Parental origin of chromosome 22 alleles lost in meningioma

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Alpha galactosidase A activity in Parkinson's disease.

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Rare susceptibility variants for bipolar disorder suggest a role for G protein-coupled receptors.

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Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.

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Neurons derived from patients with bipolar disorder divide into intrinsically different sub-populations of neurons, predicting the patients' responsiveness to lithium.

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Loss of the proprioception and touch sensation channel PIEZO2 in siblings with a progressive form of contractures.

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Integrating clinical diagnostics with interventional genetics for neurodevelopmental disorders.

American journal of human genetics·2026

Effect heterogeneity reveals complex pleiotropic effects of rare coding variants.

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Monoallelic variants in BRSK1 are associated with a neurodevelopmental disorder with or without epilepsy.

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Genetic data sharing by clinical laboratories in Canada: A position statement by the Canadian College of Medical Geneticists.

American journal of human genetics·2026

Robust cis-by-trans epistasis in the human plasma proteome highlights an ABO-centered interaction network.

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International experiences of genomic newborn screening: Lessons from over 10,800 newborns.

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Pediatric Spinal Cord Astrocytoma With Granular Cell-Like Morphology and KIAA1549::BRAF Fusion.

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Selective vulnerability and resilience of thalamic neuronal populations in Frontotemporal Dementia.

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Parental origin of chromosome 22 alleles lost in meningioma

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Posttranslational modifications & lithium's therapeutic effect-Potential biomarkers for clinical responses in psychiatric & neurodegenerative disorders.

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