Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Publikationen
Suchbegriffe: MIDDLE AGED - GENETICS , . Treffer: 131
2008
Bink, K; Haralambieva, E; Kremer, M; Ott, G; Beham-Schmid, C; de Leval, L; Peh, SC; Laeng, HR; Jütting, U; Hutzler, P; Quintanilla-Martinez, L; Fend, F
Primary extramedullary plasmacytoma: similarities with and differences from multiple myeloma revealed by interphase cytogenetics.
Haematologica. 2008; 93(4): 623-626.
Doi: 10.3324/haematol.12005
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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
Doi: 10.1007/s10549-007-9808-0
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2007
Briganti, A; Shariat, SF; Chun, FK; Hutterer, GC; Roehrborn, CG; Gallina, A; Rigatti, P; Valiquette, L; Montorsi, F; Karakiewicz, PI
Differences in the rate of lymph node invasion in men with clinically localized prostate cancer might be related to the continent of origin.
BJU Int. 2007; 100(3):528-532
Doi: 10.1111/j.1464-410X.2007.07005.x
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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.
Doi: 10.1016/j.thromres.2007.03.007
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Gugatschka, M; Hoeller, A; Fahrleitner-Pammer, A; Dobnig, H; Pietschmann, P; Kudlacek, S; Obermayer-Pietsch, B
Calcium supply, bone mineral density and genetically defined lactose maldigestion in a cohort of elderly men.
J Endocrinol Invest. 2007; 30(1): 46-51.
Doi: 10.1007/BF03347395
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Heitzer, E; Lassacher, A; Quehenberger, F; Kerl, H; Wolf, P
UV fingerprints predominate in the PTCH mutation spectra of basal cell carcinomas independent of clinical phenotype.
J Invest Dermatol. 2007; 127(12): 2872-2881.
Doi: 10.1038/sj.jid.5700923
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Lackner, A; Raggam, RB; Stammberger, H; Beham, A; Braun, H; Kleinhappl, B; Buzina, W; Kittinger, C; Reinisch, S; Berghold, A; Freudenschuss, K; Barth, S; Marth, E
The role of interleukin-16 in eosinophilic chronic rhinosinusitis.
Eur Arch Otorhinolaryngol. 2007; 264(8): 887-893.
Doi: 10.1007/s00405-007-0300-6
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Miltenberger-Miltenyi, G; Janecke, AR; Wanschitz, JV; Timmerman, V; Windpassinger, C; Auer-Grumbach, M; Löscher, WN
Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL gene.
Arch Neurol. 2007; 64(7):966-970
Doi: 10.1001/archneur.64.7.966
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Nohara, A; Kawashiri, MA; Claudel, T; Mizuno, M; Tsuchida, M; Takata, M; Katsuda, S; Miwa, K; Inazu, A; Kuipers, F; Kobayashi, J; Koizumi, J; Yamagishi, M; Mabuchi, H
High frequency of a retinoid X receptor gamma gene variant in familial combined hyperlipidemia that associates with atherogenic dyslipidemia.
Arterioscler Thromb Vasc Biol. 2007; 27(4): 923-928.
Doi: 10.1161/01.ATV.0000258945.76141.8a
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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
Doi: 10.1016/j.atherosclerosis.2006.07.001
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Uhrig, S; Schlembach, D; Waldispuehl-Geigl, J; Schaffer, W; Geigl, J; Klopocki, E; Mundlos, S; Speicher, MR
Impact of array comparative genomic hybridization-derived information on genetic counseling demonstrated by prenatal diagnosis of the TAR (thrombocytopenia-absent-radius) syndrome-associated microdeletion 1q21.1.
Am J Hum Genet. 2007; 81(4): 866-868.
Doi: 10.1086/521338
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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.
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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.
