E. Redeker

2.4k citations

29 papers · 823 · h-index 16

Impact in

Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Molecular Biology
- Genomics and Chromatin Dynamics
- DNA Repair Mechanisms
- RNA Research and Splicing
- Epigenetics and DNA Methylation

Papers in

Molecular Biology 17
- Genomics and Chromatin Dynamics 4
- DNA Repair Mechanisms 3
- Epigenetics and DNA Methylation 3
Genetics 8
- Genomic variations and chromosomal abnormalities 3

Co-authors: Marcel M. A. M. Mannens (6 shared papers)Christa Heyting (5 shared papers)A. J. J. Dietrich (3 shared papers)A. C. G. Vink (3 shared papers)Peter B. Møens (2 shared papers)Raoul C. M. Hennekam (2 shared papers)Sylvia Huisman (1 shared paper)Saskia M. Maas (1 shared paper)
Journals: Genomics (3 papers)Human Molecular Genetics (2 papers)Human Mutation (1 paper)Atherosclerosis (1 paper)Familial Cancer (1 paper)
Partner nations: Netherlands United States Belgium

In The Last Decade

E. Redeker

29 papers receiving 808 citations

Peers

Countries citing papers authored by E. Redeker

Since Specialization

Citations

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

Fields of papers citing papers by E. Redeker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Increased DNA damage sensitivity of Cornelia de Lange syndrome cells: evidence for impaired recombinational repair Human Molecular Genetics ·Mischa G. Vrouwe, Elhaam Elghalbzouri-Maghrani, Matty Meijers, Peter Schouten, Barbara C. Godthelp, Zahurul A. Bhuiyan, E. Redeker, Marcel M. A. M. Mannens, Leon H.F. Mullenders, Albert Pastink, F. Darroudi	2007	88
2	Synaptonemal complex proteins Genome ·Christa Heyting, A. J. J. Dietrich, Peter B. Møens, R. Dettmers, Hildo H. Offenberg, E. Redeker, A. C. G. Vink	1989	84
3	High rate of mosaicism in individuals with Cornelia de Lange syndrome Journal of Medical Genetics ·Sylvia Huisman, E. Redeker, Saskia M. Maas, Marcel M. A. M. Mannens, Raoul C. M. Hennekam	2013	84
4	Identification of two major components of the lateral elements of synaptonemal complexes of the rat. PubMed ·Christa Heyting, Peter B. Møens, W. van Raamsdonk, A. J. J. Dietrich, A. C. G. Vink, E. Redeker	1987	74
5	Two major components of synaptonemal complexes are specific for meiotic prophase nuclei Chromosoma ·Christa Heyting, R. Dettmers, A. J. J. Dietrich, E. Redeker, A. C. G. Vink	1988	62
6	Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly BMC Medical Genomics ·Patrick Rump, Omid Jazayeri, Krista K. van Dijk-Bos, Lennart Johansson, Anthonie J. van Essen, Johanna B. G. M. Verheij, Hermine E. Veenstra‐Knol, E. Redeker, Marcel M. A. M. Mannens, Morris A. Swertz, Behrooz Z. Alizadeh, Conny M.A. van Ravenswaaij‐Arts, Richard J. Sinke, Birgit Sikkema‐Raddatz	2015	61
7	Multiplex ligation-dependent probe amplification (MLPA) enhances the molecular diagnosis of aniridia and related disorders. PubMed ·E. Redeker, Annette S H de Visser, Arthur A. Bergen, Marcel M. A. M. Mannens	2008	54
8	High-Resolution Chromosomal Localization of the Human Calcitonin/CGRP/IAPP Gene Family Members Genomics ·J.M.N. Hoovers, E. Redeker, Frank Speleman, Jo W.M. Höppener, Shama L. Bhola, Jet Bliek, Nadine Van Roy, N. J. Leschot, A. Westerveld, M. Mannens	1993	31
9	Microfluidic Amplification as a Tool for Massive Parallel Sequencing of the Familial Hypercholesterolemia Genes Clinical Chemistry ·Silke Hollants, E. Redeker, Gert Matthijs	2012	28
10	Targeted carrier screening for four recessive disorders: High detection rate within a founder population European Journal of Medical Genetics ·Inge B. Mathijssen, Lidewij Henneman, Janneke M. C. van Eeten-Nijman, Phillis Lakeman, Cecile P. E. Ottenheim, E. Redeker, Winnie Ottenhof, Hanne Meijers‐Heijboer, Merel C. van Maarle	2015	25
11	Mitochondrial Encephalopathy and Transient 3-Methylglutaconic Aciduria in ECHS1 Deficiency: Long-Term Follow-Up JIMD Reports ·Irene C. Huffnagel, E. Redeker, Liesbeth Reneman, Frédéric M. Vaz, Sacha Ferdinandusse, Bwee Tien Poll‐The	2017	24
12	An Integrated Physical Map of 210 Markers Assigned to the Short Arm of Human Chromosome 11 Genomics ·E. Redeker, J.M.N. Hoovers, Mariëlle Alders, C.J.A. van Moorsel, Alasdair Ivens, Simon G. Gregory, Linda M. Kalikin, Jet Bliek, L. de Galan, R. van den Bogaard, Jenny A. Visser, Robbert van der Voort, Andrew P. Feinberg, Peter Little, A. Westerveld, M. Mannens	1994	23
13	DNA analysis of the SH3BP2 gene in patients with aggressive central giant cell granuloma British Journal of Oral and Maxillofacial Surgery ·Jan de Lange, Merel C. van Maarle, Hans P. van den Akker, E. Redeker	2006	23
14	A new mutation in the SH3BP2 gene showing reduced penetrance in a family affected with cherubism Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology ·Jan de Lange, Merel C. van Maarle, Hans P. van den Akker, E. Redeker	2006	22
15	The distal region of 11p13 and associated genetic diseases Genomics ·M. Mannens, J.M.N. Hoovers, E. M. Bleeker‐Wagemakers, E. Redeker, Jet Bliek, M. Overbeeke-Melkert, G F Saunders, Bryan R.G. Williams, V. van Heynigen, Claudine Junien, Daniel A. Haber, Frank Speleman, Christa Heyting, Rosalyn Slater, N. J. Leschot, A. Westerveld	1991	20
16	Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands Familial Cancer ·Charlotte J. Dommering, Lidewij Henneman, Annemarie H. van der Hout, Marianne A. Jonker, Carli M.J. Tops, Ans M.W. van den Ouweland, Rob B. van der Luijt, Arjen R. Mensenkamp, Frans B.L. Hogervorst, E. Redeker, Christine de Die‐Smulders, Annette C. Moll, Hanne Meijers‐Heijboer	2016	17
17	Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange Syndrome European Journal of Human Genetics ·Zahurul A. Bhuiyan, Helen Stewart, E. Redeker, Marcel M. A. M. Mannens, Raoul C. M. Hennekam	2007	15
18	Development of NIPBL Locus-Specific Database Using LOVD: From Novel Mutations to Further Genotype-Phenotype Correlations in Cornelia de Lange Syndrome Human Mutation ·Jorge Oliveira, Cristina Dias, E. Redeker, Eurico Leandro Bandeirinha Pinto da Costa, João Silva, Margarida Reis Lima, Johan T. den Dunnen, Rosário Santos	2010	15
19	Successful Growth Hormone Therapy in Cornelia de Lange Syndrome Journal of Clinical Research in Pediatric Endocrinology ·Michael de Graaf, Sarina G. Kant, Jan M. Wit, E. Redeker, Gijs W.E. Santen, Annemieke Johanna Maria Henriëtta Verkerk, André G. Uitterlinden, Monique Losekoot, Wilma Oostdijk	2017	14
20	Molecular Genetic Testing for Familial Hypercholesterolemia in The Netherlands: A Stepwise Screening Strategy Enhances the Mutation Detection Rate Genetic Testing ·Maria Lombardi, E. Redeker, David H. Gent, K.L. Smeele, R. Weerdesteijn, Marcel M. A. M. Mannens	2006	13

