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

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Suchbegriffe: SNP, . Treffer: 219

Matzhold, EM; Drexler-Helmberg, C; Helmberg, W; Wagner, A; Wagner, T Allele-specific long-range sequencing as a method for ABO haplotyping in clinical blood group diagnosis and immunohematology research.
MOL GENET GENOM MED. 2023; e2286 Doi: 10.1002/mgg3.2286 [OPEN ACCESS]
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Merle, DA; Sen, M; Armento, A; Stanton, CM; Thee, EF; Meester-Smoor, MA; Kaiser, M; Clark, SJ; Klaver, CCW; Keane, PA; Wright, AF; Ehrmann, M; Ueffing, M 10q26 - The enigma in age-related macular degeneration.
Prog Retin Eye Res. 2023; 96: 101154 Doi: 10.1016/j.preteyeres.2022.101154
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Ortiz, M; Jauset-Rubio, M; Trummer, O; Foessl, I; Kodr, D; Acero, JL; Botero, ML; Biggs, P; Lenartowicz, D; Trajanoska, K; Rivadeneira, F; Hocek, M; Obermayer-Pietsch, B; O'Sullivan, CK Generic Platform for the Multiplexed Targeted Electrochemical Detection of Osteoporosis-Associated Single Nucleotide Polymorphisms Using Recombinase Polymerase Solid-Phase Primer Elongation and Ferrocene-Modified Nucleoside Triphosphates
ACS CENTRAL SCI. 2023; 9(8): 1591-1602. Doi: 10.1021/acscentsci.3c00243 [OPEN ACCESS]
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Schweighofer, N; Strasser, M; Obermayer, A; Trummer, O; Sourij, H; Sourij, C; Obermayer-Pietsch, B Identification of Novel Intronic SNPs in Transporter Genes Associated with Metformin Side Effects.
Genes (Basel). 2023; 14(8): 1609 Doi: 10.3390/genes14081609 [OPEN ACCESS]
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Yenice, CP; Chahin, N; Jauset-Rubio, M; Hall, M; Biggs, P; Dimai, HP; Obermayer-Pietsch, B; Ortiz, M; O'Sullivan, CK Semiautomated Electrochemical Melting Curve Analysis Device for the Detection of an Osteoporosis Associated Single Nucleotide Polymorphism in Blood.
Anal Chem. 2023; 95(38): 14192-14202. Doi: 10.1021/acs.analchem.3c01668 [OPEN ACCESS]
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Zheng, J; Wheeler, E; Pietzner, M; Andlauer, TFM; Yau, MS; Hartley, AE; Brumpton, BM; Rasheed, H; Kemp, JP; Frysz, M; Robinson, J; Reppe, S; Prijatelj, V; Gautvik, KM; Falk, L; Maerz, W; Gergei, I; Peyser, PA; Kavousi, M; de, Vries, PS; Miller, CL; Bos, M; van, der, Laan, SW; Malhotra, R; Herrmann, M; Scharnagl, H; Kleber, M; Dedoussis, G; Zeggini, E; Nethander, M; Ohlsson, C; Lorentzon, M; Wareham, N; Langenberg, C; Holmes, MV; Davey, Smith, G; Tobias, JH Lowering of Circulating Sclerostin May Increase Risk of Atherosclerosis and Its Risk Factors: Evidence From a Genome-Wide Association Meta-Analysis Followed by Mendelian Randomization.
ARTHRITIS RHEUMATOL. 2023; 75(10): 1781-1792. Doi: 10.1002/art.42538 [OPEN ACCESS]
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2022

Alberts, T; Antipova, V; Holzmann, C; Hawlitschka, A; Schmitt, O; Kurth, J; Stenzel, J; Lindner, T; Krause, BJ; Wree, A; Witt, M Olfactory Bulb D₂/D₃ Receptor Availability after Intrastriatal Botulinum Neurotoxin-A Injection in a Unilateral 6-OHDA Rat Model of Parkinson's Disease.
