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Scientific Reports|October 19, 2017
Minimal methylation classifier (MIMIC): A novel method for derivation and rapid diagnostic detection of disease-associated DNA methylation signaturesE C Schwalbe, D Hicks, G Rafiee, et al.
The Journal of Clinical Investigation|May 4, 2021
Huntington's disease mice and human brain tissue exhibit increased G3BP1 granules and TDP43 mislocalizationIsabella I Sanchez, Thai B Nguyen, Whitney E England, et al.
Communications Biology|March 18, 2022
Characterisation of PDGF-BB:PDGFRβ signalling pathways in human brain pericytes: evidence of disruption in Alzheimer's diseaseLeon C D Smyth, Blake Highet, Deidre Jansson, et al.
Acta Neuropathologica Communications|March 25, 2022
Neutrophil-vascular interactions drive myeloperoxidase accumulation in the brain in Alzheimer's diseaseLeon C D Smyth, Helen C Murray, Madison Hill, et al.
Science Advances|July 19, 2024
Huntingtin is an RNA binding protein and participates in <i>NEAT1</i>-mediated paraspecklesManisha Yadav, Rachel J Harding, Tiantian Li, et al.
Clinical Oral Implants Research|February 24, 2026
Consensus Report of Group 4 of the 1st Global Consensus for Clinical Guidelines for the Rehabilitation of the Edentulous Maxilla: Conventional Dentures, Implant Overdentures and Implant-Supported Fixed Dental ProsthesesCharlotte Stilwell, Ronald E Jung, Florian Beuer, et al.
Science Advances|February 13, 2019
<i>Porphyromonas gingivalis</i> in Alzheimer's disease brains: Evidence for disease causation and treatment with small-molecule inhibitorsStephen S Dominy, Casey Lynch, Florian Ermini, et al.
Nature Communications|April 9, 2025
Mutant huntingtin induces neuronal apoptosis via derepressing the non-canonical poly(A) polymerase PAPD5Zhefan Stephen Chen, Shaohong Isaac Peng, Lok I Leong, et al.
Human Molecular Genetics|July 13, 1999
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndromeD J Marsh, J B Kum, K L Lunetta, et al.
American Journal of Human Genetics|July 1, 1996
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeatsD C Rubinsztein, J Leggo, R Coles, et al.
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