Suchergebnisse - "Anxiety Disorders genetics"

Heritability and polygenic load for comorbid anxiety and depression

Autoren: Fara Tabrizi Jörgen Rosén Hampus Grönvall et al.

Quelle: Transl Psychiatry
Translational Psychiatry, Vol 15, Iss 1, Pp 1-10 (2025)
Tabrizi, F, Rosén, J, Grönvall, H, William-Olsson, V R, Arner, E, Magnusson, P K, Palm, C, Larsson, H, Viktorin, A, Bernhardsson, J, Björkdahl, J, Jansson, B, Sundin, Ö, Zhou, X, Speed, D & Åhs, F 2025, 'Heritability and polygenic load for comorbid anxiety and depression', Translational Psychiatry, vol. 15, no. 1, 98, pp. 98. https://doi.org/10.1038/s41398-025-03325-3

Schlagwörter: Adult, Male, Multifactorial Inheritance, Anxiety/genetics, Twins, Monozygotic/genetics, Neurosciences. Biological psychiatry. Neuropsychiatry, Comorbidity, Anxiety, Antidepressive Agents/therapeutic use, Predictive markers, Twins, Dizygotic/genetics, Psykiatri, Article, Medical Genetics and Genomics, Depressive Disorder/genetics, Anti-Anxiety Agents/therapeutic use, Twins, Dizygotic, Humans, Diseases in Twins/genetics, Genetic Predisposition to Disease, Aged, Psychiatry, Aged, 80 and over, Depressive Disorder, Depression, Depression/genetics, Twins, Monozygotic, Polygenic Scores, Middle Aged, Anxiety Disorders, Medicinsk genetik och genomik, Antidepressive Agents, Female, Anxiety Disorders/genetics, RC321-571

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/40140358
https://doaj.org/article/4549d93b801b4fd2a13e7b115a260c56
http://urn.kb.se/resolve?urn=urn:nbn:se:miun:diva-54107

Role of inflammation in depressive and anxiety disorders, affect, and cognition:genetic and non-genetic findings in the lifelines cohort study

Autoren: Mac Giollabhui, Naoise Slaney, Chloe Hemani, Gibran et al.

Quelle: Mac Giollabhui, N, Slaney, C, Hemani, G, Foley, É M, van der Most, P J, Nolte, I M, Snieder, H, Davey Smith, G, Khandaker, G M & Hartman, C A 2025, 'Role of inflammation in depressive and anxiety disorders, affect, and cognition : genetic and non-genetic findings in the lifelines cohort study', Translational Psychiatry, vol. 15, 164. https://doi.org/10.1038/s41398-025-03372-w

Schlagwörter: Humans, Female, Male, Anxiety Disorders/genetics, Inflammation/genetics, C-Reactive Protein/metabolism, Middle Aged, Adult, Executive Function, Interleukin-6/blood, Mendelian Randomization Analysis, Netherlands, Cognition, Depressive Disorder/genetics, Receptors, Affect, Cohort Studies, Attention, Memory, Episodic, Prospective Studies, Biomarkers/blood

Dateibeschreibung: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/40348744; info:eu-repo/semantics/altIdentifier/hdl/https://hdl.handle.net/11370/c9e30010-3067-4789-9cb1-4c383cc6c70d; info:eu-repo/semantics/altIdentifier/pissn/2158-3188; info:eu-repo/semantics/altIdentifier/eissn/2158-3188

Verfügbarkeit: https://hdl.handle.net/11370/c9e30010-3067-4789-9cb1-4c383cc6c70d
https://research.rug.nl/en/publications/c9e30010-3067-4789-9cb1-4c383cc6c70d
https://doi.org/10.1038/s41398-025-03372-w
https://pure.rug.nl/ws/files/1310669236/s41398-025-03372-w.pdf

Molecular Basis of Anxiety:A Comprehensive Review of 2014-2024 Clinical and Preclinical Studies

Autoren: Merkouris, Ermis Brasinika, Alexandra Patsiavoura, Meropi et al.

Quelle: Merkouris, E, Brasinika, A, Patsiavoura, M, Siniosoglou, C, Tsiptsios, D, Triantafyllis, A S, Mueller, C, Mpikou, I, Samara, M T, Christodoulou, N & Tsamakis, K 2025, 'Molecular Basis of Anxiety : A Comprehensive Review of 2014-2024 Clinical and Preclinical Studies', International Journal of Molecular Sciences, vol. 26, no. 11, 5417. https://doi.org/10.3390/ijms26115417

Schlagwörter: Humans, Anxiety/genetics, Animals, Anxiety Disorders/genetics, Epigenesis, Genetic, Hypothalamo-Hypophyseal System/metabolism, Pituitary-Adrenal System/metabolism, gamma-Aminobutyric Acid/metabolism

Verfügbarkeit: https://kclpure.kcl.ac.uk/portal/en/publications/828c90b6-9abe-4f64-8314-f216f33cd2f1
https://doi.org/10.3390/ijms26115417
http://www.scopus.com/inward/record.url?scp=105007662853&partnerID=8YFLogxK

Can flow proneness be protective against mental and cardiovascular health problems? A genetically informed prospective cohort study: A genetically informed prospective cohort study

Autoren: Emma Gaston Fredrik Ullén Laura W. Wesseldijk et al.

Quelle: Transl Psychiatry
Translational Psychiatry, Vol 14, Iss 1, Pp 1-8 (2024)
Translational Psychiatry
Translational Psychiatry, 14(1):144

Schlagwörter: 05 social sciences, Twins, Dizygotic/genetics, Neurosciences. Biological psychiatry. Neuropsychiatry, Twins, Monozygotic, Anxiety, Anxiety Disorders, Article, 692/699/476/1333, Humans [MeSH], Prospective Studies [MeSH], 631/477/2811, 692/53/2421, Cross-Sectional Studies [MeSH], 692/699/476/1799, 692/699/476/1414, Anxiety [MeSH], Twins, Monozygotic/genetics [MeSH], Twins, Dizygotic/genetics [MeSH], Anxiety Disorders/genetics [MeSH], article, 3. Good health, 03 medical and health sciences, Cross-Sectional Studies, 0302 clinical medicine, Twins, Dizygotic, Humans, 0501 psychology and cognitive sciences, Prospective Studies, Anxiety Disorders/genetics, Monozygotic/genetics, RC321-571

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/38480692
https://doaj.org/article/954ebeb87d5649b2a67cc921d8d96e89
https://pure.amsterdamumc.nl/en/publications/27e4e2ae-f81b-4216-8b8a-636f29e08110
https://doi.org/10.1038/s41398-024-02855-6
http://hdl.handle.net/21.11116/0000-000F-1FDC-8
http://hdl.handle.net/21.11116/0000-000F-1FDA-A
https://repository.publisso.de/resource/frl:6503931

Role of Inflammation in Depressive and Anxiety Disorders, Affect, and Cognition: Genetic and Non-Genetic Findings in the Lifelines Cohort Study: Genetic and Non-Genetic Findings in the Lifelines Cohort Study

Autoren: Naoise Mac Giollabhui Chloe Slaney Gibran Hemani et al.

