Viviana Pensato

Fondazione IRCCS Istituto Neurologico Carlo Besta

Italy

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Articles (17)

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2024

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2023

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2022

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2020

Collaborators (41)

Franco Taroni

Head

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Ashley Jones

King’s College London

UNITED KINGDOM

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Nilo Riva

ITALY

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Frank Baas

Professor of Genome Diagnostics

Leiden University

NETHERLANDS

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Marka van Blitterswijk

Associate Professor

Mayo Clinic

UNITED STATES

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Jennifer Phillips-Cremins

Associate Professor

University of Pennsylvania

UNITED STATES

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Silvia Fenu

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Daniela Di Bella

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Pierpaola Tannorella

Istituto Auxologico Italiano

ITALY

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Charles Curtis

King’s College London

UNITED KINGDOM

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Dominic Rowe

Macquarie University

AUSTRALIA

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Bradley Smith

King’s College London

UNITED KINGDOM

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Stéphanie Millecamps

Sorbonne Université

FRANCE

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Russell McLaughlin

Ussher Assistant Professor in Genome Analysis

Trinity College Dublin

IRELAND

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Sandra D'Alfonso

Università degli Studi del Piemonte Orientale Amedeo Avogadro

ITALY

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Paola Caroppo

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Paolo Volanti

Head

Istituti Clinici Scientifici Maugeri SpA IRCCS Lumezzane

ITALY

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Michael Sendtner

Professor for Clinical Neurobiology

University of Würzburg

GERMANY

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Mariarita Galbiati

Associate Professor

Università degli Studi di Torino

ITALY

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Danny Miller

Assistant Professor

University of Washington

UNITED STATES

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simon topp

King’s College London

UNITED KINGDOM

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Ewout J. N. Groen

NETHERLANDS

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Frederik Steyn

Senior Lecturer/Group Leader

University of Queensland

AUSTRALIA

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Kelly Williams

Macquarie University

AUSTRALIA

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Anna Maria Aloisi

University of Siena

ITALY

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Lyle Ostrow

Associate Professor

Temple University

UNITED STATES

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Julian Großkreutz

University of Lübeck

GERMANY

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Mark K Bakker

NETHERLANDS

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Jonathan Mill

Professor

University of Exeter

UNITED KINGDOM

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Garth Nicholson

Professor

AUSTRALIA

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Julia Kraft

Charité - Universitätsmedizin Berlin

GERMANY

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Marcella Zollino

Università Cattolica del Sacro Cuore

ITALY

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Sarah Furlong

Macquarie University

AUSTRALIA

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John Landers

University of Massachusetts Chan Medical School

UNITED STATES

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Stuart Pickering-Brown

The University of Manchester

UNITED KINGDOM

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Caroline Vance

King’s College London

UNITED KINGDOM

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Angelica Nordin

University Hospital of Umeå

SWEDEN

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Oleg Butovsky

Associate Professor of Neurology

Brigham and Women's Hospital

UNITED STATES

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monica consonni

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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ALESSANDRA FERLINI

University of Ferrara

ITALY

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Francesca Brett

Clinical Associate Professor

IRELAND

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Viviana Pensato

Research Interests

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Articles (17)

Altered molecular and cellular mechanisms in KIF5A-associated neurodegenerative or neurodevelopmental disorders

MiR-146a in ALS: Contribution to Early Peripheral Nerve Degeneration and Relevance as Disease Biomarker

Behavioral and Cognitive Phenotypes of Patients With Amyotrophic Lateral Sclerosis Carrying SOD1 Variants

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.

Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects

Identification of a cytokine profile in serum and cerebrospinal fluid of pediatric and adult spinal muscular atrophy patients and its modulation upon nusinersen treatment

Missense mutation in ATXN2 gene (c.2860C &gt; T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotype

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Dysregulation of Muscle-Specific MicroRNAs as Common Pathogenic Feature Associated with Muscle Atrophy in ALS, SMA and SBMA: Evidence from Animal Models and Human Patients

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis.

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Duplication of exons 15 and 16 in Matrin-3: a phenotype bridging amyotrophic lateral sclerosis and immune-mediated disorders

Pain Study in X-Linked Adrenoleukodystrophy in Males and Females.

Optical coherence tomography in adult adrenoleukodystrophy: a cross-sectional and longitudinal study

Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms

Asymptomatic adrenoleukodystrophy in elderly males

Collaborators (41)

Franco Taroni

Ashley Jones

Nilo Riva

Frank Baas

Marka van Blitterswijk

Jennifer Phillips-Cremins

Silvia Fenu

Daniela Di Bella

Pierpaola Tannorella

Charles Curtis

Dominic Rowe

Bradley Smith

Stéphanie Millecamps

Russell McLaughlin

Sandra D'Alfonso

Paola Caroppo

Paolo Volanti

Michael Sendtner

Mariarita Galbiati

Danny Miller

simon topp

Ewout J. N. Groen

Frederik Steyn

Kelly Williams

Anna Maria Aloisi

Lyle Ostrow

Julian Großkreutz

Mark K Bakker

Jonathan Mill

Garth Nicholson

Julia Kraft

Marcella Zollino

Sarah Furlong

John Landers

Stuart Pickering-Brown

Caroline Vance

Angelica Nordin

Oleg Butovsky

monica consonni

ALESSANDRA FERLINI

Francesca Brett

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Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotype