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1Academic Journal
Authors: Leblond, Claire, Rolland, Thomas, Barthome, Eli, Mougin, Zakaria, Fleury, Mathis, Ecker, Christine, Bonnot-Briey, Stéf, Cliquet, Freddy, Tabet, Anne-Claude, Maruani, Anna, Chaumette, Boris, Green, Jonathan, Delorme, Richard, Bourgeron, Thomas
Contributors: Cliquet, Freddy
Source: Leblond, C S, Rolland, T, Barthome, E, Mougin, Z, Fleury, M, Ecker, C, Bonnot-Briey, S, Cliquet, F, Tabet, A-C, Maruani, A, Chaumette, B, Green, J, Delorme, R & Bourgeron, T 2024, 'A Genetic Bridge Between Medicine and Neurodiversity for Autism', Annual Review of Genetics, vol. 58, no. 1, pp. 487-512. https://doi.org/10.1146/annurev-genet-111523-102614
Annual ReviewsSubject Terms: 0301 basic medicine, Autism Spectrum Disorder, [SDV.MHEP.PSM] Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health, autism, common genetic variants, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, rare genetic variants, 03 medical and health sciences, Intellectual Disability, Humans, Genetic Predisposition to Disease, neurodiversity, Autistic Disorder, Child, Multidisciplinary research, 0303 health sciences, [SCCO.NEUR] Cognitive science/Neuroscience, Genetic Variation, participative research, Intellectual Disability/genetics, Autism Spectrum Disorder/genetics, Phenotype, Genetic Variation/genetics, Attention Deficit Disorder with Hyperactivity, Attention Deficit Disorder with Hyperactivity/genetics, Autistic Disorder/genetics
File Description: application/pdf
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2Academic Journal
Authors: Konzok, Julian, Gorski, Mathias, Winkler, Thomas W., Baumeister, Sebastian E., Warrier, Varun, Leitzmann, Michael F., Baurecht, Hansjörg
Contributors: Apollo - University of Cambridge Repository
Source: Mol Psychiatry
Subject Terms: Male, Conduct Disorder, 0301 basic medicine, ddc:610, Substance-Related Disorders, Antisocial Personality Disorder/epidemiology [MeSH], Antisocial Personality Disorder/genetics [MeSH], Risk Factors [MeSH], 692/699/476, Attention Deficit Disorder with Hyperactivity/genetics [MeSH], Polymorphism, Single Nucleotide/genetics [MeSH], Genome-Wide Association Study/methods [MeSH], Male [MeSH], Conduct Disorder/epidemiology [MeSH], 45/43, Child Abuse/psychology [MeSH], Phenotype [MeSH], Child [MeSH], Genetic Predisposition to Disease/genetics [MeSH], Substance-Related Disorders/psychology [MeSH], Gene-Environment Interaction [MeSH], Female [MeSH], Conduct Disorder/genetics [MeSH], 631/208, Humans [MeSH], 631/477, Article, Substance-Related Disorders/genetics [MeSH], Mendelian Randomization Analysis/methods [MeSH], article, 610 Medizin, Antisocial Personality Disorder, Mendelian Randomization Analysis, Polymorphism, Single Nucleotide, 3. Good health, 03 medical and health sciences, Phenotype, 0302 clinical medicine, Risk Factors, Attention Deficit Disorder with Hyperactivity, Humans, Female, Genetic Predisposition to Disease, Gene-Environment Interaction, Child Abuse, Child, Genome-Wide Association Study
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3Academic Journal
Authors: Luis M. García-Marín, Adrian I. Campos, Santiago Diaz-Torres, Jill A. Rabinowitz, Zuriel Ceja, Brittany L. Mitchell, Katrina L. Grasby, Jackson G. Thorp, Ingrid Agartz, Saud Alhusaini, David Ames, Philippe Amouyel, Ole A. Andreassen, Konstantinos Arfanakis, Alejandro Arias-Vasquez, Nicola J. Armstrong, Lavinia Athanasiu, Mark E. Bastin, Alexa S. Beiser, David A. Bennett, Joshua C. Bis, Marco P. M. Boks, Dorret I. Boomsma, Henry Brodaty, Rachel M. Brouwer, Jan K. Buitelaar, Ralph Burkhardt, Wiepke Cahn, Vince D. Calhoun, Owen T. Carmichael, Mallar Chakravarty, Qiang Chen, Christopher R. K. Ching, Sven Cichon, Benedicto Crespo-Facorro, Fabrice Crivello, Anders M. Dale, George Davey Smith, Eco J. C. de Geus, Philip L. De Jager, Greig I. de Zubicaray, Stéphanie Debette, Charles DeCarli, Chantal Depondt, Sylvane Desrivières, Srdjan Djurovic, Stefan Ehrlich, Susanne Erk, Thomas Espeseth, Guillén Fernández, Irina Filippi, Simon E. Fisher, Debra A. Fleischman, Evan Fletcher, Myriam Fornage, Andreas J. Forstner, Clyde Francks, Barbara Franke, Tian Ge, Aaron L. Goldman, Hans J. Grabe, Robert C. Green, Oliver Grimm, Nynke A. Groenewold, Oliver Gruber, Vilmundur Gudnason, Asta K. Håberg, Unn K. Haukvik, Andreas Heinz, Derrek P. Hibar, Saima Hilal, Jayandra J. Himali, Beng-Choon Ho, David F. Hoehn, Pieter J. Hoekstra, Edith Hofer, Wolfgang Hoffmann, Avram J. Holmes, Georg Homuth, Norbert Hosten, M. Kamran Ikram, Jonathan C. Ipser, Clifford R. Jack Jr, Neda Jahanshad, Erik G. Jönsson, Rene S. Kahn, Ryota Kanai, Marieke Klein, Maria J. Knol, Lenore J. Launer, Stephen M. Lawrie, Stephanie Le Hellard, Phil H. Lee, Hervé Lemaître, Shuo Li, David C. M. Liewald, Honghuang Lin, W. T. Longstreth, Oscar L. Lopez, Michelle Luciano, Pauline Maillard, Andre F. Marquand, Nicholas G. Martin, Jean-Luc Martinot, Karen A. Mather, Venkata S. Mattay, Katie L. McMahon, Patrizia Mecocci, Ingrid Melle, Andreas Meyer-Lindenberg, Nazanin Mirza-Schreiber, Yuri Milaneschi, Thomas H. Mosley, Thomas W. Mühleisen, Bertram Müller-Myhsok, Susana Muñoz Maniega, Matthias Nauck, Kwangsik Nho, Wiro J. Niessen, Markus M. Nöthen, Paul A. Nyquist, Jaap Oosterlaan, Massimo Pandolfo, Tomas Paus, Zdenka Pausova, Brenda W. J. H. Penninx, G. Bruce Pike, Bruce M. Psaty, Benno Pütz, Simone Reppermund, Marcella D. Rietschel, Shannon L. Risacher, Nina Romanczuk-Seiferth, Rafael Romero-Garcia, Gennady V. Roshchupkin, Jerome I. Rotter, Perminder S. Sachdev, Philipp G. Sämann, Arvin Saremi, Muralidharan Sargurupremraj, Andrew J. Saykin, Lianne Schmaal, Helena Schmidt, Reinhold Schmidt, Peter R. Schofield, Markus Scholz, Gunter Schumann, Emanuel Schwarz, Li Shen, Jean Shin, Sanjay M. Sisodiya, Albert V. Smith, Jordan W. Smoller, Hilkka S. Soininen, Vidar M. Steen, Dan J. Stein, Jason L. Stein, Sophia I. Thomopoulos, Arthur W. Toga, Diana Tordesillas-Gutiérrez, Julian N. Trollor, Maria C. Valdes-Hernandez, Dennis van ′t Ent, Hans van Bokhoven, Dennis van der Meer, Nic J. A. van der Wee, Javier Vázquez-Bourgon, Dick J. Veltman, Meike W. Vernooij, Arno Villringer, Louis N. Vinke, Henry Völzke, Henrik Walter, Joanna M. Wardlaw, Daniel R. Weinberger, Michael W. Weiner, Wei Wen, Lars T. Westlye, Eric Westman, Tonya White, A. Veronica Witte, Christiane Wolf, Jingyun Yang, Marcel P. Zwiers, M. Arfan Ikram, Sudha Seshadri, Paul M. Thompson, Claudia L. Satizabal, Sarah E. Medland, Miguel E. Rentería
Contributors: European Commission, European Research Council, National Institutes of Health (US), Department of Energy (US), Fundación Marques de Valdecilla, Instituto de Investigación Marqués de Valdecilla, Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72], Onderzoek, Brain, Onderzoeksgroep 11, Admin, Oskar
Source: medRxiv
Digital.CSIC. Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Nature genetics 56(11), 2333-2344 (2024). doi:10.1038/s41588-024-01951-z
Nature Genetics, 56, 11, pp. 2333-2344
Nature Genetics, vol 56, iss 11Subject Terms: Male, Organ Size/genetics, Multifactorial Inheritance, Biological Psychology, 270 Language and Computation in Neural Systems, Human Genetics - Radboud University Medical Center - DCMN, genetics [Attention Deficit Disorder with Hyperactivity], Medical and Health Sciences, Psychiatry - Radboud University Medical Center - DCMN, pathology [Brain], genetics [Parkinson Disease], Psychology, 2.1 Biological and endogenous factors, Parkinson Disease/genetics, genetics [Multifactorial Inheritance], methods [Genomics], 220 Statistical Imaging Neuroscience, Cognitive Neuroscience - Radboud University Medical Center - DCMN, Brain, Parkinson Disease, Pharmacology and Pharmaceutical Sciences, Single Nucleotide, Organ Size, Genomics, Biological Sciences, Middle Aged, Mental Illness, Bioinformatics and computational biology, Mental Health, Neurological, Mental health, Female, [SHS] Humanities and Social Sciences, Attention Deficit Disorder with Hyperactivity/genetics, White People/genetics, Biotechnology, Adult, Agricultural biotechnology, genetics [White People], Polymorphism, Single Nucleotide, 150 000 MR Techniques in Brain Function, Article, White People, ddc:570, Journal Article, Genetics, Humans, Brain/pathology, Genetic Predisposition to Disease, Polymorphism, Multifactorial Inheritance/genetics, Biomedical and Clinical Sciences, genetics [Organ Size], Human Genome, Neurosciences, pathology [Attention Deficit Disorder with Hyperactivity], Genomics/methods, Brain Disorders, pathology [Parkinson Disease], Good Health and Well Being, [SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie, Attention Deficit Disorder with Hyperactivity, name=Bristol Population Health Science Institute, Developmental Biology, Genome-Wide Association Study
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https://doi.org/10.1038/s41588-024-01951-z
https://repository.ubn.ru.nl//bitstream/handle/2066/313586/313586.pdf
https://hdl.handle.net/2066/313586
https://juser.fz-juelich.de/record/1032350
https://hdl.handle.net/11391/1589699
https://doi.org/10.1038/s41588-024-01951-z
https://hal.science/hal-04797532v1
https://doi.org/10.1038/s41588-024-01951-z
https://escholarship.org/uc/item/4g85k360
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https://escholarship.org/uc/item/9bp1077g -
4Academic Journal
Authors: Francesca Furia, Amanda M. Levy, Miel Theunis, Michael J. Bamshad, Meghan N. Bartos, Emilia K. Bijlsma, Francesco Brancati, Lucile Cejudo, Jessica X. Chong, Chiara De Luca, Sarah Joy Dean, Alena Egense, Himanshu Goel, Adam J. Guenzel, Ulrike Hüffmeier, Eric Legius, Grazia M. S. Mancini, Iñigo Marcos‐Alcalde, Tanguy Niclass, Marc Planes, Sylvia Redon, David Ros‐Pardo, Karen Rouault, Rachel Schot, Sarah Schuhmann, Joseph J. Shen, Alice M. Tao, Isabelle Thiffault, Hilde Van Esch, Ingrid M. Wentzensen, Tahsin Stefan Barakat, Rikke S. Møller, Paulino Gomez‐Puertas, Wendy K. Chung, Elena Gardella, Zeynep Tümer
Contributors: Netherlands Organisation for Health Research and Development, Governo Italiano, Ministerio de Ciencia e Innovación (España), Agencia Estatal de Investigación (España), Ministerio de Ciencia, Innovación y Universidades (España), Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72], The University of Newcastle. College of Health, Medicine & Wellbeing, School of Medicine and Public Health
Source: Furia, F, Levy, A M, Theunis, M, Bamshad, M J, Bartos, M N, Bijlsma, E K, Brancati, F, Cejudo, L, Chong, J X, De Luca, C, Dean, S J, Egense, A, Goel, H, Guenzel, A J, Hüffmeier, U, Legius, E, Mancini, G M S, Marcos-Alcalde, I, Niclass, T, Planes, M, Redon, S, Ros-Pardo, D, Rouault, K, Schot, R, Schuhmann, S, Shen, J J, Tao, A M, Thiffault, I, Van Esch, H, Wentzensen, I M, Barakat, T S, Møller, R S, Gomez-Puertas, P, Chung, W K, Gardella, E & Tümer, Z 2024, ' The phenotypic and genotypic spectrum of individuals with mono-or biallelic ANK3 variants ', Clinical Genetics, vol. 106, no. 5, pp. 574-584 . https://doi.org/10.1111/cge.14587
Subject Terms: Male, 0301 basic medicine, Autism Spectrum Disorder, Epilepsy/genetics, Ankyrins/genetics, aggressivity, ankyrin‐G, autism spectrum disorder, epilepsy, hypotonia, intellectual disability, language delay, neurodevelopmental disorder, sleep disturbances, Child, epilespy, Genetics & Heredity, 0303 health sciences, Phenotype, Child, Preschool, Female, Attention Deficit Disorder with Hyperactivity/genetics, Life Sciences & Biomedicine, Adult, Ankyrins, Mutation/genetics, Adolescent, Genotype, 3105 Genetics, 03 medical and health sciences, Intellectual Disability, Humans, Genetic Predisposition to Disease, Language Development Disorders, Preschool, Alleles, Genetic Association Studies, 0604 Genetics, Science & Technology, ankyrin-G, Epilepsy, 3202 Clinical sciences, Infant, 1103 Clinical Sciences, GENE, Intellectual Disability/genetics, Autism Spectrum Disorder/genetics, DE-NOVO MUTATIONS, Neurodevelopmental Disorders, Attention Deficit Disorder with Hyperactivity, Language Development Disorders/genetics, Mutation, ANKYRIN
File Description: application/pdf
Linked Full TextAccess URL: https://pubmed.ncbi.nlm.nih.gov/38988293
https://hdl.handle.net/1887/4210430
https://lirias.kuleuven.be/handle/20.500.12942/748352
https://doi.org/10.1111/cge.14587
https://curis.ku.dk/ws/files/407596628/Clinical_Genetics_2024_Furia_The_phenotypic_and_genotypic_spectrum_of_individuals_with_mono_or_biallelic_ANK3.pdf
https://portal.findresearcher.sdu.dk/da/publications/8bd5234c-9b77-4773-a84b-a00885d3d21d
https://doi.org/10.1111/cge.14587 -
5Academic Journal
Authors: Verhoef, Ellen, Allegrini, Andrea G., Jansen, Philip R., Lange, Katherine, Wang, Carol A., Morgan, Angela T., Ahluwalia, Tarunveer S., Symeonides, Christos, Andreassen, Ole A., Bartels, Meike, Boomsma, Dorret, Dale, Philip S., Ehli, Erik, Fernandez-Orth, Dietmar, Guxens, Mònica, Hakulinen, Christian, Harris, Kathleen Mullan, Haworth, Simon, de Hoyos, Lucía, Jaddoe, Vincent, Keltikangas-Järvinen, Liisa, Lehtimäki, Terho, Middeldorp, Christel, Min, Josine L., Mishra, Pashupati P., Njølstad, Pål Rasmus, Sunyer, Jordi, Tate, Ashley E., Timpson, Nicholas, van der Laan, Camiel, Vrijheid, Martine, Vuoksimaa, Eero, Whipp, Alyce, Ystrom, Eivind, ACTION Consortium, Barwon Infant Study investigator group, Eising, Else, Franken, Marie-Christine, Hypponen, Elina, Mansell, Toby, Olislagers, Mitchell, Omerovic, Emina, Rimfeld, Kaili, Schlag, Fenja, Selzam, Saskia, Shapland, Chin Yang, Tiemeier, Henning, Whitehouse, Andrew J.O., Saffery, Richard, Bønnelykke, Klaus, Reilly, Sheena, Pennell, Craig E., Wake, Melissa, Cecil, Charlotte A.M., Plomin, Robert, Fisher, Simon E., St. Pourcain, Beate
Contributors: The University of Newcastle. College of Health, Medicine & Wellbeing, School of Medicine and Public Health
Source: Verhoef, E, Allegrini, A G, Jansen, P R, Lange, K, Wang, C A, Morgan, A T, Ahluwalia, T S, Symeonides, C, Andreassen, O A, Bartels, M, Boomsma, D, Dale, P S, Ehli, E, Fernandez-Orth, D, Guxens, M N, Hakulinen, C, Harris, K M, Haworth, S, de Hoyos, L, Jaddoe, V, Keltikangas-Järvinen, L, Lehtimäki, T, Middeldorp, C, Min, J L, Mishra, P P, Njølstad, P L R, Sunyer, J, Tate, A E, Timpson, N, van der Laan, C, Vrijheid, M, Vuoksimaa, E, Whipp, A, Ystrom, E, ACTION Consortium & EAGLE Working Group 2024, 'Genome-Wide Analyses of Vocabulary Size in Infancy and Toddlerhood : Associations With Attention-Deficit/Hyperactivity Disorder, Literacy, and Cognition-Related Traits', Biological Psychiatry, vol. 95, no. 9, pp. 859-869. https://doi.org/10.1016/j.biopsych.2023.11.025
Biological Psychiatry, 95, 9, pp. 859-869
Verhoef, E, Allegrini, A G, Jansen, P R, Lange, K, Wang, C A, Morgan, A T, Ahluwalia, T S, Symeonides, C, Eising, E, Franken, M-C, Hypponen, E, Mansell, T, Olislagers, M, Omerovic, E, Rimfeld, K, Schlag, F, Selzam, S, Shapland, C Y, Tiemeier, H, Whitehouse, A J O, Saffery, R, Bønnelykke, K, Reilly, S, Pennell, C E, Wake, M, Cecil, C A M, Plomin, R, Fisher, S E, St Pourcain, B, EAGLE Working Group, ACTION consortium & Barwon Infant Study Investigator Group 2024, ' Genome-Wide Analyses of Vocabulary Size in Infancy and Toddlerhood : Associations With Attention-Deficit/Hyperactivity Disorder, Literacy, and Cognition-Related Traits ', Biological Psychiatry, vol. 95, no. 9, pp. 859-869 . https://doi.org/10.1016/j.biopsych.2023.11.025
Biological PsychiatrySubject Terms: cognition, Netherlands Twin Register (NTR), Biomedical and clinical sciences, Adolescent, Development, Vocabulary, Cognition, Neurobiology, Literacy, Psychology, ADHD, GWAS, Humans, Longitudinal Studies, 10. No inequality, development, vocabulary, 4. Education, Infant, 3. Good health, Biological sciences, Phenotype, Attention Deficit Disorder with Hyperactivity, SEM, Attention Deficit Disorder with Hyperactivity/genetics, Genome-Wide Association Study
File Description: application/pdf
Linked Full TextAccess URL: https://pubmed.ncbi.nlm.nih.gov/38070845
https://research.vumc.nl/en/publications/3c6825e6-4538-4ee4-a62f-ca036eb5905f
https://hdl.handle.net/2066/307187
https://repository.ubn.ru.nl//bitstream/handle/2066/307187/307187.pdf
https://curis.ku.dk/ws/files/387838362/1_s2.0_S0006322323017572_main.pdf -
6Academic Journal
Authors: Sonja LaBianca, Isabell Brikell, Dorte Helenius, Robert Loughnan, Joel Mefford, Clare E. Palmer, Rebecca Walker, Jesper R. Gådin, Morten Krebs, Vivek Appadurai, Morteza Vaez, Esben Agerbo, Marianne Giørtz Pedersen, Anders D. Børglum, David M. Hougaard, Ole Mors, Merete Nordentoft, Preben Bo Mortensen, Kenneth S. Kendler, Terry L. Jernigan, Daniel H. Geschwind, Andrés Ingason, Andrew W. Dahl, Noah Zaitlen, Søren Dalsgaard, Thomas M. Werge, Andrew J. Schork
Source: LaBianca, S, Brikell, I, Helenius, D, Loughnan, R, Mefford, J, Palmer, C E, Walker, R, Gådin, J R, Krebs, M, Appadurai, V, Vaez, M, Agerbo, E, Pedersen, M G, Børglum, A D, Hougaard, D M, Mors, O, Nordentoft, M, Mortensen, P B, Kendler, K S, Jernigan, T L, Geschwind, D H, Ingason, A, Dahl, A W, Zaitlen, N, Dalsgaard, S, Werge, T M & Schork, A J 2024, ' Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder ', Nature Genetics, vol. 56, no. 2, pp. 234-244 . https://doi.org/10.1038/s41588-023-01593-7
Nature Genetics, vol 56, iss 2
LaBianca, S, Brikell, I, Helenius, D, Loughnan, R, Mefford, J, Palmer, C E, Walker, R, Gådin, J R, Krebs, M, Appadurai, V, Vaez, M, Agerbo, E, Pedersen, M G, Børglum, A D, Hougaard, D M, Mors, O, Nordentoft, M, Mortensen, P B, Kendler, K S, Jernigan, T L, Geschwind, D H, Ingason, A, Dahl, A W, Zaitlen, N, Dalsgaard, S, Werge, T M & Schork, A J 2024, 'Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder', Nature Genetics, vol. 56, no. 2, pp. 234-244. https://doi.org/10.1038/s41588-023-01593-7Subject Terms: Multifactorial Inheritance, Autism Spectrum Disorder, Intellectual and Developmental Disabilities (IDD), Autism, Agricultural biotechnology, Medical and Health Sciences, Clinical Research, 2.3 Psychological, Behavioral and Social Science, Genetics, 2.1 Biological and endogenous factors, Humans, Multifactorial Inheritance/genetics, Pediatric, Prevention, Human Genome, Biological Sciences, Mental Illness, Attention Deficit Hyperactivity Disorder (ADHD), Bioinformatics and computational biology, 3. Good health, Brain Disorders, Autism Spectrum Disorder/genetics, Mental Health, Good Health and Well Being, Attention Deficit Disorder with Hyperactivity, Mental health, social and economic factors, Attention Deficit Disorder with Hyperactivity/genetics, Developmental Biology
File Description: application/pdf
Access URL: https://pubmed.ncbi.nlm.nih.gov/38036780
https://curis.ku.dk/ws/files/429031412/Polygenic_profiles.pdf
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https://doi.org/10.1038/s41588-023-01593-7 -
7Academic Journal
Authors: Nielsen, Trine Tollerup, Bali, Paraskevi, Grove, Jakob, Mohr-Jensen, Christina, Werge, Thomas, Dalsgaard, Søren, Børglum, Anders, Sonuga-Barke, Edmund, Minnis, Helen, Demontis, Ditte, Corfield, Elizabeth, Tbartz van Elst, Ludger, Mattheisen, Manuel, de Wit, Melanie, Uddin, Mohammed Jashim, Anney, Richard, Scherer, Stephen, Bourgeron, Thomas, Polderman, Tinca
Contributors: Devauchelle, Benjamin
Source: Nielsen, T T, Bali, P, Grove, J, Mohr-Jensen, C, Werge, T, Dalsgaard, S, Børglum, A D, Sonuga-Barke, E, Minnis, H, Demontis, D & Autism Spectrum Working Group of the Psychiatric Genomics Consortium 2025, 'Genetic Architecture and Risk of Childhood Maltreatment Across 5 Psychiatric Diagnoses', JAMA Psychiatry, vol. 82, no. 8, e0243639, pp. 790-800. https://doi.org/10.1001/jamapsychiatry.2025.0828