Quelle: medRxiv
Transl Psychiatry
Res Sq
Translational Psychiatry, Vol 15, Iss 1, Pp 1-14 (2025)

Schlagwörter: Male, Adult, Memory, Episodic, Neurosciences. Biological psychiatry. Neuropsychiatry, Article, Cohort Studies, Executive Function, Cognition, Memory, Depressive Disorder/genetics, Inflammation/genetics, Receptors, Humans, Attention, Prospective Studies, Netherlands, Inflammation, 2. Zero hunger, Depressive Disorder, Interleukin-6, C-Reactive Protein/metabolism, Middle Aged, Mendelian Randomization Analysis, Anxiety Disorders, Receptors, Interleukin-6, 3. Good health, Affect, C-Reactive Protein, Female, Interleukin-6/blood, Episodic, Anxiety Disorders/genetics, Biomarkers/blood, RC321-571

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/38699368
https://pubmed.ncbi.nlm.nih.gov/40348744
https://pubmed.ncbi.nlm.nih.gov/39149475
https://doaj.org/article/a02add68bc7b48c098786daf84a25705
https://research.rug.nl/en/publications/1cf314c0-f00c-4f34-864c-09cd54a9f855
https://hdl.handle.net/11370/1cf314c0-f00c-4f34-864c-09cd54a9f855
https://doi.org/10.1101/2024.04.17.24305950

Genetic overlap between functional impairment and depression and anxiety symptom severity: Evidence from the GLAD Study

Autoren: Megan Skelton Jessica Mundy Abigail R. ter Kuile et al.

Quelle: Skelton, M, Mundy, J, Kuile, A R T, Adey, B N, Armour, C, Buckman, J E J, Coleman, J R I, Davies, M R, Hirsch, C R, Hotopf, M, Jones, I R, Kalsi, G, Krebs, G, Lee, S H, Lin, Y, McIntosh, A M, Peel, A J, Rayner, C, Rimes, K A, Smith, D J, Thompson, K N, Veale, D, Walters, J T R, Hübel, C, Breen, G & Eley, T C 2025, 'Genetic overlap between functional impairment and depression and anxiety symptom severity: evidence from the GLAD Study', Psychological Medicine. https://doi.org/10.1017/S0033291725101037
Skelton, M, Mundy, J, ter Kuile, A, Adey, B, Armour, C, Buckman, J E J, Coleman, J, Davies, M, Hirsch, C, Hotopf, M, Jones, I R, Kalsi, G, Krebs, G, Lee, S-H, Lin, Y, M. McIntosh, A, Peel, A, Rayner, C, Rimes, K, Smith, D J, Thompson, K, Veale, D, Walters, J, Hübel, C, Breen, G & Eley, T 2025, ' Genetic overlap between functional impairment and depression and anxiety symptom severity: Evidence from the GLAD Study ', Psychological Medicine .
Skelton, M, Mundy, J, Ter Kuile, A R, Adey, B N, Armour, C, Buckman, J E J, Coleman, J R I, Davies, M R, Hirsch, C R, Hotopf, M, Jones, I R, Kalsi, G, Krebs, G, Lee, S H, Lin, Y, McIntosh, A M, Peel, A J, Rayner, C, Rimes, K A, Smith, D J, Thompson, K N, Veale, D, Walters, J T R, Hübel, C, Breen, G & Eley, T C 2025, 'Genetic overlap between functional impairment and depression and anxiety symptom severity : evidence from the GLAD Study', Psychological Medicine, vol. 55, pp. e224. https://doi.org/10.1017/S0033291725101037

Schlagwörter: Male, Adult, Anxiety/genetics, Depression/genetics, Middle Aged, Severity of Illness Index, Polymorphism, Single Nucleotide, Activities of Daily Living, Humans, Female, Genetic Predisposition to Disease, Depressive Disorder, Major/genetics, Anxiety Disorders/genetics, Genome-Wide Association Study

Dateibeschreibung: application/pdf

Zugangs-URL: https://pure.qub.ac.uk/en/publications/391f03f3-c8eb-4b1f-91ab-e093e0421855
https://kclpure.kcl.ac.uk/portal/en/publications/6aabe09e-7f0b-4f43-ad22-a9116fc33e2f

Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders

Autoren: Eijsbouts, Chris Zheng, Tenghao Kennedy, Nicholas A. et al.

Weitere Verfasser: Eijsbouts, Chris Zheng, Tenghao Kennedy, Nicholas A. et al.

Quelle: Nat Genet
23andMe Research Team 2021, 'Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders', Nature Genetics, vol. 53, no. 11, pp. 1543-1552. https://doi.org/10.1038/s41588-021-00950-8
Nature Genetics, vol 53, iss 11

Schlagwörter: Male, 0301 basic medicine, Molecular Chaperones/genetics, 692/699/1503/1502/2071, Medical and Health Sciences, Oral and gastrointestinal, Irritable Bowel Syndrome, Bellygenes Initiative, 2.1 Biological and endogenous factors, Aged, Anxiety Disorders, CD56 Antigen, Cell Adhesion Molecules, Cytoskeletal Proteins, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Guanine Nucleotide Exchange Factors, Homeodomain Proteins, Humans, Middle Aged, Molecular Chaperones, Mood Disorders, Polymorphism, Single Nucleotide, United Kingdom, Aetiology, 692/699/476, 0303 health sciences, United Kingdom/epidemiology, Pain Research, Mood Disorders/genetics, article, Single Nucleotide, Biological Sciences, 3. Good health, Mental Health, Neurological, Mental health, Irritable Bowel Syndrome/epidemiology, Chronic Pain, Cell Adhesion Molecules/genetics, Guanine Nucleotide Exchange Factors/genetics, 631/208/205/2138, Cytoskeletal Proteins/genetics, 23andMe Research Team, Article, 38/43, 03 medical and health sciences, Behavioral and Social Science, Genetics, Polymorphism, Human Genome, Neurosciences, CD56 Antigen/genetics, Brain Disorders, Homeodomain Proteins/genetics, Digestive Diseases, Anxiety Disorders/genetics, Developmental Biology

