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Renner Wilfried |

** = Publications listed in SCI/SSCI/Pubmed

2017

Full papers/articles (Journal)

** Mangge, H; Niedrist, T; Renner, W; Lyer, S; Alexiou, C; Haybaeck, J New Diagnostic and Therapeutic Aspects of Pancreatic Ductal Adenocarcinoma.
Curr Med Chem. 2017;
PubMed FullText FullText_MUG

 

** Renner, W; Langsenlehner, U; Krenn-Pilko, S; Eder, P; Langsenlehner, T BCL2 genotypes and prostate cancer survival.
Strahlenther Onkol. 2017; 193(6):466-471 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

** Stotz, M; Herzog, SA; Pichler, M; Smolle, M; Riedl, J; Rossmann, C; Bezan, A; Stöger, H; Renner, W; Berghold, A; Gerger, A Cancer Stem Cell Gene Variants in CD44 Predict Outcome in Stage II and Stage III Colon Cancer Patients.
Anticancer Res. 2017; 37(4):2011-2018
Web of Science PubMed FullText FullText_MUG

 

Letters

** Schulz, E; Lind, K; Renner, W; Petersen, BS; Quehenberger, F; Dill, C; Hofer, S; Lal, R; Hoefler, G; Schlenke, P; Ehninger, G; Schetelig, J; Middeke, JM; Stölzel, F; Sill, H The TP53 Pro72Arg SNP in de novo acute myeloid leukaemia - results of two cohort studies involving 215 patients and 3759 controls.
Br J Haematol. 2017; 129(18):
PubMed FullText FullText_MUG

 

2016

Full papers/articles (Journal)

** Auer-Grumbach, M; Toegel, S; Schabhüttl, M; Weinmann, D; Chiari, C; Bennett, DL; 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 Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies.
AM J HUM GENET. 2016; 99(3): 607-623. [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

** Renner, W; Jahrbacher, R; Marx-Neuhold, E; Tischler, S; Zulus, B A novel exonuclease (TaqMan) assay for rapid haptoglobin genotyping.
CLIN CHEM LAB MED. 2016; 54(5): 781-783.
Web of Science PubMed FullText FullText_MUG

 

** Trummer, O; Langsenlehner, U; Krenn-Pilko, S; Pieber, TR; Obermayer-Pietsch, B; Gerger, A; Renner, W; Langsenlehner, T Vitamin D and prostate cancer prognosis: a Mendelian randomization study.
World J Urol. 2016; 34(4):607-611
Web of Science PubMed FullText FullText_MUG

 

** Wenzl, K; Hofer, S; Troppan, K; Lassnig, M; Steinbauer, E; Wiltgen, M; Zulus, B; Renner, W; Beham-Schmid, C; Neumeister, P; Deutsch, A Higher incidence of the SNP Met 788 Ile in the coding region of A20 in diffuse large B cell lymphomas.
Tumour Biol. 2016; 37(4):4785-4789
Web of Science PubMed FullText FullText_MUG

 

Letters

** Trummer, O; Renner, W; Langsenlehner, T Rebuttal to "Causal effect of vitamin D on prostate cancer using Mendelian randomization approach".
World J Urol. 2016; 34(4):615-615
Web of Science PubMed FullText FullText_MUG

 

Abstracts (Journal)

** Schulz, E; Lind, K; Renner, W; Petersen, BS; Dill, C; Hofer, S; Lal, R; Quehenberger, F; Stolzel, F; Sill, H THE HOMOZYGOUS TP53 P72R SNP IS ASSOCIATED WITH NON-FAVORABLE CYTOGENETIC RISK GROUPS IN ACUTE MYELOID LEUKEMIA
HAEMATOLOGICA. 2016; 101: 383-383. [Poster]
Web of Science

 

** Tobias, N; Martini, CV; Renner, W; Posch, U; Schaffellner, S; Stauber, R; Muller, H; Kniepeiss, D EVALUATION OF DONOR AND RECEPTOR PNPLA3 (RS738409) -POLYMORPHISM DURING LIVER TRANSPLANTATION
TRANSPL INT. 2016; 29: 12-12.-Austrotransplant 2016; 19 - 21 OCT, 2016; [Poster]
Web of Science

 

2015

Full papers/articles (Journal)

** Ewald, L; Beate, LW; Stephanie, S; Wilfried, R; Yosuf, el-S Analysis of a Functional IL-6 Gene Polymorphism in HLAB27 Associated and Intermediate Uveitis Gives New Insight in Disease Pathogenesis and Commonality with Other Autoimmune Diseases.
J Immunol Res. 2015; 2015:174062-174062 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

** Langsenlehner, U; Hofmann, G; Renner, W; Gerger, A; Krenn-Pilko, S; Thurner, EM; Krippl, P; Langsenlehner, T Association of vascular endothelial growth factor - A gene polymorphisms and haplotypes with breast cancer metastases.
Acta Oncol. 2015; 54(3): 368-376.
Web of Science PubMed FullText FullText_MUG

 

** Lindner, E; Weger, M; Ardjomand, N; Renner, W; El-Shabrawi, Y Associations of Independent IL2RA Gene Variants with Intermediate Uveitis.
PLoS One. 2015; 10(7):e0130737-e0130737 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

** Szkandera, J; Herzog, S; Pichler, M; Stiegelbauer, V; Stotz, M; Schaberl-Moser, R; Samonigg, H; Asslaber, M; Lax, S; Leitner, G; Renner, W; Lenz, HJ; Berghold, A; Gerger, A LGR5 rs17109924 is a predictive genetic biomarker for time to recurrence in patients with colon cancer treated with 5-fluorouracil-based adjuvant chemotherapy.
Pharmacogenomics J. 2015; 15(5): 391-396. [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

** Troppan, K; Hofer, S; Wenzl, K; Lassnig, M; Pursche, B; Steinbauer, E; Wiltgen, M; Zulus, B; Renner, W; Beham-Schmid, C; Deutsch, A; Neumeister, P Frequent down regulation of the tumor suppressor gene a20 in multiple myeloma.
PLoS One. 2015; 10(4):e0123922-e0123922 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Abstracts (Journal)

** Kniepeiss, D; Renner, W; Jakoby, E; Grgic, R; Strugger, A; Muller, H; Schaffellner, S; Pfeiffer, KP IMPLEMENTATION OF A TRANSPLANT - APP FOR LIVER TRANSPLANT PATIENTS
TRANSPL INT. 2015; 28: 16-16. [Poster]
Web of Science

 

2014

Full papers/articles (Journal)

** Absenger, G; Benhaim, L; Szkandera, J; Zhang, W; Yang, D; Labonte, MJ; Pichler, M; Stotz, M; Samonigg, H; Renner, W; Gerger, A; Lenz, HJ The cyclin D1 (CCND1) rs9344 G>A polymorphism predicts clinical outcome in colon cancer patients treated with adjuvant 5-FU-based chemotherapy.
Pharmacogenomics J. 2014; 14(2):130-134
Web of Science PubMed FullText FullText_MUG Google Scholar

 

** Langsenlehner, T; Thurner, EM; Renner, W; Gerger, A; Kapp, KS; Langsenlehner, U Association of genetic variants in VEGF-A with clinical recurrence in prostate cancer patients treated with definitive radiotherapy.
Strahlenther Onkol. 2014; 190(4):364-369
Web of Science PubMed FullText FullText_MUG

 

** Pereira, TV; Kimura, L; Suwazono, Y; Nakagawa, H; Daimon, M; Oizumi, T; Kayama, T; Kato, T; Li, L; Chen, S; Gu, D; Renner, W; März, W; Yamada, Y; Bagos, PG; Mingroni-Netto, RC Multivariate meta-analysis of the association of G-protein beta 3 gene (GNB3) haplotypes with cardiovascular phenotypes.
MOL BIOL REP. 2014; 41(5): 3113-3125.
Web of Science PubMed FullText FullText_MUG

 

** Province, MA; Goetz, MP; Brauch, H; Flockhart, DA; Hebert, JM; Whaley, R; Suman, VJ; Schroth, W; Winter, S; Zembutsu, H; Mushiroda, T; Newman, WG; Lee, MT; Ambrosone, CB; Beckmann, MW; Choi, JY; Dieudonné, AS; Fasching, PA; Ferraldeschi, R; Gong, L; Haschke-Becher, E; Howell, A; Jordan, LB; Hamann, U; Kiyotani, K; Krippl, P; Lambrechts, D; Latif, A; Langsenlehner, U; Lorizio, W; Neven, P; Nguyen, AT; Park, BW; Purdie, CA; Quinlan, P; Renner, W; Schmidt, M; Schwab, M; Shin, JG; Stingl, JC; Wegman, P; Wingren, S; Wu, AH; Ziv, E; Zirpoli, G; Thompson, AM; Jordan, VC; Nakamura, Y; Altman, RB; Ames, MM; Weinshilboum, RM; Eichelbaum, M; Ingle, JN; Klein, TE CYP2D6 Genotype and Adjuvant Tamoxifen: Meta-Analysis of Heterogeneous Study Populations.
Clin Pharmacol Ther. 2014; 95(2):216-227 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

** Prüller, F; Weiss, EC; Raggam, RB; Cervar-Zivkovic, M; Renner, W; Wagner, J; Michaelis, S; März, W; Mangge, H Activated protein C resistance assay and factor V Leiden.
N Engl J Med. 2014; 371(7): 685-686. [OPEN ACCESS]
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** Scharnagl, H; Kleber, ME; Genser, B; Kickmaier, S; Renner, W; Weihrauch, G; Grammer, T; Rossmann, C; Winkelmann, BR; Boehm, BO; Sattler, W; März, W; Malle, E Association of myeloperoxidase with total and cardiovascular mortality in individuals undergoing coronary angiography--the LURIC study.
Int J Cardiol. 2014; 174(1):96-105 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

** Schulz, E; Klampfl, P; Holzapfel, S; Janecke, AR; Ulz, P; Renner, W; Kashofer, K; Nojima, S; Leitner, A; Zebisch, A; Wölfler, A; Hofer, S; Gerger, A; Lax, S; Beham-Schmid, C; Steinke, V; Heitzer, E; Geigl, JB; Windpassinger, C; Hoefler, G; Speicher, MR; Boland, CR; Kumanogoh, A; Sill, H Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X.
Nat Commun. 2014; 5(10):5191-5191 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

** Szkandera, J; Pichler, M; Absenger, G; Stotz, M; Weissmueller, M; Samonigg, H; Asslaber, M; Lax, S; Leitner, G; Winder, T; Renner, W; Gerger, A A functional germline variant in GLI1 implicates hedgehog signaling in clinical outcome of stage II and III colon carcinoma patients.
Clin Cancer Res. 2014; 20(6):1687-1697 [OPEN ACCESS]
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** Thurner, EM; Krenn-Pilko, S; Langsenlehner, U; Renner, W; Gerger, A; Kapp, KS; Langsenlehner, T Association of genetic variants in apoptosis genes FAS and FASL with radiation-induced late toxicity after prostate cancer radiotherapy.
Strahlenther Onkol. 2014; 190(3):304-309
Web of Science PubMed FullText FullText_MUG

 

Reviews

** Domej, W; Oettl, K; Renner, W Oxidative stress and free radicals in COPD--implications and relevance for treatment.
Int J Chron Obstruct Pulmon Dis. 2014; 9(11):1207-1224 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Abstracts (Journal)

** Schulz, E; Klampfl, P; Holzapfel, S; Janecke, AR; Ulz, P; Renner, W; Kashofer, K; Najima, S; Leitner, A; Zebisch, A; Wölfler, A; Hofer, S; Gerger, A; Lax, S; Beham-Schmid, C; Steinke, V; Geigl, JB; Höfler, G; Speicher, MR; Boland, CR; Kumanogoh, A; Sill, H Germline variants in the semaphorin SEMA4A confer susceptibility to familial colorectal cancer type X
Oncol Res Treat. 2014; 37(S5):105-105.-Annual Meeting of the German, Austrian and Swiss Associations of Hematology and Medical Oncology; OCT 10-14, 2014; Hamburg, GERMANY. (ISBN: 978-3-318-02811-9 ) [Oral Communication]
Web of Science

 

** Thurner, EM; Krenn-Pilko, S; Langsenlehner, U; Renner, W; Gerger, A; Kapp, KS; Langsenlehner, T; Relation between Polymorphisms in the Apoptotic Genes FAS and FASL and radiogenic Long-Terms-Effects in Prostate Cancer Patients.
STRAHLENTHER ONKOL. 2014; 190(1):127-127.-30th OEGRO Annual Conference; SEP 20-21, 2013; Bregenz, AUSTRIA. [Poster]
Web of Science

 

2013

Full papers/articles (Journal)

** Absenger, G; Szkandera, J; Stotz, M; Pichler, M; Winder, T; Langsenlehner, T; Langsenlehner, U; Samonigg, H; Renner, W; Gerger, A A common and functional gene variant in the vascular endothelial growth factor a predicts clinical outcome in early-stage breast cancer.
Mol Carcinog. 2013; 52 Suppl 1(9):E96-102
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** Kniepeiss, D; Wagner, D; Wasler, A; Tscheliessnigg, KH; Renner, W The role of CYP2C8 genotypes in dose requirement and levels of everolimus after heart transplantation.
Wien Klin Wochenschr. 2013; 125(13-14):393-395
Web of Science PubMed FullText FullText_MUG

 

** Steinwender, G; Lindner, E; Weger, M; Plainer, S; Renner, W; Ardjomand, N; El-Shabrawi, Y Association between polymorphism of the vitamin D metabolism gene CYP27B1 and HLA-B27-associated uveitis. Is a state of relative immunodeficiency pathogenic in HLA B27-positive uveitis?
PLoS One. 2013; 8(4):e62244-e62244 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

** Szkandera, J; Absenger, G; Liegl-Atzwanger, B; Pichler, M; Stotz, M; Gerger, S; Zacherl, M; Renner, W; Haijun, M; Leithner, A; Gerger, A Common gene variants in RAD51, XRCC2 and XPD are not associated with clinical outcome in soft-tissue sarcoma patients.
Cancer Epidemiol. 2013; 37(6):1003-1009
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** Szkandera, J; Absenger, G; Pichler, M; Stotz, M; Langsenlehner, T; Samonigg, H; Renner, W; Gerger, A Association of common gene variants in vitamin D modulating genes and colon cancer recurrence.
J Cancer Res Clin Oncol. 2013; 139(9):1457-1464
Web of Science PubMed FullText FullText_MUG

