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| 37525358 | Senile plaque-associated transactive response DNA-binding protein 43 in Alzheimer's disease: A case report spanning 16â¿¿years of memory loss. | Neuropathology | 2024 |
| 37831661 | Uncovering the distinct macro-scale anatomy of dysexecutive and behavioural degenerative diseases. | Brain | 2024 |
| 37827570 | Temporal course of cognitive and behavioural changes in motor neuron diseases. | J Neurol Neurosurg Psychiatry | 2024 |
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| 38093787 | Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions in Alzheimer's disease. | Free Neuropathol | 2023 |
| 37563165 | Frontotemporal lobar degeneration. | Nat Rev Dis Primers | 2023 |
| 37386798 | Psychotic symptoms in frontotemporal dementia with TDP-43 tend to be associated with type B pathology. | Neuropathol Appl Neurobiol | 2023 |
| 37182869 | Comparison of Clinical, Genetic, and Pathologic Features of Limbic and Diffuse Transactive Response DNA-Binding Protein 43 Pathology in Alzheimer's Disease Neuropathologic Spectrum. | J Alzheimers Dis | 2023 |
| 37077569 | Case report: TMEM106B haplotype alters penetrance of GRN mutation in frontotemporal dementia family. | Front Neurol | 2023 |
| 37171891 | NanoPack2: population-scale evaluation of long-read sequencing data. | Bioinformatics | 2023 |
| 37171635 | Limbic-predominant age-related TDP-43 proteinopathy (LATE-NC) is associated with abundant TMEM106B pathology. | Acta Neuropathol | 2023 |
| 37100087 | C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypes. | Brain | 2023 |
| 37163045 | Creating the Pick's disease International Consortium: Association study of <i>MAPT</i> H2 haplotype with risk of Pick's disease. | medRxiv | 2023 |
| 37327267 | The SERPINA5 coding variant E228Q does not contribute to clinicopathologic characteristics in Alzheimer's disease: A cross-sectional study. | Medicine (Baltimore) | 2023 |
| 36546684 | APOE2 Exacerbates TDP-43 Related Toxicity in the Absence of Alzheimer Pathology. | Ann Neurol | 2023 |
| 36607424 | Correction to: Accumulation of TMEM106B Câ¿¿terminal fragments in neurodegenerative disease and aging. | Acta Neuropathol | 2023 |
| 34823271 | Concurrent tau pathologies in frontotemporal lobar degeneration with TDP-43 pathology. | Neuropathol Appl Neurobiol | 2022 |
| 35790423 | Differences in Motor Features of <i>C9orf72</i>, <i>MAPT</i>, or <i>GRN</i> Variant Carriers With Familial Frontotemporal Lobar Degeneration. | Neurology | 2022 |
| 35810449 | GRN Mutations Are Associated with Lewy Body Dementia. | Mov Disord | 2022 |
| 36632182 | White-matter abnormalities in presymptomatic <i>GRN</i> and <i>C9orf72</i> mutation carriers. | Brain Commun | 2022 |
| 36001141 | Atypical Alzheimer's disease phenotypes with normal or borderline PET biomarker profiles. | J Neurol | 2022 |
| 36056242 | Identification of TMEM106B amyloid fibrils provides an updated view of TMEM106B biology in health and disease. | Acta Neuropathol | 2022 |
| 34918030 | Shared brain transcriptomic signature in TDP-43 type A FTLD patients with or without GRN mutations. | Brain | 2022 |
| 35247328 | Homotypic fibrillization of TMEM106B across diverse neurodegenerative diseases. | Cell | 2022 |
| 35047667 | Revealing the Mutational Spectrum in Southern Africans With Amyotrophic Lateral Sclerosis. | Neurol Genet | 2022 |
| 32843152 | Underlying genetic variation in familial frontotemporal dementia: sequencing of 198 patients. | Neurobiol Aging | 2021 |
| 33568542 | Association of Mitochondrial DNA Genomic Variation With Risk of Pick Disease. | Neurology | 2021 |
| 33709463 | Loss of Tmem106b leads to cerebellum Purkinje cell death and motor deficits. | Brain Pathol | 2021 |
| 33756466 | Neurobehavioral Characteristics of FDG-PET Defined Right-Dominant Semantic Dementia: A Longitudinal Study. | Dement Geriatr Cogn Disord | 2021 |
| 33889947 | Long-read targeted sequencing uncovers clinicopathological associations for C9orf72-linked diseases. | Brain | 2021 |
| 33861770 | Impact of variant-level batch effects on identification of genetic risk factors in large sequencing studies. | PLoS One | 2021 |
| 33635380 | Latent trait modeling of tau neuropathology in progressive supranuclear palsy. | Acta Neuropathol | 2021 |
| 34687211 | SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration. | Brain | 2021 |
| 33969528 | Old age genetically confirmed frontotemporal lobar degeneration with TDP-43 has limbic predominant TDP-43 deposition. | Neuropathol Appl Neurobiol | 2021 |
| 34103532 | A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speech. | Nat Commun | 2021 |
| 34049163 | FDG-PET in presymptomatic C9orf72 mutation carriers. | Neuroimage Clin | 2021 |
| 33433878 | Lysosomal Dysfunction and Other Pathomechanisms in FTLD: Evidence from Progranulin Genetics and Biology. | Adv Exp Med Biol | 2021 |
| 33247623 | Brain volumetric deficits in MAPT mutation carriers: a multisite study. | Ann Clin Transl Neurol | 2021 |
| 33274526 | Lewy Body Disease is a Contributor to Logopenic Progressive Aphasia Phenotype. | Ann Neurol | 2021 |
| 33270986 | Machine learning suggests polygenic risk for cognitive dysfunction in amyotrophic lateral sclerosis. | EMBO Mol Med | 2021 |
| 31272932 | Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration. | Alzheimers Dement | 2020 |
| 32000838 | Elevated methylation levels, reduced expression levels, and frequent contractions in a clinical cohort of C9orf72 expansion carriers. | Mol Neurodegener | 2020 |
| 31810826 | Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study. | Lancet Neurol | 2020 |
| 31784375 | Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration. | Alzheimers Dement | 2020 |
| 31636026 | The longitudinal evaluation of familial frontotemporal dementia subjects protocol: Framework and methodology. | Alzheimers Dement | 2020 |
| 31955222 | Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity. | Acta Neuropathol | 2020 |
| 31918955 | Trajectory of lobar atrophy in asymptomatic and symptomatic GRN mutation carriers: a longitudinal MRI study. | Neurobiol Aging | 2020 |
| 31857710 | Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein. | Nat Neurosci | 2020 |
| 31914230 | Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint. | Alzheimers Dement | 2020 |