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Maria Anfossi

Frontotemporal dementia and its subtypes: a genome-wide association study
2014 · Raffaele Ferrari, Dena G Hernandez, et al. · The Lancet Neurology · 397
Early diagnosis of Alzheimer’s disease: the role of biomarkers including advanced EEG signal analysis. Report from the IFCN-sponsored panel of experts
2020 · P.M. Rossini, R. Di Iorio, et al. · Clinical Neurophysiology · 257
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Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study
2018 · Cyril Pottier, Xiaolai Zhou, et al. · The Lancet Neurology · 142
Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia
2018 · Vivek Swarup, Flora I. Hinz, et al. · Nature Medicine · 133
Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation
2013 · Daniela Galimberti, Chiara Fenoglio, et al. · Biological Psychiatry · 120
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CXCR4 involvement in neurodegenerative diseases
2018 · Luke W. Bonham, Celeste M. Karch, et al. · Translational Psychiatry · 98
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Heterogeneity within a large kindred with frontotemporal dementia: A novel progranulin mutation
2007 · A. C. Bruni, P. Momeni, et al. · Neurology · 77
Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia
2008 · Livia Bernardi, Carmine Tomaino, et al. · Neurobiology of Aging · 62
Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood
2022 · Yi-Jun Ge, Ya-Nan Ou, et al. · Biological Psychiatry · 56
Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease
2019 · Irene Rosas, Carmen Martínez, et al. · Neurobiology of Aging · 56
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
2018 · Ming Zhang, Raffaele Ferrari, et al. · Brain · 52
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Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in Southern Italy
2012 · Livia Bernardi, Francesca Frangipane, et al. · Neurobiology of Aging · 48
Exploring Links Between Psychosis and Frontotemporal Dementia Using Multimodal Machine Learning: Dementia Praecox Revisited
2022 · Nikolaos Koutsouleris, Christos Pantelis, et al. · JAMA Psychiatry · 42
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS
2017 · E. Taskesen, A. Mishra, et al. · Scientific Reports · 42
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Worldwide distribution of PSEN1 Met146Leu mutation: A large variability for a founder mutation
2010 · A. C. Bruni, L. Bernardi, et al. · Neurology · 40
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Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family
2015 · Maria E. Conidi, Livia Bernardi, et al. · Neurology · 33
Role of Niemann-Pick Type C Disease Mutations in Dementia
2016 · Chiara Cupidi, Francesca Frangipane, et al. · Journal of Alzheimer s Disease · 31
AβPP A713T Mutation in Late Onset Alzheimer's Disease with Cerebrovascular Lesions
2009 · Livia Bernardi, Silvana Geracitano, et al. · Journal of Alzheimer s Disease · 26
The Genetic Variability of UCP4 Affects the Individual Susceptibility to Late-Onset Alzheimer’s Disease and Modifies the Disease’s Risk in APOE- ɛ 4 Carriers
2016 · Alberto Montesanto, Paolina Crocco, et al. · Journal of Alzheimer s Disease · 24
Presenilin 2 Ser130Leu mutation in a case of late-onset “sporadic” Alzheimer’s disease
2007 · Carmine Tomaino, Livia Bernardi, et al. · Journal of Neurology · 22
Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes
2021 · Lianne M. Reus, Bogdan Pasaniuc, et al. · Biological Psychiatry · 21
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Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome
2014 · Livia Bernardi, Chiara Cupidi, et al. · Neurobiology of Aging · 20
The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family
2017 · Maura Gallo, Francesca Frangipane, et al. · Neurobiology of Aging · 19
Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia
2009 · Maura Gallo, Carmine Tomaino, et al. · Neurological Sciences · 18
Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia
2011 · Maria Anfossi, Romina Vuono, et al. · Neurobiology of Aging · 17
Works count: 59
Citation count: 2,038
H-index: 21
I10-index: 34
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