 

** Szkandera, J; Winder, T; Stotz, M; Weissmueller, M; Langsenlehner, T; Pichler, M; Samonigg, H; Renner, W; Gerger, A; Absenger, G A common gene variant in PLS3 predicts colon cancer recurrence in women.
Tumour Biol. 2013; 34(4):2183-2188
Web of Science PubMed FullText FullText_MUG

 

** Trummer, O; Pilz, S; Hoffmann, MM; Winkelmann, BR; Boehm, BO; März, W; Pieber, TR; Obermayer-Pietsch, B; Renner, W Vitamin D and Mortality: A Mendelian Randomization Study.
Clin Chem. 2013; 59(5):793-797 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

** Wallner-Liebmann, SJ; Grammer, TB; Siekmeier, R; Mangge, H; März, W; Renner, W Smoking denial in cardiovascular disease studies.
Adv Exp Med Biol. 2013; 788(32):35-38
Web of Science PubMed FullText FullText_MUG

 

** Weger, M; Steinbrugger, I; Renner, W; Pöschl, EM; Brockmann, T; Rabensteiner, DF; El-Shabrawi, Y; Haas, A Role of the vitamin K epoxide reductase complex subunit 1 (VKORC1) -1639G>A gene polymorphism in patients with retinal vein occlusion.
Curr Eye Res. 2013; 38(12):1278-1282
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Letters

** Lindner, E; Steinwender, G; Plainer, S; Poeschl, EM; Weger, M; Ardjomand, N; Renner, W; El-Shabrawi, Y Role of IL-10 gene polymorphisms in intermediate and HLA-B27-associated uveitis.
Acta Ophthalmol. 2013; 91(5):e415-e417 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

** Prüller, F; Raggam, RB; Mangge, H; Truschnig-Wilders, M; Matzhold, EM; Weiss, EC; Hasiba, B; Summers, KL; Renner, W; Siegert, G; Kostka, H A novel factor V mutation causes a normal activated protein C ratio despite the presence of a heterozygous F5 R506Q (factor V Leiden) mutation.
Br J Haematol. 2013; 163(3):414-417 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Abstracts (Journal)

** Krenn-Pilko, S; Thurner, EM; Ehammer-Rosenkranz, A; Renner, W; Kapp, KS; Langsenlehner, U; Langsenlehner, T Genetic polymorphisms in the vascular endothelial growth factor gene and breast cancer metastases. An update of the Austrian "tumor of breast tissue: incidence, genetics, and environmental risk factors" study
EUR J CANCER. EJC, Abstract book, Proceedings of the 17th European Cancer Congress. 2013; 49(2):S403-S403.-17th ECCO / 38th ESMO / 32nd ESTRO European Cancer Congress on Reinforcing Multidisciplinarity; SEP 27-OCT 01, 2013; Amsterdam, NETHERLANDS. [Oral Communication]
Web of Science

 

** Krenn-Pilko, S; Thurner, EM; Renner, W; Gerger, A; Kapp, KS; Langsenlehner, U; Langsenlehner, T The Relationship between VEGF Gene polymorphisms and Haplotypes with the Development of Distant metastases in postmenopausal Breast cancer patients
STRAHLENTHER ONKOL. . 2013; 189(2):182-183.-29th Annual Meeting of the Austrian-Society-of-Radiation-Oncology-Radiobiology-and-Medical-Radiophysics (OGRO); SEP 28-29, 2012; Gnunden, AUSTRIA. [Poster]
Web of Science

 

** Langsenlehner, T; Thurner, EM; Krenn-Pilko, S; Ehammer-Rosenkranz, A; Renner, W; Gerger, A; Kapp, KS; Langsenlehner, U Association between VEGF-A gene variants and clinical outcome in prostate cancer patients treated with definitive radiotherapy
EUR J CANCER. 2013; 49: S689-S689.-17th ECCO / 38th ESMO / 32nd ESTRO European Cancer Congress on Reinforcing Multidisciplinarity; SEP 27-OCT 01, 2013; Amsterdam, NETHERLANDS. [Poster]
Web of Science

 

** Thurner, EM; Krenn-Pilko, S; Renner, W; Gerger, A; Langsenlehner, U; Kapp, KS; Langsenlehner, T Genetic variants in DNA repair genes and radiation-induced late toxicity in prostate cancer patients
EUR J CANCER. 2013; 49: S693-S693.-17th ECCO / 38th ESMO / 32nd ESTRO European Cancer Congress on Reinforcing Multidisciplinarity; SEP 27-OCT 01, 2013; Amsterdam, NETHERLANDS. [Poster]
Web of Science

 

** Wallner-Liebmann, S; Siekmeier, R; Grammer, T; Mangge, H; Marz, W; Renner, W; Discrepancy between history and biochemically specific Smoking status in Patients of LURIC Study.
INTERNIST. 2013; 54: 106-106.-Jahrestagung der ÖKG; Juni 5-8, 2013; Salzburg, AUSTRIA. [Poster]
Web of Science

 

2012

Full papers/articles (Journal)

** Demirkan, A; van Duijn, CM; Ugocsai, P; Isaacs, A; Pramstaller, PP; Liebisch, G; Wilson, JF; Johansson, Å; Rudan, I; Aulchenko, YS; Kirichenko, AV; Janssens, AC; Jansen, RC; Gnewuch, C; Domingues, FS; Pattaro, C; Wild, SH; Jonasson, I; Polasek, O; Zorkoltseva, IV; Hofman, A; Karssen, LC; Struchalin, M; Floyd, J; Igl, W; Biloglav, Z; Broer, L; Pfeufer, A; Pichler, I; Campbell, S; Zaboli, G; Kolcic, I; Rivadeneira, F; Huffman, J; Hastie, ND; Uitterlinden, A; Franke, L; Franklin, CS; Vitart, V; DIAGRAM Consortium; Nelson, CP; Preuss, M; CARDIoGRAM Consortium; Bis, JC; O'Donnell, CJ; Franceschini, N; CHARGE Consortium; Witteman, JC; Axenovich, T; Oostra, BA; Meitinger, T; Hicks, AA; Hayward, C; Wright, AF; Gyllensten, U; Campbell, H; Schmitz, G; EUROSPAN consortium Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
PLoS Genet. 2012; 8(2):e1002490-e1002490 [OPEN ACCESS]
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** Haijun, M; Xiaohui, Z; Ting, M; Renner, W; Abulizi, P; Baopeng, T Association between KCNE1 (G38S) genetic polymorphism and non-valvular atrial fibrillation in an Uygur population.
Wien Klin Wochenschr. 2012; 124(21-22):737-741
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** Lu, X; Wang, L; Chen, S; He, L; Yang, X; Shi, Y; Cheng, J; Zhang, L; Gu, CC; Huang, J; Wu, T; Ma, Y; Li, J; Cao, J; Chen, J; Ge, D; Fan, Z; Li, Y; Zhao, L; Li, H; Zhou, X; Chen, L; Liu, D; Chen, J; Duan, X; Hao, Y; Wang, L; Lu, F; Liu, Z; Yao, C; Shen, C; Pu, X; Yu, L; Fang, X; Xu, L; Mu, J; Wu, X; Zheng, R; Wu, N; Zhao, Q; Li, Y; Liu, X; Wang, M; Yu, D; Hu, D; Ji, X; Guo, D; Sun, D; Wang, Q; Yang, Y; Liu, F; Mao, Q; Liang, X; Ji, J; Chen, P; Mo, X; Li, D; Chai, G; Tang, Y; Li, X; Du, Z; Liu, X; Dou, C; Yang, Z; Meng, Q; Wang, D; Wang, R; Yang, J; Schunkert, H; Samani, NJ; Kathiresan, S; Reilly, MP; Erdmann, J; Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium; Peng, X; Wu, X; Liu, D; Yang, Y; Chen, R; Qiang, B; Gu, D Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
Nat Genet. 2012; 44(8):890-894 [OPEN ACCESS]
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** Szkandera, J; Absenger, G; Dandachi, N; Regitnig, P; Lax, S; Stotz, M; Samonigg, H; Renner, W; Gerger, A Analysis of functional germline polymorphisms for prediction of response to anthracycline-based neoadjuvant chemotherapy in breast cancer.
Mol Genet Genomics. 2012; 287(9):755-764
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** Szkandera, J; Absenger, G; Stotz, M; Weissmueller, M; Winder, T; Langsenlehner, T; Samonigg, H; Renner, W; Schippinger, W; Gerger, A The Functional Polymorphism of Erythropoietin Gene rs1617640 G>T Is Not Associated with Susceptibility and Clinical Outcome of Early-stage Breast Cancer.
Anticancer Res. 2012; 32(8):3473-3478
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** Trummer, O; Schwetz, V; Walter-Finell, D; Lerchbaum, E; Renner, W; Gugatschka, M; Dobnig, H; Pieber, TR; Obermayer-Pietsch, B Allelic Determinants of Vitamin D Insufficiency, Bone Mineral Density, and Bone Fractures.
J Clin Endocrinol Metab. 2012; 97(7): E1234-E1240. [OPEN ACCESS]
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** Zimmermann, C; Weger, M; Faschinger, C; Renner, W; Mossböck, G Role of interleukin 6-174G>C polymorphism 
in primary open-angle glaucoma.
Eur J Ophthalmol. 2012; 23(2):183-186
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Editorials

** Hoffmann, MM; Renner, W Insight from genome-wide association studies into coronary heart disease
PHARMACOGENOMICS. 2012; 13(4): 361-363.
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Abstracts (Journal)

** Hofmann, G; Langsenlehner, T; Moazedi-Fuerst, F; Gerger, A; Kielhauser, S; Absenger, G; Szkandera, J; Samonigg, H; Krippl, P; Renner, W; COMMON VEGF GENE POLYMORPHISMS ARE NOT ASSOCIATED WITH RELAPSE-FREE SURVIVAL IN COLORECTAL CANCER PATIENTS.
ANN ONCOL. 2012; 23: 86-87.-14th World Congress on Gastrointestinal Cancer of the European-Society-for-Medical-Oncology (ESMO); JUN 27-30, 2012; Barcelona, SPAIN. [Poster]
Web of Science

 

** Hofmann, G; Langsenlehner, T; Moazedi-Fuerst, F; Gerger, A; Kielhauser, S; Thurner, E-M; Absenger, G; Szkandera, J; Samonigg, H; Glehr, M; Krippl, P; Renner, W Genetic variants of UGT1A4 and their impact on relapse-free survival in Tamoxifen treated breast cancer patients.
Onkologie. 2012; 35(S 6):64-64.-Jahrestagung der Deutschen, Österreichischen und Schweizerischen Gesellschaften für Hämatologie und Onkologie; OCT 19-23, 2012; Stuttgart, GERMANY. [Poster]
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** Krenn-Pilko, S; Hofmann, G; Renner, W; Gerger, A; Thurner, EM; Kapp, KS; Langsenlehner, U; Langsenlehner, T The Role of VEGF Gene Polymorphisms in the Development of Distant Metastases in Postmenopausal Breast Cancer Patients
EUR J CANCER. .... 2012; 48(1):S184-S185.-8th European Breast Cancer Conference (EBCC); MAR 21-24, 2012; Vienna, AUSTRIA. [Poster]
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** Krenn-Pilko, S; Thurner, EM; Absenger, G; Renner, W; Gerger, A; Kapp, KS; Langsenlehner, U; Langsenlehner, T; Association Between Variants in the VEGF Gene and Distant Metastases in Postmenopausal Breast Cancer Patients.
EUR J CANCER. EUROPEAN JOURNAL OF CANCER48: S271-S271. OXFORD: ELSEVIER SCI LTD; ( Presented at: 22nd Biennial Congress of the European-Association-for-Cancer-Research, Barcelona, SPAIN, JUL 07-10, 2012) [Poster]
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** Krenn-Pilko, S; Thurner, EM; Renner, W; Absenger, G; Gerger, A; Kapp, KS; Langsenlehner, T; Langsenlehner, U The Development of Distant Metastases in Postmenopausal Woman with Breast Cancer in Association with VEGF Gene Polymorphisms
EUR J CANCER. 2012; 48: 63-63.-24th EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics; NOV 06-09, 2012; Dublin, IRELAND. [Poster]
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** Szkandera, J; Absenger, G; Dandachi, N; Regitnig, P; Lax, S; Stotz, M; Winder, T; Samonigg, H; Renner, W; Gerger, A Analysis of functional germline polymorphisms for prediction of response to anthracycline-based neoadjuvant chemotherapy in breast cancer
WIEN KLIN WOCHENSCHR. 2012; 124(15-16):575-575. [Poster]
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** Szkandera, J; Absenger, G; Stotz, M; Weissmuller, M; Winder, T; Langsenlehner, T; Samonigg, H; Renner, W; Schippinger, W; Gerger, A The functional polymorphism of erythropoietin gene rs1617640 G > T is not associated with susceptibility and clinical outcome of early-stage breast cancer
WIEN KLIN WOCHENSCHR. 2012; 124(15-16):575-575. [Poster]
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** Szkandera, J; Winder, T; Absenger, G; Stotz, M; Weissmuller, M; Langsenlehner, T; Hofmann, G; Samonigg, H; Renner, W; Gerger, A; A COMMON GENE VARIANT IN PLS3 PREDICTS COLON CANCER RECURRENCE IN WOMEN.
ANN ONCOL. 2012; 23: 83-83.-14th World Congress on Gastrointestinal Cancer of the European-Society-for-Medical-Oncology (ESMO); JUN 27-30, 2012; Barcelona, SPAIN. [Poster]
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** Thurner, EM; Krenn-Pilko, S; Renner, W; Gerger, A; Kapp, KS; Langsenlehner, U; Langsenlehner, T Genetic Variants in the TGF-beta 1 Gene and the Risk of Late Toxicity After Radiotherapy in Prostate Cancer Patients
EUR J CANCER. 2012; 48: 87-87.-24th EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics; NOV 06-09, 2012; Dublin, IRELAND. [Poster]
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** Thurner, EM; Krenn-Pilko, S; Renner, W; Langsenlehner, U; Gerger, A; Kapp, KS; Langsenlehner, T Role of ERCC2 Gene polymorphisms in the development of radiation-induced Late effects in Prostate cancer patients.
Strahlentherapie und Onkologie. 2012; 188(1):107-107.-18. Jahrestagung der Deutschen Gesellschaft für Radioonkologie; JUN 7-10, 2012; Wiesbaden, GERMANY. [Poster]
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** Thurner, EM; Krenn-Pilko, S; Renner, W; Szkandera, J; Gerger, A; Langsenlehner, U; Kapp, KS; Langsenlehner, T; Role of Polymorphisms in the ERCC2 Gene in the Development of Severe Side Effects After Radiotherapy of Prostate Cancer Patients.
EUR J CANCER. EUROPEAN JOURNAL OF CANCER48: S271-S271. OXFORD: ELSEVIER SCI LTD; ( Presented at: 22nd Biennial Congress of the European-Association-for-Cancer-Research, Barcelona, SPAIN, JUL 07-10, 2012) [Poster]
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** Thurner, EM; Renner, W; Krenn-Pilko, S; Langsenlehner, U; Kapp, K; Langsenlehner, T Influence of VEGF gene variants on the risk for Development of Radiation-induced late effects in Prostate cancer patients
STRAHLENTHER ONKOL. 2012; 188: 195-195.-18th Annual Congress of the German-Society-for-Radiation-Oncology; JUN 07-10, 2012; Wiesbaden, GERMANY. [Poster]
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** Trummer, O; Pilz, S; Hoffmann, M; Winkelmann, B; Boehm, B; Marz, W; Pieber, TR; Renner, W; Obermayer-Pietsch, B; Vitamin D levels, vitamin D insufficiency genotypes and mortality: A Mendelian randomization study.
BONE. 2012; 50: S108-S109.-39th Annual Congress of the European-Calcified-Tissue-Society (ECTS); MAY 19-23, 2012; Stockholm, SWEDEN. [Poster]
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** Trummer, O; Pilz, S; Hoffmann, MM; Winkelmann, BR; Boehm, BO; Marz, W; Pieber, TR; Renner, W; Obermayer-Pietsch, B Vitamin D levels, Vitamin D Insufficiency Genotypes and Mortality
WIEN KLIN WOCHENSCHR. 2012; 124(15-16):564-564. [Poster]
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Abstracts (Proceedings)

