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Search Items: SINGLE NUCLEOTIDE POLYMORPHISMS, . hits: 51

2019

Aspelund, T; Grübler, MR; Smith, AV; Gudmundsson, EF; Keppel, M; Cotch, MF; Harris, TB; Jorde, R; Grimnes, G; Joakimsen, R; Schirmer, H; Wilsgaard, T; Mathiesen, EB; Njølstad, I; Løchen, ML; März, W; Kleber, ME; Tomaschitz, A; Grove-Laugesen, D; Rejnmark, L; Swart, KMA; Brouwer, IA; Lips, P; van Schoor, NM; Sempos, CT; Durazo-Arvizu, RA; Škrabáková, Z; Dowling, KG; Cashman, KD; Kiely, M; Pilz, S; Gudnason, V; Eiriksdottir, G Effect of Genetically Low 25-Hydroxyvitamin D on Mortality Risk: Mendelian Randomization Analysis in 3 Large European Cohorts.
Nutrients. 2019; 11(1): [OPEN ACCESS]
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2017

Hofer, P; Hagmann, M; Brezina, S; Dolejsi, E; Mach, K; Leeb, G; Baierl, A; Buch, S; Sutterlüty-Fall, H; Karner-Hanusch, J; Bergmann, MM; Bachleitner-Hofmann, T; Stift, A; Gerger, A; Rötzer, K; Karner, J; Stättner, S; Waldenberger, M; Meitinger, T; Strauch, K; Linseisen, J; Gieger, C; Frommlet, F; Gsur, A Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas.
Oncotarget. 2017; 8(58):98623-98634 [OPEN ACCESS]
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Kerbert, AJ; Schaapman, JJ; van der Reijden, JJ; Amorós Navarro, À; McCormick, A; van Hoek, B; Arroyo, V; Ginès, P; Jalan, R; Vargas, V; Stauber, R; Verspaget, HW; Coenraad, MJ; CANONIC Study Investigators of the EASL-CLIF Consortium Short article: Impact of genetic variation in the vasopressin 1a receptor on the development of organ failure in patients admitted for acute decompensation of liver cirrhosis.
Eur J Gastroenterol Hepatol. 2017; 29(5):535-538
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Lienhart, WD; Strandback, E; Gudipati, V; Koch, K; Binter, A; Uhl, MK; Rantasa, DM; Bourgeois, B; Madl, T; Zangger, K; Gruber, K; Macheroux, P Catalytic competence, structure and stability of the cancer-associated R139W variant of the human NAD(P)H:quinone oxidoreductase 1 (NQO1).
FEBS J. 2017; 284(8): 1233-1245. [OPEN ACCESS]
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Phuah, CL; Dave, T; Malik, R; Raffeld, MR; Ayres, AM; Goldstein, JN; Viswanathan, A; Greenberg, SM; Jagiella, JM; Hansen, BM; Norrving, B; Jimenez-Conde, J; Roquer, J; Pichler, A; Enzinger, C; Montaner, J; Fernandez-Cadenas, I; Lindgren, A; Slowik, A; Schmidt, R; Biffi, A; Rost, N; Langefeld, CD; Markus, HS; Mitchell, BD; Worrall, BB; Kittner, SJ; Woo, D; Dichgans, M; Rosand, J; Anderson, CD; METASTROKE; NINDS-SiGN Consortium; International Stroke Genetics Consortium Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke.
Brain. 2017; 140(10):2663-2672 [OPEN ACCESS]
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Robinson-Cohen, C; Lutsey, PL; Kleber, ME; Nielson, CM; Mitchell, BD; Bis, JC; Eny, KM; Portas, L; Eriksson, J; Lorentzon, M; Koller, DL; Milaneschi, Y; Teumer, A; Pilz, S; Nethander, M; Selvin, E; Tang, W; Weng, LC; Wong, HS; Lai, D; Peacock, M; Hannemann, A; Völker, U; Homuth, G; Nauk, M; Murgia, F; Pattee, JW; Orwoll, E; Zmuda, JM; Riancho, JA; Wolf, M; Williams, F; Penninx, B; Econs, MJ; Ryan, KA; Ohlsson, C; Paterson, AD; Psaty, BM; Siscovick, DS; Rotter, JI; Pirastu, M; Streeten, E; März, W; Fox, C; Coresh, J; Wallaschofski, H; Pankow, JS; de Boer, IH; Kestenbaum, B Genetic Variants Associated with Circulating Parathyroid Hormone.
J Am Soc Nephrol. 2017; 28(5):1553-1565 [OPEN ACCESS]
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2016