About E. Redeker

E. Redeker is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Rheumatology and Surgery, having authored 29 papers that have together received 823 indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (4 papers), DNA Repair Mechanisms (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Epigenetics and DNA Methylation (3 papers), Lipoproteins and Cardiovascular Health (3 papers), Prenatal Screening and Diagnostics (3 papers), Folate and B Vitamins Research (2 papers) and Cancer Genomics and Diagnostics (2 papers). The work is most often cited by research in Genetics (260 citations), Molecular Biology (538 citations), Reproductive Medicine (46 citations), Oral Surgery (27 citations) and Pediatrics, Perinatology and Child Health (66 citations). E. Redeker has collaborated with scholars based in Netherlands, United States and Belgium. Frequent co-authors include Marcel M. A. M. Mannens, Christa Heyting, A. J. J. Dietrich, A. C. G. Vink, Peter B. Møens, Raoul C. M. Hennekam, Sylvia Huisman, Saskia M. Maas, Merel C. van Maarle and Arthur A. Bergen. Their work appears in journals such as Genomics, Human Molecular Genetics, Human Mutation, Atherosclerosis and Familial Cancer.

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.

Explore authors with similar magnitude of impact

E. Redeker

Impact in

Papers in i

In The Last Decade

E. Redeker

Peers

Countries citing papers authored by E. Redeker

Fields of papers citing papers by E. Redeker

All Works

About E. Redeker

Explore authors with similar magnitude of impact

Papers in