Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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Publikationen

Suchbegriffe: POLYMORPHISMS, . Treffer: 250

2020

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; Cantwell, L; 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; Valladares, O; Vardarajan, B; Wang, LS; 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. 2020; 25(8):1859-1875 [OPEN ACCESS]
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Kälsch, AI; Scharnagl, H; Kleber, ME; Windpassinger, C; Sattler, W; Leipe, J; Krämer, BK; März, W; Malle, E Long- and short-term association of low-grade systemic inflammation with cardiovascular mortality in the LURIC study.
Clin Res Cardiol. 2020; 109(3):358-373
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Karras, SN; Koufakis, T; Antonopoulou, V; Goulis, DG; Alaylıoğlu, M; Dursun, E; Gezen-Ak, D; Annweiler, C; Pilz, S; Fakhoury, H; Al Anouti, F; Harizopoulou, V; Naughton, DP; Zebekakis, P; Kotsa, K Vitamin D receptor Fokl polymorphism is a determinant of both maternal and neonatal vitamin D concentrations at birth.
J Steroid Biochem Mol Biol. 2019; 199(1): 105568-105568.
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Mashbat, B; Bellos, E; Hodeib, S; Bidmos, F; Thwaites, RS; Lu, Y; Wright, VJ; Herberg, JA; Klobassa, DS; Zenz, W; Hansel, TT; Nadel, S; Langford, PR; Schlapbach, LJ; Li, MS; Redinbo, MR; Di, YP; Levin, M; Sancho-Shimizu, V A Rare Mutation in SPLUNC1 Affects Bacterial Adherence and Invasion in Meningococcal Disease.
Clin Infect Dis. 2020; 70(10):2045-2053 [OPEN ACCESS]
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Matušková, V; Zeman, T; Ewerlingová, L; Hlinomazová, Z; Souček, J; Vlková, E; Goswami, N; Balcar, VJ; Šerý, O An association of neovascular age-related macular degeneration with polymorphisms of CFH, ARMS2, HTRA1 and C3 genes in Czech population.
Acta Ophthalmol. 2020;
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Trummer, O; Schweighofer, N; Haudum, CW; Trummer, C; Pilz, S; Theiler-Schwetz, V; Keppel, MH; Grübler, M; Pieber, TR; Renner, W; Obermayer-Pietsch, B; Lerchbaum, E Genetic Components of 25-Hydroxyvitamin D Increase in Three Randomized Controlled Trials.
J Clin Med. 2020; 9(2): [OPEN ACCESS]
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2019

Ahmed, J; Windpassinger, C; Salim, M; Wiener, M; Petek, E; Schaflinger, E; Taj, S; Hussain, S; Abbas, S; Abbas, M; Younis, I; Muhammad, N; Khan, S; Khan, MA Genetic study of Khyber-Pukhtunkhwa resident Pakistani families presenting primary microcephaly with intellectual disability.
J Pak Med Assoc. 2019; 69(12): 1812-1816. [OPEN ACCESS]
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Argemi, J; Latasa, MU; Atkinson, SR; Blokhin, IO; Massey, V; Gue, JP; Cabezas, J; Lozano, JJ; Van Booven, D; Bell, A; Cao, S; Vernetti, LA; Arab, JP; Ventura-Cots, M; Edmunds, LR; Fondevilla, C; Stärkel, P; Dubuquoy, L; Louvet, A; Odena, G; Gomez, JL; Aragon, T; Altamirano, J; Caballeria, J; Jurczak, MJ; Taylor, DL; Berasain, C; Wahlestedt, C; Monga, SP; Morgan, MY; Sancho-Bru, P; Mathurin, P; Furuya, S; Lackner, C; Rusyn, I; Shah, VH; Thursz, MR; Mann, J; Avila, MA; Bataller, R Defective HNF4alpha-dependent gene expression as a driver of hepatocellular failure in alcoholic hepatitis.
NAT COMMUN. 2019; 10(1): 3126-3126. [OPEN ACCESS]
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Arriga, R; Caratelli, S; Lanzilli, G; Ottaviani, A; Cenciarelli, C; Sconocchia, T; Spagnoli, GC; Iezzi, G; Roselli, M; Lauro, D; Coppola, A; Dotti, G; Ferrone, S; Sconocchia, G CD16-158-valine chimeric receptor T cells overcome the resistance of KRAS-mutated colorectal carcinoma cells to cetuximab.
INT J CANCER. 2019; 14(8):
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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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Borghini, L; Png, E; Binder, A; Wright, VJ; Pinnock, E; de Groot, R; Hazelzet, J; Emonts, M; Van der Flier, M; Schlapbach, LJ; Anderson, S; Secka, F; Salas, A; Fink, C; Carrol, ED; Pollard, AJ; Coin, LJ; Kuijpers, TW; Martinon-Torres, F; Zenz, W; Levin, M; Hibberd, ML; Davila, S; EUCLIDS consortium Identification of regulatory variants associated with genetic susceptibility to meningococcal disease.
Sci Rep. 2019; 9(1):6966-6966 [OPEN ACCESS]
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Pfeifer, B; Kapan, DD Estimates of introgression as a function of pairwise distances.
BMC BIOINFORMATICS. 2019; 20(1): 207-207. [OPEN ACCESS]
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Sammar, M; Drobnjak, T; Mandala, M; Gizurarson, S; Huppertz, B; Meiri, H Galectin 13 (PP13) Facilitates Remodeling and Structural Stabilization of Maternal Vessels during Pregnancy.
INT J MOL SCI. 2019; 20(13): [OPEN ACCESS]
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Zheng, J; Maerz, W; Gergei, I; Kleber, M; Drechsler, C; Wanner, C; Brandenburg, V; Reppe, S; Gautvik, KM; Medina-Gomez, C; Shevroja, E; Gilly, A; Park, YC; Dedoussis, G; Zeggini, E; Lorentzon, M; Henning, P; Lerner, UH; Nilsson, KH; Movérare-Skrtic, S; Baird, D; Elsworth, B; Falk, L; Groom, A; Capellini, TD; Grundberg, E; Nethander, M; Ohlsson, C; Davey Smith, G; Tobias, JH Mendelian Randomization Analysis Reveals a Causal Influence of Circulating Sclerostin Levels on Bone Mineral Density and Fractures.
J BONE MINER RES. 2019; 53(4): [OPEN ACCESS]
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2018