Toxins (Basel). 2022; 14(2): Doi: 10.3390/toxins14020094 [OPEN ACCESS]
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Kumar, V; Pouw, RB; Autio, MI; Sagmeister, MG; Phua, ZY; Borghini, L; Wright, VJ; Hoggart, C; Pan, B; Tan, AKY; Binder, A; Brouwer, MC; Pinnock, E; De, Groot, R; Hazelzet, J; Emonts, M; Van, Der, Flier, M; Reiter, K; Nöthen, MM; Hoffmann, P; Schlapbach, LJ; Bellos, E; Anderson, S; Secka, F; Martinón-Torres, F; Salas, A; Fink, C; Carrol, ED; Pollard, AJ; Coin, LJ; Zenz, W; Wouters, D; Ang, LT; Hibberd, ML; Levin, M; Kuijpers, TW; Davila, S, , EUCLIDS, consortium Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrations.
Am J Hum Genet. 2022; 109(9): 1680-1691. Doi: 10.1016/j.ajhg.2022.08.001 [OPEN ACCESS]
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Muzammal, M; Ali, MZ; Brugger, B; Blatterer, J; Ahmad, S; Taj, S; Shah, SK; Khan, S; Enzinger, C; Petek, E; Wagner, K; Khan, MA; Windpassinger, C A novel protein truncating mutation in L2HGDH causes L-2-hydroxyglutaric aciduria in a consanguineous Pakistani family.
Metab Brain Dis. 2022; 37(1):243-252 Doi: 10.1007/s11011-021-00832-2 [OPEN ACCESS]
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Posch-Pertl, L; List, W; Michelitsch, M; Pinter-Hausberger, S; Berisha, B; Posch, F; Kloeckl, L; Renner, W; Weger, M Heme oxygenase-1 gene rs2071746 polymorphism in retinal vein occlusion.
Ophthalmic Genet. 2022; 43(5):627-632 Doi: 10.1080/13816810.2022.2092754
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Ritsch, A; Hunjadi, M; Stojakovic, T; Scherberich, JE; Silbernagel, G; Scharnagl, H; Delgado, GE; Kleber, ME; März, W Independent Effects of Kidney Function and Cholesterol Efflux on Cardiovascular Mortality.
Biomedicines. 2022; 10(8): Doi: 10.3390/biomedicines10081832 [OPEN ACCESS]
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Wetzstein, N; Diricks, M; Kohl, TA; Wichelhaus, TA; Andres, S; Paulowski, L; Schwarz, C; Lewin, A; Kehrmann, J; Kahl, BC; Dichtl, K; Hügel, C; Eickmeier, O; Smaczny, C; Schmidt, A; Zimmermann, S; Nährlich, L; Hafkemeyer, S; Niemann, S; Maurer, FP; Hogardt, M Molecular Epidemiology of Mycobacterium abscessus Isolates Recovered from German Cystic Fibrosis Patients.
Microbiol Spectr. 2022; 10(4):e0171422 Doi: 10.1128/spectrum.01714-22 [OPEN ACCESS]
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Yengo, L; Vedantam, S; Marouli, E; Sidorenko, J; Bartell, E; Sakaue, S; Graff, M; Eliasen, AU; Jiang, Y; Raghavan, S; Miao, J; Arias, JD; Graham, SE; Mukamel, RE; Spracklen, CN; Yin, X; Chen, SH; Ferreira, T; Highland, HH; Ji, Y; Karaderi, T; Lin, K; Lüll, K; Malden, DE; Medina-Gomez, C; Machado, M; Moore, A; Rüeger, S; Sim, X; Vrieze, S; Ahluwalia, TS; Akiyama, M; Allison, MA; Alvarez, M; Andersen, MK; Ani, A; Appadurai, V; Arbeeva, L; Bhaskar, S; Bielak, LF; Bollepalli, S; Bonnycastle, LL; Bork-Jensen, J; Bradfield, JP; Bradford, Y; Braund, PS; Brody, JA; Burgdorf, KS; Cade, BE; Cai, H; Cai, Q; Campbell, A