Peter Van den Bergh

ORCID: 0000-0003-1954-4617

MedicineNeuroscienceBiochemistry, Genetics and Molecular Biology

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 10 papers. Top paper: “Predicting Outcome in Guillain-Barré Syndrome”.

Predicting Outcome in Guillain-Barré Syndrome

Neurology(2021)10.1212/wnl.0000000000013139

N/A

2.5DataRank · unranked

68 citations

Hester F. Lingsma, Christa Walgaard, Badrul Islam, Nowshin Papri, Amy Davidson +95 more

Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy

Nature Genetics(2024)10.1038/s41588-023-01651-0

N/A

0.901DataRank · unranked

33 citations

Dan Cox, Irina Zaharieva, Valeria Di Leo, J. Sarparanta, Per Harald Jonson +80 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

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

Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophy

Brain(2023)10.1093/brain/awad312

N/A

0DataRank · unranked

16 citations

Russell J. Butterfield, Patrick J. van der Vliet, Jan De Bleecker, Ludo van der Pol, Diane M. Dunn +18 more

Human skeletal myopathy myosin mutations disrupt myosin head sequestration

JCI Insight(2023)10.1172/jci.insight.172322

N/A

0DataRank · unranked

15 citations

Abbi Hau, Sarah Kosta, Hannah F. Dugdale, Francesco Muntoni, Adele D’Amico +14 more

Electrodiagnostic subtyping in Guillain–Barré syndrome patients in the International Guillain–Barré Outcome Study

European Journal of Neurology(2024)10.1111/ene.16335

N/A

0DataRank · unranked

11 citations

Judith Drenthen, Laura de Koning, Peter Van den Bergh, Robert D. M. Hadden, Satoshi Kuwabara +34 more

The most bothersome symptoms in neuromuscular diseases: the ERN EURO NMD Survey

Orphanet Journal of Rare Diseases(2025)10.1186/s13023-025-03742-z

N/A

0DataRank · unranked

5 citations

Alessandro Colitta, Manuela Lavorato, Peter Van den Bergh, Janbernd Kirschner, Cornelia Kornblum +13 more

Making sense of missense variants in TTN-related congenital myopathies

Acta Neuropathologica(2021)10.1007/s00401-020-02257-0

N/A

0DataRank · unranked

67 citations

Roksana Nikoopour, Atsushi Fukuzawa, Ay Lin Kho, Miguel A. Fernandez-Garcia, Elizabeth Wraige +40 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