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M. Anfossi · SciRah

Researcher profile · Semantic Scholar

M. Anfossi

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M. Anfossi — researcher profile on SciRah

h-index: 20
Works: 50
Citations: 1,578

Most-cited papers

Frontotemporal dementia and its subtypes: a genome-wide association study
R. Ferrari, D. Hernandez, M. Nalls, J. Rohrer +154 more
2014Lancet Neurology350 citations Open access
Semantic Scholar
Early diagnosis of Alzheimer's disease: the role of biomarkers including advanced EEG signal analysis. Report from the IFCN-sponsored panel of experts.
P. M. Rossini, R. Di Iorio, F. Vecchio, M. Anfossi +15 more
2020Clinical Neurophysiology207 citations Open access
Semantic Scholar
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation.
D. Galimberti, C. Fenoglio, M. Serpente, C. Villa +38 more
2013Biological Psychiatry122 citations Open access
Semantic Scholar
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal dementia and GRN mutations: a genome-wide association study
C. Pottier, Xiaolai Zhou, R. B. Perkerson, M. Baker +129 more
2018Lancet Neurology118 citations Open access
Semantic Scholar
Heterogeneity within a large kindred with frontotemporal dementia
A. C. Bruni, P. Momeni, L. Bernardi, C. Tomaino +20 more
2007Neurology81 citations
Semantic Scholar
Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia.
L. Bernardi, C. Tomaino, M. Anfossi, M. Gallo +11 more
2009Neurobiology of Aging62 citations
Semantic Scholar
The process of truth disclosure: an assessment of the results of information during the diagnostic phase in patients with cancer.
G. Numico, M. Anfossi, G. Bertelli, E. Russi +10 more
2009Annals of Oncology57 citations Open access
Semantic Scholar
Epidemiology and genetics of FTD: a door-to-door survey in Southern Italy
L. Bernardi, F. Frangipane, N. Smirne, R. Colao +24 more
2012Neurobiology of Aging48 citations Open access
Semantic Scholar
Worldwide distribution of PSEN1 Met146Leu mutation
A. Bruni, L. Bernardi, R. Colao, E. Rubino +31 more
2010Neurology42 citations Open access
Semantic Scholar
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS
E. Taskesen, A. Mishra, S. van der Sluis, R. Ferrari +158 more
2017Scientific Reports40 citations Open access
Semantic Scholar
The Relationship between Stress and Diabetes Mellitus
G. Falco, Piero Stanley Pirro, E. Castellano, M. Anfossi +2 more
201536 citations Open access
Semantic Scholar
Empathy in the doctor-patient relationship.
M. Anfossi, G. Numico
2004Journal of Clinical Oncology33 citations
Semantic Scholar
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family
M. E. Conidi, L. Bernardi, G. Puccio, N. Smirne +17 more
2015Neurology32 citations Open access
Semantic Scholar
Role of Niemann-Pick Type C Disease Mutations in Dementia
C. Cupidi, F. Frangipane, M. Gallo, A. Clodomiro +17 more
2016Journal of Alzheimer's Disease29 citations
Semantic Scholar
AβPP A713T Mutation in Late Onset Alzheimer's Disease with Cerebrovascular Lesions
L. Bernardi, S. Geracitano, R. Colao, G. Puccio +10 more
2009Journal of Alzheimer's Disease28 citations
Semantic Scholar
author-version of: Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease
Irene Rosas, C. Martínez, J. Clarimón, A. Lleó +31 more
202323 citations Open access
Semantic Scholar
Presenilin 2 Ser130Leu mutation in a case of late-onset “sporadic” Alzheimer’s disease
C. Tomaino, L. Bernardi, M. Anfossi, A. Costanzo +15 more
2007Journal of Neurology23 citations
Semantic Scholar
The Genetic Variability of UCP4 Affects the Individual Susceptibility to Late-Onset Alzheimer's Disease and Modifies the Disease's Risk in APOE-ɛ4 Carriers.
A. Montesanto, Paolina Crocco, M. Anfossi, N. Smirne +6 more
2016Journal of Alzheimer's Disease22 citations
Semantic Scholar
The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family.
M. Gallo, F. Frangipane, C. Cupidi, M. De Bartolo +22 more
2017Neurobiology of Aging21 citations
Semantic Scholar
MAPT V363I Variation in a Sporadic Case of Frontotemporal Dementia: Variable Penetrant Mutation or Rare Polymorphism?
M. Anfossi, L. Bernardi, M. Gallo, S. Geracitano +9 more
2011Alzheimer Disease and Associated Disorders20 citations
Semantic Scholar
Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism
L. Bernardi, C. Tomaino, M. Anfossi, M. Gallo +8 more
2008Journal of Neurology20 citations
Semantic Scholar
Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome.
L. Bernardi, C. Cupidi, F. Frangipane, M. Anfossi +12 more
2014Neurobiology of Aging18 citations
Semantic Scholar
A Novel Pathogenic PSEN1 Mutation in a Family with Alzheimer's Disease: Phenotypical and Neuropathological Features
M. Gallo, N. Marcello, S. Curcio, R. Colao +17 more
2011Journal of Alzheimer's Disease18 citations
Semantic Scholar
Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia.
M. Anfossi, R. Vuono, R. Maletta, K. Virdee +15 more
2011Neurobiology of Aging18 citations
Semantic Scholar
Role of TOMM40 rs10524523 Polymorphism in Onset of Alzheimer's Disease Caused by the PSEN1 M146L Mutation
L. Bernardi, M. Gallo, M. Anfossi, M. E. Conidi +11 more
2013Journal of Alzheimer's Disease17 citations
Semantic Scholar
Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia
M. Gallo, C. Tomaino, G. Puccio, F. Frangipane +10 more
2010Neurological Sciences17 citations
Semantic Scholar
Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia.
Irene Rosas, C. Martínez, E. Coto, J. Clarimón +34 more
