Foernzler D - Search Results

1

Pharmacogenetic analysis of adverse drug effect reveals genetic variant for susceptibility to liver toxicity.

Acuña G, Foernzler D, Leong D, Rabbia M, Smit R, Dorflinger E, Gasser R, Hoh J, Ott J, Borroni E, To Z, Thompson A, Li J, Hashimoto L, Lindpaintner K. Acuña G, et al. Among authors: foernzler d. Pharmacogenomics J. 2002;2(5):327-34. doi: 10.1038/sj.tpj.6500123. Pharmacogenomics J. 2002. PMID: 12439739

2

A semi-automated system for analysis and storage of SNPs.

Lehnert V, Holzwarth J, Ott M, Thompson A, Demmak S, Foernzler D. Lehnert V, et al. Among authors: foernzler d. Hum Mutat. 2001 Apr;17(4):243-54. doi: 10.1002/humu.20. Hum Mutat. 2001. PMID: 11295821

3

Lack of association between the SOST gene and bone mineral density in perimenopausal women: analysis of five polymorphisms.

Balemans W, Foernzler D, Parsons C, Ebeling M, Thompson A, Reid DM, Lindpaintner K, Ralston SH, Van Hul W. Balemans W, et al. Among authors: foernzler d. Bone. 2002 Oct;31(4):515-9. doi: 10.1016/s8756-3282(02)00844-x. Bone. 2002. PMID: 12398949

4

Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposis.

Heinimann K, Thompson A, Locher A, Furlanetto T, Bader E, Wolf A, Meier R, Walter K, Bauerfeind P, Marra G, Müller H, Foernzler D, Dobbie Z. Heinimann K, et al. Among authors: foernzler d. Cancer Res. 2001 Oct 15;61(20):7616-22. Cancer Res. 2001. PMID: 11606402

5

Interaction between CYP1A1 T3801C and AHR G1661A polymorphisms according to smoking status on blood pressure in the Stanislas cohort.

Gambier N, Marteau JB, Batt AM, Marie B, Thompson A, Siest G, Foernzler D, Visvikis-Siest S. Gambier N, et al. Among authors: foernzler d. J Hypertens. 2006 Nov;24(11):2199-205. doi: 10.1097/01.hjh.0000249697.26983.aa. J Hypertens. 2006. PMID: 17053541

6

Molecular genetics of pseudoxanthoma elasticum: type and frequency of mutations in ABCC6.

Miksch S, Lumsden A, Guenther UP, Foernzler D, Christen-Zäch S, Daugherty C, Ramesar RK, Lebwohl M, Hohl D, Neldner KH, Lindpaintner K, Richards RI, Struk B. Miksch S, et al. Among authors: foernzler d. Hum Mutat. 2005 Sep;26(3):235-48. doi: 10.1002/humu.20206. Hum Mutat. 2005. PMID: 16086317

7

Genetic Polymorphism of CYP2C19 gene in the Stanislas cohort. A link with inflammation.

Bertrand-Thiébault C, Berrahmoune H, Thompson A, Marie B, Droesch S, Siest G, Foernzler D, Visvikis-Siest S. Bertrand-Thiébault C, et al. Among authors: foernzler d. Ann Hum Genet. 2008 Mar;72(Pt 2):178-83. doi: 10.1111/j.1469-1809.2007.00417.x. Epub 2008 Jan 20. Ann Hum Genet. 2008. PMID: 18205890

8

Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST).

Balemans W, Ebeling M, Patel N, Van Hul E, Olson P, Dioszegi M, Lacza C, Wuyts W, Van Den Ende J, Willems P, Paes-Alves AF, Hill S, Bueno M, Ramos FJ, Tacconi P, Dikkers FG, Stratakis C, Lindpaintner K, Vickery B, Foernzler D, Van Hul W. Balemans W, et al. Among authors: foernzler d. Hum Mol Genet. 2001 Mar 1;10(5):537-43. doi: 10.1093/hmg/10.5.537. Hum Mol Genet. 2001. PMID: 11181578

9

Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease.

Balemans W, Patel N, Ebeling M, Van Hul E, Wuyts W, Lacza C, Dioszegi M, Dikkers FG, Hildering P, Willems PJ, Verheij JB, Lindpaintner K, Vickery B, Foernzler D, Van Hul W. Balemans W, et al. Among authors: foernzler d. J Med Genet. 2002 Feb;39(2):91-7. doi: 10.1136/jmg.39.2.91. J Med Genet. 2002. PMID: 11836356 Free PMC article.

10

Which are the best tools for specific clinical application (chips, multiplex, mass spec profile, etc.)?

Ferrari M, Michel G, Foernzler D, Leininger-Muller B, Noyer-Weidner M, Frueh F, Visvikis S, Lambert C, Shenoi H, Hinnen A, Siest G. Ferrari M, et al. Among authors: foernzler d. Clin Chem Lab Med. 2003 Apr;41(4):492-5. doi: 10.1515/CCLM.2003.074. Clin Chem Lab Med. 2003. PMID: 12747592 No abstract available.

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