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

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Publikationen

Suchbegriffe: POLYMORPHISM, SINGLE NUCLEOTIDE - GENETICS , . Treffer: 81

2019

Berroterán-Infante, N; Tadić, M; Hacker, M; Wadsak, W; Mitterhauser, M Binding Affinity of Some Endogenous and Synthetic TSPO Ligands Regarding the rs6971 Polymorphism.
Int J Mol Sci. 2019; 20(3): [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 (- Case Report) [OPEN ACCESS]
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Hamilton, EMC; Bertini, E; Kalaydjieva, L; Morar, B; Dojčáková, D; Liu, J; Vanderver, A; Curiel, J; Persoon, CM; Diodato, D; Pinelli, L; van der Meij, NL; Plecko, B; Blaser, S; Wolf, NI; Waisfisz, Q; Abbink, TEM; van der Knaap, MS; Recessive H-ABC Research Group UFM1 founder mutation in the Roma population causes recessive variant of H-ABC.
Neurology. 2017; 89(17):1821-1828 [OPEN ACCESS]
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Renner, W; Langsenlehner, U; Krenn-Pilko, S; Eder, P; Langsenlehner, T BCL2 genotypes and prostate cancer survival.
Strahlenther Onkol. 2017; 193(6):466-471 [OPEN ACCESS]
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Saleheen, D; Zhao, W; Young, R; Nelson, CP; Ho, W; Ferguson, JF; Rasheed, A; Ou, K; Nurnberg, ST; Bauer, RC; Goel, A; Do, R; Stewart, AFR; Hartiala, J; Zhang, W; Thorleifsson, G; Strawbridge, RJ; Sinisalo, J; Kanoni, S; Sedaghat, S; Marouli, E; Kristiansson, K; Hua Zhao, J; Scott, R; Gauguier, D; Shah, SH; Smith, AV; van Zuydam, N; Cox, AJ; Willenborg, C; Kessler, T; Zeng, L; Province, MA; Ganna, A; Lind, L; Pedersen, NL; White, CC; Joensuu, A; Edi Kleber, M; Hall, AS; März, W; Salomaa, V; O'Donnell, C; Ingelsson, E; Feitosa, MF; Erdmann, J; Bowden, DW; Palmer, CNA; Gudnason, V; Faire, U; Zalloua, P; Wareham, N; Thompson, JR; Kuulasmaa, K; Dedoussis, G; Perola, M; Dehghan, A; Chambers, JC; Kooner, J; Allayee, H; Deloukas, P; McPherson, R; Stefansson, K; Schunkert, H; Kathiresan, S; Farrall, M; Marcel Frossard, P; Rader, DJ; Samani, NJ; Reilly, MP Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions.
Circulation. 2017; 135(24):2336-2353 [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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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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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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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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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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Schweiger, R; Kaufman, S; Laaksonen, R; Kleber, ME; März, W; Eskin, E; Rosset, S; Halperin, E Fast and Accurate Construction of Confidence Intervals for Heritability.
Am J Hum Genet. 2016; 98(6):1181-1192 [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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Walford, GA; Gustafsson, S; Rybin, D; Stančáková, A; Chen, H; Liu, CT; Hong, J; Jensen, RA; Rice, K; Morris, AP; Mägi, R; Tönjes, A; Prokopenko, I; Kleber, ME; Delgado, G; Silbernagel, G; Jackson, AU; Appel, EV; Grarup, N; Lewis, JP; Montasser, ME; Landenvall, C; Staiger, H; Luan, J; Frayling, TM; Weedon, MN; Xie, W; Morcillo, S; Martínez-Larrad, MT; Biggs, ML; Chen, YD; Corbaton-Anchuelo, A; Færch, K; Gómez-Zumaquero, JM; Goodarzi, MO; Kizer, JR; Koistinen, HA; Leong, A; Lind, L; Lindgren, C; Machicao, F; Manning, AK; Martín-Núñez, GM; Rojo-Martínez, G; Rotter, JI; Siscovick, DS; Zmuda, JM; Zhang, Z; Serrano-Rios, M; Smith, U; Soriguer, F; Hansen, T; Jørgensen, TJ; Linnenberg, A; Pedersen, O; Walker, M; Langenberg, C; Scott, RA; Wareham, NJ; Fritsche, A; Häring, HU; Stefan, N; Groop, L; O'Connell, JR; Boehnke, M; Bergman, RN; Collins, FS; Mohlke, KL; Tuomilehto, J; März, W; Kovacs, P; Stumvoll, M; Psaty, BM; Kuusisto, J; Laakso, M; Meigs, JB; Dupuis, J; Ingelsson, E; Florez, JC Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci.
Diabetes. 2016; 65(10):3200-3211 [OPEN ACCESS]
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2015

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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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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Debette, S; Ibrahim Verbaas, CA; Bressler, J; Schuur, M; Smith, A; Bis, JC; Davies, G; Wolf, C; Gudnason, V; Chibnik, LB; Yang, Q; deStefano, AL; de Quervain, DJ; Srikanth, V; Lahti, J; Grabe, HJ; Smith, JA; Priebe, L; Yu, L; Karbalai, N; Hayward, C; Wilson, JF; Campbell, H; Petrovic, K; Fornage, M; Chauhan, G; Yeo, R; Boxall, R; Becker, J; Stegle, O; Mather, KA; Chouraki, V; Sun, Q; Rose, LM; Resnick, S; Oldmeadow, C; Kirin, M; Wright, AF; Jonsdottir, MK; Au, R; Becker, A; Amin, N; Nalls, MA; Turner, ST; Kardia, SL; Oostra, B; Windham, G; Coker, LH; Zhao, W; Knopman, DS; Heiss, G; Griswold, ME; Gottesman, RF; Vitart, V; Hastie, ND; Zgaga, L; Rudan, I; Polasek, O; Holliday, EG; Schofield, P; Choi, SH; Tanaka, T; An, Y; Perry, RT; Kennedy, RE; Sale, MM; Wang, J; Wadley, VG; Liewald, DC; Ridker, PM; Gow, AJ; Pattie, A; Starr, JM; Porteous, D; Liu, X; Thomson, R; Armstrong, NJ; Eiriksdottir, G; Assareh, AA; Kochan, NA; Widen, E; Palotie, A; Hsieh, YC; Eriksson, JG; Vogler, C; van Swieten, JC; Shulman, JM; Beiser, A; Rotter, J; Schmidt, CO; Hoffmann, W; Nöthen, MM; Ferrucci, L; Attia, J; Uitterlinden, AG; Amouyel, P; Dartigues, JF; Amieva, H; Räikkönen, K; Garcia, M; Wolf, PA; Hofman, A; Longstreth, WT; Psaty, BM; Boerwinkle, E; DeJager, PL; Sachdev, PS; Schmidt, R; Breteler, MM; Teumer, A; Lopez, OL; Cichon, S; Chasman, DI; Grodstein, F; Müller-Myhsok, B; Tzourio, C; Papassotiropoulos, A; Bennett, DA; Ikram, MA; Deary, IJ; van Duijn, CM; Launer, L; Fitzpatrick, AL; Seshadri, S; Mosley, TH; Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium.
