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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 4
2009 3
2010 2
2011 1
2013 2
2014 5
2015 3
2016 1
2017 2
2018 1
2019 1
2020 3
2021 2
2022 3
2024 0

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29 results

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Page 1
Evidence for correlations between BMI-associated SNPs and circRNAs.
Rajcsanyi LS, Diebels I, Pastoors L, Kanber D, Peters T, Volckmar AL, Zheng Y, Grosse M, Dieterich C, Hebebrand J, Kaiser FJ, Horsthemke B, Hinney A. Rajcsanyi LS, et al. Among authors: kanber d. Sci Rep. 2022 Jul 25;12(1):12643. doi: 10.1038/s41598-022-16495-7. Sci Rep. 2022. PMID: 35879369 Free PMC article.
Imprinting of RB1 (the new kid on the block).
Buiting K, Kanber D, Horsthemke B, Lohmann D. Buiting K, et al. Among authors: kanber d. Brief Funct Genomics. 2010 Jul;9(4):347-53. doi: 10.1093/bfgp/elq014. Epub 2010 Jun 15. Brief Funct Genomics. 2010. PMID: 20551090 Review.
The origin of the RB1 imprint.
Kanber D, Buiting K, Roos C, Gromoll J, Kaya S, Horsthemke B, Lohmann D. Kanber D, et al. PLoS One. 2013 Nov 25;8(11):e81502. doi: 10.1371/journal.pone.0081502. eCollection 2013. PLoS One. 2013. PMID: 24282601 Free PMC article.
TFF1 in Aqueous Humor-A Potential New Biomarker for Retinoblastoma.
Busch MA, Haase A, Miroschnikov N, Doege A, Biewald E, Bechrakis NE, Beier M, Kanber D, Lohmann D, Metz K, Dünker N. Busch MA, et al. Among authors: kanber d. Cancers (Basel). 2022 Jan 28;14(3):677. doi: 10.3390/cancers14030677. Cancers (Basel). 2022. PMID: 35158945 Free PMC article.
Clinical utility gene card for: Angelman Syndrome.
Buiting K, Clayton-Smith J, Driscoll DJ, Gillessen-Kaesbach G, Kanber D, Schwinger E, Williams C, Horsthemke B. Buiting K, et al. Among authors: kanber d. Eur J Hum Genet. 2015 Feb;23(2). doi: 10.1038/ejhg.2014.93. Epub 2014 Jun 4. Eur J Hum Genet. 2015. PMID: 24896151 Free PMC article. No abstract available.
Clinical utility gene card for: Prader-Willi Syndrome.
Buiting K, Cassidy SB, Driscoll DJ, Gillessen-Kaesbach G, Kanber D, Tauber M, Schwinger E, Horsthemke B. Buiting K, et al. Among authors: kanber d. Eur J Hum Genet. 2014 Sep;22(9). doi: 10.1038/ejhg.2014.66. Epub 2014 Apr 16. Eur J Hum Genet. 2014. PMID: 24736734 Free PMC article. No abstract available.
A familial disorder of altered DNA-methylation.
Caliebe A, Richter J, Ammerpohl O, Kanber D, Beygo J, Bens S, Haake A, Jüttner E, Korn B, Mackay DJ, Martin-Subero JI, Nagel I, Sebire NJ, Seidmann L, Vater I, von Kaisenberg CS, Temple IK, Horsthemke B, Buiting K, Siebert R. Caliebe A, et al. Among authors: kanber d. J Med Genet. 2014 Jun;51(6):407-12. doi: 10.1136/jmedgenet-2013-102149. Epub 2014 Apr 10. J Med Genet. 2014. PMID: 24721835
The human retinoblastoma gene is imprinted.
Kanber D, Berulava T, Ammerpohl O, Mitter D, Richter J, Siebert R, Horsthemke B, Lohmann D, Buiting K. Kanber D, et al. PLoS Genet. 2009 Dec;5(12):e1000790. doi: 10.1371/journal.pgen.1000790. Epub 2009 Dec 24. PLoS Genet. 2009. PMID: 20041224 Free PMC article.
29 results