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Brain : a Journal of Neurology|May 1, 2019
Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group reportPeter T Nelson, Dennis W Dickson, John Q Trojanowski, et al.
Nature Communications|July 11, 2024
The transcriptional co-repressor Runx1t1 is essential for MYCN-driven neuroblastoma tumorigenesisJayne E Murray, Emanuele Valli, Giorgio Milazzo, et al.
Neuron|August 18, 2017
TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule DynamicsIan R Mackenzie, Alexandra M Nicholson, Mohona Sarkar, et al.
Molecular Neurodegeneration|September 21, 2014
Genetic modifiers in carriers of repeat expansions in the C9ORF72 geneMarka van Blitterswijk, Bianca Mullen, Aleksandra Wojtas, et al.
Acta Neuropathologica|January 4, 2014
TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementiaMarka van Blitterswijk, Bianca Mullen, Alexandra M Nicholson, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 6, 2023
Pathogenic variants in the Longitudinal Early-onset Alzheimer's Disease Study cohortKelly N H Nudelman, Trever Jackson, Malia Rumbaugh, et al.
American Journal of Human Genetics|December 4, 2018
DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable ImmunodeficiencyClare V Logan, Jennie E Murray, David A Parry, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|September 1, 2023
Influence of amyloid and diagnostic syndrome on non-traditional memory scores in early-onset Alzheimer's diseaseJustin Bushnell, Dustin B Hammers, Paul Aisen, et al.
Science Translational Medicine|September 29, 2021
APOE3-Jacksonville (V236E) variant reduces self-aggregation and risk of dementiaChia-Chen Liu, Melissa E Murray, Xia Li, et al.
Neurology|September 13, 2013
C9ORF72 repeat expansions in cases with previously identified pathogenic mutationsMarka van Blitterswijk, Matthew C Baker, Mariely DeJesus-Hernandez, et al.
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