2020Neurobiology of Aging13 citations Open access
Semantic Scholar
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
L. Bonham, Natasha Z. R. Steele, C. Karch, Iris J. Broce +166 more
2019Scientific Reports13 citations Open access
Semantic Scholar
Association of the Variant Cys139Arg at GRN Gene to the Clinical Spectrum of Frontotemporal Lobar Degeneration
I. Piaceri, S. Pradella, C. Cupidi, Serena Nannucci +12 more
2014Journal of Alzheimer's Disease13 citations
Semantic Scholar
PSEN1 and PRNP Gene Mutations Co-occurrence Makes Onset Very Early in a Family with FTD Phenotype
L. Bernardi, M. Anfossi, M. Gallo, S. Geracitano +11 more
2011Journal of Alzheimer's Disease10 citations
Semantic Scholar
C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts
Beatrice Costa, C. Manzoni, M. Bernal-Quirós, D. Kia +106 more
2020Neurology9 citations Open access
Semantic Scholar
Estimating the Inheritance of Frontotemporal Lobar Degeneration in the Italian Population
B. Borroni, M. Grassi, M. Bianchi, A. Bruni +17 more
2014Journal of Alzheimer's Disease7 citations
Semantic Scholar
Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis
Yixin Gao, Ting Wang, Xing-Hao Yu, R. Ferrari +158 more
2020Scientific Reports6 citations Open access
Semantic Scholar
Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia
R. Maletta, N. Smirne, L. Bernardi, M. Anfossi +17 more
2018Journal of Alzheimer's Disease6 citations
Semantic Scholar
Angela R.: a familial Alzheimer’s disease case in the days of Auguste D.
L. Borrello, C. Cupidi, V. Laganà, M. Anfossi +5 more
2016Journal of Neurology6 citations Open access
Semantic Scholar
Identification of Three Novel LRRK2 Mutations associated with Parkinson's Disease in a Calabrian Population
M. Anfossi, R. Colao, M. Gallo, L. Bernardi +12 more
2013Journal of Alzheimer's Disease6 citations
Semantic Scholar
Perinatal loss from the health workers point of view: Perception and reaction to an unexpected and potentially traumatic event
G. Gandino, M. Anfossi, I. Vanni, B. Loera
20145 citations
Semantic Scholar
Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS
E. Taskesen, A. Mishra, S. van der Sluis, R. Ferrari +158 more
2018Scientific Reports2 citations Open access
Semantic Scholar
Phenotypic expressions of Alzheimer’s disease: a gender perspective
N. Smirne, P. Notaro, Desirée Addesi, V. Laganà +19 more
20182 citations
Semantic Scholar
P3‐279: A novel progranulin mutation in a large frontotemporal dementia calabrian kindred
F. Frangipane, R. Colao, M. Mirabelli, G. Puccio +18 more
20082 citations
Semantic Scholar
HBV SEROLOGICAL MARKERS IN OCCULT HEPATITIS B: COMPARISON BETWEEN HBV NAT RR AND IR BLOOD DONORS IN THE CALABRIA REGION
L. Bernardi, A. Dominijanni, M. Anfossi, A. Muraca +6 more
2026Transfusion and Apheresis Science0 citations
Semantic Scholar
Psychological care of the diabetic patient
G. Falco, C. Giordana, F. Cavalleri, A. Piacenza +4 more
20180 citations Open access
Semantic Scholar
Immune-related genetic enrichment in frontotemporal dementia
Iris J. Broce, C. Karch, Natalie Wen, C. Fan +181 more
2017bioRxiv0 citations Open access
Semantic Scholar
Primary progressive crossed aphasia in dextrals: report of three cases
T. Piccoli, S. Realmuto, S. Curcio, C. Cupidi +9 more
20130 citations
Semantic Scholar
P3‐277: TAU V363I mutation: Pathogenic or not?
M. Anfossi, L. Bernardi, M. Gallo, S. Geracitano +10 more
20080 citations Open access
Semantic Scholar
Two novel tau mutations associated to a Frontotemporal Dementia Sporadic case: a molecular study
M. Losso, M. Anfossi, L. Bernardi, A. C. Bruni +4 more
20080 citations
Semantic Scholar
A Clinical, Pathological And Molecular Study Of A Frontotemporal Dementia Sporadic Case
M. Losso, R. Vuono, M. Anfossi, L. Bernardi +13 more
20080 citations
Semantic Scholar
P3‐286: Subcortical ischemic vascular dementia: A search for APP gene mutations
S. Geracitano, L. Bernardi, R. Maletta, C. Tomaino +13 more
20080 citations Open access
Semantic Scholar
P3–404: Presenilins mutations are frequent in early–onset familial frontotemporal dementia
R. Maletta, R. Colao, S. Curcio, F. Frangipane +12 more
20060 citations
Semantic Scholar
A two year experience of support group for family members (FM) of cancer patients (CP)
M. Anfossi, R. Peano
19990 citations
Semantic Scholar

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R. Maletta×40
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R. Maletta — researcher profile on SciRah
L. Bernardi×37
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F. Frangipane×34
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M. Gallo×34
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×33

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N. Smirne — researcher profile on SciRah

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R. Colao — researcher profile on SciRah

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A. Bruni — researcher profile on SciRah

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G. Puccio — researcher profile on SciRah

M. Mirabelli×24

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M. Mirabelli — researcher profile on SciRah

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S. Curcio — researcher profile on SciRah

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C. Cupidi — researcher profile on SciRah

M. E. Conidi×17

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M. E. Conidi — researcher profile on SciRah