Biol Psychiatry. 2015; 77(8):749-763 [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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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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Locke, AE; Kahali, B; Berndt, SI; Justice, AE; Pers, TH; Day, FR; Powell, C; Vedantam, S; Buchkovich, ML; Yang, J; Croteau-Chonka, DC; Esko, T; Fall, T; Ferreira, T; Gustafsson, S; Kutalik, Z; Luan, J; Mägi, R; Randall, JC; Winkler, TW; Wood, AR; Workalemahu, T; Faul, JD; Smith, JA; Zhao, JH; Zhao, W; Chen, J; Fehrmann, R; Hedman, ÅK; Karjalainen, J; Schmidt, EM; Absher, D; Amin, N; Anderson, D; Beekman, M; Bolton, JL; Bragg-Gresham, JL; Buyske, S; Demirkan, A; Deng, G; Ehret, GB; Feenstra, B; Feitosa, MF; Fischer, K; Goel, A; Gong, J; Jackson, AU; Kanoni, S; Kleber, ME; Kristiansson, K; Lim, U; Lotay, V; Mangino, M; Leach, IM; Medina-Gomez, C; Medland, SE; Nalls, MA; Palmer, CD; Pasko, D; Pechlivanis, S; Peters, MJ; Prokopenko, I; Shungin, D; Stančáková, A; Strawbridge, RJ; Sung, YJ; Tanaka, T; Teumer, A; Trompet, S; van der Laan, SW; van Setten, J; Van Vliet-Ostaptchouk, JV; Wang, Z; Yengo, L; Zhang, W; Isaacs, A; Albrecht, E; Ärnlöv, J; Arscott, GM; Attwood, AP; Bandinelli, S; Barrett, A; Bas, IN; Bellis, C; Bennett, AJ; Berne, C; Blagieva, R; Blüher, M; Böhringer, S; Bonnycastle, LL; Böttcher, Y; Boyd, HA; Bruinenberg, M; Caspersen, IH; Chen, YI; Clarke, R; Daw, EW; de Craen, AJM; Delgado, G; Dimitriou, M; Doney, ASF; Eklund, N; Estrada, K; Eury, E; Folkersen, L; Fraser, RM; Garcia, ME; Geller, F; Giedraitis, V; Gigante, B; Go, AS; Golay, A; Goodall, AH; Gordon, SD; Gorski, M; Grabe, HJ; Grallert, H; Grammer, TB; Gräßler, J; Grönberg, H; Groves, CJ; Gusto, G; Haessler, J; Hall, P; Haller, T; Hallmans, G; Hartman, CA; Hassinen, M; Hayward, C; Heard-Costa, NL; Helmer, Q; Hengstenberg, C; Holmen, O; Hottenga, JJ; James, AL; Jeff, JM; Johansson, Å; Jolley, J; Juliusdottir, T; Kinnunen, L; Koenig, W; Koskenvuo, M; Kratzer, W; Laitinen, J; Lamina, C; Leander, K; Lee, NR; Lichtner, P; Lind, L; Lindström, J; Lo, KS; Lobbens, S; Lorbeer, R; Lu, Y; Mach, F; Magnusson, PKE; Mahajan, A; McArdle, WL; McLachlan, S; Menni, C; Merger, S; Mihailov, E; Milani, L; Moayyeri, A; Monda, KL; Morken, MA; Mulas, A; Müller, G; Müller-Nurasyid, M; Musk, AW; Nagaraja, R; Nöthen, MM; Nolte, IM; Pilz, S; Rayner, NW; Renstrom, F; Rettig, R; Ried, JS; Ripke, S; Robertson, NR; Rose, LM; Sanna, S; Scharnagl, H; Scholtens, S; Schumacher, FR; Scott, WR; Seufferlein, T; Shi, J; Smith, AV; Smolonska, J; Stanton, AV; Steinthorsdottir, V; Stirrups, K; Stringham, HM; Sundström, J; Swertz, MA; Swift, AJ; Syvänen, AC; Tan, ST; Tayo, BO; Thorand, B; Thorleifsson, G; Tyrer, JP; Uh, HW; Vandenput, L; Verhulst, FC; Vermeulen, SH; Verweij, N; Vonk, JM; Waite, LL; Warren, HR; Waterworth, D; Weedon, MN; Wilkens, LR; Willenborg, C; Wilsgaard, T; Wojczynski, MK; Wong, A; Wright, AF; Zhang, Q; LifeLines Cohort Study; Brennan, EP; Choi, M; Dastani, Z; Drong, AW; Eriksson, P; Franco-Cereceda, A; Gådin, JR; Gharavi, AG; Goddard, ME; Handsaker, RE; Huang, J; Karpe, F; Kathiresan, S; Keildson, S; Kiryluk, K; Kubo, M; Lee, JY; Liang, L; Lifton, RP; Ma, B; McCarroll, SA; McKnight, AJ; Min, JL; Moffatt, MF; Montgomery, GW; Murabito, JM; Nicholson, G; Nyholt, DR; Okada, Y; Perry, JRB; Dorajoo, R; Reinmaa, E; Salem, RM; Sandholm, N; Scott, RA; Stolk, L; Takahashi, A; Tanaka, T; van 't Hooft, FM; Vinkhuyzen, AAE; Westra, HJ; Zheng, W; Zondervan, KT; ADIPOGen Consortium; AGEN-BMI Working Group; CARDIOGRAMplusC4D Consortium; CKDGen Consortium; GLGC; ICBP; MAGIC Investigators; MuTHER Consortium; MIGen Consortium; PAGE Consortium; ReproGen Consortium; GENIE Consortium; International Endogene Consort ... Genetic studies of body mass index yield new insights for obesity biology.