Doi: 10.1111/j.1600-0625.2007.00620.x
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2006
Beetz, C; Nygren, AO; Schickel, J; Auer-Grumbach, M; Bürk, K; Heide, G; Kassubek, J; Klimpe, S; Klopstock, T; Kreuz, F; Otto, S; Schüle, R; Schöls, L; Sperfeld, AD; Witte, OW; Deufel, T
High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia.
Neurology. 2006; 67(11):1926-1930
Doi: 10.1212/01.wnl.0000244413.49258.f5
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Brücher, BL; Geddert, H; Langner, C; Höfler, H; Fink, U; Siewert, JR; Sarbia, M
Hypermethylation of hMLH1, HPP1, p14(ARF), p16(INK4A) and APC in primary adenocarcinomas of the small bowel.
Int J Cancer. 2006; 119(6): 1298-1302.
Doi: 10.1002/ijc.21990
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Coen, K; Pareyson, D; Auer-Grumbach, M; Buyse, G; Goemans, N; Claeys, KG; Verpoorten, N; Laura, M; Scaioli, V; Salmhofer, W; Pieber, TR; Nelis, E; De Jonghe, P; Timmerman, V
Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II.
NEUROLOGY. 2006; 66(5): 748-751.
Doi: 10.1212/01.wnl.0000201191.57519.47
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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.
Doi: 10.1016/j.ophtha.2006.01.004
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Laimer, M; Klausegger, A; Aberer, W; Oender, K; Steinhuber, M; Lanschuetzer, CM; Wally, V; Hintner, H; Bauer, JW
Haploinsufficiency due to deletion within the 3'-UTR of C1-INH-gene associated with hereditary angioedema.
GENET MED. 2006; 8: 249-254.
Doi: 10.1097/01.gim.0000214302.90076.fa
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Loew, M; Hoffmann, MM; Hahmann, H; Maerz, W; Brenner, H; Rothenbacher, D
Genotype combinations of plasminogen activator inhibitor-1 and angiotensin-converting enzyme genes and risk for early onset of coronary heart disease.
Eur J Cardiovasc Prev Rehabil. 2006; 13(3):449-456
Doi: 10.1097/00149831-200606000-00023
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Schneider, J; Ruschhaupt, M; Buness, A; Asslaber, M; Regitnig, P; Zatloukal, K; Schippinger, W; Ploner, F; Poustka, A; Sültmann, H
Identification and meta-analysis of a small gene expression signature for the diagnosis of estrogen receptor status in invasive ductal breast cancer.
Int J Cancer. 2006; 119(12):2974-2979
Doi: 10.1002/ijc.22234
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Todt, I; Hennies, HC; Küster, W; Smolle, J; Rademacher, G; Mutze, S; Basta, D; Eisenschenk, A; Ernst, A
Neurotological and neuroanatomical changes in the connexin-26-related HID/KID syndrome.
Audiol Neurootol. 2006; 11(4):242-248
Doi: 10.1159/000093110
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Verhoeven, K; Claeys, KG; Züchner, S; Schröder, JM; Weis, J; Ceuterick, C; Jordanova, A; Nelis, E; De Vriendt, E; Van Hul, M; Seeman, P; Mazanec, R; Saifi, GM; Szigeti, K; Mancias, P; Butler, IJ; Kochanski, A; Ryniewicz, B; De Bleecker, J; Van den Bergh, P; Verellen, C; Van Coster, R; Goemans, N; Auer-Grumbach, M; Robberecht, W; Milic Rasic, V; Nevo, Y; Tournev, I; Guergueltcheva, V; Roelens, F; Vieregge, P; Vinci, P; Moreno, MT; Christen, HJ; Shy, ME; Lupski, JR; Vance, JM; De Jonghe, P; Timmerman, V
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2.
Brain. 2006; 129(Pt 8):2093-2102
Doi: 10.1093/brain/awl126
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2005
Auer-Grumbach, M; Schlotter-Weigel, B; Lochmüller, H; Strobl-Wildemann, G; Auer-Grumbach, P; Fischer, R; Offenbacher, H; Zwick, EB; Robl, T; Hartl, G; Hartung, HP; Wagner, K; Windpassinger, C; Austrian Peripheral Neuropathy Study Group
Phenotypes of the N88S Berardinelli-Seip congenital lipodystrophy 2 mutation.
