The Neurogenetics Collection: emerging themes and future considerations for the field in Brain

Strenuous physical activity is associated with a younger age of amyotrophic lateral sclerosis onset in two independent cohorts.

Brain communications·2026

Pathology and Genetics in a Global Cohort of Parkinsonian Disorders.

JAMA neurology·2026

The Motor Neuron Disease Register for England, Wales, and Northern Ireland: Protocol for a Population Register.

JMIR research protocols·2026

CYP2D6 variants in amyotrophic lateral sclerosis: an association study of risk and survival.

Brain : a journal of neurology·2026

Machine learning model based on plasma proteomics for the identification of Parkinson's disease.

Brain : a journal of neurology·2026

Pathology and genetics in a global cohort of Parkinsonian Disorders.

medRxiv : the preprint server for health sciences·2026

Neurological disease progression in adults with ataxia telangiectasia: a longitudinal study.

Brain : a journal of neurology·2026

Diabetes and neurodegeneration in cognitively unimpaired older adults: implications for cognition.

Brain : a journal of neurology·2026

Lytic Epstein-Barr virus infection and emerging autoantibodies precede multiple sclerosis prodrome.

Brain : a journal of neurology·2026

Divergent tau pathology profiles induced by distinct alpha-synuclein aggregates in non-human primates.

Brain : a journal of neurology·2026

Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

Brain : a journal of neurology·2026

Mechanochemical endothelial-astrocyte signalling via Piezo1-Epac1 drives neurovascular injury after stroke.

Brain : a journal of neurology·2026

Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.

Bioinformatics (Oxford, England)·2026

Association of HTR2A (rs6313) gene polymorphism with autism spectrum disorder in Jordanian children: a case-control study.

Drug metabolism and personalized therapy·2026

Single-cell Transcriptome-wide Mendelian Randomization and Colocalization Converge on Astrocytic TRIM66 as a Candidate Driver and Potential Therapeutic Target for Trigeminal Neuralgia.

Current medicinal chemistry·2026

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

American journal of medical genetics. Part A·2026

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

Human mutation·2026

Functional genomics in Xenopus identifies ARHGAP10 as a congenital heart disease and ciliopathy gene.

iScience·2026

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The Neurogenetics Collection: emerging themes and future considerations for the field in Brain

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Strenuous physical activity is associated with a younger age of amyotrophic lateral sclerosis onset in two independent cohorts.

Pathology and Genetics in a Global Cohort of Parkinsonian Disorders.

The Motor Neuron Disease Register for England, Wales, and Northern Ireland: Protocol for a Population Register.

CYP2D6 variants in amyotrophic lateral sclerosis: an association study of risk and survival.

Machine learning model based on plasma proteomics for the identification of Parkinson's disease.

Pathology and genetics in a global cohort of Parkinsonian Disorders.

Neurological disease progression in adults with ataxia telangiectasia: a longitudinal study.

Diabetes and neurodegeneration in cognitively unimpaired older adults: implications for cognition.

Lytic Epstein-Barr virus infection and emerging autoantibodies precede multiple sclerosis prodrome.

Divergent tau pathology profiles induced by distinct alpha-synuclein aggregates in non-human primates.

Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

Mechanochemical endothelial-astrocyte signalling via Piezo1-Epac1 drives neurovascular injury after stroke.

Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.

Association of HTR2A (rs6313) gene polymorphism with autism spectrum disorder in Jordanian children: a case-control study.

Single-cell Transcriptome-wide Mendelian Randomization and Colocalization Converge on Astrocytic TRIM66 as a Candidate Driver and Potential Therapeutic Target for Trigeminal Neuralgia.

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

Functional genomics in Xenopus identifies ARHGAP10 as a congenital heart disease and ciliopathy gene.

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The Neurogenetics Collection: emerging themes and future considerations for the field in Brain

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