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Search Items: POLYMORPHISMS, . hits: 226

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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2018

Bis, JC; Jian, X; Kunkle, BW; Chen, Y; Hamilton-Nelson, KL; Bush, WS; Salerno, WJ; Lancour, D; Ma, Y; Renton, AE; Marcora, E; Farrell, JJ; Zhao, Y; Qu, L; Ahmad, S; Amin, N; Amouyel, P; Beecham, GW; Below, JE; Campion, D; Charbonnier, C; Chung, J; Crane, PK; Cruchaga, C; Cupples, LA; Dartigues, JF; Debette, S; Deleuze, JF; Fulton, L; Gabriel, SB; Genin, E; Gibbs, RA; Goate, A; Grenier-Boley, B; Gupta, N; Haines, JL; Havulinna, AS; Helisalmi, S; Hiltunen, M; Howrigan, DP; Ikram, MA; Kaprio, J; Konrad, J; Kuzma, A; Lander, ES; Lathrop, M; Lehtimäki, T; Lin, H; Mattila, K; Mayeux, R; Muzny, DM; Nasser, W; Neale, B; Nho, K; Nicolas, G; Patel, D; Pericak-Vance, MA; Perola, M; Psaty, BM; Quenez, O; Rajabli, F; Redon, R; Reitz, C; Remes, AM; Salomaa, V; Sarnowski, C; Schmidt, H; Schmidt, M; Schmidt, R; Soininen, H; Thornton, TA; Tosto, G; Tzourio, C; van der Lee, SJ; van Duijn, CM; Vardarajan, B; Wang, W; Wijsman, E; Wilson, RK; Witten, D; Worley, KC; Zhang, X; Alzheimer’s Disease Sequencing Project; Bellenguez, C; Lambert, JC; Kurki, MI; Palotie, A; Daly, M; Boerwinkle, E; Lunetta, KL; Destefano, AL; Dupuis, J; Martin, ER; Schellenberg, GD; Seshadri, S; Naj, AC; Fornage, M; Farrer, LA Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.
Mol Psychiatry. 2018; [OPEN ACCESS]
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Madar-Shapiro, L; Karady, I; Trahtenherts, A; Syngelaki, A; Akolekar, R; Poon, L; Cohen, R; Sharabi-Nov, A; Huppertz, B; Sammar, M; Juhasz, K; Than, NG; Papp, Z; Romero, R; Nicolaides, KH; Meiri, H Predicting the Risk to Develop Preeclampsia in the First Trimester Combining Promoter Variant -98A/C of LGALS13 (Placental Protein 13), Black Ethnicity, Previous Preeclampsia, Obesity, and Maternal Age.
Fetal Diagn Ther. 2018; 43(4):250-265 [OPEN ACCESS]
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Malle, EM; Posch-Pertl, L; Renner, W; Pinter-Hausberger, S; Singer, C; Haas, A; Wedrich, A; Weger, M Role of the tissue-type plasminogen activator -7351C > T and plasminogen activator inhibitor 1 4G/5G gene polymorphisms in central serous chorioretinopathy.
Ophthalmic Genet. 2018; 39(6): 714-716.
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Norden, J; Pearce, KF; Irving, JAE; Collin, MP; Wang, XN; Wolff, D; Kolb, HJ; Socie, G; Kuzmina, Z; Greinix, H; Holler, E; Rocha, V; Gluckman, E; Hromadnikova, I; Dickinson, AM The influence of glucocorticoid receptor single nucleotide polymorphisms on outcome after haematopoietic stem cell transplantation
INT J IMMUNOGENET. 2018; 45(5): 247-256.
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2017

Blazevic, S; Horvaticek, M; Kesic, M; Zill, P; Hranilovic, D; Ivanisevic, M; Desoye, G; Stefulj, J Epigenetic adaptation of the placental serotonin transporter gene (SLC6A4) to gestational diabetes mellitus.
PLoS One. 2017; 12(6):e0179934-e0179934 [OPEN ACCESS]
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Herrmann, M; Farrell, CL; Pusceddu, I; Fabregat-Cabello, N; Cavalier, E Assessment of vitamin D status - a changing landscape.
