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

Navigation/Suche

• Forscher*innen.
• Institutionen.
• Projekte.
• Publikationen.
• Partner.
• Geldgeber.
• Ausstattung.
• Knowhow.
• Forschungsfelder.

Publikationen

Suchbegriffe: GENETIC PREDISPOSITION TO DISEASE - , . Treffer: 188

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]
Web of Science PubMed FullText FullText_MUG

 

van de Putte, R; van Rooij, IALM; Marcelis, CLM; Guo, M; Brunner, HG; Addor, MC; Cavero-Carbonell, C; Dias, CM; Draper, ES; Etxebarriarteun, L; Gatt, M; Haeusler, M; Khoshnood, B; Klungsoyr, K; Kurinczuk, JJ; Lanzoni, M; Latos-Bielenska, A; Luyt, K; O'Mahony, MT; Miller, N; Mullaney, C; Nelen, V; Neville, AJ; Perthus, I; Pierini, A; Randrianaivo, H; Rankin, J; Rissmann, A; Rouget, F; Schaub, B; Tucker, D; Wellesley, D; Wiesel, A; Zymak-Zakutnia, N; Loane, M; Barisic, I; de Walle, HEK; Roeleveld, N; Bergman, JEH Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study.
Pediatr Res. 2020; 87(3):541-549 Doi: 10.1038/s41390-019-0561-y [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

2018

Day, F; Karaderi, T; Jones, MR; Meun, C; He, C; Drong, A; Kraft, P; Lin, N; Huang, H; Broer, L; Magi, R; Saxena, R; Laisk, T; Urbanek, M; Hayes, MG; Thorleifsson, G; Fernandez-Tajes, J; Mahajan, A; Mullin, BH; Stuckey, BGA; Spector, TD; Wilson, SG; Goodarzi, MO; Davis, L; Obermayer-Pietsch, B; Uitterlinden, AG; Anttila, V; Neale, BM; Jarvelin, MR; Fauser, B; Kowalska, I; Visser, JA; Andersen, M; Ong, K; Stener-Victorin, E; Ehrmann, D; Legro, RS; Salumets, A; McCarthy, MI; Morin-Papunen, L; Thorsteinsdottir, U; Stefansson, K; 23andMe Research Team; Styrkarsdottir, U; Perry, JRB; Dunaif, A; Laven, J; Franks, S; Lindgren, CM; Welt, CK Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.
PLoS Genet. 2018; 14(12):e1007813-e1007813 Doi: 10.1371/journal.pgen.1007813 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Kashofer, K; Gornicec, M; Lind, K; Caraffini, V; Schauer, S; Beham-Schmid, C; Wölfler, A; Hoefler, G; Sill, H; Zebisch, A Detection of prognostically relevant mutations and translocations in myeloid sarcoma by next generation sequencing.
Leuk Lymphoma. 2018; 59(2):501-504 Doi: 10.1080/10428194.2017.1339879 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Koentges, C; Pepin, ME; Müsse, C; Pfeil, K; Alvarez, SVV; Hoppe, N; Hoffmann, MM; Odening, KE; Sossalla, S; Zirlik, A; Hein, L; Bode, C; Wende, AR; Bugger, H Gene expression analysis to identify mechanisms underlying heart failure susceptibility in mice and humans.
Basic Res Cardiol. 2018; 113(1):8-8 Doi: 10.1007/s00395-017-0666-6 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Madar-Shapiro, L; Karady, I; Trahtenherts, A; Syngelaki, A; Akolekar, R; Poon, L; Cohen, R; Sharabi-Nov, A; Huppertz, B; Sammar, M; Juhasz, K; Than, NG; Papp, Z; Romero, R; Nicolaides, KH; Meiri, H Predicting the Risk to Develop Preeclampsia in the First Trimester Combining Promoter Variant -98A/C of LGALS13 (Placental Protein 13), Black Ethnicity, Previous Preeclampsia, Obesity, and Maternal Age.
Fetal Diagn Ther. 2018; 43(4):250-265 Doi: 10.1159/000477933 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

2017

Aung, T; Ozaki, M; Lee, MC; Schlötzer-Schrehardt, U; Thorleifsson, G; Mizoguchi, T; Igo, RP; Haripriya, A; Williams, SE; Astakhov, YS; Orr, AC; Burdon, KP; Nakano, S; Mori, K; Abu-Amero, K; Hauser, M; Li, Z; Prakadeeswari, G; Bailey, JNC; Cherecheanu, AP; Kang, JH; Nelson, S; Hayashi, K; Manabe, SI; Kazama, S; Zarnowski, T; Inoue, K; Irkec, M; Coca-Prados, M; Sugiyama, K; Järvelä, I; Schlottmann, P; Lerner, SF; Lamari, H; Nilgün, Y; Bikbov, M; Park, KH; Cha, SC; Yamashiro, K; Zenteno, JC; Jonas, JB; Kumar, RS; Perera, SA; Chan, ASY; Kobakhidze, N; George, R; Vijaya, L; Do, T; Edward, DP; de Juan Marcos, L; Pakravan, M; Moghimi, S; Ideta, R; Bach-Holm, D; Kappelgaard, P; Wirostko, B; Thomas, S; Gaston, D; Bedard, K; Greer, WL; Yang, Z; Chen, X; Huang, L; Sang, J; Jia, H; Jia, L; Qiao, C; Zhang, H; Liu, X; Zhao, B; Wang, YX; Xu, L; Leruez, S; Reynier, P; Chichua, G; Tabagari, S; Uebe, S; Zenkel, M; Berner, D; Mossböck, G; Weisschuh, N; Hoja, U; Welge-Luessen, UC; Mardin, C; Founti, P; Chatzikyriakidou, A; Pappas, T; Anastasopoulos, E; Lambropoulos, A; Ghosh, A; Shetty, R; Porporato, N; Saravanan, V; Venkatesh, R; Shivkumar, C; Kalpana, N; Sarangapani, S; Kanavi, MR; Beni, AN; Yazdani, S; Lashay, A; Naderifar, H; Khatibi, N; Fea, A; Lavia, C; Dallorto, L; Rolle, T; Frezzotti, P; Paoli, D; Salvi, E; Manunta, P; Mori, Y; Miyata, K; Higashide, T; Chihara, E; Ishiko, S; Yoshida, A; Yanagi, M; Kiuchi, Y; Ohashi, T; Sakurai, T; Sugimoto, T; Chuman, H; Aihara, M; Inatani, M; Miyake, M; Gotoh, N; Matsuda, F; Yoshimura, N; Ikeda, Y; Ueno, M; Sotozono, C; Jeoung, JW; Sagong, M; Park, KH; Ahn, J; Cruz-Aguilar, M; Ezzouhairi, SM; Rafei, A; Chong, YF; Ng, XY; Goh, SR; Chen, Y; Yong, VHK; Khan, MI; Olawoye, OO; Ashaye, AO; Ugbede, I; Onakoya, A; Kizor-Akaraiwe, N; Teekhasaenee, C; Suwan, Y; Supakontanasan, W; Okeke, S; Uche, NJ; Asimadu, I; Ayub, H; Akhtar, F; Kosior-Jarecka, E; Lukasik, U; Lischinsky, I; Castro, V; Grossmann, RP; Sunaric Megevand, G; Roy, S; Dervan, E; Silke, E; Rao, A; Sahay, P; Fornero, P; Cuello, O; Sivori, D; Zompa, T; Mills, RA; Souzeau, E; Mitchell, P; Wang, JJ; Hewitt, AW; Coote, M; Crowston, JG; Astakhov, SY; Akopov, EL; Emelyanov, A; Vysochinskaya, V; Kazakbaeva, G; Fayzrakhmanov, R; Al-Obeidan, SA; Owaidhah, O; Aljasim, LA; Chowbay, B; Foo, JN; Soh, RQ; Sim, KS; Xie, Z; Cheong, AWO; Mok, SQ; Soo, HM; Chen, XY; Peh, SQ; Heng, KK; Husain, R; Ho, SL; Hillmer, AM; Cheng, CY; Escudero-Domínguez, FA; González-Sarmiento, R; Martinon-Torres, F; Salas, A; Pathanapitoon, K; Hansapinyo, L; Wanichwecharugruang, B; Kitnarong, N; Sakuntabhai, A; Nguyn, HX; Nguyn, GTT; Nguyn, TV; Zenz, W; Binder, A; Klobassa, DS; Hibberd, ML; Davila, S; Herms, S; Nöthen, MM; Moebus, S; Rautenbach, RM; Ziskind, A; Carmichael, TR; Ramsay, M; Álvarez, L; García, M; González-Iglesias, H; Rodríguez-Calvo, PP; Fernández-Vega Cueto, L; Oguz, Ç; Tamcelik, N; Atalay, E; Batu, B; Aktas, D; Kasım, B; Wilson, MR; Coleman, AL; Liu, Y; Challa, P; Herndon, L; Kuchtey, RW; Kuchtey, J; Curtin, K; Chaya, CJ; Crandall, A; Zangwill, LM; Wong, TY; Nakano, M; Kinoshita, S; den Hollander, AI; Vesti, E; Fingert, JH; Lee, RK; Sit, AJ; Shingleton, BJ; Wang, N; Cusi, D; Qamar, R; Kraft, P; Pericak-Vance, MA; Raychaudhuri, S; Heegaard, S; Kivelä, T; Reis, A; Kruse, FE; Weinreb, RN; Pasquale, LR; Haines, JL; Thorsteinsdottir, U; Jonasson, F; Allingham, RR; Milea, D; Ritch, R; Kubota, T; Tashiro, K; Vithana, EN; Micheal, S; Topouzis, F; Craig, JE; Dubina, M; Sundaresan, P; Stefansson, K Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
Nat Genet. 2017; 49(7):993-1004 Doi: 10.1038/ng.3875 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Christophersen, IE; Rienstra, M; Roselli, C; Yin, X; Geelhoed, B; Barnard, J; Lin, H; Arking, DE; Smith, AV; Albert, CM; Chaffin, M; Tucker, NR; Li, M; Klarin, D; Bihlmeyer, NA; Low, SK; Weeke, PE; Müller-Nurasyid, M; Smith, JG; Brody, JA; Niemeijer, MN; Dörr, M; Trompet, S; Huffman, J; Gustafsson, S; Schurmann, C; Kleber, ME; Lyytikäinen, LP; Seppälä, I; Malik, R; Horimoto, ARVR; Perez, M; Sinisalo, J; Aeschbacher, S; Thériault, S; Yao, J; Radmanesh, F; Weiss, S; Teumer, A; Choi, SH; Weng, LC; Clauss, S; Deo, R; Rader, DJ; Shah, SH; Sun, A; Hopewell, JC; Debette, S; Chauhan, G; Yang, Q; Worrall, BB; Paré, G; Kamatani, Y; Hagemeijer, YP; Verweij, N; Siland, JE; Kubo, M; Smith, JD; Van Wagoner, DR; Bis, JC; Perz, S; Psaty, BM; Ridker, PM; Magnani, JW; Harris, TB; Launer, LJ; Shoemaker, MB; Padmanabhan, S; Haessler, J; Bartz, TM; Waldenberger, M; Lichtner, P; Arendt, M; Krieger, JE; Kähönen, M; Risch, L; Mansur, AJ; Peters, A; Smith, BH; Lind, L; Scott, SA; Lu, Y; Bottinger, EB; Hernesniemi, J; Lindgren, CM; Wong, JA; Huang, J; Eskola, M; Morris, AP; Ford, I; Reiner, AP; Delgado, G; Chen, LY; Chen, YI; Sandhu, RK; Li, M; Boerwinkle, E; Eisele, L; Lannfelt, L; Rost, N; Anderson, CD; Taylor, KD; Campbell, A; Magnusson, PK; Porteous, D; Hocking, LJ; Vlachopoulou, E; Pedersen, NL; Nikus, K; Orho-Melander, M; Hamsten, A; Heeringa, J; Denny, JC; Kriebel, J; Darbar, D; Newton-Cheh, C; Shaffer, C; Macfarlane, PW; Heilmann-Heimbach, S; Almgren, P; Huang, PL; Sotoodehnia, N; Soliman, EZ; Uitterlinden, AG; Hofman, A; Franco, OH; Völker, U; Jöckel, KH; Sinner, MF; Lin, HJ; Guo, X; METASTROKE Consortium of the ISGC; Neurology Working Group of the CHARGE Consortium; Dichgans, M; Ingelsson, E; Kooperberg, C; Melander, O; Loos, RJF; Laurikka, J; Conen, D; Rosand, J; van der Harst, P; Lokki, ML; Kathiresan, S; Pereira, A; Jukema, JW; Hayward, C; Rotter, JI; März, W; Lehtimäki, T; Stricker, BH; Chung, MK; Felix, SB; Gudnason, V; Alonso, A; Roden, DM; Kääb, S; Chasman, DI; Heckbert, SR; Benjamin, EJ; Tanaka, T; Lunetta, KL; Lubitz, SA; Ellinor, PT; AFGen Consortium Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
