Molecular genetic studies of schizophrenia

Genetic risk for schizophrenia is associated with increased proportion of indirect connections in brain networks revealed by a semi-metric analysis: evidence from population sample stratified for polygenic risk.

Cerebral cortex (New York, N.Y. : 1991)·2022

Genetic risk for schizophrenia is associated with altered visually-induced gamma band activity: evidence from a population sample stratified polygenic risk.

Translational psychiatry·2021

Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS).

Psychological medicine·2019

Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation.

Psychological medicine·2018

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.

Molecular psychiatry·2018

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.

Translational psychiatry·2017

Critical role of actin in modulating BBB permeability.

Brain research. Brain research reviews·2005

Dual role of nitric oxide in adult neurogenesis.

Brain research. Brain research reviews·2005

Dopamine-glutamate reciprocal modulation of release and motor responses in the rat caudate-putamen and nucleus accumbens of "intact" animals.

Brain research. Brain research reviews·2005

CNS injury research; reviewing the last decade: methodological errors and a proposal for a new strategy.

Brain research. Brain research reviews·2005

Contribution from neurophysiological and psychological methods to the study of motor imagery.

Brain research. Brain research reviews·2005

Ceruloplasmin in neurodegenerative diseases.

Brain research. Brain research reviews·2005

Wilson disease associated with a novel variant in the ATP7B gene.

Frontiers in neurology·2026

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Scientific reports·2026

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Journal of genetics and genomics = Yi chuan xue bao·2026

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Clinica chimica acta; international journal of clinical chemistry·2026

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

Brain & development·2026

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

The Journal of heredity·2026

Related Experiment Videos

Molecular genetic studies of schizophrenia

Related Concept Videos

Genetic risk for schizophrenia is associated with increased proportion of indirect connections in brain networks revealed by a semi-metric analysis: evidence from population sample stratified for polygenic risk.

Genetic risk for schizophrenia is associated with altered visually-induced gamma band activity: evidence from a population sample stratified polygenic risk.

Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS).

Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation.

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.

Critical role of actin in modulating BBB permeability.

Dual role of nitric oxide in adult neurogenesis.

Dopamine-glutamate reciprocal modulation of release and motor responses in the rat caudate-putamen and nucleus accumbens of "intact" animals.

CNS injury research; reviewing the last decade: methodological errors and a proposal for a new strategy.

Contribution from neurophysiological and psychological methods to the study of motor imagery.

Ceruloplasmin in neurodegenerative diseases.

Wilson disease associated with a novel variant in the ATP7B gene.

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

Related Experiment Videos

Molecular genetic studies of schizophrenia

Related Concept Videos

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