** Krenn-Pilko, S; Hofmann, G; Renner, W; Gerger, A; Thurner, EM; Kapp, KS; Langsenlehner, U; Langsenlehner, T The role of VEGF Gene Polymorphism in the development of distant metastases in postmenopausal Breast cancer patients.
Strahlentherapie und Onkologie. 2012. 2012; 188(1):65-65.-Jahrestagung der Deutschen Gesellschaft für Radioonkologie; JUN 7-10, 2012; Wiesbaden, GERMANY. (ISBN: 0179-7158 ) [Poster]
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2011

Full papers/articles (Journal)

** Grammer, TB; Hoffmann, MM; Renner, W; Kleber, ME; Winkelmann, BR; Böhm, BO; März, W Apolipoprotein E genotypes, circulating C-reactive protein and angiographic coronary artery disease: the Ludwigshafen Risk and Cardiovascular Health Study.
Atherosclerosis. 2011; 215(2):487-493
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** Gugatschka, M; Dehchamani, D; Wascher, TC; Friedrich, G; Renner, W DNA repair gene ERCC2 polymorphisms and risk of squamous cell carcinoma of the head and neck.
Exp Mol Pathol. 2011; 91(1): 331-334.
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** Hausberger, S; Steinbrugger, I; Haas, A; Rabensteiner, DF; Luger, T; Borkenstein, AF; Renner, W; Wedrich, A; El-Shabrawi, Y; Schmut, O; Weger, M Role of TNF-alpha-308G > A and-238G > A gene polymorphisms in patients with retinal artery occlusion
SPEKTRUM AUGENHEILKD. 2011; 25(4): 273-276.
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** Herder, C; Peeters, W; Illig, T; Baumert, J; de Kleijn, DP; Moll, FL; Poschen, U; Klopp, N; Müller-Nurasyid, M; Roden, M; Preuss, M; CARDIoGRAM Consortium; Karakas, M; Meisinger, C; Thorand, B; Pasterkamp, G; Koenig, W; Assimes, TL; Deloukas, P; Erdmann, J; Holm, H; Kathiresan, S; König, IR; McPherson, R; Reilly, MP; Roberts, R; Samani, NJ; Schunkert, H; Stewart, AF RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studies.
PLoS One. 2011; 6(12):e25734-e25734 [OPEN ACCESS]
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** Hofmann, G; Langsenlehner, U; Langsenlehner, T; Glehr, M; Gerger, A; Absenger, G; Szkandera, J; Fuerst, F; Samonigg, H; Krippl, P; Renner, W Single nucleotide polymorphisms of integrin alpha-2 and beta-3 genes are not associated with relapse-free and overall survival in colorectal cancer patients.
Anticancer Res. 2011; 31(4):1373-1377
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** International Consortium for Blood Pressure Genome-Wide Association Studies; Ehret, GB; Munroe, PB; Rice, KM; Bochud, M; Johnson, AD; Chasman, DI; Smith, AV; Tobin, MD; Verwoert, GC; Hwang, SJ; Pihur, V; Vollenweider, P; O'Reilly, PF; Amin, N; Bragg-Gresham, JL; Teumer, A; Glazer, NL; Launer, L; Zhao, JH; Aulchenko, Y; Heath, S; Sõber, S; Parsa, A; Luan, J; Arora, P; Dehghan, A; Zhang, F; Lucas, G; Hicks, AA; Jackson, AU; Peden, JF; Tanaka, T; Wild, SH; Rudan, I; Igl, W; Milaneschi, Y; Parker, AN; Fava, C; Chambers, JC; Fox, ER; Kumari, M; Go, MJ; van der Harst, P; Kao, WH; Sjögren, M; Vinay, DG; Alexander, M; Tabara, Y; Shaw-Hawkins, S; Whincup, PH; Liu, Y; Shi, G; Kuusisto, J; Tayo, B; Seielstad, M; Sim, X; Nguyen, KD; Lehtimäki, T; Matullo, G; Wu, Y; Gaunt, TR; Onland-Moret, NC; Cooper, MN; Platou, CG; Org, E; Hardy, R; Dahgam, S; Palmen, J; Vitart, V; Braund, PS; Kuznetsova, T; Uiterwaal, CS; Adeyemo, A; Palmas, W; Campbell, H; Ludwig, B; Tomaszewski, M; Tzoulaki, I; Palmer, ND; CARDIoGRAM consortium; CKDGen Consortium; KidneyGen Consortium; EchoGen consortium; CHARGE-HF consortium; Aspelund, T; Garcia, M; Chang, YP; O'Connell, JR; Steinle, NI; Grobbee, DE; Arking, DE; Kardia, SL; Morrison, AC; Hernandez, D; Najjar, S; McArdle, WL; Hadley, D; Brown, MJ; Connell, JM; Hingorani, AD; Day, IN; Lawlor, DA; Beilby, JP; Lawrence, RW; Clarke, R; Hopewell, JC; Ongen, H; Dreisbach, AW; Li, Y; Young, JH; Bis, JC; Kähönen, M; Viikari, J; Adair, LS; Lee, NR; Chen, MH; Olden, M; Pattaro, C; Bolton, JA; Köttgen, A; Bergmann, S; Mooser, V; Chaturvedi, N; Frayling, TM; Islam, M; Jafar, TH; Erdmann, J; Kulkarni, SR; Bornstein, SR; Grässler, J; Groop, L; Voight, BF; Kettunen, J; Howard, P; Taylor, A; Guarrera, S; Ricceri, F; Emilsson, V; Plump, A; Barroso, I; Khaw, KT; Weder, AB; Hunt, SC; Sun, YV; Bergman, RN; Collins, FS; Bonnycastle, LL; Scott, LJ; Stringham, HM; Peltonen, L; Perola, M; Vartiainen, E; Brand, SM; Staessen, JA; Wang, TJ; Burton, PR; Soler Artigas, M; Dong, Y; Snieder, H; Wang, X; Zhu, H; Lohman, KK; Rudock, ME; Heckbert, SR; Smith, NL; Wiggins, KL; Doumatey, A; Shriner, D; Veldre, G; Viigimaa, M; Kinra, S; Prabhakaran, D; Tripathy, V; Langefeld, CD; Rosengren, A; Thelle, DS; Corsi, AM; Singleton, A; Forrester, T; Hilton, G; McKenzie, CA; Salako, T; Iwai, N; Kita, Y; Ogihara, T; Ohkubo, T; Okamura, T; Ueshima, H; Umemura, S; Eyheramendy, S; Meitinger, T; Wichmann, HE; Cho, YS; Kim, HL; Lee, JY; Scott, J; Sehmi, JS; Zhang, W; Hedblad, B; Nilsson, P; Smith, GD; Wong, A; Narisu, N; Stančáková, A; Raffel, LJ; Yao, J; Kathiresan, S; O'Donnell, CJ; Schwartz, SM; Ikram, MA; Longstreth, WT; Mosley, TH; Seshadri, S; Shrine, NR; Wain, LV; Morken, MA; Swift, AJ; Laitinen, J; Prokopenko, I; Zitting, P; Cooper, JA; Humphries, SE; Danesh, J; Rasheed, A; Goel, A; Hamsten, A; Watkins, H; Bakker, SJ; van Gilst, WH; Janipalli, CS; Mani, KR; Yajnik, CS; Hofman, A; Mattace-Raso, FU; Oostra, BA; Demirkan, A; Isaacs, A; Rivadeneira, F; Lakatta, EG; Orru, M; Scuteri, A; Ala-Korpela, M; Kangas, AJ; Lyytikäinen, LP; Soininen, P; Tukiainen, T; Würtz, P; Ong, RT; Dörr, M; Kroemer, HK; Völker, U; Völzke, H; Galan, P; Hercberg, S; Lathrop, M; Zelenika, D; Deloukas, P; Mangino, M; Spector, TD; Zhai, G; Meschia, JF; Nalls, MA; Sharma, P; Terzic, J; Kumar, MV; Denniff, M; Zukowska-Szczechowska, E; Wagenknecht, LE; Fowkes, FG; Charchar, FJ; Schwarz, PE; Hayward, C; Guo, X; Rotimi, C; Bots, ML; Brand, E; Samani, NJ; Polasek, O; Talmud, PJ; Nyberg, F; Kuh, D; Laan, M; ... Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Nature. 2011; 478(7367):103-109 [OPEN ACCESS]
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** Kniepeiss, D; Renner, W; Trummer, O; Wagner, D; Wasler, A; Khoschsorur, GA; Truschnig-Wilders, M; Tscheliessnigg, KH The role of CYP3A5 genotypes in dose requirements of tacrolimus and everolimus after heart transplantation.
Clin Transplant. 2011; 25(1): 146-150.
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** Langsenlehner, T; Renner, W; Gerger, A; Hofmann, G; Thurner, EM; Kapp, KS; Langsenlehner, U Impact of VEGF gene polymorphisms and haplotypes on radiation-induced late toxicity in prostate cancer patients.
Strahlenther Onkol. 2011; 187(12):784-791
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** Langsenlehner, T; Renner, W; Gerger, A; Hofmann, G; Thurner, EM; Kapp, KS; Langsenlehner, U Association between single nucleotide polymorphisms in the gene for XRCC1 and radiation-induced late toxicity in prostate cancer patients.
Radiother Oncol. 2011; 98(3):387-393
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** Maier, R; Steinbrugger, I; Haas, A; Selimovic, M; Renner, W; El-Shabrawi, Y; Werner, C; Wedrich, A; Schmut, O; Weger, M Role of inflammation-related gene polymorphisms in patients with central retinal vein occlusion.
Ophthalmology. 2011; 118(6): 1125-1129.
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** Mangge, H; Renner, W; Almer, G; Weghuber, D; Möller, R; Horejsi, R Rs9939609 variant of the fat mass and obesity-associated gene and trunk obesity in adolescents.
J Obes. 2011; 2011(8):186368-186368 [OPEN ACCESS]
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** Mossbock, G; Weger, M; Faschinger, C; Schmut, O; Renner, W; Wedrich, A; Zimmermann, C; El-Shabrawi, Y Role of cholesterol 24S-hydroxylase gene polymorphism (rs754203) in primary open angle glaucoma.
MOL VIS. 2011; 17(12): 616-620. [OPEN ACCESS]
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** Parmar, S; Stingl, JC; Huber-Wechselberger, A; Kainz, A; Renner, W; Langsenlehner, U; Krippl, P; Brockmöller, J; Haschke-Becher, E Impact of UGT2B7 His268Tyr polymorphism on the outcome of adjuvant epirubicin treatment in breast cancer.
Breast Cancer Res. 2011; 13(3):R57-R57 [OPEN ACCESS]
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** Silbernagel, G; Renner, W; Grammer, TB; Hugl, SR; Bertram, J; Kleber, ME; Hoffmann, MM; Winkelmann, BR; Marz, W; Boehm, BO Association of TCF7L2 SNPs with age at onset of type 2 diabetes and proinsulin/insulin ratio but not with glucagon-like peptide 1
DIABETES-METAB RES. 2011; 27(5): 499-505.
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** Suhre, K; Shin, SY; Petersen, AK; Mohney, RP; Meredith, D; Wägele, B; Altmaier, E; CARDIoGRAM; Deloukas, P; Erdmann, J; Grundberg, E; Hammond, CJ; de Angelis, MH; Kastenmüller, G; Köttgen, A; Kronenberg, F; Mangino, M; Meisinger, C; Meitinger, T; Mewes, HW; Milburn, MV; Prehn, C; Raffler, J; Ried, JS; Römisch-Margl, W; Samani, NJ; Small, KS; Wichmann, HE; Zhai, G; Illig, T; Spector, TD; Adamski, J; Soranzo, N; Gieger, C; Assimes, TL; Deloukas, P; Erdmann, J; Holm, H; Kathiresan, S; König, IR; McPherson, R; Reilly, MP; Roberts, R; Samani, NJ; Schunkert, H; Stewart, AF Human metabolic individuality in biomedical and pharmaceutical research.
Nature. 2011; 477(7362):54-60 [OPEN ACCESS]
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** Weger, M; Steinbrugger, I; El-Shabrawi, Y; Haas, A; Renner, W To the Editor.
Retina. 2011; 31(8): 1743-1743
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Abstracts (Journal)