Nat Genet. 2017; 49(6):946-952 Doi: 10.1038/ng.3843 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Del Greco M, F; Foco, L; Pichler, I; Eller, P; Eller, K; Benyamin, B; Whitfield, JB; Genetics of Iron Status Consortium; CKDGen Consortium; Pramstaller, PP; Thompson, JR; Pattaro, C; Minelli, C Serum iron level and kidney function: a Mendelian randomization study.
Nephrol Dial Transplant. 2017; 32(2):273-278 Doi: 10.1093/ndt/gfw215 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Graff, M; Scott, RA; Justice, AE; Young, KL; Feitosa, MF; Barata, L; Winkler, TW; Chu, AY; Mahajan, A; Hadley, D; Xue, L; Workalemahu, T; Heard-Costa, NL; den Hoed, M; Ahluwalia, TS; Qi, Q; Ngwa, JS; Renström, F; Quaye, L; Eicher, JD; Hayes, JE; Cornelis, M; Kutalik, Z; Lim, E; Luan, J; Huffman, JE; Zhang, W; Zhao, W; Griffin, PJ; Haller, T; Ahmad, S; Marques-Vidal, PM; Bien, S; Yengo, L; Teumer, A; Smith, AV; Kumari, M; Harder, MN; Justesen, JM; Kleber, ME; Hollensted, M; Lohman, K; Rivera, NV; Whitfield, JB; Zhao, JH; Stringham, HM; Lyytikäinen, LP; Huppertz, C; Willemsen, G; Peyrot, WJ; Wu, Y; Kristiansson, K; Demirkan, A; Fornage, M; Hassinen, M; Bielak, LF; Cadby, G; Tanaka, T; Mägi, R; van der Most, PJ; Jackson, AU; Bragg-Gresham, JL; Vitart, V; Marten, J; Navarro, P; Bellis, C; Pasko, D; Johansson, Å; Snitker, S; Cheng, YC; Eriksson, J; Lim, U; Aadahl, M; Adair, LS; Amin, N; Balkau, B; Auvinen, J; Beilby, J; Bergman, RN; Bergmann, S; Bertoni, AG; Blangero, J; Bonnefond, A; Bonnycastle, LL; Borja, JB; Brage, S; Busonero, F; Buyske, S; Campbell, H; Chines, PS; Collins, FS; Corre, T; Smith, GD; Delgado, GE; Dueker, N; Dörr, M; Ebeling, T; Eiriksdottir, G; Esko, T; Faul, JD; Fu, M; Færch, K; Gieger, C; Gläser, S; Gong, J; Gordon-Larsen, P; Grallert, H; Grammer, TB; Grarup, N; van Grootheest, G; Harald, K; Hastie, ND; Havulinna, AS; Hernandez, D; Hindorff, L; Hocking, LJ; Holmens, OL; Holzapfel, C; Hottenga, JJ; Huang, J; Huang, T; Hui, J; Huth, C; Hutri-Kähönen, N; James, AL; Jansson, JO; Jhun, MA; Juonala, M; Kinnunen, L; Koistinen, HA; Kolcic, I; Komulainen, P; Kuusisto, J; Kvaløy, K; Kähönen, M; Lakka, TA; Launer, LJ; Lehne, B; Lindgren, CM; Lorentzon, M; Luben, R; Marre, M; Milaneschi, Y; Monda, KL; Montgomery, GW; De Moor, MHM; Mulas, A; Müller-Nurasyid, M; Musk, AW; Männikkö, R; Männistö, S; Narisu, N; Nauck, M; Nettleton, JA; Nolte, IM; Oldehinkel, AJ; Olden, M; Ong, KK; Padmanabhan, S; Paternoster, L; Perez, J; Perola, M; Peters, A; Peters, U; Peyser, PA; Prokopenko, I; Puolijoki, H; Raitakari, OT; Rankinen, T; Rasmussen-Torvik, LJ; Rawal, R; Ridker, PM; Rose, LM; Rudan, I; Sarti, C; Sarzynski, MA; Savonen, K; Scott, WR; Sanna, S; Shuldiner, AR; Sidney, S; Silbernagel, G; Smith, BH; Smith, JA; Snieder, H; Stančáková, A; Sternfeld, B; Swift, AJ; Tammelin, T; Tan, ST; Thorand, B; Thuillier, D; Vandenput, L; Vestergaard, H; van