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K. Claeys · SciRah

Researcher profile · Semantic Scholar

K. Claeys

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K. Claeys — researcher profile on SciRah

h-index: 50
Works: 327
Citations: 9,087

Most-cited papers

FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice
M. Momenilandi, R. Lévy, Steicy Sobrino, Jingwei J. Li +69 more
2024Cell51 citations Open access
Semantic Scholar
Patient-reported burden of myasthenia gravis: baseline results of the international prospective, observational, longitudinal real-world digital study MyRealWorld-MG
S. Dewilde, Glenn Philips, S. Paci, J. Beauchamp +14 more
2023BMJ Open51 citations Open access
Semantic Scholar
Unraveling undiagnosed rare disease cases by HiFi long-read genome sequencing
W. Steyaert, L. Sagath, G. Demidov, V. Yépez +49 more
2025Genome Research34 citations Open access
Semantic Scholar
International Validation of the Erasmus Guillain–Barré Syndrome Respiratory Insufficiency Score
A. Doets, C. Walgaard, Hester F. Lingsma, B. Islam +173 more
2022Annals of Neurology33 citations Open access
Semantic Scholar
Recommendations for the management of myasthenia gravis in Belgium
J. De Bleecker, G. Remiche, A. Alonso-Jiménez, V. Van Parys +3 more
2024Acta Neurologica Belgica31 citations Open access
Semantic Scholar
Biochemical and clinical biomarkers in adult SMA 3–4 patients treated with nusinersen for 22 months
B. De Wel, M. De Schaepdryver, K. Poesen, K. Claeys
2022Annals of Clinical and Translational Neurology30 citations Open access
Semantic Scholar
The emerging spectrum of fetal acetylcholine receptor antibody-related disorders (FARAD)
N. Allen, M. O’Rahelly, B. Eymard, M. Chouchane +43 more
2023Brain : a journal of neurology29 citations Open access
Semantic Scholar
104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07)
B. Schoser, Priya S. Kishnani, D. Bratkovic, Barry J. Byrne +79 more
2024Journal of Neurology28 citations Open access
Semantic Scholar
NEB mutations disrupt the super-relaxed state of myosin and remodel the muscle metabolic proteome in nemaline myopathy
N. Ranu, J. Laitila, H. Dugdale, J. Mariano +19 more
2022Acta Neuropathologica Communications27 citations Open access
Semantic Scholar
Automated MRI quantification of volumetric per-muscle fat fractions in the proximal leg of patients with muscular dystrophies
L. Huysmans, B. De Wel, K. Claeys, F. Maes
2023Frontiers in Neurology25 citations Open access
Semantic Scholar
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing
B. Yaldiz, Erdi Kucuk, J. Hampstead, T. Hofste +296 more
2023Human Genomics24 citations Open access
Semantic Scholar
EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disorders
A. Atalaia, D. Wandrei, Nawel Lalout, R. Thompson +34 more
2024Orphanet Journal of Rare Diseases23 citations Open access
Semantic Scholar
Patient-reported impact of myasthenia gravis in the real world: findings from a digital observational survey-based study (MyRealWorld MG)
S. Berrih-Aknin, Jacqueline A Palace, A. Meisel, K. Claeys +10 more
2023BMJ Open23 citations Open access
Semantic Scholar
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy
A. Töpf, D. Cox, I. Zaharieva, Valeria Di Leo +81 more
2024Nature Genetics21 citations Open access
Semantic Scholar
Identification of new telomere- and telomerase-associated autoantigens in systemic sclerosis.
J. Vulsteke, V. Smith, C. Bonroy, R. Derua +11 more
2023Journal of Autoimmunity21 citations
Semantic Scholar
Anti-Ku + myositis: an acquired inflammatory protein-aggregate myopathy
Marie-Therese Holzer, A. Uruha, Andreas Roos, Andreas Hentschel +16 more
2024Acta Neuropathologica20 citations Open access
Semantic Scholar
Impact of Vutrisiran on Quality of Life and Physical Function in Patients with Hereditary Transthyretin-Mediated Amyloidosis with Polyneuropathy
L. Obici, S. Ajroud-Driss, Kon-ping Lin, J. Berk +337 more
2023Neurological Therapeutics19 citations Open access
Semantic Scholar
