E. Redeker

2.4k citations

29 papers · 808 indexed · h-index 17

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

Oral Surgery 3
- Oral and Maxillofacial Pathology 3
Genetics 8
- Genomic variations and chromosomal abnormalities 4

Co-authors: 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
Journals: Genomics (3 papers)Human Molecular Genetics (2 papers)European Journal of Human Genetics (1 paper)Familial Cancer (1 paper)Atherosclerosis (1 paper)
Partner nations: Netherlands United States Belgium

In The Last Decade

E. Redeker

29 papers receiving 798 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-authorship network

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

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20 of 20 papers shown

#	Work
1	A novel pathogenic frameshift variant in AXIN2 in a man with polyposis and hypodontia Hereditary Cancer in Clinical Practice ·Marjoleine F. Broekema, E. Redeker, Fernando Peña Silva, Liselotte P. van Hest	2023	1
2	Framing the potential of public frameshift peptides as immunotherapy targets in colon cancer PLoS ONE ·Shakiba Ghadir Jamal Abad, A. Kumar, Aldo Jongejan, E. Redeker, Cornelis J.A. Punt, Adriaan D. Bins	2021	7
3	With expanded carrier screening, founder populations run the risk of being overlooked Journal of Community Genetics ·Inge B. Mathijssen, Merel C. van Maarle, Novi Ratna Sari, E. Redeker, Leo P. ten Kate, Lidewij Henneman, Hanne Meijers‐Heijboer	2017	9
4	Successful Growth Hormone Therapy in Cornelia de Lange Syndrome Journal of Clinical Research in Pediatric Endocrinology ·Muhammad Nawaz Tunio, Sarina G. Kant, Jan M. Wit, E. Redeker, Gijs W.E. Santen, V.A. Ivanov, André G. Uitterlinden, Monique Losekoot, Wilma Oostdijk	2017	14
5	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
6	Targeted carrier screening for four recessive disorders: High detection rate within a founder population European Journal of Medical Genetics ·Inge B. Mathijssen, Lidewij Henneman, Sam Woodhouse, Phillis Lakeman, Sébastien Roland, E. Redeker, G. Fabiani, Hanne Meijers‐Heijboer, Merel C. van Maarle	2015	23
7	Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly BMC Medical Genomics ·Patrick Rump, A. Kozlov, Krista K. van Dijk-Bos, Lennart Johansson, Anthonie J. van Essen, Tanya Vandale, 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	59
8	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	81
9	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, Aha Gilang Nugraha, João Silva, مهرانوش امامیان طبرستانی, Johan T. den Dunnen, Rosário Santos	2010	15
10	Increased DNA damage sensitivity of Cornelia de Lange syndrome cells: evidence for impaired recombinational repair Human Molecular Genetics ·Mischa G. Vrouwe, Francisco Pérez Daza, 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	87
11	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
12	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, Paul Edeghoghon Umolu, Rui Diogo, Marcel M. A. M. Mannens	2006	13
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	Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3 Cytogenetic and Genome Research ·E. Redeker, Mariëlle Alders, J.M.N. Hoovers, Charles W. Richard, A. Westerveld, M. Mannens	1995	18
15	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, Kanayama Kiichi, Alasdair Ivens, Simon G. Gregory, Linda M. Kalikin, Jet Bliek, L. de Galan, Christian Eitzinger, Jenny A. Visser, Robbert van der Voort, Andrew P. Feinberg, Peter Little, A. Westerveld, M. Mannens	1994	23
16	The distal region of 11p13 and associated genetic diseases Genomics ·M. Mannens, J.M.N. Hoovers, E. M. Bleeker‐Wagemakers, E. Redeker, Jet Bliek, Lanwei Zhu, G F Saunders, Bryan R.G. Williams, Ngenroda Mön, Claudine Junien, Daniel A. Haber, Frank Speleman, Christa Heyting, Rosalyn Slater, N. J. Leschot, A. Westerveld	1991	19
17	DNA diagnosis in a family with autosomal dominant aniridia Ophthalmic Paediatrics and Genetics ·Frank D. Verbraak, D. Richards, E. Redeker, G F Saunders, E. M. Bleeker‐Wagemakers	1991	3
18	Synaptonemal complex proteins Genome ·Christa Heyting, A. J. J. Dietrich, Peter B. Møens, بوزرورة ليندة, Hildo H. Offenberg, E. Redeker, A. C. G. Vink	1989	79
19	Two major components of synaptonemal complexes are specific for meiotic prophase nuclei Chromosoma ·Christa Heyting, بوزرورة ليندة, A. J. J. Dietrich, E. Redeker, A. C. G. Vink	1988	58
20	Amniotic fluid gel acetylcholinesterase determination in prenatal diagnosis: Dark field illumination as a method for improving the detection of precipitation bands Prenatal Diagnosis ·John Bosco Odongo, Christa Heyting, J. D. Kalen, E. Redeker	1985	3

About E. Redeker

E. Redeker is a scholar working on Oral Surgery, Genetics, Molecular Biology, Rheumatology and Reproductive Medicine, having authored 29 papers that have together received 808 indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (5 papers), Genomic variations and chromosomal abnormalities (4 papers), DNA Repair Mechanisms (3 papers), Epigenetics and DNA Methylation (3 papers), Prenatal Screening and Diagnostics (3 papers), Lipoproteins and Cardiovascular Health (3 papers), Oral and Maxillofacial Pathology (3 papers) and RNA Research and Splicing (3 papers). The work is most often cited by research in Genetics (284 citations), Molecular Biology (571 citations), Reproductive Medicine (46 citations), Oral Surgery (34 citations) and Pediatrics, Perinatology and Child Health (77 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 W. van Raamsdonk. Their work appears in journals such as Genomics, Human Molecular Genetics, European Journal of Human Genetics, Familial Cancer and Atherosclerosis.

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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