Volleth M - Search Results

1

Evidence for multi-copy Mega-NUMTs in the human genome.

Lutz-Bonengel S, Niederstätter H, Naue J, Koziel R, Yang F, Sänger T, Huber G, Berger C, Pflugradt R, Strobl C, Xavier C, Volleth M, Weiß SC, Irwin JA, Romsos EL, Vallone PM, Ratzinger G, Schmuth M, Jansen-Dürr P, Liehr T, Lichter P, Parsons TJ, Pollak S, Parson W. Lutz-Bonengel S, et al. Among authors: volleth m. Nucleic Acids Res. 2021 Feb 22;49(3):1517-1531. doi: 10.1093/nar/gkaa1271. Nucleic Acids Res. 2021. PMID: 33450006 Free PMC article.

2

Long-term Culture of EBV-induced Human Lymphoblastoid Cell Lines Reveals Chromosomal Instability.

Volleth M, Zenker M, Joksic I, Liehr T. Volleth M, et al. J Histochem Cytochem. 2020 Apr;68(4):239-251. doi: 10.1369/0022155420910113. Epub 2020 Feb 28. J Histochem Cytochem. 2020. PMID: 32108534 Free PMC article.

3

High-resolution chromosome painting reveals the first genetic signature for the chiropteran suborder Pteropodiformes (Mammalia: Chiroptera).

Volleth M, Yang F, Müller S. Volleth M, et al. Chromosome Res. 2011 May;19(4):507-19. doi: 10.1007/s10577-011-9196-5. Epub 2011 Mar 11. Chromosome Res. 2011. PMID: 21394511

4

The human genome puzzle - the role of copy number variation in somatic mosaicism.

Mkrtchyan H, Gross M, Hinreiner S, Polytiko A, Manvelyan M, Mrasek K, Kosyakova N, Ewers E, Nelle H, Liehr T, Bhatt S, Thoma K, Gebhart E, Wilhelm S, Fahsold R, Volleth M, Weise A. Mkrtchyan H, et al. Among authors: volleth m. Curr Genomics. 2010 Sep;11(6):426-31. doi: 10.2174/138920210793176047. Curr Genomics. 2010. PMID: 21358987 Free PMC article.

5

Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?

Guilherme RS, Klein E, Venner C, Hamid AB, Bhatt S, Melaragno MI, Volleth M, Polityko A, Kulpanovich A, Kosyakova N, Liehr T. Guilherme RS, et al. Among authors: volleth m. Chromosome Res. 2012 Oct;20(7):825-35. doi: 10.1007/s10577-012-9316-x. Epub 2012 Oct 18. Chromosome Res. 2012. PMID: 23076733

6

16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2.

Barber JC, Hall V, Maloney VK, Huang S, Roberts AM, Brady AF, Foulds N, Bewes B, Volleth M, Liehr T, Mehnert K, Bateman M, White H. Barber JC, et al. Among authors: volleth m. Eur J Hum Genet. 2013 Feb;21(2):182-9. doi: 10.1038/ejhg.2012.144. Epub 2012 Jul 25. Eur J Hum Genet. 2013. PMID: 22828807 Free PMC article.

7

Genotype/phenotype analysis in a patient with pure and complete trisomy 12p.

Zumkeller W, Volleth M, Muschke P, Tönnies H, Heller A, Liehr T, Wieacker P, Stumm M. Zumkeller W, et al. Among authors: volleth m. Am J Med Genet A. 2004 Sep 1;129A(3):261-4. doi: 10.1002/ajmg.a.30125. Am J Med Genet A. 2004. PMID: 15326625

8

Early embryonic chromosome instability results in stable mosaic pattern in human tissues.

Mkrtchyan H, Gross M, Hinreiner S, Polytiko A, Manvelyan M, Mrasek K, Kosyakova N, Ewers E, Nelle H, Liehr T, Volleth M, Weise A. Mkrtchyan H, et al. Among authors: volleth m. PLoS One. 2010 Mar 9;5(3):e9591. doi: 10.1371/journal.pone.0009591. PLoS One. 2010. PMID: 20231887 Free PMC article.

9

Mitotic stability of small supernumerary marker chromosomes depends on their shape and telomeres - a long term in vitro study.

Hussein SS, Kreskowski K, Ziegler M, Klein E, Hamid AB, Kosyakova N, Volleth M, Liehr T, Fan X, Piaszinski K. Hussein SS, et al. Among authors: volleth m. Gene. 2014 Dec 1;552(2):246-8. doi: 10.1016/j.gene.2014.09.041. Epub 2014 Sep 20. Gene. 2014. PMID: 25245454

10

Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors.

Hochstenbach R, Nowakowska B, Volleth M, Ummels A, Kutkowska-Kaźmierczak A, Obersztyn E, Ziemkiewicz K, Gerloff C, Schanze D, Zenker M, Muschke P, Schanze I, Poot M, Liehr T. Hochstenbach R, et al. Among authors: volleth m. Mol Syndromol. 2016 Feb;6(5):210-21. doi: 10.1159/000441408. Epub 2015 Oct 31. Mol Syndromol. 2016. PMID: 26997941 Free PMC article.

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