Validation of an Artificial Intelligence driven framework to automatically detect red flag symptoms in screening for rare diseases in electronic health records: hereditary transthyretin amyloidosis polyneuropathy as a key example
Dries Hens, L. Wyers, K. Claeys
2022Journal of the peripheral nervous system19 citations Open access
Semantic Scholar
Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing
W. Steyaert, L. Sagath, G. Demidov, V. Yépez +49 more
2024medRxiv18 citations Open access
Semantic Scholar
ADAPT NXT: Fixed Cycles or Every‐Other‐Week IV Efgartigimod in Generalized Myasthenia Gravis
A. Habib, K. Claeys, V. Bril, Y. Hussain +12 more
2025Annals of Clinical and Translational Neurology17 citations Open access
Semantic Scholar
Six-Minute Walk Distance Is a Useful Outcome Measure to Detect Motor Decline in Treated Late-Onset Pompe Disease Patients
K. Claeys, A. D'Hondt, Lucas Fache, K. Peers +1 more
2022Cells15 citations Open access
Semantic Scholar
Congenital Myasthenic Syndromes in Belgium: Genetic and Clinical Characterization of Pediatric and Adult Patients.
Nathalie Smeets, A. Gheldof, B. Dequeker, Margaux Poleur +20 more
2024Pediatric Neurology13 citations Open access
Semantic Scholar
Histopathological correlations and fat replacement imaging patterns in recessive limb‐girdle muscular dystrophy type 12
B. De Wel, L. Huysmans, C. Depuydt, V. Goosens +6 more
2023Journal of Cachexia, Sarcopenia and Muscle13 citations Open access
Semantic Scholar
What Are the Normal Serum Creatine Kinase Values for Skeletal Muscle? A Worldwide Systematic Review
K. Aleksovska, T. Kyriakides, Corrado Angelini, Zohar Argov +12 more
2025European Journal of Neurology12 citations Open access
Semantic Scholar
Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP-mediated disease reveals characteristic features useful for diagnosis
D. Esteller, M. Schiava, J. Verdú-Díaz, R. Villar-Quiles +62 more
2023Journal of Neurology12 citations Open access
Semantic Scholar
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD
A. Cortese, M. Dohrn, R. Curro', Sara Negri +77 more
2025Brain : a journal of neurology11 citations Open access
Semantic Scholar
Lessons for future clinical trials in adults with Becker muscular dystrophy: Disease progression detected by muscle magnetic resonance imaging, clinical and patient‐reported outcome measures
B. De Wel, L. Iterbeke, L. Huysmans, Ronald Peeters +9 more
2024European Journal of Neurology11 citations Open access
Semantic Scholar
Switching treatment to cipaglucosidase alfa plus miglustat positively affects patient-reported outcome measures in patients with late-onset Pompe disease
Priya S. Kishnani, Barry J. Byrne, K. Claeys, J. Diaz-Manera +73 more
2024Journal of Patient-Reported Outcomes10 citations Open access
Semantic Scholar
Anoctamin-5 related muscle disease: Clinical and genetic findings in a large European cohort.
Alexander de Bruyn, F. Montagnese, Sonja Holm-Yildiz, N. Poulsen +29 more
2023Brain : a journal of neurology10 citations Open access
Semantic Scholar
Two-year Risdiplam treatment in adults with spinal muscular atrophy: improvements in motor and respiratory function, quality of life and fatigue.
L. Iterbeke, K. Claeys
2025Neuromuscular Disorders9 citations
Semantic Scholar
A retrospective survey of patients with hereditary transthyretin-mediated (hATTR) amyloidosis treated with patisiran in real-world clinical practice in Belgium
J. De Bleecker, K. Claeys, S. Delstanche, V. Van Parys +3 more
2023Acta Neurologica Belgica9 citations Open access
Semantic Scholar
Unraveling the Molecular Basis of the Dystrophic Process in Limb-Girdle Muscular Dystrophy LGMD-R12 by Differential Gene Expression Profiles in Diseased and Healthy Muscles
C. Depuydt, V. Goosens, Rekin's Janky, A. D'Hondt +5 more
2022Cells9 citations Open access
Semantic Scholar
Novel OBSCN variants associated with a risk to exercise-intolerance and rhabdomyolysis.
F. Zemorshidi, A. Topf, K. Claeys, Adam Mc Farlane +3 more
2023Neuromuscular Disorders8 citations Open access
Semantic Scholar
Switching Enzyme Replacement Therapy for Late‐Onset Pompe Disease From Alglucosidase Alfa to Cipaglucosidase Alfa Plus Miglustat: Post Hoc Effect Size Analysis of PROPEL