Hou, L; Heilbronner, U; Degenhardt, F; Adli, M; Akiyama, K; Akula, N; Ardau, R; Arias, B; Backlund, L; Banzato, CE; Benabarre, A; Bengesser, S; Bhattacharjee, AK; Biernacka, JM; Birner, A; Brichant-Petitjean, C; Bui, ET; Cervantes, P; Chen, GB; Chen, HC; Chillotti, C; Cichon, S; Clark, SR; Colom, F; Cousins, DA; Cruceanu, C; Czerski, PM; Dantas, CR; Dayer, A; Étain, B; Falkai, P; Forstner, AJ; Frisén, L; Fullerton, JM; Gard, S; Garnham, JS; Goes, FS; Grof, P; Gruber, O; Hashimoto, R; Hauser, J; Herms, S; Hoffmann, P; Hofmann, A; Jamain, S; Jiménez, E; Kahn, JP; Kassem, L; Kittel-Schneider, S; Kliwicki, S; König, B; Kusumi, I; Lackner, N; Laje, G; Landén, M; Lavebratt, C; Leboyer, M; Leckband, SG; Jaramillo, CA; MacQueen, G; Manchia, M; Martinsson, L; Mattheisen, M; McCarthy, MJ; McElroy, SL; Mitjans, M; Mondimore, FM; Monteleone, P; Nievergelt, CM; Nöthen, MM; Ösby, U; Ozaki, N; Perlis, RH; Pfennig, A; Reich-Erkelenz, D; Rouleau, GA; Schofield, PR; Schubert, KO; Schweizer, BW; Seemüller, F; Severino, G; Shekhtman, T; Shilling, PD; Shimoda, K; Simhandl, C; Slaney, CM; Smoller, JW; Squassina, A; Stamm, T; Stopkova, P; Tighe, SK; Tortorella, A; Turecki, G; Volkert, J; Witt, S; Wright, A; Young, LT; Zandi, PP; Potash, JB; DePaulo, JR; Bauer, M; Reininghaus, EZ; Novák, T; Aubry, JM; Maj, M; Baune, BT; Mitchell, PB; Vieta, E; Frye, MA; Rybakowski, JK; Kuo, PH; Kato, T; Grigoroiu-Serbanescu, M; Reif, A; Del Zompo, M; Bellivier, F; Schalling, M; Wray, NR; Kelsoe, JR; Alda, M; Rietschel, M; McMahon, FJ; Schulze, TG Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study.
Lancet. 2016; 387(10023):1085-1093 [OPEN ACCESS]
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Keenan, T; Zhao, W; Rasheed, A; Ho, WK; Malik, R; Felix, JF; Young, R; Shah, N; Samuel, M; Sheikh, N; Mucksavage, ML; Shah, O; Li, J; Morley, M; Laser, A; Mallick, NH; Zaman, KS; Ishaq, M; Rasheed, SZ; Memon, FU; Ahmed, F; Hanif, B; Lakhani, MS; Fahim, M; Ishaq, M; Shardha, NK; Ahmed, N; Mahmood, K; Iqbal, W; Akhtar, S; Raheel, R; O'Donnell, CJ; Hengstenberg, C; März, W; Kathiresan, S; Samani, N; Goel, A; Hopewell, JC; Chambers, J; Cheng, YC; Sharma, P; Yang, Q; Rosand, J; Boncoraglio, GB; Kazmi, SU; Hakonarson, H; Köttgen, A; Kalogeropoulos, A; Frossard, P; Kamal, A; Dichgans, M; Cappola, T; Reilly, MP; Danesh, J; Rader, DJ; Voight, BF; Saleheen, D Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study.
J AM COLL CARDIOL. 2016; 67(4): 407-416. [OPEN ACCESS]
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NINDS Stroke Genetics Network (SiGN); International Stroke Genetics Consortium (ISGC) Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
Lancet Neurol. 2016; 15(2):174-184 [OPEN ACCESS]
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Paar, C; Hammerl, V; Blessberger, H; Stekel, H; Steinwender, C; Berg, J Conditions of High Resolution Melting Analysis on the Cobas z480 Instrument for the Genotyping of VKORC1 in the Clinical Routine Laboratory.
Clin Lab. 2016; 62(12):2461-2467 [OPEN ACCESS]
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Pirpamer, L; Hofer, E; Gesierich, B; De Guio, F; Freudenberger, P; Seiler, S; Duering, M; Jouvent, E; Duchesnay, E; Dichgans, M; Ropele, S; Schmidt, R Determinants of iron accumulation in the normal aging brain.
Neurobiol Aging. 2016; 43(32):149-155
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Traylor, M; Zhang, CR; Adib-Samii, P; Devan, WJ; Parsons, OE; Lanfranconi, S; Gregory, S; Cloonan, L; Falcone, GJ; Radmanesh, F; Fitzpatrick, K; Kanakis, A; Barrick, TR; Moynihan, B; Lewis, CM; Boncoraglio, GB; Lemmens, R; Thijs, V; Sudlow, C; Wardlaw, J; Rothwell, PM; Meschia, JF; Worrall, BB; Levi, C; Bevan, S; Furie, KL; Dichgans, M; Rosand, J; Markus, HS; Rost, N; International Stroke Genetics Consortium Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.
Neurology. 2016; 86(2):146-153 [OPEN ACCESS]
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Tsang-A-Sjoe, MW; Nagelkerke, SQ; Bultink, IE; Geissler, J; Tanck, MW; Tacke, CE; Ellis, JA; Zenz, W; Bijl, M; Berden, JH; de Leeuw, K; Derksen, RH; Kuijpers, TW; Voskuyl, AE Fc-gamma receptor polymorphisms differentially influence susceptibility to systemic lupus erythematosus and lupus nephritis.
Rheumatology (Oxford). 2016; 55(5): 939-948. [OPEN ACCESS]
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2015

