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Publikationen

Suchbegriffe: SNP, . Treffer: 161

2018

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. [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. [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. [OPEN ACCESS]
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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.
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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 (- 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 [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): [OPEN ACCESS]
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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 [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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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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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
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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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Wild, PS; Felix, JF; Schillert, A; Teumer, A; Chen, MH; Leening, MJG; Völker, U; Großmann, V; Brody, JA; Irvin, MR; Shah, SJ; Pramana, S; Lieb, W; Schmidt, R; Stanton, AV; Malzahn, D; Smith, AV; Sundström, J; Minelli, C; Ruggiero, D; Lyytikäinen, LP; Tiller, D; Smith, JG; Monnereau, C; Di Tullio, MR; Musani, SK; Morrison, AC; Pers, TH; Morley, M; Kleber, ME; Aragam, J; Benjamin, EJ; Bis, JC; Bisping, E; Broeckel, U; Cheng, S; Deckers, JW; Del Greco M, F; Edelmann, F; Fornage, M; Franke, L; Friedrich, N; Harris, TB; Hofer, E; Hofman, A; Huang, J; Hughes, AD; Kähönen, M; Investigators, K; Kruppa, J; Lackner, KJ; Lannfelt, L; Laskowski, R; Launer, LJ; Leosdottir, M; Lin, H; Lindgren, CM; Loley, C; MacRae, CA; Mascalzoni, D; Mayet, J; Medenwald, D; Morris, AP; Müller, C; Müller-Nurasyid, M; Nappo, S; Nilsson, PM; Nuding, S; Nutile, T; Peters, A; Pfeufer, A; Pietzner, D; Pramstaller, PP; Raitakari, OT; Rice, KM; Rivadeneira, F; Rotter, JI; Ruohonen, ST; Sacco, RL; Samdarshi, TE; Schmidt, H; Sharp, ASP; Shields, DC; Sorice, R; Sotoodehnia, N; Stricker, BH; Surendran, P; Thom, S; Töglhofer, AM; Uitterlinden, AG; Wachter, R; Völzke, H; Ziegler, A; Münzel, T; März, W; Cappola, TP; Hirschhorn, JN; Mitchell, GF; Smith, NL; Fox, ER; Dueker, ND; Jaddoe, VWV; Melander, O; Russ, M; Lehtimäki, T; Ciullo, M; Hicks, AA; Lind, L; Gudnason, V; Pieske, B; Barron, AJ; Zweiker, R; Schunkert, H; Ingelsson, E; Liu, K; Arnett, DK; Psaty, BM; Blankenberg, S; Larson, MG; Felix, SB; Franco, OH; Zeller, T; Vasan, RS; Dörr, M Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
J Clin Invest. 2017; 127(5):1798-1812 [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

Barban, N; Jansen, R; de Vlaming, R; Vaez, A; Mandemakers, JJ; Tropf, FC; Shen, X; Wilson, JF; Chasman, DI; Nolte, IM; Tragante, V; van der Laan, SW; Perry, JR; Kong, A; BIOS