Výsledky vyhledávání - "Attention Deficit Disorder with Hyperactivity genetics"

A Genetic Bridge Between Medicine and Neurodiversity for Autism

Autoři: Leblond, Claire Rolland, Thomas Barthome, Eli a další

Přispěvatelé: Leblond, Claire Rolland, Thomas Barthome, Eli a další

Zdroj: 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 Reviews

Témata: 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

Popis souboru: application/pdf

Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/39585908
https://pasteur.hal.science/pasteur-05129876v1/document
https://pasteur.hal.science/pasteur-05129876v1
https://doi.org/10.1146/annurev-genet-111523-102614

Child maltreatment as a transdiagnostic risk factor for the externalizing dimension: a Mendelian randomization study

Autoři: Konzok, Julian Gorski, Mathias Winkler, Thomas W. a další

Přispěvatelé: Konzok, Julian Gorski, Mathias Winkler, Thomas W. a další

Zdroj: Mol Psychiatry

Témata: 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

Popis souboru: text/xml; application/zip; application/pdf

Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/39174650
https://repository.publisso.de/resource/frl:6492158
https://epub.uni-regensburg.de/59015/

Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries

Autoři: Luis M. García-Marín Adrian I. Campos Santiago Diaz-Torres a další

Přispěvatelé: Luis M. García-Marín Adrian I. Campos Santiago Diaz-Torres a další

Zdroj: 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 11

Témata: 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

Popis souboru: application/pdf

Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/39433889
https://pubmed.ncbi.nlm.nih.gov/39371125
http://hdl.handle.net/10261/382948
https://pure.eur.nl/en/publications/410f7986-f65f-42aa-af38-d460c51e1f6e
https://doi.org/10.1038/s41588-024-01951-z
https://research.vu.nl/en/publications/58f7979b-939d-43c2-803d-c9907b080eb4
https://doi.org/10.1038/s41588-024-01951-z
https://hdl.handle.net/1871.1/58f7979b-939d-43c2-803d-c9907b080eb4
https://cris.maastrichtuniversity.nl/en/publications/7059d74f-7105-4417-827c-58fdf7a066b9
https://doi.org/10.1038/s41588-024-01951-z
https://cris.maastrichtuniversity.nl/en/publications/df387d7a-d54e-41be-97eb-9535da578ecd
https://doi.org/10.1101/2024.08.13.24311922
https://dspace.library.uu.nl/handle/1874/459118
https://dspace.library.uu.nl/handle/1874/461144
https://pure.amsterdamumc.nl/en/publications/c860cd0e-54aa-4ba2-975d-b1ba9e2199c1
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
https://escholarship.org/content/qt4g85k360/qt4g85k360.pdf
https://escholarship.org/content/qt9bp1077g/qt9bp1077g.pdf
https://escholarship.org/uc/item/9bp1077g

The phenotypic and genotypic spectrum of individuals with mono‐ or biallelic ANK3 variants

Autoři: Francesca Furia Amanda M. Levy Miel Theunis a další

Přispěvatelé: Francesca Furia Amanda M. Levy Miel Theunis a další

Zdroj: 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

Témata: 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

Popis souboru: application/pdf

Přístupová URL adresa: 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

Genome-Wide Analyses of Vocabulary Size in Infancy and Toddlerhood: Associations With Attention-Deficit/Hyperactivity Disorder, Literacy, and Cognition-Related Traits: Associations With Attention-Deficit/Hyperactivity Disorder, Literacy, and Cognition-Related Traits