Nature. 2015; 518(7538):197-206 [OPEN ACCESS]
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Lopez, LM; Hill, WD; Harris, SE; Valdes Hernandez, M; Munoz Maniega, S; Bastin, ME; Bailey, E; Smith, C; McBride, M; McClure, J; Graham, D; Dominiczak, A; Yang, Q; Fornage, M; Ikram, MA; Debette, S; Launer, L; Bis, JC; Schmidt, R; Seshadri, S; Porteous, DJ; Starr, J; Deary, IJ; Wardlaw, JM Genes from a translational analysis support a multifactorial nature of white matter hyperintensities.
Stroke. 2015; 46(2):341-347 [OPEN ACCESS]
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Marth, C; Hubalek, M; Petru, E; Polterauer, S; Reinthaller, A; Schauer, C; Scholl-Firon, T; Singer, CF; Zschocke, J; Zeimet, AG AGO Austria recommendations for genetic testing of patients with ovarian cancer.
Wien Klin Wochenschr. 2015; 127(15-16):652-654 [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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Shungin, D; Winkler, TW; Croteau-Chonka, DC; Ferreira, T; Locke, AE; Mägi, R; Strawbridge, RJ; Pers, TH; Fischer, K; Justice, AE; Workalemahu, T; Wu, JMW; Buchkovich, ML; Heard-Costa, NL; Roman, TS; Drong, AW; Song, C; Gustafsson, S; Day, FR; Esko, T; Fall, T; Kutalik, Z; Luan, J; Randall, JC; Scherag, A; Vedantam, S; Wood, AR; Chen, J; Fehrmann, R; Karjalainen, J; Kahali, B; Liu, CT; Schmidt, EM; Absher, D; Amin, N; Anderson, D; Beekman, M; Bragg-Gresham, JL; Buyske, S; Demirkan, A; Ehret, GB; Feitosa, MF; Goel, A; Jackson, AU; Johnson, T; Kleber, ME; Kristiansson, K; Mangino, M; Leach, IM; Medina-Gomez, C; Palmer, CD; Pasko, D; Pechlivanis, S; Peters, MJ; Prokopenko, I; Stančáková, A; Sung, YJ; Tanaka, T; Teumer, A; Van Vliet-Ostaptchouk, JV; Yengo, L; Zhang, W; Albrecht, E; Ärnlöv, J; Arscott, GM; Bandinelli, S; Barrett, A; Bellis, C; Bennett, AJ; Berne, C; Blüher, M; Böhringer, S; Bonnet, F; Böttcher, Y; Bruinenberg, M; Carba, DB; Caspersen, IH; Clarke, R; Daw, EW; Deelen, J; Deelman, E; Delgado, G; Doney, AS; Eklund, N; Erdos, MR; Estrada, K; Eury, E; Friedrich, N; Garcia, ME; Giedraitis, V; Gigante, B; Go, AS; Golay, A; Grallert, H; Grammer, TB; Gräßler, J; Grewal, J; Groves, CJ; Haller, T; Hallmans, G; Hartman, CA; Hassinen, M; Hayward, C; Heikkilä, K; Herzig, KH; Helmer, Q; Hillege, HL; Holmen, O; Hunt, SC; Isaacs, A; Ittermann, T; James, AL; Johansson, I; Juliusdottir, T; Kalafati, IP; Kinnunen, L; Koenig, W; Kooner, IK; Kratzer, W; Lamina, C; Leander, K; Lee, NR; Lichtner, P; Lind, L; Lindström, J; Lobbens, S; Lorentzon, M; Mach, F; Magnusson, PK; Mahajan, A; McArdle, WL; Menni, C; Merger, S; Mihailov, E; Milani, L; Mills, R; Moayyeri, A; Monda, KL; Mooijaart, SP; Mühleisen, TW; Mulas, A; Müller, G; Müller-Nurasyid, M; Nagaraja, R; Nalls, MA; Narisu, N; Glorioso, N; Nolte, IM; Olden, M; Rayner, NW; Renstrom, F; Ried, JS; Robertson, NR; Rose, LM; Sanna, S; Scharnagl, H; Scholtens, S; Sennblad, B; Seufferlein, T; Sitlani, CM; Smith, AV; Stirrups, K; Stringham, HM; Sundström, J; Swertz, MA; Swift, AJ; Syvänen, AC; Tayo, BO; Thorand, B; Thorleifsson, G; Tomaschitz, A; Troffa, C; van Oort, FV; Verweij, N; Vonk, JM; Waite, LL; Wennauer, R; Wilsgaard, T; Wojczynski, MK; Wong, A; Zhang, Q; Zhao, JH; Brennan, EP; Choi, M; Eriksson, P; Folkersen, L; Franco-Cereceda, A; Gharavi, AG; Hedman, ÅK; Hivert, MF; Huang, J; Kanoni, S; Karpe, F; Keildson, S; Kiryluk, K; Liang, L; Lifton, RP; Ma, B; McKnight, AJ; McPherson, R; Metspalu, A; Min, JL; Moffatt, MF; Montgomery, GW; Murabito, JM; Nicholson, G; Nyholt, DR; Olsson, C; Perry, JR; Reinmaa, E; Salem, RM; Sandholm, N; Schadt, EE; Scott, RA; Stolk, L; Vallejo, EE; Westra, HJ; Zondervan, KT; ADIPOGen Consortium; CARDIOGRAMplusC4D Consortium; CKDGen Consortium; GEFOS Consortium; GENIE Consortium; GLGC; ICBP; International Endogene Consortium; LifeLines Cohort Study; MAGIC Investigators; MuTHER Consortium; PAGE Consortium; ReproGen Consortium; Amouyel, P; Arveiler, D; Bakker, SJ; Beilby, J; Bergman, RN; Blangero, J; Brown, MJ; Burnier, M; Campbell, H; Chakravarti, A; Chines, PS; Claudi-Boehm, S; Collins, FS; Crawford, DC; Danesh, J; de Faire, U; de Geus, EJ; Dörr, M; Erbel, R; Eriksson, JG; Farrall, M; Ferrannini, E; Ferrières, J; Forouhi, NG; Forrester, T; Franco, OH; Gansevoort, RT; Gieger, C; Gudnason, V; Haiman, CA; Harris, TB; Hattersley, AT; Heliövaara, M; Hicks, AA; Hingorani, AD; Hoffmann, W; Hofman, A; Homuth, G; Humphries, SE; Hyppönen, E; Illig, T; Jarvelin, MR; Johansen, B; Jousilahti ... New genetic loci link adipose and insulin biology to body fat distribution.
