Neuroimaging and the genetics of schizophrenia

Advance-care-planning and end-of-life discussions in the perioperative period: a review of healthcare professionals' knowledge, attitudes, and training.

British journal of anaesthesia·2018

Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia.

Molecular psychiatry·2017

Bridging the translational divide: identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous gene.

Scientific reports·2015

708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits.

Molecular psychiatry·2013

The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data.

Translational psychiatry·2012

The influence of polygenic risk for bipolar disorder on neural activation assessed using fMRI.

Translational psychiatry·2012

CSF p-tau205: a biomarker of Alzheimer's disease progression and biological staging.

Molecular psychiatry·2026

Higher frequencies of CNV deletions in bipolar disorder among Chinese Population.

Molecular psychiatry·2026

Sexual dimorphism of midbrain catecholaminergic metabolism revealed by neuromelanin-sensitive MRI.

Molecular psychiatry·2026

In vivo imaging of synaptic density in psychotropic-free adults with autism spectrum disorder: a [¹¹C]UCB-J PET study.

Molecular psychiatry·2026

Cognitive and synaptic impairment induced by deficiency of autism risk gene Smarcc2 and its rescue by histone deacetylase inhibition.

Molecular psychiatry·2026

A prefrontal cortex-piriform cortex circuit mediates diminished interest.

Molecular psychiatry·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

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Molecular genetics & genomic medicine·2026

Related Experiment Videos

Neuroimaging and the genetics of schizophrenia

Related Concept Videos

Advance-care-planning and end-of-life discussions in the perioperative period: a review of healthcare professionals' knowledge, attitudes, and training.

Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia.

Bridging the translational divide: identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous gene.

708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits.

The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data.

The influence of polygenic risk for bipolar disorder on neural activation assessed using fMRI.

CSF p-tau205: a biomarker of Alzheimer's disease progression and biological staging.

Higher frequencies of CNV deletions in bipolar disorder among Chinese Population.

Sexual dimorphism of midbrain catecholaminergic metabolism revealed by neuromelanin-sensitive MRI.

In vivo imaging of synaptic density in psychotropic-free adults with autism spectrum disorder: a [¹¹C]UCB-J PET study.

Cognitive and synaptic impairment induced by deficiency of autism risk gene Smarcc2 and its rescue by histone deacetylase inhibition.

A prefrontal cortex-piriform cortex circuit mediates diminished interest.

[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.

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Related Experiment Videos

Neuroimaging and the genetics of schizophrenia

Related Concept Videos

Related Articles