Kleber, ME; Delgado, G; Grammer, TB; Silbernagel, G; Huang, J; Krämer, BK; Ritz, E; März, W Uric Acid and Cardiovascular Events: A Mendelian Randomization Study.
J Am Soc Nephrol. 2015; 26(11):2831-2838 [OPEN ACCESS]
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Rannikmäe, K; Davies, G; Thomson, PA; Bevan, S; Devan, WJ; Falcone, GJ; Traylor, M; Anderson, CD; Battey, TW; Radmanesh, F; Deka, R; Woo, JG; Martin, LJ; Jimenez-Conde, J; Selim, M; Brown, DL; Silliman, SL; Kidwell, CS; Montaner, J; Langefeld, CD; Slowik, A; Hansen, BM; Lindgren, AG; Meschia, JF; Fornage, M; Bis, JC; Debette, S; Ikram, MA; Longstreth, WT; Schmidt, R; Zhang, CR; Yang, Q; Sharma, P; Kittner, SJ; Mitchell, BD; Holliday, EG; Levi, CR; Attia, J; Rothwell, PM; Poole, DL; Boncoraglio, GB; Psaty, BM; Malik, R; Rost, N; Worrall, BB; Dichgans, M; Van Agtmael, T; Woo, D; Markus, HS; Seshadri, S; Rosand, J; Sudlow, CL; METASTROKE Consortium; CHARGE WMH Group; ISGC ICH GWAS Study Collaboration; WMH in Ischemic Stroke GWAS Study Collaboration; International Stroke Genetics Consortium Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease.
Neurology. 2015; 84(9):918-926 [OPEN ACCESS]
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Saternus, R; Pilz, S; Gräber, S; Kleber, M; März, W; Vogt, T; Reichrath, J A closer look at evolution: Variants (SNPs) of genes involved in skin pigmentation, including EXOC2, TYR, TYRP1, and DCT, are associated with 25(OH)D serum concentration.
Endocrinology. 2015; 156(1):39-47 [OPEN ACCESS]
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2014