Nature. 2015; 518(7538):187-196 [OPEN ACCESS]
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2014

Ibrahim-Verbaas, CA; Fornage, M; Bis, JC; Choi, SH; Psaty, BM; Meigs, JB; Rao, M; Nalls, M; Fontes, JD; O'Donnell, CJ; Kathiresan, S; Ehret, GB; Fox, CS; Malik, R; Dichgans, M; Schmidt, H; Lahti, J; Heckbert, SR; Lumley, T; Rice, K; Rotter, JI; Taylor, KD; Folsom, AR; Boerwinkle, E; Rosamond, WD; Shahar, E; Gottesman, RF; Koudstaal, PJ; Amin, N; Wieberdink, RG; Dehghan, A; Hofman, A; Uitterlinden, AG; Destefano, AL; Debette, S; Xue, L; Beiser, A; Wolf, PA; Decarli, C; Ikram, MA; Seshadri, S; Mosley, TH; Longstreth, WT; van Duijn, CM; Launer, LJ Predicting stroke through genetic risk functions: the CHARGE Risk Score Project.
Stroke. 2014; 45(2):403-412 [OPEN ACCESS]
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Langsenlehner, T; Thurner, EM; Renner, W; Gerger, A; Kapp, KS; Langsenlehner, U Association of genetic variants in VEGF-A with clinical recurrence in prostate cancer patients treated with definitive radiotherapy.
Strahlenther Onkol. 2014; 190(4):364-369
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Oei, L; Estrada, K; Duncan, EL; Christiansen, C; Liu, CT; Langdahl, BL; Obermayer-Pietsch, B; Riancho, JA; Prince, RL; van Schoor, NM; McCloskey, E; Hsu, YH; Evangelou, E; Ntzani, E; Evans, DM; Alonso, N; Husted, LB; Valero, C; Hernandez, JL; Lewis, JR; Kaptoge, SK; Zhu, K; Cupples, LA; Medina-Gómez, C; Vandenput, L; Kim, GS; Hun Lee, S; Castaño-Betancourt, MC; Oei, EH; Martinez, J; Daroszewska, A; van der Klift, M; Mellström, D; Herrera, L; Karlsson, MK; Hofman, A; Ljunggren, Ö; Pols, HA; Stolk, L; van Meurs, JB; Ioannidis, JP; Zillikens, MC; Lips, P; Karasik, D; Uitterlinden, AG; Styrkarsdottir, U; Brown, MA; Koh, JM; Richards, JB; Reeve, J; Ohlsson, C; Ralston, SH; Kiel, DP; Rivadeneira, F Genome-wide association study for radiographic vertebral fractures: a potential role for the 16q24 BMD locus.
Bone. 2014; 59(3):20-27 [OPEN ACCESS]
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Seppälä, I; Kleber, ME; Lyytikäinen, LP; Hernesniemi, JA; Mäkelä, KM; Oksala, N; Laaksonen, R; Pilz, S; Tomaschitz, A; Silbernagel, G; Boehm, BO; Grammer, TB; Koskinen, T; Juonala, M; Hutri-Kähönen, N; Alfthan, G; Viikari, JS; Kähonen, M; Raitakari, OT; März, W; Meinitzer, A; Lehtimäki, T; AtheroRemo Consortium Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.
Eur Heart J. 2014; 35(8):524-531 [OPEN ACCESS]
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2013

Absenger, G; Szkandera, J; Stotz, M; Pichler, M; Winder, T; Langsenlehner, T; Langsenlehner, U; Samonigg, H; Renner, W; Gerger, A A common and functional gene variant in the vascular endothelial growth factor a predicts clinical outcome in early-stage breast cancer.
Mol Carcinog. 2013; 52 Suppl 1(9):E96-102
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Anderson, CD; Biffi, A; Nalls, MA; Devan, WJ; Schwab, K; Ayres, AM; Valant, V; Ross, OA; Rost, NS; Saxena, R; Viswanathan, A; Worrall, BB; Brott, TG; Goldstein, JN; Brown, D; Broderick, JP; Norrving, B; Greenberg, SM; Silliman, SL; Hansen, BM; Tirschwell, DL; Lindgren, A; Slowik, A; Schmidt, R; Selim, M; Roquer, J; Montaner, J; Singleton, AB; Kidwell, CS; Woo, D; Furie, KL; Meschia, JF; Rosand, J; on behalf of the International Stroke Genetics Consortium Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral Hemorrhage.
