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by Demontis, Ditte and Walters, Raymond K and Martin, Joanna and Mattheisen, Manuel and Als, Thomas D and Agerbo, Esben and Baldursson, Gísli and Belliveau, Rich and Bybjerg-Grauholm, Jonas and Bækvad-Hansen, Marie and Cerrato, Felecia and Chambert, Kimberly and Churchhouse, Claire and Dumont, Ashley and Eriksson, Nicholas and Gandal, Michael and Goldstein, Jacqueline I and Grasby, Katrina L and Grove, Jakob and Gudmundsson, Olafur O and Hansen, Christine S and Hauberg, Mads Engel and Hollegaard, Mads V and Howrigan, Daniel P and Huang, Hailiang and Maller, Julian B and Martin, Alicia R and Martin, Nicholas G and Moran, Jennifer and Pallesen, Jonatan and Palmer, Duncan S and Pedersen, Carsten Bøcker and Pedersen, Marianne Giørtz and Poterba, Timothy and Poulsen, Jesper Buchhave and Ripke, Stephan and Robinson, Elise B and Satterstrom, F. Kyle and Stefansson, Hreinn and Stevens, Christine and Turley, Patrick and Walters, G. Bragi and Won, Hyejung and Wright, Margaret J and Albayrak, Özgür and Anney, Richard J. L and Arranz, Maria Jesús and Banaschewski, Tobias J and Bau, Claiton and Biederman, Joseph and Buitelaar, Jan K and Casas, Miguel and Charach, Alice and Crosbie, Jennifer and Dempfle, Astrid and Doyle, Alysa E and Ebstein, Richard P and Elia, Josephine and Freitag, Christine and Föcker, Manuel and Gill, Michael and Grevet, Eugenio and Hawi, Ziarih and Hebebrand, Johannes and Herpertz-Dahlmann, Beate and Hervas, Amaia and Hinney, Anke and Hohmann, Sarah and Holmans, Peter and Hutz, Mara and Ickowitz, Abel and Johansson, Stefan and Kent, Lindsey and Kittel-Schneider, Sarah and Lambregts-Rommelse, Nanda and Lehmkuhl, Gerd and Loo, Sandra K and McGough, James J and Meyer, Jobst and Mick, Eric and Middletion, Frank and Miranda, Ana and Mota, Nina Roth and Mulas, Fernando and Mulligan, Aisling and Nelson, Freimer and Nguyen, T. Trang and Oades, Robert D and O’Donovan, Michael C and Owen, Michael J and Palmason, Haukur and Ramos-Quiroga, Josep Antoni and Renner, Tobias J and Ribasés, Marta and Rietschel, Marcella and Rivero, Olga and Romanos, Jasmin and Romanos, Marcel and Rothenberger, Aribert and Royers, Herbert and ... and Early Lifecourse Genetic and ADHD Working Grp Psychiat Genomics and 23andMe Res Team and Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium and 23andMe Research Team and ADHD Working Group of the Psychiatric Genomics Consortium (PGC)
Nature Genetics, ISSN 1061-4036, 01/2019, Volume 51, Issue 1, pp. 63 - 75
Journal Article
by Savage, Jeanne E and Jansen, Philip R and Stringer, Sven and Watanabe, Kyoko and Bryois, Julien and De Leeuw, Christiaan A and Nagel, Mats and Awasthi, Swapnil and Barr, Peter B and Coleman, Jonathan R. I and Grasby, Katrina L and Hammerschlag, Anke R and Kaminski, Jakob A and Karlsson, Robert and Krapohl, Eva and Lam, Max and Nygaard, Marianne and Reynolds, Chandra A and Trampush, Joey W and Young, Hannah and Zabaneh, Delilah and Hägg, Sara and Hansell, Narelle K and Karlsson, Ida K and Linnarsson, Sten and Montgomery, Grant W and Muñoz-Manchado, Ana B and Quinlan, Erin B and Schumann, Gunter and Skene, Nathan G and Webb, Bradley T and White, Tonya and Arking, Dan E and Avramopoulos, Dimitrios and Bilder, Robert M and Bitsios, Panos and Burdick, Katherine E and Cannon, Tyrone D and Chiba-Falek, Ornit and Christoforou, Andrea and Cirulli, Elizabeth T and Congdon, Eliza and Corvin, Aiden and Davies, Gail and Deary, Ian J and Derosse, Pamela and Dickinson, Dwight and Djurovic, Srdjan and Donohoe, Gary and Conley, Emily Drabant and Eriksson, Johan G and Espeseth, Thomas and Freimer, Nelson A and Giakoumaki, Stella and Giegling, Ina and Gill, Michael and Glahn, David C and Hariri, Ahmad R and Hatzimanolis, Alex and Keller, Matthew C and Knowles, Emma and Koltai, Deborah and Konte, Bettina and Lahti, Jari and Le Hellard, Stephanie and Lencz, Todd and Liewald, David C and London, Edythe and Lundervold, Astri J and Malhotra, Anil K and Melle, Ingrid and Morris, Derek and Need, Anna C and Ollier, William and Palotie, Aarno and Payton, Antony and Pendleton, Neil and Poldrack, Russell A and Räikkönen, Katri and Reinvang, Ivar and Roussos, Panos and Rujescu, Dan and Sabb, Fred W and Scult, Matthew A and Smeland, Olav B and Smyrnis, Nikolaos and Starr, John M and Steen, Vidar M and Stefanis, Nikos C and Straub, Richard E and Sundet, Kjetil and Tiemeier, Henning and Voineskos, Aristotle N and Weinberger, Daniel R and Widen, Elisabeth and Yu, Jin and Abecasis, Goncalo and Andreassen, Ole A and Breen, Gerome and Christiansen, Lene and ...