Vliet-Ostaptchouk, JV; Vohl, MC; Völker, U; Waeber, G; Walker, M; Wild, S; Wong, A; Wright, AF; Zillikens, MC; Zubair, N; Haiman, CA; Lemarchand, L; Gyllensten, U; Ohlsson, C; Hofman, A; Rivadeneira, F; Uitterlinden, AG; Pérusse, L; Wilson, JF; Hayward, C; Polasek, O; Cucca, F; Hveem, K; Hartman, CA; Tönjes, A; Bandinelli, S; Palmer, LJ; Kardia, SLR; Rauramaa, R; Sørensen, TIA; Tuomilehto, J; Salomaa, V; Penninx, BWJH; de Geus, EJC; Boomsma, DI; Lehtimäki, T; Mangino, M; Laakso, M; Bouchard, C; Martin, NG; Kuh, D; Liu, Y; Linneberg, A; März, W; Strauch, K; Kivimäki, M; Harris, TB; Gudnason, V; Völzke, H; Qi, L; Järvelin, MR; Chambers, JC; Kooner, JS; Froguel, P; Kooperberg, C; Vollenweider, P; Hallmans, G; Hansen, T; Pedersen, O; Metspalu, A; Wareham, NJ; Langenberg, C; Weir, DR; Porteous, DJ; Boerwinkle, E; Chasman, DI; CHARGE Consortium; EPIC-InterAct Consortium; PAGE Consortium; Abecasis, GR; Barroso, I; McCarthy, MI; Frayling, TM; O'Connell, JR; van Duijn, CM; Boehnke, M; Heid, IM; Mohlke, KL; Strachan, DP; Fox, CS; Liu, CT; Hirschhorn, JN; Klein, RJ; Johnson, AD; Borecki, IB; Franks, PW; North, KE; C Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
PLoS Genet. 2017; 13(4): e1006528-e1006528. Doi: 10.1371/journal.pgen.1006528 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Hibar, DP; Adams, HHH; Jahanshad, N; Chauhan, G; Stein, JL; Hofer, E; Renteria, ME; Bis, JC; Arias-Vasquez, A; Ikram, MK; Desrivières, S; Vernooij, MW; Abramovic, L; Alhusaini, S; Amin, N; Andersson, M; Arfanakis, K; Aribisala, BS; Armstrong, NJ; Athanasiu, L; Axelsson, T; Beecham, AH; Beiser, A; Bernard, M; Blanton, SH; Bohlken, MM; Boks, MP; Bralten, J; Brickman, AM; Carmichael, O; Chakravarty, MM; Chen, Q; Ching, CRK; Chouraki, V; Cuellar-Partida, G; Crivello, F; Den Braber, A; Doan, NT; Ehrlich, S; Giddaluru, S; Goldman, AL; Gottesman, RF; Grimm, O; Griswold, ME; Guadalupe, T; Gutman, BA; Hass, J; Haukvik, UK; Hoehn, D; Holmes, AJ; Hoogman, M; Janowitz, D; Jia, T; Jørgensen, KN; Karbalai, N; Kasperaviciute, D; Kim, S; Klein, M; Kraemer, B; Lee, PH; Liewald, DCM; Lopez, LM; Luciano, M; Macare, C; Marquand, AF; Matarin, M; Mather, KA; Mattheisen, M; McKay, DR; Milaneschi, Y; Muñoz Maniega, S; Nho, K; Nugent, AC; Nyquist, P; Loohuis, LMO; Oosterlaan, J; Papmeyer, M; Pirpamer, L; Pütz, B; Ramasamy, A; Richards, JS; Risacher, SL; Roiz-Santiañez, R; Rommelse, N; Ropele, S; Rose, EJ; Royle, NA; Rundek, T; Sämann, PG; Saremi, A; Satizabal, CL; Schmaal, L; Schork, AJ; Shen, L; Shin, J; Shumskaya, E; Smith, AV; Sprooten, E; Strike, LT; Teumer, A; Tordesillas-Gutierrez, D; Toro, R; Trabzuni, D; Trompet, S; Vaidya, D; Van