Ieke B. Ginjaar

3.7k citations

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

Molecular Biology top 5%
Cardiology and Cardiovascular Medicine top 5%
Genetics top 2%
Genetics top 5%
Cellular and Molecular Neuroscience top 5%

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
Topics: Muscle Physiology and Disorders (27 papers)Cardiomyopathy and Myosin Studies (17 papers)Neurogenetic and Muscular Disorders Research (9 papers)
Cited by: Genetics Molecular Biology Cardiology and Cardiovascular Medicine
Journals: New England Journal of Medicine Cell The Journal of Immunology
Partner nations: Netherlands United Kingdom Belgium

In The Last Decade

Ieke B. Ginjaar

35 papers receiving 2.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Local Dystrophin Restoration with Antisense Oligonucleotide PRO051

2007 577 citations Judith C. van Deutekom, Anneke A. M. Janson et al. New England Journal of Medicine profile →

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 of co-authors of Ieke B. Ginjaar

This figure shows the co-authorship network connecting the top 25 collaborators of Ieke B. Ginjaar. A scholar is included among the top collaborators of Ieke B. Ginjaar 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 Ieke B. Ginjaar. Ieke B. Ginjaar 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

#	Work	Indexed citations
1	Significance of incidental copy number variants in the Duchenne muscular dystrophy gene 2025 ·Neuromuscular Disorders ·Ieke B. Ginjaar,Marjolein Kriek,(unknown),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,(unknown),Joanne Verheij,Trijnie Dijkhuizen,Hermine A. van Duyvenvoorde	0
2	Autosomal recessive limb‐girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients 2019 ·Clinical Genetics ·(unknown),(unknown),Wim H.J.P. Linssen,C.S.M. Straathof,E. Niks,(unknown),(unknown),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	32
3	Clinical Experience With Long-Term Acetazolamide Treatment in Children With Nondystrophic Myotonias: A Three-Case Report 2014 ·Pediatric Neurology ·(unknown),Bas C. Stunnenberg,Ieke B. Ginjaar,Gea Drost,Corrie E. Erasmus,L.T.L. Sie	20
4	Brain natriuretic peptide is not predictive of dilated cardiomyopathy in Becker and Duchenne muscular dystrophy patients and carriers 2013 ·BMC Neurology ·(unknown),Lukas Dekker,Rob de Haan,Erik Endert,Ieke B. Ginjaar,Marianne de Visser,Anneke J. van der Kooi	14
5	Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle disease 2012 ·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	46
6	Therapeutic exon skipping for dysferlinopathies? 2010 ·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	33
7	In tandem analysis of CLCN1 and SCN4A greatly enhances mutation detection in families with non-dystrophic myotonia 2008 ·European Journal of Human Genetics ·J. Trip,Gea Drost,(unknown),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	58
8	A novel GLRA1 mutation in a recessive hyperekplexia pedigree 2007 ·Movement Disorders ·Rob Forsyth,Artemis Gika,Ieke B. Ginjaar,Marina A.J. Tijssen	13
9	Local Dystrophin Restoration with Antisense Oligonucleotide PRO051breakdown → 2007 ·New England Journal of Medicine ·Judith C. van Deutekom,Anneke A. M. Janson,Ieke B. Ginjaar,(unknown),Annemieke Aartsma‐Rus,(unknown),Johan T. den Dunnen,Klaas Koop,Anneke J. van der Kooi,Nathalie Goemans,Sjef J. de Kimpe,(unknown),(unknown),Gerard Platenburg,Jan J.G.M. Verschuuren,Gert‐Jan B. van Ommen	577
10	CAV3 gene mutation analysis in patients with idiopathic hyper‐CK‐emia 2006 ·Muscle & Nerve ·Jaap C. Reijneveld,Ieke B. Ginjaar,(unknown),Nicolette C. Notermans	18
11	Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display 2005 ·European Journal of Human Genetics ·Yanchao Huang,Peter Verheesen,Andreas Roussis,(unknown),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	52
12	Sarcoglycanopathies and the risk of undetected deletion alleles in diagnosis 2005 ·Human Mutation ·Stefan J. White,Shirley Uitte de Willige,(unknown),(unknown),Ieke B. Ginjaar,Martijn H. Breuning,Johan T. den Dunnen	8
13	Novel mutations in three patients with LGMD2C with phenotypic differences 2004 ·Pediatric Neurology ·Sascha Vermeer,Aad Verrips,Michèl A.A.P. Willemsen,H. J. ter Laak,Ieke B. Ginjaar,Ben C.J. Hamel	10
14	Duchenne and Becker Muscular Dystrophy 2004 ·Humana Press eBooks ·Alexander L.J. Kneppers,Ieke B. Ginjaar,Egbert Bakker	10
15	DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients 2003 ·Human Mutation ·Robert M.W. Hofstra,(unknown),Rolf H. A. M. Vossen,(unknown),(unknown),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	39
16	Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family 2000 ·European Journal of Human Genetics ·Ieke B. Ginjaar,Alexander L.J. Kneppers,(unknown),Louise V.B. Anderson,(unknown),Judith C. van Deutekom,(unknown),Johan T. den Dunnen,Egbert Bakker	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. 1996 ·Journal of Medical Genetics ·Pauline A.M. Roest,(unknown),(unknown),Ieke B. Ginjaar,Egbert Bakker,F.B.L. Hogervorst,G J van Ommen,Johan T. den Dunnen	19
18	Different localization of dystrophin in developing and adult human skeletal muscle 1991 ·Muscle & Nerve ·Andy Wessels,Ieke B. Ginjaar,Antoon F.M. Moorman,Gert‐Jan B. van Ommen	54
19	Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies 1990 ·Cell ·(unknown),Hélène Gilgenkrantz,(unknown),Ghislaine Hamard,Philippe Chafey,Dominique Récan,(unknown),Albert de la Chapelle,(unknown),Ieke B. Ginjaar,(unknown),F. Tomé,Axel Kahn,(unknown)	141
20	Detection of Truncated Dystrophin in Fetal DMD Myotubes 1990 ·Advances in experimental medicine and biology ·Ieke B. Ginjaar,Egbert Bakker,Johan T. den Dunnen,Andy Wessels,(unknown),(unknown),Elizabeth E. Zubrzycka‐Gaarn,Kenneth H. Fischbeck,A. F. M. Moorman,Gert‐Jan B. van Ommen	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) and Neurogenetic and Muscular Disorders Research (9 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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