Ann Neurol. 2005; 57(3):415-424
Doi: 10.1002/ana.20410
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Grünig, E; Dehnert, C; Mereles, D; Koehler, R; Olschewski, H; Bärtsch, P; Janssen, B
Enhanced hypoxic pulmonary vasoconstriction in families of adults or children with idiopathic pulmonary arterial hypertension.
Chest. 2005; 128(6 Suppl):630S-6633
Doi: 10.1378/chest.128.6_suppl.630S-a
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Kahraman, G; Krepler, K; Franz, C; Ries, E; Maar, N; Wedrich, A; Rieger, A; Dejaco-Ruhswurm, I
Seven years of HAART impact on ophthalmic management of HIV-infected patients.
OCUL IMMUNOL INFLAMM. 2005; 13: 213-218.
Doi: 10.1080/09273940490912443
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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.
Doi: 10.1158/1055-9965.EPI-05-0204
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Monson, NL; Brezinschek, HP; Brezinschek, RI; Mobley, A; Vaughan, GK; Frohman, EM; Racke, MK; Lipsky, PE
Receptor revision and atypical mutational characteristics in clonally expanded B cells from the cerebrospinal fluid of recently diagnosed multiple sclerosis patients.
J NEUROIMMUNOL. 2005; 158(1-2): 170-181.
Doi: 10.1016/j.jneuroim.2004.04.022
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Quehenberger, F; Vasen, HF; van Houwelingen, HC
Risk of colorectal and endometrial cancer for carriers of mutations of the hMLH1 and hMSH2 gene: correction for ascertainment.
J Med Genet. 2005; 42(6):491-496
Doi: 10.1136/jmg.2004.024299
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Reich, O; Regauer, S
Endometrial stromal sarcoma--observational evidence of a genetic background?
Eur J Gynaecol Oncol. 2005; 26(3):288-290
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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.
Doi: 10.1016/j.ophtha.2005.05.019
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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.
Doi: 10.1161/01.STR.0000151329.84830.37
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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.
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Zotz, RB; Winkelmann, BR; Müller, C; Boehm, BO; März, W; Scharf, RE
Association of polymorphisms of platelet membrane integrins alpha IIb(beta)3 (HPA-1b/Pl) and alpha2(beta)1 (alpha807TT) with premature myocardial infarction.
J THROMB HAEMOST 2005 3: 1522-1529.
Doi: 10.1111/j.1538-7836.2005.01432.x
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2004
Dandachi, N; Dietze, O; Hauser-Kronberger, C
Evaluation of the clinical significance of HER2 amplification by chromogenic in situ hybridisation in patients with primary breast cancer.
ANTICANCER RES. 2004; 24: 2401-2406.
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Ehling, R; Gassner, Ch; Lutterotti, A; Strasser-Fuchs, S; Kollegger, H; Kristoferitsch, W; Reindl, M; Berger, T
Genetic variants in the tumor necrosis factor receptor II gene in patients with multiple sclerosis.
Tissue Antigens. 2004; 63(1):28-33
Doi: 10.1111/j.1399-0039.2004.00166.x
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Hendriks, YM; Wagner, A; Morreau, H; Menko, F; Stormorken, A; Quehenberger, F; Sandkuijl, L; Møller, P; Genuardi, M; Van Houwelingen, H; Tops, C; Van Puijenbroek, M; Verkuijlen, P; Kenter, G; Van Mil, A; Meijers-Heijboer, H; Tan, GB; Breuning, MH; Fodde, R; Wijnen, JT; Bröcker-Vriends, AH; Vasen, H
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance.
