Zhongbo Chen

United Kingdom

Research Interests

Explore related searches

Professors in United Kingdom Professors in Medical Science Medical Science professors in United Kingdom

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

Articles (25)

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Collaborators (13)

Sebastian R. Schreglmann

GERMANY

View details

Aude Deydier

Institut Pasteur de Lille

FRANCE

View details

Andre Altmann

University College London

UNITED KINGDOM

View details

Juan A. Botía

University College London

UNITED KINGDOM

View details

Selina Wray

Professor of Molecular Neuroscience

UCL Institute of Neurology, University College London

UNITED KINGDOM

View details

Tom Fowler

Queen Mary University of London

UNITED KINGDOM

View details

Anu Suomalainen-Wartiovaara

Academy Professor

University of Helsinki

FINLAND

View details

Mario Ezquerra

SPAIN

View details

Alexandra Durr

Professor, MD, PhD,

Sorbonne Université

FRANCE

View details

Arianna Tucci

Clinical Reader in Genomic Medicine

Queen Mary University of London

UNITED KINGDOM

View details

Johan Jakobsson

Lund University

SWEDEN

View details

Martin Paucar

Karolinska Institutet

SWEDEN

View details

Leonardo Collado-Torres

Assistant Professor

Johns Hopkins University

UNITED STATES

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Zhongbo Chen

Research Interests

Explore related searches

Contact this professor

Articles (25)

Splicing accuracy varies across human introns, tissues, age and disease.

Identification of GGC Repeat Expansions in ZFHX3 among Chilean Movement Disorder Patients

The annotation of GBA1 has been concealed by its protein-coding pseudogene GBAP1

Adaptive Long‐Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4

A Population‐Wide Exploration of the <scp><i>THAP11</i> CAG</scp> Repeat Size and Structure in the 100,000 Genomes Project and <scp>UK</scp> Biobank

The <scp><i>ZFHX3</i> GGC</scp> Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder

Repeat expansion disorders

Genetic topography and cortical cell loss in Huntington’s disease link development and neurodegeneration

aws-s3-integrity-check: an open-source bash tool to verify the integrity of a dataset stored on Amazon S3

Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia

Deep Intronic &lt;i&gt;FGF14&lt;/i&gt; GAA Repeat Expansion in Late-Onset Cerebellar Ataxia

Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia

IntroVerse: a comprehensive database of introns across human tissues

The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases

PhenoExam: gene set analyses through integration of different phenotype databases

Mitochondrial-nuclear cross-talk in the human brain is modulated by cell type and perturbed in neurodegenerative disease.

Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage.

Reply: Genetic heterogeneity of neuronal intranuclear inclusion disease. What about the infantile variant?

Concordance of CSF measures of Alzheimer's pathology with amyloid PET status in a preclinical cohort: A comparison of Lumipulse and established immunoassays.

Leveraging omic features with F3UTER enables identification of unannotated 3\textquoterightUTRs for synaptic genes

Novel variants broaden the phenotypic spectrum of PLEKHG5‐ associated neuropathies

Reply to: No evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease

Neuronal intranuclear inclusion disease is genetically heterogeneous.

GGC Repeat Expansion in NOTCH2NLC is rare in European Leukoencephalopathy.

GGC repeat expansion in NOTCH2NLC is rare in European patients with essential tremor.

Collaborators (13)

Sebastian R. Schreglmann

Aude Deydier

Andre Altmann

Juan A. Botía

Selina Wray

Tom Fowler

Anu Suomalainen-Wartiovaara

Mario Ezquerra

Alexandra Durr

Arianna Tucci

Johan Jakobsson

Martin Paucar

Leonardo Collado-Torres

Make your next move.

Deep Intronic <i>FGF14</i> GAA Repeat Expansion in Late-Onset Cerebellar Ataxia