Dateibeschreibung: application/pdf; application/zip; text/xml

Zugangs-URL: https://www.nature.com/articles/s41588-021-00950-8.pdf
https://pubmed.ncbi.nlm.nih.gov/34741163
https://research.manchester.ac.uk/en/publications/3dd6a1aa-4bf8-4587-8b27-76e526cab9a7
https://doi.org/10.1038/s41588-021-00950-8
https://hdl.handle.net/11588/902307
https://research.rug.nl/en/publications/c5f9c3c9-4872-44a9-bf39-1a826ffbb3f0
https://hdl.handle.net/11370/c5f9c3c9-4872-44a9-bf39-1a826ffbb3f0
https://doi.org/10.1038/s41588-021-00950-8
https://cris.maastrichtuniversity.nl/en/publications/f12f3adc-8833-4857-a924-5111261abb5f
https://doi.org/10.1038/s41588-021-00950-8
https://www.bdi.ox.ac.uk/publications/1198470
https://www.ndm.ox.ac.uk/publications/1198470
https://pubmed.ncbi.nlm.nih.gov/34741163/
https://europepmc.org/article/PMC/PMC8571093
https://www.repository.cam.ac.uk/handle/1810/330402
https://www.nature.com/articles/s41588-021-00950-8.pdf
https://www.nature.com/articles/s41588-021-00950-8
https://hdl.handle.net/11564/763316
https://doi.org/10.1038/s41588-021-00950-8
https://ora.ox.ac.uk/objects/uuid:0a831c34-5c9d-40b6-afa2-640f7587638d
https://doi.org/10.1038/s41588-021-00950-8
https://www.nature.com/articles/s41588-021-00950-8
https://hdl.handle.net/11568/1117653
https://doi.org/10.1038/s41588-021-00950-8
https://hdl.handle.net/11588/902307
https://doi.org/10.1038/s41588-021-00950-8
https://www.nature.com/articles/s41588-021-00950-8
https://hdl.handle.net/11585/856276
https://doi.org/10.1038/s41588-021-00950-8
https://www.repository.cam.ac.uk/handle/1810/330840
https://doi.org/10.17863/cam.78283
https://doi.org/10.1038/s41588-021-00950-8
https://www.repository.cam.ac.uk/handle/1810/330402
https://doi.org/10.17863/cam.77845
https://doi.org/10.1038/s41588-021-00950-8
https://escholarship.org/uc/item/59j5q88x
https://escholarship.org/content/qt59j5q88x/qt59j5q88x.pdf

Genetic correlates of socio-economic status influence the pattern of shared heritability across mental health traits

Autoren: Abdel Abdellaoui Wim van den Brink Eske M. Derks et al.

Quelle: Nat Hum Behav

Schlagwörter: 0301 basic medicine, Obsessive-Compulsive Disorder, Schizophrenia/genetics, Anorexia Nervosa, Bipolar Disorder, Alcohol Drinking, Autism Spectrum Disorder, Smoking/genetics, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Genetic, SDG 3 - Good Health and Well-being, Models, Anorexia Nervosa/genetics, Humans, Genetic Predisposition to Disease, Polymorphism, Substance-Related Disorders/genetics, Obsessive-Compulsive Disorder/genetics, Mental Disorders/genetics, Depressive Disorder, Depressive Disorder, Major, 0303 health sciences, Models, Genetic, Bipolar Disorder/genetics, Mental Disorders, Genetic Variation, Major/genetics, Single Nucleotide, Alcohol Drinking/genetics, Anxiety Disorders, 3. Good health, Autism Spectrum Disorder/genetics, Mental Health, Social Class, Attention Deficit Disorder with Hyperactivity, Latent Class Analysis, Tourette Syndrome/genetics, Income, Schizophrenia, Educational Status, Smoking Cessation, Attention Deficit Disorder with Hyperactivity/genetics, Anxiety Disorders/genetics, Genome-Wide Association Study

Zugangs-URL: https://www.medrxiv.org/content/medrxiv/early/2020/02/27/2020.02.26.20028092.full.pdf
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376746
https://pubmed.ncbi.nlm.nih.gov/33686200
https://pure.eur.nl/en/publications/6d2d29bf-258d-4eb3-aa43-bf1b80bdcd9e
https://doi.org/10.1038/s41562-021-01053-4
https://research.vu.nl/en/publications/d74cd188-9df7-4ff0-9539-d05644d474fd
https://doi.org/10.1038/s41562-021-01053-4
https://hdl.handle.net/1871.1/d74cd188-9df7-4ff0-9539-d05644d474fd
https://www.medrxiv.org/content/10.1101/2020.02.26.20028092v1
https://www.medrxiv.org/content/medrxiv/early/2020/02/27/2020.02.26.20028092.full.pdf
https://www.nature.com/articles/s41562-021-01053-4
https://pubmed.ncbi.nlm.nih.gov/33686200/
https://www.nature.com/articles/s41562-021-01053-4.pdf
https://www.narcis.nl/publication/RecordID/oai%3Aresearch.vu.nl%3Apublications%2Fd74cd188-9df7-4ff0-9539-d05644d474fd
http://www.ncbi.nlm.nih.gov/pubmed/33686200
https://europepmc.org/article/PPR/PPR114798
https://pure.amsterdamumc.nl/en/publications/5811324b-96ff-49cd-9430-4b8b733177e4
https://doi.org/10.1038/s41562-021-01053-4

Gene discovery and biological insights into anxiety disorders from a large-scale multi-ancestry genome-wide association study.

Autoren: Friligkou, E. Løkhammer, S. Cabrera-Mendoza, B. et al.

Schlagwörter: Genome-Wide Association Study, Humans, Anxiety Disorders/genetics, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Multifactorial Inheritance/genetics, Male, Bipolar Disorder/genetics, Transcriptome, Female, Schizophrenia/genetics, White People/genetics

Relation: Nature Genetics; https://iris.unil.ch/handle/iris/251300; serval:BIB_EDBAC44C578C; 001315666000004

Verfügbarkeit: https://iris.unil.ch/handle/iris/251300
https://doi.org/10.1038/s41588-024-01908-2

Genetic correlates of socio-economic status influence the pattern of shared heritability across mental health traits

Autoren: Marees, Andries T Smit, Dirk J A Abdellaoui, Abdel et al.

Quelle: Marees , A T , Smit , D J A , Abdellaoui , A , Nivard , M G , van den Brink , W , Denys , D , Galama , T J , Verweij , K J H & Derks , E M 2021 , ' Genetic correlates of socio-economic status influence the pattern of shared heritability across mental health traits ' , Nature Human Behaviour , vol. 5 , no. 8 , pp. 1065-1073 . https://doi.org/10.1038/s41562-021-01053-4

Schlagwörter: Alcohol Drinking/genetics, Anorexia Nervosa/genetics, Anxiety Disorders/genetics, Attention Deficit Disorder with Hyperactivity/genetics, Autism Spectrum Disorder/genetics, Bipolar Disorder/genetics, Depressive Disorder, Major/genetics, Educational Status, Genetic Predisposition to Disease, Genetic Variation, Genome-Wide Association Study, Humans, Income, Latent Class Analysis, Mental Disorders/genetics, Mental Health, Models, Genetic, Obsessive-Compulsive Disorder/genetics, Polymorphism, Single Nucleotide, Schizophrenia/genetics, Smoking/genetics, Smoking Cessation, Social Class, Substance-Related Disorders/genetics, Tourette Syndrome/genetics

Dateibeschreibung: application/pdf

Verfügbarkeit: https://research.vu.nl/en/publications/d74cd188-9df7-4ff0-9539-d05644d474fd
https://doi.org/10.1038/s41562-021-01053-4
https://hdl.handle.net/1871.1/d74cd188-9df7-4ff0-9539-d05644d474fd
https://research.vu.nl/ws/files/152996088/Genetic_correlates_of_socioeconomic_status_influence_the_pattern_of_shared_heritability_across_mental_health_traits.pdf

Serotonin synthesis rate and the tryptophan hydroxylase-2: G-703T polymorphism in social anxiety disorder: G-703T polymorphism in social anxiety disorder

Autoren: Ina Marteinsdottir Tomas Furmark Gunnar Antoni et al.

Quelle: Furmark, T, Marteinsdottir, I, Frick, A, Heurling, K, Tillfors, M, Appel, L, Antoni, G, Hartvig, P, Fischer, H, Roland Långström, B, Eriksson, E & Fredrikson, M 2016, ' Serotonin synthesis rate and the tryptophan hydroxylase-2 : G-703T polymorphism in social anxiety disorder ', Journal of Psychopharmacology, vol. 30, no. 10, pp. 1028-1035 . https://doi.org/10.1177/0269881116648317

Schlagwörter: Adult, Male, Serotonin, positron emission tomography, Serotonin synthesis, Genotype, Phobia, brain, Hippocampus/metabolism, Tryptophan Hydroxylase, Gyrus Cinguli, Hippocampus, Serotonin/metabolism, Basal Ganglia, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Journal Article, Serotonin synthesis [C-11]5-HTP brain anxiety gene positron emission tomography human tryptophan-hydroxylase-2 gene predicts amygdala reactivity positron-emission-tomography human brain in-vivo transporter phobia system stress pet Neurosciences & Neurology Pharmacology & Pharmacy Psychiatry, Humans, Polymorphism, gene, Polymorphism, Genetic/genetics, 10. No inequality, Alleles, Genetic/genetics, Polymorphism, Genetic, [ C]5-HTP, Gyrus Cinguli/metabolism, Phobia, Social, anxiety, Amygdala, Anxiety Disorders, 3. Good health, Social/genetics, Phobia, Social/genetics, Basal Ganglia/metabolism, Female, Tryptophan Hydroxylase/genetics, Amygdala/metabolism, Anxiety Disorders/genetics

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/27189957
http://journals.sagepub.com/doi/abs/10.1177/0269881116648317
https://journals.sagepub.com/doi/10.1177/0269881116648317
https://core.ac.uk/display/80329816
https://portal.findresearcher.sdu.dk/da/publications/serotonin-synthesis-rate-and-the-tryptophan-hydroxylase-2-g-703t-
http://journals.sagepub.com/doi/10.1177/0269881116648317
http://findresearcher.sdu.dk/portal/da/publications/serotonin-synthesis-rate-and-the-tryptophan-hydroxylase2(3249f605-94ce-4e5b-8a57-89e7d559c7d1).html
https://portal.findresearcher.sdu.dk/da/publications/3249f605-94ce-4e5b-8a57-89e7d559c7d1
https://portal.findresearcher.sdu.dk/da/publications/3249f605-94ce-4e5b-8a57-89e7d559c7d1
https://doi.org/10.1177/0269881116648317

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Autoren: Alana Cavadino Frits R. Rosendaal Joseph K. Pickrell et al.

Weitere Verfasser: Alana Cavadino Frits R. Rosendaal Joseph K. Pickrell et al.