Clin Chem Lab Med. 2017; 55(1): 3-26. [OPEN ACCESS]
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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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Jüngst, C; Stadlbauer, V; Reichert, MC; Zimmer, V; Weber, SN; Ofner-Ziegenfuß, L; Voigtländer, T; Spindelböck, W; Fickert, P; Kirchner, GI; Lammert, F; Lankisch, TO; Krawczyk, M NOD2 gene variants confer risk for secondary sclerosing cholangitis in critically ill patients.
Sci Rep. 2017; 7(1):7026-7026 [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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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
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Zewinger, S; Kleber, ME; Tragante, V; McCubrey, RO; Schmidt, AF; Direk, K; Laufs, U; Werner, C; Koenig, W; Rothenbacher, D; Mons, U; Breitling, LP; Brenner, H; Jennings, RT; Petrakis, I; Triem, S; Klug, M; Filips, A; Blankenberg, S; Waldeyer, C; Sinning, C; Schnabel, RB; Lackner, KJ; Vlachopoulou, E; Nygård, O; Svingen, GFT; Pedersen, ER; Tell, GS; Sinisalo, J; Nieminen, MS; Laaksonen, R; Trompet, S; Smit, RAJ; Sattar, N; Jukema, JW; Groesdonk, HV; Delgado, G; Stojakovic, T; Pilbrow, AP; Cameron, VA; Richards, AM; Doughty, RN; Gong, Y; Cooper-DeHoff, R; Johnson, J; Scholz, M; Beutner, F; Thiery, J; Smith, JG; Vilmundarson, RO; McPherson, R; Stewart, AFR; Cresci, S; Lenzini, PA; Spertus, JA; Olivieri, O; Girelli, D; Martinelli, NI; Leiherer, A; Saely, CH; Drexel, H; Mündlein, A; Braund, PS; Nelson, CP; Samani, NJ; Kofink, D; Hoefer, IE; Pasterkamp, G; Quyyumi, AA; Ko, YA; Hartiala, JA; Allayee, H; Tang, WHW; Hazen, SL; Eriksson, N; Held, C; Hagström, E; Wallentin, L; Åkerblom, A; Siegbahn, A; Karp, I; Labos, C; Pilote, L; Engert, JC; Brophy, JM; Thanassoulis, G; Bogaty, P; Szczeklik, W; Kaczor, M; Sanak, M; Virani, SS; Ballantyne, CM; Lee, VV; Boerwinkle, E; Holmes, MV; Horne, BD; Hingorani, A; Asselbergs, FW; Patel, RS; GENIUS-CHD consortium; Krämer, BK; Scharnagl, H; Fliser, D; März, W; Speer, T Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study.
Lancet Diabetes Endocrinol. 2017; 5(7):534-543 [OPEN ACCESS]
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2016

Bengesser, SA; Fuchs, R; Lackner, N; Birner, A; Reininghaus, B; Meier-Allard, N; Stracke, A; Kapfhammer, HP; Reininghaus, EZ; Wallner-Liebmann, S Endoplasmic Reticulum Stress and Bipolar Disorder - Almost Forgotten Therapeutic Drug Targets in the Unfolded Protein Response Pathway Revisited.
CNS Neurol Disord Drug Targets. 2016; 15(4):403-413
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Brownbill, P; Chernyavsky, I; Bottalico, B; Desoye, G; Hansson, S; Kenna, G; Knudsen, LE; Markert, UR; Powles-Glover, N; Schneider, H; Leach, L An international network (PlaNet) to evaluate a human placental testing platform for chemicals safety testing in pregnancy.