; Cañadas-Garre, M; Catamo, E; Chai, JF; Chai, X; Chang, LC; Chang, YC; Chen, CH; Chesi, A; Choi, SH; Chung, RH; Cocca, M; Concas, MP; Couture, C; Cuellar-Partida, G; Danning, R; Daw, EW; Degenhard, F; Delgado, GE; Delitala, A; Demirkan, A; Deng, X; Devineni, P; Dietl, A; Dimitriou, M; Dimitrov, L; Dorajoo, R; Ekici, AB; Engmann, JE; Fairhurst-Hunter, Z; Farmaki, AE; Faul, JD; Fernandez-Lopez, JC; Forer, L; Francescatto, M; Freitag-Wolf, S; Fuchsberger, C; Galesloot, TE; Gao, Y; Gao, Z; Geller, F; Giannakopoulou, O; Giulianini, F; Gjesing, AP; Goel, A; Gordon, SD; Gorski, M; Grove, J; Guo, X; Gustafsson, S; Haessler, J; Hansen, TF; Havulinna, AS; Haworth, SJ; He, J; Heard-Costa, N; Hebbar, P; Hindy, G; Ho, YA; Hofer, E; Holliday, E; Horn, K; Hornsby, WE; Hottenga, JJ; Huang, H; Huang, J; Huerta-Chagoya, A; Huffman, JE; Hung, YJ; Huo, S; Hwang, MY; Iha, H; Ikeda, DD; Isono, M; Jackson, AU; Jäger, S; Jansen, IE; Johansson, I; Jonas, JB; Jonsson, A; Jørgensen, T; Kalafati, IP; Kanai, M; Kanoni, S; Kårhus, LL; Kasturiratne, A; Katsuya, T; Kawaguchi, T; Kember, RL; Kentistou, KA; Kim, HN; Kim, YJ; Kleber, ME; Knol, MJ; Kurbasic, A; Lauzon, M; Le, P; Lea, R; Lee, JY; Leonard, HL; Li, SA; Li, X; Li, X; Liang, J; Lin, H; Lin, SY; Liu, J; Liu, X; Lo, KS; Long, J; Lores-Motta, L; Luan, J; Lyssenko, V; Lyytikäinen, LP; Mahajan, A; Mamakou, V; Mangino, M; Manichaikul, A; Marten, J; Mattheisen, M; Mavarani, L; McDaid, AF; Meidtner, K; Melendez, TL; Mercader, JM; Milaneschi, Y; Miller, JE; Millwood, IY; Mishra, PP; Mitchell, RE; Møllehave, LT; Morgan, A; Mucha, S; Munz, M; Nakatochi, M; Nelson, CP; Nethander, M; Nho, CW; Nielsen, AA; Nolte, IM; Nongmaithem, SS; Noordam, R; Ntalla, I; Nutile, T; Pandit, A; Christofidou, P; Pärna, K; Pauper, M; Petersen, ERB; Petersen, LV; Pitkänen, N; Polašek, O; Poveda, A; Preuss, MH; Pyarajan, S; Raffield, LM; Rakugi, H; Ramirez, J; Rasheed, A; Raven, D; Rayner, NW; Riveros, C; Rohde, R; Ruggiero, D; Ruotsalainen, SE; Ryan, KA; Sabater-Lleal, M; Saxena, R; Scholz, M; Sendamarai, A; Shen, B; Shi, J; Shin, JH; Sidore, C; Sitlani, CM; Slieker, RC; Smit, RAJ; Smith, AV; Smith, JA; Smyth, LJ; Southam, L; Steinthorsdottir, V; Sun, L; Takeuchi, F; Tallapragada, DSP; Taylor, KD; Tayo, BO; Tcheandjieu, C; Terzikhan, N; Tesolin, P; Teumer, A; Theusch, E; Thompson, DJ; Thorleifsson, G; Timmers, PRHJ; Trompet, S; Turman, C; Vaccargiu, S; van, der, Laan, SW; van, der, Most, PJ; van, Klinken, JB; van, Setten, J; Verma, SS; Verweij, N; Veturi, Y; Wang, CA; Wang, C; Wang, L; Wang, Z; Warren, HR; Bin, Wei, W; Wickremasinghe, AR; Wielscher, M; Wiggins, KL; Winsvold, BS; Wong, A; Wu, Y; Wuttke, M; Xia, R; Xie, T; Yamamoto, K; Yang, J; Yao, J; Young, H; Yousri, NA; Yu, L; Zeng, L; Zhang, W; Zhang, X; Zhao, JH; Zhao, W; Zhou, W; Zimmermann, ME; Zoledziewska, M; Adair, LS; Adams, HHH; Aguilar-Salinas, CA; Al-Mulla, F; Arnett, DK; Asse ... A saturated map of common genetic variants associated with human height.
