| Incidence and impact of subclinical epileptiform activity in Alzheimer's disease KA Vossel, KG Ranasinghe, AJ Beagle, D Mizuiri, SM Honma, ... Annals of neurology 80 (6), 858-870, 2016 | 447 | 2016 |
| Neuropathology of autosomal dominant Alzheimer disease in the national Alzheimer coordinating center database JM Ringman, S Monsell, DW Ng, Y Zhou, A Nguyen, G Coppola, ... Journal of Neuropathology & Experimental Neurology 75 (3), 284-290, 2016 | 94 | 2016 |
| Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases EM Ramos, DR Dokuru, V Van Berlo, K Wojta, Q Wang, AY Huang, ... Alzheimer's & Dementia 16 (1), 118-130, 2020 | 55 | 2020 |
| Peripheral blood gene expression reveals an inflammatory transcriptomic signature in Friedreich’s ataxia patients D Nachun, F Gao, C Isaacs, C Strawser, Z Yang, D Dokuru, V Van Berlo, ... Human molecular genetics 27 (17), 2965-2977, 2018 | 46 | 2018 |
| Genetic screen in a large series of patients with primary progressive aphasia EM Ramos, DR Dokuru, V Van Berlo, K Wojta, Q Wang, AY Huang, ... Alzheimer's & Dementia 15 (4), 553-560, 2019 | 43 | 2019 |
| Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia EG Geier, M Bourdenx, NJ Storm, JN Cochran, DW Sirkis, JH Hwang, ... Acta neuropathologica 137, 71-88, 2019 | 30 | 2019 |
| Frontotemporal dementia spectrum: first genetic screen in a Greek cohort EM Ramos, C Koros, DR Dokuru, V Van Berlo, C Kroupis, K Wojta, ... Neurobiology of aging 75, 224. e1-224. e8, 2019 | 23 | 2019 |
| Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian family EM Ramos, A Roca, N Chumchim, DR Dokuru, V Van Berlo, ... Neurogenetics 20, 99-102, 2019 | 19 | 2019 |
| Linking tuberous sclerosis complex, excessive mTOR signaling, and age-related neurodegeneration: a new association between TSC1 mutation and … NT Olney, C Alquezar, EM Ramos, AL Nana, JC Fong, AM Karydas, ... Acta neuropathologica 134, 813-816, 2017 | 18 | 2017 |
| Two novel mutations in the first transmembrane domain of presenilin1 cause young-onset Alzheimer’s disease CY Liu, Y Ohki, T Tomita, S Osawa, BR Reed, W Jagust, V Van Berlo, ... Journal of Alzheimer's Disease 58 (4), 1035-1041, 2017 | 18 | 2017 |
| Systems-level analysis of peripheral blood gene expression in dementia patients reveals an innate immune response shared across multiple disorders D Nachun, EM Ramos, A Karydas, D Dokuru, F Gao, Z Yang, V Van Berlo, ... bioRxiv, 2019.12. 13.875112, 2019 | 11 | 2019 |
| A novel PSEN1 (S230N) mutation causing early-onset Alzheimer’s Disease associated with prosopagnosia, hoarding, and Parkinsonism JM Ringman, M Casado, V Van Berlo, J Pa, N Joseph-Mathurin, ... Neuroscience letters 657, 11-15, 2017 | 11 | 2017 |
| Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases. Alzheimers Dement. 2020; 16 (1): 118–30 EM Ramos, DR Dokuru, V Van Berlo, K Wojta, Q Wang, AY Huang | 6 | |
| Frontotemporal lobar degeneration spectrum: the first genetic screen in a Greek cohort S Lee, EM Ramos, C Kroupis, C Koros, V Van Berlo, K Wojta, Q Wang, ... JOURNAL OF NEUROCHEMISTRY 138, 308-308, 2016 | | 2016 |
| Frontotemporal lobar degeneration spectrum: first genetic screen in a Greek cohort EM Ramos, S Lee, C Kroupis, C Koros, V Van Berlo, K Wojta, Q Wang, ... JOURNAL OF NEUROCHEMISTRY 138, 324-324, 2016 | | 2016 |
| P2‐067: A novel mutation in the first transmembrane portion of PSEN1 causing young‐onset Alzheimer's disease CY Liu, V Van Berlo, G Coppola, JM Ringman Alzheimer's & Dementia 11 (7S_Part_11), P508-P508, 2015 | | 2015 |