Reprod Toxicol. 2016; 64(5):191-202
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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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Okbay, A; Baselmans, BM; De Neve, JE; Turley, P; Nivard, MG; Fontana, MA; Meddens, SF; Linnér, RK; Rietveld, CA; Derringer, J; Gratten, J; Lee, JJ; Liu, JZ; de Vlaming, R; Ahluwalia, TS; Buchwald, J; Cavadino, A; Frazier-Wood, AC; Furlotte, NA; Garfield, V; Geisel, MH; Gonzalez, JR; Haitjema, S; Karlsson, R; van der Laan, SW; Ladwig, KH; Lahti, J; van der Lee, SJ; Lind, PA; Liu, T; Matteson, L; Mihailov, E; Miller, MB; Minica, CC; Nolte, IM; Mook-Kanamori, D; van der Most, PJ; Oldmeadow, C; Qian, Y; Raitakari, O; Rawal, R; Realo, A; Rueedi, R; Schmidt, B; Smith, AV; Stergiakouli, E; Tanaka, T; Taylor, K; Thorleifsson, G; Wedenoja, J; Wellmann, J; Westra, HJ; Willems, SM; Zhao, W; LifeLines Cohort Study; Amin, N; Bakshi, A; Bergmann, S; Bjornsdottir, G; Boyle, PA; Cherney, S; Cox, SR; Davies, G; Davis, OS; Ding, J; Direk, N; Eibich, P; Emeny, RT; Fatemifar, G; Faul, JD; Ferrucci, L; Forstner, AJ; Gieger, C; Gupta, R; Harris, TB; Harris, JM; Holliday, EG; Hottenga, JJ; De Jager, PL; Kaakinen, MA; Kajantie, E; Karhunen, V; Kolcic, I; Kumari, M; Launer, LJ; Franke, L; Li-Gao, R; Liewald, DC; Koini, M; Loukola, A; Marques-Vidal, P; Montgomery, GW; Mosing, MA; Paternoster, L; Pattie, A; Petrovic, KE; Pulkki-Råback, L; Quaye, L; Räikkönen, K; Rudan, I; Scott, RJ; Smith, JA; Sutin, AR; Trzaskowski, M; Vinkhuyzen, AE; Yu, L; Zabaneh, D; Attia, JR; Bennett, DA; Berger, K; Bertram, L; Boomsma, DI; Snieder, H; Chang, SC; Cucca, F; Deary, IJ; van Duijn, CM; Eriksson, JG; Bültmann, U; de Geus, EJ; Groenen, PJ; Gudnason, V; Hansen, T; Hartman, CA; Haworth, CM; Hayward, C; Heath, AC; Hinds, DA; Hyppönen, E; Iacono, WG; Järvelin, MR; Jöckel, KH; Kaprio, J; Kardia, SL; Keltikangas-Järvinen, L; Kraft, P; Kubzansky, LD; Lehtimäki, T; Magnusson, PK; Martin, NG; McGue, M; Metspalu, A; Mills, M; de Mutsert, R; Oldehinkel, AJ; Pasterkamp, G; Pedersen, NL; Plomin, R; Polasek, O; Power, C; Rich, SS; Rosendaal, FR; den Ruijter, HM; Schlessinger, D; Schmidt, H; Svento, R; Schmidt, R; Alizadeh, BZ; Sørensen, TI; Spector, TD; Starr, JM; Stefansson, K; Steptoe, A; Terracciano, A; Thorsteinsdottir, U; Thurik, AR; Timpson, NJ; Tiemeier, H; Uitterlinden, AG; Vollenweider, P; Wagner, GG; Weir, DR; Yang, J; Conley, DC; Smith, GD; Hofman, A; Johannesson, M; Laibson, DI; Medland, SE; Meyer, MN; Pickrell, JK; Esko, T; Krueger, RF; Beauchamp, JP; Koellinger, PD; Benjamin, DJ; Bartels, M; Cesarini, D Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.
Nat Genet. 2016; 48(6):624-633 [OPEN ACCESS]
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Okbay, A; Beauchamp, JP; Fontana, MA; Lee, JJ; Pers, TH; Rietveld, CA; Turley, P; Chen, GB; Emilsson, V; Meddens, SF; Oskarsson, S; Pickrell, JK; Thom, K; Timshel, P; de Vlaming, R; Abdellaoui, A; Ahluwalia, TS; Bacelis, J; Baumbach, C; Bjornsdottir, G; Brandsma, JH; Pina Concas, M; Derringer, J; Furlotte, NA; Galesloot, TE; Girotto, G; Gupta, R; Hall, LM; Harris, SE; Hofer, E; Horikoshi, M; Huffman, JE; Kaasik, K; Kalafati, IP; Karlsson, R; Kong, A; Lahti, J; van der Lee, SJ; deLeeuw, C; Lind, PA; Lindgren, KO; Liu, T; Mangino, M; Marten, J; Mihailov, E; Miller, MB; van der Most, PJ; Oldmeadow, C; Payton, A; Pervjakova, N; Peyrot, WJ; Qian, Y; Raitakari, O; Rueedi, R; Salvi, E; Schmidt, B; Schraut, KE; Shi, J; Smith, AV; Poot, RA; St Pourcain, B; Teumer, A; Thorleifsson, G; Verweij, N; Vuckovic, D; Wellmann, J; Westra, HJ; Yang, J; Zhao, W; Zhu, Z; Alizadeh, BZ; Amin, N; Bakshi, A; Baumeister, SE; Biino, G; Bønnelykke, K; Boyle, PA; Campbell, H; Cappuccio, FP; Davies, G; De Neve, JE; Deloukas, P; Demuth, I; Ding, J; Eibich, P; Eisele, L; Eklund, N; Evans, DM; Faul, JD; Feitosa, MF; Forstner, AJ; Gandin, I; Gunnarsson, B; Halldórsson, BV; Harris, TB; Heath, AC; Hocking, LJ; Holliday, EG; Homuth, G; Horan, MA; Hottenga, JJ; de Jager, PL; Joshi, PK; Jugessur, A; Kaakinen, MA; Kähönen, M; Kanoni, S; Keltigangas-Järvinen, L; Kiemeney, LA; Kolcic, I; Koskinen, S; Kraja, AT; Kroh, M; Kutalik, Z; Latvala, A; Launer, LJ; Lebreton, MP; Levinson, DF; Lichtenstein, P; Lichtner, P; Liewald, DC; LifeLines Cohort Study; Loukola, A; Madden, PA; Mägi, R; Mäki-Opas, T; Marioni, RE; Marques-Vidal, P; Meddens, GA; McMahon, G; Meisinger, C; Meitinger, T; Milaneschi, Y; Milani, L; Montgomery, GW; Myhre, R; Nelson, CP; Nyholt, DR; Ollier, WE; Palotie, A; Paternoster, L; Pedersen, NL; Petrovic, KE; Porteous, DJ; Räikkönen, K; Ring, SM; Robino, A; Rostapshova, O; Rudan, I; Rustichini, A; Salomaa, V; Sanders, AR; Sarin, AP; Schmidt, H; Scott, RJ; Smith, BH; Smith, JA; Staessen, JA; Steinhagen-Thiessen, E; Strauch, K; Terracciano, A; Tobin, MD; Ulivi, S; Vaccargiu, S; Quaye, L; van Rooij, FJ; Venturini, C; Vinkhuyzen, AA; Völker, U; Völzke, H; Vonk, JM; Vozzi, D; Waage, J; Ware, EB; Willemsen, G; Attia, JR; Bennett, DA; Berger, K; Bertram, L; Bisgaard, H; Boomsma, DI; Borecki, IB; Bültmann, U; Chabris, CF; Cucca, F; Cusi, D; Deary, IJ; Dedoussis, GV; van Duijn, CM; Eriksson, JG; Franke, B; Franke, L; Gasparini, P; Gejman, PV; Gieger, C; Grabe, HJ; Gratten, J; Groenen, PJ; Gudnason, V; van der Harst, P; Hayward, C; Hinds, DA; Hoffmann, W; Hyppönen, E; Iacono, WG; Jacobsson, B; Järvelin, MR; Jöckel, KH; Kaprio, J; Kardia, SL; Lehtimäki, T; Lehrer, SF; Magnusson, PK; Martin, NG; McGue, M; Metspalu, A; Pendleton, N; Penninx, BW; Perola, M; Pirastu, N; Pirastu, M; Polasek, O; Posthuma, D; Power, C; Province, MA; Samani, NJ; Schlessinger, D; Schmidt, R; Sørensen, TI; Spector, TD; Stefansson, K; Thorsteinsdottir, U; Thurik, AR; Timpson, NJ; Tiemeier, H; Tung, JY; Uitterlinden, AG; Vitart, V; Vollenweider, P; Weir, DR; Wilson, JF; Wright, AF; Conley, DC; Krueger, RF; Davey Smith, G; Hofman, A; Laibson, DI; Medland, SE; Meyer, MN; Yang, J; Johannesson, M; Visscher, PM; Esko, T; Koellinger, PD; Cesarini, D; Benjamin, DJ Genome-wide association study identifies 74 loci associated with educational attainment.
Nature. 2016; 533(7604): 539-542. [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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Pearce, KF; Balavarca, Y; Norden, J; Jackson, G; Holler, E; Dressel, R; Greinix, H; Toubert, A; Gluckman, E; Hromadnikova, I; Sedlacek, P; Wolff, D; Holtick, U; Bickeböller, H; Dickinson, AM Impact of genomic risk factors on survival after haematopoietic stem cell transplantation for patients with acute leukaemia.
Int J Immunogenet. 2016; 43(6):404-412
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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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Reichmann, F; Holzer, P Neuropeptide Y: A stressful review.
Neuropeptides. 2016; 55(6):99-109 [OPEN ACCESS]
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Roeseler, E; Julius, U; Heigl, F; Spitthoever, R; Heutling, D; Breitenberger, P; Leebmann, J; Lehmacher, W; Kamstrup, PR; Nordestgaard, BG; Maerz, W; Noureen, A; Schmidt, K; Kronenberg, F; Heibges, A; Klingel, R; Pro(a)LiFe-Study Group Lipoprotein Apheresis for Lipoprotein(a)-Associated Cardiovascular Disease: Prospective 5 Years of Follow-Up and Apolipoprotein(a) Characterization.
Arterioscler Thromb Vasc Biol. 2016; 36(9):2019-2027 [OPEN ACCESS]
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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

Balavarca, Y; Pearce, K; Norden, J; Collin, M; Jackson, G; Holler, E; Dressel, R; Kolb, HJ; Greinix, H; Socie, G; Toubert, A; Rocha, V; Gluckman, E; Hromadnikova, I; Sedlacek, P; Wolff, D; Holtick, U; Dickinson, A; Bickeböller, H Predicting survival using clinical risk scores and non-HLA immunogenetics.
Bone Marrow Transplant. 2015; 50(11):1445-1452 [OPEN ACCESS]
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Benhaim, L; Zhang, W; Wakatsuki, T; Yang, D; Gerger, A; Bohanes, P; Paez, D; Loupakis, F; LaBonte, MJ; Ning, Y; El-Khoueiry, R; Ladner, R; Wilson, P; Zhang, H; Giamas, G; Stebbing, J; Lenz, HJ Genetic variants of kinase suppressors of Ras (KSR1) to predict survival in patients with ERα-positive advanced breast cancer.
Pharmacogenomics J. 2015; 15(3):235-240
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Benke, K; Ágg, B; Mátyás, G; Szokolai, V; Harsányi, G; Szilveszter, B; Odler, B; Pólos, M; Maurovich-Horvat, P; Radovits, T; Merkely, B; Nagy, ZB; Szabolcs, Z Gene polymorphisms as risk factors for predicting the cardiovascular manifestations in Marfan syndrome. Role of folic acid metabolism enzyme gene polymorphisms in Marfan syndrome.
Thromb Haemost. 2015; 114(4):748-756
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Biebl, A; Muendlein, A; Kinz, E; Drexel, H; Kabesch, M; Zenz, W; Elling, R; Müller, C; Keil, T; Lau, S; Simma, B Confirmation of Host Genetic Determinants in the CFH Region and Susceptibility to Meningococcal Disease in a Central European Study Sample.
Pediatr Infect Dis J. 2015; 34(10):1115-1117
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Bohanes, P; Yang, D; Loupakis, F; LaBonte, MJ; Gerger, A; Ning, Y; Lenz, C; Lenz, F; Wakatsuki, T; Zhang, W; Benhaim, L; El-Khoueiry, A; El-Khoueiry, R; Lenz, HJ Integrin genetic variants and stage-specific tumor recurrence in patients with stage II and III colon cancer.
Pharmacogenomics J. 2015; 15(3):226-234
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Ebner, S; Mangge, H; Langhof, H; Halle, M; Siegrist, M; Aigner, E; Paulmichl, K; Paulweber, B; Datz, C; Sperl, W; Kofler, B; Weghuber, D Mitochondrial Haplogroup T Is Associated with Obesity in Austrian Juveniles and Adults.
PLoS One. 2015; 10(8):e0135622-e0135622 [OPEN ACCESS]
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Gaberscek, S; Zaletel, K; Schwetz, V; Pieber, T; Obermayer-Pietsch, B; Lerchbaum, E MECHANISMS IN ENDOCRINOLOGY Thyroid and polycystic ovary syndrome
EUR J ENDOCRINOL. 2015; 172(1): R9-21. [OPEN ACCESS]
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Gorski, M; Tin, A; Garnaas, M; McMahon, GM; Chu, AY; Tayo, BO; Pattaro, C; Teumer, A; Chasman, DI; Chalmers, J; Hamet, P; Tremblay, J; Woodward, M; Aspelund, T; Eiriksdottir, G; Gudnason, V; Harris, TB; Launer, LJ; Smith, AV; Mitchell, BD; O'Connell, JR; Shuldiner, AR; Coresh, J; Li, M; Freudenberger, P; Hofer, E; Schmidt, H; Schmidt, R; Holliday, EG; Mitchell, P; Wang, JJ; de Boer, IH; Li, G; Siscovick, DS; Kutalik, Z; Corre, T; Vollenweider, P; Waeber, G; Gupta, J; Kanetsky, PA; Hwang, SJ; Olden, M; Yang, Q; de Andrade, M; Atkinson, EJ; Kardia, SL; Turner, ST; Stafford, JM; Ding, J; Liu, Y; Barlassina, C; Cusi, D; Salvi, E; Staessen, JA; Ridker, PM; Grallert, H; Meisinger, C; Müller-Nurasyid, M; Krämer, BK; Kramer, H; Rosas, SE; Nolte, IM; Penninx, BW; Snieder, H; Fabiola Del Greco, M; Franke, A; Nöthlings, U; Lieb, W; Bakker, SJ; Gansevoort, RT; van der Harst, P; Dehghan, A; Franco, OH; Hofman, A; Rivadeneira, F; Sedaghat, S; Uitterlinden, AG; Coassin, S; Haun, M; Kollerits, B; Kronenberg, F; Paulweber, B; Aumann, N; Endlich, K; Pietzner, M; Völker, U; Rettig, R; Chouraki, V; Helmer, C; Lambert, JC; Metzger, M; Stengel, B; Lehtimäki, T; Lyytikäinen, LP; Raitakari, O; Johnson, A; Parsa, A; Bochud, M; Heid, IM; Goessling, W; Köttgen, A; Kao, WH; Fox, CS; Böger, CA Genome-wide association study of kidney function decline in individuals of European descent.
Kidney Int. 2015; 87(5):1017-1029 [OPEN ACCESS]
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Hernesniemi, JA; Lyytikäinen, LP; Oksala, N; Seppälä, I; Kleber, ME; Mononen, N; März, W; Mikkelsson, J; Pessi, T; Louhelainen, AM; Martiskainen, M; Nikus, K; Klopp, N; Waldenberger, M; Illig, T; Kähönen, M; Laaksonen, R; Karhunen, PJ; Lehtimäki, T Predicting sudden cardiac death using common genetic risk variants for coronary artery disease.
Eur Heart J. 2015; 36(26):1669-1675 [OPEN ACCESS]
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Hofer, E; Cavalieri, M; Bis, JC; DeCarli, C; Fornage, M; Sigurdsson, S; Srikanth, V; Trompet, S; Verhaaren, BF; Wolf, C; Yang, Q; Adams, HH; Amouyel, P; Beiser, A; Buckley, BM; Callisaya, M; Chauhan, G; de Craen, AJ; Dufouil, C; van Duijn, CM; Ford, I; Freudenberger, P; Gottesman, RF; Gudnason, V; Heiss, G; Hofman, A; Lumley, T; Martinez, O; Mazoyer, B; Moran, C; Niessen, WJ; Phan, T; Psaty, BM; Satizabal, CL; Sattar, N; Schilling, S; Shibata, DK; Slagboom, PE; Smith, A; Stott, DJ; Taylor, KD; Thomson, R; Töglhofer, AM; Tzourio, C; van Buchem, M; Wang, J; Westendorp, RG; Windham, BG; Vernooij, MW; Zijdenbos, A; Beare, R; Debette, S; Ikram, MA; Jukema, JW; Launer, LJ; Longstreth, WT; Mosley, TH; Seshadri, S; Schmidt, H; Schmidt, R; Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium White Matter Lesion Progression: Genome-Wide Search for Genetic Influences.