Quelle: Nat Genet
Nature genetics, vol. 48, no. 6, pp. 624-633
Okbay, A, Baselmans, B M L, De Neve, J-E, Turley, P, Nivard, M G, Fontana, M A, Meddens, S F W, Linnér, R K, Rietveld, C A, Derringer, J, Gratten, J, Lee, J J, Liu, J Z, de Vlaming, R, Ahluwalia, T S, Buchwald, J, Cavadino, A, Frazier-Wood, A C, Furlotte, N A, Garfield, V, Geisel, M H, Gonzalez, J R, Haitjema, S, Karlsson, R, van der Laan, S W, Ladwig, K-H, Lahti, J, van der Lee, S J, Lind, P A, Liu, T, Matteson, L, Mihailov, E, Miller, M B, Minica, C C, Nolte, I M, Mook-Kanamori, D, van der Most, P J, Oldmeadow, C, Qian, Y, Raitakari, O, Rawal, R, Stergiakouli, E, Davis, O S P, Fatemifar, G, Paternoster, L, Haworth, C M A, Sorensen, T, Timpson, N J, Smith, G D, Medland, S E 2016, 'Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses', Nature Genetics, vol. 48, no. 6, pp. 624-633. https://doi.org/10.1038/ng.3552
Okbay, A, Baselmans, B M L, De Neve, J, Turley, P, Nivard, M G, Fontana, M A, Meddens, S F W, Linnér, R K, Rietveld, C A, Derringer, J, Gratten, J, Lees, J, Liu, J Z, De Vlaming, R, Ahluwalia, T S, Buchwald, J, Cavadino, A, Frazier-wood, A C, Furlotte, N A, Garfield, V, Geisel, M H, Gonzalez, J R, Haitjema, S, Karlsson, R, Van Der Laan, S W, Ladwig, K, Lahti, J, Van Der Lee, S J, Lind, P A, Liu, T, Matteson, L, Mihailov, E, Miller, M B, Minica, C C, Nolte, I M, Mook-kanamori, D, Van Der Most, P J, Oldmeadow, C, Qian, Y, Raitakari, O, Rawal, R, Realo, A, Rueedi, R, Schmidt, B, Smith, A V, Stergiakouli, E, Tanaka, T, Taylor, K, Wedenoja, J, Wellmann, J, Westra, H, Willems, S M, Zhao, W, Amin, N, Bakshi, A, Boyle, P A, Cherney, S, Cox, S R, Davies, G, Davis, O S P, Ding, J, Direk, N, Eibich, P, Emeny, R T, Fatemifar, G, Faul, J D, Ferrucci, L, Forstner, A, Gieger, C, Gupta, R, Harris, T B, Harris, J M, Holliday, E G, Hottenga, J, De Jager, P L, Kaakinen, M A, Kajantie, E, Karhunen, V, Kolcic, I, Kumari, M, Launer, L J, Franke, L, Li-gao, R, Koini, M, Loukola, A, Marques-vidal, P, Montgomery, G W, Mosing, M A, Paternoster, L, Pattie, A, Petrovic, K E, Pulkki-råback, L, Quaye, L, Räikkönen, K, Rudan, I, Scott, R J, Smith, J A, Sutin, A R, Trzaskowski, M, Vinkhuyzen, A E, Yu, L, Zabaneh, D, Attia, J R, Bennett, D A, Berger, K, Bertram, L, Boomsma, D I, Snieder, H, Chang, S, Cucca, F, Deary, I J, Van Duijn, C M, Eriksson, J G, Bültmann, U, De Geus, E J C, Groenen, P J F, Gudnason, V, Hansen, T, Hartman, C A, Haworth, C M A, Hayward, C, Heath, A C, Hinds, D A, Hyppönen, E, Iacono, W G, Järvelin, M, Jöckel, K, Kaprio, J, Kardia, S L R, Keltikangas-järvinen, L, Kraft, P, Kubzansky, L D, Lehtimäki, T, Magnusson, P K E, Martin, N G, Mcgue, M, Metspalu, A, Mills, M, De Mutsert, R, Oldehinkel, A J, Pasterkamp, G, Pedersen, N L, Plomin, R, Polasek, O, Power, C, Rich, S S, Rosendaal, F R, Den Ruijter, H M, Schlessinger, D, Schmidt, H, Svento, R, Schmidt, R, Alizadeh, B Z, Sørensen, T I A, Spector, T D, Steptoe, A, Terracciano, A, Thurik, A R, Timpson, N J, Tiemeier, H, Uitterlinden, A G, Vollenweider, P, Wagner, G G, Weir, D R, Yang, J, Conley, D C, Smith, G D, Hofman, A, Johannesson, M, Laibson, D I, Medland, S E, Meyer, M N, Pickrell, J K, Esko, T, Krueger, R F, Beauchamp, J P, Koellinger, P D, Benjamin, D J, Bartels, M & Cesarini, D 2016, ' Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses ', Nature Genetics . https://doi.org/10.1038/ng.3552
Okbay, A, Baselmans, B M L, De Neve, J, Turley, P, Nivard, M G, Fontana, M A, Meddens, S F W, Linnér, R K, Rietveld, C A, Derringer, J, Gratten, J, Lees, J, Liu, J Z, De Vlaming, R, Ahluwalia, T S, Buchwald, J, Cavadino, A, Frazier-wood, A C, Furlotte, N A, Garfield, V, Geisel, M H, Gonzalez, J R, Haitjema, S, Karlsson, R, Van Der Laan, S W, Ladwig, K, Lahti, J, Van Der Lee, S J, Lind, P A, Liu, T, Matteson, L, Mihailov, E, Miller, M B, Minica, C C, Nolte, I M, Mook-kanamori, D, Van Der Most, P J, Oldmeadow, C, Qian, Y, Raitakari, O, Rawal, R, Realo, A, Rueedi, R, Schmidt, B, Smith, A V, Stergiakouli, E, Tanaka, T, Taylor, K, Wedenoja, J, Wellmann, J, Westra, H, Willems, S M, Zhao, W, Amin, N, Bakshi, A, Boyle, P A, Cherney, S, Cox, S R, Davies, G, Davis, O S P, Ding, J, Direk, N, Eibich, P, Emeny, R T, Fatemifar, G, Faul, J D, Ferrucci, L, Forstner, A, Gieger, C, Gupta, R, Harris, T B, Harris, J M, Holliday, E G, Hottenga, J, De Jager, P L, Kaakinen, M A, Kajantie, E, Karhunen, V, Kolcic, I, Kumari, M, Launer, L J, Franke, L, Li-gao, R, Koini, M, Loukola, A, Marques-vidal, P, Montgomery, G W, Mosing, M A, Paternoster, L, Pattie, A, Petrovic, K E, Pulkki-råback, L, Quaye, L, Räikkönen, K, Rudan, I, Scott, R J, Smith, J A, Sutin, A R, Trzaskowski, M, Vinkhuyzen, A E, Yu, L, Zabaneh, D, Attia, J R, Bennett, D A, Berger, K, Bertram, L, Boomsma, D I, Snieder, H, Chang, S, Cucca, F, Deary, I J, Van Duijn, C M, Eriksson, J G, Bültmann, U, De Geus, E J C, Groenen, P J F, Gudnason, V, Hansen, T, Hartman, C A, Haworth, C M A, Hayward, C, Heath, A C, Hinds, D A, Hyppönen, E, Iacono, W G, Järvelin, M, Jöckel, K, Kaprio, J, Kardia, S L R, Keltikangas-järvinen, L, Kraft, P, Kubzansky, L D, Lehtimäki, T, Magnusson, P K E, Martin, N G, Mcgue, M, Metspalu, A, Mills, M, De Mutsert, R, Oldehinkel, A J, Pasterkamp, G, Pedersen, N L, Plomin, R, Polasek, O, Power, C, Rich, S S, Rosendaal, F R, Den Ruijter, H M, Schlessinger, D, Schmidt, H, Svento, R, Schmidt, R, Alizadeh, B Z, Sørensen, T I A, Spector, T D, Steptoe, A, Terracciano, A, Thurik, A R, Timpson, N J, Tiemeier, H, Uitterlinden, A G, Vollenweider, P, Wagner, G G, Weir, D R, Yang, J, Conley, D C, Smith, G D, Hofman, A, Johannesson, M, Laibson, D I, Medland, S E, Meyer, M N, Pickrell, J K, Esko, T, Krueger, R F, Beauchamp, J P, Koellinger, P D, Benjamin, D J, Bartels, M & Cesarini, D 2016, 'Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses', Nature Genetics. https://doi.org/10.1038/ng.3552
Nature Genetics, vol 48, iss 6
Nature Genetics

Schlagwörter: Netherlands Twin Register (NTR), Medizin, Medical and Health Sciences, Genome-wide association studies, DISEASE, depressive symptoms, well-being, GWAS, neuroticism, Anxiety Disorders/genetics, Bayes Theorem, Depression/genetics, Genome-Wide Association Study, Humans, Phenotype, Polymorphism, Single Nucleotide, Genetics & Heredity, RISK, PERSONALITY, HERITABILITY, Depression, COMMON VARIANTS, Single Nucleotide, 11 Medical And Health Sciences, Biological Sciences, Mental Illness, Bioinformatics and computational biology, Anxiety Disorders, 3. Good health, Mental Health, depression, Behavioural genetics, epidemiology, Life Sciences & Biomedicine, EMC NIHES-01-64-01, Agricultural biotechnology, QH426 Genetics, personality, genetic, ta3111, EMC NIHES-04-55-01, Article, 1311 Genetics, SDG 3 - Good Health and Well-being, RESOURCE, Journal Article, Genetics, EUR ESE 31, Polymorphism, behavioural genetics, METAANALYSIS, HAPPINESS, Neuroticism, EMC ONWAR-01-58-02, Science & Technology, Human Genome, MAJOR DEPRESSION, 06 Biological Sciences, Brain Disorders, genome-wide association studies, EMC MM-01-39-09-A, HUMAN HEIGHT, genome-wide analysis, LifeLines Cohort Study, Developmental Biology

