Ieke B. Ginjaar

3.7k citations

37 papers · 2.6k indexed · 1 hit paper · h-index 21

Genetics top 2%
- Neurogenetic and Muscular Disorders Research 9
- Virus-based gene therapy research 3
Molecular Biology top 5%
- Muscle Physiology and Disorders 27
- Ion channel regulation and function 4
- RNA Research and Splicing 3
- Mitochondrial Function and Pathology 2
Cardiology and Cardiovascular Medicine top 5%
- Cardiomyopathy and Myosin Studies 17
Aging top 5%
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases 8

Co-authors: Annemieke Aartsma‐Rus Johan T. den Dunnen Gert‐Jan B. van Ommen Jan J.G.M. Verschuuren Kate Bushby Ivo F.A.C. Fokkema J. van Deutekom Anneke J. van der Kooi
Cited by: Genetics Molecular Biology Cardiology and Cardiovascular Medicine
Journals: New England Journal of Medicine (1 paper)Cell (1 paper)The Journal of Immunology (1 paper)
Partner nations: Netherlands United Kingdom Belgium

In The Last Decade

Ieke B. Ginjaar

35 papers receiving 2.5k citations

Hit Papers

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Peers

Countries citing papers authored by Ieke B. Ginjaar

Since Specialization

Citations

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

Fields of papers citing papers by Ieke B. Ginjaar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ieke B. Ginjaar. 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 Ieke B. Ginjaar. The network helps show where Ieke B. Ginjaar may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Ieke B. Ginjaar, 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 Ieke B. Ginjaar Line = papers co-authored together Ieke B. Ginjaar links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Significance of incidental copy number variants in the Duchenne muscular dystrophy gene Neuromuscular Disorders ·Ieke B. Ginjaar,Marjolein Kriek,Mariette J. V. Hoffer,Renske Oegema,Ellen van Binsbergen,Karin E. M. Diderich,Laura J. C. M. van Zutven,Floor A.M. Duijkers,Alida C. Knegt,Corrie E. Erasmus,Nicole de Leeuw,Joanne Verheij,Trijnie Dijkhuizen,Hermine A. van Duyvenvoorde	2025	0
2	Autosomal recessive limb‐girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients Clinical Genetics ·Leroy ten Dam,Wendy S. Frankhuizen,Wim H.J.P. Linssen,C.S.M. Straathof,E. Niks,Karin G. Faber,Annemarie Fock,Jan B. M. Kuks,Esther Brusse,I.F.M. de Coo,Nicol C. Voermans,Aad Verrips,Jessica E. Hoogendijk,Ludo van der Pol,Dineke Westra,Marianne de Visser,Anneke J. van der Kooi,Ieke B. Ginjaar	2019	32
3	Clinical Experience With Long-Term Acetazolamide Treatment in Children With Nondystrophic Myotonias: A Three-Case Report Pediatric Neurology ·Joekie M. Markhorst,Bas C. Stunnenberg,Ieke B. Ginjaar,Gea Drost,Corrie E. Erasmus,L.T.L. Sie	2014	20
4	Brain natriuretic peptide is not predictive of dilated cardiomyopathy in Becker and Duchenne muscular dystrophy patients and carriers BMC Neurology ·Steven Schade van Westrum,Lukas Dekker,Rob de Haan,Erik Endert,Ieke B. Ginjaar,Marianne de Visser,Anneke J. van der Kooi	2013	14
5	Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle disease Neurobiology of Disease ·Victoria M. James,Anna Bode,Seo‐Kyung Chung,Jennifer Gill,Maartje Nielsen,Frances M. Cowan,Mihailo Vujic,Rhys H. Thomas,Mark I. Rees,Kirsten Harvey,Angelo Keramidas,Maya Topf,Ieke B. Ginjaar,Joseph W. Lynch,Victoria L. Harvey	2012	46
6	Therapeutic exon skipping for dysferlinopathies? European Journal of Human Genetics ·Annemieke Aartsma‐Rus,Kavita Singh,Ivo F.A.C. Fokkema,Ieke B. Ginjaar,Gert‐Jan B. van Ommen,Johan T. den Dunnen,Silvère M. van der Maarel	2010	33
7	In tandem analysis of CLCN1 and SCN4A greatly enhances mutation detection in families with non-dystrophic myotonia European Journal of Human Genetics ·J. Trip,Gea Drost,Dennis J Verbove,Anneke J. van der Kooi,Jan B. M. Kuks,Nicolette C. Notermans,Jan J.G.M. Verschuuren,Marianne de Visser,Baziel G.M. van Engelen,Carin G. Faber,Ieke B. Ginjaar	2008	58
8	A novel GLRA1 mutation in a recessive hyperekplexia pedigree Movement Disorders ·Rob Forsyth,Artemis Gika,Ieke B. Ginjaar,Marina A.J. Tijssen	2007	13
