BACKGROUND: The Depression Network Study (DeNt) is a multicentre study designed to identify genes and/or loci linked to and/or associated with susceptibility to unipolar depression in Caucasian families. This study presents the method and socio-demographic details of the first 470 affected sibling pairs recruited from 8 different sites in Europe and the United States of America. METHODS: Probands fulfilling either the Diagnostic and Statistical Manual 4th edition (DSM-IV) or the International Classification of Diseases 10th edition (ICD-10) criteria for recurrent unipolar depression of moderate or severe degree and who had at least one similarly affected sibling were eligible for the study. Detailed clinical and psychological assessments we...
OBJECTIVE: The authors studied a dense map of single nucleotide polymorphism (SNP) DNA markers o...
The Genesis 12–19 (G1219) Study is an ongoing longitudinal study of a sample of UK twin pairs, non-t...
Objective: The authors carried out a genomewide linkage scan to identify chromosomal regions likely ...
BACKGROUND: The Depression Network Study (DeNt) is a multicentre study designed to identify genes an...
The Depression Network Study (DeNt) is a multicentre study designed to identify genes and/or loci li...
Objective Studies of major depression in twins and families have shown moderate to high heritabilit...
OBJECTIVE: The purpose of this study was to find loci for major depression via linkage analysis of a...
Objective: Studies of major depression in twins and families have shown moderate to high heritabilit...
OBJECTIVE: Studies of major depression in twins and families have shown moderate to high heritabilit...
Monozygotic (MZ) twin studies constitute a key resource for the dissection of environmental and biol...
OBJECTIVE: The purpose of this study was to find loci for major depression via linkage analysis of a...
Genome-wide linkage analysis was carried out in a sample of 497 sib pairs concordant for recurrent m...
Background: Both clinical care and genome-wide studies need to account for levels of severity in the...
Depression is a polygenic trait that causes extensive periods of disability. Previous genetic studie...
Depression is the most common psychiatric disorder and the leading cause of disability worldwide. D...
OBJECTIVE: The authors studied a dense map of single nucleotide polymorphism (SNP) DNA markers o...
The Genesis 12–19 (G1219) Study is an ongoing longitudinal study of a sample of UK twin pairs, non-t...
Objective: The authors carried out a genomewide linkage scan to identify chromosomal regions likely ...
BACKGROUND: The Depression Network Study (DeNt) is a multicentre study designed to identify genes an...
The Depression Network Study (DeNt) is a multicentre study designed to identify genes and/or loci li...
Objective Studies of major depression in twins and families have shown moderate to high heritabilit...
OBJECTIVE: The purpose of this study was to find loci for major depression via linkage analysis of a...
Objective: Studies of major depression in twins and families have shown moderate to high heritabilit...
OBJECTIVE: Studies of major depression in twins and families have shown moderate to high heritabilit...
Monozygotic (MZ) twin studies constitute a key resource for the dissection of environmental and biol...
OBJECTIVE: The purpose of this study was to find loci for major depression via linkage analysis of a...
Genome-wide linkage analysis was carried out in a sample of 497 sib pairs concordant for recurrent m...
Background: Both clinical care and genome-wide studies need to account for levels of severity in the...
Depression is a polygenic trait that causes extensive periods of disability. Previous genetic studie...
Depression is the most common psychiatric disorder and the leading cause of disability worldwide. D...
OBJECTIVE: The authors studied a dense map of single nucleotide polymorphism (SNP) DNA markers o...
The Genesis 12–19 (G1219) Study is an ongoing longitudinal study of a sample of UK twin pairs, non-t...
Objective: The authors carried out a genomewide linkage scan to identify chromosomal regions likely ...