** Hofmann, G; Langsenlehner, T; Fuerst, F; Gerger, A; Langsenlehner, U; Bitsche, S; Absenger, G; Samonigg, H; Krippl, P; Renner, W RELAPSE-FREE SURVIVAL IN COLORECTAL CANCER PATIENTS IS NOT ASSOCIATED WITH SINGLE NUCLEOTIDE POLYMORPHISMS IN INTEGRIN RECEPTOR SUBUNITS
ANN ONCOL. 2011; 22: v109-v109.-ESMO 13th World Congress on Gastrointestinal Cancer ; JUN 22-25, 2011; Barcelona, SPAIN. [Poster]
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** Hofmann, G; Langsenlehner, T; Fuerst, F; Gerger, A; Langsenlehner, U; Szkandera, J; Absenger, G; Samonigg, H; Krippl, P; Renner, W A COMMON HEREDITARY SINGLE NUCLEOTIDE POLYMORPHISM IN THE IN THE GENE OF DEATH RECEPTOR 4 (TNFRSF10A) AND ITS IMPACT ON OVERALL SURVIVAL IN RECTAL CANCER PATIENTS
ANN ONCOL. . 2011; 22: v129-v129.-ESMO 13th World Congress on Gastrointestinal Cancer; JUN 22-25, 2011; Barcelona, SPAIN. [Poster]
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** Hofmann, G; Langsenlehner, T; Fuerst, F; Gerger, A; Langsenlehner, U; Szkandera, J; Absenger, G; Samonigg, H; Krippl, P; Renner, W Common single nucleotide polymorphisms in the genes of integrin alpha-2 and beta-3 subunits are not associated with overall survival in rectal cancer patients
ONKOLOGIE. 2011; 34: 245-246.-Gemeinsame Jahrestagung 2011 der DGHO, ÖGHO, SGMO und SGH+SSH; SEP 30-OCT 4, 2011; Basel, SWITZERLAND. [Poster]
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** Kniepeiss, D; Trummer, O; Wagner, D; Wasler, A; Truschnig-Wilders, M; Iberer, F; Tscheliessnigg, KH; Renner, W The Role of CYP2C8 Genotypes in Dose Requirement and Levels of Everolimus after Heart Transplantation.
AM J TRANSPLANT. 2011; 11: 683- [Oral Communication]
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** Thurner, EM; Renner, W; Hofmann, G; Gerger, A; Langsenlehner, U; Kapp, KS; Langsenlehner, T Side effects - Prevention and Management.
STRAHLENTHER ONKOL. 2011; 187(1):78-78. [Oral Communication]
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2010

Full papers/articles (Journal)

** Bahadori, B; Uitz, E; Dehchamani, D; Pilger, E; Renner, W The fibrinogen gamma 10034C>T polymorphism is not associated with Peripheral Arterial Disease
THROMB RES. 2010; 126(4): 350-352.
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** Bahadori, B; Uitz, E; Mayer, A; Harauer, J; Dam, K; Truschnig-Wilders, M; Pilger, E; Renner, W Polymorphisms of the hypoxia-inducible factor 1 gene and peripheral artery disease.
Vasc Med. 2010; 15(5):371-374
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** Gerger, A; Renner, W; Langsenlehner, T; Hofmann, G; Knechtel, G; Szkandera, J; Samonigg, H; Krippl, P; Langsenlehner, U Association of interleukin-10 gene variation with breast cancer prognosis.
Breast Cancer Res Treat. 2010; 119(3):701-705
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** Gruber, HJ; Bernecker, C; Lechner, A; Weiss, S; Wallner-Blazek, M; Meinitzer, A; Hobarth, G; Renner, W; Fauler, G; Horejsi, R; Fazekas, F; Truschnig-Wilders, M Increased nitric oxide stress is associated with migraine.
CEPHALALGIA. 2010; 30(4): 486-492.
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** Haschke-Becher, E; Kirchheiner, J; Trummer, O; Grunbacher, G; Kainz, A; Boehm, BO; Marz, W; Renner, W Impact of CYP2C8 and 2C9 polymorphisms on coronary artery disease and myocardial infarction in the LURIC cohort.
PHARMACOGENOMICS. 2010; 11(10): 1359-1365.
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** Kleber, ME; Grammer, TB; Renner, W; Marz, W 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)
BMC MED GENET. 2010; 11: 157 [OPEN ACCESS]
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** Kleber, ME; Renner, W; Grammer, TB; Linsel-Nitschke, P; Boehm, BO; Winkelmann, BR; Bugert, P; Hoffmann, MM; Marz, W Association of the single nucleotide polymorphism rs599839 in the vicinity of the sortilin 1 gene with LDL and triglyceride metabolism, coronary heart disease and myocardial infarction The Ludwigshafen Risk and Cardiovascular Health Study
ATHEROSCLEROSIS. 2010; 209(2): 492-497.
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** Knechtel, G; Hofmann, G; Gerger, A; Renner, W; Langsenlehner, T; Szkandera, J; Wolf, G; Samonigg, H; Krippl, P; Langsenlehner, U Analysis of common germline polymorphisms as prognostic factors in patients with lymph node-positive breast cancer.
J Cancer Res Clin Oncol. 2010; 136(12):1813-1819
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** Knechtel, G; Szkandera, J; Stotz, M; Hofmann, G; Langsenlehner, U; Krippl, P; Samonigg, H; Renner, W; Langner, C; Dehchamani, D; Gerger, A Single nucleotide polymorphisms in the hypoxia-inducible factor-1 gene and colorectal cancer risk.
Mol Carcinog. 2010; 49(9):805-809
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** Mossböck, G; Weger, M; Faschinger, C; Zimmermann, C; Schmut, O; Renner, W; El-Shabrawi, Y Role of functional single nucleotide polymorphisms of MMP1, MMP2, and MMP9 in open angle glaucomas.
Mol Vis. 2010; 16(12): 1764-1770. [OPEN ACCESS]
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** Saleheen, D; Soranzo, N; Rasheed, A; Scharnagl, H; Gwilliam, R; Alexander, M; Inouye, M; Zaidi, M; Potter, S; Haycock, P; Bumpstead, S; Kaptoge, S; Di Angelantonio, E; Sarwar, N; Hunt, SE; Sheikh, N; Shah, N; Samuel, M; Haider, SR; Murtaza, M; Thompson, A; Gobin, R; Butterworth, A; Ahmad, U; Hakeem, A; Zaman, KS; Kundi, A; Yaqoob, Z; Cheema, LA; Qamar, N; Faruqui, A; Mallick, NH; Azhar, M; Samad, A; Ishaq, M; Rasheed, SZ; Jooma, R; Niazi, JH; Gardezi, AR; Memon, NA; Ghaffar, A; Rehman, FU; Hoffmann, MM; Renner, W; Kleber, ME; Grammer, TB; Stephens, J; Attwood, A; Koch, K; Hussain, M; Kumar, K; Saleem, A; Kumar, K; Daood, MS; Gul, AA; Abbas, S; Zafar, J; Shahid, F; Bhatti, SM; Ali, SS; Fahim, M; Sagoo, G; Bray, S; McGinnis, R; Dudbridge, F; Winkelmann, BR; Boehm, B; Thompson, S; Ouwehand, W; Marz, W; Frossard, P; Danesh, J; Deloukas, P Genetic determinants of major blood lipids in Pakistanis compared with Europeans.
CIRC-CARDIOVASC GENET. 2010; 3(4): 348-357. [OPEN ACCESS]
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** Stingl, JC; Parmar, S; Huber-Wechselberger, A; Kainz, A; Renner, W; Seeringer, A; Brockmöller, J; Langsenlehner, U; Krippl, P; Haschke-Becher, E Impact of CYP2D6*4 genotype on progression free survival in tamoxifen breast cancer treatment.
Curr Med Res Opin. 2010; 26(11):2535-2542
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** Szkandera, J; Knechtel, G; Stotz, M; Hofmann, G; Langsenlehner, U; Krippl, P; Langsenlehner, T; Dehchamani, D; Samonigg, H; Renner, W; Gerger, A Association of hypoxia-inducible factor 1-alpha gene polymorphisms and colorectal cancer prognosis.
Anticancer Res. 2010; 30(6):2393-2397
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** Tomaschitz, A; Maerz, W; Pilz, S; Ritz, E; Scharnagl, H; Renner, W; Boehm, BO; Fahrleitner-Pammer, A; Weihrauch, G; Dobnig, H Aldosterone/renin ratio determines peripheral and central blood pressure values over a broad range.
J Am Coll Cardiol. 2010; 55(19): 2171-2180. [OPEN ACCESS]
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** Yazdani-Biuki, B; Krippl, P; Brickmann, K; Fuerst, F; Langsenlehner, U; Paulweber, B; Pilger, E; Wascher, TC; Brezinschek, HP; Renner, W The functional promoter polymorphism of the coagulation factor XII gene is not associated with peripheral arterial disease.
Angiology. 2010; 61(2):211-215
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Letters

** Steinbrugger, I; Haas, A; Maier, R; Renner, W; Mattes, D; El-Shabrawi, Y; Wedrich, A; Schmut, O; Weger, M Thrombophilic gene variants.
Ophthalmology. 2010; 117(4): 856-856.
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Abstracts (Journal)

** Dobnig, H; Scharnagl, H; Renner, W; Seelhorst, U; Wellnitz, B; Kinkeldei, J; Bohm, B; Fahrleitner-Pammer, A; Marz, W INFLUENCE OF 25-HYDROXYVITAMIN D STATUS ON SERUM PARATHYROID HORMONE LEVELS VARIES WITH KDOQI CLASSIFICATION OF RENAL FUNCTION AND IS INDEPENDENT OF 1,25 DIHYDROXYVITAMIN D CONCENTRATIONS
OSTEOPOROSIS INT. 2010; 21: 11-11. -IOF World Congress on Osteoporosis 10Th European Congress on Clinical an Economic Aspects of Osteoporosis and Osteoarthritis ; 5-8 May ; Florence, Italy. [Oral Communication]
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** Hofmann, G; Langsenlehner, T; Fuerst, F; Bitsche, S; Gerger, A; Langsenlehner, U; Krippl, P; Renner, W Hereditary variants of VEGF receptor genes and their impact on overall survival in rectal cancer.
Onkologie2010; 33(S 6):174-174.-Jahrestagung der Deutschen, Österreichischen und Schweizerischen Gesellschaften für Hämatologie und Onkologie; OCT 1-5, 2010; Berlin, GERMANY. [Poster]
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** Hofmann, G; Langsenlehner, T; Fuerst, F; Gerger, A; Langsenlehner, U; Knechtel, G; Samonigg, H; Krippl, P; Renner, W COMMON VEGF RECEPTOR GENE POLYMORPHISMS AND THEIR INFLUENCE ON OVERALL SURVIVAL IN COLORECTAL CANCER PATIENTS
Annals of Oncology2010; 21(S 6):35-35.-12th World Congress on Gastrointestinal Cancer; June 30-July 3, 2010; Barcelona, SPAIN. [Poster]
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** Hofmann, G; Langsenlehner, T; Fuerst, F; Gerger, A; Langsenlehner, U; Knechtel, G; Samonigg, H; Krippl, P; Renner, W ASSOCIATION OF COMMON SINGLE NUCLEOTIDE POLYMORPHISMS IN INTEGRINS WITH METASTASIS-FREE SURVIVAL IN RECTAL CANCER PATIENTS
Annals of Oncology2010; 21(S 6):59-59.-12th World Congress on Gastrointestinal Cancer; June 30-July 3, 2010; Barcelona, SPAIN. [Poster]
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** Hofmann, G; Langsenlehner, T; Fuerst, F; Szkandera, J; Gerger, A; Langsenlehner, U; Krippl, P; Renner, W Association of a single nucleotide polymorphism in the gene of TNFRSF10A (TRAILR-1) with relapse-free survival in colorectal cancer.
Onkologie2010; 33(S 6):173-173.-Jahrestagung der Deutschen, Österreichischen und Schweizerischen Gesellschaften für Hämatologie und Onkologie; OCT 1-5, 2010; Berlin, GERMANY. (ISBN: 0378-584X ) [Poster]
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** Knechtel, G; Szkandera, J; Stotz, M; Hofmann, G; Langsenlehner, U; Krippl, P; Samonigg, H; Renner, W; Dehchamani, D; Gerger, A Single nucleotide polymorphisms in the hypoxia-inducible factor 1 gene and colorectal cancer risk
Onkologie-International Journal for Cancer Research and Treatment2010; 33(S6):225-226.-Jahrestagung der Deutschen, Österreichischen und Schweizerischen Gesellschaften für Hämatologie und Onkologie; OKT 1-5, 2010; Berlin, GERMANY. (ISBN: 978-3-8055-9633-6 ) [Oral Communication]
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** Langsenlehner, T; Renner, W; Hofmann, G; Thurner, EM; Kapp, KS; Langsenlehner, U The XRCC1 Arg280His polymorphism is associated with high-grade radiation-induced late toxicity in prostate cancer patients.
EJC SUPPL. 2010; 8(7):167-167.-22nd EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics; NOV 16-19, 2010; Berlin, GERMANY. [Oral Communication]
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** Szkandera, J; Knechtel, G; Stotz, M; Hofmann, G; Langsenlehner, U; Krippl, P; Langsenlehner, T; Dehchamani, D; Samonigg, H; Renner, W; Gerger, A Association of Hypoxia Inducible Factor 1-alpha Gene Polymorphisms and Colorectal Cancer Prognosis.
Onkologie-International Journal for Cancer Research and Treatment2010; 33(S6):226-226.-Jahrestagung der Deutschen, Österreichischen und Schweizerischen Gesellschaften für Hämatologie und Onkologie; OKT 1-5, 2010; Berlin, GERMANY. (ISBN: 978-3-8055-9633-6 ) [Oral Communication]
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** Thurner, EM; Partl, R; Tauber, G; Renner, W; Kapp, KS; Langsenlehner, U; Langsenlehner, T The role of DNA repair gene polymorphisms in the development of radiation-induced late toxicity in prostate cancer patients
EJC SUPPL. 2010; 8(5):850--21st Meeting of the European Association for Cancer Research.; JUN 26-29, 2010; Oslo, NORWAY. [Poster]
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2009

Full papers/articles (Journal)

