Genetics of bipolar affective disorder: time for another reinvention?

Alcohol consumption and telomere length: Mendelian randomization clarifies alcohol's effects.

Molecular psychiatry·2022

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls.

Psychological medicine·2018

Trauma exposure interacts with the genetic risk of bipolar disorder in alcohol misuse of US soldiers.

Acta psychiatrica Scandinavica·2017

Genome-wide association study identifies a novel locus for cannabis dependence.

Molecular psychiatry·2017

Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence.

Molecular psychiatry·2017

A genome-wide gene-by-trauma interaction study of alcohol misuse in two independent cohorts identifies PRKG1 as a risk locus.

Molecular psychiatry·2017

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

American journal of human genetics·2026

Beyond exons: Linking noncoding heritability and polygenicity across complex human traits and disorders.

American journal of human genetics·2026

Phenome- and laboratory-wide meta-analyses of sickle cell trait reveal multi-system disease associations.

American journal of human genetics·2026

Mutation rate heterogeneity biases variant effect prediction and reveals genuine mutational robustness.

American journal of human genetics·2026

A phenotypic paradigm for cerebral palsy genetics.

American journal of human genetics·2026

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson syndrome.

American journal of human genetics·2026

Spatial isoform sequencing at single-cell resolution reveals cell-type-specific spatial isoform variability in multiple brain cell types.

Nature methods·2026

Large-scale single-molecule analysis of tau proteoforms.

Nature methods·2026

Gene-Chronos: parameter-efficient developmental time inference using a pretrained single-cell foundation model.

Briefings in bioinformatics·2026

Improving long-read somatic structural variant calling with pangenome and de novo personal genome assembly.

Cancer research communications·2026

Glycemic and bodyweight effects of GIPR coding variation reflect differences in surface expression and intrinsic functional impairment.

Science advances·2026

Upscaling Genotyping by Amplicon Sequencing With GBAS-GUI.

Molecular ecology resources·2026

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Genetics of bipolar affective disorder: time for another reinvention?

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Alcohol consumption and telomere length: Mendelian randomization clarifies alcohol's effects.

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls.

Trauma exposure interacts with the genetic risk of bipolar disorder in alcohol misuse of US soldiers.

Genome-wide association study identifies a novel locus for cannabis dependence.

Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence.

A genome-wide gene-by-trauma interaction study of alcohol misuse in two independent cohorts identifies PRKG1 as a risk locus.

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

Beyond exons: Linking noncoding heritability and polygenicity across complex human traits and disorders.

Phenome- and laboratory-wide meta-analyses of sickle cell trait reveal multi-system disease associations.

Mutation rate heterogeneity biases variant effect prediction and reveals genuine mutational robustness.

A phenotypic paradigm for cerebral palsy genetics.

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson syndrome.

Spatial isoform sequencing at single-cell resolution reveals cell-type-specific spatial isoform variability in multiple brain cell types.

Large-scale single-molecule analysis of tau proteoforms.

Gene-Chronos: parameter-efficient developmental time inference using a pretrained single-cell foundation model.

Improving long-read somatic structural variant calling with pangenome and de novo personal genome assembly.

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