A double dominant genetic mechanism for schizophrenia

Mental abilities of male relatives of psychotic patients.

Acta psychiatrica Scandinavica·2002

Relation of mathematical ability to psychosis in Iceland.

Clinical genetics·2000

Partly dominant transmission of schizophrenia in Iceland.

The British journal of psychiatry : the journal of mental science·1988

Family transmission of schizophrenia: a review and synthesis.

The British journal of psychiatry : the journal of mental science·1982

Genetic factors in myopia.

Acta geneticae medicae et gemellologiae·1976

Influence of the myopia gene on brain development.

Clinical genetics·1975

Haplotype-based validation of genomic regions for breeding of new Nordic apples.

Hereditas·2026

miR-335-3p acts as a tumor suppressor in esophageal squamous cell carcinoma and predicts favorable prognosis.

Hereditas·2026

SNP rs7430456 mediated LINC00578 drives triple negative breast cancer through regulating miR-143-5p expression.

Hereditas·2026

BFLF1 gene polymorphisms are associated with increased mortality in patients with EBV-associated diseases.

Hereditas·2026

miR-1-3p, as a novel diagnostic and prognostic biomarker, aggravates pancreatic acinar cell injury in acute pancreatitis by targeting GNPTAB.

Hereditas·2026

Identification of FOXK1 and SEMA7A as key genes associated with m6A-related programmed cell death in diabetic retinopathy.

Hereditas·2026

A Novel de Novo WAC Frameshift Variant in DeSanto-Shinawi Syndrome With Temporo-Occipital Epileptiform Activity and Congenital Cardiac Anomalies.

American journal of medical genetics. Part A·2026

PLCG2 downregulation impairs synaptic function and increases Alzheimer's disease hallmarks in neuronal cultures.

Nature genetics·2026

A Young Child With Global Developmental Delay and Epilepsy Secondary to a Novel Variant of KBG Syndrome.

Cureus·2026

Comprehensive Evaluation of Clinical, Developmental, Genetic, and Reproductive Characteristics of 133 Patients with Klinefelter Syndrome.

Molecular syndromology·2026

Deficiency in circulating T cells in four core genotypes mice with Sry translocation.

Journal of immunology (Baltimore, Md. : 1950)·2026

When to think of genetic causes for rhabdomyolysis? A Brazilian single-center exploratory study.

Arquivos de neuro-psiquiatria·2026

Related Experiment Videos

A double dominant genetic mechanism for schizophrenia

Related Concept Videos

Mental abilities of male relatives of psychotic patients.

Relation of mathematical ability to psychosis in Iceland.

Partly dominant transmission of schizophrenia in Iceland.

Family transmission of schizophrenia: a review and synthesis.

Genetic factors in myopia.

Influence of the myopia gene on brain development.

Haplotype-based validation of genomic regions for breeding of new Nordic apples.

miR-335-3p acts as a tumor suppressor in esophageal squamous cell carcinoma and predicts favorable prognosis.

SNP rs7430456 mediated LINC00578 drives triple negative breast cancer through regulating miR-143-5p expression.

BFLF1 gene polymorphisms are associated with increased mortality in patients with EBV-associated diseases.

miR-1-3p, as a novel diagnostic and prognostic biomarker, aggravates pancreatic acinar cell injury in acute pancreatitis by targeting GNPTAB.

Identification of FOXK1 and SEMA7A as key genes associated with m6A-related programmed cell death in diabetic retinopathy.

A Novel de Novo WAC Frameshift Variant in DeSanto-Shinawi Syndrome With Temporo-Occipital Epileptiform Activity and Congenital Cardiac Anomalies.

PLCG2 downregulation impairs synaptic function and increases Alzheimer's disease hallmarks in neuronal cultures.

A Young Child With Global Developmental Delay and Epilepsy Secondary to a Novel Variant of KBG Syndrome.

Comprehensive Evaluation of Clinical, Developmental, Genetic, and Reproductive Characteristics of 133 Patients with Klinefelter Syndrome.

Deficiency in circulating T cells in four core genotypes mice with Sry translocation.

When to think of genetic causes for rhabdomyolysis? A Brazilian single-center exploratory study.

Related Experiment Videos

A double dominant genetic mechanism for schizophrenia

Related Concept Videos

Related Articles