** Amouyel, P; Arveiler, D; Boekholdt, SM; Braund, P; Bruse, P; Bumpstead, SJ; Bugert, P; Cambien, F; Danesh, J; Deloukas, P; Doering, A; Ducimetiere, P; Dunn, RM; El Mokhtari, NE; Erdmann, J; Evans, A; Ewels, P; Ferrieres, J; Fischer, M; Frossard, P; Garner, S; Gieger, C; Gohri, MJR; Goodall, AH; Grosshennig, A; Hall, A; Hardwick, R; Haukijarvi, A; Hengstenberg, C; Illig, T; Karvanen, J; Kastelein, J; Kee, F; Khaw, KT; Kluter, H; Konig, IR; Kuulasmaa, K; Laiho, P; Luc, G; Marz, W; McGinnis, R; McLaren, W; Meisinger, C; Morrison, C; Ou, X; Ouwehand, WH; Preuss, M; Proust, C; Ravindrarajah, R; Renner, W; Rice, K; Ruidavets, JB; Saleheen, D; Salomaa, V; Samani, NJ; Sandhu, MS; Schafer, AS; Scholz, M; Schreiber, S; Schunkert, H; Silander, K; Singh, R; Soranzo, N; Stark, K; Stegmayr, B; Stephens, J; Thompson, J; Tiret, L; Trip, MD; van der Schoot, E; Virtamo, J; Wareham, NJ; Wichmann, HE; Wiklund, PG; Wright, B; Ziegler, A; Zwaginga, JJ Large scale association analysis of novel genetic loci for coronary artery disease.
Arterioscler Thromb Vasc Biol. 2009; 29(5):774-780 [OPEN ACCESS]
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** Erdmann, J; Grosshennig, A; Braund, PS; König, IR; Hengstenberg, C; Hall, AS; Linsel-Nitschke, P; Kathiresan, S; Wright, B; Trégouët, DA; Cambien, F; Bruse, P; Aherrahrou, Z; Wagner, AK; Stark, K; Schwartz, SM; Salomaa, V; Elosua, R; Melander, O; Voight, BF; O'Donnell, CJ; Peltonen, L; Siscovick, DS; Altshuler, D; Merlini, PA; Peyvandi, F; Bernardinelli, L; Ardissino, D; Schillert, A; Blankenberg, S; Zeller, T; Wild, P; Schwarz, DF; Tiret, L; Perret, C; Schreiber, S; El Mokhtari, NE; Schäfer, A; März, W; Renner, W; Bugert, P; Klüter, H; Schrezenmeir, J; Rubin, D; Ball, SG; Balmforth, AJ; Wichmann, HE; Meitinger, T; Fischer, M; Meisinger, C; Baumert, J; Peters, A; Ouwehand, WH; Italian Atherosclerosis, Thrombosis, and Vascular Biology Working Group; Myocardial Infarction Genetics Consortium; Wellcome Trust Case Control Consortium; Cardiogenics Consortium; Deloukas, P; Thompson, JR; Ziegler, A; Samani, NJ; Schunkert, H New susceptibility locus for coronary artery disease on chromosome 3q22.3.
Nat Genet. 2009; 41(3):280-282 [OPEN ACCESS]
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** Gerger, A; Hofmann, G; Langsenlehner, U; Renner, W; Weitzer, W; Wehrschütz, M; Wascher, T; Samonigg, H; Krippl, P Integrin alpha-2 and beta-3 gene polymorphisms and colorectal cancer risk.
Int J Colorectal Dis. 2009; 24(2):159-163
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** Grammer, TB; März, W; Renner, W; Böhm, BO; Hoffmann, MM C-reactive protein genotypes associated with circulating C-reactive protein but not with angiographic coronary artery disease: the LURIC study.
Eur Heart J. 2009; 30(2):170-182 [OPEN ACCESS]
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** Grammer, TB; Renner, W; Hoffmann, MM; Kleber, M; Winkelhofer-Roob, BM; Boehm, BO; Maerz, W SOD3 R231G polymorphism associated with coronary artery disease and myocardial infarction. The Ludwigshafen Risk and Cardiovascular Health (LURIC) study
FREE RADICAL RES. 2009; 43(7): 677-684.
Web of Science Google Scholar

 

** Hoffmann, MM; Winkler, K; Renner, W; Winkelmann, BR; Seelhorst, U; Wellnitz, B; Boehm, BO; März, W Genetic variants and haplotypes of lipoprotein associated phospholipase A2 and their influence on cardiovascular disease (The Ludwigshafen Risk and Cardiovascular Health Study).
J Thromb Haemost. 2009; 7(1):41-48 [OPEN ACCESS]
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** Hofmann, G; Langsenlehner, U; Langsenlehner, T; Yazdani-Biuki, B; Clar, H; Gerger, A; Fuerst, F; Samonigg, H; Krippl, P; Renner, W A common hereditary single-nucleotide polymorphism in the gene of FAS and colorectal cancer survival.
J Cell Mol Med. 2009; 13(9B):3699-3702
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** Kofler, B; Mueller, EE; Eder, W; Stanger, O; Maier, R; Weger, M; Haas, A; Winker, R; Schmut, O; Paulweber, B; Iglseder, B; Renner, W; Wiesbauer, M; Aigner, I; Santic, D; Zimmermann, FA; Mayr, JA; Sperl, W Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: a case control study
BMC MED GENET. 2009; 10: 35 [OPEN ACCESS]
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** Mattes, D; Haas, A; Renner, W; Steinbrugger, I; El-Shabrawi, Y; Wedrich, A; Werner, C; Schmut, O; Weger, M Analysis of three pigment epithelium-derived factor gene polymorphisms in patients with exudative age-related macular degeneration.
Mol Vis. 2009; 15: 343-348. [OPEN ACCESS]
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** Matzhold, EM; Trummer, O; Grünbacher, G; Zulus, B; Boehm, BO; März, W; Renner, W Association of polymorphisms in the chemokine receptor CX3CR1 gene with coronary artery disease.
Cytokine. 2009; 47(3): 224-227.
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** Mossböck, G; Renner, W; El-Shabrawi, Y; Faschinger, C; Schmut, O; Wedrich, A; Zimmermann, C; Weger, M TNF-alpha -308 G>A and -238 G>A polymorphisms are not major risk factors in Caucasian patients with exfoliation glaucoma.
Mol Vis. 2009; 15(10): 518-522. [OPEN ACCESS]
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** Mossbock, G; Weger, M; Meinitzer, A; Semmelrock, J; Schmut, O; Faschinger, C; Zimmermann, C; Renner, W; Stanger, O Asymmetric dimethylarginine and homocysteine in primary open angle glaucoma
SPEKTRUM AUGENHEILKD. 2009; 23(5): 333-336.
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** Pilz, S; Dobnig, H; Winklhofer-Roob, BM; Renner, W; Seelhorst, U; Wellnitz, B; Boehm, BO; März, W Low serum zinc concentrations predict mortality in patients referred to coronary angiography.
Br J Nutr. 2009; 101(10): 1534-1540.
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** Silbernagel, G; Fauler, G; Renner, W; Landl, EM; Hoffmann, MM; Winkelmann, BR; Boehm, BO; März, W The relationships of cholesterol metabolism and plasma plant sterols with the severity of coronary artery disease.
J Lipid Res. 2009; 50(2):334-341 [OPEN ACCESS]
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** Steinbrugger, I; Haas, A; Maier, R; Renner, W; Mayer, M; Werner, C; Wedrich, A; El-Shabrawi, Y; Schmut, O; Weger, M Analysis of inflammation- and atherosclerosis-related gene polymorphisms in branch retinal vein occlusion.
Mol Vis. 2009; 15: 609-618. [OPEN ACCESS]
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** Steinbrugger, I; Haas, A; Renner, W; Mayer, M; Wedrich, A; El-Shabrawi, Y; Werner, C; Schmut, O; Weger, M Die Bedeutung des C3 Arg102Gly Genpolymorphismus als Risikofaktor für die exsudative altersabhängige Makuladegeneration.
Spektrum der Augenheilkunde. 2009; 23(5): 353-357.
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** Wehrschuetz, M; Schöllnast, H; Wehrschuetz, E; Renner, W; Luschin, G VEGF 936C > T Polymorphism and Association of BI-RADS Score in Women with Suspected Breast Cancer.
Breast Cancer (Auckl). 2009; 3(3):77-81 [OPEN ACCESS]
PubMed PUBMED Central FullText

 

Letters

** Clar, H; Krippl, P; Renner, W; Langsenlehner, T; Clar, V; Windhager, R; Langsenlehner, U Association of polymorphisms of angiogenesis genes with breast cancer.
Breast Cancer Res Treat. 2009; 113(1): 197-198.
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** Weger, W; Hofer, A; Wolf, P; El-Shabrawi, Y; Renner, W; Kerl, H; Salmhofer, W Common polymorphisms in the interleukin-22 gene are not associated with chronic plaque psoriasis.
Exp Dermatol. 2009; 18(9): 796-798.
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Abstracts (Journal)

** Dobnig, H; Pilz, S; Scharnagl, H; Renner, W; Seelhorst, U; Wellnitz, B; Fahrleitner-Pammer, A; Bohm, BO; Marz, W 25-hydroxyvitamin D levels and association with all-cause mortality in patients with type 2 diabetes mellitus
DIABETOLOGIA. 2009; 52: 316--44th General Assembly of the European Association for the Study of Diabetes (EASD); SEP 7-11, 2009; Rome, ITALY. [Poster]
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** Dobnig, H; Pilz, S; Scharnagl, H; Renner, W; Seelhorst, U; Wellnitz, B; Kinkeldei, J; Bohm, B; Fahrleitner-Pammer, A; Marz, W Influence of 25-hydroxyvitamin D and 1,25 dihydroxyvitamin D status on serum parathyroid hormone levels varies at different levels of renal function
BONE. 2009; 44(2):S360-S360.-36th European Symposium on Calcified Tissue; MAY 23-27, 2009; Vienna, Austria. [Poster]
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** Hofmann, G; Langsenlehner, T; Fuerst, F; Gerger, A; Langsenlehner, U; Knechtel, G; Szkandera, J; Krippl, P; Renner, W The 683A>C polymorphism in the ligand binding domain of TRAILR-1 (TNFRSF10A) is not associated with colorectal cancer survival.
Annals of Oncology2009; 20(S 7):31-31.-11th World Congress on Gastrointestinal Cancer ; JUNE 24-27, 2009; Barcelona, SPAIN. [Poster]
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** Hofmann, G; Langsenlehner, T; Fuerst, F; Gerger, A; Langsenlehner, U; Samonigg, H; Clar, H; Krippl, P; Renner, W A hereditary single nucleotide polymorphism in the FAS gene and its impact on developing metastases in rectal cancer patients.
Annals of Oncology. 2009; 20(S 7):58-58.-11th World Congress on Gastrointestinal Cancer ; JUNE 24-27; Barcelona, SPAIN. [Poster]
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** Langsenlehner, T; Partl, R; Tauber, G; Gerger, A; Hofmann, G; Renner, W; Kapp, KS; Langsenlehner, U Single nucleotide polymorphisms in the gene for vascular endothelial growth factor and radiation induced late toxicity
EJC Supplements 20092009; 7(2):155-155.-Joint ECCO15-34th ESMO Multidisciplinary Congress; SEP 20-24, 2009; Berlin, GERMANY. [Oral Communication]
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2008

Full papers/articles (Journal)

** Boehm, BO; Möller, P; Högel, J; Winkelmann, BR; Renner, W; Rosinger, S; Seelhorst, U; Wellnitz, B; März, W; Melzner, J; Brüderlein, S Lymphocytes of type 2 diabetic women carry a high load of stable chromosomal aberrations: a novel risk factor for disease-related early death.
Diabetes. 2008; 57(11): 2950-2957. [OPEN ACCESS]
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** Clar, H; Langsenlehner, U; Krippl, P; Renner, W; Leithner, A; Gruber, G; Hofmann, G; Yazdani-Biuki, B; Langsenlehner, T; Windhager, R A polymorphism in the G protein beta3-subunit gene is associated with bone metastasis risk in breast cancer patients.
Breast Cancer Res Treat. 2008; 111(3):449-452
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** Dobnig, H; Pilz, S; Scharnagl, H; Renner, W; Seelhorst, U; Wellnitz, B; Kinkeldei, J; Boehm, BO; Weihrauch, G; Maerz, W Independent association of low serum 25-hydroxyvitamin d and 1,25-dihydroxyvitamin d levels with all-cause and cardiovascular mortality.
Arch Intern Med. 2008; 168(12): 1340-1349. [OPEN ACCESS]
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** Hofmann, G; Langsenlehner, U; Renner, W; Langsenlehner, T; Yazdani-Biuki, B; Clar, H; Gerger, A; Wehrschuetz, M; Samonigg, H; Krippl, P Common single nucleotide polymorphisms in the vascular endothelial growth factor gene and colorectal cancer risk.
J Cancer Res Clin Oncol. 2008; 134(5):591-595
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** Langdahl, BL; Uitterlinden, AG; Ralston, SH; Trikalinos, TA; Balcells, S; Brandi, ML; Scollen, S; Lips, P; Lorenc, R; Obermayer-Pietsch, B; Reid, DM; Armas, JB; Arp, PP; Bassiti, A; Bustamante, M; Husted, LB; Carey, AH; Pérez Cano, R; Dobnig, H; Dunning, AM; Fahrleitner-Pammer, A; Falchetti, A; Karczmarewicz, E; Kruk, M; van Leeuwen, JP; Masi, L; van Meurs, JB; Mangion, J; McGuigan, FE; Mellibovsky, L; Mosekilde, L; Nogués, X; Pols, HA; Reeve, J; Renner, W; Rivadeneira, F; van Schoor, NM; Ioannidis, JP; APOSS investigators; DOPS investigators; EPOS investigators; EPOLOS investigators; FAMOS investigators; LASA investigators; ERGO investigators; for the GENOMOS Study Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: the GENOMOS study.
Bone. 2008; 42(5): 969-981.
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** Langsenlehner, T; Langsenlehner, U; Renner, W; Kapp, KS; Krippl, P; Hofmann, G; Clar, H; Pummer, K; Mayer, R The Glu228Ala polymorphism in the ligand binding domain of death receptor 4 is associated with increased risk for prostate cancer metastases.
Prostate. 2008; 68(3):264-268
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** Langsenlehner, T; Langsenlehner, U; Renner, W; Krippl, P; Mayer, R; Wascher, TC; Kapp, KS Single nucleotide polymorphisms and haplotypes in the gene for vascular endothelial growth factor and risk of prostate cancer.
Eur J Cancer. 2008; 44(11):1572-1576
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** Langsenlehner, U; Wolf, G; Langsenlehner, T; Gerger, A; Hofmann, G; Clar, H; Wascher, TC; Paulweber, B; Samonigg, H; Krippl, P; Renner, W Genetic polymorphisms in the vascular endothelial growth factor gene and breast cancer risk. The Austrian "tumor of breast tissue: incidence, genetics, and environmental risk factors" study.
Breast Cancer Res Treat. 2008; 109(2):297-304
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** Mossböck, G; Renner, W; Faschinger, C; Schmut, O; Wedrich, A; Weger, M Lysyl oxidase-like protein 1 (LOXL1) gene polymorphisms and exfoliation glaucoma in a Central European population.
Mol Vis. 2008; 14(10): 857-861. [OPEN ACCESS]
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** Mossböck, G; Weger, M; Faschinger, C; Schmut, O; Renner, W Plasminogen activator inhibitor-1 4G/5G gene polymorphism and primary open-angle glaucoma.
Mol Vis. 2008; 14(10): 1240-1244. [OPEN ACCESS]
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** van Meurs, JB; Trikalinos, TA; Ralston, SH; Balcells, S; Brandi, ML; Brixen, K; Kiel, DP; Langdahl, BL; Lips, P; Ljunggren, O; Lorenc, R; Obermayer-Pietsch, B; Ohlsson, C; Pettersson, U; Reid, DM; Rousseau, F; Scollen, S; Van Hul, W; Agueda, L; Akesson, K; Benevolenskaya, LI; Ferrari, SL; Hallmans, G; Hofman, A; Husted, LB; Kruk, M; Kaptoge, S; Karasik, D; Karlsson, MK; Lorentzon, M; Masi, L; McGuigan, FE; Mellström, D; Mosekilde, L; Nogues, X; Pols, HA; Reeve, J; Renner, W; Rivadeneira, F; van Schoor, NM; Weber, K; Ioannidis, JP; Uitterlinden, AG; GENOMOS Study Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis.
JAMA. 2008; 299(11): 1277-1290. [OPEN ACCESS]
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** Weger, W; Hofer, A; Stanger, O; Wolf, P; El-Shabrawi, Y; Renner, W; Kerl, H; Salmhofer, W The methylenetetrahydrofolate reductase 677C>T gene polymorphism is not associated with chronic plaque psoriasis.
Exp Dermatol. 2008; 17(9): 748-751.
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Letters