der Grond, J; Van der Lee, SJ; Van der Meer, D; Van Donkelaar, MMJ; Van Eijk, KR; Van Erp, TGM; Van Rooij, D; Walton, E; Westlye, LT; Whelan, CD; Windham, BG; Winkler, AM; Wittfeld, K; Woldehawariat, G; Wolf, C; Wolfers, T; Yanek, LR; Yang, J; Zijdenbos, A; Zwiers, MP; Agartz, I; Almasy, L; Ames, D; Amouyel, P; Andreassen, OA; Arepalli, S; Assareh, AA; Barral, S; Bastin, ME; Becker, DM; Becker, JT; Bennett, DA; Blangero, J; van Bokhoven, H; Boomsma, DI; Brodaty, H; Brouwer, RM; Brunner, HG; Buckner, RL; Buitelaar, JK; Bulayeva, KB; Cahn, W; Calhoun, VD; Cannon, DM; Cavalleri, GL; Cheng, CY; Cichon, S; Cookson, MR; Corvin, A; Crespo-Facorro, B; Curran, JE; Czisch, M; Dale, AM; Davies, GE; De Craen, AJM; De Geus, EJC; De Jager, PL; De Zubicaray, GI; Deary, IJ; Debette, S; DeCarli, C; Delanty, N; Depondt, C; DeStefano, A; Dillman, A; Djurovic, S; Donohoe, G; Drevets, WC; Duggirala, R; Dyer, TD; Enzinger, C; Erk, S; Espeseth, T; Fedko, IO; Fernández, G; Ferrucci, L; Fisher, SE; Fleischman, DA; Ford, I; Fornage, M; Foroud, TM; Fox, PT; Francks, C; Fukunaga, M; Gibbs, JR; Glahn, DC; Gollub, RL; Göring, HHH; Green, RC; Gruber, O; Gudnason, V; Guelfi, S; Håberg, AK; Hansell, NK; Hardy, J; Hartman, CA; Hashimoto, R; Hegenscheid, K; Heinz, A; Le Hellard, S; Hernandez, DG; Heslenfeld, DJ; Ho, BC; Hoekstra, PJ; Hoffmann, W; Hofman, A; Holsboer, F; Homuth, G; Hosten, N; Hottenga, JJ; Huentelman, M; Hulshoff Pol, HE; Ikeda, M; Jack, CR; Jenkinson, M; Johnson, R; Jönsson, EG; Jukema, JW; Kahn, RS; Kanai, R; Kloszewska, I; Knopman, DS; Kochunov, P; Kwok, JB; Lawrie, SM; Lemaître, H; Liu, X; Longo, DL; Lopez, OL; Lovestone, S; Martinez, O; Martinot, JL; Mattay, VS; McDonald, C; McIntosh, AM; McMahon, FJ; McMahon, KL; Mecocci, P; Melle, I; Meyer-Lindenberg, A; Mohnke, S; Montgomery, GW; Morris, DW; Mosley, TH; Mühleisen, TW; Müller-Myhsok, B; Nalls, MA; Nauck, M; Nichols, TE; Niessen, WJ; Nöthen, MM; Nyberg, L; Ohi, K; Olvera, RL; Ophoff, RA; Pandolfo, M; Paus, T; Pausova, Z; Penninx, BWJH; Pike, GB; Potkin, SG; Psaty, BM; Reppermund, S; Rietschel, M; Roffman, JL; Romanczuk-Seiferth, N; Rotter, JI; Ryten, M; Sacco, RL; Sachdev, PS; Saykin, AJ; ... Novel genetic loci associated with hippocampal volume.
Nat Commun. 2017; 8(6):13624-13624 Doi: 10.1038/ncomms13624 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Jahic, A; Hinreiner, S; Emberger, W; Hehr, U; Zuchner, S; Beetz, C Doublet-Mediated DNA Rearrangement-A Novel and Potentially Underestimated Mechanism for the Formation of Recurrent Pathogenic Deletions.
Hum Mutat. 2017; 38(3):275-278 Doi: 10.1002/humu.23162
Web of Science PubMed FullText FullText_MUG