Consortium; Ahluwalia, TS; Albrecht, E; Yerges-Armstrong, L; Atzmon, G; Auro, K; Ayers, K; Bakshi, A; Ben-Avraham, D; Berger, K; Bergman, A; Bertram, L; Bielak, LF; Bjornsdottir, G; Bonder, MJ; Broer, L; Bui, M; Barbieri, C; Cavadino, A; Chavarro, JE; Turman, C; Concas, MP; Cordell, HJ; Davies, G; Eibich, P; Eriksson, N; Esko, T; Eriksson, J; Falahi, F; Felix, JF; Fontana, MA; Franke, L; Gandin, I; Gaskins, AJ; Gieger, C; Gunderson, EP; Guo, X; Hayward, C; He, C; Hofer, E; Huang, H; Joshi, PK; Kanoni, S; Karlsson, R; Kiechl, S; Kifley, A; Kluttig, A; Kraft, P; Lagou, V; Lecoeur, C; Lahti, J; Li-Gao, R; Lind, PA; Liu, T; Makalic, E; Mamasoula, C; Matteson, L; Mbarek, H; McArdle, PF; McMahon, G; Meddens, SF; Mihailov, E; Miller, M; Missmer, SA; Monnereau, C; van der Most, PJ; Myhre, R; Nalls, MA; Nutile, T; Kalafati, IP; Porcu, E; Prokopenko, I; Rajan, KB; Rich-Edwards, J; Rietveld, CA; Robino, A; Rose, LM; Rueedi, R; Ryan, KA; Saba, Y; Schmidt, D; Smith, JA; Stolk, L; Streeten, E; Tönjes, A; Thorleifsson, G; Ulivi, S; Wedenoja, J; Wellmann, J; Willeit, P; Yao, J; Yengo, L; Zhao, JH; Zhao, W; Zhernakova, DV; Amin, N; Andrews, H; Balkau, B; Barzilai, N; Bergmann, S; Biino, G; Bisgaard, H; Bønnelykke, K; Boomsma, DI; Buring, JE; Campbell, H; Cappellani, S; Ciullo, M; Cox, SR; Cucca, F; Toniolo, D; Davey-Smith, G; Deary, IJ; Dedoussis, G; Deloukas, P; van Duijn, CM; de Geus, EJ; Eriksson, JG; Evans, DA; Faul, JD; Sala, CF; Froguel, P; Gasparini, P; Girotto, G; Grabe, HJ; Greiser, KH; Groenen, PJ; de Haan, HG; Haerting, J; Harris, TB; Heath, AC; Heikkilä, K; Hofman, A; Homuth, G; Holliday, EG; Hopper, J; Hyppönen, E; Jacobsson, B; Jaddoe, VW; Johannesson, M; Jugessur, A; Kähönen, M; Kajantie, E; Kardia, SL; Keavney, B; Kolcic, I; Koponen, P; Kovacs, P; Kronenberg, F; Kutalik, Z; La Bianca, M; Lachance, G; Iacono, WG; Lai, S; Lehtimäki, T; Liewald, DC; LifeLines Cohort Study; Lindgren, CM; Liu, Y; Luben, R; Lucht, M; Luoto, R; Magnus, P; Magnusson, PK; Martin, NG; McGue, M; McQuillan, R; Medland, SE; Meisinger, C; Mellström, D; Metspalu, A; Traglia, M; Milani, L; Mitchell, P; Montgomery, GW; Mook-Kanamori, D; de Mutsert, R; Nohr, EA; Ohlsson, C; Olsen, J; Ong, KK; Paternoster, L; Pattie, A; Penninx, BW; Perola, M; Peyser, PA; Pirastu, M; Polasek, O; Power, C; Kaprio, J; Raffel, LJ; Räikkönen, K; Raitakari, O; Ridker, PM; Ring, SM; Roll, K; Rudan, I; Ruggiero, D; Rujescu, D; Salomaa, V; Schlessinger, D; Schmidt, H; Schmidt, R; Schupf, N; Smit, J; Sorice, R; Spector, TD; Starr, JM; Stöckl, D; Strauch, K; Stumvoll, M; Swertz, MA; Thorsteinsdottir, U; Thurik, AR; Timpson, NJ; Tung, JY; Uitterlinden, AG; Vaccargiu, S; Viikari, J; Vitart, V; Völzke, H; Vollenweider, P; Vuckovic, D; Waage, J; Wagner, GG; Wang, JJ; Wareham, NJ; Weir, DR; Willemsen, G; Willeit, J; Wright, AF; Zondervan, KT; Stefansson, K; Krueger, RF; Lee, JJ; Benjamin, DJ; Cesarini, D; Koellinger, PD; den Hoed, M; Snieder, H; Mills, MC Genome-wide analysis identifies 12 loci influencing human reproductive behavior.
Nat Genet. 2016; 48(12):1462-1472 [OPEN ACCESS]
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Bogen, D; Brunner, C; Walder, D; Ziegler, A; Abbasi, R; Ladenstein, RL; Noguera, R; Martinsson, T; Amann, G; Schilling, FH; Ussowicz, M; Benesch, M; Ambros, PF; Ambros, IM The genetic tumor background is an important determinant for heterogeneous MYCN-amplified neuroblastoma.
Int J Cancer. 2016; 139(1):153-163 [OPEN ACCESS]
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Bonin, S; Donada, M; Bussolati, G; Nardon, E; Annaratone, L; Pichler, M; Chiaravalli, AM; Capella, C; Hoefler, G; Stanta, G A synonymous EGFR polymorphism predicting responsiveness to anti-EGFR therapy in metastatic colorectal cancer patients.
