Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.
about
Genetic determinants of depression: recent findings and future directions16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions.Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping DataGenomic structural variation in psychiatric disorders.Rare copy number variation in treatment-resistant major depressive disorderInvestigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy.Prioritization of Copy Number Variation Loci Associated with Autism from AutDB-An Integrative Multi-Study Genetic Database.Copy number variants in German patients with schizophreniaPhenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder.Copy number variation in bipolar disorder.Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets.Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders.Effect of copy number variants on outcomes for infants with single ventricle heart defects.Recent advances in nutrition, genes and brain health.Genomic structural variation in affective, anxiety, and stress-related disorders.Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2.Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication.Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred.Redefining the endophenotype concept to accommodate transdiagnostic vulnerabilities and etiological complexity.A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders.
P2860
Q27027836-4665586B-5F77-40ED-BC1B-7ABE8C8C9C95Q30362781-9BB54A29-BE47-464C-9435-30DEB8D17222Q30578002-E4E65D16-BDE1-4A59-A65A-7F266DD748E6Q33354553-C1AF5477-07D1-4CB4-BB3B-2450AE5A6C47Q33922682-5D9B29CA-ECD5-4D4E-AC29-E22AD5E14014Q34257185-AEDFD654-DDC0-4DBC-A955-94C0A2B64DEEQ34794203-51A2E8C5-5D90-4672-8826-988400783809Q34811896-BDB08F0E-D047-4059-83F2-B935AEE1DFF9Q36498543-66A01BDC-55B5-471D-BABE-34086C7BCEC1Q37287371-FAE83F57-0277-4044-85B1-E6C9CF6E1AD7Q37362339-9260EABF-46F0-4C94-B2A9-407216AF4BEEQ37508181-E4A6A75E-0DC9-47AC-A87D-0965CF0CA0A5Q37704931-C60FBBED-4471-4274-A1F5-63E4B8E60CE6Q38020256-DC4D8803-6E34-4215-B5DC-FC179267374BQ38248716-4FCB180D-2CAD-4D2D-91F6-582756508D13Q40699271-FB5D99A4-E2ED-4358-9192-52A58E8A1B62Q46936151-1987FA3A-30AE-4E6A-9CC0-CF5B94485206Q47706855-2C41DD2B-D383-43F4-A658-6196970FDF6CQ47772593-B88C07B3-960C-40FB-AECA-74FBC7588F0BQ48309066-161F8739-212A-4406-980B-39D9319FC9D2
P2860
Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Association between copy numbe ...... a German case-control sample.
@en
Association between copy numbe ...... a German case-control sample.
@nl
type
label
Association between copy numbe ...... a German case-control sample.
@en
Association between copy numbe ...... a German case-control sample.
@nl
prefLabel
Association between copy numbe ...... a German case-control sample.
@en
Association between copy numbe ...... a German case-control sample.
@nl
P2093
P2860
P50
P356
P1476
Association between copy numbe ...... a German case-control sample.
@en
P2093
Andreas Heinz
Christiane Wolf
Christoph Lange
Henrik Walter
Jana Strohmaier
Lutz Priebe
Magdalena Groß
René Breuer
Sandra Meier
Susanne Lucae
P2860
P304
P356
10.1002/AJMG.B.32034
P407
P50
P577
2012-02-17T00:00:00Z