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Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2025
RRP12 Variants Are Associated With Autosomal Recessive Brain CalcificationsEdoardo Monfrini, Paola Rinchetti, Mathieu Anheim, et al.
Nature Medicine|October 26, 2021
Neurological complications after first dose of COVID-19 vaccines and SARS-CoV-2 infectionMartina Patone, Lahiru Handunnetthi, Defne Saatci, et al.
Molecular Psychiatry|January 30, 2023
Pathogenic TRIO variants associated with neurodevelopmental disorders perturb the molecular regulation of TRIO and axon pathfinding in vivoMaxime Bonnet, Fiona Roche, Christine Fagotto-Kaufmann, et al.
Human Molecular Genetics|January 5, 2002
Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosaChristina F Chakarova, Matthew M Hims, Hanno Bolz, et al.
Medrxiv : the Preprint Server for Health Sciences|July 9, 2024
Cortical Lesion Expansion in Chronic Traumatic Brain InjuryHolly J Freeman, Alexander S Atalay, Jian Li, et al.
Frontiers in Neurology|October 31, 2025
Unsupervised semi-automated MRI segmentation detects cortical lesion expansion in chronic traumatic brain injuryHolly J Freeman, Alexander S Atalay, Jian Li, et al.
Biodiversity Data Journal|October 29, 2014
Fauna europaea: helminths (animal parasitic)David I Gibson, Rodney A Bray, David Hunt, et al.
Nature Genetics|May 29, 2025
Analysis of R-loop forming regions identifies RNU2-2 and RNU5B-1 as neurodevelopmental disorder genesAdam Jackson, Nishi Thaker, Alexander Blakes, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 5, 2025
Biomarker discovery using NUcleic Acid-Linked Immuno-Sandwich Assay in multiple sclerosis patients experiencing progression independent of relapse activitySofia Sandgren, Aleksandra Maleska Maceski, Pascal Benkert, et al.
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