Schizophrenia: new phenes and new genes

Genetic vulnerability to DUSP22 promoter hypermethylation is involved in the relation between in utero famine exposure and schizophrenia.

NPJ schizophrenia·2018

GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.

Molecular psychiatry·2017

Longitudinal analyses of the DNA methylome in deployed military servicemen identify susceptibility loci for post-traumatic stress disorder.

Molecular psychiatry·2017

Investigating the neuroimmunogenic architecture of schizophrenia.

Molecular psychiatry·2017

Altered expression of histamine signaling genes in autism spectrum disorder.

Translational psychiatry·2017

GAD1 alternative transcripts and DNA methylation in human prefrontal cortex and hippocampus in brain development, schizophrenia.

Molecular psychiatry·2017

Stress-related psychopathology shapes episodic memory development in youth: Network-level brain predictors and relations with early-life stress.

Biological psychiatry·2026

Recent progress of large-scale biomarker consortia and paths forward in biomarker development for autism.

Biological psychiatry·2026

Revisiting the Links Between Asthma and the Psychosis Spectrum: shared molecular mechanisms.

Biological psychiatry·2026

A Contrastive Framework for Modeling Brain Heterogeneity in Precision Mental Health.

Biological psychiatry·2026

Neuromodulation in Alzheimer's disease: a review with illustrative pilot data using focused ultrasound.

Biological psychiatry·2026

Cortical Hub Vulnerability and Molecular Signatures of Sulcal Widening in Schizophrenia.

Biological psychiatry·2026

Hyperexcitability in hippocampal CA1 pyramidal cells OF Fmr1 knockout mice emerges during late postnatal development.

Neuroscience·2026

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

American journal of medical genetics. Part A·2026

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

International journal of molecular sciences·2026

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

International journal of molecular sciences·2026

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

Cells·2026

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

Related Experiment Videos

Schizophrenia: new phenes and new genes

Related Concept Videos

Genetic vulnerability to DUSP22 promoter hypermethylation is involved in the relation between in utero famine exposure and schizophrenia.

GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.

Longitudinal analyses of the DNA methylome in deployed military servicemen identify susceptibility loci for post-traumatic stress disorder.

Investigating the neuroimmunogenic architecture of schizophrenia.

Altered expression of histamine signaling genes in autism spectrum disorder.

GAD1 alternative transcripts and DNA methylation in human prefrontal cortex and hippocampus in brain development, schizophrenia.

Stress-related psychopathology shapes episodic memory development in youth: Network-level brain predictors and relations with early-life stress.

Recent progress of large-scale biomarker consortia and paths forward in biomarker development for autism.

Revisiting the Links Between Asthma and the Psychosis Spectrum: shared molecular mechanisms.

A Contrastive Framework for Modeling Brain Heterogeneity in Precision Mental Health.

Neuromodulation in Alzheimer's disease: a review with illustrative pilot data using focused ultrasound.

Cortical Hub Vulnerability and Molecular Signatures of Sulcal Widening in Schizophrenia.

Hyperexcitability in hippocampal CA1 pyramidal cells OF Fmr1 knockout mice emerges during late postnatal development.

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Related Experiment Videos

Schizophrenia: new phenes and new genes

Related Concept Videos

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