Stroke. 2013; 44(3):612-619 [OPEN ACCESS]
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Köttgen, A; Albrecht, E; Teumer, A; Vitart, V; Krumsiek, J; Hundertmark, C; Pistis, G; Ruggiero, D; Oeaghdha, CM; Haller, T; Yang, Q; Tanaka, T; Johnson, AD; Kutalik, Z; Smith, AV; Shi, J; Struchalin, M; Middelberg, RP; Brown, MJ; Gaffo, AL; Pirastu, N; Li, G; Hayward, C; Zemunik, T; Huffman, J; Yengo, L; Zhao, JH; Demirkan, A; Feitosa, MF; Liu, X; Malerba, G; Lopez, LM; van der Harst, P; Li, X; Kleber, ME; Hicks, AA; Nolte, IM; Johansson, A; Murgia, F; Wild, SH; Bakker, SJ; Peden, JF; Dehghan, A; Steri, M; Tenesa, A; Lagou, V; Salo, P; Mangino, M; Rose, LM; Lehtimäki, T; Woodward, OM; Okada, Y; Tin, A; Müller, C; Oldmeadow, C; Putku, M; Czamara, D; Kraft, P; Frogheri, L; Thun, GA; Grotevendt, A; Gislason, GK; Harris, TB; Launer, LJ; McArdle, P; Shuldiner, AR; Boerwinkle, E; Coresh, J; Schmidt, H; Schallert, M; Martin, NG; Montgomery, GW; Kubo, M; Nakamura, Y; Tanaka, T; Munroe, PB; Samani, NJ; Jacobs, DR; Liu, K; D'Adamo, P; Ulivi, S; Rotter, JI; Psaty, BM; Vollenweider, P; Waeber, G; Campbell, S; Devuyst, O; Navarro, P; Kolcic, I; Hastie, N; Balkau, B; Froguel, P; Esko, T; Salumets, A; Khaw, KT; Langenberg, C; Wareham, NJ; Isaacs, A; Kraja, A; Zhang, Q; Wild, PS; Scott, RJ; Holliday, EG; Org, E; Viigimaa, M; Bandinelli, S; Metter, JE; Lupo, A; Trabetti, E; Sorice, R; Döring, A; Lattka, E; Strauch, K; Theis, F; Waldenberger, M; Wichmann, HE; Davies, G; Gow, AJ; Bruinenberg, M; LifeLines Cohort Study; Stolk, RP; Kooner, JS; Zhang, W; Winkelmann, BR; Boehm, BO; Lucae, S; Penninx, BW; Smit, JH; Curhan, G; Mudgal, P; Plenge, RM; Portas, L; Persico, I; Kirin, M; Wilson, JF; Leach, IM; van Gilst, WH; Goel, A; Ongen, H; Hofman, A; Rivadeneira, F; Uitterlinden, AG; Imboden, M; von Eckardstein, A; Cucca, F; Nagaraja, R; Piras, MG; Nauck, M; Schurmann, C; Budde, K;Ernst, F; Farrington, SM; Theodoratou, E; Prokopenko, I; Stumvoll, M; Jula, A; Perola, M; Salomaa, V; Shin, SY; Spector, TD; Sala, C; Ridker, PM; Kähönen, M; Viikari, J; Hengstenberg, C; Nelson, CP; CARDIoGRAM Consortium;DIAGRAM Consortium;ICBP Consortium MAGIC Consortium;Meschia, JF;Nalls, MA;Sharma, P;Singleton, AB;Kamatani, N;Zeller, T;Burnier, M;Attia, J;Laan, M;Klopp, N;Hillege, HL;Kloiber, S;Choi, H Pirastu, M Tore, S Probst-Hensch, NM Völzke, H; Gudnason, V; Parsa, A; Schmidt, R; Whitfield, JB; Fornage, M; Gasparini, P; Siscovick, DS; Polasek, O; Campbell, H; Rudan, I; Bouatia-Naji, N; Metspalu, A; Loos, RJ; van Duijn, CM; Borecki, IB; Ferrucci, L; Gambaro, G;Deary, IJ; Wolffenbuttel, BH; Chambers, JC; März, W;Pramstaller, PP; Snieder, H; Gyllensten, U; Wright, AF; Navis, G; Watkins, H; Witteman, JCM; Sanna, S; Schipf, S; Dunlop, MG; Tönjes, A; Ripatti, S; Soranzo, N; Toniolo, D; Chasman, DI; Raitakari, O; Kao, WHL; Ciullo, M; Fox, CS; Caulfield, M; Bochud, M; Gieger, C Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
Nat Genet. 2013; 45(2): 145-154. [OPEN ACCESS]
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Lieb, W; Jansen, H; Loley, C; Pencina, MJ; Nelson, CP; Newton-Cheh, C; Kathiresan, S; Reilly, MP; Assimes, TL; Boerwinkle, E; Hall, AS; Hengstenberg, C; Laaksonen, R; McPherson, R; Thorsteinsdottir, U; Ziegler, A; Peters, A; Thompson, JR; König, IR; Erdmann, J; Samani, NJ; Vasan, RS; Schunkert, H; CARDIoGRAM; Assimes, TL; Deloukas, P; Erdmann, J; Holm, H; Kathiresan, S; König, IR; McPherson, R; Reilly, MP; Roberts, R; Samani, NJ; Schunkert, H; Stewart, AF Genetic predisposition to higher blood pressure increases coronary artery disease risk.
Hypertension. 2013; 61(5):995-1001 [OPEN ACCESS]
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Sabater-Lleal, M; Huang, J; Chasman, D; Naitza, S; Dehghan, A; Johnson, AD; Teumer, A; Reiner, AP; Folkersen, L; Basu, S; Rudnicka, AR; Trompet, S; Mälarstig, A; Baumert, J; Bis, JC; Guo, X; Hottenga, JJ; Shin, SY; Lopez, LM; Lahti, J; Tanaka, T; Yanek, LR; Oudot-Mellakh, T; Wilson, JF; Navarro, P; Huffman, JE; Zemunik, T; Redline, S; Mehra, R; Pulanic, D; Rudan, I; Wright, AF; Kolcic, I; Polasek, O; Wild, SH; Campbell, H; Curb, JD; Wallace, R; Liu, S; Eaton, CB; Becker, DM; Becker, LC; Bandinelli, S; Räikkönen, K; Widen, E; Palotie, A; Fornage, M; Green, D; Gross, M; Davies, G; Harris, SE; Liewald, DC; Starr, JM; Williams, FM; Grant, PJ; Spector, TD; Strawbridge, RJ; Silveira, A; Sennblad, B; Rivadeneira, F; Uitterlinden, AG; Franco, OH; Hofman, A; van Dongen, J; Willemsen, G; Boomsma, DI; Yao, J; Swords Jenny, N; Haritunians, T; McKnight, B; Lumley, T; Taylor, KD; Rotter, JI; Psaty, BM; Peters, A; Gieger, C; Illig, T; Grotevendt, A; Homuth, G; Völzke, H; Kocher, T; Goel, A; Franzosi, MG; Seedorf, U; Clarke, R; Steri, M; Tarasov, KV; Sanna, S; Schlessinger, D; Stott, DJ; Sattar, N; Buckley, BM; Rumley, A; Lowe, GD; McArdle, WL; Chen, MH; Tofler, GH; Song, J; Boerwinkle, E; Folsom, AR; Rose, LM; Franco-Cereceda, A; Teichert, M; Ikram, MA; Mosley, TH; Bevan, S; Dichgans, M; Rothwell, PM; Sudlow, CL; Hopewell, JC; Chambers, JC; Saleheen, D; Kooner, JS; Danesh, J; Nelson, CP; Erdmann, J; Reilly, MP; Kathiresan, S; Schunkert, H; Morange, PE; Ferrucci, L; Eriksson, JG; Jacobs, D; Deary, IJ; Soranzo, N; Witteman, JC; de Geus, EJ; Tracy, RP; Hayward, C; Koenig, W; Cucca, F; Jukema, JW; Eriksson, P; Seshadri, S; Markus, HS; Watkins, H; Samani, NJ; VTE Consortium; STROKE Consortium; Wellcome Trust Case Control Consortium 2 (WTCCC2); C4D Consortium; CARDIoGRAM Consortium; Wallaschofski, H; Smith, NL; Tregouet, D; Ridker, PM; Tang, W; Strachan, DP; Hamsten, A; O'Donnell, CJ Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.
