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Victoria Van Berlo
Victoria Van Berlo
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Cited by
Cited by
Year
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
4462016
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
942016
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
542020
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
472018
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
442019
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
302019
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
232019
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
212017
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
192019
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
182017
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
112019
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
112017
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
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Articles 1–16