Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsVivianna M. Van Deerlin, Howard Feldman, John C. van Swieten et al.|Nature Genetics|2010Cited by 608
TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13AAnna‐Leigh Brown, Mary Poss, Pietro Fratta et al.|Nature|2022Cited by 510
Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated GliaOliver H. Tam, Molly Hammell, Robert W. Baloh et al.|Cell Reports|2019Cited by 333
T cell lymphoma and secondary primary malignancy risk after commercial CAR T cell therapyGuido Ghilardi, Marco Ruella, Joseph A. Fraietta et al.|Nature Medicine|2024Cited by 254
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiativeRosa Rademakers, Mike Hutton, Matt Baker et al.|The Lancet Neurology|2007Cited by 217