Nielsen, T T, Bali, P, Grove, J, Mohr-Jensen, C, Werge, T, Dalsgaard, S, Børglum, A D, Sonuga-Barke, E, Minnis, H, Corfield, E C, Tbartz van Elst, L, Mattheisen, M, de Wit, M M, Uddin, M J, Anney, R J L, Scherer, S W, Bourgeron, T, Polderman, T J C, Autism Spectrum Working Group of the Psychiatric Genomics Consortium & Demontis, D 2025, 'Genetic Architecture and Risk of Childhood Maltreatment Across 5 Psychiatric Diagnoses', JAMA Psychiatry. https://doi.org/10.1001/jamapsychiatry.2025.0828Subject Terms: Male, Adult, Mental Disorders/genetics, Schizophrenia/genetics, Adolescent, Bipolar Disorder/genetics, [SCCO.NEUR] Cognitive science/Neuroscience, Young Adult, Child Abuse/statistics & numerical data, Risk Factors, Case-Control Studies, Humans, Educational Status, Female, Genetic Predisposition to Disease, Adult Survivors of Child Abuse/psychology, Child, Attention Deficit Disorder with Hyperactivity/genetics, Multifactorial Inheritance/genetics, Substance-Related Disorders/genetics, Genome-Wide Association Study
Access URL: https://pubmed.ncbi.nlm.nih.gov/40341348
https://vbn.aau.dk/da/publications/ef2e8192-d82c-4222-bdc2-a7bc70b34dae
https://doi.org/10.1001/jamapsychiatry.2025.0828
https://pure.amsterdamumc.nl/en/publications/bb46cecf-7df0-4803-8f48-63299544fa29
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http://www.scopus.com/inward/record.url?scp=105005290238&partnerID=8YFLogxK
https://doi.org/10.1001/jamapsychiatry.2025.0828
https://pasteur.hal.science/pasteur-05228329v1
https://doi.org/10.1001/jamapsychiatry.2025.0828
https://pure.au.dk/portal/en/publications/9eb7cba1-b489-40b7-b1f6-be67358eeccc
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https://doi.org/10.1001/jamapsychiatry.2025.0828 -
8Academic Journal
Authors: Dinkelbach, Lars, Peters, Triinu, Grasemann, Corinna, Hebebrand, Johannes, Hinney, Anke, Hirtz, Raphael
Source: Eur Child Adolesc Psychiatry
Subject Terms: ADHD, Female [MeSH], Mendelian randomization, Adult [MeSH], Humans [MeSH], Testosterone/blood [MeSH], Middle Aged [MeSH], Sex effects, Attention Deficit Disorder with Hyperactivity/genetics [MeSH], Polymorphism, Single Nucleotide/genetics [MeSH], Genome-Wide Association Study [MeSH], United Kingdom/epidemiology [MeSH], Male [MeSH], Original Contribution, Testosterone, Mendelian Randomization Analysis [MeSH], Sex Factors [MeSH], Male, Adult, 0301 basic medicine, 0303 health sciences, Medizin, Mendelian Randomization Analysis, Middle Aged, Polymorphism, Single Nucleotide, United Kingdom, 03 medical and health sciences, Sex Factors, Attention Deficit Disorder with Hyperactivity, Humans, Female, Genome-Wide Association Study
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9Academic Journal
Authors: Yilmaz, Zeynep, Quattlebaum, Mary J., Pawar, Pratiksha S., Thornton, Laura M., Bulik, Cynthia M., Javaras, Kristin N., Yao, Shuyang, Lichtenstein, Paul, Larsson, Henrik, Baker, Jessica H.
Source: Yilmaz, Z, Quattlebaum, M J, Pawar, P S, Thornton, L M, Bulik, C M, Javaras, K N, Yao, S, Lichtenstein, P, Larsson, H & Baker, J H 2023, 'Associations Between Attention Deficit Hyperactivity Disorder Symptom Dimensions and Disordered Eating Symptoms in Adolescence : A Population-Based Twin Study', Behavior Genetics, vol. 53, no. 2, pp. 143-153. https://doi.org/10.1007/s10519-022-10128-5
Subject Terms: 0301 basic medicine, Male, 0303 health sciences, Adolescent, Feeding and Eating Disorders/genetics, Bulimia/complications, Twins, Symptom-level associations, Twin study, Comorbidity, Disordered eating, 3. Good health, Feeding and Eating Disorders, 03 medical and health sciences, Attention-deficit/hyperactivity disorder, Attention Deficit Disorder with Hyperactivity, Sex differences, Genetics, Population cohort, Humans, Female, Bulimia, Attention Deficit Disorder with Hyperactivity/genetics, Twins/genetics
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https://doi.org/10.1007/s10519-022-10128-5
http://www.scopus.com/inward/record.url?scp=85143604736&partnerID=8YFLogxK -
10Academic Journal
Authors: Barbara J. Coffey, Julie Hagstrøm, Frank Visscher, Pieter J. Hoekstra, Andrea Dietrich, Thomas V. Fernandez, Mohamed Abdulkadir, Dongmei Yu, Lawrence W. Brown, Jay A. Tischfield, Eun-Young Shin, Keun-Ah Cheon, Athanasios Maras, Dong-Ho Song, Samuel H. Zinner, Astrid Morer, Jeremiah M. Scharf, Samuel Kuperman, Robert A. King, Isobel Heyman, Tammy Hedderly, Dorothy E. Grice, Kerstin J. Plessen, Yun-Joo Koh, Donald L. Gilbert, Hyun Ju Hong, Laura Ibanez-Gomez, Gary A. Heiman, Alexander Münchau, Young Shin Kim, Carol A. Mathews, Blanca Garcia-Delgar, Bennett L. Leventhal, Sodahm Kook, Young Key Kim, Marcos Madruga-Garrido, Veit Roessner, Chaim Huyser, Lisa Osiecki, Pablo Mir, Jungeun Song
Contributors: National Institute of Mental Health (US), Tourette Syndrome Association of New Jersey, Judah Foundation, Tourette Association of America, National Institutes of Health (US), Instituto de Salud Carlos III, Junta de Andalucía, Sociedad Andaluza de Neurología, Fundación Alicia Koplowitz, Fundación Mutua Madrileña, Jacques and Gloria Gossweiler Foundation, Generalitat de Catalunya, German Research Foundation, National Institute of Environmental Health Sciences (US), Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72], Consejeria de Salud y Bienestar Social de la Junta de Andalucia, Consejeria de Economia, Innovacion, Ciencia y Empresa de la Junta de Andalucia, Instituto de Salud Carlos III. Spanish Government, Mohamed Abdulkadir, Dongmei Yu, Lisa Osiecki, Robert A King, Thomas V Fernandez, Lawrence W Brown, Keun-Ah Cheon, Barbara J Coffey, Blanca Garcia-Delgar, Donald L Gilbert, Dorothy E Grice, Julie Hagstrøm, Tammy Hedderly, Isobel Heyman, Hyun Ju Hong, Chaim Huyser, Laura Ibanez-Gomez, Young Key Kim, Young-Shin Kim, Yun-Joo Koh, Sodahm Kook, Samuel Kuperman, Bennett Leventhal, Marcos Madruga-Garrido, Athanasios Maras, Pablo Mir, Astrid Morer, Alexander Münchau, Kerstin J Plessen, Veit Roessner, Eun-Young Shin, Dong-Ho Song, Jungeun Song, Frank Visscher, Samuel H Zinner, Carol A Mathews, Jeremiah M Scharf, Jay A Tischfield, Gary A Heiman, Andrea Dietrich, Pieter J Hoekstra, Cheon, Keun Ah
Source: J Neural Transm (Vienna)
Digital.CSIC. Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
instname
RISalud-ANDALUCIA. Repositorio Institucional de Salud de Andalucía
Journal of neural transmission, vol. 128, no. 11, pp. 1757-1765
Abdulkadir, M, Yu, D, Osiecki, L, King, R A, Fernandez, T V, Brown, L W, Cheon, K A, Coffey, B J, Garcia-Delgar, B, Gilbert, D L, Grice, D E, Hagstrøm, J, Hedderly, T, Heyman, I, Hong, H J, Huyser, C, Ibanez-Gomez, L, Kim, Y K, Kim, Y S, Koh, Y J, Kook, S, Kuperman, S, Leventhal, B, Madruga-Garrido, M, Maras, A, Mir, P, Morer, A, Münchau, A, Plessen, K J, Roessner, V, Shin, E Y, Song, D H, Song, J, Visscher, F, Zinner, S H, Mathews, C A, Scharf, J M, Tischfield, J A, Heiman, G A, Dietrich, A & Hoekstra, P J 2021, ' Investigation of gene–environment interactions in relation to tic severity ', Journal of Neural Transmission, vol. 128, no. 11, pp. 1757-1765 . https://doi.org/10.1007/s00702-021-02396-y