Nature Genetics, ISSN 1061-4036, 07/2018, Volume 50, Issue 7, pp. 912 - 919
Intelligence is highly heritable(1) and a major determinant of human health and well-being(2). Recent genome-wide meta-analyses have identified 24 genomic loci... 
GENERAL COGNITIVE FUNCTION | CONSORTIUM | TEST BATTERIES | GWAS | ANNOTATION | GENETICS & HEREDITY | RISK | LOCI | EDUCATIONAL-ATTAINMENT | TRAITS | HERITABILITY | Genetic Predisposition to Disease | Humans | Middle Aged | Adolescent | Female | Male | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Intelligence - genetics | Quantitative Trait Loci | Brain - physiology | Brain | Chromatin | Neurosciences | Intelligence | Synaptogenesis | Mental disorders | Genomics | Genes | Cognitive ability | Schizophrenia | Association analysis | Nervous system | Identification | Mapping | Genomes | Genetic effects | Annotations | Coding | Genetic analysis | Neostriatum | Alzheimer's disease | Bioinformatics | Neurodegenerative diseases | Neurons | Attention deficit hyperactivity disorder | Causation | Gene expression | Spiny neurons | Loci | Educational attainment | Meta-analysis | Quantitative trait loci | Neurological diseases | Studies | Pyramidal cells | Gene loci | Gene mapping | Alzheimers disease | Hippocampus | Medical and Health Sciences | Medicin och hälsovetenskap | Alzheimer disease | Article | nervous system development | genetic association | gene location | schizophrenia | Klinisk medicin | pleiotropy | gene mapping | genetic correlation | priority journal | human | Neurologi | corpus striatum | hippocampus | synapse | chromatin | heredity | genetic variability | intelligence | pyramidal nerve cell | gene locus | Mendelian randomization analysis | Clinical Medicine | Neurology | expression quantitative trait locus | medium spiny neuron | genome-wide association study | attention deficit disorder | exon | conserved sequence | gene expression
Journal Article
Journal of Health Psychology, ISSN 1359-1053, 06/2019, p. 135910531985904
Journal Article
Behavior Genetics, ISSN 0001-8244, 7/2019, Volume 49, Issue 4, pp. 386 - 398
This study assessed the heritability of 25 hydroxyvitamin D3 (25(OH)D3) in a large twin cohort and the shared effect of sun exposure and skin colour on... 
Public Health | Vitamin D | Sun exposure | Psychology | Genetics | Clinical Psychology | Health Psychology | Heritability | Skin colour | Twin | Analysis | Genes | Resveratrol | Genetic research | Calcifediol | Skin | Alfacalcidol | Research institutes | Twins | Genetic variation | Environmental aspects | Summer | Genetic diversity | Concentration | Sun | Environmental effects | Genetic variance | Winter | Genetic analysis | Siblings
Journal Article
Journal Article
Journal Article
Journal of health psychology, 06/2019, p. 1359105319859048
This study examined the extent to which psychosocial impact of nausea and vomiting during pregnancy predicts postpartum depression using a retrospective... 
Journal Article
Brain Sciences, ISSN 2076-3425, 12/2016, Volume 6, Issue 4, pp. 63 - 63
Loss of function of the hippocampus or frontal cortex is associated with reduced performance on memory tasks, in which subjects are incidentally exposed to... 
Source memory | Episodic memory | Spatial learning | Sensory preconditioning | BRAIN ACTIVITY |