Papers authored by Hoischen A

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Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.
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Vissers LE, Bhatt SS, Janssen IM, Xia Z, Lalani SR, Pfundt R, Derwinska K, de Vries BB, Gilissen C, Hoischen A, Nesteruk M, Wisniowiecka-Kowalnik B, Smyk M, Brunner HG, Cheung SW, van Kessel AG, 
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Human molecular genetics 18(19):3579-93, 2009 Oct 1 - Who cited this? | PubMed ID: 19578123 | Fulltext
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Array-CGH in unclear syndromic nephropathies identifies a microdeletion in Xq22.3-q23.
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Hoischen A, Landwehr C, Kabisch S, Ding XQ, Trost D, Stropahl G, Wigger M, Radlwimmer B, Weber RG, and Haffner D
Pediatric nephrology (Berlin, Germany) 24(9):1673-81, 2009 Sep - Who cited this? | PubMed ID: 19444485 | Fulltext
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[Pain staging, gender, and rehabilitation outcome in chronic low back pain. A pilot study].
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Hampel P, Brunnberg A, Krohn-Grimberghe B, Mantel F, Thomsen M, Hoischen A, Hrkac M, Tlach L, Morfeld M, and Mohr B
Der Orthopade 38(8):742-51, 2009 Aug - Who cited this? | PubMed ID: 19618164 | Fulltext
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Rosetted glioneuronal tumor of the spine with overtly anaplastic histological features.
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Scholz M, Hoischen A, Radlwimmer B, Weber RG, Harders A, Reifenberger G, and Riemenschneider MJ
Acta neuropathologica 117(5):591-3, 2009 May - Who cited this? | PubMed ID: 19266208 | Fulltext
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Transchromosomic cell model of Down syndrome shows aberrant migration, adhesion and proteome response to extracellular matrix.
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Delom F, Burt E, Hoischen A, Veltman J, Groet J, Cotter FE, and Nizetic D
Proteome science 7:31, 2009 - Who cited this? | PubMed ID: 19715584 | Fulltext
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Comprehensive characterization of genomic aberrations in gangliogliomas by CGH, array-based CGH and interphase FISH.
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Hoischen A, Ehrler M, Fassunke J, Simon M, Baudis M, Landwehr C, Radlwimmer B, Lichter P, Schramm J, Becker AJ, and Weber RG
Brain pathology (Zurich, Switzerland) 18(3):326, 2008 Jul - Who cited this? | PubMed ID: 18371186 | Fulltext
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Angiocentric glioma: report of clinico-pathologic and genetic findings in 8 cases.
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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, and Hans VH
The American journal of surgical pathology 31(11):1709-18, 2007 Nov - Who cited this? | PubMed ID: 18059228 | Fulltext
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Genome-wide analysis for micro-aberrations in familial exstrophy of the bladder using array-based comparative genomic hybridization.
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Reutter H, Hoischen A, Ludwig M, Stein R, Radlwimmer B, Engels H, Wolffenbuttel KP, and Weber RG
BJU international 100(3):646-50, 2007 Sep - Who cited this? | PubMed ID: 17669146 | Fulltext
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Severe mental retardation with breathing abnormalities (Pitt-Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4.
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Brockschmidt A, Todt U, Ryu S, Hoischen A, Landwehr C, Birnbaum S, Frenck W, Radlwimmer B, Lichter P, Engels H, Driever W, Kubisch C, and Weber RG
Human molecular genetics 16(12):1488-94, 2007 Jun 15 - Who cited this? | PubMed ID: 17478476 | Fulltext
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DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation.
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Engels H, Brockschmidt A, Hoischen A, Landwehr C, Bosse K, Walldorf C, Toedt G, Radlwimmer B, Propping P, Lichter P, and Weber RG
Neurology 68(10):743-50, 2007 Mar 6 - Who cited this? | PubMed ID: 17339581 | Fulltext
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Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomas.
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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, and Reifenberger G
Oncogene 26(7):1088-97, 2007 Feb 15 - Who cited this? | PubMed ID: 16909113 | Fulltext
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Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.
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Brenk CH, Prott EC, Trost D, Hoischen A, Walldorf C, Radlwimmer B, Wieczorek D, Propping P, Gillessen-Kaesbach G, Weber RG, and Engels H
European journal of human genetics : EJHG 15(1):35-44, 2007 Jan - Who cited this? | PubMed ID: 17024214 | Fulltext
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Comprehensive genomic analysis of desmoplastic medulloblastomas: identification of novel amplified genes and separate evaluation of the different histological components.
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Ehrbrecht A, Müller U, Wolter M, Hoischen A, Koch A, Radlwimmer B, Actor B, Mincheva A, Pietsch T, Lichter P, Reifenberger G, and Weber RG
The Journal of pathology 208(4):554-63, 2006 Mar - Who cited this? | PubMed ID: 16400626 | Fulltext
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Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.
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Engels H, Bosse K, Ehrbrecht A, Zahn S, Hoischen A, Propping P, Bindl L, and Reutter H
American journal of medical genetics 111(2):205-9, 2002 Aug 1 - Who cited this? | PubMed ID: 12210352 | Fulltext
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