Jonathan Baets

Also affiliated with Antwerp University Hospital

NeuroscienceBiochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 18 papers. Top paper: “BiP inactivation due to loss of the deAMPylation function of FICD causes a motor neuron disease”.

BiP inactivation due to loss of the deAMPylation function of FICD causes a motor neuron disease

Genetics in Medicine(2022)10.1016/j.gim.2022.08.019

N/A

1.0DataRank · unranked

30 citations

Ariel Ruiz, Maike F. Dohrn, Melanie Wayand, Amjad Farooq, Matt C. Danzi +14 more

Clinico‐Genetic, Imaging and Molecular Delineation of COQ8A‐Ataxia: A Multicenter Study of 59 Patients

Annals of Neurology(2020)10.1002/ana.25751

N/A

0.654DataRank · unranked

77 citations

Tommaso Schirinzi, Lucia Laugwitz, Nathan H. Murray, C.A. Bingman, Selina Reich +37 more

Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation

JCI Insight(2021)10.1172/jci.insight.148363

N/A

0.648DataRank · unranked

74 citations

Hong Joo Kim, Lin Guo, Kevin J. O’Donovan, Inès Mademan, Tine Deconinck +21 more

Pathogenic Variants in the Myosin Chaperone UNC-45B Cause Progressive Myopathy with Eccentric Cores

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.11.002

N/A

0.578DataRank · unranked

46 citations

Carl Elias Kutzner, Ying Hu, Xavière Lornage, John Rendu, Tanya Stojkovic +42 more

De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia

Movement Disorders(2022)10.1002/mds.28959

N/A

0.494DataRank · unranked

26 citations

Jonathan De Winter, Danique Beijer, Giulia Coarelli, Melanie Wayand, Robin Palvadeau +33 more

C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD

Acta Neuropathologica(2023)10.1007/s00401-023-02565-1

N/A

0DataRank · unranked

24 citations

Nika Schuermans, Antoon Meylemans, Pontus LeBlanc, Lauren Versluys, Katie E. Copley +17 more

Non-muscle myosin II regulates presynaptic actin assemblies and neuronal mechanobiology in Drosophila

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.10.566609

N/A

0DataRank · unranked

1 citations

Jonathan Baets, Avital A. Rodal, Biljana Ermanoska

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

Brain Communications(2024)10.1093/braincomms/fcae070

N/A

0DataRank · unranked

18 citations

Sheila Marte, Jiaxin C Li, Willem De Ridder, Jessie Z Chen, Abigail L. D. Tadenev +12 more

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

Journal of the Peripheral Nervous System(2024)10.1111/jns.12621

N/A

0DataRank · unranked

1 citations

Matt C. Danzi, Ariel Ruiz, Jacquelyn Raposo, Yeisha Arcia de Jesus, Mary M. Reilly +16 more

Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features

medRxiv(2024)10.1101/2024.09.23.24313872

N/A

0DataRank · unranked

3 citations

Liedewei Van de Vondel, Biljana Ermanoska, Alice Monticelli, Arnaud Isapof, Enzo Cohen +33 more

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

Genetics in Medicine(2025)10.1016/j.gim.2025.101399

N/A

0DataRank · unranked

5 citations

Liedewei Van de Vondel, Biljana Ermanoska, Alice Monticelli, Arnaud Isapof, Enzo Cohen +32 more

Nonmuscle myosin II regulates presynaptic actin and neuronal mechanobiology in Drosophila

The Journal of Cell Biology(2025)10.1083/jcb.202501211

N/A

0DataRank · unranked

2 citations

Jonathan Baets, Avital A. Rodal, Biljana Ermanoska

Asparaginyl-tRNA synthetase (NARS1) variants implicated in dominant neurological phenotypes display dominant-negative properties

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100519

N/A

0DataRank · unranked

0 citations

Keyana Blake, Brendan L M Sutton, Marina Konyukh, Stephan Züchner, Tanya Stojkovic +3 more

Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy

Journal of Clinical Investigation(2025)10.1172/jci184474

N/A

0DataRank · unranked

0 citations

Stéphanie Efthymiou, Christopher J. Record, Xinyu Miao, Renee Q. Lin, J. Parmar +76 more

The genetic landscape of axonal neuropathies in the middle-aged and elderly

Neurology(2020)10.1212/wnl.0000000000011132

N/A

0DataRank · unranked

31 citations

Petra Laššuthová, Dagmara Kabzińska, Lisa Abreu, Jonathan Baets, Christian Beetz +52 more

Unrestrained poly-ADP-ribosylation provides insights into chromatin regulation and human disease

Molecular Cell(2021)10.1016/j.molcel.2021.04.028

N/A

0DataRank · unranked

108 citations

Thomas Agnew, Anne R. Wondisford, Michael Tellier, Nicole Kaminski, Danique Beijer +15 more

Efficacy and Safety of Bimagrumab in Sporadic Inclusion Body Myositis

Neurology(2021)10.1212/wnl.0000000000011626

N/A

0DataRank · unranked

37 citations

Michael G. Hanna, Pedro Machado, Umesh A. Badrising, Hector Chinoy, Olivier Benvéniste +93 more

DEFINING THE DIVERSITY OF HNRNPA1 MUTATIONS IN CLINICAL PHENOTYPE AND PATHOMECHANISM

medRxiv(2021)10.1101/2021.02.02.21250330

N/A

0DataRank · unranked

1 citations

Hyung Jun Kim, Lin Guo, Kevin J. O’Donovan, Inès Mademan, Tine Deconinck +21 more