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1دورية أكاديمية
المؤلفون: de Witte, Lot D., Wang, Zhaoyu, Snijders, Gijsje L.J.L., Mendelev, Natalia, Liu, Qingkun, Sneeboer, Marjolein A.M., Boks, Marco P.M., Ge, Yongchao, Haghighi, Fatemeh
المساهمون: MMB Research line 3b, AIOS Psychiatrie, TN groep Pasterkamp, Onderzoeksgroep 2, Brain
مصطلحات موضوعية: Bipolar disorder, Brain region, Depression, Methylation, Microglia, Transcriptome, DNA Methylation, Microglia/metabolism, Mood Disorders/genetics, Humans, Epigenome, Brain/metabolism, Biological Psychiatry, Research Support, U.S. Gov't, Non-P.H.S, Journal Article
وصف الملف: application/pdf
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2دورية أكاديمية
المصدر: 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/s41588-021-00950-8Test
مصطلحات موضوعية: Aged, Anxiety Disorders/genetics, CD56 Antigen/genetics, Cell Adhesion Molecules/genetics, Cytoskeletal Proteins/genetics, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Guanine Nucleotide Exchange Factors/genetics, Homeodomain Proteins/genetics, Humans, Irritable Bowel Syndrome/epidemiology, Male, Middle Aged, Molecular Chaperones/genetics, Mood Disorders/genetics, Polymorphism, Single Nucleotide, United Kingdom/epidemiology
الإتاحة: https://doi.org/10.1038/s41588-021-00950-8Test
https://research.manchester.ac.uk/en/publications/3dd6a1aa-4bf8-4587-8b27-76e526cab9a7Test -
3دورية أكاديمية
المؤلفون: Dlugauskas, Edgaras, Strumila, Robertas, Lengvenyte, Aiste, Ambrozaityte, Laima, Dagyte, Evelina, Molyte, Alma, Navickas, Alvydas, Utkus, Algirdas
المصدر: Nordic Journal of Psychiatry. 73(1):31
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4دورية أكاديمية
المؤلفون: Chang, H., Hoshina, N., Zhang, C., Ma, Y., Cao, H., Wang, Y., Wu, D.D., Bergen, S.E., Landén, M., Hultman, C.M., Preisig, M., Kutalik, Z., Castelao, E., Grigoroiu-Serbanescu, M., Forstner, A.J., Strohmaier, J., Hecker, J., Schulze, T.G., Müller-Myhsok, B., Reif, A., Mitchell, P.B., Martin, N.G., Schofield, P.R., Cichon, S., Nöthen, M.M., Walter, H., Erk, S., Heinz, A., Amin, N., van Duijn, C.M., Meyer-Lindenberg, A., Tost, H., Xiao, X., Yamamoto, T., Rietschel, M., Li, M.
المساهمون: Swedish Bipolar Study Group, MooDS Bipolar Consortium, Backlund, L., Frisén, L., Lavebratt, C., Schalling, M., Ösby, U., Mühleisen, T.W., Leber, M., Degenhardt, F., Treutlein, J., Mattheisen, M., Maaser, A., Meier, S., Herms, S., Hoffmann, P., Lacour, A., Witt, S.H., Streit, F., Lucae, S., Maier, W., Schwarz, M., Vedder, H., Kammerer-Ciernioch, J., Pfennig, A., Bauer, M., Hautzinger, M., Wright, A., Fullerton, J.M., Montgomery, G.W., Medland, S.E., Gordon, S.D., Becker, T., Schumacher, J., Propping, P.
