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Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2012
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's diseaseLaura L Kilarski, Justin P Pearson, Victoria Newsway, et al.
EMBO Reports|January 4, 2024
The NSP3 protein of SARS-CoV-2 binds fragile X mental retardation proteins to disrupt UBAP2L interactionsDimitriya H Garvanska, R Elias Alvarado, Filip Oskar Mundt, et al.
Brain : a Journal of Neurology|April 13, 2026
Data-driven modelling of tau pathology reveals distinct progressive supranuclear palsy subtypesPatrick W Cullinane, Jacy Bezerra Parmera, Hemanth Nelvagal, et al.
Clinical Epigenetics|June 9, 2015
The GALNT9, BNC1 and CCDC8 genes are frequently epigenetically dysregulated in breast tumours that metastasise to the brainRajendra P Pangeni, Prasanna Channathodiyil, David S Huen, et al.
Nature Communications|September 16, 2024
USP50 suppresses alternative RecQ helicase use and deleterious DNA2 activity during replicationHannah L Mackay, Helen R Stone, George E Ronson, et al.
Scientific Reports|January 4, 2023
Prevalence of pre-eclampsia and adverse pregnancy outcomes in women with pre-existing cardiomyopathy: a multi-centre retrospective cohort studyLaura Ormesher, Sarah Vause, Suzanne Higson, et al.
Cell Stem Cell|September 5, 2025
Nanobioreactor detection of space-associated hematopoietic stem and progenitor cell agingJessica Pham, Jane Isquith, Larisa Balaian, et al.
Human Molecular Genetics|August 16, 2012
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's diseaseMargaux F Keller, Mohamad Saad, Jose Bras, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
CNV-Finder: Streamlining Copy Number Variation DiscoveryNicole Kuznetsov, Kensuke Daida, Mary B Makarious, et al.
Human Molecular Genetics|December 11, 2012
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's diseasePeter Holmans, Valentina Moskvina, Lesley Jones, et al.
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