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المؤلفون: Ingason A; Research Institute of Biological Psychiatry, Mental Health Center Sct. Hans, Copenhagen University Hospital, Roskilde, Denmark., Kirov G, Giegling I, Hansen T, Isles AR, Jakobsen KD, Kristinsson KT, le Roux L, Gustafsson O, Craddock N, Möller HJ, McQuillin A, Muglia P, Cichon S, Rietschel M, Ophoff RA, Djurovic S, Andreassen OA, Pietiläinen OP, Peltonen L, Dempster E, Collier DA, St Clair D, Rasmussen HB, Glenthøj BY, Kiemeney LA, Franke B, Tosato S, Bonetto C, Saemundsen E, Hreidarsson SJ, Nöthen MM, Gurling H, O'Donovan MC, Owen MJ, Sigurdsson E, Petursson H, Stefansson H, Rujescu D, Stefansson K, Werge T

مؤلفون مشاركون: GROUP Investigators

المصدر: The American journal of psychiatry [Am J Psychiatry] 2011 Apr; Vol. 168 (4), pp. 408-17. Date of Electronic Publication: 2011 Feb 15.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: American Psychiatric Association Country of Publication: United States NLM ID: 0370512 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1535-7228 (Electronic) Linking ISSN: 0002953X NLM ISO Abbreviation: Am J Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Pair 15/*genetics , DNA Copy Number Variations/*genetics , Schizophrenia/*genetics, Adolescent ; Adult ; Age of Onset ; Blotting, Southern ; Child ; Denmark ; Female ; Genetic Association Studies ; Genotype ; Humans ; Male ; Mothers ; Prader-Willi Syndrome/genetics ; Psychotic Disorders/genetics ; Uniparental Disomy/genetics ; United Kingdom ; Young Adult

المؤلفون: Perlis RH; Department of Psychiatry, Massachusetts General Hospital, Boston, 02114, USA. rperlis@partners.org, Huang J, Purcell S, Fava M, Rush AJ, Sullivan PF, Hamilton SP, McMahon FJ, Schulze TG, Potash JB, Zandi PP, Willour VL, Penninx BW, Boomsma DI, Vogelzangs N, Middeldorp CM, Rietschel M, Nöthen M, Cichon S, Gurling H, Bass N, McQuillin A, Hamshere M, Craddock N, Sklar P, Smoller JW

مؤلفون مشاركون: Wellcome Trust Case Control Consortium Bipolar Disorder Group

المصدر: The American journal of psychiatry [Am J Psychiatry] 2010 Dec; Vol. 167 (12), pp. 1499-507. Date of Electronic Publication: 2010 Nov 01.

نوع المنشور: Journal Article; Meta-Analysis; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural

بيانات الدورية: Publisher: American Psychiatric Association Country of Publication: United States NLM ID: 0370512 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1535-7228 (Electronic) Linking ISSN: 0002953X NLM ISO Abbreviation: Am J Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Suicide, Attempted*, Genome-Wide Association Study/*methods , Mood Disorders/*genetics, Genetic Predisposition to Disease ; Genotype ; Humans ; Polymorphism, Single Nucleotide

المؤلفون: Feyder M; Section on Behavioral Science and Genetics, Laboratory for Integrative Neuroscience, National Institute on Alcoholism and Alcohol Abuse, Rockville, MD 20852-9411, USA. michael.feyder@ki.se, Karlsson RM, Mathur P, Lyman M, Bock R, Momenan R, Munasinghe J, Scattoni ML, Ihne J, Camp M, Graybeal C, Strathdee D, Begg A, Alvarez VA, Kirsch P, Rietschel M, Cichon S, Walter H, Meyer-Lindenberg A, Grant SG, Holmes A

المصدر: The American journal of psychiatry [Am J Psychiatry] 2010 Dec; Vol. 167 (12), pp. 1508-17. Date of Electronic Publication: 2010 Oct 15.

نوع المنشور: Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: American Psychiatric Association Country of Publication: United States NLM ID: 0370512 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1535-7228 (Electronic) Linking ISSN: 0002953X NLM ISO Abbreviation: Am J Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Gene Deletion* , Genetic Variation*, Child Development Disorders, Pervasive/*genetics , Intracellular Signaling Peptides and Proteins/*genetics , Membrane Proteins/*genetics , Williams Syndrome/*genetics, Adult ; Amygdala/pathology ; Amygdala/physiopathology ; Amygdala/ultrastructure ; Animals ; Behavior, Animal ; Child ; Child Development Disorders, Pervasive/pathology ; Dendritic Spines/ultrastructure ; Disease Models, Animal ; Disks Large Homolog 4 Protein ; Female ; Guanylate Kinases ; Humans ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Nerve Tissue Proteins/metabolism ; Neural Pathways/pathology ; Parietal Lobe/pathology ; Phenotype ; Polymorphism, Single Nucleotide ; Prosencephalon/metabolism ; Williams Syndrome/pathology ; Williams Syndrome/physiopathology

المؤلفون: Rietschel M; Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, University of Heidelberg, Mannheim, Germany., Beckmann L, Strohmaier J, Georgi A, Karpushova A, Schirmbeck F, Boesshenz KV, Schmäl C, Bürger C, Jamra RA, Schumacher J, Höfels S, Kumsta R, Entringer S, Krug A, Markov V, Maier W, Propping P, Wüst S, Kircher T, Nöthen MM, Cichon S, Schulze TG

المصدر: The American journal of psychiatry [Am J Psychiatry] 2008 Jun; Vol. 165 (6), pp. 753-62. Date of Electronic Publication: 2008 Mar 17.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: American Psychiatric Association Country of Publication: United States NLM ID: 0370512 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1535-7228 (Electronic) Linking ISSN: 0002953X NLM ISO Abbreviation: Am J Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Anxiety Disorders/*genetics , Carrier Proteins/*genetics , Depressive Disorder, Major/*genetics , Neurotic Disorders/*genetics, Adult ; Anxiety Disorders/epidemiology ; Cross-Sectional Studies ; Depressive Disorder, Major/epidemiology ; Female ; Gene Frequency ; Genetic Predisposition to Disease/genetics ; Genetics, Population ; Germany ; Haplotypes ; Humans ; Intracellular Signaling Peptides and Proteins ; Male ; Middle Aged ; Neurotic Disorders/epidemiology ; Phenotype