Hani Kushlaf, J. Díaz-Manera, D. Bratkovic, Barry J. Byrne +13 more
2025Muscle and Nerve7 citations Open access
Semantic Scholar
Small fiber involvement is independent from clinical pain in late-onset Pompe disease
E. Enax-Krumova, Iris Dahlhaus, J. Görlach, K. Claeys +17 more
2022Orphanet Journal of Rare Diseases7 citations Open access
Semantic Scholar
Prospective Natural History Study in 24 Adult Patients With LGMDR12 Over 2 Years of Follow-up
B. De Wel, L. Huysmans, R. Peeters, V. Goosens +8 more
2022Neurology6 citations
Semantic Scholar
Fixed-cycle and Continuous Dosing of Intravenous Efgartigimod for Generalized Myasthenia Gravis: Study Design of ADAPT NXT (P10-11.010)
V. Bril, Y. Hussain, Kelly Gwathmey, G. Sahagian +9 more
2024Neurology5 citations
Semantic Scholar
IFN-α2 Autoantibody Screening and Functional Evaluation in Viral and Bacterial Infections.
M. Cockx, S. Steels, Birthe Michiels, J. Van Elslande +6 more
2024The Journal of Applied Laboratory Medicine4 citations
Semantic Scholar
EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemia
T. Kyriakides, K. Aleksovska, C. Angelini, Z. Argov +12 more
2026European Journal of Neurology3 citations Open access
Semantic Scholar
Transition from childhood to adulthood in neuromuscular disorders: results from the ERN EURO-NMD survey
Teresinha Evangelista, Houda Ali, C. Handberg, Thomas Sejersen +7 more
2025Orphanet Journal of Rare Diseases3 citations Open access
Semantic Scholar
Improving outcome measures in late onset Pompe disease: Modified Rasch‐Built Pompe‐Specific Activity scale
H. V. van Kooten, Mike C Horton, S. Wenninger, H. Babačić +15 more
2024European Journal of Neurology3 citations Open access
Semantic Scholar
Heterozygous POLG variant Ser1181Asn co-segregating in a family with autosomal dominant axonal neuropathy, proximal muscle fatigability, ptosis, and ragged red fibers
M. Dohrn, Corina Heller, D. Zengeler, C. Obermaier +11 more
2022Neurological Research and Practice3 citations Open access
Semantic Scholar
Real-world evidence on utilization and clinical outcomes of efgartigimod in patients with generalized myasthenia gravis.
L. Miguet, Martijn De Merlier, K. Claeys
2026Journal of Neuroimmunology2 citations Open access
Semantic Scholar
Clinically important improvements in 6-minute walk distance and forced vital capacity in adults with late-onset Pompe disease switching from alglucosidase alfa to cipaglucosidase alfa plus miglustat in the PROPEL study.
S. Wenninger, H. Kushlaf, N. Hummel, Brian Fox +6 more
2026Neuromuscular Disorders2 citations Open access
Semantic Scholar
Fractures in Hereditary Neuromuscular Disorders: Frequency, Risk Factors, and Implications
M. Opsomer, L. Iterbeke, H. Borghs, Tine De Cuyper +3 more
2025European Journal of Neurology2 citations Open access
Semantic Scholar
Muscle Biopsy Findings in Valosin-Containing Protein Multisystem Proteinopathy
M. Schiava, Y. Parkhurst, Matthew Henderson, T. Polvikoski +63 more
2025Neurology: Genetics2 citations Open access
Semantic Scholar
Automated Classification of Neuromuscular Diseases Using Thigh Muscle MRI With Model Interpretations
L. Huysmans, L. Iterbeke, B. De Wel, M. Opsomer +2 more
2025Journal of Cachexia, Sarcopenia and Muscle2 citations Open access
Semantic Scholar
Editorial: Implementing new technologies for neuromuscular disorders
N. Dubuisson, K. Claeys, B. Schoser
2024Frontiers in Neurology2 citations Open access
Semantic Scholar
Phenotype variability and therapeutic response to Patisiran in patients with hereditary transthyretin amyloidosis: a Belgian real-world experience
Stéphanie Delstanche, K. Claeys, J. De Bleecker, G. Remiche +3 more
2024Acta Clinica Belgica2 citations Open access
Semantic Scholar
Peptides From the Variable Domain of Immunoglobulin G as Biomarkers in Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Joris Godelaine, Yamini Chitale, B. De Moor, C. Mathieu +6 more
2023Neurology: Neuroimmunology & Neuroinflammation2 citations Open access
Semantic Scholar

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