Deniz Kanber

1.6k total citations
33 papers, 999 citations indexed

About

Deniz Kanber is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Deniz Kanber has authored 33 papers receiving a total of 999 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 22 papers in Genetics and 17 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Deniz Kanber's work include Genetic Syndromes and Imprinting (21 papers), Epigenetics and DNA Methylation (20 papers) and Prenatal Screening and Diagnostics (17 papers). Deniz Kanber is often cited by papers focused on Genetic Syndromes and Imprinting (21 papers), Epigenetics and DNA Methylation (20 papers) and Prenatal Screening and Diagnostics (17 papers). Deniz Kanber collaborates with scholars based in Germany, United Kingdom and Netherlands. Deniz Kanber's co-authors include Bernhard Horsthemke, Karin Buiting, Jörg Gromoll, Frank Tüttelmann, Dietmar Lohmann, Diana Mitter, Reiner Siebert, Jasmin Beygo, Thomas Eggermann and Gabriele Gillessen‐Kaesbach and has published in prestigious journals such as PLoS ONE, Scientific Reports and PLoS Genetics.

In The Last Decade

Deniz Kanber

32 papers receiving 959 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Deniz Kanber Germany 17 712 662 403 117 94 33 999
Anna Newlin United States 12 147 0.2× 210 0.3× 96 0.2× 37 0.3× 64 0.7× 17 425
Shlomit Rienstein Israel 14 277 0.4× 161 0.2× 107 0.3× 67 0.6× 12 0.1× 28 559
Anita S. Kulharya United States 14 509 0.7× 452 0.7× 147 0.4× 85 0.7× 7 0.1× 31 843
Miho Ishida United Kingdom 11 415 0.6× 315 0.5× 167 0.4× 11 0.1× 22 0.2× 28 703
Kristin Bosse Germany 14 244 0.3× 312 0.5× 62 0.2× 40 0.3× 23 0.2× 24 526
Sophia Kitsiou‐Tzeli Greece 16 422 0.6× 407 0.6× 77 0.2× 44 0.4× 10 0.1× 39 656
Derek Lim United Kingdom 13 651 0.9× 546 0.8× 293 0.7× 13 0.1× 5 0.1× 24 928
Roel Hordijk Netherlands 15 409 0.6× 520 0.8× 184 0.5× 62 0.5× 4 0.0× 22 739
Sandra Chantot‐Bastaraud France 24 759 1.1× 939 1.4× 404 1.0× 304 2.6× 3 0.0× 67 1.4k
Carmelilia De Bernardo Italy 16 336 0.5× 261 0.4× 41 0.1× 32 0.3× 24 0.3× 32 612

Countries citing papers authored by Deniz Kanber

Since Specialization
Citations

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

Fields of papers citing papers by Deniz Kanber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Deniz Kanber

