Ilse Wieland

Ilse Wieland

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Ilse Wieland

Ilse Wieland

Publications by authors named "Ilse Wieland"

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Detection of a multilineage mosaic NRAS mutation c.181C>A (p.Gln61Lys) in an individual with a complex congenital nevus syndrome.

Pigment Cell Melanoma Res 2019 05 21;32(3):470-473. Epub 2018 Dec 21.

Institute of Human Genetics, University Hospital Otto-von-Guericke-University, Magdeburg, Germany.

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http://dx.doi.org/10.1111/pcmr.12761DOI Listing
May 2019

A Postzygotic SMO Mutation Caused the Original Case of Happle-Tinschert Syndrome.

Acta Derm Venereol 2018 Apr;98(5):534-535

Institute of Human Genetics, University Hospital Magdeburg, Otto-von-Guericke University, Leipziger Str. 44, DE-39120 Magdeburg, Germany.

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http://dx.doi.org/10.2340/00015555-2883DOI Listing
April 2018

Genetic Variants of DICE1/INTS6 in German Prostate Cancer Families with Linkage to 13q14.

Urol Int 2015 31;95(4):386-9. Epub 2015 Jan 31.

Klinik fx00FC;r Urologie, Otto-von-Guericke-Universitx00E4;t, Magdeburg, Germany.

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http://dx.doi.org/10.1159/000366229DOI Listing
September 2016

Hereditary diffuse leukoencephalopathy with spheroids (HDLS) with a novel CSF1R mutation and spinal cord involvement.

J Neurol Sci 2015 Nov 28;358(1-2):515-7. Epub 2015 Sep 28.

German Center for Neurodegenerative Disease, Leipziger Straße 44, 39120 Magdeburg, Germany.

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http://dx.doi.org/10.1016/j.jns.2015.09.370DOI Listing
November 2015

Craniofrontonasal Syndrome: Atrial Septal Defect With a Novel EFNB1 Gene Mutation.

Cleft Palate Craniofac J 2015 Mar 11;52(2):234-6. Epub 2014 Jun 11.

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http://dx.doi.org/10.1597/13-354DOI Listing
March 2015

Clinical and genetic evaluation of patients with KATP channel mutations from the German registry for congenital hyperinsulinism.

Horm Res Paediatr 2014 7;81(3):156-68. Epub 2014 Jan 7.

Department of Pediatrics, Otto von Guericke University Magdeburg, Magdeburg, Germany.

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https://www.karger.com/Article/FullText/356905
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http://dx.doi.org/10.1159/000356905DOI Listing
December 2014

A cryptic unbalanced translocation der(4)t(4;17)(p16.1;q25.3) identifies Wittwer syndrome as a variant of Wolf-Hirschhorn syndrome.

Am J Med Genet A 2014 Dec 23;164A(12):3213-4. Epub 2014 Sep 23.

Institute of Human Genetics, University Hospital Magdeburg, Otto-von-Guericke University, Magdeburg, Germany.

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http://doi.wiley.com/10.1002/ajmg.a.36765
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http://dx.doi.org/10.1002/ajmg.a.36765DOI Listing
December 2014

Potocki-Shaffer deletion encompassing ALX4 in a patient with frontonasal dysplasia phenotype.

Am J Med Genet A 2014 Feb 13;164A(2):346-52. Epub 2013 Dec 13.

Division of Pediatrics, San Giovanni Hospital, Bellinzona, Switzerland.

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http://dx.doi.org/10.1002/ajmg.a.36140DOI Listing
February 2014

High-level somatic mosaicism of AKT1 c.49G>A mutation in skin scrapings from epidermal nevi enables non-invasive molecular diagnosis in patients with Proteus syndrome.

Am J Med Genet A 2013 Apr 22;161A(4):889-91. Epub 2013 Feb 22.

Institute of Human Genetics, University Hospital Magdeburg, Otto-von-Guericke University, Magdeburg, Germany.

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http://dx.doi.org/10.1002/ajmg.a.35764DOI Listing
April 2013

The impact of CFNS-causing EFNB1 mutations on ephrin-B1 function.

BMC Med Genet 2010 Jun 17;11:98. Epub 2010 Jun 17.

Institut für Humangenetik, Universitätsklinikum, Otto-von-Guericke-Universität, Magdeburg, Germany.

