Genetic epidemiology of psychiatric disorders

[Diagnosis and management of cervical paragangliomas: the Freiburg experience].

Laryngo- rhino- otologie·2004

Altered levels of plasma 24S- and 27-hydroxycholesterol in demented patients.

Neuroscience letters·2004

[Tumour staged surgery of endolymphatic sac tumors (ELST)].

Laryngo- rhino- otologie·2004

[Paragangliomas of the head and neck. Part 2: Therapy and follow-up].

HNO·2004

The efficacy of inhibitors involved in spermidine metabolism in Plasmodium falciparum, Anopheles stephensi and Trypanosoma evansi.

Parasitology research·2004

[Paragangliomas in the head-/neck region. I: Classification and diagnosis].

HNO·2004

Untargeted plasma metabolomics identifies metabolite signatures associated with suicidality status in chronic schizophrenia.

European archives of psychiatry and clinical neuroscience·2026

Association between antidepressant use and the risk of type 2 diabetes: a multi-stage Mendelian randomization study.

European archives of psychiatry and clinical neuroscience·2026

Esketamine-based treatment, depression-specific metacognitive training, and their combination in treatment-resistant depression: 6-month trajectories of depressive symptoms and rumination in a multicenter observational study.

European archives of psychiatry and clinical neuroscience·2026

Depressive symptom heterogeneity and mortality in a prospective U.S. cohort.

European archives of psychiatry and clinical neuroscience·2026

Integrated multi-omics and functional analyses reveal a GDCA-TGR5-mediated immunometabolic signature in anorexia nervosa.

European archives of psychiatry and clinical neuroscience·2026

Suicidal ideation and cognitive function: a comparative study in adolescents with unipolar versus bipolar depression.

European archives of psychiatry and clinical neuroscience·2026

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

Pharmacology & therapeutics·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Related Experiment Videos

Genetic epidemiology of psychiatric disorders

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[Diagnosis and management of cervical paragangliomas: the Freiburg experience].

Altered levels of plasma 24S- and 27-hydroxycholesterol in demented patients.

[Tumour staged surgery of endolymphatic sac tumors (ELST)].

[Paragangliomas of the head and neck. Part 2: Therapy and follow-up].

The efficacy of inhibitors involved in spermidine metabolism in Plasmodium falciparum, Anopheles stephensi and Trypanosoma evansi.

[Paragangliomas in the head-/neck region. I: Classification and diagnosis].

Untargeted plasma metabolomics identifies metabolite signatures associated with suicidality status in chronic schizophrenia.

Association between antidepressant use and the risk of type 2 diabetes: a multi-stage Mendelian randomization study.

Esketamine-based treatment, depression-specific metacognitive training, and their combination in treatment-resistant depression: 6-month trajectories of depressive symptoms and rumination in a multicenter observational study.

Depressive symptom heterogeneity and mortality in a prospective U.S. cohort.

Integrated multi-omics and functional analyses reveal a GDCA-TGR5-mediated immunometabolic signature in anorexia nervosa.

Suicidal ideation and cognitive function: a comparative study in adolescents with unipolar versus bipolar depression.

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

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Genetic epidemiology of psychiatric disorders

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