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Journal of Neural Transmission (Vienna, Austria : 1996)|September 21, 2014
Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortiumIrina Alafuzoff, Maria Pikkarainen, Manuela Neumann, et al.
Experimental Gerontology|June 19, 2012
The need to unify neuropathological assessments of vascular alterations in the ageing brain: multicentre survey by the BrainNet Europe consortiumIrina Alafuzoff, Ellen Gelpi, Safa Al-Sarraj, et al.
Neurobiology of Aging|June 13, 2016
ABCA7 p.G215S as potential protective factor for Alzheimer's diseaseCeleste Sassi, Michael A Nalls, Perry G Ridge, et al.
Nature Medicine|July 4, 2018
Functional diversity and cooperativity between subclonal populations of pediatric glioblastoma and diffuse intrinsic pontine glioma cellsMara Vinci, Anna Burford, Valeria Molinari, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 10, 2025
The spectrum of IDH- and H3-wildtype high-grade glioma subgroups occurring across teenage and young adult patient populationsRita Pereira, Alan Mackay, Yura Grabovska, et al.
Neuro-Oncology Advances|March 30, 2026
Characterization of patient-derived site-specific <i>in vivo</i> models of pediatric-type diffuse high-grade glioma using magnetic resonance imagingJessica K R Boult, Diana M Carvalho, Ketty Kessler, et al.
Human Molecular Genetics|June 29, 2014
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodiesJose Bras, Rita Guerreiro, Lee Darwent, et al.
Nature Communications|May 7, 2025
Genomic landscape of diffuse glioma revealed by whole genome sequencingBen Kinnersley, Josephine Jung, Alex J Cornish, et al.
Neurobiology of Aging|December 9, 2015
Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseasesRita Guerreiro, Valentina Escott-Price, Lee Darwent, et al.
European Journal of Human Genetics : EJHG|June 14, 2012
The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founderBradley N Smith, Stephen Newhouse, Aleksey Shatunov, et al.
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