Holliday, EG; Traylor, M; Malik, R; Bevan, S; Maguire, J; Koblar, SA; Sturm, J; Hankey, GJ; Oldmeadow, C; McEvoy, M; Sudlow, C; Rothwell, PM; Coresh, J; Hamet, P; Tremblay, J; Turner, ST; de Andrade, M; Rao, M; Schmidt, R; Crick, PA; Robino, A; Peralta, CA; Jukema, JW; Mitchell, P; Rosas, SE; Wang, JJ; Scott, RJ; Dichgans, M; Mitchell, BD; Kao, WH; Fox, CS; Levi, C; Attia, J; Markus, HS; CKDGen Consortium and the International Stroke Genetics Consortium Polygenic overlap between kidney function and large artery atherosclerotic stroke.
Stroke. 2014; 45(12):3508-3513 [OPEN ACCESS]
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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
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Moayyeri, A; Hsu, YH; Karasik, D; Estrada, K; Xiao, SM; Nielson, C; Srikanth, P; Giroux, S; Wilson, SG; Zheng, HF; Smith, AV; Pye, SR; Leo, PJ; Teumer, A; Hwang, JY; Ohlsson, C; McGuigan, F; Minster, RL; Hayward, C; Olmos, JM; Lyytikäinen, LP; Lewis, JR; Swart, KM; Masi, L; Oldmeadow, C; Holliday, EG; Cheng, S; van Schoor, NM; Harvey, NC; Kruk, M; del Greco M, F; Igl, W; Trummer, O; Grigoriou, E; Luben, R; Liu, CT; Zhou, Y; Oei, L; Medina-Gomez, C; Zmuda, J; Tranah, G; Brown, SJ; Williams, FM; Soranzo, N; Jakobsdottir, J; Siggeirsdottir, K; Holliday, KL; Hannemann, A; Go, MJ; Garcia, M; Polasek, O; Laaksonen, M; Zhu, K; Enneman, AW; McEvoy, M; Peel, R; Sham, PC; Jaworski, M; Johansson, Å; Hicks, AA; Pludowski, P; Scott, R; Dhonukshe-Rutten, RA; van der Velde, N; Kähönen, M; Viikari, JS; Sievänen, H; Raitakari, OT; González-Macías, J; Hernández, JL; Mellström, D; Ljunggren, O; Cho, YS; Völker, U; Nauck, M; Homuth, G; Völzke, H; Haring, R; Brown, MA; McCloskey, E; Nicholson, GC; Eastell, R; Eisman, JA; Jones, G; Reid, IR; Dennison, EM; Wark, J; Boonen, S; Vanderschueren, D; Wu, FC; Aspelund, T; Richards, JB; Bauer, D; Hofman, A; Khaw, KT; Dedoussis, G; Obermayer-Pietsch, B; Gyllensten, U; Pramstaller, PP; Lorenc, RS; Cooper, C; Kung, AW; Lips, P; Alen, M; Attia, J; Brandi, ML; de Groot, LC; Lehtimäki, T; Riancho, JA; Campbell, H; Liu, Y; Harris, TB; Akesson, K; Karlsson, M; Lee, JY; Wallaschofski, H; Duncan, EL; O'Neill, TW; Gudnason, V; Spector, TD; Rousseau, F; Orwoll, E; Cummings, SR; Wareham, NJ; Rivadeneira, F; Uitterlinden, AG; Prince, RL; Kiel, DP; Reeve, J; Kaptoge, SK Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium.
Hum Mol Genet. 2014; 23(11):3054-3068 [OPEN ACCESS]
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Paar, C; Enko, D; Zahel, B; Mayr, R; Berg, J Reliable analysis of the single nucleotide polymorphism of lactase persistence LPH(-13910) C/T from saliva derived DNA: validation of a standardized saliva collection system.
Clin Lab. 2014; 60(12):1977-1982
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Stättermayer, AF; Strassl, R; Maieron, A; Rutter, K; Stauber, R; Strasser, M; Beinhardt, S; Datz, C; Scherzer, TM; Steindl-Munda, P; Gschwantler, M; Trauner, M; Hofer, H; Ferenci, P Polymorphisms of interferon-λ4 and IL28B - effects on treatment response to interferon/ribavirin in patients with chronic hepatitis C.
Aliment Pharmacol Ther. 2014; 39(1):104-111 [OPEN ACCESS]
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2013

