Search Results - "Multifactorial Inheritance/genetics [MeSH]"

A meta-analysis of genome-wide studies of resilience in the German population

Authors: Marisol Herrera-Rivero Linda Garvert Katrin Horn et al.

Source: Mol Psychiatry
Molecular psychiatry 30(2), 497-505 (2025). doi:10.1038/s41380-024-02688-1

Subject Terms: Male, Adult, 0301 basic medicine, 0303 health sciences, Resilience, Psychological, Middle Aged, methods [Genome-Wide Association Study], Article, ddc, 3. Good health, Female [MeSH], Multifactorial Inheritance/genetics [MeSH], 631/208, Personality/genetics [MeSH], Resilience, Psychological [MeSH], Adult [MeSH], Humans [MeSH], Mental Health [MeSH], Middle Aged [MeSH], 692/699/476, Polymorphism, Single Nucleotide/genetics [MeSH], Cohort Studies [MeSH], 631/477, Genome-Wide Association Study/methods [MeSH], Male [MeSH], 45/43, Germany [MeSH], article, Cohort Studies, 03 medical and health sciences, Mental Health, Germany, genetics [Polymorphism, Single Nucleotide], Humans, genetics [Personality], Female, ddc:610, genetics [Multifactorial Inheritance]

File Description: application/pdf

Access URL: https://pubmed.ncbi.nlm.nih.gov/39112778
https://cris.maastrichtuniversity.nl/en/publications/6705496c-b5a2-468c-a0ae-f49f18427510
https://doi.org/10.1038/s41380-024-02688-1
https://pub.dzne.de/record/276147
https://repository.publisso.de/resource/frl:6503734
https://mediatum.ub.tum.de/doc/1769787/document.pdf

The interplay between polygenic score for tumor necrosis factor-α, brain structural connectivity, and processing speed in major depression

Authors: Flinkenflügel, Kira Gruber, Marius Meinert, Susanne et al.

Source: Mol Psychiatry
Molecular psychiatry 29, 3151-3159 (2024). doi:10.1038/s41380-024-02577-7
Molecular Psychiatry

Subject Terms: Male, Adult, 0301 basic medicine, Multifactorial Inheritance, Female [MeSH], Multifactorial Inheritance/genetics [MeSH], 59/57, Adult [MeSH], Humans [MeSH], Nerve Net/physiopathology [MeSH], Depressive Disorder, Major/metabolism [MeSH], Depressive Disorder, Major/genetics [MeSH], Middle Aged [MeSH], Processing Speed [MeSH], 692/699/476/1414, Article, Brain/physiopathology [MeSH], Depressive Disorder, Major/physiopathology [MeSH], Male [MeSH], Nerve Net/metabolism [MeSH], Nerve Net/diagnostic imaging [MeSH], Brain/metabolism [MeSH], Magnetic Resonance Imaging/methods [MeSH], Tumor Necrosis Factor-alpha/metabolism [MeSH], 631/378, article, Neuropsychological Tests [MeSH], Neuropsychological Tests, Magnetic Resonance Imaging/methods, Nerve Net/metabolism, 03 medical and health sciences, 0302 clinical medicine, Brain/metabolism, Humans, Multifactorial Inheritance/genetics, Processing Speed, Tumor Necrosis Factor-alpha/metabolism, Depressive Disorder, Depressive Disorder, Major, Tumor Necrosis Factor-alpha, Brain, Major/genetics, Middle Aged, Magnetic Resonance Imaging, Female, Nerve Net

Access URL: https://pubmed.ncbi.nlm.nih.gov/38693319
https://research.vu.nl/en/publications/3ca947ed-9539-4dfc-bc88-7e6616c75d05
https://doi.org/10.1038/s41380-024-02577-7
https://hdl.handle.net/1871.1/3ca947ed-9539-4dfc-bc88-7e6616c75d05
https://juser.fz-juelich.de/record/1026976
https://repository.publisso.de/resource/frl:6521043

Comparison of subjective cognitive decline and polygenic risk score in the prediction of all-cause dementia, Alzheimer’s disease and vascular dementia

Authors: Trares, Kira Stocker, Hannah Stevenson-Hoare, Joshua et al.

