Renner W - Search Results

1

Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies.

Auer-Grumbach M, Toegel S, Schabhüttl M, Weinmann D, Chiari C, Bennett DLH, Beetz C, Klein D, Andersen PM, Böhme I, Fink-Puches R, Gonzalez M, Harms MB, Motley W, Reilly MM, Renner W, Rudnik-Schöneborn S, Schlotter-Weigel B, Themistocleous AC, Weishaupt JH, Ludolph AC, Wieland T, Tao F, Abreu L, Windhager R, Zitzelsberger M, Strom TM, Walther T, Scherer SS, Züchner S, Martini R, Senderek J. Auer-Grumbach M, et al. Among authors: renner w. Am J Hum Genet. 2016 Sep 1;99(3):607-623. doi: 10.1016/j.ajhg.2016.07.008. Am J Hum Genet. 2016. PMID: 27588448 Free PMC article.

2

The angiotensin-I converting enzyme I/D polymorphism is not associated with type 2 diabetes in individuals undergoing coronary angiography. (The Ludwigshafen Risk and Cardiovascular Health Study).

Grammer TB, Renner W, von Karger S, Boehm BO, Winkelmann BR, Maerz W. Grammer TB, et al. Among authors: renner w. Mol Genet Metab. 2006 Aug;88(4):378-83. doi: 10.1016/j.ymgme.2006.01.008. Epub 2006 Jun 12. Mol Genet Metab. 2006. PMID: 16765625

3

A polymorphism in the G protein beta3-subunit gene is associated with bone metastasis risk in breast cancer patients.

Clar H, Langsenlehner U, Krippl P, Renner W, Leithner A, Gruber G, Hofmann G, Yazdani-Biuki B, Langsenlehner T, Windhager R. Clar H, et al. Among authors: renner w. Breast Cancer Res Treat. 2008 Oct;111(3):449-52. doi: 10.1007/s10549-007-9808-0. Epub 2007 Nov 4. Breast Cancer Res Treat. 2008. PMID: 17978878

4

Heme oxygenase-1 gene rs2071746 polymorphism in retinal vein occlusion.

Posch-Pertl L, List W, Michelitsch M, Pinter-Hausberger S, Berisha B, Posch F, Kloeckl L, Renner W, Weger M. Posch-Pertl L, et al. Among authors: renner w. Ophthalmic Genet. 2022 Oct;43(5):627-632. doi: 10.1080/13816810.2022.2092754. Epub 2022 Jun 27. Ophthalmic Genet. 2022. PMID: 35762119

5

Role of the tissue-type plasminogen activator -7351C > T and plasminogen activator inhibitor 1 4G/5G gene polymorphisms in central serous chorioretinopathy.

Malle EM, Posch-Pertl L, Renner W, Pinter-Hausberger S, Singer C, Haas A, Wedrich A, Weger M. Malle EM, et al. Among authors: renner w. Ophthalmic Genet. 2018 Dec;39(6):714-716. doi: 10.1080/13816810.2018.1536219. Epub 2018 Nov 15. Ophthalmic Genet. 2018. PMID: 30442055

6

Interindividual differences of response to statin treatment cannot be explained by variations of the human gene for RhoA.

Oliyarnyk O, Renner W, Paulweber B, Wascher TC. Oliyarnyk O, et al. Among authors: renner w. Biochem Genet. 2005 Apr;43(3-4):143-8. doi: 10.1007/s10528-005-1507-0. Biochem Genet. 2005. PMID: 15932062 No abstract available.

7

Single nucleotide polymorphisms in the hypoxia-inducible factor-1 gene and colorectal cancer risk.

Knechtel G, Szkandera J, Stotz M, Hofmann G, Langsenlehner U, Krippl P, Samonigg H, Renner W, Langner C, Dehchamani D, Gerger A. Knechtel G, et al. Among authors: renner w. Mol Carcinog. 2010 Sep;49(9):805-9. doi: 10.1002/mc.20655. Mol Carcinog. 2010. PMID: 20572162

8

Effect of the rs2259816 polymorphism in the HNF1A gene on circulating levels of c-reactive protein and coronary artery disease (the ludwigshafen risk and cardiovascular health study).

Kleber ME, Grammer TB, Renner W, März W. Kleber ME, et al. Among authors: renner w. BMC Med Genet. 2010 Nov 9;11:157. doi: 10.1186/1471-2350-11-157. BMC Med Genet. 2010. PMID: 21062467 Free PMC article.

9

Dysfunctional nitric oxide signalling increases risk of myocardial infarction.

Erdmann J, Stark K, Esslinger UB, Rumpf PM, Koesling D, de Wit C, Kaiser FJ, Braunholz D, Medack A, Fischer M, Zimmermann ME, Tennstedt S, Graf E, Eck S, Aherrahrou Z, Nahrstaedt J, Willenborg C, Bruse P, Brænne I, Nöthen MM, Hofmann P, Braund PS, Mergia E, Reinhard W, Burgdorf C, Schreiber S, Balmforth AJ, Hall AS, Bertram L, Steinhagen-Thiessen E, Li SC, März W, Reilly M, Kathiresan S, McPherson R, Walter U; CARDIoGRAM; Ott J, Samani NJ, Strom TM, Meitinger T, Hengstenberg C, Schunkert H. Erdmann J, et al. Nature. 2013 Dec 19;504(7480):432-6. doi: 10.1038/nature12722. Epub 2013 Nov 10. Nature. 2013. PMID: 24213632

10

Association of polymorphisms in the chemokine receptor CX3CR1 gene with coronary artery disease.

Matzhold EM, Trummer O, Grünbacher G, Zulus B, Boehm BO, März W, Renner W. Matzhold EM, et al. Among authors: renner w. Cytokine. 2009 Sep;47(3):224-7. doi: 10.1016/j.cyto.2009.06.010. Epub 2009 Jul 22. Cytokine. 2009. PMID: 19628406

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