Nature. 2022; 610(7933):704-712 Doi: 10.1038/s41586-022-05275-y [OPEN ACCESS]
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2021

Hall, IF; Climent, M; Anselmi, CV; Papa, L; Tragante, V; Lambroia, L; Farina, FM; Kleber, ME; Marz, W; Biguori, C; Condorelli, G; Elia, L rs41291957 controls miR-143 and miR-145 expression and impacts coronary artery disease risk
EMBO MOL MED. 2021; e14060 Doi: 10.15252/emmm.202114060 [OPEN ACCESS]
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Katzmann, JL; Mason, AM; März, W; Kleber, ME; Niessner, A; Blüher, M; Speer, T; Laufs, U Genetic Variation in Sodium-glucose Cotransporter 2 and Heart Failure.
CLIN PHARMACOL THER. 2021; 11(2): Doi: 10.1002/cpt.2153 [OPEN ACCESS]
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Quinodoz, M; Peter, VG; Bedoni, N; Royer, Bertrand, B; Cisarova, K; Salmaninejad, A; Sepahi, N; Rodrigues, R; Piran, M; Mojarrad, M; Pasdar, A; Ghanbari, Asad, A; Sousa, AB; Coutinho, Santos, L; Superti-Furga, A; Rivolta, C AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data.
Nat Commun. 2021; 12(1): 518 Doi: 10.1038/s41467-020-20584-4 [OPEN ACCESS]
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Wendel, B; Papiol, S; Andlauer, TFM; Zimmermann, J; Wiltfang, J; Spitzer, C; Senner, F; Schulte, EC; Schmauß, M; Schaupp, SK; Repple, J; Reininghaus, E; Reimer, J; Reich-Erkelenz, D; Opel, N; Nenadić, I; Meinert, S; Konrad, C; Klöhn-Saghatolislam, F; Kircher, T; Kalman, JL; Juckel, G; Jansen, A; Jäger, M; Heilbronner, M; von, Hagen, M; Gade, K; Figge, C; Fallgatter, AJ; Dietrich, DE; Dannlowski, U; Comes, AL; Budde, M; Baune, BT; Arolt, V; Anghelescu, IG; Anderson-Schmidt, H; Adorjan, K; Falkai, P; Schulze, TG; Bickeböller, H; Heilbronner, U A genome-wide association study of the longitudinal course of executive functions.
Transl Psychiatry. 2021; 11(1): 386 Doi: 10.1038/s41398-021-01510-8 [OPEN ACCESS]
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2020

Falcone, GJ; Kirsch, E; Acosta, JN; Noche, RB; Leasure, A; Marini, S; Chung, J; Selim, M; Meschia, JF; Brown, DL; Worrall, BB; Tirschwell, DL; Jagiella, JM; Schmidt, H; Jimenez-Conde, J; Fernandez-Cadenas, I; Lindgren, A; Slowik, A; Gill, D; Holmes, M; Phuah, CL; Petersen, NH; Matouk Md, CN; Gunel, M; Sansing, L; Bennett, D; Chen, Z; Sun, LL; Clarke, R; Walters, RG; Gill, TM; Biffi, A; Kathiresan, S; Langefeld, CD; Woo, D; Rosand, J; Sheth, KN; Anderson, CD; International Stroke Genetics Consortium Genetically Elevated LDL Associates with Lower Risk of Intracerebral Hemorrhage.
Ann Neurol. 2020; 88(1):56-66 Doi: 10.1002/ana.25740 [OPEN ACCESS]
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Hässler, S; Bachelet, D; Duhaze, J; Szely, N; Gleizes, A; Hacein-Bey Abina, S; Aktas, O; Auer, M; Avouac, J; Birchler, M; Bouhnik, Y; Brocq, O; Buck-Martin, D; Cadiot, G; Carbonnel, F; Chowers, Y; Comabella, M; Derfuss, T; De Vries, N; Donnellan, N; Doukani, A; Guger, M; Hartung, HP; Kubala Havrdova, E; Hemmer, B; Huizinga, T; Ingenhoven, K; Hyldgaard-Jensen, PE; Jury, EC; Khalil, M; Kieseier, B; Laurén, A; Lindberg, R; Loercher, A; Maggi, E; Manson, J; Mauri, C; Mohand Oumoussa, B; Montalban, X; Nachury, M; Nytrova, P; Richez, C; Ryner, M; Sellebjerg, F; Sievers, C; Sikkema, D; Soubrier, M; Tourdot, S; Trang, C; Vultaggio, A; Warnke, C; Spindeldreher, S; Dönnes, P; Hickling, TP; Hincelin Mery, A; Allez, M; Deisenhammer, F; Fogdell-Hahn, A; Mariette, X; Pallardy, M; Broët, P; ABIRISK consortium Clinicogenomic factors of biotherapy immunogenicity in autoimmune disease: A prospective multicohort study of the ABIRISK consortium.