Tumour Biol. 2016; 37(6):7295-7303
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Feichtinger, J; Hernández, I; Fischer, C; Hanscho, M; Auer, N; Hackl, M; Jadhav, V; Baumann, M; Krempl, PM; Schmidl, C; Farlik, M; Schuster, M; Merkel, A; Sommer, A; Heath, S; Rico, D; Bock, C; Thallinger, GG; Borth, N Comprehensive genome and epigenome characterization of CHO cells in response to evolutionary pressures and over time.
Biotechnol Bioeng. 2016; 113(10): 2241-2253. [OPEN ACCESS]
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Gandolfi, G; Longo, C; Moscarella, E; Zalaudek, I; Sancisi, V; Raucci, M; Manzotti, G; Gugnoni, M; Piana, S; Argenziano, G; Ciarrocchi, A The extent of whole-genome copy number alterations predicts aggressive features in primary melanomas.
Pigment Cell Melanoma Res. 2016; 29(2):163-175
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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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Ibrahim-Verbaas, CA; Bressler, J; Debette, S; Schuur, M; Smith, AV; Bis, JC; Davies, G; Trompet, S; Smith, JA; Wolf, C; Chibnik, LB; Liu, Y; Vitart, V; Kirin, M; Petrovic, K; Polasek, O; Zgaga, L; Fawns-Ritchie, C; Hoffmann, P; Karjalainen, J; Lahti, J; Llewellyn, DJ; Schmidt, CO; Mather, KA; Chouraki, V; Sun, Q; Resnick, SM; Rose, LM; Oldmeadow, C; Stewart, M; Smith, BH; Gudnason, V; Yang, Q; Mirza, SS; Jukema, JW; deJager, PL; Harris, TB; Liewald, DC; Amin, N; Coker, LH; Stegle, O; Lopez, OL; Schmidt, R; Teumer, A; Ford, I; Karbalai, N; Becker, JT; Jonsdottir, MK; Au, R; Fehrmann, R; Herms, S; Nalls, M; Zhao, W; Turner, ST; Yaffe, K; Lohman, K; van Swieten, JC; Kardia, S; Knopman, DS; Meeks, WM; Heiss, G; Holliday, EG; Schofield, PW; Tanaka, T; Stott, DJ; Wang, J; Ridker, P; Gow, AJ; Pattie, A; Starr, JM; Hocking, LJ; Armstrong, NJ; McLachlan, S; Shulman, JM; Pilling, LC; Eiriksdottir, G; Scott, RJ; Kochan, NA; Palotie, A; Hsieh, YC; Eriksson, JG; Penman, A; Gottesman, RF; Oostra, BA; Yu, L; DeStefano, AL; Beiser, A; Garcia, M; Rotter, JI; Nöthen, MM; Hofman, A; Slagboom, PE; Westendorp, R; Buckley, BM; Wolf, PA; Uitterlinden, AG; Psaty, BM; Grabe, HJ; Bandinelli, S; Chasman, DI; Grodstein, F; Räikkönen, K; Lambert, JC; Porteous, DJ; Generation Scotland; Price, JF; Sachdev, PS; Ferrucci, L; Attia, JR; Rudan, I; Hayward, C; Wright, AF; Wilson, JF; Cichon, S; Franke, L; Schmidt, H; Ding, J; de Craen, A; Fornage, M; Bennett, DA; Deary, IJ; Ikram, MA; Launer, LJ; Fitzpatrick, AL; Seshadri, S; van Duijn, CM; Mosley, TH GWAS for executive function and processing speed suggests involvement of the CADM2 gene.