Scherzer, TM; Stättermayer, AF; Stauber, R; Maieron, A; Strasser, M; Laferl, H; Schwarzer, R; Datz, C; Rutter, K; Beinhardt, S; Steindl-Munda, P; Hofer, H; Ferenci, P Effect of gender and ITPA polymorphisms on ribavirin-induced anemia in chronic hepatitis C patients.
J Hepatol. 2013; 59(5):964-971
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Silbernagel, G; Chapman, MJ; Genser, B; Kleber, ME; Fauler, G; Scharnagl, H; Grammer, TB; Boehm, BO; Mäkelä, KM; Kähönen, M; Carmena, R; Rietzschel, ER; Bruckert, E; Deanfield, JE; Miettinen, TA; Raitakari, OT; Lehtimäki, T; März, W High intestinal cholesterol absorption is associated with cardiovascular disease and risk alleles in ABCG8 and ABO: evidence from the LURIC and YFS cohorts and from a meta-analysis.
J Am Coll Cardiol. 2013; 62(4):291-299 [OPEN ACCESS]
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2012

Heitzer, E; Seidl, H; Bambach, I; Schmidbauer, U; Cerroni, L; Wolf, P Infrequent p53 gene mutation but UV gradient-like p53 protein positivity in keloids.
Exp Dermatol. 2012; 21(4):277-280
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Huang, J; Sabater-Lleal, M; Asselbergs, FW; Tregouet, D; Shin, SY; Ding, J; Baumert, J; Oudot-Mellakh, T; Folkersen, L; Johnson, AD; Smith, NL; Williams, SM; Ikram, MA; Kleber, ME; Becker, DM; Truong, V; Mychaleckyj, JC; Tang, W; Yang, Q; Sennblad, B; Moore, JH; Williams, FM; Dehghan, A; Silbernagel, G; Schrijvers, EM; Smith, S; Karakas, M; Tofler, GH; Silveira, A; Navis, GJ; Lohman, K; Chen, MH; Peters, A; Goel, A; Hopewell, JC; Chambers, JC; Saleheen, D; Lundmark, P; Psaty, BM; Strawbridge, RJ; Boehm, BO; Carter, AM; Meisinger, C; Peden, JF; Bis, JC; McKnight, B; Öhrvik, J; Taylor, K; Franzosi, MG; Seedorf, U; Collins, R; Franco-Cereceda, A; Syvänen, AC; Goodall, AH; Yanek, LR; Cushman, M; Müller-Nurasyid, M; Folsom, AR; Basu, S; Matijevic, N; van Gilst, WH; Kooner, JS; Hofman, A; Danesh, J; Clarke, R; Meigs, JB; DIAGRAM Consortium; Kathiresan, S; Reilly, MP; CARDIoGRAM Consortium; Klopp, N; Harris, TB; Winkelmann, BR; Grant, PJ; Hillege, HL; Watkins, H; C4D Consortium; Spector, TD; Becker, LC; Tracy, RP; März, W; Uitterlinden, AG; Eriksson, P; Cambien, F; CARDIOGENICS Consortium; Morange, PE; Koenig, W; Soranzo, N; van der Harst, P; Liu, Y; O'Donnell, CJ; Hamsten, A Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation.
Blood. 2012; 120(24):4873-4881 [OPEN ACCESS]
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2011

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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Pröll, J; Danzer, M; Stabentheiner, S; Niklas, N; Hackl, C; Hofer, K; Atzmüller, S; Hufnagl, P; Gülly, C; Hauser, H; Krieger, O; Gabriel, C Sequence capture and next generation resequencing of the MHC region highlights potential transplantation determinants in HLA identical haematopoietic stem cell transplantation.
DNA Res. 2011; 18(4):201-210 [OPEN ACCESS]
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Schmidt, H; Zeginigg, M; Wiltgen, M; Freudenberger, P; Petrovic, K; Cavalieri, M; Gider, P; Enzinger, C; Fornage, M; Debette, S; Rotter, JI; Ikram, MA; Launer, LJ; Schmidt, R; CHARGE consortium Neurology working group Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease.
Brain. 2011; 134(Pt 11): 3384-3397. [OPEN ACCESS]
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2010