Dateibeschreibung: application/pdf; text

Zugangs-URL: https://europepmc.org/articles/pmc4884152?pdf=render
https://pubmed.ncbi.nlm.nih.gov/27089181
https://hdl.handle.net/11370/9a0a221a-d502-4093-92c6-ce7096f6130e
https://doi.org/10.1038/ng.3552
https://research.rug.nl/en/publications/9a0a221a-d502-4093-92c6-ce7096f6130e
https://www.rug.nl/research/portal/publications/genetic-variants-associated-with-subjective-wellbeing-depressive-symptoms-and-neuroticism-identified-through-genomewide-analyses(9a0a221a-d502-4093-92c6-ce7096f6130e).html
https://research.vu.nl/en/publications/genetic-variants-associated-with-subjective-well-being-depressive
https://experts.umn.edu/en/publications/genetic-variants-associated-with-subjective-well-being-depressive
https://ifs.org.uk/publications/13371
https://europepmc.org/articles/PMC4884152
https://escholarship.org/content/qt3m65775d/qt3m65775d.pdf?t=qhcuv3
https://hdl.handle.net/1887/113142
https://pure.amsterdamumc.nl/en/publications/58fcc10b-66cc-4965-b3d1-168cf3c37d64
https://doi.org/10.1038/ng.3552
http://hdl.handle.net/10044/1/45805
https://hdl.handle.net/11541.2/118776
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https://doi.org/10.1038/ng.3552
https://hdl.handle.net/11388/178377
https://serval.unil.ch/resource/serval:BIB_749211F19289.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_749211F192891
https://serval.unil.ch/notice/serval:BIB_749211F19289
https://avesis.deu.edu.tr/publication/details/5ef75e82-9d00-4caf-adaa-b75a95c29dc3/oai
https://research-information.bris.ac.uk/ws/files/77942650/Genetic_Associations_with_Subjective_Well_Being.pdf
https://hdl.handle.net/1983/d0c789cd-41f1-4eee-a18b-9bc31d106b90
https://kclpure.kcl.ac.uk/ws/files/51187425/Okbay_et_al_Nature_Genet_2016_pre_print.pdf
https://escholarship.org/uc/item/3m65775d
https://escholarship.org/content/qt3m65775d/qt3m65775d.pdf
https://publications.scilifelab.se/publication/b81caa63626b43ad8892ec30746fb70a

Preliminary study of anxiety symptoms, family dysfunction, and the brain-derived neurotrophic factor (BDNF) Val66Met genotype in offspring of parents with bipolar disorder

Autoren: Joachim Hallmayer Eunjoo Kim Seung Chul Hong et al.

Weitere Verfasser: Joachim Hallmayer Eunjoo Kim Seung Chul Hong et al.

Quelle: Journal of Psychiatric Research. 61:81-88

Schlagwörter: Risk, Adult, Male, Parents, Bipolar Disorder, Adolescent, Pediatric bipolar, Anxiety, Polymorphism, Single Nucleotide, Brain-derived neurotrophic factor, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Child of Impaired Parents, Risk Factors, Humans, Family, Genetic Predisposition to Disease, Anxiety Disorders/genetics, Polymorphism, Gene–environment interaction, Child, 10. No inequality, Brain-Derived Neurotrophic Factor/genetics, Bipolar Disorder/genetics, Brain-Derived Neurotrophic Factor, Single Nucleotide, Anxiety Disorders, Child of Impaired Parents/psychology, Female, Family/psychology, Parents/psychology

Dateibeschreibung: 81~88

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/25498133
https://ir.ymlib.yonsei.ac.kr/handle/22282913/139524
http://www.sciencedirect.com/science/article/pii/S0022395614003367
https://europepmc.org/article/MED/25498133
https://www.sciencedirect.com/science/article/abs/pii/S0022395614003367

Genetic variation in CADM2 as a link between psychological traits and obesity

Autoren: Fabrizio Veglia Julia Morris Bruna Gigante et al.

Weitere Verfasser: Fabrizio Veglia Julia Morris Bruna Gigante et al.

Quelle: Sci Rep
Morris, J, Bailey, M E S, Baldassarre, D, Cullen, B, de Faire, U, Ferguson, A, Gigante, B, Giral, P, Goel, A, Graham, N, Hamsten, A, Humphries, S E, Johnston, K J A, Lyall, D M, Lyall, L M, Sennblad, B, Silveira, A, Smit, A J, Tremoli, E, Veglia, F, Ward, J, Watkins, H, Smith, D J & Strawbridge, R J 2019, ' Genetic variation in CADM2 as a link between psychological traits and obesity ', Scientific Reports, vol. 9, no. 1, pp. 7339 . https://doi.org/10.1038/s41598-019-43861-9

Schlagwörter: EXPRESSION, Male, 0301 basic medicine, Bipolar Disorder, Quantitative Trait Loci, Obesity/genetics, LOCI, [SDV.GEN] Life Sciences [q-bio]/Genetics, Polymorphism, Single Nucleotide, Article, Medical Genetics and Genomics, 03 medical and health sciences, Risk-Taking, Genetics research, Humans, Genetic Predisposition to Disease, Obesity, GENOME-WIDE ASSOCIATION, COMMON, METAANALYSIS, Medicinsk genetik, Aged, RISK, Neuroticism, 2. Zero hunger, Depressive Disorder, Major, 0303 health sciences, Bipolar Disorder/genetics, ENERGY HOMEOSTASIS, Endocrine system and metabolic diseases, Genetic Variation, Middle Aged, Anxiety Disorders, Medicinsk genetik och genomik, [SDV.MHEP.CSC] Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular system, 3. Good health, [SDV] Life Sciences [q-bio], BODY-MASS INDEX, INSIGHTS, Affect, Cardiovascular diseases, VISUALIZATION, Female, Psychiatric disorders, Cell Adhesion Molecules/genetics, Depressive Disorder, Major/genetics, Medical Genetics, Anxiety Disorders/genetics, Cell Adhesion Molecules