** Clar, H; Renner, W; Krippl, P; Leithner, A; Gruber, G; Langsenlehner, T; Hofmann, G; Yazdani-Biuki, B; Clar, V; Windhager, R; Langsenlehner, U The LCT 13910 C/T polymorphism as a risk factor for osteoporosis, has no impact on metastatic bone disease in breast cancer.
Breast Cancer Res Treat. 2008; 112(2): 363-365.
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** Langsenlehner, T; Renner, W; Yazdani-Biuki, B; Langsenlehner, U Methylenetetrahydrofolate reductase (MTHFR) and breast cancer risk: a nested-case-control study and a pooled meta-analysis.
Breast Cancer Res Treat. 2008; 107(3): 459-460.
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** Weger, W; Hofer, A; Wolf, P; El-Shabrawi, Y; Renner, W; Kerl, H; Salmhofer, W Role of the interleukin 15 96516A>T and IL15 96330C>A gene polymorphisms in Caucasian patients with chronic plaque psoriasis.
J Dermatol Sci. 2008; 51(2): 147-149.
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** Yazdani-Biuki, B; Brickmann, K; Langsenlehner, U; Renner, W; Truschnig, M; Krippl, P; Fürst, F; Graninger, WB; Brezinschek, HP The Glu228Ala polymorphism in the ligand-binding domain of death receptor 4 is not associated with rheumatoid arthritis.
Ann Rheum Dis. 2008; 67(7): 1053-1054. [OPEN ACCESS]
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Reviews

** Mossbock, G; Faschinger, C; Weger, M; Renner, W Role of genetic factors in glaucomas
SPEKTRUM AUGENHEILKD. 2008; 22(4): 227-232.
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Abstracts (Journal)

** Hofmann, G; Langsenlehner, T; Fuerst, F; Gerger, A; Langsenlehner, U; Samonigg, H; Clar, H; Krippl, P; Renner, W Hereditary gene polymorphisms of vascular endothelial growth factor and colorectal cancer.
ANN ONCOL. 2008; 19(S6):68-68.-10th World Congress on Gastrointestinal Cancer; JUNE 25-28, 2008; Barcelona, SPAIN. [Poster]
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** Hofmann, G; Langsenlehner, T; Fuerst, F; Gerger, A; Langsenlehner, U; Samonigg, H; Clar, H; Krippl, P; Renner, W Association of a common-670 A > G polymorphism in the gene of TNFRSF6 (FAS) with overall survival in colorectal cancer patients
ANN ONCOL. 2008; 19(S 6):68-68. [Oral Communication]
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** Langsenlehner, T; Langsenlehner, U; Renner, W; Mayer, R; Kapp, KS Association of SNPs in the genes of VEGF, IL-10, COX-2, FAS, FASL and TRAIL-R1 with radio-gene after-effects for prostate carcinoma patients.
STRAHLENTHER ONKOL. 14. Jahreskongress der Deutschen Gesellschaft für Radioonkologie, 25. Jahrestagung der Österreichischen Gesellschaft für Radioonkologie, Radiobiologie und Medizinische Strahlenphysik2008; 184: 147-147.-14. Jahreskongress der Deutschen Gesellschaft für Radioonkologie, 25. Jahrestagung der Österreichischen Gesellschaft für Radioonkologie, Radiobiologie und Medizinische Strahlenphysik; MAI 1-4, 2008; Wien, AUSTRIA. [Poster]
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** Meilinger, M; Schweighofer, N; Wehr, E; Renner, W; Obermayer-Pietsch, B Genetics of metabolic bone disease - Lipoprotein receptor related protein 5 & 6 and osteoporosis
WIEN KLIN WOCHENSCHR. 2008; 120(15-16):A46-A46.-ÖGIM; 17.-21.9.2008; g. [Poster]
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2007

Full papers/articles (Journal)

** Eder, T; Mayer, R; Langsenlehner, U; Renner, W; Krippl, P; Wascher, TC; Pummer, K; Kapp, KS Interleukin-10 ATA promoter haplotype and prostate cancer risk: a population-based study.
Eur J Cancer. 2007; 43(3): 472-475.
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** Gerger, A; Langsenlehner, U; Renner, W; Weitzer, W; Eder, T; Yazdani-Biuki, B; Hofmann, G; Samonigg, H; Krippl, P A multigenic approach to predict breast cancer risk.
Breast Cancer Res Treat. 2007; 104(2):159-164
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** Grünbacher, G; Weger, W; Marx-Neuhold, E; Pilger, E; Köppel, H; Wascher, T; März, W; Renner, W The fibrinogen gamma (FGG) 10034C>T polymorphism is associated with venous thrombosis.
Thromb Res. 2007; 121(1): 33-36.
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** März, W; Seelhorst, U; Wellnitz, B; Tiran, B; Obermayer-Pietsch, B; Renner, W; Boehm, BO; Ritz, E; Hoffmann, MM Alanine to serine polymorphism at position 986 of the calcium-sensing receptor associated with coronary heart disease, myocardial infarction, all-cause, and cardiovascular mortality.
J Clin Endocrinol Metab. 2007; 92(6):2363-2369 [OPEN ACCESS]
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** Obermayer-Pietsch, BM; Gugatschka, M; Reitter, S; Plank, W; Strele, A; Walter, D; Bonelli, C; Goessler, W; Dobnig, H; Högenauer, C; Renner, W; Fahrleitner-Pammer, A Adult-type hypolactasia and calcium availability: decreased calcium intake or impaired calcium absorption?
Osteoporos Int. 2007; 18(4): 445-451.
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** Renner, W; Hoffmann, MM; Grünbacher, G; Winkelmann, BR; Boehm, BO; März, W G-protein beta3 subunit (GNB3) gene polymorphisms and cardiovascular disease: the Ludwigshafen Risk and Cardiovascular Health (LURIC) study.
Atherosclerosis. 2007; 192(1):108-112
Web of Science PubMed FullText FullText_MUG

 

** Weger, M; Renner, W; Steinbrugger, I; Köfer, K; Wedrich, A; Groselj-Strele, A; El-Shabrawi, Y; Schmut, O; Haas, A Association of the HTRA1 -625G>A promoter gene polymorphism with exudative age-related macular degeneration in a Central European population.
Mol Vis. 2007; 13(4): 1274-1279. [OPEN ACCESS]
Web of Science PubMed

 

** Weger, M; Steinbrugger, I; El-Shabrawi, Y; Wegscheider, BJ; Weger, W; Renner, W; Schmut, O; Haas, A Haplotype-tagging interleukin-10 promoter polymorphism is associated with reduced risk of retinal artery occlusion.
Mol Vis. 2007; 13(7): 549-552. [OPEN ACCESS]
Web of Science PubMed PUBMED Central Google Scholar

 

** Weger, W; Hofer, A; Wolf, P; El-Shabrawi, Y; Renner, W; Kerl, H; Salmhofer, W The angiotensin-converting enzyme insertion/deletion and the endothelin -134 3A/4A gene polymorphisms in patients with chronic plaque psoriasis.
Exp Dermatol. 2007; 16(12): 993-998.
Web of Science PubMed FullText FullText_MUG

 

** Wegscheider, BJ; Weger, M; Renner, W; Steinbrugger, I; März, W; Mossböck, G; Temmel, W; El-Shabrawi, Y; Schmut, O; Jahrbacher, R; Haas, A Association of complement factor H Y402H gene polymorphism with different subtypes of exudative age-related macular degeneration.
Ophthalmology. 2007; 114(4):738-742
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Abstracts (Journal)

** Dobnig, H; Scharnagl, H; Renner, W; Seelhorst, U; Wellnitz, B; Riedmuller, G; Bruck, C; Tiran, B; Boehm, B; Maerz, W Serum concentrations of vitamin D are significant and independent predictors of mortality: The Ludwigshafen Risk and Cardiovascular Health (LURIC) study
EXP CLIN ENDOCRINOL DIABETES. 115: S91-S91.-51. Annual Meeting of the German Society of Endocrinology (DGE); MAR 7-10, 2007; Salzburg, Austria. [Poster]
Web of Science

 

** Hofmann, G; Gerger, A; Weitzer, W; Langsenlehner, T; Fuerst, F; Renner, W; Samonigg, H; Krippl, P; Langsenlehner, U The ITGA2 807C > T polymorphism is associated with reduced colorectal cancer susceptibility
ANN ONCOL. 2007; 18: VII38-VII38.-2007 World Congress on Gastrointestinal Cancer; JUN 27-30, 2007; Barcelona, SPAIN. [Poster]
Web of Science

 

** Obermayer-Pietsch, B; Gugatschka, M; Groselj-Strele, A; Goessler, W; Dobnig, H; Hoegenauer, C; Fahrleitner-Pammer, A; Renner, W Genetically defined adult-type hypolactasia and calcium balance: High amounts of lactose decrease calcium absorption
EXP CLIN ENDOCRINOL DIABETES. 2007; 115: S7-S7. [Poster]
Web of Science

 

** Zimmermann, F; Stanger, O; Muller, E; Wiesbauer, M; Mayr, JA; Paulweber, B; Iglseder, B; Renner, W; Eder, W; Sperl, W; Kofler, B Distribution of mitochondrial haplogroups in coronary artery disease
FEBS J. 2007; 274: 229-229. [Poster]
Web of Science

 

2006

Full papers/articles (Journal)

** El-Shabrawi, Y; Wegscheider, BJ; Weger, M; Renner, W; Posch, U; Ulrich, S; Ardjomand, N; Hermann, J Polymorphisms within the tumor necrosis factor-alpha promoter region in patients with HLA-B27-associated uveitis: association with susceptibility and clinical manifestations.
OPHTHALMOLOGY. 2006; 113(4): 695-700.
Web of Science PubMed FullText FullText_MUG

 

** Grammer, TB; Renner, W; von Karger, S; Boehm, BO; Winkelmann, BR; Maerz, W 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).
Mol Genet Metab. 2006; 88(4):378-383
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** Langsenlehner, U; Renner, W; Yazdani-Biuki, B; Eder, T; Wascher, TC; Paulweber, B; Clar, H; Hofmann, G; Samonigg, H; Krippl, P Integrin alpha-2 and beta-3 gene polymorphisms and breast cancer risk.
Breast Cancer Res Treat. 2006; 97(1):67-72
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** Langsenlehner, U; Yazdani-Biuki, B; Eder, T; Renner, W; Wascher, TC; Paulweber, B; Weitzer, W; Samonigg, H; Krippl, P The cyclooxygenase-2 (PTGS2) 8473T>C polymorphism is associated with breast cancer risk.
Clin Cancer Res. 2006; 12(4):1392-1394 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

** Mossbock, G; Weger, M; Faschinger, C; Steinbrugger, I; Temmel, W; Schmut, O; Renner, W; Hufnagel, C; Stanger, O Methylenetetrahydrofolatereductase (MTHFR) 677C>T polymorphism and open angle glaucoma.
MOL VIS. 2006; 12(11): 356-359. [OPEN ACCESS]
Web of Science PubMed

 