Journal of neural transmission (Vienna, Austria : 1996), vol 128, iss 11Subject Terms: 0301 basic medicine, Polimorfismo de nucleótido simple, Autism Spectrum Disorder, Autism, Neurodegenerative, Severity of Illness Index, Attention Deficit Disorder with Hyperactivity/genetics, Autism Spectrum Disorder/genetics, Female, Gene-Environment Interaction, Genome-Wide Association Study, Humans, Pregnancy, Tics, Tourette Syndrome, Gene–environment interaction, Pre- and perinatal complications, Tic severity, Tourette syndrome, 2.1 Biological and endogenous factors, Psychology, Predicción, Aetiology, Pediatric, 0303 health sciences, Serious Mental Illness, 3. Good health, Mental Health, Nucleótidos, Sitios genéticos, Mental health, Intellectual and Developmental Disabilities (IDD), Attention Deficit Disorder with Hyperactivity* / genetics, 03 medical and health sciences, Genetics, Metaanálisis, Neurotransmisores, Neurology & Neurosurgery, Autism Spectrum Disorder* / genetics, Human Genome, Psychiatry and Preclinical Psychiatric Studies - Original Article, Neurosciences, Trastorno obsesivo compulsivo, Gene-environment interaction, Brain Disorders, Genes, Attention Deficit Disorder with Hyperactivity, Trastorno del espectro autista, Síndrome de Tourette
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11Academic Journal
Source: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie. 50:203-217
Subject Terms: 0301 basic medicine, 03 medical and health sciences, 0302 clinical medicine, ADHD, Genetik, Pleiotropie, Attention Deficit Disorder with Hyperactivity/diagnosis [MeSH], Multifactorial Inheritance/genetics [MeSH], Übersichtsarbeit, Humans [MeSH], genetics, polygenetische Risikoscores, Komorbidität, ADHS, Attention Deficit Disorder with Hyperactivity/genetics [MeSH], comorbidities, Attention Deficit Disorder with Hyperactivity/epidemiology [MeSH], Genome-Wide Association Study [MeSH], Comorbidity [MeSH], pleiotropy, comorbidity, Genetic Predisposition to Disease/genetics [MeSH], polygenic risk scores
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12Academic Journal
Authors: Zhang, J., Chen, Z. K., Triatin, R. D., Snieder, H., Thio, C. H. L., Hartman, C. A.
Source: Epidemiol Psychiatr Sci
Epidemiology and Psychiatric Sciences, Vol 33 (2024)
Epidemiology and Psychiatric SciencesSubject Terms: Type 2/genetics, Male, Pediatric Obesity, Blood Pressure/genetics, Neurosciences. Biological psychiatry. Neuropsychiatry, Blood Pressure, Polymorphism, Single Nucleotide, Body Mass Index, SDG 3 - Good Health and Well-being, Risk Factors, Pediatric Obesity/genetics, Diabetes Mellitus, health outcomes, Humans, Genetic Predisposition to Disease, Polymorphism, Child, Single Nucleotide, Mendelian Randomization Analysis, chronic conditions, attention deficit hyperactivity disorder, Diabetes Mellitus, Type 2, Attention Deficit Disorder with Hyperactivity, Original Article, Female, Public aspects of medicine, RA1-1270, Sedentary Behavior, Attention Deficit Disorder with Hyperactivity/genetics, metabolism, RC321-571
Linked Full TextAccess URL: https://pubmed.ncbi.nlm.nih.gov/39465621
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https://doi.org/10.1017/S2045796024000593
https://research-portal.uu.nl/en/publications/3c6aba55-7e55-473c-8fd2-9f3223cb538c
https://doi.org/10.1017/S2045796024000593 -
13Academic Journal
Authors: Ditte Demontis, G. Bragi Walters, Georgios Athanasiadis, Raymond Walters, Karen Therrien, Trine Tollerup Nielsen, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biau Zeng, Wen Zhang, Jakob Grove, Thomas D. Als, Jinjie Duan, F. Kyle Satterstrom, Jonas Bybjerg-Grauholm, Marie Bækved-Hansen, Olafur O. Gudmundsson, Sigurdur H. Magnusson, Gisli Baldursson, Katrin Davidsdottir, Gyda S. Haraldsdottir, Esben Agerbo, Gabriel E. Hoffman, Søren Dalsgaard, Joanna Martin, Marta Ribasés, Dorret I. Boomsma, Maria Soler Artigas, Nina Roth Mota, Daniel Howrigan, Sarah E. Medland, Tetyana Zayats, Veera M. Rajagopal, Alexandra Havdahl, Alysa Doyle, Andreas Reif, Anita Thapar, Bru Cormand, Calwing Liao, Christie Burton, Claiton H. D. Bau, Diego Luiz Rovaris, Edmund Sonuga-Barke, Elizabeth Corfield, Eugenio Horacio Grevet, Henrik Larsson, Ian R. Gizer, Irwin Waldman, Isabell Brikell, Jan Haavik, Jennifer Crosbie, James McGough, Jonna Kuntsi, Joseph Glessner, Kate Langley, Klaus-Peter Lesch, Luis Augusto Rohde, Mara H. Hutz, Marieke Klein, Mark Bellgrove, Martin Tesli, Michael C. O’Donovan, Ole Andreas Andreassen, Patrick W. L. Leung, Pedro M. Pan, Ridha Joober, Russel Schachar, Sandra Loo, Stephanie H. Witt, Ted Reichborn-Kjennerud, Tobias Banaschewski, Ziarih Hawi, Mark J. Daly, Ole Mors, Merete Nordentoft, David M. Hougaard, Preben Bo Mortensen, Stephen V. Faraone, Hreinn Stefansson, Panos Roussos, Barbara Franke, Thomas Werge, Benjamin M. Neale, Kari Stefansson, Anders D. Børglum
Source: Nature Genetics, 55, 2, pp. 198-208
Nature Genetics, vol 55, iss 2
Demontis, D, Walters, G B, Athanasiadis, G, Walters, R, Therrien, K, Nielsen, T T, Farajzadeh, L, Voloudakis, G, Bendl, J, Zeng, B, Zhang, W, Grove, J, Als, T D, Duan, J, Satterstrom, F K, Bybjerg-Grauholm, J, Bækved-Hansen, M, Gudmundsson, O O, Magnusson, S H, Baldursson, G, Davidsdottir, K, Haraldsdottir, G S, Agerbo, E, Hoffman, G E, Dalsgaard, S, Martin, J, Ribasés, M, Boomsma, D I, Soler Artigas, M, Roth Mota, N, Howrigan, D, Medland, S E, Zayats, T, Rajagopal, V M, Nordentoft, M, Mors, O, Hougaard, D M, Mortensen, P B, Daly, M J, Faraone, S V, Stefansson, H, Roussos, P, Franke, B, Werge, T, Neale, B M, Stefansson, K, Børglum, A D & ADHD Working Group of the Psychiatric Genomics Consortium 2023, 'Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains', Nature Genetics, vol. 55, no. 2, pp. 198-208. https://doi.org/10.1038/s41588-022-01285-8
Nat GenetSubject Terms: Netherlands Twin Register (NTR), 0301 basic medicine, 0303 health sciences, Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience, 4. Education, Radboud University Medical Center, Brain, 3. Good health, 03 medical and health sciences, Cognition, 0302 clinical medicine, SDG 3 - Good Health and Well-being, Attention Deficit Disorder with Hyperactivity, Humans, Genetic Predisposition to Disease, Attention Deficit Disorder with Hyperactivity/genetics, 10. No inequality, Genome-Wide Association Study
File Description: application/pdf
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14Academic Journal
Authors: Kittel-Schneider, S., Arteaga-Henriquez, G., Arias Vasquez, A., Asherson, P., Banaschewski, T., Brikell, I., Buitelaar, J.K., Cormand, B., Faraone, S.V, Freitag, C.M., Ginsberg, Y., Haavik, J., Hartman, Catharina A., Kuntsi, J., Larsson, H., Matura, S., McNeill, R.V., Ramos-Quiroga, J.A., Ribases, M., Romanos, M., Vainieri, I., Franke, B., Reif, A.