Dateibeschreibung: application/pdf

Zugangs-URL: https://www.nature.com/articles/s41598-019-43861-9.pdf
https://pubmed.ncbi.nlm.nih.gov/31089183
https://eprints.gla.ac.uk/185776/11/185776.pdf
https://research.rug.nl/en/publications/099147fe-bd68-4784-9bf7-a8ee79f51eef
https://hdl.handle.net/11370/099147fe-bd68-4784-9bf7-a8ee79f51eef
https://doi.org/10.1038/s41598-019-43861-9
https://research.rug.nl/en/publications/genetic-variation-in-cadm2-as-a-link-between-psychological-traits
https://www.rdm.ox.ac.uk/publications/998914
http://eprints.gla.ac.uk/185776/
https://air.unimi.it/handle/2434/644417
https://www.well.ox.ac.uk/publications/998914
http://ui.adsabs.harvard.edu/abs/2019NatSR...9.7339M/abstract
https://hdl.handle.net/2434/644417
https://doi.org/10.1038/s41598-019-43861-9
https://www.pure.ed.ac.uk/ws/files/218233548/s41598_019_43861_9.pdf
https://hdl.handle.net/20.500.11820/ceabc318-e424-45bf-afb5-13787549ac75
https://hal.sorbonne-universite.fr/hal-02149513v1
https://hal.sorbonne-universite.fr/hal-02149513v1/document
https://doi.org/10.1038/s41598-019-43861-9
https://discovery-pp.ucl.ac.uk/id/eprint/10075814/
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-387288
https://publications.scilifelab.se/publication/5c89b2604ecd4e0eb9cbc8a13f7b3b5a

A genome-wide linkage study of individuals with high scores on NEO personality traits

Autoren: Aaron Isaacs Elena S. Gusareva Irina V. Zorkoltseva et al.

Weitere Verfasser: Aaron Isaacs Elena S. Gusareva Irina V. Zorkoltseva et al.

Quelle: Amin, N, Schuur, M, Gusareva, E S, Isaacs, A, Aulchenko, Y S, Kirichenko, A V, Zorkoltseva, I V, Axenovich, T I, Oostra, B A, Janssens, A C J W & Van Duijn, C M 2012, 'A genome-wide linkage study of individuals with high scores on NEO personality traits', Molecular Psychiatry, vol. 17, no. 10, pp. 1031-1041. https://doi.org/10.1038/mp.2011.97

Schlagwörter: Male, 0301 basic medicine, haplotype, family, Personality Inventory, Genetic Linkage, [SDV.MHEP.PSM] Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health, Consciousness/physiology, Cohort Studies, Extraversion, Psychological, Chromosomes, Human, Human health sciences, Child, EMC MGC-02-96-01, Emotional Intelligence, Netherlands, Psychiatry, Genetic Linkage/genetics, 0303 health sciences, Human/genetics, pedigree, Middle Aged, Anxiety Disorders, Aggression, Phenotype, Genome-Wide Association Study/methods, Female, linkage, EMC NIHES-01-64-03, Adult, EMC NIHES-01-64-02, Adolescent, Consciousness, DNA Copy Number Variations, Genotype, CNV, Aggression/physiology, DNA Copy Number Variations/genetics, Sciences de la santé humaine, Chromosomes, Young Adult, 03 medical and health sciences, Personality/genetics, Humans, Extraversion, Neuroticism, Family Health, NEO, Psychological, Anxiety Disorders/genetics, Psychiatrie, Genome-Wide Association Study

Dateibeschreibung: application/pdf

Zugangs-URL: https://www.nature.com/articles/mp201197.pdf
https://pubmed.ncbi.nlm.nih.gov/21826060
https://hal.science/hal-00668053v1
https://doi.org/10.1038/mp.2011.97
https://hal.science/hal-00668053v1/document
https://cris.maastrichtuniversity.nl/en/publications/d67d897f-7509-45a0-9328-f741c01325cb
https://doi.org/10.1038/mp.2011.97
https://www.ncbi.nlm.nih.gov/pubmed/21826060
https://hal.archives-ouvertes.fr/hal-00668053
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https://pubmed.ncbi.nlm.nih.gov/21826060/
https://www.nature.com/articles/mp201197
https://repub.eur.nl/pub/31208
https://research.vumc.nl/en/publications/cae2dd9d-9da7-43ea-88b3-ed42086185d5
https://pure.amsterdamumc.nl/en/publications/3466cfab-c3bf-4a4d-ab23-85b8bbbc5548
https://doi.org/10.1038/mp.2011.97
https://hdl.handle.net/2268/108429
https://doi.org/10.1038/mp.2011.97

Expanding the range of ZNF804A variants conferring risk of psychosis

Autoren: Markus M. Nöthen Anders D. Børglum Robin M. Murray et al.

Weitere Verfasser: Markus M. Nöthen Anders D. Børglum Robin M. Murray et al.

Quelle: Molecular Psychiatry; Vol 16
Molecular Psychiatry
Molecular Psychiatry, 16, 1, pp. 59-66
Molecular psychiatry 16, 59-66 (2011). doi:10.1038/mp.2009.149
Steinberg, S, Mors, O, Børglum, A D, Gustafsson, O, Werge, T, Mortensen, P B, Andreassen, O A, Sigurdsson, E, Thorgeirsson, T E, Böttcher, Y, Olason, P, Ophoff, R A, Cichon, S, Gudjonsdottir, I H, Pietiläinen, O P H, Nyegaard, M, Tuulio-Henriksson, A, Ingason, A, Hansen, T, Athanasiu, L, Suvisaari, J, Lonnqvist, J, Paunio, T, Hartmann, A, Jürgens, G, Nordentoft, M, Hougaard, D, Norgaard-Pedersen, B, Breuer, R, Möller, H-J, Giegling, I, Glenthøj, A B, Rasmussen, H B, Mattheisen, M, Bitter, I, Réthelyi, J M, Sigmundsson, T, Fossdal, R, Thorsteinsdottir, U, Ruggeri, M, Tosato, S, Strengman, E, Kiemeney, L A, Melle, I, Djurovic, S, Abramova, L, Kaleda, V, Walshe, M, Bramon, E, Vassos, E & Genetic Risk and Outcome in Psychosis 2011, 'Expanding the range of ZNF804A variants conferring risk of psychosis', Molecular Psychiatry, vol. 16, no. 1, pp. 59-66. https://doi.org/10.1038/mp.2009.149

Schlagwörter: 0301 basic medicine, NCEBP 1: Molecular epidemiology ONCOL 5: Aetiology, screening and detection, Bipolar Disorder, DNA Copy Number Variations, Kruppel-Like Transcription Factors: genetics, CNV, Kruppel-Like Transcription Factors, Bipolar Disorder: genetics, 03 medical and health sciences, Schizophrenia: genetics, Reference Values, Humans, DNA Copy Number Variations: genetics, Genetic Predisposition to Disease, bipolar disorder, 0303 health sciences, Anxiety Disorders: genetics, association, Anxiety Disorders, 3. Good health, schizophrenia, ZNF804A, Case-Control Studies, ZNF804A protein, human, Schizophrenia, Genome-Wide Association Study