Mol Psychiatry. 2016; 21(2):189-197 [OPEN ACCESS]
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Jun, G; Ibrahim-Verbaas, CA; Vronskaya, M; Lambert, JC; Chung, J; Naj, AC; Kunkle, BW; Wang, LS; Bis, JC; Bellenguez, C; Harold, D; Lunetta, KL; Destefano, AL; Grenier-Boley, B; Sims, R; Beecham, GW; Smith, AV; Chouraki, V; Hamilton-Nelson, KL; Ikram, MA; Fievet, N; Denning, N; Martin, ER; Schmidt, H; Kamatani, Y; Dunstan, ML; Valladares, O; Laza, AR; Zelenika, D; Ramirez, A; Foroud, TM; Choi, SH; Boland, A; Becker, T; Kukull, WA; van der Lee, SJ; Pasquier, F; Cruchaga, C; Beekly, D; Fitzpatrick, AL; Hanon, O; Gill, M; Barber, R; Gudnason, V; Campion, D; Love, S; Bennett, DA; Amin, N; Berr, C; Tsolaki, M; Buxbaum, JD; Lopez, OL; Deramecourt, V; Fox, NC; Cantwell, LB; Tárraga, L; Dufouil, C; Hardy, J; Crane, PK; Eiriksdottir, G; Hannequin, D; Clarke, R; Evans, D; Mosley, TH; Letenneur, L; Brayne, C; Maier, W; De Jager, P; Emilsson, V; Dartigues, JF; Hampel, H; Kamboh, MI; de Bruijn, RF; Tzourio, C; Pastor, P; Larson, EB; Rotter, JI; O'Donovan, MC; Montine, TJ; Nalls, MA; Mead, S; Reiman, EM; Jonsson, PV; Holmes, C; St George-Hyslop, PH; Boada, M; Passmore, P; Wendland, JR; Schmidt, R; Morgan, K; Winslow, AR; Powell, JF; Carasquillo, M; Younkin, SG; Jakobsdóttir, J; Kauwe, JS; Wilhelmsen, KC; Rujescu, D; Nöthen, MM; Hofman, A; Jones, L; IGAP Consortium; Haines, JL; Psaty, BM; Van Broeckhoven, C; Holmans, P; Launer, LJ; Mayeux, R; Lathrop, M; Goate, AM; Escott-Price, V; Seshadri, S; Pericak-Vance, MA; Amouyel, P; Williams, J; van Duijn, CM; Schellenberg, GD; Farrer, LA A novel Alzheimer disease locus located near the gene encoding tau protein.
Mol Psychiatry. 2016; 21(1):108-117 [OPEN ACCESS]
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Khan, MA; Khan, S; Windpassinger, C; Badar, M; Nawaz, Z; Mohammad, RM The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future Recommendations.
Ann Hum Genet. 2016; 80(6):342-368 [OPEN ACCESS]
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Khan, MA; Mohan, S; Zubair, M; Windpassinger, C Homozygosity mapping identified a novel protein truncating mutation (p.Ser100Leufs*24) of the BBS9 gene in a consanguineous Pakistani family with Bardet Biedl syndrome.
BMC Med Genet. 2016; 17(6): 10-10. [OPEN ACCESS]
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Lin, H; Mueller-Nurasyid, M; Smith, AV; Arking, DE; Barnard, J; Bartz, TM; Lunetta, KL; Lohman, K; Kleber, ME; Lubitz, SA; Geelhoed, B; Trompet, S; Niemeijer, MN; Kacprowski, T; Chasman, DI; Klarin, D; Sinner, MF; Waldenberger, M; Meitinger, T; Harris, TB; Launer, LJ; Soliman, EZ; Chen, LY; Smith, JD; Van Wagoner, DR; Rotter, JI; Psaty, BM; Xie, Z; Hendricks, AE; Ding, J; Delgado, GE; Verweij, N; van der Harst, P; Macfarlane, PW; Ford, I; Hofman, A; Uitterlinden, A; Heeringa, J; Franco, OH; Kors, JA; Weiss, S; Völzke, H; Rose, LM; Natarajan, P; Kathiresan, S; Kääb, S; Gudnason, V; Alonso, A; Chung, MK; Heckbert, SR; Benjamin, EJ; Liu, Y; März, W; Rienstra, M; Jukema, JW; Stricker, BH; Dörr, M; Albert, CM; Ellinor, PT Gene-gene Interaction Analyses for Atrial Fibrillation.
Sci Rep. 2016; 6(24):35371-35371 [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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Rossberg, W; Saternus, R; Wagenpfeil, S; Kleber, M; März, W; Reichrath, S; Vogt, T; Reichrath, J Human Pigmentation, Cutaneous Vitamin D Synthesis and Evolution: Variants of Genes (SNPs) Involved in Skin Pigmentation Are Associated with 25(OH)D Serum Concentration.
Anticancer Res. 2016; 36(3):1429-1437
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Trummer, O; Langsenlehner, U; Krenn-Pilko, S; Pieber, TR; Obermayer-Pietsch, B; Gerger, A; Renner, W; Langsenlehner, T Vitamin D and prostate cancer prognosis: a Mendelian randomization study.