Source: Articles publicats en revistes (Genètica, Microbiologia i Estadística)
Dipòsit Digital de la UB
instname
Neuroscience and Biobehavioral Reviews, 132, pp. 1157-1180
Kittel-Schneider, S, Arteaga-Henriquez, G, Vasquez, A A, Asherson, P, Banaschewski, T, Brikell, I, Buitelaar, J, Cormand, B, Faraone, S V, Freitag, C M, Ginsberg, Y, Haavik, J, Hartman, C A, Kuntsi, J, Larsson, H, Matura, S, McNeill, R V, Ramos-Quiroga, J A, Ribases, M, Romanos, M, Vainieri, I, Franke, B & Reif, A 2022, 'Non-mental diseases associated with ADHD across the lifespan : Fidgety Philipp and Pippi Longstocking at risk of multimorbidity?', Neuroscience and Biobehavioral Reviews, vol. 132, pp. 1157-1180. https://doi.org/10.1016/j.neubiorev.2021.10.035Subject Terms: Diabetes mellitus type II, Longevity, 03 medical and health sciences, 0302 clinical medicine, Humans, Cognitive Neuroscience - Radboud University Medical Center, Obesity, Somatic disorders, Asma, Migraine, Diabetis, Epilepsy, Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience, Diabetes, Brain, Multimorbidity, Psychiatry - Radboud University Medical Center, Non-mental disease, Asthma, 3. Good health, Epilèpsia, Attention-deficit/hyperactivity disorder, Elimination disorders, Migranya, Attention Deficit Disorder with Hyperactivity, Trastorns per dèficit d'atenció amb hiperactivitat en els adults, Obesitat, Attention deficit disorder with hyperactivity in adults, Human Genetics - Radboud University Medical Center, Attention Deficit Disorder with Hyperactivity/genetics
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https://pure.au.dk/portal/en/publications/ac0842c5-6274-45b7-8fb3-71837cf65678
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15Academic Journal
Authors: Patel, Kejal H.S., Walters, G. Bragi, Stefánsson, Hreinn, Stefánsson, Kári, Degenhardt, Franziska, Nothen, Markus, Van Der Veen, Tracey, Demontis, Ditte, Borglum, Anders, Kristiansen, Mark, Bass, Nicholas J., McQuillin, Andrew
Source: Patel, K H S, Walters, G B, Stefánsson, H, Stefánsson, K, Degenhardt, F, Nothen, M, Van Der Veen, T, Demontis, D, Borglum, A, Kristiansen, M, Bass, N J & McQuillin, A 2024, 'Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD', American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, vol. 195, no. 4, e32967. https://doi.org/10.1002/ajmg.b.32967
Subject Terms: ADHD, alcohol dependence, co-morbidity, co-occurring disorders, polygenic risk scores, Genetic Predisposition to Disease, Comorbidity, Humans, Risk Factors, Middle Aged, Male, Multifactorial Inheritance/genetics, Case-Control Studies, Attention Deficit Disorder with Hyperactivity/genetics, Female, Adult, Genetic Risk Score, Alcoholism/genetics
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16Academic Journal
Authors: Sheng Wang, Belinda Wang, Vanessa Drury, Sam Drake, Nawei Sun, Hasan Alkhairo, Juan Arbelaez, Clif Duhn, Yana Bromberg, Lawrence W. Brown, Xiaolong Cao, Keun-Ah Cheon, Kyungun Cheong, Hannyung Choi, Barbara J. Coffey, Li Deng, Carolin Fremer, Blanca Garcia-Delgar, Donald L. Gilbert, Danea Glover, Dorothy E. Grice, Julie Hagstrøm, Tammy Hedderly, Isobel Heyman, Hyun Ju Hong, Chaim Huyser, Heejoo Kim, Young Key Kim, Eunjoo Kim, Young-Shin Kim, Robert A. King, Yun-Joo Koh, Sodahm Kook, Samuel Kuperman, Junghan Lee, Bennett L. Leventhal, Marcos Madruga-Garrido, Dararat Mingbunjerdsuk, Pablo Mir, Astrid Morer, Tara L. Murphy, Kirsten Müller-Vahl, Alexander Münchau, Cara Nasello, Dong Hun Oh, Kerstin J. Plessen, Veit Roessner, Eun-Young Shin, Dong-Ho Song, Jungeun Song, Joshua K. Thackray, Frank Visscher, Samuel H. Zinner, Vanessa H. Bal, Kate Langley, Joanna Martin, Pieter J. Hoekstra, Andrea Dietrich, Jinchuan Xing, Gary A. Heiman, Jay A. Tischfield, Thomas V. Fernandez, Michael J. Owen, Michael C. O’Donovan, Anita Thapar, Matthew W. State, A. Jeremy Willsey
Contributors: National Institute of Mental Health (US), Tourette Association of America, Human Genetics Institute of New Jersey, Tourette Syndrome Association of New Jersey, Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72], Tourette International Collaborative Genetics (TIC Genetics), Bromberg, Y., Brown, L.W., Cao, X., Cheon, K.A., Cheong, K., Choi, H., Coffey, B.J., Deng, L., Fremer, C., Garcia-Delgar, B., Gilbert, D.L., Glover, D., Grice, D.E., Hagstrøm, J., Hedderly, T., Heyman, I., Hong, H.J., Huyser, C., Kim, H., Kim, Y.K., Kim, E., Kim, Y.S., King, R.A., Koh, Y.J., Kook, S., Kuperman, S., Lee, J., Leventhal, B.L., Madruga-Garrido, M., Mingbunjerdsuk, D., Mir, P., Morer, A., Murphy, T.L., Müller-Vahl, K., Münchau, A., Nasello, C., Oh, D.H., Plessen, K.J., Roessner, V., Shin, E.Y., Song, D.H., Song, J., Thackray, J.K., Visscher, F., Zinner, S.H.