** Mossböck, G; Weger, M; Moray, M; Renner, W; Haller-Schober, EM; Mattes, D; Schmut, O; Wegscheider, B; El-Shabrawi, Y TNF-alpha promoter polymorphisms and primary open-angle glaucoma.
EYE. 2006; 20(9): 1040-1043.
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** Ralston, SH; Uitterlinden, AG; Brandi, ML; Balcells, S; Langdahl, BL; Lips, P; Lorenc, R; Obermayer-Pietsch, B; Scollen, S; Bustamante, M; Husted, LB; Carey, AH; Diez-Perez, A; Dunning, AM; Falchetti, A; Karczmarewicz, E; Kruk, M; van Leeuwen, JPTM; van Meurs, JBJ; Mangion, J; McGuigan, FEA; Mellibovsky, L; del Monte, F; Pols, HAP; Reeve, J; Reid, DM; Renner, W; Rivadeneira, F; van Schoor, NM; Sherlock, RE; Ioannidis, JPA Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: The GENOMOS study
PLOS MED. 2006; 3: 515-523. [OPEN ACCESS]
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** Schäfer, E; Weger, M; Birgül, T; Renner, W; Stanger, O; Steinbrugger, I; Schmut, O; Temmel, W; Haas, A Angiotensin-converting enzyme insertion/deletion polymorphism and retinal artery occlusion.
Acta Ophthalmol Scand. 2006; 84(3):305-308
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** Trummer, O; Köppel, H; Wascher, TC; Grünbacher, G; Gutjahr, M; Stanger, O; Ramschak-Schwarzer, S; Boehm, BO; Winkelmann, BR; März, W; Renner, W The serotonin transporter gene polymorphism is not associated with smoking behavior.
Pharmacogenomics J. 2006; 6(6):397-400
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** Uitterlinden, AG; Ralston, SH; Brandi, ML; Carey, AH; Grinberg, D; Langdahl, BL; Lips, P; Lorenc, R; Obermayer-Pietsch, B; Reeve, J; Reid, DM; Amedei, A; Amidei, A; Bassiti, A; Bustamante, M; Husted, LB; Diez-Perez, A; Dobnig, H; Dunning, AM; Enjuanes, A; Fahrleitner-Pammer, A; Fang, Y; Karczmarewicz, E; Kruk, M; van Leeuwen, JP; Mavilia, C; van Meurs, JB; Mangion, J; McGuigan, FE; Pols, HA; Renner, W; Rivadeneira, F; van Schoor, NM; Scollen, S; Sherlock, RE; Ioannidis, JP; APOSS Investigators; EPOS Investigators; EPOLOS Investigators; FAMOS Investigators; LASA Investigators; Rotterdam Study Investigators; GENOMOS Study The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysis.
Ann Intern Med. 2006; 145(4):255-264 [OPEN ACCESS]
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** Yazdani-Biuki, B; Brickmann, K; Wohlfahrt, K; Mueller, T; März, W; Renner, W; Gutjahr, M; Langsenlehner, U; Krippl, P; Wascher, TC; Paulweber, B; Graninger, W; Brezinschek, HP The MHC2TA -168A>G gene polymorphism is not associated with rheumatoid arthritis in Austrian patients.
Arthritis Res Ther. 2006; 8(4): R97-R97. [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Abstracts (Journal)

** Langsenlehner, U; Eder, T; Renner, W; Gerger, A; Hofmann, G; Samonigg, H; Krippl, P The cyclooxygenase-2 (PTGS2) 8473T > C polymorphism increases breast cancer risk.
BREAST CANCER RES TREAT. 2006; 100: S251-S252.-29th Annual San Antonio Breast Cancer Symposium; DEC 14-17, 2006; San Antonio, USA. [Poster]
Web of Science

 

2005

Full papers/articles (Journal)

** Högenauer, C; Hammer, HF; Mellitzer, K; Renner, W; Krejs, GJ; Toplak, H Evaluation of a new DNA test compared with the lactose hydrogen breath test for the diagnosis of lactase non-persistence.
Eur J Gastroenterol Hepatol. 2005; 17(3):371-376
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** Langsenlehner, U; Krippl, P; Renner, W; Yazdani-Biuki, B; Eder, T; Köppel, H; Wascher, TC; Paulweber, B; Samonigg, H Interleukin-10 promoter polymorphism is associated with decreased breast cancer risk.
Breast Cancer Res Treat. 2005; 90(2):113-115
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** Oliyarnyk, O; Renner, W; Paulweber, B; Wascher, TC Interindividual differences of response to statin treatment cannot be explained by variations of the human gene for RhoA.
Biochem Genet. 2005; 43(3-4):143-148
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** Renner, W; Nauck, M; Winkelmann, BR; Hoffmann, MM; Scharnagl, H; Mayer, V; Boehm, BO; März, W; LURIC Study team Association of angiotensinogen haplotypes with angiotensinogen levels but not with blood pressure or coronary artery disease: the Ludwigshafen Risk and Cardiovascular Health Study.
J Mol Med (Berl). 2005; 83(3):235-239
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** Weger, M; Renner, W; Steinbrugger, I; Cichocki, L; Temmel, W; Stanger, O; El-Shabrawi, Y; Lechner, H; Schmut, O; Haas, A Role of thrombophilic gene polymorphisms in branch retinal vein occlusion.
OPHTHALMOLOGY. 2005; 112(11): 1910-1915.
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** Weger, M; Steinbrugger, I; Haas, A; März, W; El-Shabrawi, Y; Weger, W; Schmut, O; Renner, W Role of the interleukin-6 -174 G>C gene polymorphism in retinal artery occlusion.
STROKE. 2005; 36(2): 249-252. [OPEN ACCESS]
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** Wegscheider, BJ; Weger, M; Renner, W; Posch, U; Ulrich, S; Hermann, J; Ardjomand, N; Haller-Schober, EM; El-Shabrawi, Y Role of the CCL2/MCP-1 -2518A>G gene polymorphism in HLA-B27 associated uveitis.
MOL VIS. 2005; 11(9-10): 896-900. [OPEN ACCESS]
Web of Science PubMed

 

** Wölfler, A; Erkeland, SJ; Bodner, C; Valkhof, M; Renner, W; Leitner, C; Olipitz, W; Pfeilstöcker, M; Tinchon, C; Emberger, W; Linkesch, W; Touw, IP; Sill, H A functional single-nucleotide polymorphism of the G-CSF receptor gene predisposes individuals to high-risk myelodysplastic syndrome.
Blood. 2005; 105(9):3731-3736 [OPEN ACCESS]
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Letters

** Grunbacher, G; Marx-Neuhold, E; Pilger, E; Koppel, H; Renner, W The functional-4C > T polymorphism of the coagulation factor XII gene is not associated with deep venous thrombosis
J THROMB HAEMOST. 2005; 3: 2815-2817.
Web of Science

 

** Langsenlehner, U; Hofmann, G; Samonigg, H; Krippl, P; Renner, W; Clar, H Cyclin D1 genotype and breast cancer metastasis.
CANCER EPIDEM BIOMARKER PREV. 2005; 14: 1844-1845. [OPEN ACCESS]
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** Mattes, D; Weger, M; Renner, W; Cichocki, L; Haas, A Role of angiotensin-converting enzyme insertion/deletion and plasminogen activator inhibitor-1 4G/5G gene polymorphisms in retinal vein occlusion.
J THROMB HAEMOST. 2005; 3: 2583-2584. [OPEN ACCESS]
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Abstracts (Journal)

** Hofmann, G; Langsenlehner, U; Renner, W; Greimel, A; Samonigg, H; Krippl, P Breast cancer metastasis-free survival and its association to a common hereditary gene polymorphism of cyclin D1
BREAST CANCER RES TREAT. 94: S-78-S-79.
Web of Science

 

** Hofmann, G; Langsenlehner, U; Renner, W; Greimel, A; Samonigg, H; Krippl, P A single nucleotide polymorphism in the CCND1 gene is associated with decreased risk of developing metastases in female breast cancer patients
EJC SUPPL. 2005; 3(2): 46-47.
Web of Science

 

** Obermayer-Pietsch, BM; Gugatschka, M; Strele, A; Fahrleitner-Pammer, A; Dobnig, H; Kudlacek, S; Pietschmann, P; Renner, W Osteoporosis and genetic disposition for primary adult lactose intolerance in men
BONE. 36: S252-S252.-2nd Joint Meeting of the European-Calcified-Tissue-Society/International-Bone-and-Mineral-Society; JUN 25-29, 2005; Geneva, SWITZERLAND.
Web of Science

 

** Obermayer-Pietsch, BM; Gugatschka, M; Strele, A; Reitter, S; Plank, W; Fahrleitner-Pammer, A; Dobnig, H; Goessler, W; Renner, W Lactose intolerance and skeletal calcium balance - Decreased calcium intake or impaired calcium resorption?
J BONE MINER RES. 20: S391-S391.-27th Annual Meeting of the American-Society-for-Bone-and-Mineral-Research; SEP 23-27, 2005; Nashville, TN.
Web of Science

 

** Renner, W; Nauck, M; Winkelmann, BR; Hoffmann, MH; Scharnagl, H; Mayer, V; Boehm, BO; Marz, W Angiotensinogen haplotypes and angiotensinogen levels
ATHEROSCLER SUPPL 2005 6: 59-59. [Poster]
Web of Science

 

2004

Full papers/articles (Journal)

** Köppel, H; Renner, W; Gugl, A; Cichocki, L; Gasser, R; Wascher, TC; Pilger, E The angiotensin-converting-enzyme insertion/deletion polymorphism is not related to venous thrombosis.
Thromb Haemost. 2004; 91(1):76-79
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** Köppel, H; Renner, W; Krippl, P; Wascher, TC; Pilger, E Diminished response to activated protein C is not correlated with severity of peripheral arterial occlusive disease.
Clin Lab. 2004; 50(11-12): 689-693.
PubMed Google Scholar

 

** Krippl, P; Langsenlehner, U; Renner, W; Yazdani-Biuki, B; Köppel, H; Leithner, A; Wascher, TC; Paulweber, B; Samonigg, H The 5A/6A polymorphism of the matrix metalloproteinase 3 gene promoter and breast cancer.
Clin Cancer Res. 2004; 10(10):3518-3520 [OPEN ACCESS]
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** Krippl, P; Langsenlehner, U; Renner, W; Yazdani-Biuki, B; Wolf, G; Wascher, TC; Paulweber, B; Samonigg, H The 825C>T polymorphism of the G-protein beta-3 subunit gene (GNB3) and breast cancer.
CANCER LETT. 2004; 206(1): 59-62.
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** Langsenlehner, U; Krippl, P; Renner, W; Yazdani-Biuki, B; Eder, T; Wolf, G; Wascher, TC; Paulweber, B; Weitzer, W; Samonigg, H Genetic variants of the sulfotransferase 1A1 and breast cancer risk.
Breast Cancer Res Treat. 2004; 87(1):19-22
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** Obermayer-Pietsch, BM; Bonelli, CM; Walter, DE; Kuhn, RJ; Fahrleitner-Pammer, A; Berghold, A; Goessler, W; Stepan, V; Dobnig, H; Leb, G; Renner, W Genetic predisposition for adult lactose intolerance and relation to diet, bone density, and bone fractures.
J BONE MINER RES. 2004; 19(1): 42-47. [OPEN ACCESS]
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** Wolf, G; Aigner, RM; Schaffler, G; Langsenlehner, U; Renner, W; Samonigg, H; Yazdani-Biuki, B; Krippl, P The 936C>T polymorphism of the gene for vascular endothelial growth factor is associated with 18F-fluorodeoxyglucose uptake.
BREAST CANCER RES TREAT. 2004; 88(3): 205-208.
Web of Science PubMed FullText FullText_MUG

 

Letters

** Köppel, H; Krippl, P; Gasser, R; Wascher, TC; Paulweber, B; Pilger, E; Renner, W Hemochromatosis gene (HFE) polymorphisms are not associated with peripheral arterial disease.
Thromb Haemost. 2004; 91(6):1258-1259
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** Krippl, P; Langsenlehner, U; Renner, W; Köppel, H; Samonigg, H Re: Polymorphisms of death pathway genes FAS and FASL in esophageal squamous-cell carcinoma.
J NAT CANCER INST 2004 96: 1478-1479. [OPEN ACCESS]
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** Krippl, P; Langsenlehner, U; Samonigg, H; Renner, W; Köppel, H Vascular endothelial growth factor in predicting outcome in breast cancer.
CLIN CANCER RES 2004 10: 8752-8753. [OPEN ACCESS]
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** Obermayer-Pietsch, BM; Bonelli, CM; Walter, D; Fahrleitner, A; Stepan, V; Dobnig, H; Leb, G; Renner, W Genetic components of lactose intolerance and community frequency
J BONE MINER RES. 2004; 19: 1747-1747.
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** Renner, W; Grammer, T; Hoffmann, MM; Nauck, MS; Winkelmann, BR; Boehm, BO; März, W Association analysis of the polymorphism T1128C in the signal peptide of neuropeptide Y in a Swedish hypertensive population.
J Hypertens. 2004; 22(12):2398-2399
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** Renner, W; Pressl, H; Wascher, TC; Paulweber, B; Malaimare, L; Iglseder, B The role of the A54T polymorphism of the intestinal fatty acid binding protein for lipid levels, insulin sensitivity and carotid atherosclerosis.
Atherosclerosis. 2004; 173(1):137-139
Web of Science PubMed FullText FullText_MUG

 

Reviews

** Mangge, H; Hubmann, H; Pilz, S; Schauenstein, K; Renner, W; März, W Beyond cholesterol--inflammatory cytokines, the key mediators in atherosclerosis.
Clin Chem Lab Med. 2004; 42(5):467-474
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Abstracts (Journal)

** Knez, I; Dacar, D; Trantina-Yates, A; Renner, W; Maier, R; Rehak, P; Rienmuller, R; Rigler, B Prosthesis-patient mismatch in aortic valve surgery: variables influencing postoperative changes of left ventricular myocardial mass
EUR HEART J 2004 25: 656-657.
Web of Science

 

** Marz, W; Hoffmann, M; Renner, W; Boehm, B; Winkelman, B Alanine to serine polymorphism at position 986 of the calcium sensing receptor associated with coronary heart disease and myocardial infarction. (The Ludwigshafen Risk and Cardiovascular Health Atudy)
ATHEROSCLER SUPPL 2004 5: 87-87.
Web of Science

 

** Obermayer-Pietsch, BM; Bonelli, CM; Walter, DE; Kuhn, RJ; Fahrleitner-Pammer, A; Berghold, A; Stepan, V; Dobnig, H; Leb, G; Renner, W GENETIC DISPOSITION FOR ADULT LACTOSE INTOLERANCE AND RELATION TO BONE PROPERTIES AND FRACTURES DURING LIFETIME
CALCIFIED TISSUE INT. 2004; 74: S128-S128.
Web of Science

 

** Renner, W; Hoffmann, M; Winkelmann, B; Scharnagl, H; Bohm, B; Marz, W The P12A polymorphism of the peroxisome proliferator-activated receptor gamma-2 gene associated premature coronary heart disease and myocardial infraction. (The Ludwigshafen Risk and Cardiovascular Health Study)
ATHEROSCLER SUPPL 2004 5: 89-89.
Web of Science

 

2003

Full papers/articles (Journal)