9	Local Dystrophin Restoration with Antisense Oligonucleotide PRO051breakdown → New England Journal of Medicine ·Judith C. van Deutekom,Anneke A. M. Janson,Ieke B. Ginjaar,Wendy S. Frankhuizen,Annemieke Aartsma‐Rus,Mattie Bremmer-Bout,Johan T. den Dunnen,Klaas Koop,Anneke J. van der Kooi,Nathalie Goemans,Sjef J. de Kimpe,Peter F. Ekhart,Edna H. Venneker,Gerard Platenburg,Jan J.G.M. Verschuuren,Gert‐Jan B. van Ommen	2007	577
10	CAV3 gene mutation analysis in patients with idiopathic hyper‐CK‐emia Muscle & Nerve ·Jaap C. Reijneveld,Ieke B. Ginjaar,Wendy S. Frankhuizen,Nicolette C. Notermans	2006	18
11	Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display European Journal of Human Genetics ·Yanchao Huang,Peter Verheesen,Andreas Roussis,Wendy S. Frankhuizen,Ieke B. Ginjaar,Faye Haldane,Steve Laval,Louise V.B. Anderson,Theo Verrips,Rune R. Frants,Hans de Haard,Kate Bushby,Johan T. den Dunnen,Silvère M. van der Maarel	2005	52
12	Sarcoglycanopathies and the risk of undetected deletion alleles in diagnosis Human Mutation ·Stefan J. White,Shirley Uitte de Willige,Dennis J Verbove,Luisa Politano,Ieke B. Ginjaar,Martijn H. Breuning,Johan T. den Dunnen	2005	8
13	Novel mutations in three patients with LGMD2C with phenotypic differences Pediatric Neurology ·Sascha Vermeer,Aad Verrips,Michèl A.A.P. Willemsen,H. J. ter Laak,Ieke B. Ginjaar,Ben C.J. Hamel	2004	10
14	Duchenne and Becker Muscular Dystrophy Humana Press eBooks ·Alexander L.J. Kneppers,Ieke B. Ginjaar,Egbert Bakker	2004	10
15	DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients Human Mutation ·Robert M.W. Hofstra,Inge M. Mulder,Rolf H. A. M. Vossen,Pia A. M. de Koning-Gans,Marian M.J. Kraak,Ieke B. Ginjaar,Annemarie H. van der Hout,Egbert Bakker,Charles H.C.M. Buys,Gert‐Jan B. van Ommen,Anthonie J. van Essen,Johan T. den Dunnen	2003	39
16	Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family European Journal of Human Genetics ·Ieke B. Ginjaar,Alexander L.J. Kneppers,Jan-Douwe M v d Meulen,Louise V.B. Anderson,Mattie Bremmer-Bout,Judith C. van Deutekom,Jitske Weegenaar,Johan T. den Dunnen,Egbert Bakker	2000	73
17	Splicing mutations in DMD/BMD detected by RT-PCR/PTT: detection of a 19AA insertion in the cysteine rich domain of dystrophin compatible with BMD. Journal of Medical Genetics ·Pauline A.M. Roest,M. Bout,Astrid C. van der Tuijn,Ieke B. Ginjaar,Egbert Bakker,F.B.L. Hogervorst,G J van Ommen,Johan T. den Dunnen	1996	19
18	Different localization of dystrophin in developing and adult human skeletal muscle Muscle & Nerve ·Andy Wessels,Ieke B. Ginjaar,Antoon F.M. Moorman,Gert‐Jan B. van Ommen	1991	54
19	Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies Cell ·Jamel Chelly,Hélène Gilgenkrantz,Martine Lambert,Ghislaine Hamard,Philippe Chafey,Dominique Récan,Pierre Katz,Albert de la Chapelle,Michel Koenig,Ieke B. Ginjaar,Michel Fardeau,F. Tomé,Axel Kahn,Jean-Claude Kaplan	1990	141
20	Detection of Truncated Dystrophin in Fetal DMD Myotubes Advances in experimental medicine and biology ·Ieke B. Ginjaar,Egbert Bakker,Johan T. den Dunnen,Andy Wessels,Marleen M. B. van Paassen,Maarten D. Kloosterman,Elizabeth E. Zubrzycka‐Gaarn,Kenneth H. Fischbeck,A. F. M. Moorman,Gert‐Jan B. van Ommen	1990	2

About Ieke B. Ginjaar

Ieke B. Ginjaar is a scholar working on Cardiology and Cardiovascular Medicine, Genetics and Cellular and Molecular Neuroscience, having authored 37 papers that have together received 2.6k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (27 papers), Cardiomyopathy and Myosin Studies (17 papers), Neurogenetic and Muscular Disorders Research (9 papers), Genetic Neurodegenerative Diseases (8 papers), Ion channel regulation and function (4 papers), Virus-based gene therapy research (3 papers), RNA Research and Splicing (3 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Genetics (477 citations), Molecular Biology (2.2k citations) and Cardiology and Cardiovascular Medicine (593 citations). Ieke B. Ginjaar has collaborated with scholars based in Netherlands, United Kingdom and Belgium. Frequent co-authors include Annemieke Aartsma‐Rus, Johan T. den Dunnen, Gert‐Jan B. van Ommen, Jan J.G.M. Verschuuren, Kate Bushby, Ivo F.A.C. Fokkema, J. van Deutekom, Anneke J. van der Kooi, Egbert Bakker and Judith C. van Deutekom. Their work appears in journals such as New England Journal of Medicine, Cell and The Journal of Immunology.

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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