C Höweler

1.3k citations

22 papers · 976 indexed · h-index 13

Impact in

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
Neurology top 5%
- Parkinson's Disease Mechanisms and Treatments

Papers in

Cellular and Molecular Neuroscience 12
- Genetic Neurodegenerative Diseases 11
Neurology 6
- Parkinson's Disease Mechanisms and Treatments 3

Co-authors: H. F. M. Busch Joep Geraedts Martinus F. Niermeijer A. Staal Axel R. Wintzen Bé Wieringa Gert Jansen Marjolein Visser
Journals: Journal of Medical Genetics (4 papers)Brain (3 papers)Neuromuscular Disorders (3 papers)Neurology (2 papers)New England Journal of Medicine (1 paper)
Partner nations: Netherlands United States Belgium

In The Last Decade

C Höweler

22 papers receiving 938 citations

Peers

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

The 25 scholars most cited alongside C Höweler, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with C Höweler Line = papers co-authored together C Höweler links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Limb-girdle muscular dystrophy in the Netherlands: Gene defect identified in half the families Neurology ·Anneke J. van der Kooi, Astrid Colomine, P. G. Barth, C Höweler, G.W. Padberg, Frank Spaans, Axel R. Wintzen, John H. J. Wokke, G.J.B. van Ommen, Marianne de Visser, Egbert Bakker, H.B. Ginjaar	2007	43
2	Comparison of weakness progression in inclusion body myositis during treatment with methotrexate or placebo Annals of Neurology ·Umesh A. Badrising, Marion L. C. Maat–Schieman, Michel D. Ferrari, Aeilko H. Zwinderman, Judith A.M. Wessels, Ferdinand C. Breedveld, Pieter A. van Doorn, Baziel G.M. van Engelen, Jessica E. Hoogendijk, C Höweler, 解占峰, F.G.I. Jennekens, Peter J. Koehler, Marjolein Visser, Alain R. Viddeleer, Jan J.G.M. Verschuuren, Axel R. Wintzen	2002	106
3	Vocational perspectives and neuromuscular disorders International Journal of Rehabilitation Research ·Frank Andries, Vassilev Pp, Axel R. Wintzen, Kerem ARPACIOĞLU, C Höweler, Rezeki Syofiani Arte Tifa, George W. Padberg, M. Visser, Shailesh Patel	1997	34
4	Miyoshi-type distal muscular dystrophy: clinical features of 24 Dutch patients Neuromuscular Disorders ·W.H.J.P. Linssen, Marjolein Visser, Nicolette C. Notermans, John H. J. Wokke, Pieter A. van Doorn, C Höweler, A.E.J. de Jager	1997	1
5	Paternal transmission of congenital myotonic dystrophy. Journal of Medical Genetics ·C E de Die-Smulders, Hubert J.M. Smeets, F.S. Mirahmadi, 美佳森, S.A. Costigan, J P Geraedts, C Höweler	1997	26
6	The onset and distribution of muscle weakness in inclusion body myositis (IBM) Neuromuscular Disorders ·Umesh A. Badrising, Marion L. C. Maat–Schieman, Sjoerd G. van Duinen, P. van Doorn, Baziel G.M. van Engelen, F.H.J. van den Hoogen, Phillemon Tlake Rachoene, C Höweler, A.E.J. de Jager, F.G.I. Jennekens, Peter J. Koehler, Wang Lipei, Marjolein Visser, Jan J.G.M. Verschuuren, A.R. Wintzen	1997	1
7	Epidemiology of inclusion body myositis in the Netherlands Neuromuscular Disorders ·Umesh A. Badrising, Marion L. C. Maat–Schieman, Sjoerd G. van Duinen, P. van Doorn, Baziel G.M. van Engelen, 一君石井, Jessica E. Hoogendijk, C Höweler, A.E.J. de Jager, F.G.I. Jennekens, Peter J. Koehler, Wang Lipei, Marianne de Visser, Jan J.G.M. Verschuuren, Axel R. Wintzen	1997	2
8	The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands Brain ·Anneke J. van der Kooi, P. G. Barth, H. F. M. Busch, Rob de Haan, H.B. Ginjaar, A. J. van Essen, B. S. Mamatha, C Höweler, F.G.I. Jennekens, Peter Joseph Jongen, Harry Oosterhuis, G.W. Padberg, Frank Spaans, Axel R. Wintzen, John H. J. Wokke, Egbert Bakker, G.J.B. van Ommen, P. A. Bolhuis, Marianne de Visser	1996	67