** Gugl, A; Renner, W; Seinost, G; Brodmann, M; Pabst, E; Wascher, TC; Paulweber, B; Iglseder, B; Pilger, E Two polymorphisms in the fracalkine receptor CX3CR1 are not associated with peripheral arterial disease.
Atherosclerosis. 2003; 166(2):339-343
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** Knez, I; Renner, W; Maier, R; Rehak, P; Rienmüller, R; Pilsl, M; Stanger, O; Mircic, A; Dacar, D; Szalay, Z; Martinovic, I; Vogt, PR; Rigler, B Angiotensin-converting enzyme polymorphisms and their potential impact on left ventricular myocardial geometry after aortic valve surgery.
J Heart Valve Dis. 2003; 12(6):687-695
Web of Science PubMed

 

** Krippl, P; Langsenlehner, U; Renner, W; Yazdani-Biuki, B; Wolf, G; Wascher, TC; Paulweber, B; Bahadori, B; Samonigg, H The L10P polymorphism of the transforming growth factor-beta 1 gene is not associated with breast cancer risk.
Cancer Lett. 2003; 201(2):181-184
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** Krippl, P; Langsenlehner, U; Renner, W; Yazdani-Biuki, B; Wolf, G; Wascher, TC; Paulweber, B; Haas, J; Samonigg, H A common 936 C/T gene polymorphism of vascular endothelial growth factor is associated with decreased breast cancer risk.
Int J Cancer. 2003; 106(4):468-471
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** Krippl, P; Langsenlehner, U; Renner, W; Yazdani-Biuki, B; Wolf, G; Wascher, TC; Paulweber, B; Weitzer, W; Leithner, A; Samonigg, H The 870G>A polymorphism of the cyclin D1 gene is not associated with breast cancer.
Breast Cancer Res Treat. 2003; 82(3):165-168
Web of Science PubMed FullText FullText_MUG

 

** Langsenlehner, U; Krippl, P; Renner, W; Yazdani-Biuki, B; Wolf, G; Wascher, TC; Paulweber, B; Weitzer, W; Samonigg, H The common 677C>T gene polymorphism of methylenetetrahydrofolate reductase gene is not associated with breast cancer risk.
Breast Cancer Res Treat. 2003; 81(2):169-172
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** Schmoelzer, I; Renner, W; Paulweber, B; Malaimare, L; Iglseder, B; Schmid, P; Schallmoser, K; Wascher, TC Lack of association of the Glu298Asp polymorphism of endothelial nitric oxide synthase with manifest coronary artery disease, carotid atherosclerosis and forearm vascular reactivity in two Austrian populations.
EUR J CLIN INVEST 2003 33: 191-198.
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** Wascher, TC; Paulweber, B; Malaimare, L; Stadlmayr, A; Iglseder, B; Schmoelzer, I; Renner, W Associations of a human G protein beta3 subunit dimorphism with insulin resistance and carotid atherosclerosis.
Stroke. 2003; 34(3):605-609 [OPEN ACCESS]
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** Weger, M; Renner, W; Pinter, O; Stanger, O; Temmel, W; Fellner, P; Schmut, O; Haas, A Role of factor V Leiden and prothrombin 20210A in patients with retinal artery occlusion.
Eye. 2003; 17(6):731-734
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Letters

** Weger, M; Stanger, O; Renner, W; Schmut, O; Haas, A Hyperhomocysteinemia and BRVO - Author reply
OPHTHALMOLOGY. 2003; 110(10): 2069-2069.
Web of Science

 

Abstracts (Journal)

** Hoegenauer, C; Hammer, HF; Mellitzer, K; Renner, W; Toplak, H Evaluation of a new genetic test compared to lactose hydrogen breath test for the diagnosis of acquired primary lactase deficiency
GASTROENTEROLOGY. 2003; 124(4): A64-A64.
Web of Science

 

** Krippl, P; Langsenlehner, U; Renner, W; Samonigg, H A common 936 C/T gene polymorphism of vascular endothelial growth factor is associated with decreased breast cancer risk.
BREAST CANCER RES TREAT 2003 82: S140-S140.
Web of Science

 

** Obermayer-Pietsch, BM; Bonelli, CM; Walter, DE; Kuhn, RJ; Fahrleitner-Pammer, A; Berghold, A; Goessler, W; Stepan, V; Dobnig, H; Renner, W; Leb, G Genetic disposition for adult lactose intolerance, calcium metabolism, bone density, and bone fractures
BONE 2003 33: S12-S12.
Web of Science

 

** Renner, W; Schmolzer, I; Pressl, H; Paulweber, B; Wascher, TC The human G-protein beta-3 subunit gene 825 C/T dimorphism is associated with Type 2 diabetes.
DIABETOLOGIA 2003 46: 365-365.
Web of Science

 

2002

Full papers/articles (Journal)

** Brodmann, M; Renner, W; Seinost, G; Pabst, E; Stark, G; Pilger, E Genetic evaluation of the common variant of the endothelial nitric oxide synthase (Glu(298)->
INT ANGIOL 2002 21: 169-172.
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** Renner, W; Brodmann, M; Pabst, E; Stanger, O; Wascher, TC; Pilger, E The V34L polymorphism of factor XIII and peripheral arterial disease.
Int Angiol. 2002; 21(1):53-57
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** Renner, W; Cichocki, L; Forjanics, A; Köppel, H; Gasser, R; Pilger, E G-455A polymorphism of the fibrinogen beta gene and deep vein thrombosis.
Eur J Clin Invest. 2002; 32(10):755-758
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** Renner, W; Pabst, E; Paulweber, B; Malaimare, L; Iglseder, B; Wascher, TC; Pilger, E The angiotensin-converting-enzyme insertion/deletion polymorphism is not a risk factor for peripheral arterial disease.
Atherosclerosis. 2002; 165(1):175-178
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** Weger, M; Stanger, O; Deutschmann, H; Leitner, FJ; Renner, W; Schmut, O; Semmelrock, J; Haas, A The role of hyperhomocysteinemia and methylenetetrahydrofolate reductase (MTHFR) C677T mutation in patients with retinal artery occlusion.
Am J Ophthalmol. 2002; 134(1):57-61
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** Weger, M; Stanger, O; Deutschmann, H; Temmel, W; Renner, W; Schmut, O; Quehenberger, F; Semmelrock, J; Haas, A Hyperhomocyst(e)inemia, but not methylenetetrahydrofolate reductase C677T mutation, as a risk factor in branch retinal vein occlusion.
Ophthalmology. 2002; 109(6):1105-1109
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** Weger, M; Stanger, O; Deutschmann, H; Temmel, W; Renner, W; Schmut, O; Semmelrock, J; Haas, A Hyperhomocyst(e)inemia and MTHFR C677T genotypes in patients with central retinal vein occlusion.
Graefes Arch Clin Exp Ophthalmol. 2002; 240(4):286-290
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Letters

** Brodmann, M; Renner, W; Stark, G; Seinost, G; Pilger, E C 677T methylentetrahydrofolate reductase (MTHFR) polymorphism and thrombangiitis obliterans.
Int J Cardiol. 2002; 83(3):275-276
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Abstracts (Journal)

** Schmoelzer, I; Renner, W; Paulweber, B; Iglseder, B; Wascher, TC Different contribution of the C825T-polymorphism of GNB3 to the risk for advanced carotid atherosclerosis in individuals with and without metabolic syndrome.
DIABETOLOGIA 2002 45: 1175-1175.
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** Weger, M; Renner, W; Fellner, P; Stanger, O; Schmut, O; Haas, A The role of factor V Leiden and prothrombin 20210A in retinal artery occlusion
INVEST OPHTHALMOL VISUAL SCI 2002 43: 494-494.
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2001

Full papers/articles (Journal)

** Brodmann, M; Renner, W; Stark, G; Seinost, G; Pilger, E Vascular endothelial growth factor expression in patients suffering from thrombangitis obliterans.
Int J Cardiol. 2001; 80(2-3):185-186
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** Renner, W; Kotschan, S; Hoffmann, C; Obermayer-Pietsch, B; Pilger, E A common 936 C/T mutation in the gene for vascular endothelial growth factor is associated with vascular endothelial growth factor plasma levels.
J VASC RES. 2001; 37(6): 443-448.
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** Renner, W; Winkler, M; Hoffmann, C; Köppel, H; Seinost, G; Brodmann, M; Pilger, E The PlA1/A2 polymorphism of platelet glycoprotein IIIa is not associated with deep venous thrombosis.
Int Angiol. 2001; 20(2):148-151
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** Stanger, O; Renner, W; Khoschsorur, G; Rigler, B; Wascher, TC NADH/NADPH oxidase p22 phox C242T polymorphism and lipid peroxidation in coronary artery disease.
Clin Physiol. 2001; 21(6):718-722
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** Stanger, O; Weger, M; Renner, W; Konetschny, R Vascular dysfunction in hyperhomocyst(e)inemia. Implications for atherothrombotic disease.
Clin Chem Lab Med. 2001; 39(8):725-733
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** Weger, M; Renner, W; Stanger, O; Schmut, O; Deutschmann, H; Wascher, TC; Haas, A Role of factor XIII Val34Leu polymorphism in retinal artery occlusion.
Stroke. 2001; 32(12):2759-2761 [OPEN ACCESS]
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** Weger, M; Stanger, O; Deutschmann, H; Simon, M; Renner, W; Schmut, O; Semmelrock, J; Haas, A Hyperhomocyst(e)inaemia, but not MTHFR C677T mutation, as a risk factor for non-arteritic ischaemic optic neuropathy.
Br J Ophthalmol. 2001; 85(7):803-806 [OPEN ACCESS]
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Letters

** Brodmann, M; Renner, W; Stark, G; Ramschak, H; Seinost, G; Pilger, E Coinheritance of factor V Leiden (F5 1691A) and prothrombin 20210 A (F2 20210A) in an Austrian family as cause for early onset of venous thromboembolism.
Thromb Res. 2001; 101(5):421-422 (- Case Report)
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** Köppel, H; Renner, W; Seinost, G; Pilger, E Idiopathic deep vein thrombosis in siblings with homozygous factor V Leiden mutation.
Thromb Haemost. 2001; 85(3):562-563 (- Case Report)
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** Renner, W; Brodmann, M; Winkler, M; Washer, TC; Pilger, E The PLA1/A2 polymorphism of platelet glycoprotein IIIa is not associated with peripheral arterial disease.
Thromb Haemost. 2001; 85(4):745-746
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** Roller, RE; Renner, W; Dorr, A; Pilger, E; Schnedl, WJ Oxidative stress and increase of vascular endothelial growth factor in plasma of patients with peripheral arterial occlusive disease.
Thromb Haemost. 2001; 85(2):368-368
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** Roller, RE; Renner, W; Tischler, R; Pilger, E; Schnedl, WJ Vascular endothelial growth factor in plasma of patients undergoing peripheral angioplasty.
Thromb Haemost. 2001; 85(6):1119-1120 [Poster]
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Abstracts (Journal)

** Schmoelzer, I; Wascher, TC; Francesconi, M; Francesconi, C; Schmid, P; Schallmoser, K; Renner, W Association of the Glu298Asp polymorphism of endothelial nitric oxide synthase with cardiovascular risk in type-II diabetes.
DIABETOLOGIA 2001 44: 1199-1199.
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** Wascher, TC; Schmoelzer, I; Paulweber, B; Malaimare, L; Stadlmayr, A; Iglseder, B; Renner, W Association of a human G-protein beta 3 subunit polymorphism with reduced insulin sensitivity.
DIABETOLOGIA 2001 44: 364-364.
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2000

Full papers/articles (Journal)

** Brodmann, M; Renner, W; Stark, G; Winkler, M; Pabst, E; Hofmann, C; Pilger, E Prothrombotic risk factors in patients with thrombangitis obliterans.
Thromb Res. 2000; 99(5):483-486
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** Obermayer-Pietsch, BM; Frühauf, GE; Chararas, K; Mikhail-Reinisch, S; Renner, W; Berghold, A; Kenner, L; Lackner, C Association of the vitamin D receptor genotype BB with low bone density in hyperthyroidism.
J Bone Miner Res. 2000; 15(10):1950-1955 [OPEN ACCESS]
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** Renner, W; Köppel, H; Brodmann, M; Pabst, E; Schallmoser, K; Toplak, H; Wascher, TC; Pilger, E Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease.
THROMB HAEMOST 2000 83: 20-22.
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** Renner, W; Köppel, H; Hoffmann, C; Schallmoser, K; Stanger, O; Toplak, H; Wascher, TC; Pilger, E Prothrombin G20210A, factor V Leiden, and factor XIII Val34Leu: common mutations of blood coagulation factors and deep vein thrombosis in Austria.
THROMB RES 2000 99: 35-39.
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** Renner, W; Schallmoser, K; Gallippi, P; Krauss, C; Toplak, H; Wascher, TC; Pilger, E C242T polymorphism of the p22 phox gene is not associated with peripheral arterial occlusive disease.
ATHEROSCLEROSIS. 2000; 152: 175-179.
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** Seinost, G; Renner, W; Brodmann, M; Winkler, M; Köppel, H; Pilger, E C677T mutation in the methylene tetrahydrofolate reductase gene as a risk factor for venous thrombotic disease in Austrian patients.
Thromb Res. 2000; 100(5):405-407
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Abstracts (Journal)

** Stanger, O; Renner, W; Khoschsorur, GA; Pilger, E; Rigler, B p22 phox C242T polymorphism and lipid peroxidation in coronary artery disease
EUR HEART J 2000 21: 276-276.
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1999

Full papers/articles (Journal)

** Renner, W; Pilger, E Simultaneous in vivo quantitation of vascular endothelial growth factor mRNA splice variants.
J Vasc Res. 1999; 36(2):133-138
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1997

Full papers/articles (Journal)

** Pölzleitner, E; Zechner, EL; Renner, W; Fratte, R; Jauk, B; Högenauer, G; Koraimann, G TraM of plasmid R1 controls transfer gene expression as an integrated control element in a complex regulatory network.
Mol Microbiol. 1997; 25(3): 495-507. [OPEN ACCESS]
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1995

Full papers/articles (Journal)

** Strohmaier, H; Remler, P; Renner, W; Högenauer, G Expression of genes kdsA and kdsB involved in 3-deoxy-D-manno-octulosonic acid metabolism and biosynthesis of enterobacterial lipopolysaccharide is growth phase regulated primarily at the transcriptional level in Escherichia coli K-12.
J Bacteriol. 1995; 177(15):4488-4500 [OPEN ACCESS]
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