Source: Nat Commun
Digital.CSIC. Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Nature Communications, Vol 14, Iss 1, Pp 1-18 (2023)
Wang, S, Wang, B, Drury, V, Drake, S, Sun, N, Alkhairo, H, Arbelaez, J, Duhn, C, Bromberg, Y, Brown, L W, Cao, X, Cheon, K-A, Cheong, K, Choi, H, Coffey, B J, Deng, L, Fremer, C, Garcia-Delgar, B, Gilbert, D L, Glover, D, Grice, D E, Hagstrøm, J, Hedderly, T, Heyman, I, Hong, H J, Huyser, C, Kim, H, Kim, Y K, Kim, E, Kim, Y-S, King, R A, Koh, Y-J, Kook, S, Kuperman, S, Lee, J, Leventhal, B L, Madruga-Garrido, M, Mingbunjerdsuk, D, Mir, P, Morer, A, Murphy, T L, Müller-Vahl, K, Münchau, A, Nasello, C, Oh, D H, Plessen, K J, Roessner, V, Shin, E-Y, Song, D-H, Song, J, Thackray, J K, Visscher, F, Zinner, S H, Bal, V H, Langley, K, Martin, J, Hoekstra, P J, Dietrich, A, Xing, J, Heiman, G A, Tischfield, J A, Fernandez, T V, Owen, M J, O’Donovan, M C, Thapar, A, State, M W & Willsey, A J 2023, 'Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD', Nature Communications, vol. 14, no. 1, 8077. https://doi.org/10.1038/s41467-023-43776-0
Nature communications, vol. 14, no. 1, pp. 8077
Nature Communications, vol 14, iss 1Subject Terms: Male, Autism Spectrum Disorder, Science, Neurodevelopmental disorders, Autism spectrum disorders, Article, Humans, Female, Attention Deficit Disorder with Hyperactivity/genetics, Tourette Syndrome/genetics, Autistic Disorder/genetics, Autism Spectrum Disorder/genetics, Neurodevelopmental Disorders, Attention Deficit Disorder with Hyperactivity, Autistic Disorder, Tourette Syndrome
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17Academic Journal
Authors: Faltraco, Frank, Palm, Denise, Uzoni, Adriana, Borchert, Lena, Simon, Frederick, Tucha, Oliver, Thome, Johannes
Source: J Neural Transm (Vienna)
Journal of Neural TransmissionSubject Terms: 0301 basic medicine, 03 medical and health sciences, 0302 clinical medicine, Attention Deficit Disorder with Hyperactivity, Dopamine, Psychiatry and Preclinical Psychiatric Studies - Original Article, Gene Expression, Humans, Period Circadian Proteins, Fibroblasts, Period Circadian Proteins/genetics [MeSH], Circadian rhythm, Humans [MeSH], Circadian Rhythm [MeSH], Period Circadian Proteins/metabolism [MeSH], ADHD Dopamine, Human dermal fibroblasts, Gene Expression [MeSH], Attention Deficit Disorder with Hyperactivity/genetics [MeSH], Dopamine [MeSH], Fibroblasts/metabolism [MeSH], Circadian Rhythm, 3. Good health
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18Academic Journal
Authors: Faltraco, Frank, Palm, Denise, Uzoni, Adriana, Simon, Frederick, Tucha, Oliver, Thome, Johannes
Source: J Neural Transm (Vienna)
Journal of Neural TransmissionSubject Terms: Fibroblasts [MeSH], Circadian rhythm, Attention Deficit Disorder with Hyperactivity/drug therapy [MeSH], Humans [MeSH], Psychiatry and Preclinical Psychiatric Studies - Original Article, Atomoxetine Hydrochloride [MeSH], Circadian Rhythm [MeSH], Human dermal fibroblasts, Atomoxetine, Gene Expression [MeSH], Sleep [MeSH], Attention Deficit Disorder with Hyperactivity/genetics [MeSH], 0301 basic medicine, 03 medical and health sciences, 0302 clinical medicine, Attention Deficit Disorder with Hyperactivity, Gene Expression, Humans, Fibroblasts, Atomoxetine Hydrochloride, Sleep, 16. Peace & justice, Circadian Rhythm
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https://pubmed.ncbi.nlm.nih.gov/34273025/
https://link.springer.com/content/pdf/10.1007/s00702-021-02373-5.pdf
https://link.springer.com/article/10.1007/s00702-021-02373-5
https://paperity.org/p/269413082/atomoxetine-and-circadian-gene-expression-in-human-dermal-fibroblasts-from-study
https://repository.publisso.de/resource/frl:6446548 -
19Academic Journal
Authors: Clara Albiñana, Zhihong Zhu, Andrew J. Schork, Andrés Ingason, Hugues Aschard, Isabell Brikell, Cynthia M. Bulik, Liselotte V. Petersen, Esben Agerbo, Jakob Grove, Merete Nordentoft, David M. Hougaard, Thomas Werge, Anders D. Børglum, Preben Bo Mortensen, John J. McGrath, Benjamin M. Neale, Florian Privé, Bjarni J. Vilhjálmsson
Contributors: Lassailly-Bondaz, Anne
Source: Nat Commun
Nature Communications, Vol 14, Iss 1, Pp 1-11 (2023)
Albiñana, C, Zhu, Z, Schork, A J, Ingason, A, Aschard, H, Brikell, I, Bulik, C M, Petersen, L V, Agerbo, E, Grove, J, Nordentoft, M, Hougaard, D M, Werge, T, Børglum, A D, Mortensen, P B, McGrath, J J, Neale, B M, Privé, F & Vilhjálmsson, B J 2023, 'Multi-PGS enhances polygenic prediction by combining 937 polygenic scores', Nature Communications, vol. 14, no. 1, 4702. https://doi.org/10.1038/s41467-023-40330-w
Albiñana, C, Zhu, Z, Schork, A J, Ingason, A, Aschard, H, Brikell, I, Bulik, C M, Petersen, L V, Agerbo, E, Grove, J, Nordentoft, M, Hougaard, D M, Werge, T, Børglum, A D, Mortensen, P B, McGrath, J J, Neale, B M, Privé, F & Vilhjálmsson, B J 2023, ' Multi-PGS enhances polygenic prediction by combining 937 polygenic scores ', Nature Communications, vol. 14, 4702 . https://doi.org/10.1038/s41467-023-40330-wSubject Terms: Multifactorial Inheritance, Phenotype, Attention Deficit Disorder with Hyperactivity, Science, Humans, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, Attention Deficit Disorder with Hyperactivity/genetics, Multifactorial Inheritance/genetics, Article, 3. Good health, Genome-Wide Association Study
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https://pure.au.dk/ws/files/375677753/s41467-023-40330-w.pdf
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https://doi.org/10.1038/s41467-023-40330-w
https://pure.au.dk/ws/files/375677753/s41467-023-40330-w.pdf
https://pure.au.dk/portal/en/publications/d85efb37-046e-4114-a4ff-c395324194fd -
20Academic Journal
Authors: Shelley D. Smith, Urs Maurer, Yves Chaix, Darina Czamara, Jean-François Démonet, Per Hoffmann, Fabien Fauchereau, Anthony P. Monaco, Anniek Vaessen, Joel B. Talcott, Andrew P. Morris, Bent Müller, Myriam Peyrard-Janvid, Stéphanie Iannuzzi, Juha Kere, Till F. M. Andlauer, Daniel Brandeis, Jessica Becker, Guillaume Huguet, Simon E. Fisher, Bertram Müller-Myhsok, Thomas S. Scerri, Arndt Wilcke, Jacqueline Hulslander, Holger Kirsten, Heikki Lyytinen, Beate St Pourcain, Valéria Csépe, Karin Landerl, Richard K. Olson, Erik G. Willcutt, Alessandro Gialluisi, Gerd Schulte-Körne, Ferenc Honbolygó, Silvia Paracchini, Johannes Schumacher, Kerstin U. Ludwig, Nazanin Mirza-Schreiber, John C. DeFries, Franck Ramus, Clyde Francks, Markus M. Nöthen, Milene Bonte, Dénes Tóth, Paavo H.T. Leppänen, John F. Stein, Bruce F. Pennington, Thomas Bourgeron, Kristina Moll
