Hoischen A - Search Results

1

Genome-wide analysis for micro-aberrations in familial exstrophy of the bladder using array-based comparative genomic hybridization.

Reutter H, Hoischen A, Ludwig M, Stein R, Radlwimmer B, Engels H, Wolffenbuttel KP, Weber RG. Reutter H, et al. Among authors: hoischen a. BJU Int. 2007 Sep;100(3):646-50. doi: 10.1111/j.1464-410X.2007.07086.x. BJU Int. 2007. PMID: 17669146

2

Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.

Engels H, Bosse K, Ehrbrecht A, Zahn S, Hoischen A, Propping P, Bindl L, Reutter H. Engels H, et al. Among authors: hoischen a. Am J Med Genet. 2002 Aug 1;111(2):205-9. doi: 10.1002/ajmg.10560. Am J Med Genet. 2002. PMID: 12210352 Review.

3

Comprehensive genomic analysis of desmoplastic medulloblastomas: identification of novel amplified genes and separate evaluation of the different histological components.

Ehrbrecht A, Müller U, Wolter M, Hoischen A, Koch A, Radlwimmer B, Actor B, Mincheva A, Pietsch T, Lichter P, Reifenberger G, Weber RG. Ehrbrecht A, et al. Among authors: hoischen a. J Pathol. 2006 Mar;208(4):554-63. doi: 10.1002/path.1925. J Pathol. 2006. PMID: 16400626

4

Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomas.

Weber RG, Hoischen A, Ehrler M, Zipper P, Kaulich K, Blaschke B, Becker AJ, Weber-Mangal S, Jauch A, Radlwimmer B, Schramm J, Wiestler OD, Lichter P, Reifenberger G. Weber RG, et al. Among authors: hoischen a. Oncogene. 2007 Feb 15;26(7):1088-97. doi: 10.1038/sj.onc.1209851. Epub 2006 Aug 7. Oncogene. 2007. PMID: 16909113

5

Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.

Brenk CH, Prott EC, Trost D, Hoischen A, Walldorf C, Radlwimmer B, Wieczorek D, Propping P, Gillessen-Kaesbach G, Weber RG, Engels H. Brenk CH, et al. Among authors: hoischen a. Eur J Hum Genet. 2007 Jan;15(1):35-44. doi: 10.1038/sj.ejhg.5201718. Epub 2006 Oct 4. Eur J Hum Genet. 2007. PMID: 17024214

6

DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation.

Engels H, Brockschmidt A, Hoischen A, Landwehr C, Bosse K, Walldorf C, Toedt G, Radlwimmer B, Propping P, Lichter P, Weber RG. Engels H, et al. Among authors: hoischen a. Neurology. 2007 Mar 6;68(10):743-50. doi: 10.1212/01.wnl.0000256367.70365.e0. Neurology. 2007. PMID: 17339581

7

Severe mental retardation with breathing abnormalities (Pitt-Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4.

Brockschmidt A, Todt U, Ryu S, Hoischen A, Landwehr C, Birnbaum S, Frenck W, Radlwimmer B, Lichter P, Engels H, Driever W, Kubisch C, Weber RG. Brockschmidt A, et al. Among authors: hoischen a. Hum Mol Genet. 2007 Jun 15;16(12):1488-94. doi: 10.1093/hmg/ddm099. Epub 2007 May 3. Hum Mol Genet. 2007. PMID: 17478476

8

Angiocentric glioma: report of clinico-pathologic and genetic findings in 8 cases.

Preusser M, Hoischen A, Novak K, Czech T, Prayer D, Hainfellner JA, Baumgartner C, Woermann FG, Tuxhorn IE, Pannek HW, Bergmann M, Radlwimmer B, Villagrán R, Weber RG, Hans VH. Preusser M, et al. Among authors: hoischen a. Am J Surg Pathol. 2007 Nov;31(11):1709-18. doi: 10.1097/PAS.0b013e31804a7ebb. Am J Surg Pathol. 2007. PMID: 18059228

9

Comprehensive characterization of genomic aberrations in gangliogliomas by CGH, array-based CGH and interphase FISH.

Hoischen A, Ehrler M, Fassunke J, Simon M, Baudis M, Landwehr C, Radlwimmer B, Lichter P, Schramm J, Becker AJ, Weber RG. Hoischen A, et al. Brain Pathol. 2008 Jul;18(3):326-37. doi: 10.1111/j.1750-3639.2008.00122.x. Epub 2008 Mar 26. Brain Pathol. 2008. PMID: 18371186 Free PMC article.

10

Rosetted glioneuronal tumor of the spine with overtly anaplastic histological features.

Scholz M, Hoischen A, Radlwimmer B, Weber RG, Harders A, Reifenberger G, Riemenschneider MJ. Scholz M, et al. Among authors: hoischen a. Acta Neuropathol. 2009 May;117(5):591-3. doi: 10.1007/s00401-009-0510-7. Epub 2009 Mar 6. Acta Neuropathol. 2009. PMID: 19266208 No abstract available.

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