World J Urol. 2016; 34(4):607-611 [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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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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Chauhan, G; Adams, HHH; Bis, JC; Weinstein, G; Yu, L; Töglhofer, AM; Smith, AV; van der Lee, SJ; Gottesman, RF; Thomson, R; Wang, J; Yang, Q; Niessen, WJ; Lopez, OL; Becker, JT; Phan, TG; Beare, RJ; Arfanakis, K; Fleischman, D; Vernooij, MW; Mazoyer, B; Schmidt, H; Srikanth, V; Knopman, DS; Jack, CR; Amouyel, P; Hofman, A; DeCarli, C; Tzourio, C; van Duijn, CM; Bennett, DA; Schmidt, R; Longstreth, WT; Mosley, TH; Fornage, M; Launer, LJ; Seshadri, S; Ikram, MA; Debette, S Association of Alzheimer's disease GWAS loci with MRI markers of brain aging.
Neurobiol Aging. 2015; 36(4):1765.e7-1761765 [OPEN ACCESS]
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Davies, G; Armstrong, N; Bis, JC; Bressler, J; Chouraki, V; Giddaluru, S; Hofer, E; Ibrahim-Verbaas, CA; Kirin, M; Lahti, J; van der Lee, SJ; Le Hellard, S; Liu, T; Marioni, RE; Oldmeadow, C; Postmus, I; Smith, AV; Smith, JA; Thalamuthu, A; Thomson, R; Vitart, V; Wang, J; Yu, L; Zgaga, L; Zhao, W; Boxall, R; Harris, SE; Hill, WD; Liewald, DC; Luciano, M; Adams, H; Ames, D; Amin, N; Amouyel, P; Assareh, AA; Au, R; Becker, JT; Beiser, A; Berr, C; Bertram, L; Boerwinkle, E; Buckley, BM; Campbell, H; Corley, J; De Jager, PL; Dufouil, C; Eriksson, JG; Espeseth, T; Faul, JD; Ford, I; Generation Scotland; Gottesman, RF; Griswold, ME; Gudnason, V; Harris, TB; Heiss, G; Hofman, A; Holliday, EG; Huffman, J; Kardia, SL; Kochan, N; Knopman, DS; Kwok, JB; Lambert, JC; Lee, T; Li, G; Li, SC; Loitfelder, M; Lopez, OL; Lundervold, AJ; Lundqvist, A; Mather, KA; Mirza, SS; Nyberg, L; Oostra, BA; Palotie, A; Papenberg, G; Pattie, A; Petrovic, K; Polasek, O; Psaty, BM; Redmond, P; Reppermund, S; Rotter, JI; Schmidt, H; Schuur, M; Schofield, PW; Scott, RJ; Steen, VM; Stott, DJ; van Swieten, JC; Taylor, KD; Trollor, J; Trompet, S; Uitterlinden, AG; Weinstein, G; Widen, E; Windham, BG; Jukema, JW; Wright, AF; Wright, MJ; Yang, Q; Amieva, H; Attia, JR; Bennett, DA; Brodaty, H; de Craen, AJ; Hayward, C; Ikram, MA; Lindenberger, U; Nilsson, LG; Porteous, DJ; Räikkönen, K; Reinvang, I; Rudan, I; Sachdev, PS; Schmidt, R; Schofield, PR; Srikanth, V; Starr, JM; Turner, ST; Weir, DR; Wilson, JF; van Duijn, C; Launer, L; Fitzpatrick, AL; Seshadri, S; Mosley, TH; Deary, IJ Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).
Mol Psychiatry. 2015; 20(2):183-192 [OPEN ACCESS]
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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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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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Iyengar, SK; Sedor, JR; Freedman, BI; Kao, WH; Kretzler, M; Keller, BJ; Abboud, HE; Adler, SG; Best, LG; Bowden, DW; Burlock, A; Chen, YD; Cole, SA; Comeau, ME; Curtis, JM; Divers, J; Drechsler, C; Duggirala, R; Elston, RC; Guo, X; Huang, H; Hoffmann, MM; Howard, BV; Ipp, E; Kimmel, PL; Klag, MJ; Knowler, WC; Kohn, OF; Leak, TS; Leehey, DJ; Li, M; Malhotra, A; März, W; Nair, V; Nelson, RG; Nicholas, SB; O'Brien, SJ; Pahl, MV; Parekh, RS; Pezzolesi, MG; Rasooly, RS; Rotimi, CN; Rotter, JI; Schelling, JR; Seldin, MF; Shah, VO; Smiles, AM; Smith, MW; Taylor, KD; Thameem, F; Thornley-Brown, DP; Truitt, BJ; Wanner, C; Weil, EJ; Winkler, CA; Zager, PG; Igo, RP; Hanson, RL; Langefeld, CD; Family Investigation of Nephropathy and Diabetes (FIND) Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND).
