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Plos One|May 3, 2014
Marine litter distribution and density in European seas, from the shelves to deep basinsChristopher K Pham, Eva Ramirez-Llodra, Claudia H S Alt, et al.
Archives of Disease in Childhood|December 23, 2020
COVID-19 in children treated with immunosuppressive medication for kidney diseasesMatko Marlais, Tanja Wlodkowski, Samhar Al-Akash, et al.
Plos Genetics|September 20, 2008
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosisNicola J Rutherford, Yong-Jie Zhang, Matt Baker, et al.
Neurobiology of Aging|July 31, 2012
Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotypeNicola J Rutherford, Michael G Heckman, Mariely Dejesus-Hernandez, et al.
Neurobiology of Aging|May 29, 2014
Ataxin-2 as potential disease modifier in C9ORF72 expansion carriersMarka van Blitterswijk, Bianca Mullen, Michael G Heckman, 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.
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.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
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