Debette, S; Bis, JC; Fornage, M; Schmidt, H; Ikram, MA; Sigurdsson, S; Heiss, G; Struchalin, M; Smith, AV; van der Lugt, A; Decarli, C; Lumley, T; Knopman, DS; Enzinger, C; Eiriksdottir, G; Koudstaal, PJ; Destefano, AL; Psaty, BM; Dufouil, C; Catellier, DJ; Fazekas, F; Aspelund, T; Aulchenko, YS; Beiser, A; Rotter, JI; Tzourio, C; Shibata, DK; Tscherner, M; Harris, TB; Rivadeneira, F; Atwood, LD; Rice, K; Gottesman, RF; van Buchem, MA; Uitterlinden, AG; Kelly-Hayes, M; Cushman, M; Zhu, Y; Boerwinkle, E; Gudnason, V; Hofman, A; Romero, JR; Lopez, O; van Duijn, CM; Au, R; Heckbert, SR; Wolf, PA; Mosley, TH; Seshadri, S; Breteler, MM; Schmidt, R; Launer, LJ; Longstreth, WT Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium.
Stroke. 2010; 41(2): 210-217. [OPEN ACCESS]
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Guertl, B; Leuschner, I; Guelly, C; Ebner, B; Kronberger, C; Hoefler, G Is Predisposition for Nephroblastoma Linked to Polymorphisms of the WTX Gene?
Pathol Oncol Res. 2010; 16(2):189-191
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Trottier, J; El Husseini, D; Perreault, M; Pâquet, S; Caron, P; Bourassa, S; Verreault, M; Inaba, TT; Poirier, GG; Bélanger, A; Guillemette, C; Trauner, M; Barbier, O The human UGT1A3 enzyme conjugates norursodeoxycholic acid into a C23-ester glucuronide in the liver.
J Biol Chem. 2010; 285(2):1113-1121 [OPEN ACCESS]
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2009

Biebl, A; Muendlein, A; Kazakbaeva, Z; Heuberger, S; Sonderegger, G; Drexel, H; Lau, S; Nickel, R; Kabesch, M; Simma, B CD14 C-159T and toll-like receptor 4 Asp299Gly polymorphisms in surviving meningococcal disease patients.
PLoS One. 2009; 4(10):e7374-e7374 [OPEN ACCESS]
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Müssig, K; Staiger, H; Machicao, F; Kirchhoff, K; Guthoff, M; Schäfer, SA; Kantartzis, K; Silbernagel, G; Stefan, N; Holst, JJ; Gallwitz, B; Häring, HU; Fritsche, A Association of type 2 diabetes candidate polymorphisms in KCNQ1 with incretin and insulin secretion.
Diabetes. 2009; 58(7):1715-1720 [OPEN ACCESS]
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2008

Hildebrandt, GC; Granell, M; Urbano-Ispizua, A; Wolff, D; Hertenstein, B; Greinix, HT; Brenmoehl, J; Schulz, C; Dickinson, AM; Hahn, J; Rogler, G; Andreesen, R; Holler, E Recipient NOD2/CARD15 variants: a novel independent risk factor for the development of bronchiolitis obliterans after allogeneic stem cell transplantation.
Biol Blood Marrow Transplant. 2008; 14(1): 67-74.
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Keck, ME; Kern, N; Erhardt, A; Unschuld, PG; Ising, M; Salyakina, D; Müller, MB; Knorr, CC; Lieb, R; Hohoff, C; Krakowitzky, P; Maier, W; Bandelow, B; Fritze, J; Deckert, J; Holsboer, F; Müller-Myhsok, B; Binder, EB Combined effects of exonic polymorphisms in CRHR1 and AVPR1B genes in a case/control study for panic disorder.
Am J Med Genet B Neuropsychiatr Genet. 2008; 147B(7): 1196-1204.
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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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Mezger, M; Steffens, M; Beyer, M; Manger, C; Eberle, J; Toliat, MR; Wienker, TF; Ljungman, P; Hebart, H; Dornbusch, HJ; Einsele, H; Loeffler, J Polymorphisms in the chemokine (C-X-C motif) ligand 10 are associated with invasive aspergillosis after allogeneic stem-cell transplantation and influence CXCL10 expression in monocyte-derived dendritic cells.
Blood. 2008; 111(2):534-536 [OPEN ACCESS]
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Staiger, H; Machicao, F; Kantartzis, K; Schäfer, SA; Kirchhoff, K; Guthoff, M; Silbernagel, G; Stefan, N; Fritsche, A; Häring, HU Novel meta-analysis-derived type 2 diabetes risk loci do not determine prediabetic phenotypes.
PLoS One. 2008; 3(8):e3019-e3019 [OPEN ACCESS]
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Staiger, H; Machicao, F; Schäfer, SA; Kirchhoff, K; Kantartzis, K; Guthoff, M; Silbernagel, G; Stefan, N; Häring, HU; Fritsche, A Polymorphisms within the novel type 2 diabetes risk locus MTNR1B determine beta-cell function.
PLoS One. 2008; 3(12): e3962-e3962. [OPEN ACCESS]
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2007

