Hinreiner S - Search Results

1

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: hinreiner s. PLoS One. 2010 Mar 9;5(3):e9591. doi: 10.1371/journal.pone.0009591. PLoS One. 2010. PMID: 20231887 Free PMC article.

2

Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level.

Weise A, Gross M, Mrasek K, Mkrtchyan H, Horsthemke B, Jonsrud C, Von Eggeling F, Hinreiner S, Witthuhn V, Claussen U, Liehr T. Weise A, et al. Among authors: hinreiner s. Int J Mol Med. 2008 Feb;21(2):189-200. doi: 10.3892/ijmm.21.2.189. Int J Mol Med. 2008. PMID: 18204785

3

Characterization of chromosomal rearrangements using multicolor-banding (MCB/m-band).

Liehr T, Weise A, Hinreiner S, Mkrtchyan H, Mrasek K, Kosyakova N. Liehr T, et al. Among authors: hinreiner s. Methods Mol Biol. 2010;659:231-8. doi: 10.1007/978-1-60761-789-1_16. Methods Mol Biol. 2010. PMID: 20809315

4

POD-FISH: a new technique for parental origin determination based on copy number variation polymorphism.

Weise A, Gross M, Hinreiner S, Witthuhn V, Mkrtchyan H, Liehr T. Weise A, et al. Among authors: hinreiner s. Methods Mol Biol. 2010;659:291-8. doi: 10.1007/978-1-60761-789-1_22. Methods Mol Biol. 2010. PMID: 20809321

5

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: hinreiner s. Curr Genomics. 2010 Sep;11(6):426-31. doi: 10.2174/138920210793176047. Curr Genomics. 2010. PMID: 21358987 Free PMC article.

6

Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literature.

Liehr T, Mrasek K, Hinreiner S, Reich D, Ewers E, Bartels I, Seidel J, Emmanuil N, Petesen M, Polityko A, Dufke A, Iourov I, Trifonov V, Vermeesch J, Weise A. Liehr T, et al. Among authors: hinreiner s. Sex Dev. 2007;1(6):353-62. doi: 10.1159/000111767. Epub 2008 Jan 18. Sex Dev. 2007. PMID: 18391547 Review.

7

10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.

Liehr T, Stumm M, Wegner RD, Bhatt S, Hickmann P, Patsalis PC, Meins M, Morlot S, Klaschka V, Ewers E, Hinreiner S, Mrasek K, Kosyakova N, Cai WW, Cheung SW, Weise A. Liehr T, et al. Among authors: hinreiner s. Cytogenet Genome Res. 2009;124(1):102-5. doi: 10.1159/000200094. Epub 2009 Apr 15. Cytogenet Genome Res. 2009. PMID: 19372675

8

Novel complex t(V;9;22) rearrangements in three cases with chronic myeloid leukemia and a rare translocation in a case with classical Philadelphia chromosome.

Mkrtchyan H, Ghazaryan S, Avetisyan G, Hovhannisyan A, Muradyan L, Daghbashyan S, Karst C, Gross M, Hinreiner S, Aroutiounian R, Liehr T. Mkrtchyan H, et al. Among authors: hinreiner s. Oncol Rep. 2008 Jul;20(1):99-104. Oncol Rep. 2008. PMID: 18575724

9

An unexpected finding in a child with neurological problems: mosaic ring chromosome 18.

Koç A, Kan D, Karaer K, Ergün MA, Karaoğuz MY, Gücüyener K, Hinreiner S, Liehr T, Perçin EF. Koç A, et al. Among authors: hinreiner s. Eur J Pediatr. 2008 Jun;167(6):655-9. doi: 10.1007/s00431-007-0568-y. Epub 2007 Aug 1. Eur J Pediatr. 2008. PMID: 17668239

10

High Frequency of Pathogenic Rearrangements in SPG11 and Extensive Contribution of Mutational Hotspots and Founder Alleles.

Günther S, Elert-Dobkowska E, Soehn AS, Hinreiner S, Yoon G, Heller R, Hellenbroich Y, Hübner CA, Ray PN, Hehr U, Bauer P, Sulek A, Beetz C. Günther S, et al. Among authors: hinreiner s. Hum Mutat. 2016 Jul;37(7):703-9. doi: 10.1002/humu.23000. Epub 2016 Apr 28. Hum Mutat. 2016. PMID: 27071356

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