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

All Works

20 of 20 papers shown
1.
Budeus, Bettina, Saskia Ting, Deniz Kanber, et al.. (2024). In vitro model of retinoblastoma derived tumor and stromal cells for tumor microenvironment (TME) studies. Cell Death and Disease. 15(12). 905–905.
2.
Afanasyeva, Elena, M. Schneider, Christopher Schröder, et al.. (2024). A MYCN-driven de-differentiation profile identifies a subgroup of aggressive retinoblastoma. Communications Biology. 7(1). 919–919. 2 indexed citations
3.
Busch, Maike, Eva Biewald, Nikolaos E. Bechrakis, et al.. (2022). TFF1 in Aqueous Humor—A Potential New Biomarker for Retinoblastoma. Cancers. 14(3). 677–677. 14 indexed citations
4.
Kanber, Deniz, Alexandra Brenzel, Janine Altmüller, et al.. (2022). RB1-Negative Retinal Organoids Display Proliferation of Cone Photoreceptors and Loss of Retinal Differentiation. Cancers. 14(9). 2166–2166. 8 indexed citations
5.
Kanber, Deniz, Triinu Peters, Anna‐Lena Volckmar, et al.. (2022). Evidence for correlations between BMI-associated SNPs and circRNAs. Scientific Reports. 12(1). 12643–12643. 1 indexed citations
6.
Kanber, Deniz, et al.. (2020). Biallelic and monoallelic deletion of the RB1 promoter in six isogenic clonal H9 hESC lines. Stem Cell Research. 45. 101779–101779. 2 indexed citations
7.
Reschke, Madlen, Eva Biewald, Alma Kuechler, et al.. (2020). 13q deletion syndrome resulting from balanced chromosomal rearrangement in father: the significance of parental karyotyping. Molecular Cytogenetics. 13(1). 31–31. 4 indexed citations
8.
Beygo, Jasmin, Karin Buiting, Simon Ramsden, et al.. (2019). Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromes. European Journal of Human Genetics. 27(9). 1326–1340. 38 indexed citations
9.
Beygo, Jasmin, Gabriele Gillessen‐Kaesbach, Beate Albrecht, et al.. (2017). New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome. European Journal of Human Genetics. 25(8). 935–945. 31 indexed citations
10.
Fryssira, Helen, Deniz Kanber, Christalena Sofocleous, et al.. (2015). A novel large deletion of the ICR1 region including H19 and putative enhancer elements. BMC Medical Genetics. 16(1). 30–30. 6 indexed citations
11.
Buiting, Karin, Suzanne B. Cassidy, Daniel J. Driscoll, et al.. (2014). Clinical utility gene card for: Prader-Willi Syndrome. European Journal of Human Genetics. 22(9). 1153–1153. 15 indexed citations
12.
Schröder, Christopher, Deniz Kanber, Ludger Klein‐Hitpaß, et al.. (2014). Evolutionary Origin and Methylation Status of Human Intronic CpG Islands that Are Not Present in Mouse. Genome Biology and Evolution. 6(7). 1579–1588. 12 indexed citations
13.
Buiting, Karin, Jill Clayton‐Smith, Daniel J. Driscoll, et al.. (2014). Clinical utility gene card for: Angelman Syndrome. European Journal of Human Genetics. 23(2). 3–3. 24 indexed citations
14.
Kanber, Deniz, Karin Buiting, Christian Roos, et al.. (2013). The Origin of the RB1 Imprint. PLoS ONE. 8(11). e81502–e81502. 21 indexed citations
15.
Mitter, Diana, Reinhard Ullmann, Ludger Klein‐Hitpaß, et al.. (2011). Genotype–phenotype correlations in patients with retinoblastoma and interstitial 13q deletions. European Journal of Human Genetics. 19(9). 947–958. 76 indexed citations
16.
Irving, Melita, Karin Buiting, Deniz Kanber, et al.. (2010). Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14. American Journal of Medical Genetics Part A. 152A(8). 1942–1950. 27 indexed citations
17.
Buiting, Karin, Deniz Kanber, Bernhard Horsthemke, & Dietmar Lohmann. (2010). Imprinting of RB1 (the new kid on the block). Briefings in Functional Genomics. 9(4). 347–353. 26 indexed citations
18.
Begemann, Matthias, Sabrina Spengler, Deniz Kanber, et al.. (2010). Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues. Clinical Genetics. 80(1). 83–88. 48 indexed citations
19.
Kanber, Deniz, Karin Buiting, Michael Zeschnigk, Michael Ludwig, & Bernhard Horsthemke. (2008). Low frequency of imprinting defects in ICSI children born small for gestational age. European Journal of Human Genetics. 17(1). 22–29. 38 indexed citations
20.
Zeschnigk, Michael, Beate Albrecht, Karin Buiting, et al.. (2007). IGF2/H19 hypomethylation in Silver–Russell syndrome and isolated hemihypoplasia. European Journal of Human Genetics. 16(3). 328–334. 49 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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