Mangold E - Search Results

1

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.

Mangold E, Ludwig KU, Birnbaum S, Baluardo C, Ferrian M, Herms S, Reutter H, de Assis NA, Chawa TA, Mattheisen M, Steffens M, Barth S, Kluck N, Paul A, Becker J, Lauster C, Schmidt G, Braumann B, Scheer M, Reich RH, Hemprich A, Pötzsch S, Blaumeiser B, Moebus S, Krawczak M, Schreiber S, Meitinger T, Wichmann HE, Steegers-Theunissen RP, Kramer FJ, Cichon S, Propping P, Wienker TF, Knapp M, Rubini M, Mossey PA, Hoffmann P, Nöthen MM. Mangold E, et al. Nat Genet. 2010 Jan;42(1):24-6. doi: 10.1038/ng.506. Epub 2009 Dec 20. Nat Genet. 2010. PMID: 20023658

2

[Hereditary colorectal carcinoma: predictive diagnosis and genetic counseling].

Mangold E, Friedl W, Propping P. Mangold E, et al. Praxis (Bern 1994). 2001 Mar 22;90(12):490-6. Praxis (Bern 1994). 2001. PMID: 11324308 German.

3

A modified multiplex PCR assay for detection of large deletions in MSH2 and MLH1.

Wang Y, Friedl W, Sengteller M, Jungck M, Filges I, Propping P, Mangold E. Wang Y, et al. Among authors: mangold e. Hum Mutat. 2002 Mar;19(3):279-86. doi: 10.1002/humu.10042. Hum Mutat. 2002. PMID: 11857745

4

Loss of DNA mismatch repair proteins in skin tumors from patients with Muir-Torre syndrome and MSH2 or MLH1 germline mutations: establishment of immunohistochemical analysis as a screening test.

Mathiak M, Rütten A, Mangold E, Fischer HP, Ruzicka T, Friedl W, Propping P, Kruse R. Mathiak M, et al. Among authors: mangold e. Am J Surg Pathol. 2002 Mar;26(3):338-43. doi: 10.1097/00000478-200203000-00007. Am J Surg Pathol. 2002. PMID: 11859205

5

Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers.

Friedl W, Uhlhaas S, Schulmann K, Stolte M, Loff S, Back W, Mangold E, Stern M, Knaebel HP, Sutter C, Weber RG, Pistorius S, Burger B, Propping P. Friedl W, et al. Among authors: mangold e. Hum Genet. 2002 Jul;111(1):108-11. doi: 10.1007/s00439-002-0748-9. Epub 2002 Jun 13. Hum Genet. 2002. PMID: 12136244

6

Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes.

Wang Y, Friedl W, Lamberti C, Jungck M, Mathiak M, Pagenstecher C, Propping P, Mangold E. Wang Y, et al. Among authors: mangold e. Int J Cancer. 2003 Feb 20;103(5):636-41. doi: 10.1002/ijc.10869. Int J Cancer. 2003. PMID: 12494471 Free article.

7

Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis.

Aretz S, Uhlhaas S, Caspari R, Mangold E, Pagenstecher C, Propping P, Friedl W. Aretz S, et al. Among authors: mangold e. Eur J Hum Genet. 2004 Jan;12(1):52-8. doi: 10.1038/sj.ejhg.5201088. Eur J Hum Genet. 2004. PMID: 14523376

8

Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.

Aretz S, Uhlhaas S, Sun Y, Pagenstecher C, Mangold E, Caspari R, Möslein G, Schulmann K, Propping P, Friedl W. Aretz S, et al. Among authors: mangold e. Hum Mutat. 2004 Nov;24(5):370-80. doi: 10.1002/humu.20087. Hum Mutat. 2004. PMID: 15459959

9

Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes.

Wehner M, Mangold E, Sengteller M, Friedrichs N, Aretz S, Friedl W, Propping P, Pagenstecher C. Wehner M, et al. Among authors: mangold e. Eur J Hum Genet. 2005 Aug;13(8):983-6. doi: 10.1038/sj.ejhg.5201421. Eur J Hum Genet. 2005. PMID: 15870828

10

Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining.

Mangold E, Pagenstecher C, Friedl W, Fischer HP, Merkelbach-Bruse S, Ohlendorf M, Friedrichs N, Aretz S, Buettner R, Propping P, Mathiak M. Mangold E, et al. J Pathol. 2005 Dec;207(4):385-95. doi: 10.1002/path.1858. J Pathol. 2005. PMID: 16216036

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