 

Plecko, B; Zweier, M; Begemann, A; Mathis, D; Schmitt, B; Striano, P; Baethmann, M; Vari, MS; Beccaria, F; Zara, F; Crowther, LM; Joset, P; Sticht, H; Papuc, SM; Rauch, A Confirmation of mutations in PROSC as a novel cause of vitamin B 6 -dependent epilepsy.
J Med Genet. 2017; 54(12): 809-814. Doi: 10.1136/jmedgenet-2017-104521 (- Case Report)
Web of Science PubMed FullText FullText_MUG

 

Redin, C; Brand, H; Collins, RL; Kammin, T; Mitchell, E; Hodge, JC; Hanscom, C; Pillalamarri, V; Seabra, CM; Abbott, MA; Abdul-Rahman, OA; Aberg, E; Adley, R; Alcaraz-Estrada, SL; Alkuraya, FS; An, Y; Anderson, MA; Antolik, C; Anyane-Yeboa, K; Atkin, JF; Bartell, T; Bernstein, JA; Beyer, E; Blumenthal, I; Bongers, EM; Brilstra, EH; Brown, CW; Brüggenwirth, HT; Callewaert, B; Chiang, C; Corning, K; Cox, H; Cuppen, E; Currall, BB; Cushing, T; David, D; Deardorff, MA; Dheedene, A; D'Hooghe, M; de Vries, BB; Earl, DL; Ferguson, HL; Fisher, H; FitzPatrick, DR; Gerrol, P; Giachino, D; Glessner, JT; Gliem, T; Grady, M; Graham, BH; Griffis, C; Gripp, KW; Gropman, AL; Hanson-Kahn, A; Harris, DJ; Hayden, MA; Hill, R; Hochstenbach, R; Hoffman, JD; Hopkin, RJ; Hubshman, MW; Innes, AM; Irons, M; Irving, M; Jacobsen, JC; Janssens, S; Jewett, T; Johnson, JP; Jongmans, MC; Kahler, SG; Koolen, DA; Korzelius, J; Kroisel, PM; Lacassie, Y; Lawless, W; Lemyre, E; Leppig, K; Levin, AV; Li, H; Li, H; Liao, EC; Lim, C; Lose, EJ; Lucente, D; Macera, MJ; Manavalan, P; Mandrile, G; Marcelis, CL; Margolin, L; Mason, T; Masser-Frye, D; McClellan, MW; Mendoza, CJ; Menten, B; Middelkamp, S; Mikami, LR; Moe, E; Mohammed, S; Mononen, T; Mortenson, ME; Moya, G; Nieuwint, AW; Ordulu, Z; Parkash, S; Pauker, SP; Pereira, S; Perrin, D; Phelan, K; Aguilar, RE; Poddighe, PJ; Pregno, G; Raskin, S; Reis, L; Rhead, W; Rita, D; Renkens, I; Roelens, F; Ruliera, J; Rump, P; Schilit, SL; Shaheen, R; Sparkes, R; Spiegel, E; Stevens, B; Stone, MR; Tagoe, J; Thakuria, JV; van Bon, BW; van de Kamp, J; van Der Burgt, I; van Essen, T; van Ravenswaaij-Arts, CM; van Roosmalen, MJ; Vergult, S; Volker-Touw, CM; Warburton, DP; Waterman, MJ; Wiley, S; Wilson, A; Yerena-de Vega, MC; Zori, RT; Levy, B; Brunner, HG; de Leeuw, N; Kloosterman, WP; Thorland, EC; Morton, CC; Gusella, JF; Talkowski, ME The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.
Nat Genet. 2017; 49(1):36-45 Doi: 10.1038/ng.3720 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Salminen, A; Vlachopoulou, E; Havulinna, AS; Tervahartiala, T; Sattler, W; Lokki, ML; Nieminen, MS; Perola, M; Salomaa, V; Sinisalo, J; Meri, S; Sorsa, T; Pussinen, PJ Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases: A Genome-Wide Analysis.
Circ Cardiovasc Genet. 2017; 10(6): Doi: 10.1161/CIRCGENETICS.117.001731 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Saraggi, D; Salmaso, R; Valentini, E; Munari, G; Vindigni, V; Rugge, M; Fassan, M; Cerroni, L Pigmented trichoblastoma developed in a sebaceous nevus: HRAS mutation as a common molecular driver.
Pathol Res Pract. 2017; 213(7):860-862 Doi: 10.1016/j.prp.2017.03.012 (- Case Report)
Web of Science PubMed FullText FullText_MUG

 

Schmidt, N; Grammer, T; Gouni-Berthold, I; Julius, U; Kassner, U; Klose, G; König, C; Laufs, U; Otte, B; Steinhagen-Thiessen, E; Wanner, C; März, W CaRe high - Cascade screening and registry for high cholesterol in Germany.
Atheroscler Suppl. 2017; 30(1):72-76 Doi: 10.1016/j.atherosclerosissup.2017.05.015
Web of Science PubMed FullText FullText_MUG

 

Toib, A; Zhang, C; Borghetti, G; Zhang, X; Wallner, M; Yang, Y; Troupes, CD; Kubo, H; Sharp, TE; Feldsott, E; Berretta, RM; Zalavadia, N; Trappanese, DM; Harper, S; Gross, P; Chen, X; Mohsin, S; Houser, SR Remodeling of repolarization and arrhythmia susceptibility in a myosin-binding protein C knockout mouse model.
Am J Physiol Heart Circ Physiol. 2017; 313(3):H620-H630 Doi: 10.1152/ajpheart.00167.2017 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Widhalm, K; Benke, IM; Fritz, M; Geiger, H; Helk, O; Fritsch, M; Hoermann, G; Kostner, G Homozygous familial hypercholesterolemia: Summarized case reports.
Atherosclerosis. 2017; 257:86-89 Doi: 10.1016/j.atherosclerosis.2017.01.002 (- Case Report)
Web of Science PubMed FullText FullText_MUG

 