PLoS Med. 2020; 17(10): e1003348-e1003348. Doi: 10.1371/journal.pmed.1003348 [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 Doi: 10.1007/s00392-019-01516-9
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Ledermann, K; Hasler, G; Jenewein, J; Sprott, H; Schnyder, U; Martin-Soelch, C 5'UTR polymorphism in the serotonergic receptor HTR3A gene is differently associated with striatal Dopamine D2/D3 receptor availability in the right putamen in Fibromyalgia patients and healthy controls-Preliminary evidence.
Synapse. 2020; 74(5):e22147-e22147 Doi: 10.1002/syn.22147
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Mehrjardi, NZ; Molcanyi, M; Hatay, FF; Timmer, M; Shahbazi, E; Ackermann, JP; Herms, S; Heilmann-Heimbach, S; Wunderlich, TF; Prochnow, N; Haghikia, A; Lampert, A; Hescheler, J; Neugebauer, EAM; Baharvand, H; Šarić, T Acquisition of chromosome 1q duplication in parental and genome-edited human-induced pluripotent stem cell-derived neural stem cells results in their higher proliferation rate in vitro and in vivo.
Cell Prolif. 2020; e12892-e12892. Doi: 10.1111/cpr.12892 [OPEN ACCESS]
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Schweighofer, N; Genser, B; Maerz, W; Kleber, ME; Trummer, O; Pieber, TR; Obermayer-Pietsch, B Intronic Variants in OCT1 are Associated with All-Cause and Cardiovascular Mortality in Metformin Users with Type 2 Diabetes.
Diabetes Metab Syndr Obes. 2020; 13:2069-2080 Doi: 10.2147/DMSO.S235663 [OPEN ACCESS]
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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): Doi: 10.3390/jcm9020570 [OPEN ACCESS]
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Zhou, J; Passero, K; Palmiero, NE; Müller-Myhsok, B; Kleber, ME; Maerz, W; Hall, MA Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study.
PLoS One. 2020; 15(9):e0238304-e0238304 Doi: 10.1371/journal.pone.0238304 [OPEN ACCESS]
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2019

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 Doi: 10.1038/s41598-019-43292-6 [OPEN ACCESS]
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Karlsson Linnér, R; Biroli, P; Kong, E; Meddens, SFW; Wedow, R; Fontana, MA; Lebreton, M; Tino, SP; Abdellaoui, A; Hammerschlag, AR; Nivard, MG; Okbay, A; Rietveld, CA; Timshel, PN; Trzaskowski, M; Vlaming, R; Zünd, CL; Bao, Y; Buzdugan, L; Caplin, AH; Chen, CY; Eibich, P; Fontanillas, P; Gonzalez, JR; Joshi, PK; Karhunen, V; Kleinman, A; Levin, RZ; Lill, CM; Meddens, GA; Muntané, G; Sanchez-Roige, S; Rooij, FJV; Taskesen, E; Wu, Y; Zhang, F; 23and Me Research Team; eQTLgen Consortium; International Cannabis Consortium; Social Science Genetic Association Consortium; Auton, A; Boardman, JD; Clark, DW; Conlin, A; Dolan, CC; Fischbacher, U; Groenen, PJF; Harris, KM; Hasler, G; Hofman, A; Ikram, MA; Jain, S; Karlsson, R; Kessler, RC; Kooyman, M; MacKillop, J; Männikkö, M; Morcillo-Suarez, C; McQueen, MB; Schmidt, KM; Smart, MC; Sutter, M; Thurik, AR; Uitterlinden, AG; White, J; Wit, H; Yang, J; Bertram, L; Boomsma, DI; Esko, T; Fehr, E; Hinds, DA; Johannesson, M; Kumari, M; Laibson, D; Magnusson, PKE; Meyer, MN; Navarro, A; Palmer, AA; Pers, TH; Posthuma, D; Schunk, D; Stein, MB; Svento, R; Tiemeier, H; Timmers, PRHJ; Turley, P; Ursano, RJ; Wagner, GG; Wilson, JF; Gratten, J; Lee, JJ; Cesarini, D; Benjamin, DJ; Koellinger, PD; Beauchamp, JP Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.
