Confirmatory evidence for linkage of relative hand skill to 2p12-q11

Variations of global brain asymmetry are associated with aging and related diseases.

Science advances·2026

Patterns of language and visuospatial lateralisation in three-year-old children.

Neuropsychologia·2026

Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes.

Human genetics·2025

Evaluating the effects of archaic protein-altering variants in living human adults.

Science advances·2025

Functional characterization of pathogenic SATB2 missense variants identifies distinct effects on chromatin binding and transcriptional activity.

HGG advances·2025

Large-scale genetic mapping for human brain asymmetry.

Handbook of clinical neurology·2025

A highly prevalent lupus risk haplotype increases IRF7-dependent induction of IFN-α, enhancing antiviral defense and exacerbating autoimmunity.

American journal of human genetics·2026

CanVar-UK: A collaborative platform for germline interpretation in cancer susceptibility genes.

American journal of human genetics·2026

Distinct cochlear cell types associated with genetic susceptibility to sensory and metabolic hearing loss in older adults.

American journal of human genetics·2026

Functional characterization of the 9q34.13 locus identifies RAPGEF1 as a candidate gene modulating risk for melanoma and nevi via RAS activation.

American journal of human genetics·2026

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

Further delineation of 2p13.2-p11.2 deletion syndrome by optical genome mapping.

Neurogenetics·2026

Bidirectional associations between brain functional networks and sleep disorders: A bidirectional Mendelian randomization study.

Medicine·2026

Duodenal fluid analysis of 13 patients with progressive familial intrahepatic cholestasis type 2 from a single institution.

Medicine·2026

Genetic evidence for CTSH as a potential therapeutic target in sepsis: A Mendelian randomization and colocalization study.

Medicine·2026

Genetic and clinical spectrum of progressive familial intrahepatic cholestasis type 1: novel ATP8B1 variants and genotype-phenotype correlations.

European journal of pediatrics·2026

Genetically supported targets and drug repurposing for sleep disorders: a Mendelian randomization systematic study.

Naunyn-Schmiedeberg's archives of pharmacology·2026

Related Experiment Videos

Confirmatory evidence for linkage of relative hand skill to 2p12-q11

Related Concept Videos

Variations of global brain asymmetry are associated with aging and related diseases.

Patterns of language and visuospatial lateralisation in three-year-old children.

Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes.

Evaluating the effects of archaic protein-altering variants in living human adults.

Functional characterization of pathogenic SATB2 missense variants identifies distinct effects on chromatin binding and transcriptional activity.

Large-scale genetic mapping for human brain asymmetry.

A highly prevalent lupus risk haplotype increases IRF7-dependent induction of IFN-α, enhancing antiviral defense and exacerbating autoimmunity.

CanVar-UK: A collaborative platform for germline interpretation in cancer susceptibility genes.

Distinct cochlear cell types associated with genetic susceptibility to sensory and metabolic hearing loss in older adults.

Functional characterization of the 9q34.13 locus identifies RAPGEF1 as a candidate gene modulating risk for melanoma and nevi via RAS activation.

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.

Further delineation of 2p13.2-p11.2 deletion syndrome by optical genome mapping.

Bidirectional associations between brain functional networks and sleep disorders: A bidirectional Mendelian randomization study.

Duodenal fluid analysis of 13 patients with progressive familial intrahepatic cholestasis type 2 from a single institution.

Genetic evidence for CTSH as a potential therapeutic target in sepsis: A Mendelian randomization and colocalization study.

Genetic and clinical spectrum of progressive familial intrahepatic cholestasis type 1: novel ATP8B1 variants and genotype-phenotype correlations.

Genetically supported targets and drug repurposing for sleep disorders: a Mendelian randomization systematic study.

Related Experiment Videos

Confirmatory evidence for linkage of relative hand skill to 2p12-q11

Related Concept Videos

Related Articles