ALESSANDRA FERLINI

University of Ferrara

Italy

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Articles (10)

Year:

2025

Year:

2024

Year:

2024

Year:

2023

Year:

2023

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2023

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Collaborators (13)

Maria Chiara Zatelli

Associate Professor

University of Ferrara

ITALY

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Viviana Pensato

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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M R Ambrosio

University of Ferrara

ITALY

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Frederik Steyn

Senior Lecturer/Group Leader

University of Queensland

AUSTRALIA

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Miriam Rebecca Hübner

Charité - Universitätsmedizin Berlin

GERMANY

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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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John Landers

University of Massachusetts Chan Medical School

UNITED STATES

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Cristina Al-Khalili Szigyarto

Associated Professor

Royal Institute of Technology

SWEDEN

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Daniela Benati

University of Modena and Reggio Emilia

ITALY

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Angelica Nordin

University Hospital of Umeå

SWEDEN

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Alice Margutti

University of Ferrara

ITALY

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ALESSANDRA FERLINI

Research Interests

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Contact this professor

Articles (10)

<i>MECP2</i> mRNA Profile in Brain Tissues from a Rett Syndrome Patient and Three Human Controls: Mutated Allele Preferential Transcription and In Situ RNA Mapping

Restored Collagen VI Microfilaments Network in the Extracellular Matrix of CRISPR-Edited Ullrich Congenital Muscular Dystrophy Fibroblasts

Relevance of Next-Generation Sequencing in the Diagnosis of Thalassemia and Hemoglobinopathies: The Experience of Four Italian Diagnostic Hubs

A Proof of Principle Proteomic Study Detects Dystrophin in Human Plasma: Implications in DMD Diagnosis and Clinical Monitoring

Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project

263rd ENMC International Workshop: Focus on female carriers of dystrophinopathy: refining recommendations for prevention, diagnosis, surveillance, and treatment. Hoofddorp, The Netherlands, 13-15 May 2022

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

Communicating the diagnosis of Klinefelter syndrome to children and adolescents: when, how, and who?

Newborn Screening by Genomic Sequencing: Opportunities and Challenges

Calculating and comparing codon usage values in rare disease genes highlights codon clustering with disease-and tissue- specific hierarchy

Collaborators (13)

Maria Chiara Zatelli

Viviana Pensato

M R Ambrosio

Frederik Steyn

Miriam Rebecca Hübner

Julian Großkreutz

Mark K Bakker

Jonathan Mill

John Landers

Cristina Al-Khalili Szigyarto

Daniela Benati

Angelica Nordin

Alice Margutti

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