المصدر: Molecular psychiatry, vol. 23, no. 2, pp. 400-412
مصطلحات موضوعية: Adult, Amygdala/physiopathology, Bipolar Disorder/genetics, Brain/physiopathology, Cadherins/genetics, Cadherins/metabolism, Cognition/physiology, Dendrites, Dendritic Spines, Depressive Disorder, Major/genetics, Female, Genetic Predisposition to Disease/genetics, Genotype, Humans, Male, Middle Aged, Mood Disorders/genetics, Neuronal Plasticity, Neurons, Personality/genetics, Polymorphism, Single Nucleotide/genetics, Risk Factors, Synapses/genetics, Synapses/metabolism
وصف الملف: application/pdf
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28070120; info:eu-repo/semantics/altIdentifier/eissn/1476-5578; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_4137137BE5F60; https://serval.unil.ch/notice/serval:BIB_4137137BE5F6Test; urn:issn:1359-4184; https://serval.unil.ch/resource/serval:BIB_4137137BE5F6.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_4137137BE5F60Test
الإتاحة: https://doi.org/10.1038/mp.2016.231Test
https://serval.unil.ch/notice/serval:BIB_4137137BE5F6Test
https://serval.unil.ch/resource/serval:BIB_4137137BE5F6.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_4137137BE5F60Test -
5دورية أكاديمية
المؤلفون: Xiao, X., Wang, L., Wang, C., Yuan, T.F., Zhou, D., Zheng, F., Li, L., Grigoroiu-Serbanescu, M., Ikeda, M., Iwata, N., Takahashi, A., Kamatani, Y., Kubo, M., Preisig, M., Kutalik, Z., Castelao, E., Pistis, G., Amin, N., van Duijn, C.M., Forstner, A.J., Strohmaier, J., Hecker, J., Schulze, T.G., Müller-Myhsok, B., Reif, A., Mitchell, P.B., Martin, N.G., Schofield, P.R., Cichon, S., Nöthen, M.M., Chang, H., Luo, X.J., Fang, Y., Yao, Y.G., Zhang, C., Rietschel, M., Li, M.
المساهمون: Advanced Collaborative Study of Mood Disorder (COSMO) Team, MooDS Bipolar Consortium
المصدر: Translational psychiatry, vol. 7, no. 12, pp. 1273
مصطلحات موضوعية: Bipolar Disorder/genetics, Depressive Disorder, Major/genetics, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Mood Disorders/genetics, Polymorphism, Single Nucleotide
وصف الملف: application/pdf
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/29225345; info:eu-repo/semantics/altIdentifier/eissn/2158-3188; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_C08EB9614B490; https://serval.unil.ch/notice/serval:BIB_C08EB9614B49Test; urn:issn:2158-3188; https://serval.unil.ch/resource/serval:BIB_C08EB9614B49.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_C08EB9614B490Test
الإتاحة: https://doi.org/10.1038/s41398-017-0019-0Test
https://serval.unil.ch/notice/serval:BIB_C08EB9614B49Test
https://serval.unil.ch/resource/serval:BIB_C08EB9614B49.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_C08EB9614B490Test -
6دورية أكاديمية
المؤلفون: Hoeffding, Louise K, Duong, Linh T T, Ingason, Andrés, Rosengren, Anders, Sorbanski, Ester, Witt, Stephanie H, Djurovic, Srdjan, Andreassen, Ole A, Hansen, Thomas, Werge, Thomas, Rasmussen, Henrik B
المصدر: Nordic Journal of Psychiatry. 70(4):276
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7دورية أكاديمية
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8دورية أكاديمية
المساهمون: Jee In Kang, Chun Il Park, Kee Namkoong, Se Joo Kim, Kang, Jee In, Kim, Se Joo, Namkoong, Kee
مصطلحات موضوعية: Adolescent, Adult, Circadian Rhythm/genetics, Female, Gene Products, rev/genetics, Genotype, Humans, Male, Mood Disorders/genetics, Nuclear Receptor Subfamily 1, Group D, Member 1/genetics, Polymorphism, Single Nucleotide/genetics, Young Adult, Association, NR1D1 gene, REV-ERB慣, chronotype, circadian rhythm, genetics
العلاقة: CHRONOBIOLOGY INTERNATIONAL; J00531; OAK-2015-01136; https://ir.ymlib.yonsei.ac.kr/handle/22282913/140296Test; T201501765; CHRONOBIOLOGY INTERNATIONAL, Vol.32(4) : 568-572, 2015
الإتاحة: https://doi.org/10.3109/07420528.2015.1006327Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/140296Test -
9
المؤلفون: Cynthia Sandor, Laura M. Lyall, Valentina Escott-Price, Caleb Webber, Joey Ward, Keira J.A. Johnston, Daniel J. Smith, Michael Conlon O'Donovan, Nicholas Graham, Elizabeth M. Tunbridge, Donald M. Lyall, Paul Harrison, Amy Ferguson, Mark E.S. Bailey, Jill P. Pell, Breda Cullen, Rona J. Strawbridge
المساهمون: Harrison, P
المصدر: Ward, J, Tunbridge, E M, Sandor, C, Lyall, L M, Ferguson, A, Strawbridge, R J, Lyall, D M, Cullen, B, Graham, N, Johnston, K J A, Webber, C, Escott-Price, V, O'Donovan, M, Pell, J P, Bailey, M E S, Harrison, P J & Smith, D J 2020, ' The genomic basis of mood instability : identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function ', Molecular Psychiatry, vol. 25, no. 11, pp. 3091-3099 . https://doi.org/10.1038/s41380-019-0439-8Test
Molecular psychiatry
Molecular Psychiatryمصطلحات موضوعية: Male, 0301 basic medicine, Linkage disequilibrium, Databases, Factual, Gene Expression, Genome-wide association study, Mice, 0302 clinical medicine, 0303 health sciences, Mental Disorders, Genetic Predisposition to Disease/genetics, Mood Disorders/genetics, Genomics, Middle Aged, Polymorphism, Single Nucleotide/genetics, 3. Good health, Psychiatry and Mental health, Schizophrenia, Major depressive disorder, Female, Adult, medicine.medical_specialty, Biology, Polymorphism, Single Nucleotide, Article, Cellular and Molecular Neuroscience, 03 medical and health sciences, Genetics, medicine, Animals, Humans, Genetic Predisposition to Disease, Bipolar disorder, Psychiatry, Molecular Biology, Aged, 030304 developmental biology, Genetic association, Mental Disorders/genetics, Mood Disorders, Correction, Mental illness, medicine.disease, United Kingdom, Affect, 030104 developmental biology, Mood, Expression quantitative trait loci, 030217 neurology & neurosurgery, Neuroscience, Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c78d54c0ea7a55c8774f8e7eb0f98b7Test
https://orca.cardiff.ac.uk/id/eprint/123563/7/s41380-019-0439-8.pdfTest -
10دورية أكاديمية
المؤلفون: McMahon, F.J., Akula, N., Schulze, T.G., Muglia, P., Tozzi, F., Detera-Wadleigh, S.D., Steele, C.J., Breuer, R., Strohmaier, J., Wendland, J.R., Mattheisen, M., Mühleisen, T.W., Maier, W., Nöthen, M.M., Cichon, S., Farmer, A., Vincent, J.B., Holsboer, F., Preisig, M., Rietschel, M.
المساهمون: Bipolar Disorder Genome Study (BiGS) Consortium
المصدر: Nature genetics, vol. 42, no. 2, pp. 128-131
مصطلحات موضوعية: Chromosomes, Human, Pair 3/genetics, Genetic Loci/genetics, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Mood Disorders/genetics, Polymorphism, Single Nucleotide/genetics
وصف الملف: application/pdf
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/20081856; info:eu-repo/semantics/altIdentifier/eissn/1546-1718; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_277BDAC7A7CE1; https://serval.unil.ch/notice/serval:BIB_277BDAC7A7CETest; urn:issn:1061-4036; https://serval.unil.ch/resource/serval:BIB_277BDAC7A7CE.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_277BDAC7A7CE1Test
الإتاحة: https://doi.org/10.1038/ng.523Test
https://serval.unil.ch/notice/serval:BIB_277BDAC7A7CETest
https://serval.unil.ch/resource/serval:BIB_277BDAC7A7CE.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_277BDAC7A7CE1Test