Autoři: Verhoef, Ellen Allegrini, Andrea G. Jansen, Philip R. a další

Přispěvatelé: Verhoef, Ellen Allegrini, Andrea G. Jansen, Philip R. a další

Zdroj: 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 Psychiatry

Témata: 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

Popis souboru: application/pdf

Přístupová URL adresa: 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

Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder

Autoři: Sonja LaBianca Isabell Brikell Dorte Helenius a další

Zdroj: 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/s41588-023-01593-7

Témata: 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

Popis souboru: application/pdf

Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/38036780
https://curis.ku.dk/ws/files/429031412/Polygenic_profiles.pdf
https://escholarship.org/content/qt2xs809ct/qt2xs809ct.pdf
https://escholarship.org/uc/item/2xs809ct
https://pure.au.dk/portal/en/publications/ef2e35b5-907f-4d60-b175-a532bb6a94f7
https://doi.org/10.1038/s41588-023-01593-7

Genetic Architecture and Risk of Childhood Maltreatment Across 5 Psychiatric Diagnoses

Autoři: Nielsen, Trine Tollerup Bali, Paraskevi Grove, Jakob a další

Přispěvatelé: Nielsen, Trine Tollerup Bali, Paraskevi Grove, Jakob a další

Zdroj: 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.2025.0828

Témata: 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

Přístupová URL adresa: 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
https://doi.org/10.1001/jamapsychiatry.2025.0828
https://vbn.aau.dk/da/publications/ef2e8192-d82c-4222-bdc2-a7bc70b34dae
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
http://www.scopus.com/inward/record.url?scp=105005290238&partnerID=8YFLogxK
https://doi.org/10.1001/jamapsychiatry.2025.0828

No evidence for a causal contribution of bioavailable testosterone to ADHD in sex-combined and sex-specific two-sample Mendelian randomization studies

Autoři: Dinkelbach, Lars Peters, Triinu Grasemann, Corinna a další

Zdroj: Eur Child Adolesc Psychiatry

Témata: 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

Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/38536491
https://repository.publisso.de/resource/frl:6497221

Associations Between Attention Deficit Hyperactivity Disorder Symptom Dimensions and Disordered Eating Symptoms in Adolescence: A Population-Based Twin Study

Autoři: Yilmaz, Zeynep Quattlebaum, Mary J. Pawar, Pratiksha S. a další

Zdroj: 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

Témata: 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

Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/36484893
https://pure.au.dk/portal/en/publications/abb3b7b7-2f87-43eb-a084-1297093dad1a
https://pmc.ncbi.nlm.nih.gov/articles/PMC10167484/pdf/nihms-1896284.pdf
https://doi.org/10.1007/s10519-022-10128-5
http://www.scopus.com/inward/record.url?scp=85143604736&partnerID=8YFLogxK

Investigation of gene–environment interactions in relation to tic severity

Autoři: Barbara J. Coffey Julie Hagstrøm Frank Visscher a další

Přispěvatelé: Barbara J. Coffey Julie Hagstrøm Frank Visscher a další

Zdroj: 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 11

Témata: 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

Popis souboru: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

Přístupová URL adresa: https://link.springer.com/content/pdf/10.1007/s00702-021-02396-y.pdf
https://europepmc.org/articles/pmc8536549?pdf=render
https://pubmed.ncbi.nlm.nih.gov/34389898
http://hdl.handle.net/10261/269896
http://hdl.handle.net/10668/18374
https://research.rug.nl/en/publications/752a6a37-2bec-4452-9c76-869d5fbe516f
https://hdl.handle.net/11370/752a6a37-2bec-4452-9c76-869d5fbe516f
https://doi.org/10.1007/s00702-021-02396-y
https://link.springer.com/article/10.1007%2Fs00702-021-02396-y
https://pubmed.ncbi.nlm.nih.gov/34389898/
https://europepmc.org/article/PPR/PPR340433
https://link.springer.com/content/pdf/10.1007/s00702-021-02396-y.pdf
https://paperity.org/p/269350392/investigation-of-gene-environment-interactions-in-relation-to-tic-severity
https://www.ncbi.nlm.nih.gov/pubmed/34389898
https://www.medrxiv.org/content/10.1101/2021.05.12.21257005v1
https://medrxiv.org/content/10.1101/2021.05.12.21257005v1.full.pdf
https://serval.unil.ch/notice/serval:BIB_6D97CD3D1149
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_6D97CD3D11496
https://serval.unil.ch/resource/serval:BIB_6D97CD3D1149.P001/REF.pdf
https://hdl.handle.net/10668/18374
https://curis.ku.dk/ws/files/301347390/Investigation.pdf
https://discovery-pp.ucl.ac.uk/id/eprint/10132096/
https://escholarship.org/content/qt4177h5m7/qt4177h5m7.pdf
https://escholarship.org/uc/item/4177h5m7