Source: Alzheimers Res Ther
Alzheimer’s Research & Therapy, Vol 16, Iss 1, Pp 1-12 (2024)

Subject Terms: Male, Multifactorial Inheritance, Neurosciences. Biological psychiatry. Neuropsychiatry, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Polygenic risk score, Alzheimer Disease, Risk Factors, Subjective cognitive decline, Vascular dementia, Cohort study, Aged [MeSH], Dementia, Vascular/genetics [MeSH], Dementia/genetics [MeSH], Dementia/diagnosis [MeSH], Risk Factors [MeSH], Cohort Studies [MeSH], Alzheimer's disease, Male [MeSH], CAIDE, Dementia/epidemiology [MeSH], Dementia, Genetic Risk Score [MeSH], Female [MeSH], Multifactorial Inheritance/genetics [MeSH], Cognitive Dysfunction/diagnosis [MeSH], Humans [MeSH], Middle Aged [MeSH], Risk prediction, Research, Cognitive Dysfunction/genetics [MeSH], Alzheimer Disease/genetics [MeSH], Humans, Cognitive Dysfunction, RC346-429, Aged, Genetic Risk Score, Dementia, Vascular, Middle Aged, 3. Good health, Female, Neurology. Diseases of the nervous system, RC321-571

Access URL: https://pubmed.ncbi.nlm.nih.gov/39160600
https://doaj.org/article/2dd30935939c4e65bc30c566b652366b
https://repository.publisso.de/resource/frl:6517838

Genome-Wide Association Study of Obsessive-Compulsive Symptoms including 33,943 individuals from the general population

Authors: Nora I. Strom Christie L. Burton Conrad Iyegbe et al.

Source: Mol Psychiatry
Strom, N I, Burton, C L, Iyegbe, C, Silzer, T, Antonyan, L, Pool, R, Lemire, M, Crowley, J J, Hottenga, J J, Ivanov, V Z, Larsson, H, Lichtenstein, P, Magnusson, P, Rück, C, Schachar, R, Wu, H M, Cath, D, Crosbie, J, Mataix-Cols, D, Boomsma, D I, Mattheisen, M, Meier, S M, Smit, D J A & Arnold, P D 2024, 'Genome-Wide Association Study of Obsessive-Compulsive Symptoms including 33,943 individuals from the general population', Molecular Psychiatry, vol. 29, no. 9, pp. 2714-2723. https://doi.org/10.1038/s41380-024-02489-6

Subject Terms: Sweden, 0301 basic medicine, ddc:610, Canada, Multifactorial Inheritance, Obsessive-Compulsive Disorder, 0303 health sciences, Multifactorial Inheritance/genetics [MeSH], 631/208, England/epidemiology [MeSH], Humans [MeSH], Sweden [MeSH], 692/699/476, Polymorphism, Single Nucleotide/genetics [MeSH], Cohort Studies [MeSH], 631/477, Canada [MeSH], Article, Genome-Wide Association Study/methods [MeSH], Obsessive-Compulsive Disorder/genetics [MeSH], 45/43, Phenotype [MeSH], Genetic Predisposition to Disease/genetics [MeSH], Netherlands [MeSH], article, Polymorphism, Single Nucleotide, 3. Good health, Cohort Studies, FOS: Psychology, 03 medical and health sciences, Phenotype, England, FOS: Biological sciences, Genetics, Humans, Psychology, Genetic Predisposition to Disease, Psychiatric disorders, 610 Medizin und Gesundheit, Genome-Wide Association Study, Netherlands