Nat Genet. 2019; 51(2):245-257 Doi: 10.1038/s41588-018-0309-3 [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. Doi: 10.1186/s12859-019-2747-z [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): Doi: 10.1002/jbmr.3803 [OPEN ACCESS]
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2018

Alonso, N; Estrada, K; Albagha, OME; Herrera, L; Reppe, S; Olstad, OK; Gautvik, KM; Ryan, NM; Evans, KL; Nielson, CM; Hsu, YH; Kiel, DP; Markozannes, G; Ntzani, EE; Evangelou, E; Feenstra, B; Liu, X; Melbye, M; Masi, L; Brandi, ML; Riches, P; Daroszewska, A; Olmos, JM; Valero, C; Castillo, J; Riancho, JA; Husted, LB; Langdahl, BL; Brown, MA; Duncan, EL; Kaptoge, S; Khaw, KT; Usategui-Martín, R; Del, Pino-Montes, J; González-Sarmiento, R; Lewis, JR; Prince, RL; D'Amelio, P; García-Giralt, N; Nogués, X; Mencej-Bedrac, S; Marc, J; Wolstein, O; Eisman, JA; Oei, L; Medina-Gómez, C; Schraut, KE; Navarro, P; Wilson, JF; Davies, G; Starr, J; Deary, I; Tanaka, T; Ferrucci, L; Gianfrancesco, F; Gennari, L; Lucas, G; Elosua, R; Uitterlinden, AG; Rivadeneira, F; Ralston, SH Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density.
Ann Rheum Dis. 2018; 77(3): 378-385. Doi: 10.1136/annrheumdis-2017-212469 [OPEN ACCESS]
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de Boer, S; Baran, Y; Garcia-Garcia, HM; Eskin, I; Lenzen, MJ; Kleber, ME; Regar, E; de Jaegere, PJ; Ligthart, JM; van Geuns, RJ; Lehtimäki, T; Laaksonen, R; Boersma, E; Marz, W; Halperin, E; Serruys, PW; Koenig, W The European Collaborative Project on Inflammation and Vascular Wall Remodeling in Atherosclerosis - Intravascular Ultrasound (ATHEROREMO-IVUS) study.
EUROINTERVENTION. 2018; 14(2): 194-203. Doi: 10.4244/EIJ-D-17-00180 [OPEN ACCESS]
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Jiang, X; O'Reilly, PF; Aschard, H; Hsu, YH; Richards, JB; Dupuis, J; Ingelsson, E; Karasik, D; Pilz, S; Berry, D; Kestenbaum, B; Zheng, J; Luan, J; Sofianopoulou, E; Streeten, EA; Albanes, D; Lutsey, PL; Yao, L; Tang, W; Econs, MJ; Wallaschofski, H; Völzke, H; Zhou, A; Power, C; McCarthy, MI; Michos, ED; Boerwinkle, E; Weinstein, SJ; Freedman, ND; Huang, WY; Van Schoor, NM; van der Velde, N; Groot, LCPGM; Enneman, A; Cupples, LA; Booth, SL; Vasan, RS; Liu, CT; Zhou, Y; Ripatti, S; Ohlsson, C; Vandenput, L; Lorentzon, M; Eriksson, JG; Shea, MK; Houston, DK; Kritchevsky, SB; Liu, Y; Lohman, KK; Ferrucci, L; Peacock, M; Gieger, C; Beekman, M; Slagboom, E; Deelen, J; Heemst, DV; Kleber, ME; März, W; de Boer, IH; Wood, AC; Rotter, JI; Rich, SS; Robinson-Cohen, C; den Heijer, M; Jarvelin, MR; Cavadino, A; Joshi, PK; Wilson, JF; Hayward, C; Lind, L; Michaëlsson, K; Trompet, S; Zillikens, MC; Uitterlinden, AG; Rivadeneira, F; Broer, L; Zgaga, L; Campbell, H; Theodoratou, E; Farrington, SM; Timofeeva, M; Dunlop, MG; Valdes, AM; Tikkanen, E; Lehtimäki, T; Lyytikäinen, LP; Kähönen, M; Raitakari, OT; Mikkilä, V; Ikram, MA; Sattar, N; Jukema, JW; Wareham, NJ; Langenberg, C; Forouhi, NG; Gundersen, TE; Khaw, KT; Butterworth, AS; Danesh, J; Spector, T; Wang, TJ; Hyppönen, E; Kraft, P; Kiel, DP Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels.
