Kanber D - Search Results

1

Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues.

Begemann M, Spengler S, Kanber D, Haake A, Baudis M, Leisten I, Binder G, Markus S, Rupprecht T, Segerer H, Fricke-Otto S, Mühlenberg R, Siebert R, Buiting K, Eggermann T. Begemann M, et al. Among authors: kanber d. Clin Genet. 2011 Jul;80(1):83-8. doi: 10.1111/j.1399-0004.2010.01514.x. Epub 2010 Jul 22. Clin Genet. 2011. PMID: 20738330

2

IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia.

Zeschnigk M, Albrecht B, Buiting K, Kanber D, Eggermann T, Binder G, Gromoll J, Prott EC, Seland S, Horsthemke B. Zeschnigk M, et al. Among authors: kanber d. Eur J Hum Genet. 2008 Mar;16(3):328-34. doi: 10.1038/sj.ejhg.5201974. Epub 2008 Jan 9. Eur J Hum Genet. 2008. PMID: 18159214

3

Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprinted DLK1/GTL2 gene cluster.

Buiting K, Kanber D, Martín-Subero JI, Lieb W, Terhal P, Albrecht B, Purmann S, Gross S, Lich C, Siebert R, Horsthemke B, Gillessen-Kaesbach G. Buiting K, et al. Among authors: kanber d. Hum Mutat. 2008 Sep;29(9):1141-6. doi: 10.1002/humu.20771. Hum Mutat. 2008. PMID: 18454453

4

Low frequency of imprinting defects in ICSI children born small for gestational age.

Kanber D, Buiting K, Zeschnigk M, Ludwig M, Horsthemke B. Kanber D, et al. Eur J Hum Genet. 2009 Jan;17(1):22-9. doi: 10.1038/ejhg.2008.177. Epub 2008 Oct 22. Eur J Hum Genet. 2009. PMID: 18941474 Free PMC article.

5

A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome.

Kanber D, Giltay J, Wieczorek D, Zogel C, Hochstenbach R, Caliebe A, Kuechler A, Horsthemke B, Buiting K. Kanber D, et al. Eur J Hum Genet. 2009 May;17(5):582-90. doi: 10.1038/ejhg.2008.232. Epub 2008 Dec 10. Eur J Hum Genet. 2009. PMID: 19066619 Free PMC article.

6

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.

7

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.

8

Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14.

Irving MD, Buiting K, Kanber D, Donaghue C, Schulz R, Offiah A, Mohammed SN, Oakey RJ. Irving MD, et al. Among authors: kanber d. Am J Med Genet A. 2010 Aug;152A(8):1942-50. doi: 10.1002/ajmg.a.33449. Am J Med Genet A. 2010. PMID: 20602488 Free PMC article.

9

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.

10

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

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