PLoS Genet. 2015; 11(8):e1005352-e1005352 [OPEN ACCESS]
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Ling, H; Vincent, K; Pichler, M; Fodde, R; Berindan-Neagoe, I; Slack, FJ; Calin, GA Junk DNA and the long non-coding RNA twist in cancer genetics.
Oncogene. 2015; 34(39):5003-5011 [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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Samwald, M; Miñarro Giménez, JA; Boyce, RD; Freimuth, RR; Adlassnig, KP; Dumontier, M Pharmacogenomic knowledge representation, reasoning and genome-based clinical decision support based on OWL 2 DL ontologies.
BMC Med Inform Decis Mak. 2015; 15(12):12-12 [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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Winkler, TW; Justice, AE; Graff, M; Barata, L; Feitosa, MF; Chu, S; Czajkowski, J; Esko, T; Fall, T; Kilpeläinen, TO; Lu, Y; Mägi, R; Mihailov, E; Pers, TH; Rüeger, S; Teumer, A; Ehret, GB; Ferreira, T; Heard-Costa, NL; Karjalainen, J; Lagou, V; Mahajan, A; Neinast, MD; Prokopenko, I; Simino, J; Teslovich, TM; Jansen, R; Westra, HJ; White, CC; Absher, D; Ahluwalia, TS; Ahmad, S; Albrecht, E; Alves, AC; Bragg-Gresham, JL; de Craen, AJ; Bis, JC; Bonnefond, A; Boucher, G; Cadby, G; Cheng, YC; Chiang, CW; Delgado, G; Demirkan, A; Dueker, N; Eklund, N; Eiriksdottir, G; Eriksson, J; Feenstra, B; Fischer, K; Frau, F; Galesloot, TE; Geller, F; Goel, A; Gorski, M; Grammer, TB; Gustafsson, S; Haitjema, S; Hottenga, JJ; Huffman, JE; Jackson, AU; Jacobs, KB; Johansson, Å; Kaakinen, M; Kleber, ME; Lahti, J; Mateo Leach, I; Lehne, B; Liu, Y; Lo, KS; Lorentzon, M; Luan, J; Madden, PA; Mangino, M; McKnight, B; Medina-Gomez, C; Monda, KL; Montasser, ME; Müller, G; Müller-Nurasyid, M; Nolte, IM; Panoutsopoulou, K; Pascoe, L; Paternoster, L; Rayner, NW; Renström, F; Rizzi, F; Rose, LM; Ryan, KA; Salo, P; Sanna, S; Scharnagl, H; Shi, J; Smith, AV; Southam, L; Stančáková, A; Steinthorsdottir, V; Strawbridge, RJ; Sung, YJ; Tachmazidou, I; Tanaka, T; Thorleifsson, G; Trompet, S; Pervjakova, N; Tyrer, JP; Vandenput, L; van der Laan, SW; van der Velde, N; van Setten, J; van Vliet-Ostaptchouk, JV; Verweij, N; Vlachopoulou, E; Waite, LL; Wang, SR; Wang, Z; Wild, SH; Willenborg, C; Wilson, JF; Wong, A; Yang, J; Yengo, L; Yerges-Armstrong, LM; Yu, L; Zhang, W; Zhao, JH; Andersson, EA; Bakker, SJ; Baldassarre, D; Banasik, K; Barcella, M; Barlassina, C; Bellis, C; Benaglio, P; Blangero, J; Blüher, M; Bonnet, F; Bonnycastle, LL; Boyd, HA; Bruinenberg, M; Buchman, AS; Campbell, H; Chen, YD; Chines, PS; Claudi-Boehm, S; Cole, J; Collins, FS; de Geus, EJ; de Groot, LC; Dimitriou, M; Duan, J; Enroth, S; Eury, E; Farmaki, AE; Forouhi, NG; Friedrich, N; Gejman, PV; Gigante, B; Glorioso, N; Go, AS; Gottesman, O; Gräßler, J; Grallert, H; Grarup, N; Gu, YM; Broer, L; Ham, AC; Hansen, T; Harris, TB; Hartman, CA; Hassinen, M; Hastie, N; Hattersley, AT; Heath, AC; Henders, AK; Hernandez, D; Hillege, H; Holmen, O; Hovingh, KG; Hui, J; Husemoen, LL; Hutri-Kähönen, N; Hysi, PG; Illig, T; De