Contributors: STEMM - Stem Cells and Metabolism Research Program, Juha Kere / Principal Investigator, Research Programs Unit, University of Helsinki, Ramus, Franck, The Royal Society, University of St Andrews.School of Medicine, University of St Andrews.Centre for Biophotonics, University of St Andrews.Biomedical Sciences Research Complex, University of St Andrews.Cellular Medicine Division, Max-Planck-Institut für Psychiatrie, Max-Planck-Gesellschaft, Munich Cluster for systems neurology Munich (SyNergy), Technische Universität Munchen - Technical University Munich - Université Technique de Munich (TUM)-Ludwig Maximilian University Munich = Ludwig Maximilians Universität München (LMU), Istituto Neurologico Mediterraneo (NEUROMED I.R.C.C.S.), Università degli Studi di Roma 'La Sapienza' = Sapienza University Rome (UNIROMA)-University of Naples Federico II = Università degli studi di Napoli Federico II, Technische Universität Munchen - Technical University Munich - Université Technique de Munich (TUM), Helmholtz Zentrum München = German Research Center for Environmental Health (HMGU), Ludwig Maximilian University Munich = Ludwig Maximilians Universität München (LMU), Universität Bonn = University of Bonn, Max Planck Institute for Psycholinguistics, Radboud University Nijmegen, University of Bristol Bristol, Hungarian Academy of Sciences (MTA), Génétique humaine et fonctions cognitives - Human Genetics and Cognitive Functions (GHFC (UMR_3571 / U-Pasteur_1)), Institut Pasteur Paris (IP)-Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), Toulouse NeuroImaging Center (ToNIC), Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Toulouse Mind & Brain Institut (TMBI), Université Toulouse - Jean Jaurès (UT2J), Université de Toulouse (UT)-Université de Toulouse (UT)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université Toulouse - Jean Jaurès (UT2J), Université de Toulouse (UT)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT), Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), Université de Lausanne = University of Lausanne (UNIL), University of Liverpool, University of Manchester Manchester, University of Oxford, University of Colorado Boulder, University of Nebraska Medical Center, University of Nebraska System, University of Denver, Maastricht University Maastricht, The Chinese University of Hong Kong Hong Kong (CUHK), University of Jyväskylä (JYU), Karolinska Institutet Stockholm, Universität Zürich Zürich = University of Zurich (UZH), Eidgenössische Technische Hochschule - Swiss Federal Institute of Technology Zürich (ETH Zürich), Universität Heidelberg Heidelberg = Heidelberg University, Aston University Birmingham, Fraunhofer Institute for Cell Therapy and Immunology (Fraunhofer IZI), Fraunhofer (Fraunhofer-Gesellschaft), Leipzig University / Universität Leipzig, Tufts University Medford, Laboratoire de sciences cognitives et psycholinguistique (LSCP), Département d'Etudes Cognitives - ENS-PSL (DEC), École normale supérieure - Paris (ENS-PSL), Université Paris Sciences et Lettres (PSL)-Université Paris Sciences et Lettres (PSL)-École normale supérieure - Paris (ENS-PSL), Université Paris Sciences et Lettres (PSL)-Université Paris Sciences et Lettres (PSL)-École des hautes études en sciences sociales (EHESS)-Centre National de la Recherche Scientifique (CNRS), BioTechMed-Graz, Graz University of Technology Graz (TU Graz)-Karl-Franzens-Universität Graz-Medical University of Graz = Medizinische Universität Graz, Helsingin yliopisto = Helsingfors universitet = University of Helsinki, University of Melbourne, University of St Andrews Scotland, AG and TFMA were supported by the Munich Cluster for Systems Neurology (SyNergy). AG was supported by Fondazione Umberto Veronesi. SP is a Royal Society University Research fellow. BMM, CF, BSP and SEF are supported by the Max Planck Society. AW, BM and HK were funded by the Fraunhofer Society and the Max Planck Society within the 'Pakt für Forschung und Innovation'. HK was also supported by LIFE—Leipzig Research Center for Civilization Diseases funded by means of the European Union, the European Regional Development Fund (ERDF), and the Free State of Saxony within the excellence initiative. FR is supported by Agence Nationale de la Recherche (ANR-06-NEURO-019-01, ANR-17-EURE-0017 IEC, ANR-10-IDEX-0001-02 PSL, ANR-11-BSV4-014-01), European Commission (LSHM-CT-2005-018696). TFMA was supported by the B.M.B.F. through the DIFUTURE consortium of the Medical Informatics Initiative Germany (grant 01ZZ1804A) and by the European Union’s Horizon 2020 Research and Innovation Programme (grant MultipleMS, EU RIA 733161)., ANR-06-NEUR-0019,GENEDYS,Origines cognitives, neurologiques et génétiques des troubles développementaux du langage(2006), ANR-17-EURE-0017,FrontCog,Frontières en cognition(2017), ANR-10-IDEX-0001,PSL,Paris Sciences et Lettres(2010), ANR-11-BSV4-0014,DYSBRAIN,Le cerveau dyslexique(2011)
Source: Mol Psychiatry
Molecular Psychiatry, 26, pp. 3004-3017
Molecular Psychiatry
Molecular psychiatry, vol. 26, no. 7, pp. 3004-3017
Mol. Psychiatry 26, 3004–3017 (2021)Subject Terms: 0301 basic medicine, Multifactorial Inheritance, Intelligence, LANGUAGE, INTELLIGENCE, Educational attaintment, heritability, READING-DISABILITY, Dyslexia, MOLECULAR-GENETICS, SCHIZOPHRENIA, GWAS, Psychology, Brain cortical thickness, 10. No inequality, 2. Zero hunger, 0303 health sciences, Intracellular Signaling Peptides and Proteins, [SDV.NEU.SC]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Cognitive Sciences, developmental dyslexia, Psykologia, ddc, 3. Good health, SUSCEPTIBILITY GENE, geneettiset tekijät, BDC, RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry, Neuroinformatics, Bipolar disorder, Developmental dyslexia, NDAS, QH426 Genetics, INDIVIDUAL-DIFFERENCES, Polymorphism, Single Nucleotide, Article, Neurology and psychiatry, Heritability, 03 medical and health sciences, AGE, Genetics, LOCUS, ADHD, dysleksia, Humans, Genetic Predisposition to Disease, QH426, perinnöllisyys, Polygenic risk, genetic correlates, Transverse temporal gyrus, Reading, Attention Deficit Disorder with Hyperactivity, Schizophrenia, RC0321, Genetic Predisposition to Disease [MeSH], Intracellular Signaling Peptides and Proteins/genetics [MeSH], Neuroscience, Polymorphism, Single Nucleotide [MeSH], Dyslexia/genetics [MeSH], Humans [MeSH], Psychiatric disorders, Multifactorial Inheritance [MeSH], Attention Deficit Disorder with Hyperactivity/genetics [MeSH], Genome-Wide Association Study [MeSH], COMORBIDITY, [SDV.NEU.SC] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Cognitive Sciences, Genome-Wide Association Study
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Access URL: https://www.nature.com/articles/s41380-020-00898-x.pdf
https://pubmed.ncbi.nlm.nih.gov/33057169
https://publications.aston.ac.uk/id/eprint/42022/1/s41380_020_00898_x.pdf
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/247012
https://cris.maastrichtuniversity.nl/en/publications/8b76c901-ca76-4687-8b5d-daa0dad811ec
https://doi.org/10.1038/s41380-020-00898-x
http://www.ncbi.nlm.nih.gov/pubmed/33057169
https://experts.nebraska.edu/en/publications/genome-wide-association-study-reveals-new-insights-into-the-herit
https://www.nature.com/articles/s41380-020-00898-x
https://www.zora.uzh.ch/id/eprint/193624/
https://research-repository.st-andrews.ac.uk/handle/10023/20788
https://pure.mpg.de/pubman/faces/ViewItemOverviewPage.jsp?itemId=item_3253260
http://urn.fi/URN:NBN:fi:jyu-202010206313
https://repository.ubn.ru.nl//bitstream/handle/2066/247012/247012.pdf
https://hdl.handle.net/2066/247012
http://hdl.handle.net/10138/353203
http://hdl.handle.net/21.11116/0000-0009-9427-4
http://hdl.handle.net/21.11116/0000-0007-36E0-F
http://hdl.handle.net/21.11116/0000-0007-36E1-E
http://hdl.handle.net/21.11116/0000-0007-36E2-D
http://hdl.handle.net/21.11116/0000-0007-36DF-2
http://hdl.handle.net/21.11116/0000-0007-0A1D-F
https://serval.unil.ch/notice/serval:BIB_95BF958D027E
https://serval.unil.ch/resource/serval:BIB_95BF958D027E.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_95BF958D027E6
https://hal.science/hal-02976104v1/document
https://hal.science/hal-02976104v1
https://doi.org/10.1038/s41380-020-00898-x
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=60321
https://repository.publisso.de/resource/frl:6471324
https://epub.ub.uni-muenchen.de/76011/
https://mediatum.ub.tum.de/1585351
https://hdl.handle.net/10023/20788