip A. Wolf, Gonneke Willemsen, B. Valcarcel, Anke Hinney, Eric A.P. Steegers, Lenore J. Launer, Elina Hyppönen, Lachlan J. M. Coin, Elisabeth Thiering, Mustafa Atalay, W. T. Longstreth, Thorkild I. A. Sørensen, André G. Uitterlinden, Christel M. Middeldorp, Matthew W. Gillman, Ken K. Ong, Oliver S. P. Davis, Monique M.B. Breteler, Wei Ang, Ulla Sovio, Tuomas O. Kilpeläinen, Ioanna Ntalla, Marjo-Riitta Järvelin, Aad van der Lugt, Cornelia M. van Duijn, Cecilia M. Lindgren, Rany M. Salem, Laura H. Coker, Craig E. Pennell, Fernando Rivadeneira, Thomas S. Price, Charles DeCarli, Dorret I. Boomsma, Ellen Aagaard Nohr, Diane Berry, Rhoda Au, Yik Y. Teo, Ville Huikari, Jouke-Jan Hottenga, Matthew Kowgier, Joachim Heinrich, Nienke E. Bergen, Beate St Pourcain, Reinhold Schmidt, C Power, Kalliope Panoutsopoulou, Olli T. Raitakari, Albert Hofman, Mark I. McCarthy, Joel N. Hirschhorn, Olli Simell, Claire M. A. Haworth, Mark A. van Buchem, Anna-Liisa Hartikainen, Berthold Hocher, Debbie A Lawlor, Jennifer Pararajasingham, Toos C. E. M. van Beijsterveldt, David P. Strachan, Hanna Maaria Lakka, Timothy M. Frayling

المساهمون: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Early Growth Genetics (EGG) Consortium, Ikram, M Afran, Fornage, Myriam, Smith, Albert V, Seshadri, Sudha, Hypponen, Elina Tuulikki, Wilson, James F, Biological Psychology, Radiology & Nuclear Medicine, Epidemiology, Erasmus MC other, Internal Medicine, Obstetrics & Gynecology, Public Health, Medical Oncology

المصدر: Nature Genetics
Nature Genetics, 44(5), 539
Ikram, M A, Fornage, M, Smith, A V, Seshadri, S, Schmidt, R, Debette, S, Vrooman, H A, Sigurdsson, S, Ropele, S, Taal, H R, Mook-Kanamori, D O, Coker, L H, Longstreth, W T, Niessen, W J, DeStefano, A L, Beiser, A, Zijdenbos, A P, Struchalin, M, Jack, C R, Rivadeneira, F, Uitterlinden, A G, Knopman, D S, Hartikainen, A-L, Pennell, C E, Thiering, E, Steegers, E A P, Hakonarson, H, Heinrich, J, Palmer, L J, Jarvelin, M-R, McCarthy, M I, Grant, S F A, St Pourcain, B, Timpson, N J, Smith, G D, Sovio, U, Nalls, M A, Au, R, Hofman, A, Gudnason, H, van der Lugt, A, Harris, T B, Meeks, W M, Vernooij, M W, van Buchem, M A, Catellier, D, Jaddoe, V W V, Gudnason, V & Windham, B G & Wilson, J F 2012, ' Common variants at 6q22 and 17q21 are associated with intracranial volume ', Nature Genetics, vol. 44, no. 5, pp. 539-+ . https://doi.org/10.1038/ng.2245Test
Nature Genetics, 44(5), 539-544. Nature Publishing Group
Nature Genetics; Vol 44
Nature Genetics, 44(5), 539-+. Nature Publishing Group
Arfan Ikram, M, Fornage, M, Smith, A V, Seshadri, S, Schmidt, R, Debette, S, Vrooman, H A, Sigurdsson, S, Ropele, S, Taal, H R, Mook-Kanamori, D O, Coker, L H, Longstreth, J W T, Niessen, W J, DeStefano, A L, Beiser, A, Zijdenbos, A P, Struchalin, M, Jack, C R, Rivadeneira, F, Uitterlinden, A G, Knopman, D S, Hartikainen, A-L, Pennell, C E, Thiering, E, Steegers, E A P, Hakonarson, H, Heinrich, J, Palmer, L J, Jarvelin, M-R, McCarthy, M I, Grant, S F A, St Pourcain, B, Timpson, N J, Smith, G D, Sovio, U, van Beijsterveldt, C E M, Groen-Blokhuis, M M, Hottenga, J J, Middeldorp, C M, Nivard, M G, Willemsen, G, Boomsma, D I, Nalls, M A, Au, R, Hofman, A, Gudnason, H, van der Lugt, A, Harris, T B, Meeks, W M, Vernooij, M W, van Buchem, M A, Catellier, D, Jaddoe, V W V, Gudnason, V, Windham, B G, Wolf, P A, van Duijn, C M, Mosley, T H, Schmidt, H, Launer, L J, Breteler, M M B & DeCarli, C S 2012, ' Common variants at 6q22 and 17q21 are associated with intracranial volume ', Nature Genetics, vol. 44, no. 5, pp. 539-544 . https://doi.org/10.1038/ng.2245Test
Nature genetics 44(5), 539-544 (2012). doi:10.1038/ng.2245

مصطلحات موضوعية: Netherlands Twin Register (NTR), Genetic Markers, Male, medicine.medical_specialty, Medizin, Locus (genetics), Genome-wide association study, physiopathology [Brain], Biology, Bioinformatics, Polymorphism, Single Nucleotide, Article, genetics [Chromosomes, Human, Pair 17], 03 medical and health sciences, 0302 clinical medicine, ddc:570, Intracranial volume, Internal medicine, medicine, Genetics, Humans, 030304 developmental biology, Aged, Aged, 80 and over, 0303 health sciences, Haplotype, Chromosome, Brain, Infant, genetics [Chromosomes, Human, Pair 6], Microdeletion syndrome, ta3121, physiopathology [Head], Endocrinology, Genetic marker, Genetic Loci, Brain size, genetics [Polymorphism, Single Nucleotide], Institut für Ernährungswissenschaft, Chromosomes, Human, Pair 6, Female, Head, 030217 neurology & neurosurgery, Chromosomes, Human, Pair 17, Genome-Wide Association Study

وصف الملف: application/pdf

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

المؤلفون: 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