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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Kerber, M; Oberkanins, C; Kriegshäuser, G; Kollerits, B; Dossenbach-Glaninger, A; Fuchs, D; Ledochowski, M Hydrogen breath testing versus LCT genotyping for the diagnosis of lactose intolerance: a matter of age?
Clin Chim Acta. 2007; 383(1-2): 91-96.
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2006

Gourraud, PA; Feolo, M; Hoffman, D; Helmberg, W; Cambon-Thomsen, A The dbMHC microsatellite portal: a public resource for the storage and display of MHC microsatellite information.
TISSUE ANTIGEN 2006 67: 395-401.
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Holler, E; Rogler, G; Brenmoehl, J; Hahn, J; Herfarth, H; Greinix, H; Dickinson, AM; Socié, G; Wolff, D; Fischer, G; Jackson, G; Rocha, V; Steiner, B; Eissner, G; Marienhagen, J; Schoelmerich, J; Andreesen, R Prognostic significance of NOD2/CARD15 variants in HLA-identical sibling hematopoietic stem cell transplantation: effect on long-term outcome is confirmed in 2 independent cohorts and may be modulated by the type of gastrointestinal decontamination.
Blood. 2006; 107(10): 4189-4193.
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Leygraf, A; Hohoff, C; Freitag, C; Willis-Owen, SA; Krakowitzky, P; Fritze, J; Franke, P; Bandelow, B; Fimmers, R; Flint, J; Deckert, J Rgs 2 gene polymorphisms as modulators of anxiety in humans?
J Neural Transm. 2006; 113(12):1921-1925
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2004

Földes-Papp, Z; Costa, JM; Demel, U; Tilz, GP; Kinjo, M; Saito, K; Kii, H; Takagi, T; Tamura, M; Thyberg, P; Birch-Hirschfeld, E Specifically associated PCR products probed by coincident detection of two-color cross-correlated fluorescence intensities in human gene polymorphisms of methylene tetrahydrofolate reductase at site C677T: a novel measurement approach without follow-up mathematical analysis.
Exp Mol Pathol. 2004; 76(3):212-218
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Fröhlich, LF; Gensure, RC; Schipani, E; Jüppner, H; Bastepe, M Haplotype frequencies and linkage disequilibrium analysis of four frequent polymorphisms at the PTH/PTH-related peptide receptor gene locus.
Mol Cell Probes. 2004; 18(5): 353-357.
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Schmidt, H; Aulchenko, YS; Schweighofer, N; Schmidt, R; Frank, S; Kostner, GM; Ott, E; van Duijn, C Angiotensinogen promoter B-haplotype associated with cerebral small vessel disease enhances basal transcriptional activity.
STROKE. 2004; 35: 2592-2597. [OPEN ACCESS]
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2003

Földes-Papp, Z; Kinjo, M; Saito, K; Kii, H; Takagi, T; Tamura, M; Costa, JM; Birch-Hirschfeld, E; Demel, U; Thyberg, P; Tilz, GP C677T single nucleotide polymorphisms of the human methylene tetrahydrofolate reductase and specific identification : a novel strategy using two-color cross-correlation fluorescence spectroscopy.
Mol Diagn. 2003; 7(2): 99-111.
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Posch, PE; Cruz, I; Bradshaw, D; Medhekar, BA Novel polymorphisms and the definition of promoter 'alleles' of the tumor necrosis factor and lymphotoxin alpha loci: inclusion in HLA haplotypes.
Genes Immun. 2003; 4(8):547-558
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