Circulation. 2013; 128(12):1310-1324 [OPEN ACCESS]
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Scherzer, TM; Stättermayer, AF; Stauber, R; Maieron, A; Strasser, M; Laferl, H; Schwarzer, R; Datz, C; Rutter, K; Beinhardt, S; Steindl-Munda, P; Hofer, H; Ferenci, P Effect of gender and ITPA polymorphisms on ribavirin-induced anemia in chronic hepatitis C patients.
J Hepatol. 2013; 59(5):964-971
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Steinwender, G; Lindner, E; Weger, M; Plainer, S; Renner, W; Ardjomand, N; El-Shabrawi, Y Association between polymorphism of the vitamin D metabolism gene CYP27B1 and HLA-B27-associated uveitis. Is a state of relative immunodeficiency pathogenic in HLA B27-positive uveitis?
PLoS One. 2013; 8(4):e62244-e62244 [OPEN ACCESS]
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Szkandera, J; Absenger, G; Pichler, M; Stotz, M; Langsenlehner, T; Samonigg, H; Renner, W; Gerger, A Association of common gene variants in vitamin D modulating genes and colon cancer recurrence.
J Cancer Res Clin Oncol. 2013; 139(9):1457-1464
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Wiesner, T; Fried, I; Cerroni, L; Kutzner, H Molecular biology methods to improve diagnosis and prognosis of melanocytic tumors.
J Dtsch Dermatol Ges. 2013; 11 Suppl 4(6):19-24 (- Case Report)
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2012

Barral, S; Fernández-Cadenas, I; Bis, JC; Montaner, J; Ikram, AM; Launer, LJ; Fornage, M; Schmidt, H; Brickman, AM; Seshadri, S; Mayeux, R No association of ALOX5AP polymorphisms with risk of MRI-defined brain infarcts.
Neurobiol Aging. 2012; 33(3):629.e1-629.e3 [OPEN ACCESS]
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Estrada, K; Styrkarsdottir, U; Evangelou, E; Hsu, YH; Duncan, EL; Ntzani, EE; Oei, L; Albagha, OM; Amin, N; Kemp, JP; Koller, DL; Li, G; Liu, CT; Minster, RL; Moayyeri, A; Vandenput, L; Willner, D; Xiao, SM; Yerges-Armstrong, LM; Zheng, HF; Alonso, N; Eriksson, J; Kammerer, CM; Kaptoge, SK; Leo, PJ; Thorleifsson, G; Wilson, SG; Wilson, JF; Aalto, V; Alen, M; Aragaki, AK; Aspelund, T; Center, JR; Dailiana, Z; Duggan, DJ; Garcia, M; Garcia-Giralt, N; Giroux, S; Hallmans, G; Hocking, LJ; Husted, LB; Jameson, KA; Khusainova, R; Kim, GS; Kooperberg, C; Koromila, T; Kruk, M; Laaksonen, M; Lacroix, AZ; Lee, SH; Leung, PC; Lewis, JR; Masi, L; Mencej-Bedrac, S; Nguyen, TV; Nogues, X; Patel, MS; Prezelj, J; Rose, LM; Scollen, S; Siggeirsdottir, K; Smith, AV; Svensson, O; Trompet, S; Trummer, O; van Schoor, NM; Woo, J; Zhu, K; Balcells, S; Brandi, ML; Buckley, BM; Cheng, S; Christiansen, C; Cooper, C; Dedoussis, G; Ford, I; Frost, M; Goltzman, D; González-Macías, J; Kähönen, M; Karlsson, M; Khusnutdinova, E; Koh, JM; Kollia, P; Langdahl, BL; Leslie, WD; Lips, P; Ljunggren, Ö; Lorenc, RS; Marc, J; Mellström, D; Obermayer-Pietsch, B; Olmos, JM; Pettersson-Kymmer, U; Reid, DM; Riancho, JA; Ridker, PM; Rousseau, F; Slagboom, PE; Tang, NL; Urreizti, R; Van Hul, W; Viikari, J; Zarrabeitia, MT; Aulchenko, YS; Castano-Betancourt, M; Grundberg, E; Herrera, L; Ingvarsson, T; Johannsdottir, H; Kwan, T; Li, R; Luben, R; Medina-Gómez, C; Palsson, ST; Reppe, S; Rotter, JI; Sigurdsson, G; van Meurs, JB; Verlaan, D; Williams, FM; Wood, AR; Zhou, Y; Gautvik, KM; Pastinen, T; Raychaudhuri, S; Cauley, JA; Chasman, DI; Clark, GR; Cummings, SR; Danoy, P; Dennison, EM; Eastell, R; Eisman, JA; Gudnason, V; Hofman, A; Jackson, RD; Jones, G; Jukema, JW; Khaw, KT; Lehtimäki, T; Liu, Y; Lorentzon, M; McCloskey, E; Mitchell, BD; Nandakumar, K; Nicholson, GC; Oostra, BA; Peacock, M; Pols, HA; Prince, RL; Raitakari, O; Reid, IR; Robbins, J; Sambrook, PN; Sham, PC; Shuldiner, AR; Tylavsky, FA; van Duijn, CM; Wareham, NJ; Cupples, LA; Econs, MJ; Evans, DM; Harris, TB; Kung, AW; Psaty, BM; Reeve, J; Spector, TD; Streeten, EA; Zillikens, MC; Thorsteinsdottir, U; Ohlsson, C; Karasik, D; Richards, JB; Brown, MA; Stefansson, K; Uitterlinden, AG; Ralston, SH; Ioannidis, JP; Kiel, DP; Rivadeneira, F Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
Nat Genet. 2012; 44(5):491-501 [OPEN ACCESS]
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Haijun, M; Xiaohui, Z; Ting, M; Renner, W; Abulizi, P; Baopeng, T Association between KCNE1 (G38S) genetic polymorphism and non-valvular atrial fibrillation in an Uygur population.
