Jonathan Baets

University of Antwerp

Belgium

Research Interests

Explore related searches

Professors in Belgium

Contact this professor

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

Articles (24)

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2021

Collaborators (4)

Avital Rodal

Associate Professor of Biology

Brandeis University

UNITED STATES

View details

Vincent Timmerman

University of Antwerp

BELGIUM

View details

Sarah Weckhuysen

Associate Professor

University of Antwerp

BELGIUM

View details

Robert Burgess

Professor

Jackson Laboratory

UNITED STATES

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Jonathan Baets

Research Interests

Explore related searches

Contact this professor

Articles (24)

Nonmuscle myosin II regulates presynaptic actin and neuronal mechanobiology in Drosophila

Loss‐of‐function variants in SPTAN1 and SPTBN4 cause early‐onset hereditary myopathy

Ageing signatures and disturbed muscle regeneration in muscle proteome of inclusion body myositis

Awareness of bone strength in patients with neuromuscular disorders

Chronic sarcoid myopathy mimicking facioscapulohumeral muscular dystrophy

Clinical and imaging spectrum of non-congenital dominant <i>ACTN2</i> myopathy

Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses

Heterozygous RAB3A variants cause cerebellar ataxia by a partial loss-of-function mechanism

Heterozygous loss-of-function variants in SPTAN1 cause an early childhood onset distal myopathy

Liver function in X-linked myotubular myopathy and autosomal dominant centronuclear myopathy

Dominant <i>NARS1</i> mutations causing axonal Charcot–Marie–Tooth disease expand <i>NARS1</i>-associated diseases

Overarching pathomechanisms in inherited peripheral neuropathies, spastic paraplegias, and cerebellar ataxias

A study concept of expeditious clinical enrollment for genetic modifier studies in Charcot-Marie-Tooth neuropathy 1A

Contracturing granulomatous myositis in a patient with rheumatoid arthritis

Dominant NARS1 mutations causing axonal Charcot–Marie–Tooth disease expand NARS1 -associated diseases

Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients

Vitamin D<sub>3</sub> deficiency and osteopenia in spastic paraplegia type 5 indicate impaired bone homeostasis

Downregulation of PMP22 ameliorates myelin defects in iPSC-derived human organoid cultures of CMT1A

A retrospective survey of patients with hereditary transthyretin-mediated (hATTR) amyloidosis treated with patisiran in real-world clinical practice in Belgium

Distinct features in adult polyglucosan body disease: a case series

Myelin protein zero mutation-related hereditary neuropathies

Responsiveness of the Scale for the Assessment and Rating of Ataxia and Natural History in 884 Recessive and Early Onset Ataxia Patients

A homozygous loss of function variant in POPDC3

PCYT2 mutations disrupting etherlipid biosynthesis: phenotypes converging on the CDP-ethanolamine pathway

Collaborators (4)

Avital Rodal

Vincent Timmerman

Sarah Weckhuysen

Robert Burgess

Make your next move.