Nat Commun. 2018; 9(1): 260-260. Doi: 10.1038/s41467-017-02662-2 [OPEN ACCESS]
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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 Doi: 10.7754/Clin.Lab.2018.171212 [OPEN ACCESS]
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Lee, JJ; Wedow, R; Okbay, A; Kong, E; Maghzian, O; Zacher, M; Nguyen-Viet, TA; Bowers, P; Sidorenko, J; Karlsson Linnér, R; Fontana, MA; Kundu, T; Lee, C; Li, H; Li, R; Royer, R; Timshel, PN; Walters, RK; Willoughby, EA; Yengo, L; 23andMe Research Team; COGENT (Cognitive Genomics Consortium); Social Science Genetic Association Consortium; Alver, M; Bao, Y; Clark, DW; Day, FR; Furlotte, NA; Joshi, PK; Kemper, KE; Kleinman, A; Langenberg, C; Mägi, R; Trampush, JW; Verma, SS; Wu, Y; Lam, M; Zhao, JH; Zheng, Z; Boardman, JD; Campbell, H; Freese, J; Harris, KM; Hayward, C; Herd, P; Kumari, M; Lencz, T; Luan, J; Malhotra, AK; Metspalu, A; Milani, L; Ong, KK; Perry, JRB; Porteous, DJ; Ritchie, MD; Smart, MC; Smith, BH; Tung, JY; Wareham, NJ; Wilson, JF; Beauchamp, JP; Conley, DC; Esko, T; Lehrer, SF; Magnusson, PKE; Oskarsson, S; Pers, TH; Robinson, MR; Thom, K; Watson, C; Chabris, CF; Meyer, MN; Laibson, DI; Yang, J; Johannesson, M; Koellinger, PD; Turley, P; Visscher, PM; Benjamin, DJ; Cesarini, D Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
Nat Genet. 2018; 50(8):1112-1121 Doi: 10.1038/s41588-018-0147-3 [OPEN ACCESS]
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Melchardt, T; Magnes, T; Hufnagl, C; Thorner, AR; Ducar, M; Neureiter, D; Tränkenschuh, W; Klieser, E; Gaggl, A; Rösch, S; Rasp, G; Hartmann, TN; Pleyer, L; Rinnerthaler, G; Weiss, L; Greil, R; Egle, A Clonal evolution and heterogeneity in metastatic head and neck cancer-An analysis of the Austrian Study Group of Medical Tumour Therapy study group.
Eur J Cancer. 2018; 93: 69-78. Doi: 10.1016/j.ejca.2018.01.064
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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): Doi: 10.1111/iji.12380
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Pfeifer, B; Lercher, MJ BlockFeST: Bayesian calculation of region-specific FST to detect local adaptation.
Bioinformatics. 2018; 34(18): 3205-3207. Doi: 10.1093/bioinformatics/bty299 [OPEN ACCESS]
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2017

Abbasi, MR; Rifatbegovic, F; Brunner, C; Mann, G; Ziegler, A; Pötschger, U; Crazzolara, R; Ussowicz, M; Benesch, M; Ebetsberger-Dachs, G; Chan, GCF; Jones, N; Ladenstein, R; Ambros, IM; Ambros, PF Impact of Disseminated Neuroblastoma Cells on the Identification of the Relapse-Seeding Clone.
Clin Cancer Res. 2017; 23(15):4224-4232 Doi: 10.1158/1078-0432.CCR-16-2082 (- Case Report) [OPEN ACCESS]
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Chen, S; El-Heliebi, A; Tauber, G; Langsenlehner, T; Pötscher, M; Kashofer, K; Czyż, ZT; Polzer, B; Riethdorf, S; Kuske, A; Leitinger, G; Pantel, K; Kroneis, T; Sedlmayr, P Catch and Release: rare cell analysis from a functionalised medical wire.
