The PHF21B gene is associated with major depression and modulates the stress response

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Clinical Outcomes and Genome-Wide Association for a Brain Methylation Site in an Antidepressant Pharmacogenetics Study in Mexican Americans

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PHF21B as a candidate tumor suppressor gene in head and neck squamous cell carcinomas

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Roles of olfactory system dysfunction in depression

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Mapping the Epigenetic Basis of Complex Traits

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TRPM2 links oxidative stress to NLRP3 inflammasome activation

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Cultural Influences on Causal Beliefs About Depression Among Latino Immigrants

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Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors

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A mega-analysis of genome-wide association studies for major depressive disorder

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An efficient multi-locus mixed-model approach for genome-wide association studies in structured populations

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Genetic architectures of psychiatric disorders: the emerging picture and its implications

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The mystery of missing heritability: Genetic interactions create phantom heritability

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The current state of play on the molecular genetics of depression

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A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data

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Fluoxetine affects hippocampal plasticity, apoptosis and depressive-like behavior of chronically isolated rats

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Ancestral Components of Admixed Genomes in a Mexican Cohort

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Replication Strategies for Rare Variant Complex Trait Association Studies via Next-Generation Sequencing

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Integrating common and rare genetic variation in diverse human populations

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A method and server for predicting damaging missense mutations

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MutationTaster evaluates disease-causing potential of sequence alterations

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Involvement of α-MSH in the social isolation induced anxiety- and depression-like behaviors in rat

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De novo mutations in the gene encoding the synaptic scaffolding proteinSHANK3in patients ascertained for schizophrenia

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A Covering Method for Detecting Genetic Associations between Rare Variants and Common Phenotypes

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Identifying a High Fraction of the Human Genome to be under Selective Constraint Using GERP++

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A Novel Adaptive Method for the Analysis of Next-Generation Sequencing Data to Detect Complex Trait Associations with Rare Variants Due to Gene Main Effects and Interactions

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Fast and accurate short read alignment with Burrows-Wheeler transform

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Affective disorders and other psychiatric diagnoses in children and adolescents with 22q11.2 Deletion Syndrome

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The Rest Repression of the Neurosecretory Phenotype Is Negatively Modulated by BHC80, a Protein of the BRAF/HDAC Complex

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Sequence variations of ABCB1, SLC6A2, SLC6A3, SLC6A4, CREB1, CRHR1 and NTRK2: association with major depression and antidepressant response in Mexican-Americans

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Targeted capture and massively parallel sequencing of 12 human exomes

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Velo-cardio-facial syndrome: 30 Years of study

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Polymorphisms in inflammation-related genes are associated with susceptibility to major depression and antidepressant response

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