Wien Klin Wochenschr. 2012; 124(21-22):737-741
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Karakas, M; Baumert, J; Kleber, ME; Thorand, B; Dallmeier, D; Silbernagel, G; Grammer, TB; Rottbauer, W; Meisinger, C; Illig, T; März, W; Koenig, W A variant in the ABO gene explains the variation in soluble E-selectin levels-results from dense genotyping in two independent populations.
PLoS One. 2012; 7(12):e51441-e51441 [OPEN ACCESS]
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Schweighofer, N; Lerchbaum, E; Trummer, O; Schwetz, V; Pilz, S; Pieber, TR; Obermayer-Pietsch, B Androgen levels and metabolic parameters are associated with a genetic variant of F13A1 in women with polycystic ovary syndrome.
Gene. 2012; 504(1): 133-139.
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Taal, HR; St Pourcain, B; Thiering, E; Das, S; Mook-Kanamori, DO; Warrington, NM; Kaakinen, M; Kreiner-Møller, E; Bradfield, JP; Freathy, RM; Geller, F; Guxens, M; Cousminer, DL; Kerkhof, M; Timpson, NJ; Ikram, MA; Beilin, LJ; Bønnelykke, K; Buxton, JL; Charoen, P; Chawes, BL; Eriksson, J; Evans, DM; Hofman, A; Kemp, JP; Kim, CE; Klopp, N; Lahti, J; Lye, SJ; McMahon, G; Mentch, FD; Müller-Nurasyid, M; O'Reilly, PF; Prokopenko, I; Rivadeneira, F; Steegers, EA; Sunyer, J; Tiesler, C; Yaghootkar, H; Cohorts for Heart and Aging Research in Genetic Epidemiology Consortium; Breteler, MM; Decarli, C; Breteler, MM; Debette, S; Fornage, M; Gudnason, V; Launer, LJ; van der Lugt, A; Mosley, TH; Seshadri, S; Smith, AV; Vernooij, MW; Early Genetics & Lifecourse Epidemiology Consortium; Blakemore, AI; Chiavacci, RM; Feenstra, B; Fernandez-Banet, J; Grant, SF; Hartikainen, AL; van der Heijden, AJ; Iñiguez, C; Lathrop, M; McArdle, WL; Mølgaard, A; Newnham, JP; Palmer, LJ; Palotie, A; Pouta, A; Ring, SM; Sovio, U; Standl, M; Uitterlinden, AG; Wichmann, HE; Vissing, NH; DeCarli, C; van Duijn, CM; McCarthy, MI; Koppelman, GH; Estivill, X; Hattersley, AT; Melbye, M; Bisgaard, H; Pennell, CE; Widen, E; Hakonarson, H; Smith, GD; Heinrich, J; Jarvelin, MR; Jaddoe, VW; Early Growth Genetics Consortium Common variants at 12q15 and 12q24 are associated with infant head circumference.
Nat Genet. 2012; 44(5):532-538 [OPEN ACCESS]
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van der Harst, P; Zhang, W; Mateo Leach, I; Rendon, A; Verweij, N; Sehmi, J; Paul, DS; Elling, U; Allayee, H; Li, X; Radhakrishnan, A; Tan, ST; Voss, K; Weichenberger, CX; Albers, CA; Al-Hussani, A; Asselbergs, FW; Ciullo, M; Danjou, F; Dina, C; Esko, T; Evans, DM; Franke, L; Gögele, M; Hartiala, J; Hersch, M; Holm, H; Hottenga, JJ; Kanoni, S; Kleber, ME; Lagou, V; Langenberg, C; Lopez, LM; Lyytikäinen, LP; Melander, O; Murgia, F; Nolte, IM; O'Reilly, PF; Padmanabhan, S; Parsa, A; Pirastu, N; Porcu, E; Portas, L; Prokopenko, I; Ried, JS; Shin, SY; Tang, CS; Teumer, A; Traglia, M; Ulivi, S; Westra, HJ; Yang, J; Zhao, JH; Anni, F; Abdellaoui, A; Attwood, A; Balkau, B; Bandinelli, S; Bastardot, F; Benyamin, B; Boehm, BO; Cookson, WO; Das, D; de Bakker, PI; de Boer, RA; de Geus, EJ; de Moor, MH; Dimitriou, M; Domingues, FS; Döring, A; Engström, G; Eyjolfsson, GI; Ferrucci, L; Fischer, K; Galanello, R; Garner, SF; Genser, B; Gibson, QD; Girotto, G; Gudbjartsson, DF; Harris, SE; Hartikainen, AL; Hastie, CE; Hedblad, B; Illig, T; Jolley, J; Kähönen, M; Kema, IP; Kemp, JP; Liang, L; Lloyd-Jones, H; Loos, RJ; Meacham, S; Medland, SE; Meisinger, C; Memari, Y; Mihailov, E; Miller, K; Moffatt, MF; Nauck, M; Novatchkova, M; Nutile, T; Olafsson, I; Onundarson, PT; Parracciani, D; Penninx, BW; Perseu, L; Piga, A; Pistis, G; Pouta, A; Puc, U; Raitakari, O; Ring, SM; Robino, A; Ruggiero, D; Ruokonen, A; Saint-Pierre, A; Sala, C; Salumets, A; Sambrook, J; Schepers, H; Schmidt, CO; Silljé, HH; Sladek, R; Smit, JH; Starr, JM; Stephens, J; Sulem, P; Tanaka, T; Thorsteinsdottir, U; Tragante, V; van Gilst, WH; van Pelt, LJ; van Veldhuisen, DJ; Völker, U; Whitfield, JB; Willemsen, G; Winkelmann, BR; Wirnsberger, G; Algra, A; Cucca, F; d'Adamo, AP; Danesh, J; Deary, IJ; Dominiczak, AF; Elliott, P; Fortina, P; Froguel, P; Gasparini, P; Greinacher, A; Hazen, SL; Jarvelin, MR; Khaw, KT; Lehtimäki, T; Maerz, W; Martin, NG; Metspalu, A; Mitchell, BD; Montgomery, GW; Moore, C; Navis, G; Pirastu, M; Pramstaller, PP; Ramirez-Solis, R; Schadt, E; Scott, J; Shuldiner, AR; Smith, GD; Smith, JG; Snieder, H; Sorice, R; Spector, TD; Stefansson, K; Stumvoll, M; Tang, WH; Toniolo, D; Tönjes, A; Visscher, PM; Vollenweider, P; Wareham, NJ; Wolffenbuttel, BH; Boomsma, DI; Beckmann, JS; Dedoussis, GV; Deloukas, P; Ferreira, MA; Sanna, S; Uda, M; Hicks, AA; Penninger, JM; Gieger, C; Kooner, JS; Ouwehand, WH; Soranzo, N; Chambers, JC Seventy-five genetic loci influencing the human red blood cell.
