König IR - Search Results

1

Extended single nucleotide polymorphism and haplotype analysis of the elastin gene in Caucasians with intracranial aneurysms provides evidence for racially/ethnically based differences.

Krex D, König IR, Ziegler A, Schackert HK, Schackert G. Krex D, et al. Among authors: konig ir. Cerebrovasc Dis. 2004;18(2):104-10. doi: 10.1159/000079257. Epub 2004 Jun 22. Cerebrovasc Dis. 2004. PMID: 15218274

2

Polymorphisms of the NADPH oxidase P22PHOX gene in a Caucasian population with intracranial aneurysms.

Krex D, Ziegler A, König IR, Schackert HK, Schackert G. Krex D, et al. Among authors: konig ir. Cerebrovasc Dis. 2003;16(4):363-8. doi: 10.1159/000072558. Cerebrovasc Dis. 2003. PMID: 13130177

3

Tissue inhibitor of metalloproteinases-1, -2, and -3 polymorphisms in a white population with intracranial aneurysms.

Krex D, Röhl H, König IR, Ziegler A, Schackert HK, Schackert G. Krex D, et al. Among authors: konig ir. Stroke. 2003 Dec;34(12):2817-21. doi: 10.1161/01.STR.0000099966.51485.5F. Epub 2003 Nov 6. Stroke. 2003. PMID: 14605322

4

Matrix metalloproteinase-9 coding sequence single-nucleotide polymorphisms in caucasians with intracranial aneurysms.

Krex D, Kotteck K, König IR, Ziegler A, Schackert HK, Schackert G. Krex D, et al. Among authors: konig ir. Neurosurgery. 2004 Jul;55(1):207-12; discussion 212-3. doi: 10.1227/01.neu.0000126882.17878.6d. Neurosurgery. 2004. PMID: 15214991

5

Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).

Fitze G, Appelt H, König IR, Görgens H, Stein U, Walther W, Gossen M, Schreiber M, Ziegler A, Roesner D, Schackert HK. Fitze G, et al. Among authors: konig ir. Hum Mol Genet. 2003 Dec 15;12(24):3207-14. doi: 10.1093/hmg/ddg354. Epub 2003 Nov 4. Hum Mol Genet. 2003. PMID: 14600022

6

Analysis of SNPs in pooled DNA: a decision theoretic model.

König IR, Ziegler A. König IR, et al. Genet Epidemiol. 2004 Jan;26(1):31-43. doi: 10.1002/gepi.10290. Genet Epidemiol. 2004. PMID: 14691955

7

Compound effect of PHOX2B and RET gene variants in congenital central hypoventilation syndrome combined with Hirschsprung disease.

Fitze G, König IR, Paditz E, Serra A, Schläfke M, Roesner D, Ziegler A, Schackert HK. Fitze G, et al. Among authors: konig ir. Am J Med Genet A. 2008 Jun 1;146A(11):1486-9. doi: 10.1002/ajmg.a.32300. Am J Med Genet A. 2008. PMID: 18438890 No abstract available.

8

Analysis of the base excision repair genes MTH1, OGG1 and MUTYH in patients with squamous oral carcinomas.

Görgens H, Müller A, Krüger S, Kuhlisch E, König IR, Ziegler A, Schackert HK, Eckelt U. Görgens H, et al. Among authors: konig ir. Oral Oncol. 2007 Sep;43(8):791-5. doi: 10.1016/j.oraloncology.2006.10.004. Epub 2007 Jan 4. Oral Oncol. 2007. PMID: 17207658

9

Rare occurrence of PHOX2b mutations in sporadic neuroblastomas.

Serra A, Häberle B, König IR, Kappler R, Suttorp M, Schackert HK, Roesner D, Fitze G. Serra A, et al. Among authors: konig ir. J Pediatr Hematol Oncol. 2008 Oct;30(10):728-32. doi: 10.1097/MPH.0b013e3181772141. J Pediatr Hematol Oncol. 2008. PMID: 19011468

10

Biostatistical aspects of genome-wide association studies.

Ziegler A, König IR, Thompson JR. Ziegler A, et al. Among authors: konig ir. Biom J. 2008 Feb;50(1):8-28. doi: 10.1002/bimj.200710398. Biom J. 2008. PMID: 18217698 Free article. Review.

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