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Access URL: https://pubmed.ncbi.nlm.nih.gov/38548983
https://research.vu.nl/en/publications/6f545f81-6af7-4c40-9ec7-8b4eb6c5fd8d
https://doi.org/10.1038/s41380-024-02489-6
https://hdl.handle.net/1871.1/6f545f81-6af7-4c40-9ec7-8b4eb6c5fd8d
https://repository.publisso.de/resource/frl:6512438
http://edoc.hu-berlin.de/18452/32669
https://doi.org/10.18452/32050
http://www.scopus.com/inward/record.url?scp=85188885960&partnerID=8YFLogxK
https://pure.au.dk/portal/en/publications/6ed15da7-fa59-4926-9a34-6af8df8f0111
https://doi.org/10.1038/s41380-024-02489-6
https://publications.scilifelab.se/publication/905503ab005d4de1b7710f488a80b3af

Factor analysis of lifetime psychopathology and its brain morphometric and genetic correlates in a transdiagnostic sample

Authors: Krug, Axel Stein, Frederike David, Friederike S. et al.

Contributors: Krug, Axel Stein, Frederike David, Friederike S. et al.

Source: Transl Psychiatry
Translational Psychiatry, Vol 14, Iss 1, Pp 1-10 (2024)
Translational Psychiatry 14(1), 235 (2024). doi:10.1038/s41398-024-02936-6
Translational Psychiatry, 14(1):235

Subject Terms: Male, Adult, 0301 basic medicine, Multifactorial Inheritance, Bipolar Disorder, Medizin, Neurosciences. Biological psychiatry. Neuropsychiatry, Article, 03 medical and health sciences, 0302 clinical medicine, Humans, ddc:610, Gray Matter, 59/57, Bipolar Disorder/pathology [MeSH], Psychotic Disorders/genetics [MeSH], Gray Matter/pathology [MeSH], 631/378/340, Magnetic Resonance Imaging [MeSH], 631/208/2489, Male [MeSH], 45/43, Depressive Disorder, Major/diagnostic imaging [MeSH], Schizophrenia/pathology [MeSH], Female [MeSH], Brain/pathology [MeSH], Multifactorial Inheritance/genetics [MeSH], Brain/diagnostic imaging [MeSH], Psychotic Disorders/diagnostic imaging [MeSH], Adult [MeSH], Cerebral Cortex/pathology [MeSH], Humans [MeSH], Psychopathology [MeSH], Depressive Disorder, Major/genetics [MeSH], Middle Aged [MeSH], 692/699/476/1799, Factor Analysis, Statistical [MeSH], Bipolar Disorder/genetics [MeSH], Depressive Disorder, Major/pathology [MeSH], Genome-Wide Association Study [MeSH], Gray Matter/diagnostic imaging [MeSH], Schizophrenia/genetics [MeSH], Cerebral Cortex/diagnostic imaging [MeSH], Bipolar Disorder/diagnostic imaging [MeSH], Psychotic Disorders/pathology [MeSH], Schizophrenia/diagnostic imaging [MeSH], article, Cerebral Cortex, Depressive Disorder, Major, Psychopathology, Brain, Middle Aged, Medical sciences Medicine, Magnetic Resonance Imaging, ddc, 3. Good health, Psychotic Disorders, Schizophrenia, Female, Factor Analysis, Statistical, RC321-571, Genome-Wide Association Study

File Description: application/pdf

Access URL: https://pubmed.ncbi.nlm.nih.gov/38830892
https://doaj.org/article/d412174d62634d728bbe586b111c1f70
https://juser.fz-juelich.de/record/1028744
https://repository.publisso.de/resource/frl:6496502
https://mediatum.ub.tum.de/doc/1770236/document.pdf

Genetische Grundlagen der ADHS – ein Update

Authors: Sarah Hohmann Alexander Häge Sabina Millenet et al.

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

Access URL: https://repository.publisso.de/resource/frl:6475190