Chromosome 3 workshop

Same author

Heritable anisotropy associated with cognitive impairments among patients with schizophrenia and their non-psychotic relatives in multiplex families.

Psychological medicine·2020

Same author

Multiple rare inherited variants in a four generation schizophrenia family offer leads for complex mode of disease inheritance.

Schizophrenia research·2019

Same author

Rare variant based evidence for oligogenic contribution of neurodevelopmental pathway genes to schizophrenia.

Schizophrenia research·2019

Same author

Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study.

Schizophrenia research·2018

Same author

The complement system: a gateway to gene-environment interactions in schizophrenia pathogenesis.

Molecular psychiatry·2017

Same author

Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia.

Schizophrenia research·2017

Same journal

Dissecting causal and putative mechanistic pathways from lifestyle factors to neurological diseases via the glymphatic system: a Mendelian randomization study.

Psychiatric genetics·2026

Same journal

A rare missense variant in Bruton's tyrosine kinase is associated with bipolar disorder accompanied by psychosis.

Psychiatric genetics·2026

Same journal

Identification of rare missense variants of ionotropic glutamate receptor N-methyl-D-aspartate 2 genes in patients with schizophrenia.

Psychiatric genetics·2026

Same journal

Expression and function of miR-218-5p in the pathogenesis of postpartum depression.

Psychiatric genetics·2026

Same journal

Case report of a boy with autism spectrum disorder and lysinuric protein intolerance.

Psychiatric genetics·2026

Same journal

Familial co-occurrence of autism spectrum disorder and 47 XYY syndrome: revisiting the role of Y chromosome dosage in neurodevelopment.

Psychiatric genetics·2026

Related Experiment Videos

Chromosome 3 workshop

Related Concept Videos

Heritable anisotropy associated with cognitive impairments among patients with schizophrenia and their non-psychotic relatives in multiplex families.

Multiple rare inherited variants in a four generation schizophrenia family offer leads for complex mode of disease inheritance.

Rare variant based evidence for oligogenic contribution of neurodevelopmental pathway genes to schizophrenia.

Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study.

The complement system: a gateway to gene-environment interactions in schizophrenia pathogenesis.

Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia.

Dissecting causal and putative mechanistic pathways from lifestyle factors to neurological diseases via the glymphatic system: a Mendelian randomization study.

A rare missense variant in Bruton's tyrosine kinase is associated with bipolar disorder accompanied by psychosis.

Identification of rare missense variants of ionotropic glutamate receptor N-methyl-D-aspartate 2 genes in patients with schizophrenia.

Expression and function of miR-218-5p in the pathogenesis of postpartum depression.

Case report of a boy with autism spectrum disorder and lysinuric protein intolerance.

Familial co-occurrence of autism spectrum disorder and 47 XYY syndrome: revisiting the role of Y chromosome dosage in neurodevelopment.

Related Experiment Videos

Chromosome 3 workshop

Related Concept Videos

Related Articles

Heritable anisotropy associated with cognitive impairments among patients with schizophrenia and their non-psychotic relatives in multiplex families.

Multiple rare inherited variants in a four generation schizophrenia family offer leads for complex mode of disease inheritance.

Rare variant based evidence for oligogenic contribution of neurodevelopmental pathway genes to schizophrenia.

Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study.

The complement system: a gateway to gene-environment interactions in schizophrenia pathogenesis.

Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia.

Dissecting causal and putative mechanistic pathways from lifestyle factors to neurological diseases via the glymphatic system: a Mendelian randomization study.

A rare missense variant in Bruton's tyrosine kinase is associated with bipolar disorder accompanied by psychosis.

Identification of rare missense variants of ionotropic glutamate receptor N-methyl-D-aspartate 2 genes in patients with schizophrenia.

Expression and function of miR-218-5p in the pathogenesis of postpartum depression.

Case report of a boy with autism spectrum disorder and lysinuric protein intolerance.

Familial co-occurrence of autism spectrum disorder and 47 XYY syndrome: revisiting the role of Y chromosome dosage in neurodevelopment.