Jager, PL; Jalilzadeh, S; Jørgensen, T; Jukema, JW; Juonala, M; Kanoni, S; Karaleftheri, M; Khaw, KT; Kinnunen, L; Kittner, SJ; Koenig, W; Kolcic, I; Kovacs, P; Krarup, NT; Kratzer, W; Krüger, J; Kuh, D; Kumari, M; Kyriakou, T; Langenberg, C; Lannfelt, L; Lanzani, C; Lotay, V; Launer, LJ; Leander, K; Lindström, J; Linneberg, A; Liu, YP; Lobbens, S; Luben, R; Lyssenko, V; Männistö, S; Magnusson, PK; McArdle, WL; Menni, C; Merger, S; Milani, L; Montgomery, GW; Morris, AP; Narisu, N; Nelis, M; Ong, KK; Palotie, A; Pérusse, L; Pichler, I; Pilia, MG; Pouta, A; Rheinberger, M; Ribel-Madsen, R; Richards, M; Rice, KM; Rice, TK; Rivolta, C; Salomaa, V; Sanders, AR; Sarzynski, MA; Scholtens, S; Scott, RA; Scott, WR; Sebert, S; Sengupta, S; Sennblad, B; Seufferlein, T; Silveira, A; Slagboom, PE; Smit, JH; Sparsø, TH; Stirrups, K; Stolk, RP; Stringham, HM; Swertz, MA; Swift, AJ; Syvänen, AC; Tan, ST; Thorand, B; Tönjes, A; Tremblay, A; Tsafantakis, E; van der Most, PJ; Völker, U; Vohl, MC; Vonk, JM; Waldenberger, M; Walker, RW; Wennauer, R; Widén, E; Willemsen, G; Wilsgaard, T; Wright, AF; Zillikens, MC; van Dijk, SC; van Schoor, NM; Asselbergs, FW; de Bakker, PI; Beckmann, JS; Beilby, J; Bennett, DA; Bergma ... The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
PLoS Genet. 2015; 11(10):e1005378-e1005378 [OPEN ACCESS]
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2014

Bettermann, K; Hohensee, T; Haybaeck, J Steatosis and steatohepatitis: complex disorders.
Int J Mol Sci. 2014; 15(6):9924-9944 [OPEN ACCESS]
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Egger, G; Roetzer, KM; Noor, A; Lionel, AC; Mahmood, H; Schwarzbraun, T; Boright, O; Mikhailov, A; Marshall, CR; Windpassinger, C; Petek, E; Scherer, SW; Kaschnitz, W; Vincent, JB Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families.
Neurogenetics. 2014; 15(2):117-127
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Holmes, MV; Exeter, HJ; Folkersen, L; Nelson, CP; Guardiola, M; Cooper, JA; Sofat, R; Boekholdt, SM; Khaw, KT; Li, KW; Smith, AJ; Van't Hooft, F; Eriksson, P; Franco-Cereceda, A; Asselbergs, FW; Boer, JM; Onland-Moret, NC; Hofker, M; Erdmann, J; Kivimaki, M; Kumari, M; Reiner, AP; Keating, BJ; Humphries, SE; Hingorani, AD; Mallat, Z; Samani, NJ; Talmud, PJ; CARDIoGRAM Consortium Novel genetic approach to investigate the role of plasma secretory phospholipase A2 (sPLA2)-V isoenzyme in coronary heart disease: modified Mendelian randomization analysis using PLA2G5 expression levels.
Circ Cardiovasc Genet. 2014; 7(2):144-150 [OPEN ACCESS]
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Karastaneva, A; Urban, C; Lackner, H; Schwinger, W Dynamics of Graft Function Measured by DNA-Technology in a Patient with Severe Aplastic Anemia and Repeated Stem Cell Transplantation.
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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.
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Mandorfer, M; Reiberger, T; Payer, BA; Breitenecker, F; Aichelburg, MC; Obermayer-Pietsch, B; Rieger, A; Puoti, M; Zangerle, R; Trauner, M; Peck-Radosavljevic, M Revisiting predictors of virologic response to PEGIFN + RBV therapy in HIV-/HCV-coinfected patients: the role of metabolic factors and elevated GGT levels.
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