B. Redeker

846 total citations
11 papers, 397 citations indexed

About

B. Redeker is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, B. Redeker has authored 11 papers receiving a total of 397 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in B. Redeker's work include Genetic Syndromes and Imprinting (5 papers), Prenatal Screening and Diagnostics (4 papers) and Epigenetics and DNA Methylation (3 papers). B. Redeker is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Prenatal Screening and Diagnostics (4 papers) and Epigenetics and DNA Methylation (3 papers). B. Redeker collaborates with scholars based in Netherlands, United Kingdom and United States. B. Redeker's co-authors include Marcel M. A. M. Mannens, Marja Steenman, Shelagh Boyle, Judy Fletcher, John M. Brown, Judy Fantes, Isabel M. Hanson, Wendy A. Bickmore, Yoshimitsu Fukushima and Matthew Breen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

B. Redeker

11 papers receiving 394 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
B. Redeker Netherlands	7	316	238	101	38	30	11	397
Satoshi Ishikiriyama Japan	10	289 0.9×	283 1.2×	128 1.3×	52 1.4×	13 0.4×	21	472
Venkateswara R. Potluri United States	7	141 0.4×	195 0.8×	50 0.5×	33 0.9×	47 1.6×	10	321
Herbert Reichenbach Germany	6	308 1.0×	145 0.6×	72 0.7×	26 0.7×	38 1.3×	9	411
Hiba Risheg United States	10	374 1.2×	403 1.7×	164 1.6×	53 1.4×	28 0.9×	13	640
Kiyoshi Kikkawa Japan	12	182 0.6×	211 0.9×	103 1.0×	56 1.5×	32 1.1×	27	378
G. Del Porto Italy	12	154 0.5×	186 0.8×	64 0.6×	54 1.4×	16 0.5×	26	344
Philippe Coullin France	15	268 0.8×	208 0.9×	189 1.9×	76 2.0×	30 1.0×	28	526
Anna Sowińska‐Seidler Poland	13	254 0.8×	237 1.0×	74 0.7×	23 0.6×	12 0.4×	38	409
B. Horsthemke Germany	9	326 1.0×	321 1.3×	135 1.3×	34 0.9×	6 0.2×	13	444
C. Mignon France	11	327 1.0×	176 0.7×	74 0.7×	46 1.2×	31 1.0×	14	434

Countries citing papers authored by B. Redeker

Since Specialization

Citations

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

Fields of papers citing papers by B. Redeker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Redeker

This figure shows the co-authorship network connecting the top 25 collaborators of B. Redeker. A scholar is included among the top collaborators of B. Redeker 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 B. Redeker. B. Redeker is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Heinen, Charlotte A., Aldo Jongejan, Peter J. Watson, et al.. (2016). A specific mutation in TBL1XR1 causes Pierpont syndrome. Journal of Medical Genetics. 53(5). 330–337. 44 indexed citations

Vansenne, Fleur, Mariëtte Goddijn, B. Redeker, et al.. (2011). Knowledge and perceived risks in couples undergoing genetic testing after recurrent miscarriage or for poor semen quality. Reproductive BioMedicine Online. 23(4). 525–533. 4 indexed citations

Goddijn, Mariëtte, Heleen Schuring‐Blom, B. Redeker, et al.. (2005). Detection of Chromosome Abnormalities by Quantitative Fluorescent PCR in Ectopic Pregnancies. Gynecologic and Obstetric Investigation. 60(3). 139–144. 3 indexed citations

Speleman, Frank, Eva van den Berg, Catharina Dhooge, et al.. (1998). Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma. Genes Chromosomes and Cancer. 21(3). 265–269. 14 indexed citations

Steenman, Marja, B. Redeker, P.A. Voûte, et al.. (1997). Comparative genomic hybridization analysis of Wilms tumors. Cytogenetic and Genome Research. 77(3-4). 296–303. 53 indexed citations

Alders, Mariëlle, Jet Bliek, B. Redeker, et al.. (1996). Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors. Medical and Pediatric Oncology. 27(5). 495–497. 1 indexed citations

Mannens, Marcel M. A. M., Mariëlle Alders, B. Redeker, et al.. (1996). Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors. Medical and Pediatric Oncology. 27(5). 490–494. 16 indexed citations

Mannens, M., Mariëlle Alders, B. Redeker, et al.. (1996). Positional cloning of genes involved in the Beckwith‐Wiedemann syndrome, hemihypertrophy, and associated childhood tumors. Medical and Pediatric Oncology. 27(5). 490–494. 2 indexed citations

Fantes, Judy, B. Redeker, Matthew Breen, et al.. (1995). Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype. Human Molecular Genetics. 4(3). 415–422. 156 indexed citations

10.

Hoovers, J.M.N., Linda M. Kalikin, Laura A. Johnson, et al.. (1995). Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.. Proceedings of the National Academy of Sciences. 92(26). 12456–12460. 94 indexed citations

11.

Speleman, Frank, M. Mannens, B. Redeker, et al.. (1991). Characterization of a de novo duplication of 11p14→p13, using fluorescent in situ hybridization and Southern hybridization. Cytogenetic and Genome Research. 56(3-4). 129–131. 10 indexed citations

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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