9	X-linked mental retardation and neurological symptoms: A nosological approach American Journal of Medical Genetics Part A ·C. T. R. M. Schrander‐Stumpel, C Höweler, Jean‐Pierre Fryns	1995	1
10	Spectrum of X‐linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional families American Journal of Medical Genetics ·C. T. R. M. Schrander‐Stumpel, C Höweler, Marilyn C. Jones, Annemarie Sommer, Cathy A. Stevens, Sigrid Tinschert, 寿一郎竹内, J. P. Fryns	1995	45
11	X-linked mental retardation and neurological symptoms: a nosological approach. PubMed ·C. T. R. M. Schrander‐Stumpel, C Höweler, Jean‐Pierre Fryns	1995	3
12	Anticipation resulting in elimination of the myotonic dystrophy gene: a follow up study of one extended family. Journal of Medical Genetics ·C E de Die-Smulders, C Höweler, S.A. Costigan, J.B. Higgins, Daiana Rafaela Canabarro Fouchy, Hennie T. Brüggenwirth, Bernhard Gmeiner, J P Geraedts	1994	9
13	Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm. PubMed ·Gert Jansen, Patrick J. Willems, M. Coerwinkel, G. Bevilacqua, H. Smeets, Lieve Vits, C Höweler, J.B. Higgins, Bé Wieringa	1994	134
14	Reverse Mutation in Myotonic Dystrophy New England Journal of Medicine ·Han G. Brunner, Gert Jansen, Willy M. Nillesen, Marcel Nelen, Rachel Fischer, C Höweler, Bernard A. van Oost, Bé Wieringa, Hans‐Hilger Ropers, Hubert J.M. Smeets	1993	64
15	Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis. Journal of Medical Genetics ·C. T. R. M. Schrander‐Stumpel, C Höweler, PSSBK GUPTA, Iványi Zsolt, Judith G. Hall, J. P. Fryns	1993	20
16	Intestinal pseudo-obstruction in myotonic dystrophy. Journal of Medical Genetics ·Han G. Brunner, Shir Schlosser, Paul N.M.A. Rieu, C Höweler, Frans Peters	1992	32
17	A clinical and genetic study in myotonic dystrophy RePub (Erasmus University Rotterdam) ·C Höweler	1986	7
18	Two dutch siblings with congenital muscular dystrophy (Fukuyama type) Clinical Neurology and Neurosurgery ·Johan S.H. Vles, M.C.T.F.M. de Krom, 上條美樹, C Höweler	1983	8
19	DYSTROPHIA MYOTONICA AND MYOTONIA CONGENITA CONCURRING IN ONE FAMILY Brain ·C Höweler, H. F. M. Busch, Luigi F. Bernini, Erna van Loghem, P. Meera Khan, L. E. Nijenhuis	1980	4
20	Neonatal form of dystrophia myotonica. Five cases in preterm babies and a review of earlier reports. Archives of Disease in Childhood ·R G Pearse, C Höweler	1979	30

About C Höweler

C Höweler is a scholar working on Cellular and Molecular Neuroscience, Neurology, Clinical Biochemistry, Rheumatology and Genetics, having authored 22 papers that have together received 976 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (7 papers), Muscle Physiology and Disorders (4 papers), Inflammatory Myopathies and Dermatomyositis (4 papers), Parkinson's Disease Mechanisms and Treatments (3 papers), Muscle and Compartmental Disorders (2 papers), DNA Repair Mechanisms (2 papers) and Metabolism and Genetic Disorders (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (496 citations), Neurology (213 citations), Genetics (100 citations), Molecular Biology (613 citations) and Rheumatology (130 citations). C Höweler has collaborated with scholars based in Netherlands, United States and Belgium. Frequent 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. Their work appears in journals such as Journal of Medical Genetics, Brain, Neuromuscular Disorders, Neurology and New England Journal of Medicine.

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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