C Höweler

1.3k total citations
22 papers, 976 citations indexed

About

C Höweler is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, C Höweler has authored 22 papers receiving a total of 976 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 6 papers in Neurology. Recurrent topics in C Höweler's work include Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (7 papers) and Muscle Physiology and Disorders (4 papers). C Höweler is often cited by papers focused on Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (7 papers) and Muscle Physiology and Disorders (4 papers). C Höweler collaborates with scholars based in Netherlands, United States and Belgium. C Höweler's co-authors include H. F. M. Busch, Joep Geraedts, Martinus F. Niermeijer, A. Staal, Axel R. Wintzen, Bé Wieringa, Gert Jansen, Marjolein Visser, Peter J. Koehler and Umesh A. Badrising and has published in prestigious journals such as New England Journal of Medicine, Brain and Neurology.

In The Last Decade

C Höweler

22 papers receiving 938 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
C Höweler Netherlands	13	613	496	264	213	161	22	976
Joachim Schessl Germany	22	622 1.0×	386 0.8×	128 0.5×	310 1.5×	69 0.4×	43	1.2k
Julie T. Parke United States	12	304 0.5×	218 0.4×	59 0.2×	212 1.0×	355 2.2×	14	1.0k
Carmen Serrano Spain	14	501 0.8×	267 0.5×	82 0.3×	270 1.3×	82 0.5×	31	844
Amets Sáenz Spain	18	522 0.9×	334 0.7×	70 0.3×	222 1.0×	59 0.4×	41	949
Feza Deymeer Türkiye	25	659 1.1×	427 0.9×	57 0.2×	751 3.5×	67 0.4×	88	1.5k
Pierre‐Yves Jeannet Switzerland	14	424 0.7×	186 0.4×	106 0.4×	175 0.8×	66 0.4×	26	896
Giovanni Castelnovo France	19	375 0.6×	229 0.5×	79 0.3×	515 2.4×	39 0.2×	74	1.1k
M Puranen Finland	17	234 0.4×	148 0.3×	159 0.6×	848 4.0×	266 1.7×	30	1.6k
Phillipa J. Lamont Australia	19	1.0k 1.6×	366 0.7×	64 0.2×	118 0.6×	172 1.1×	61	1.3k
V. Decostre France	18	894 1.5×	154 0.3×	84 0.3×	65 0.3×	72 0.4×	35	1.2k

Countries citing papers authored by C Höweler

Since Specialization

Citations

This map shows the geographic impact of C Höweler'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 C Höweler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C Höweler more than expected).

Fields of papers citing papers by C Höweler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C Höweler. 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 C Höweler. The network helps show where C Höweler may publish in the future.

Co-authorship network of co-authors of C Höweler

This figure shows the co-authorship network connecting the top 25 collaborators of C Höweler. A scholar is included among the top collaborators of C Höweler 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 C Höweler. C Höweler is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Kooi, Anneke J. van der, P. G. Barth, C Höweler, et al.. (2007). Limb-girdle muscular dystrophy in the Netherlands: Gene defect identified in half the families. Neurology. 68(24). 2125–2128. 43 indexed citations

Badrising, Umesh A., Marion L. C. Maat–Schieman, Michel D. Ferrari, et al.. (2002). Comparison of weakness progression in inclusion body myositis during treatment with methotrexate or placebo. Annals of Neurology. 51(3). 369–372. 106 indexed citations

Andries, Frank, et al.. (1997). Vocational perspectives and neuromuscular disorders. International Journal of Rehabilitation Research. 20(3). 255–274. 34 indexed citations

Linssen, W.H.J.P., Marjolein Visser, Nicolette C. Notermans, et al.. (1997). Miyoshi-type distal muscular dystrophy: clinical features of 24 Dutch patients. Neuromuscular Disorders. 7(6-7). 462–462. 1 indexed citations

Die-Smulders, C E de, et al.. (1997). Paternal transmission of congenital myotonic dystrophy.. Journal of Medical Genetics. 34(11). 930–933. 26 indexed citations

Badrising, Umesh A., Marion L. C. Maat–Schieman, Sjoerd G. van Duinen, et al.. (1997). The onset and distribution of muscle weakness in inclusion body myositis (IBM). Neuromuscular Disorders. 7(6-7). 464–464. 1 indexed citations

Badrising, Umesh A., Marion L. C. Maat–Schieman, Sjoerd G. van Duinen, et al.. (1997). Epidemiology of inclusion body myositis in the Netherlands. Neuromuscular Disorders. 7(6-7). 463–464. 2 indexed citations

Kooi, Anneke J. van der, P. G. Barth, H. F. M. Busch, et al.. (1996). The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands. Brain. 119(5). 1471–1480. 67 indexed citations

Schrander‐Stumpel, C. T. R. M., C Höweler, & Jean‐Pierre Fryns. (1995). X-linked mental retardation and neurological symptoms: A nosological approach. American Journal of Medical Genetics Part A. 64(1). 16. 1 indexed citations

10.

Schrander‐Stumpel, C. T. R. M., C Höweler, Marilyn C. Jones, et al.. (1995). Spectrum of X‐linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional families. American Journal of Medical Genetics. 57(1). 107–116. 45 indexed citations

11.

Schrander‐Stumpel, C. T. R. M., C Höweler, & Jean‐Pierre Fryns. (1995). X-linked mental retardation and neurological symptoms: a nosological approach.. PubMed. 6(1). 21–32. 3 indexed citations

12.

Die-Smulders, C E de, et al.. (1994). Anticipation resulting in elimination of the myotonic dystrophy gene: a follow up study of one extended family.. Journal of Medical Genetics. 31(8). 595–601. 9 indexed citations

13.

Jansen, Gert, Patrick J. Willems, M. Coerwinkel, et al.. (1994). Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.. PubMed. 54(4). 575–85. 134 indexed citations

14.

Brunner, Han G., Gert Jansen, Willy M. Nillesen, et al.. (1993). Reverse Mutation in Myotonic Dystrophy. New England Journal of Medicine. 328(7). 476–480. 64 indexed citations

15.

Schrander‐Stumpel, C. T. R. M., et al.. (1993). Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis.. Journal of Medical Genetics. 30(1). 78–80. 20 indexed citations

16.

Brunner, Han G., et al.. (1992). Intestinal pseudo-obstruction in myotonic dystrophy.. Journal of Medical Genetics. 29(11). 791–793. 32 indexed citations

17.

Höweler, C. (1986). A clinical and genetic study in myotonic dystrophy. RePub (Erasmus University Rotterdam). 7 indexed citations

18.

Vles, Johan S.H., et al.. (1983). Two dutch siblings with congenital muscular dystrophy (Fukuyama type). Clinical Neurology and Neurosurgery. 85(3). 175–180. 8 indexed citations

19.

Höweler, C, H. F. M. Busch, Luigi F. Bernini, et al.. (1980). DYSTROPHIA MYOTONICA AND MYOTONIA CONGENITA CONCURRING IN ONE FAMILY. Brain. 103(3). 497–513. 4 indexed citations

20.

Pearse, R G & C Höweler. (1979). Neonatal form of dystrophia myotonica. Five cases in preterm babies and a review of earlier reports.. Archives of Disease in Childhood. 54(5). 331–338. 30 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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