Genetische Grundlagen der ADHS – ein Update

Autoři: Sarah Hohmann Alexander Häge Sabina Millenet a další

Zdroj: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie. 50:203-217

Témata: 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

Přístupová URL adresa: https://repository.publisso.de/resource/frl:6475190

Mediating pathways between attention deficit hyperactivity disorder and type 2 diabetes mellitus: evidence from a two-step and multivariable Mendelian randomization study: evidence from a two-step and multivariable Mendelian randomization study

Autoři: Zhang, J. Chen, Z. K. Triatin, R. D. a další

Zdroj: Epidemiol Psychiatr Sci
Epidemiology and Psychiatric Sciences, Vol 33 (2024)
Epidemiology and Psychiatric Sciences

Témata: 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

Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/39465621
https://doaj.org/article/5385d3b7ac114179aecf81e3bfa3b692
https://hdl.handle.net/11370/0199e170-9f66-4c0c-b2b5-a6be7d7d71b8
https://research.rug.nl/en/publications/0199e170-9f66-4c0c-b2b5-a6be7d7d71b8
https://doi.org/10.1017/S2045796024000593
https://research-portal.uu.nl/en/publications/3c6aba55-7e55-473c-8fd2-9f3223cb538c
https://doi.org/10.1017/S2045796024000593

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

Autoři: Ditte Demontis G. Bragi Walters Georgios Athanasiadis a další

Zdroj: 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 Genet

Témata: 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

Popis souboru: application/pdf

Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/36702997
https://hdl.handle.net/2066/290804
https://repository.ubn.ru.nl//bitstream/handle/2066/290804/290804.pdf
https://escholarship.org/uc/item/65q2q9f8
https://escholarship.org/content/qt65q2q9f8/qt65q2q9f8.pdf

Non-mental diseases associated with ADHD across the lifespan: Fidgety Philipp and Pippi Longstocking at risk of multimorbidity?

Autoři: Kittel-Schneider, S. Arteaga-Henriquez, G. Arias Vasquez, A. a další

Zdroj: 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.2021.10.035

Témata: 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

Popis souboru: application/pdf

Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/34757108
https://hdl.handle.net/2445/198170
https://www.sciencedirect.com/science/article/abs/pii/S0149763421004772
https://research.rug.nl/en/publications/non-mental-diseases-associated-with-adhd-across-the-lifespan-fidg
https://www.ncbi.nlm.nih.gov/pubmed/34757108
https://europepmc.org/article/MED/34757108
https://pubmed.ncbi.nlm.nih.gov/34757108/
https://hdl.handle.net/2066/248384
https://repository.ubn.ru.nl//bitstream/handle/2066/248384/248384.pdf
https://pure.au.dk/portal/en/publications/ac0842c5-6274-45b7-8fb3-71837cf65678
https://discovery-pp.ucl.ac.uk/id/eprint/10141860/
https://pure.au.dk/portal/en/publications/ac0842c5-6274-45b7-8fb3-71837cf65678
https://doi.org/10.1016/j.neubiorev.2021.10.035
https://pure.au.dk/ws/files/357755801/kittel-schneider2021.pdf
http://www.scopus.com/inward/record.url?scp=85119174678&partnerID=8YFLogxK

Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD

Autoři: Patel, Kejal H.S. Walters, G. Bragi Stefánsson, Hreinn a další

Zdroj: 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

Témata: 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

Dostupnost: https://pure.au.dk/portal/en/publications/b74ffd5d-74ba-46ac-8e04-11a1cc6463db
https://doi.org/10.1002/ajmg.b.32967

Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

Autoři: Sheng Wang Belinda Wang Vanessa Drury a další

Přispěvatelé: Sheng Wang Belinda Wang Vanessa Drury a další

Zdroj: 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 1

Témata: 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

Popis souboru: application/pdf

Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/38057346
http://hdl.handle.net/10261/352762
https://doaj.org/article/0f0d828cb9a44cc7a0dc9536fdc3e9b0
https://research.rug.nl/en/publications/41de5248-5bbe-43d3-9f5f-216fc4055a7a
https://doi.org/10.1038/s41467-023-43776-0
https://hdl.handle.net/11370/41de5248-5bbe-43d3-9f5f-216fc4055a7a
https://research.vumc.nl/en/publications/8865cb1b-bc85-4b85-95ee-a13a1116b107
https://serval.unil.ch/resource/serval:BIB_2A866AC1AFC8.P001/REF.pdf
https://serval.unil.ch/notice/serval:BIB_2A866AC1AFC8
https://escholarship.org/content/qt4nh8c7mh/qt4nh8c7mh.pdf
https://escholarship.org/uc/item/4nh8c7mh

Dopamine adjusts the circadian gene expression of Per2 and Per3 in human dermal fibroblasts from ADHD patients

Autoři: Faltraco, Frank Palm, Denise Uzoni, Adriana a další

Zdroj: J Neural Transm (Vienna)
Journal of Neural Transmission

Témata: 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

Přístupová URL adresa: https://link.springer.com/content/pdf/10.1007/s00702-021-02374-4.pdf
https://pubmed.ncbi.nlm.nih.gov/34275001
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295132
https://pubmed.ncbi.nlm.nih.gov/34275001/
https://link.springer.com/content/pdf/10.1007/s00702-021-02374-4.pdf
https://link.springer.com/article/10.1007/s00702-021-02374-4
https://repository.publisso.de/resource/frl:6446546

Atomoxetine and circadian gene expression in human dermal fibroblasts from study participants with a diagnosis of attention-deficit hyperactivity disorder

Autoři: Faltraco, Frank Palm, Denise Uzoni, Adriana a další

Zdroj: J Neural Transm (Vienna)
Journal of Neural Transmission

Témata: 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

Přístupová URL adresa: https://link.springer.com/content/pdf/10.1007/s00702-021-02373-5.pdf
https://pubmed.ncbi.nlm.nih.gov/34273025
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295110
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

Multi-PGS enhances polygenic prediction by combining 937 polygenic scores

Autoři: Clara Albiñana Zhihong Zhu Andrew J. Schork a další

Přispěvatelé: Clara Albiñana Zhihong Zhu Andrew J. Schork a další

Zdroj: 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-w

Témata: 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

Popis souboru: application/pdf

Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/37543680
https://hal.science/hal-04145280v1/document
https://doi.org/10.1038/s41467-023-40330-w
https://hal.science/hal-04145280v1
https://doaj.org/article/65c6fd7da745423fbb7f56199da61c83
https://pure.au.dk/ws/files/375677753/s41467-023-40330-w.pdf
https://curis.ku.dk/ws/files/362278571/s41467_023_40330_w.pdf
http://www.scopus.com/inward/record.url?scp=85166599056&partnerID=8YFLogxK
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

Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

Autoři: Shelley D. Smith Urs Maurer Yves Chaix a další

Přispěvatelé: Shelley D. Smith Urs Maurer Yves Chaix a další

Zdroj: 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)

Témata: 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

Popis souboru: application/pdf; fulltext; application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet

Přístupová URL adresa: 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