Kimbacher, C; Paar, C; Freystetter, A; Berg, J Cell Line Controls for the Genotyping of a Spectrum of Human Single Nucleotide Polymorphisms in the Clinical Laboratory.
Clin Lab. 2018; 64(5):823-834 [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; 13(8):
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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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Zeller, T; Seiffert, M; Müller, C; Scholz, M; Schäffer, A; Ojeda, F; Drexel, H; Mündlein, A; Kleber, ME; März, W; Sinning, C; Brunner, FJ; Waldeyer, C; Keller, T; Saely, CH; Sydow, K; Thiery, J; Teupser, D; Blankenberg, S; Schnabel, R Genome-Wide Association Analysis for Severity of Coronary Artery Disease Using the Gensini Scoring System.
Front Cardiovasc Med. 2017; 4(12):57-57 [OPEN ACCESS]
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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 [OPEN ACCESS]
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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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Nüesch, E; Dale, C; Palmer, TM; White, J; Keating, BJ; van Iperen, EP; Goel, A; Padmanabhan, S; Asselbergs, FW; EPIC-Netherland Investigators; Verschuren, WM; Wijmenga, C; Van der Schouw, YT; Onland-Moret, NC; Lange, LA; Hovingh, GK; Sivapalaratnam, S; Morris, RW; Whincup, PH; Wannamethe, GS; Gaunt, TR; Ebrahim, S; Steel, L; Nair, N; Reiner, AP; Kooperberg, C; Wilson, JF; Bolton, JL; McLachlan, S; Price, JF; Strachan, MW; Robertson, CM; Kleber, ME; Delgado, G; März, W; Melander, O; Dominiczak, AF; Farrall, M; Watkins, H; Leusink, M; Maitland-van der Zee, AH; de Groot, MC; Dudbridge, F; Hingorani, A; Ben-Shlomo, Y; Lawlor, DA; UCLEB Investigators; Amuzu, A; Caufield, M; Cavadino, A; Cooper, J; Davies, TL; IN Day; Drenos, F; Engmann, J; Finan, C; Giambartolomei, C; Hardy, R; Humphries, SE; Hypponen, E; Kivimaki, M; Kuh, D; Kumari, M; Ong, K; Plagnol, V; Power, C; Richards, M; Shah, S; Shah, T; Sofat, R; Talmud, PJ; Wareham, N; Warren, H; Whittaker, JC; Wong, A; Zabaneh, D; Davey Smith, G; Wells, JC; Leon, DA; Holmes, MV; Casas, JP Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis.
Int J Epidemiol. 2016; 45(6):1927-1937 [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.
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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.
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Reichmann, F; Holzer, P Neuropeptide Y: A stressful review.
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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.
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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.
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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.
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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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Beilfuss, A; Sowa, JP; Sydor, S; Beste, M; Bechmann, LP; Schlattjan, M; Syn, WK; Wedemeyer, I; Mathé, Z; Jochum, C; Gerken, G; Gieseler, RK; Canbay, A Vitamin D counteracts fibrogenic TGF-β signalling in human hepatic stellate cells both receptor-dependently and independently.
Gut. 2015; 64(5):791-799
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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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