Gastroenterology. 2004; 127(1):17-25
Doi: 10.1053/j.gastro.2004.03.068
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Irobi, J; Van den Bergh, P; Merlini, L; Verellen, C; Van Maldergem, L; Dierick, I; Verpoorten, N; Jordanova, A; Windpassinger, C; De Vriendt, E; Van Gerwen, V; Auer-Grumbach, M; Wagner, K; Timmerman, V; De Jonghe, P
The phenotype of motor neuropathies associated with BSCL2 mutations is broader than Silver syndrome and distal HMN type V.
BRAIN. 2004; 127(Pt 9): 2124-2130.
Doi: 10.1093/brain/awh232
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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.
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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
Doi: 10.1158/1078-0432.CCR-04-0010
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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.
Doi: 10.1016/j.canlet.2003.11.030
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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.
Doi: 10.1158/1078-0432.CCR-04-1211
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Leinweber, B; Colli, C; Chott, A; Kerl, H; Cerroni, L
Differential diagnosis of cutaneous infiltrates of B lymphocytes with follicular growth pattern.
AMER J DERMATOPATHOL. 2004; 26(1): 4-13.
Doi: 10.1097%2F00000372-200402000-00002
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März, W; Boehm, BO; Winkelmann, BR; Hoffmann, MM; Ludwigshafen Risk and Cardiovascular Health study
The PlA1/A2 polymorphism of platelet glycoprotein IIIa is not associated with the risk of type 2 diabetes. The Ludwigshafen Risk and Cardiovascular Health study.
Diabetologia. 2004; 47(11):1969-1973
Doi: 10.1007/s00125-004-1557-6
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März, W; Nauck, M; Hoffmann, MM; Nagel, D; Boehm, BO; Koenig, W; Rothenbacher, D; Winkelmann, BR
G(-30)A polymorphism in the pancreatic promoter of the glucokinase gene associated with angiographic coronary artery disease and type 2 diabetes mellitus.
Circulation. 2004; 109(23):2844-2849
Doi: 10.1161/01.CIR.0000129306.44085.C4
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März, W; Scharnagl, H; Hoffmann, MM; Boehm, BO; Winkelmann, BR
The apolipoprotein E polymorphism is associated with circulating C-reactive protein (the Ludwigshafen risk and cardiovascular health study).
Eur Heart J. 2004; 25(23):2109-2119
Doi: 10.1016/j.ehj.2004.08.024
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Oberkofler, H; Schraml, E; Krempler, F; Patsch, W
Restoration of sterol-regulatory-element-binding protein-1c gene expression in HepG2 cells by peroxisome-proliferator-activated receptor-gamma co-activator-1alpha.
Biochem J. 2004; 381(Pt 2): 357-363.
Doi: 10.1042/BJ20040173
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Peris, K; Fargnoli, MC; Pacifico, A; Surrenti, T; Stolz, W; Wolf, P; Soyer, HP; Chimenti, S
CDKN2A and MC1R mutations in patients with sporadic multiple primary melanoma.
J INVEST DERMATOL. 2004; 122: 1327-1330.
Doi: 10.1111/j.0022-202X.2004.22532.x
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Petzmann, S; Ullmann, R; Halbwedl, I; Popper, HH
Analysis of chromosome-11 aberrations in pulmonary and gastrointestinal carcinoids: an array comparative genomic hybridization-based study.
VIRCHOWS ARCHIV. 2004; 445(2): 151-159.
Doi: 10.1007/s00428-004-1052-y
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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
Doi: 10.1016/j.atherosclerosis.2003.11.018
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Rost, I; Fiegler, H; Fauth, C; Carr, P; Bettecken, T; Kraus, J; Meyer, C; Enders, A; Wirtz, A; Meitinger, T; Carter, NP; Speicher, MR
Tetrasomy 21pter-->q21.2 in a male infant without typical Down's syndrome dysmorphic features but moderate mental retardation.
J Med Genet. 2004; 41(3):e26-e26
Doi: 10.1136/jmg.2003.011833
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