Stroke. 2015; 46(11):3048-3057 [OPEN ACCESS]
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Kepa, S; Horvath, B; Reitter-Pfoertner, S; Schemper, M; Quehenberger, P; Grundbichler, M; Heistinger, M; Neumeister, P; Mannhalter, C; Pabinger, I Parameters influencing FVIII pharmacokinetics in patients with severe and moderate haemophilia A.
Haemophilia. 2015; 21(3):343-350
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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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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. [OPEN ACCESS]
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Lindner, E; Glatz, W; Schwab, C; El-Shabrawi, Y; Mossböck, G Analysis of functional polymorphisms in apoptosis-related genes in primary open angle glaucoma.
Mol Vis. 2015; 21(412):1340-1344 [OPEN ACCESS]
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Löbel, M; Mooslechner, AA; Bauer, S; Günther, S; Letsch, A; Hanitsch, LG; Grabowski, P; Meisel, C; Volk, HD; Scheibenbogen, C Polymorphism in COMT is associated with IgG3 subclass level and susceptibility to infection in patients with chronic fatigue syndrome.
J Transl Med. 2015; 13(10): 264-264. [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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Sebio, A; Gerger, A; Matsusaka, S; Yang, D; Zhang, W; Stremitzer, S; Stintzing, S; Sunakawa, Y; Yamauchi, S; Ning, Y; Fujimoto, Y; Ueno, M; Lenz, HJ Genetic variants within obesity-related genes are associated with tumor recurrence in patients with stages II/III colon cancer.
Pharmacogenet Genomics. 2015; 25(1):30-37 [OPEN ACCESS]
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Smolle, MA; Pichler, M; Haybaeck, J; Gerger, A Genetic markers of recurrence in colorectal cancer.
Pharmacogenomics. 2015; 16(11):1315-1328
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Verhaaren, BF; Debette, S; Bis, JC; Smith, JA; Ikram, MK; Adams, HH; Beecham, AH; Rajan, KB; Lopez, LM; Barral, S; van Buchem, MA; van der Grond, J; Smith, AV; Hegenscheid, K; Aggarwal, NT; de Andrade, M; Atkinson, EJ; Beekman, M; Beiser, AS; Blanton, SH; Boerwinkle, E; Brickman, AM; Bryan, RN; Chauhan, G; Chen, CP; Chouraki, V; de Craen, AJ; Crivello, F; Deary, IJ; Deelen, J; De Jager, PL; Dufouil, C; Elkind, MS; Evans, DA; Freudenberger, P; Gottesman, RF; Guðnason, V; Habes, M; Heckbert, SR; Heiss, G; Hilal, S; Hofer, E; Hofman, A; Ibrahim-Verbaas, CA; Knopman, DS; Lewis, CE; Liao, J; Liewald, DC; Luciano, M; van der Lugt, A; Martinez, OO; Mayeux, R; Mazoyer, B; Nalls, M; Nauck, M; Niessen, WJ; Oostra, BA; Psaty, BM; Rice, KM; Rotter, JI; von Sarnowski, B; Schmidt, H; Schreiner, PJ; Schuur, M; Sidney, SS; Sigurdsson, S; Slagboom, PE; Stott, DJ; van Swieten, JC; Teumer, A; Töglhofer, AM; Traylor, M; Trompet, S; Turner, ST; Tzourio, C; Uh, HW; Uitterlinden, AG; Vernooij, MW; Wang, JJ; Wong, TY; Wardlaw, JM; Windham, BG; Wittfeld, K; Wolf, C; Wright, CB; Yang, Q; Zhao, W; Zijdenbos, A; Jukema, JW; Sacco, RL; Kardia, SL; Amouyel, P; Mosley, TH; Longstreth, WT; DeCarli, CC; van Duijn, CM; Schmidt, R; Launer, LJ; Grabe, HJ; Seshadri, SS; Ikram, MA; Fornage, M Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI.
Circ Cardiovasc Genet. 2015; 8(2):398-409 [OPEN ACCESS]
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Wagner, B; Melzer, H; Freymüller, G; Stumvoll, S; Rendi-Wagner, P; Paulke-Korinek, M; Repa, A; Mooi, FR; Kollaritsch, H; Mittermayer, H; Kessler, HH; Stanek, G; Steinborn, R; Duchêne, M; Wiedermann, U Genetic Variation of Bordetella pertussis in Austria.
PLoS One. 2015; 10(7):e0132623-e0132623 [OPEN ACCESS]
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