Candidate-gene association 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

The dynamic interplay between sleep and mood: an intensive longitudinal study of individuals with bipolar disorder.

Psychological medicine·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

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

Investigating the genetic underpinnings of early-life irritability.

Translational psychiatry·2017

The Gabriella Miller Kids First Data Resource for genomic research in pediatric cancer and congenital anomalies.

American journal of human genetics·2026

Shared inheritance reveals landscape of somatic and germline cancer risk in TP53.

American journal of human genetics·2026

Examining gaps in institutional policies for clinical genomic data sharing: A cross-jurisdictional study.

American journal of human genetics·2026

Anthropometric and cardio-metabolic trait variation and genetic associations in sub-Saharan Africa.

American journal of human genetics·2026

Systematic and proactive evaluation of AIRE missense variant effects.

American journal of human genetics·2026

Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features.

American journal of human genetics·2026

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Pediatrics international : official journal of the Japan Pediatric Society·2026

Proteome-wide QTL mapping enables gene-protein-phenotype metabolic network construction in a genetically diverse MASLD mouse model.

bioRxiv : the preprint server for biology·2026

Sequence determinants of pathogenicity in glucose-6-phosphatase linked to glycogen storage disease type 1a.

bioRxiv : the preprint server for biology·2026

Estimating the Penetrance of PRNP Mutations in Chinese Prion Disease Patients based on the Genome Databases.

Genomics, proteomics & bioinformatics·2026

Genome-wide linkage and association mapping identified a novel candidate gene, TaGLK-A1, underlying fructan content in wheat grain.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2026

Deletion of ARPKD-associated Pkhd1 gene in mice results in decreased Tfap2b expression and eye abnormalities.

Nature communications·2026

Related Experiment Videos

Candidate-gene association 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.

The dynamic interplay between sleep and mood: an intensive longitudinal study of individuals with bipolar disorder.

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

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.

Investigating the genetic underpinnings of early-life irritability.

The Gabriella Miller Kids First Data Resource for genomic research in pediatric cancer and congenital anomalies.

Shared inheritance reveals landscape of somatic and germline cancer risk in TP53.

Examining gaps in institutional policies for clinical genomic data sharing: A cross-jurisdictional study.

Anthropometric and cardio-metabolic trait variation and genetic associations in sub-Saharan Africa.

Systematic and proactive evaluation of AIRE missense variant effects.

Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features.

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Proteome-wide QTL mapping enables gene-protein-phenotype metabolic network construction in a genetically diverse MASLD mouse model.

Sequence determinants of pathogenicity in glucose-6-phosphatase linked to glycogen storage disease type 1a.

Estimating the Penetrance of PRNP Mutations in Chinese Prion Disease Patients based on the Genome Databases.

Genome-wide linkage and association mapping identified a novel candidate gene, TaGLK-A1, underlying fructan content in wheat grain.

Deletion of ARPKD-associated Pkhd1 gene in mice results in decreased Tfap2b expression and eye abnormalities.

Related Experiment Videos

Candidate-gene association studies of schizophrenia

Related Concept Videos

Related Articles