Sci Rep. 2017; 7(2):43424-43424 Doi: 10.1038/srep43424 [OPEN ACCESS]
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Eroglu, E; Rost, R; Bischof, H; Blass, S; Schreilechner, A; Gottschalk, B; Depaoli, MR; Klec, C; Charoensin, S; Madreiter-Sokolowski, CT; Ramadani, J; Waldeck-Weiermair, M; Graier, WF; Malli, R Application of Genetically Encoded Fluorescent Nitric Oxide (NO•) Probes, the geNOps, for Real-time Imaging of NO• Signals in Single Cells.
J Vis Exp. 2017; 5(121): Doi: 10.3791/55486 [OPEN ACCESS]
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Gampenrieder, SP; Hufnagl, C; Brechelmacher, S; Huemer, F; Hackl, H; Rinnerthaler, G; Romeder, F; Monzo, Fuentes, C; Morre, P; Hauser-Kronberger, C; Mlineritsch, B; Greil, R Endothelin-1 genetic polymorphism as predictive marker for bevacizumab in metastatic breast cancer.
Pharmacogenomics J. 2017; 17(4): 344-350. Doi: 10.1038/tpj.2016.25
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Gorski, M; van der Most, PJ; Teumer, A; Chu, AY; Li, M; Mijatovic, V; Nolte, IM; Cocca, M; Taliun, D; Gomez, F; Li, Y; Tayo, B; Tin, A; Feitosa, MF; Aspelund, T; Attia, J; Biffar, R; Bochud, M; Boerwinkle, E; Borecki, I; Bottinger, EP; Chen, MH; Chouraki, V; Ciullo, M; Coresh, J; Cornelis, MC; Curhan, GC; d'Adamo, AP; Dehghan, A; Dengler, L; Ding, J; Eiriksdottir, G; Endlich, K; Enroth, S; Esko, T; Franco, OH; Gasparini, P; Gieger, C; Girotto, G; Gottesman, O; Gudnason, V; Gyllensten, U; Hancock, SJ; Harris, TB; Helmer, C; Höllerer, S; Hofer, E; Hofman, A; Holliday, EG; Homuth, G; Hu, FB; Huth, C; Hutri-Kähönen, N; Hwang, SJ; Imboden, M; Johansson, Å; Kähönen, M; König, W; Kramer, H; Krämer, BK; Kumar, A; Kutalik, Z; Lambert, JC; Launer, LJ; Lehtimäki, T; de Borst, M; Navis, G; Swertz, M; Liu, Y; Lohman, K; Loos, RJF; Lu, Y; Lyytikäinen, LP; McEvoy, MA; Meisinger, C; Meitinger, T; Metspalu, A; Metzger, M; Mihailov, E; Mitchell, P; Nauck, M; Oldehinkel, AJ; Olden, M; Wjh Penninx, B; Pistis, G; Pramstaller, PP; Probst-Hensch, N; Raitakari, OT; Rettig, R; Ridker, PM; Rivadeneira, F; Robino, A; Rosas, SE; Ruderfer, D; Ruggiero, D; Saba, Y; Sala, C; Schmidt, H; Schmidt, R; Scott, RJ; Sedaghat, S; Smith, AV; Sorice, R; Stengel, B; Stracke, S; Strauch, K; Toniolo, D; Uitterlinden, AG; Ulivi, S; Viikari, JS; Völker, U; Vollenweider, P; Völzke, H; Vuckovic, D; Waldenberger, M; Jin Wang, J; Yang, Q; Chasman, DI; Tromp, G; Snieder, H; Heid, IM; Fox, CS; Köttgen, A; Pattaro, C; Böger, CA; Fuchsberger, C 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
Sci Rep. 2017; 7(5):45040-45040 Doi: 10.1038/srep45040 [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 Doi: 10.18632/oncotarget.21697 [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 Doi: 10.1097/MEG.0000000000000834
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Nieser, M; Henopp, T; Brix, J; Stoß, L; Sitek, B; Naboulsi, W; Anlauf, M; Schlitter, AM; Klöppel, G; Gress, T; Moll, R; Bartsch, DK; Heverhagen, AE; Knoefel, WT; Kaemmerer, D; Haybaeck, J; Fend, F; Sperveslage, J; Sipos, B Loss of Chromosome 18 in Neuroendocrine Tumors of the Small Intestine: The Enigma Remains.
Neuroendocrinology. 2017; 104(3):302-312 Doi: 10.1159/000446917
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