Nature. 2012; 492(7429):369-375 [OPEN ACCESS]
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Wojciechowski, P; Lipowska, A; Rys, P; Ewens, KG; Franks, S; Tan, S; Lerchbaum, E; Vcelak, J; Attaoua, R; Straczkowski, M; Azziz, R; Barber, TM; Hinney, A; Obermayer-Pietsch, B; Lukasova, P; Bendlova, B; Grigorescu, F; Kowalska, I; Goodarzi, MO; GIANT Consortium; Strauss, JF; McCarthy, MI; Malecki, MT Impact of FTO genotypes on BMI and weight in polycystic ovary syndrome: a systematic review and meta-analysis.
Diabetologia. 2012; 55(10):2636-2645 [OPEN ACCESS]
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2011

Domschke, K; Reif, A; Weber, H; Richter, J; Hohoff, C; Ohrmann, P; Pedersen, A; Bauer, J; Suslow, T; Kugel, H; Heindel, W; Baumann, C; Klauke, B; Jacob, C; Maier, W; Fritze, J; Bandelow, B; Krakowitzky, P; Rothermundt, M; Erhardt, A; Binder, EB; Holsboer, F; Gerlach, AL; Kircher, T; Lang, T; Alpers, GW; Ströhle, A; Fehm, L; Gloster, AT; Wittchen, HU; Arolt, V; Pauli, P; Hamm, A; Deckert, J Neuropeptide S receptor gene -- converging evidence for a role in panic disorder.
Mol Psychiatry. 2011; 16(9):938-948 [OPEN ACCESS]
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Erhardt, A; Czibere, L; Roeske, D; Lucae, S; Unschuld, PG; Ripke, S; Specht, M; Kohli, MA; Kloiber, S; Ising, M; Heck, A; Pfister, H; Zimmermann, P; Lieb, R; Pütz, B; Uhr, M; Weber, P; Deussing, JM; Gonik, M; Bunck, M; Kebler, MS; Frank, E; Hohoff, C; Domschke, K; Krakowitzky, P; Maier, W; Bandelow, B; Jacob, C; Deckert, J; Schreiber, S; Strohmaier, J; Nöthen, M; Cichon, S; Rietschel, M; Bettecken, T; Keck, ME; Landgraf, R; Müller-Myhsok, B; Holsboer, F; Binder, EB TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies.
Mol Psychiatry. 2011; 16(6):647-663 [OPEN ACCESS]
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Fornage, M; Debette, S; Bis, JC; Schmidt, H; Ikram, MA; Dufouil, C; Sigurdsson, S; Lumley, T; DeStefano, AL; Fazekas, F; Vrooman, HA; Shibata, DK; Maillard, P; Zijdenbos, A; Smith, AV; Gudnason, H; de Boer, R; Cushman, M; Mazoyer, B; Heiss, G; Vernooij, MW; Enzinger, C; Glazer, NL; Beiser, A; Knopman, DS; Cavalieri, M; Niessen, WJ; Harris, TB; Petrovic, K; Lopez, OL; Au, R; Lambert, JC; Hofman, A; Gottesman, RF; Garcia, M; Heckbert, SR; Atwood, LD; Catellier, DJ; Uitterlinden, AG; Yang, Q; Smith, NL; Aspelund, T; Romero, JR; Rice, K; Taylor, KD; Nalls, MA; Rotter, JI; Sharrett, R; van Duijn, CM; Amouyel, P; Wolf, PA; Gudnason, V; van der Lugt, A; Boerwinkle, E; Psaty, BM; Seshadri, S; Tzourio, C; Breteler, MM; Mosley, TH; Schmidt, R; Longstreth, WT; DeCarli, C; Launer, LJ Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium.
Ann Neurol. 2011; 69(6): 928-939. [OPEN ACCESS]
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Graupp, M; Wehr, E; Schweighofer, N; Pieber, TR; Obermayer-Pietsch, B Association of genetic variants in the two isoforms of 5α-reductase, SRD5A1 and SRD5A2, in lean patients with polycystic ovary syndrome.
Eur J Obstet Gynecol Reprod Biol. 2011; 157(2):175-179 [OPEN ACCESS]
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Hofmann, G; Langsenlehner, U; Langsenlehner, T; Glehr, M; Gerger, A; Absenger, G; Szkandera, J; Fuerst, F; Samonigg, H; Krippl, P; Renner, W Single nucleotide polymorphisms of integrin alpha-2 and beta-3 genes are not associated with relapse-free and overall survival in colorectal cancer patients.
Anticancer Res. 2011; 31(4):1373-1377
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