Willem De Ridder

630 total citations
16 papers, 68 citations indexed

About

Willem De Ridder is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Willem De Ridder has authored 16 papers receiving a total of 68 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Cardiology and Cardiovascular Medicine and 4 papers in Cell Biology. Recurrent topics in Willem De Ridder's work include Muscle Physiology and Disorders (4 papers), Cardiomyopathy and Myosin Studies (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Willem De Ridder is often cited by papers focused on Muscle Physiology and Disorders (4 papers), Cardiomyopathy and Myosin Studies (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Willem De Ridder collaborates with scholars based in Belgium, United Kingdom and France. Willem De Ridder's co-authors include Jonathan Baets, Peter De Jonghe, Volker Straub, Luc Heytens, Nens van Alfen, Baziel G.M. van Engelen, Jan De Bleecker, Ana Töpf, Rosaline C. M. Quinlivan and Marc Snoeck and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Movement Disorders.

In The Last Decade

Willem De Ridder

11 papers receiving 66 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Willem De Ridder Belgium	6	32	22	18	12	12	16	68
Minal Jain United States	7	65 2.0×	25 1.1×	16 0.9×	6 0.5×	7 0.6×	12	109
Gaia Giribaldi Italy	7	38 1.2×	10 0.5×	27 1.5×	9 0.8×	29 2.4×	7	123
Federica Diofano Germany	4	50 1.6×	17 0.8×	10 0.6×	14 1.2×	6 0.5×	11	100
Ana Kosać Serbia	7	82 2.6×	16 0.7×	12 0.7×	31 2.6×	6 0.5×	15	120
Andrea Gangfuß Germany	6	51 1.6×	15 0.7×	14 0.8×	6 0.5×	19 1.6×	23	84
Alastair Corbett Australia	6	95 3.0×	25 1.1×	19 1.1×	5 0.4×	12 1.0×	10	128
Akihiko Mitsutake Japan	6	35 1.1×	6 0.3×	31 1.7×	10 0.8×	42 3.5×	28	89
Shigehisa Ura Japan	7	91 2.8×	14 0.6×	28 1.6×	5 0.4×	29 2.4×	14	139
Johanna L. Schmidt Italy	4	40 1.3×	6 0.3×	13 0.7×	9 0.8×	8 0.7×	6	76
V. Branković Serbia	5	50 1.6×	8 0.4×	26 1.4×	14 1.2×	7 0.6×	9	79

Countries citing papers authored by Willem De Ridder

Since Specialization

Citations

This map shows the geographic impact of Willem De Ridder's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Willem De Ridder with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Willem De Ridder more than expected).

Fields of papers citing papers by Willem De Ridder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Willem De Ridder. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Willem De Ridder. The network helps show where Willem De Ridder may publish in the future.

Co-authorship network of co-authors of Willem De Ridder

This figure shows the co-authorship network connecting the top 25 collaborators of Willem De Ridder. A scholar is included among the top collaborators of Willem De Ridder based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Willem De Ridder. Willem De Ridder is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Deconinck, Tine, Katrien Janssens, Alicia Alonso‐Jiménez, et al.. (2025). A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy. European Journal of Human Genetics. 34(1). 45–52.

Schil, Kristof Van, Tine Deconinck, Katrien Storm, et al.. (2025). TBP Repeat Expansion Analysis in Patients Carrying Heterozygous STUB1 Variants. Movement Disorders. 40(5). 980–985.

Vries, Glen M. de, Bob Asselbergh, Peter De Jonghe, et al.. (2025). Ageing Signatures and Disturbed Muscle Regeneration in Muscle Proteome of Inclusion Body Myositis. Journal of Cachexia Sarcopenia and Muscle. 16(3). e13845–e13845.

Ridder, Willem De, et al.. (2024). Contracturing granulomatous myositis in a patient with rheumatoid arthritis: a case report. Neuromuscular Disorders. 36. 38–41.

Beijer, Danique, Willem De Ridder, Abigail L. D. Tadenev, et al.. (2024). Dominant NARS1 mutations causing axonal Charcot–Marie–Tooth disease expand NARS1-associated diseases. Brain Communications. 6(2). fcae070–fcae070. 7 indexed citations

Ridder, Willem De, Geert de Vries, Kristof Van Schil, et al.. (2023). A homozygous loss of function variant in POPDC3: From invalidating exercise intolerance to a limb-girdle muscular dystrophy phenotype. Neuromuscular Disorders. 33(5). 432–439. 1 indexed citations

Jacobs, Edwin H., et al.. (2022). Distinct features in adult polyglucosan body disease: a case series. Neuromuscular Disorders. 33(2). 148–152. 3 indexed citations

Ridder, Willem De, Baziel G.M. van Engelen, & Nens van Alfen. (2022). Neurological features of Noonan syndrome and related RASopathies: Pain and nerve enlargement characterized by nerve ultrasound. American Journal of Medical Genetics Part A. 188(6). 1801–1807. 5 indexed citations

Ridder, Willem De, Peter De Jonghe, Volker Straub, & Jonathan Baets. (2021). High prevalence of sporadic late-onset nemaline myopathy in a cohort of whole-exome sequencing negative myopathy patients. Neuromuscular Disorders. 31(11). 1154–1160. 6 indexed citations

10.

Hedberg‐Oldfors, Carola, Willem De Ridder, Ognian Kalev, et al.. (2019). Functional characterization of GYG1 variants in two patients with myopathy and glycogenin-1 deficiency. Neuromuscular Disorders. 29(12). 951–960. 8 indexed citations

11.

Ridder, Willem De, et al.. (2019). Exertional rhabdomyolysis: Relevance of clinical and laboratory findings, and clues for investigation. Anaesthesia and Intensive Care. 47(2). 128–133. 5 indexed citations

12.

Küsters, Benno, Marc Snoeck, Martin Lammens, et al.. (2019). The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations. Journal of Neurology. 266(4). 876–887. 21 indexed citations

13.

Ridder, Willem De, Asfar S. Azmi, Christoph S. Clemen, et al.. (2019). Multisystem proteinopathy due to a homozygous p.Arg159His VCP mutation. Neurology. 94(8). e785–e796. 9 indexed citations

14.

Annoussamy, M., Willem De Ridder, C. Lilien, et al.. (2019). P.107Clinical changes over time in patients with centronuclear myopathy due to mutations in DNM2 gene enrolled in a European prospective natural history study. Neuromuscular Disorders. 29. S79–S80. 1 indexed citations

15.

Nelson, Isabelle, Willem De Ridder, Bob Asselbergh, et al.. (2018). LGMD AUTOSOMAL RESSESSIVE AND DOMINANT. Neuromuscular Disorders. 28. S59–S60. 1 indexed citations

16.

Ridder, Willem De, et al.. (2006). De ondertekening van Adam Willaerts’ Schepen voor een rotsachtige kust. SHILAP Revista de lepidopterología. 54(4). 382–399. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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