Zugangs-URL: https://www.nature.com/articles/mp2009149.pdf
https://pubmed.ncbi.nlm.nih.gov/20048749
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/95884
https://doi.org/10.1038/mp.2009.149
https://hdl.handle.net/1871/35777
https://research.vu.nl/en/publications/667b94c4-0140-4216-b253-1d19f9489659
https://doi.org/10.1038/mp.2009.149
https://cris.maastrichtuniversity.nl/en/publications/bb482459-c9c5-48c6-bcef-81807632345b
https://doi.org/10.1038/mp.2009.149
https://iris.univr.it/handle/11562/339999
http://ncpz.ru/siteconst/userfiles/ZNF804A.pdf
https://www.julkari.fi/handle/10024/105949
https://abdn.pure.elsevier.com/en/publications/expanding-the-range-of-znf804a-variants-conferring-risk-of-psycho
https://www.nature.com/articles/mp2009149.pdf
http://hub.hku.hk/handle/10722/141826
https://repository.ubn.ru.nl//bitstream/handle/2066/95884/95884.pdf
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http://hdl.handle.net/10722/141826
https://pure.au.dk/portal/en/publications/c0b388f9-9f83-42c4-ace6-fc1471cc05e4
https://doi.org/10.1038/mp.2009.149

The association of 5-HTTLPR and DRD4 VNTR polymorphisms with affective temperamental traits in healthy volunteers

Autoren: Kee Namkoong Jee In Kang Se Joo Kim et al.

Weitere Verfasser: Kee Namkoong Jee In Kang Se Joo Kim et al.

Quelle: Journal of Affective Disorders. 109:157-163

Schlagwörter: Adult, Male, Genotype, Asian Continental Ancestry Group/genetics, Depressive Disorder/diagnosis, Dopamine, Health Status, Minisatellite Repeats, 5-HTTLPR, Severity of Illness Index, Anxiety Disorders/epidemiology, Minisatellite Repeats/genetics, 03 medical and health sciences, 0302 clinical medicine, Asian People, Surveys and Questionnaires, Receptors, Dopamine D4/genetics, Humans, 0501 psychology and cognitive sciences, Anxiety Disorders/genetics, Serotonin Plasma Membrane Transport Proteins/genetics, Polymorphism, Temperament, Dysthymic Disorder/diagnosis, Serotonin Plasma Membrane Transport Proteins, Depressive Disorder, Polymorphism, Genetic, Affective temperament, Receptors, Dopamine D4, 05 social sciences, Dysthymic Disorder/epidemiology, Depressive Disorder/epidemiology, Depressive Disorder/genetics, Anxiety Disorders, Association study, Diagnostic and Statistical Manual of Mental Disorders, Genetic/genetics, Anxiety Disorders/diagnosis, TEMPS-A, DRD4, Female, Dysthymic Disorder, Dysthymic Disorder/genetics

Dateibeschreibung: 157~163

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/18191458
http://www.ncbi.nlm.nih.gov/pubmed/18191458
https://ir.ymlib.yonsei.ac.kr/handle/22282913/107421
https://www.sciencedirect.com/science/article/abs/pii/S0165032707004247

Facets of neuroticism and musculoskeletal symptoms. A study of middle-aged twins / Facets of neuroticism and musculoskeletal symptoms. A study of middle-aged twins

Autoren: Vassend, Olav Orvik, Benedicte Humborstad Czajkowski, Nikolai Olavi et al.

Quelle: Norsk Epidemiologi. 26(1-2):47

Anxiety disorders in women: does gender matter to treatment?

Autoren: Lisa E Wygant Gustavo Kinrys

Quelle: Brazilian Journal of Psychiatry v.27 suppl.2 2005
Brazilian Journal of Psychiatry (São Paulo. 1999. Online)
Associação Brasileira de Psiquiatria (ABP)
instacron:ABP
Revista Brasileira de Psiquiatria, Volume: 27 Supplement 2, Pages: s43-s50, Published: OCT 2005

Schlagwörter: Disease susceptibility, Antidepressivos, Comorbidity, Severity of Illness Index, Saúde da mulher, 03 medical and health sciences, Sex Factors, 0302 clinical medicine, Antidepressive agents, Pregnancy, Risk Factors, Prevalence, Anxiety disorders/genetics, Humans, Genetic Predisposition to Disease, Transtorno depressivo, Gonadal Steroid Hormones, Anxiety disorders/epidemiology, Depressive disorder, Antidepressive agents/therapeutic use, Transtornos da ansiedade, Identidade de gênero, Anxiety Disorders, Antidepressive Agents, Gender Identity Women's health, Anxiety disorders/drug therapy, Female, Anxiety disorders

Dateibeschreibung: text/html

Zugangs-URL: http://www.scielo.br/pdf/rbp/v27s2/a03v27s2.pdf
https://pubmed.ncbi.nlm.nih.gov/16302053
https://www.scielo.br/scielo.php?script=sci_abstract&pid=S1516-44462005000600003&lng=es
https://europepmc.org/article/MED/16302053
https://pubmed.ncbi.nlm.nih.gov/16302053/
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-44462005000600003
https://doaj.org/article/eb6248a8865a4ba5b6533238016801a9
https://www.ncbi.nlm.nih.gov/pubmed/16302053
http://www.scielo.br/scielo.php?pid=S1516-44462005000600003&script=sci_arttext&tlng=pt
https://www.scielo.br/scielo.php?pid=S1516-44462005000600003&script=sci_arttext&tlng=pt
https://www.scielo.br/scielo.php?pid=S1516-44462005000600003&script=sci_abstract&tlng=pt
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-44462005000600003
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-44462005000600003&lng=en&tlng=en

Association analysis of monoamine genes with measures of depression and anxiety in a selected community sample of siblings

Autoren: Nash, MW Sugden, K HuezoDiaz, P et al.

Quelle: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :33-37

Schlagwörter: Questionnaires, Male, Serotonin, 5-Ht2c - Genetics, Tryptophan Hydroxylase - Genetics, Genotype, Genetic Predisposition To Disease - Genetics, Receptor, Serotonin, 5-Ht2c - Genetics, Tryptophan Hydroxylase, Depressive Disorder - Genetics, 5-Ht1d - Genetics, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Surveys and Questionnaires, Receptor, Serotonin, 5-HT2C, Humans, Genetic Predisposition to Disease, Monoamine Oxidase, Alleles, Depressive Disorder, Siblings, Receptor, Serotonin, 5-Ht1b - Genetics, Microsatellite Repeats - Genetics, Anxiety Disorders, Receptor, Serotonin, 5-Ht1d - Genetics, Phenotype, Receptor, Serotonin, 5-HT1D, 5-Ht1b - Genetics, Anxiety Disorders - Genetics, Receptor, Serotonin, 5-HT1B, Monoamine Oxidase - Genetics, Female, Receptor, Microsatellite Repeats

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/15729745
http://hub.hku.hk/handle/10722/175920
https://core.ac.uk/display/29884165
https://onlinelibrary.wiley.com/doi/10.1002/ajmg.b.30063
http://hdl.handle.net/10722/175920