Wilhelm K - Search Results

1

Comprehensive Analyses of White-Handed Gibbon Chromosomes Enables Access to 92 Evolutionary Conserved Breakpoints Compared to the Human Genome.

Weise A, Kosyakova N, Voigt M, Aust N, Mrasek K, Löhmer S, Rubtsov N, Karamysheva TV, Trifonov VA, Hardekopf D, Jančušková T, Pekova S, Wilhelm K, Liehr T, Fan X. Weise A, et al. Among authors: wilhelm k. Cytogenet Genome Res. 2015;145(1):42-9. doi: 10.1159/000381764. Epub 2015 Apr 24. Cytogenet Genome Res. 2015. PMID: 25926034

2

New aspects on chromosomal instability: chromosomal break-points in Fanconi anemia patients co-localize on the molecular level with fragile sites.

Schoder C, Liehr T, Velleuer E, Wilhelm K, Blaurock N, Weise A, Mrasek K. Schoder C, et al. Among authors: wilhelm k. Int J Oncol. 2010 Feb;36(2):307-12. Int J Oncol. 2010. PMID: 20043063

3

BAC-probes applied for characterization of fragile sites (FS).

Mrasek K, Wilhelm K, Quintana LG, Theuss L, Liehr T, Leskovac A, Filipovic J, Joksic G, Joksic I, Weise A. Mrasek K, et al. Among authors: wilhelm k. Methods Mol Biol. 2015;1227:289-98. doi: 10.1007/978-1-4939-1652-8_15. Methods Mol Biol. 2015. PMID: 25239753

4

Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements.

Liehr T, Kosayakova N, Schröder J, Ziegler M, Kreskowski K, Pohle B, Bhatt S, Theuss L, Wilhelm K, Weise A, Mrasek K. Liehr T, et al. Among authors: wilhelm k. Balkan J Med Genet. 2011 Dec;14(2):13-6. doi: 10.2478/v10034-011-0042-z. Balkan J Med Genet. 2011. PMID: 24052707 Free PMC article.

5

Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones.

Mrasek K, Schoder C, Teichmann AC, Behr K, Franze B, Wilhelm K, Blaurock N, Claussen U, Liehr T, Weise A. Mrasek K, et al. Among authors: wilhelm k. Int J Oncol. 2010 Apr;36(4):929-40. doi: 10.3892/ijo_00000572. Int J Oncol. 2010. PMID: 20198338

6

Parental origin of deletions and duplications - about the necessity to check for cryptic inversions.

Liehr T, Schreyer I, Kuechler A, Manolakos E, Singer S, Dufke A, Wilhelm K, Jančušková T, Čmejla R, Othman MAK, Al-Rikabi AH, Mrasek K, Ziegler M, Kankel S, Kreskowski K, Weise A. Liehr T, et al. Among authors: wilhelm k. Mol Cytogenet. 2018 Mar 9;11:20. doi: 10.1186/s13039-018-0369-1. eCollection 2018. Mol Cytogenet. 2018. PMID: 29541160 Free PMC article.

7

Recombinant Chromosomes Resulting From Parental Pericentric Inversions-Two New Cases and a Review of the Literature.

Liehr T, Weise A, Mrasek K, Ziegler M, Padutsch N, Wilhelm K, Al-Rikabi A. Liehr T, et al. Among authors: wilhelm k. Front Genet. 2019 Nov 14;10:1165. doi: 10.3389/fgene.2019.01165. eCollection 2019. Front Genet. 2019. PMID: 31798640 Free PMC article.

8

MLLT10 and IL3 rearrangement together with a complex four-way translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia: A case report.

Othman MA, Melo JB, Carreira IM, Rincic M, Alhourani E, Wilhelm K, Gruhn B, Glaser A, Liehr T. Othman MA, et al. Among authors: wilhelm k. Oncol Rep. 2015 Feb;33(2):625-30. doi: 10.3892/or.2014.3624. Epub 2014 Nov 25. Oncol Rep. 2015. PMID: 25435396

9

High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia.

Othman MA, Melo JB, Carreira IM, Rincic M, Glaser A, Grygalewicz B, Gruhn B, Wilhelm K, Rittscher K, Meyer B, Silva ML, de Jesus Marques Salles T, Liehr T. Othman MA, et al. Among authors: wilhelm k. Mol Cytogenet. 2015 Jun 30;8:45. doi: 10.1186/s13039-015-0153-4. eCollection 2015. Mol Cytogenet. 2015. PMID: 26136832 Free PMC article.

10

Next generation phenotyping in Emanuel and Pallister-Killian syndrome using computer-aided facial dysmorphology analysis of 2D photos.

Liehr T, Acquarola N, Pyle K, St-Pierre S, Rinholm M, Bar O, Wilhelm K, Schreyer I. Liehr T, et al. Among authors: wilhelm k. Clin Genet. 2018 Feb;93(2):378-381. doi: 10.1111/cge.13087. Epub 2017 Nov 29. Clin Genet. 2018. PMID: 28661575

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