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http://dx.doi.org/10.1186/1471-2350-11-98DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901216PMC
June 2010

Dissecting the molecular mechanisms in craniofrontonasal syndrome: differential mRNA expression of mutant EFNB1 and the cellular mosaic.

Eur J Hum Genet 2008 Feb 28;16(2):184-91. Epub 2007 Nov 28.

Institut für Humangenetik, Otto-von-Guericke-Universität, Magdeburg, Germany.

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http://www.nature.com/articles/5201968
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http://dx.doi.org/10.1038/sj.ejhg.5201968DOI Listing
February 2008

Gene symbol: EFNB1. Disease: Craniofrontonasal syndrome.

Hum Genet 2008 Feb;123(1):105

Otto-von-Guericke-Universität, Institut für Humangenetik, Leipziger Str., 44, 39120 Magdeburg, Germany.

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February 2008

Gene symbol: EFNB1. Disease: Craniofrontonasal syndrome.

Hum Genet 2008 Feb;123(1):105

Otto-von-Guericke-Universität, Institut für Humangenetik, Leipziger Str., 44, 39120 Magdeburg, Germany.

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February 2008

The heterozygous LMNA mutation p.R471G causes a variable phenotype with features of two types of familial partial lipodystrophy.

Am J Med Genet A 2007 Dec;143A(23):2810-4

Institute of Human Genetics, Otto von Guericke University, Magdeburg, Germany.

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http://doi.wiley.com/10.1002/ajmg.a.32046
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http://dx.doi.org/10.1002/ajmg.a.32046DOI Listing
December 2007

High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11).

Genes Chromosomes Cancer 2006 Oct;45(10):945-9

Institut für Humangenetik, Otto-von-Guericke-Universität, Magdeburg, Germany.

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http://dx.doi.org/10.1002/gcc.20358DOI Listing
October 2006

Clinical and genetic aspects of craniofrontonasal syndrome: towards resolving a genetic paradox.

Mol Genet Metab 2005 Sep-Oct;86(1-2):110-6

Institut für Humangenetik, Otto-von-Guericke-Universität, Leipziger Str. 44, D-39120 Magdeburg, Germany.

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http://dx.doi.org/10.1016/j.ymgme.2005.07.017DOI Listing
January 2006

Promoter CpG hypermethylation and downregulation of DICE1 expression in prostate cancer.

Oncogene 2005 Oct;24(44):6667-75

Institute of Human Genetics, Otto-von-Guericke-University Magdeburg, Germany.

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http://dx.doi.org/10.1038/sj.onc.1208824DOI Listing
October 2005

Ectopic expression of DICE1 suppresses tumor cell growth.

Oncol Rep 2004 Aug;12(2):207-11

Institute of Human Genetics, Otto-von-Guericke-Universität, Magdeburg, Germany.

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August 2004

Molecular interactions of B-CAM (basal-cell adhesion molecule) and laminin in epithelial skin cancer.

Arch Dermatol Res 2004 Jul 15;296(2):59-66. Epub 2004 Jun 15.

Rudolf Virchow Center, DFG Research Center for Experimental Biomedicine and Department of Dermatology, University of Würzburg, Würzburg, Germany.

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http://dx.doi.org/10.1007/s00403-004-0481-4DOI Listing
July 2004

Mutations of the ephrin-B1 gene cause craniofrontonasal syndrome.

Am J Hum Genet 2004 Jun 29;74(6):1209-15. Epub 2004 Apr 29.

Institut fur Humangenetik, Otto-von-Guericke-Universitat Magdeburg, 39120 Magdeburg, Germany.

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http://dx.doi.org/10.1086/421532DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1182084PMC
June 2004

Further delineation of Wittwer syndrome and refinement of the mapping region.

Am J Med Genet A 2003 Jan;116A(1):57-60

Institut für Humangenetik, Otto-von-Guericke-Universität, Magdeburg, Germany.

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http://dx.doi.org/10.1002/ajmg.a.10874DOI Listing
January 2003

Loss of heterozygosity on chromosome 5p13-12 predicts adverse prognosis in advanced bladder cancer independent of tumor stage and grade.

J Urol 2002 Dec;168(6):2655-8

Department of Urology, Institute of Human Genetics, Ott-von-Guericke University, Magdeburg, Germany.

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http://dx.doi.org/10.1097/01.ju.0000036540.89492.88DOI Listing
December 2002