Bipolar manic-depressive psychoses: results of a genetic investigation

The relationship between attention deficit hyperactivity disorder, bipolarity and mixed features in major depressive patients: Evidence from the BRIDGE-II-Mix Study.

Journal of affective disorders·2019

Bipolar spectrum in major depressive disorders.

European archives of psychiatry and clinical neuroscience·2018

Aggressiveness in depression: a neglected symptom possibly associated with bipolarity and mixed features.

Acta psychiatrica Scandinavica·2017

Hypomania Checklist-32 - cross-validation of shorter versions screening for bipolar disorders in an epidemiological study.

Acta psychiatrica Scandinavica·2017

Screening for bipolar disorders: A public health issue.

Journal of affective disorders·2016

Relationship between personality and psychopathology in a longitudinal community study: a test of the predisposition model.

Psychological medicine·2016

Association of apolipoprotein E gene with risk, cognition, and prognosis of epilepsy.

Human genetics·2026

A case-control study on IL-8 gene polymorphisms and serum IL-8 levels in patients with age-related macular degeneration in India.

Human genetics·2026

Clinical, immunological, and molecular characteristics of severe combined immune deficiency in China.

Human genetics·2026

Mitochondrial dysfunction drives metabolic reprogramming in Gitelman syndrome: insights from proteomics and isogenic modeling.

Human genetics·2026

Polygenic risk scores in human genetics for study design discovery and translation.

Human genetics·2026

Genetic variation in BDNF is associated with opioid use disorder severity.

Human genetics·2026

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Balkan medical journal·2026

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

The Journal of allergy and clinical immunology·2026

CRP-albumin-lymphocyte index and multisystem diseases: a phenome-wide Mendelian randomization study.

Molecular genetics and genomics : MGG·2026

Congenital Hyperinsulinism With Paternally Inherited ABCC8 Variants: A Single Center Experience Over a Decade in Singapore.

Journal of the ASEAN Federation of Endocrine Societies·2026

Gestational age modifies associations between Group B Streptococcus genomic characteristics and postnatal age at disease onset.

Nature communications·2026

Related Experiment Videos

Bipolar manic-depressive psychoses: results of a genetic investigation

Related Concept Videos

The relationship between attention deficit hyperactivity disorder, bipolarity and mixed features in major depressive patients: Evidence from the BRIDGE-II-Mix Study.

Bipolar spectrum in major depressive disorders.

Aggressiveness in depression: a neglected symptom possibly associated with bipolarity and mixed features.

Hypomania Checklist-32 - cross-validation of shorter versions screening for bipolar disorders in an epidemiological study.

Screening for bipolar disorders: A public health issue.

Relationship between personality and psychopathology in a longitudinal community study: a test of the predisposition model.

Association of apolipoprotein E gene with risk, cognition, and prognosis of epilepsy.

A case-control study on IL-8 gene polymorphisms and serum IL-8 levels in patients with age-related macular degeneration in India.

Clinical, immunological, and molecular characteristics of severe combined immune deficiency in China.

Mitochondrial dysfunction drives metabolic reprogramming in Gitelman syndrome: insights from proteomics and isogenic modeling.

Polygenic risk scores in human genetics for study design discovery and translation.

Genetic variation in BDNF is associated with opioid use disorder severity.

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

CRP-albumin-lymphocyte index and multisystem diseases: a phenome-wide Mendelian randomization study.

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Bipolar manic-depressive psychoses: results of a genetic investigation

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