Rare genotype combination of the serotonin transporter gene associated with treatment response in severe personality disorder.
about
No association between COMT val158met polymorphism and suicidal behavior: meta-analysis and new data.5-HTTLPR moderates naltrexone and psychosocial treatment responses in heavy drinking men who have sex with men.Lack of association of SNPs from the FADS1-FADS2 gene cluster with major depression or suicidal behavior5-HTTLPR genotype and daily negative mood moderate the effects of sertraline on drinking intensity.Predictors for self-directed aggression in Italian prisoners include externalizing behaviors, childhood trauma and the serotonin transporter gene polymorphism 5-HTTLPR.Endophenotypes as a measure of suicidality.Neurobiology of suicide: do biomarkers exist?Pharmacogenetics of antidepressant drugs: an update after almost 20 years of research.Role of the 5-HTTLPR and SNP Promoter Polymorphisms on Serotonin Transporter Gene Expression: a Closer Look at Genetic Architecture and In Vitro Functional Studies of Common and Uncommon Allelic Variants.Extending Previous cG×I Findings on 5-HTTLPR's Moderation of Intervention Effects on Adolescent Substance Misuse Initiation.Serotonin Transporter Gene Polymorphisms and Selective Serotonin Reuptake Inhibitor Tolerability: Review of Pharmacogenetic Evidence.Addition of methylphenidate to intensive dialectical behaviour therapy for patients suffering from comorbid borderline personality disorder and ADHD: a naturalistic study.A Cross-National Tool for Assessing and Studying Suicidal Behaviors.Serotonergic 5HTTLPR/rs25531 s-allele homozygosity associates with violent suicides in male citalopram users.Interaction among childhood trauma and functional polymorphisms in the serotonin pathway moderate the risk of depressive disorders.Moderation of adult depression by the serotonin transporter promoter variant (5-HTTLPR), childhood abuse and adult traumatic events in a general population sample.Individual biological sensitivity to environmental influences: testing the differential susceptibility properties of the 5HTTLPR polymorphism in relation to depressive symptoms and delinquency in two adolescent general samples.
P2860
Q34026890-EA3FDFF4-EC6B-4055-A738-FFC053A12D25Q34255375-76AF2EAA-FBB5-40BF-B3B9-7EAA3A1B412AQ36609756-FEBD1E09-7731-4A7A-A406-A699CF647CBFQ36625432-F2135881-C9AB-496B-BCFA-9C7BC1D34F9AQ36963627-4C8F72C0-C48F-449C-8E21-675EA5D166B4Q38039966-351BC2EE-F351-4CCD-A197-7C127BACF6F7Q38083578-A9486415-1757-48D0-ACC9-E9E524B4322EQ38121519-F0D3F95A-3019-4376-A496-4D2A526B0068Q38606623-FAF5497E-D36A-4742-BFF0-B3DB2C6BE39BQ39175766-9917E6A0-0C2E-4ACE-BA27-E97C3BBD492CQ39400564-0EC22559-1817-4FF0-B24D-4CF7C672A3D3Q41507967-99B3312A-213D-4227-8D42-9D9C47207561Q41662363-A914AFD5-61A0-4FA2-B0E9-5AECD532C365Q47858460-766D848D-9E30-415E-984E-A539BAD719D0Q48214945-1EF85B2D-CCD4-4967-8CE0-B3830DFC74A3Q48733067-D94EAF50-F75B-4289-8F69-08FE3391E26AQ50090338-72EA3359-05F3-4A82-A2EE-C10C33F5AB5D
P2860
Rare genotype combination of the serotonin transporter gene associated with treatment response in severe personality disorder.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Rare genotype combination of t ...... n severe personality disorder.
@en
Rare genotype combination of t ...... n severe personality disorder.
@nl
type
label
Rare genotype combination of t ...... n severe personality disorder.
@en
Rare genotype combination of t ...... n severe personality disorder.
@nl
prefLabel
Rare genotype combination of t ...... n severe personality disorder.
@en
Rare genotype combination of t ...... n severe personality disorder.
@nl
P2093
P2860
P356
P1476
Rare genotype combination of t ...... n severe personality disorder.
@en
P2093
Alain Malafosse
Annick Salzmann
Concepción Vaquero-Lorenzo
Dominique Mouthon
European Research Consortium for Suicide (EURECA)
Isabelle Jaussent
Maria P Garcia-Portilla
Monique Vessaz
Nader Perroud
Philippe Courtet
P2860
P304
P356
10.1002/AJMG.B.31118
P577
2010-12-01T00:00:00Z