Publications by authors named "Maura Gallo"

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, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts.
Beatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, Demis A Kia, Miquel Aguilar, Maura Gallo

Neurology· December 2020

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Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.
Brian W Kunkle, Benjamin Grenier-Boley, Rebecca Sims, Joshua C Bis, Vincent Damotte, Maura Gallo

Nat Genet· September 2019

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Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.
Brian W Kunkle, Benjamin Grenier-Boley, Rebecca Sims, Joshua C Bis, Vincent Damotte, Maura Gallo

Nat Genet· March 2019

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Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia.
Raffaele Maletta, Nicoletta Smirne, Livia Bernardi, Maria Anfossi, Maura Gallo

J Alzheimers Dis· January 2019

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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.
Cyril Pottier, Xiaolai Zhou, Ralph B Perkerson, Matt Baker, Gregory D Jenkins, Maura Gallo

Lancet Neurol· June 2018

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Role of Niemann-Pick Type C Disease Mutations in Dementia.
Chiara Cupidi, Francesca Frangipane, Maura Gallo, Alessandra Clodomiro, Rosanna Colao

J Alzheimers Dis· February 2018

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Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.
Rebecca Sims, Sven J van der Lee, Adam C Naj, Céline Bellenguez, Nandini Badarinarayan, Maura Gallo

Nat Genet· September 2017

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The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family.
Maura Gallo, Francesca Frangipane, Chiara Cupidi, Matteo De Bartolo, Sabina Turone

Neurobiol Aging· August 2017

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Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family.
Maria E Conidi, Livia Bernardi, Gianfranco Puccio, Nicoletta Smirne, Maria G Muraca, Maura Gallo

Neurology· June 2015

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Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.
Irene Piaceri, Silvia Pradella, Chiara Cupidi, Serena Nannucci, Cristina Polito, Maura Gallo

J Alzheimers Dis· December 2014

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Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome.
Livia Bernardi, Chiara Cupidi, Francesca Frangipane, Maria Anfossi, Maura Gallo

Neurobiol Aging· November 2014

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Frontotemporal dementia and its subtypes: a genome-wide association study.
Raffaele Ferrari, Dena G Hernandez, Michael A Nalls, Jonathan D Rohrer, Adaikalavan Ramasamy, Maura Gallo

Lancet Neurol· July 2014

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Identification of three novel LRRK2 mutations associated with Parkinson's disease in a Calabrian population.
Maria Anfossi, Rosanna Colao, Maura Gallo, Livia Bernardi, M Elena Conidi

J Alzheimers Dis· June 2014

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Role of TOMM40 rs10524523 polymorphism in onset of alzheimer's disease caused by the PSEN1 M146L mutation.
Livia Bernardi, Maura Gallo, Maria Anfossi, Maria Elena Conidi, Rosanna Colao

J Alzheimers Dis· April 2014

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Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy.
Livia Bernardi, Francesca Frangipane, Nicoletta Smirne, Rosanna Colao, Gianfranco Puccio, Maura Gallo

Neurobiol Aging· December 2012

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A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features.
Maura Gallo, Norina Marcello, Sabrina A M Curcio, Rosanna Colao, Silvana Geracitano

J Alzheimers Dis· November 2011

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Clinical manifestations of highly prevalent corticosteroid-binding globulin mutations in a village in southern Italy.
Giovanni Cizza, Livia Bernardi, Nicoletta Smirne, Raffaele Maletta, Carmine Tomaino, Maura Gallo

J Clin Endocrinol Metab· October 2011

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PSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotype.
Livia Bernardi, Maria Anfossi, Maura Gallo, Silvana Geracitano, Rosanna Cola

J Alzheimers Dis· September 2011

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MAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism?
Maria Anfossi, Livia Bernardi, Maura Gallo, Silvana Geracitano, Rosanna Colao

Alzheimer Dis Assoc Disord· June 2011

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Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia.
Maria Anfossi, Romina Vuono, Raffaele Maletta, Kanwar Virdee, Maria Mirabelli, Maura Gallo

Neurobiol Aging· April 2011

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Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia.
Maura Gallo, Carmine Tomaino, Gianfranco Puccio, Francesca Frangipane, Sabrina A M Curcio

Neurol Sci· February 2010

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AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions.
Livia Bernardi, Silvana Geracitano, Rosanna Colao, Gianfranco Puccio, Maura Gallo

J Alzheimers Dis· December 2009

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Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia.
Livia Bernardi, Carmine Tomaino, Maria Anfossi, Maura Gallo, Silvana Geracitano

Neurobiol Aging· November 2009

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Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism.
Livia Bernardi, Carmine Tomaino, Maria Anfossi, Maura Gallo, Silvana Geracitano

J Neurol· April 2008

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Presenilin 2 Ser130Leu mutation in a case of late-onset "sporadic" Alzheimer's disease.
Carmine Tomaino, Livia Bernardi, Maria Anfossi, Angela Costanzo, Francesca Ferrise, Maura Gallo

J Neurol· March 2007

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