Contribution of genetic epidemiologic research to psychiatry

Bipolar spectrum in major depressive disorders.

European archives of psychiatry and clinical neuroscience·2018

Mood disorders and circulating levels of inflammatory markers in a longitudinal population-based study.

Psychological medicine·2017

Dysregulation of objectively assessed 24-hour motor activity patterns as a potential marker for bipolar I disorder: results of a community-based family study.

Translational psychiatry·2017

The role of genetic liability in the association of urbanicity at birth and during upbringing with schizophrenia in Denmark.

Psychological medicine·2017

Reexamining associations between mania, depression, anxiety and substance use disorders: results from a prospective national cohort.

Molecular psychiatry·2016

A population-based study of the risk of schizophrenia and bipolar disorder associated with parent-child separation during development.

Psychological medicine·2015

Schizoidism and Syntony vis-à-vis Plessner, Autopoiesis, and 4E Cognition.

Psychopathology·2026

Relationships between network analysis and psychodynamic theories: A scoping review.

Psychopathology·2026

Common and Unique Etiological Influences on Personality and Personality Disorders in Youth.

Psychopathology·2026

Distressing experiences of felt presence in Child and Adolescent Mental Health Services: Early observations from the ChUSE Trial and the challenges of assessment.

Psychopathology·2026

What is Phenomenology For? Applications in Autism Mental Health and a Pragmatist Criterion of Success.

Psychopathology·2026

Imaginative Vulnerability and Symbolic Mediation: A Phenomenological Analysis in Schizophrenia-Spectrum Conditions.

Psychopathology·2026

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Research (Washington, D.C.)·2026

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Clinical case reports·2026

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Journal of human genetics·2026

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

Nature genetics·2026

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Psychiatric genetics·2026

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Frontiers in genetics·2026

Related Experiment Videos

Contribution of genetic epidemiologic research to psychiatry

Related Concept Videos

Bipolar spectrum in major depressive disorders.

Mood disorders and circulating levels of inflammatory markers in a longitudinal population-based study.

Dysregulation of objectively assessed 24-hour motor activity patterns as a potential marker for bipolar I disorder: results of a community-based family study.

The role of genetic liability in the association of urbanicity at birth and during upbringing with schizophrenia in Denmark.

Reexamining associations between mania, depression, anxiety and substance use disorders: results from a prospective national cohort.

A population-based study of the risk of schizophrenia and bipolar disorder associated with parent-child separation during development.

Schizoidism and Syntony vis-à-vis Plessner, Autopoiesis, and 4E Cognition.

Relationships between network analysis and psychodynamic theories: A scoping review.

Common and Unique Etiological Influences on Personality and Personality Disorders in Youth.

Distressing experiences of felt presence in Child and Adolescent Mental Health Services: Early observations from the ChUSE Trial and the challenges of assessment.

What is Phenomenology For? Applications in Autism Mental Health and a Pragmatist Criterion of Success.

Imaginative Vulnerability and Symbolic Mediation: A Phenomenological Analysis in Schizophrenia-Spectrum Conditions.

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Related Experiment Videos

Contribution of genetic epidemiologic research to psychiatry

Related Concept Videos

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