2016

Adams, HH; Hibar, DP; Chouraki, V; Stein, JL; Nyquist, PA; Rentería, ME; Trompet, S; Arias-Vasquez, A; Seshadri, S; Desrivières, S; Beecham, AH; Jahanshad, N; Wittfeld, K; Van der Lee, SJ; Abramovic, L; Alhusaini, S; Amin, N; Andersson, M; Arfanakis, K; Aribisala, BS; Armstrong, NJ; Athanasiu, L; Axelsson, T; Beiser, A; Bernard, M; Bis, JC; Blanken, LM; Blanton, SH; Bohlken, MM; Boks, MP; Bralten, J; Brickman, AM; Carmichael, O; Chakravarty, MM; Chauhan, G; Chen, Q; Ching, CR; Cuellar-Partida, G; Braber, AD; Doan, NT; Ehrlich, S; Filippi, I; Ge, T; Giddaluru, S; Goldman, AL; Gottesman, RF; Greven, CU; Grimm, O; Griswold, ME; Guadalupe, T; Hass, J; Haukvik, UK; Hilal, S; Hofer, E; Hoehn, D; Holmes, AJ; Hoogman, M; Janowitz, D; Jia, T; Kasperaviciute, D; Kim, S; Klein, M; Kraemer, B; Lee, PH; Liao, J; Liewald, DC; Lopez, LM; Luciano, M; Macare, C; Marquand, A; Matarin, M; Mather, KA; Mattheisen, M; Mazoyer, B; McKay, DR; McWhirter, R; Milaneschi, Y; Mirza-Schreiber, N; Muetzel, RL; Maniega, SM; Nho, K; Nugent, AC; Loohuis, LM; Oosterlaan, J; Papmeyer, M; Pappa, I; Pirpamer, L; Pudas, S; Pütz, B; Rajan, KB; Ramasamy, A; Richards, JS; Risacher, SL; Roiz-Santiañez, R; Rommelse, N; Rose, EJ; Royle, NA; Rundek, T; Sämann, PG; Satizabal, CL; Schmaal, L; Schork, AJ; Shen, L; Shin, J; Shumskaya, E; Smith, AV; Sprooten, E; Strike, LT; Teumer, A; Thomson, R; Tordesillas-Gutierrez, D; Toro, R; Trabzuni, D; Vaidya, D; Van der Grond, J; Van der Meer, D; Van Donkelaar, MM; Van Eijk, KR; Van Erp, TG; Van Rooij, D; Walton, E; Westlye, LT; Whelan, CD; Windham, BG; Winkler, AM; Woldehawariat, G; Wolf, C; Wolfers, T; Xu, B; Yanek, LR; Yang, J; Zijdenbos, A; Zwiers, MP; Agartz, I; Aggarwal, NT; Almasy, L; Ames, D; Amouyel, P; Andreassen, OA; Arepalli, S; Assareh, AA; Barral, S; Bastin, ME; Becker, DM; Becker, JT; Bennett, DA; Blangero, J; van Bokhoven, H; Boomsma, DI; Brodaty, H; Brouwer, RM; Brunner, HG; Buckner, RL; Buitelaar, JK; Bulayeva, KB; Cahn, W; Calhoun, VD; Cannon, DM; Cavalleri, GL; Chen, C; Cheng, CY; Cichon, S; Cookson, MR; Corvin, A; Crespo-Facorro, B; Curran, JE; Czisch, M; Dale, AM; Davies, GE; De Geus, EJ; De Jager, PL; de Zubicaray, GI; Delanty, N; Depondt, C; DeStefano, AL; Dillman, A; Djurovic, S; Donohoe, G; Drevets, WC; Duggirala, R; Dyer, TD; Erk, S; Espeseth, T; Evans, DA; Fedko, IO; Fernández, G; Ferrucci, L; Fisher, SE; Fleischman, DA; Ford, I; Foroud, TM; Fox, PT; Francks, C; Fukunaga, M; Gibbs, JR; Glahn, DC; Gollub, RL; Göring, HH; Grabe, HJ; Green, RC; Gruber, O; Gudnason, V; Guelfi, S; Hansell, NK; Hardy, J; Hartman, CA; Hashimoto, R; Hegenscheid, K; Heinz, A; Le Hellard, S; Hernandez, DG; Heslenfeld, DJ; Ho, BC; Hoekstra, PJ; Hoffmann, W; Hofman, A; Holsboer, F; Homuth, G; Hosten, N; Hottenga, JJ; Hulshoff Pol, HE; Ikeda, M; Ikram, MK; Jack, CR; Jenkinson, M; Johnson, R; Jönsson, EG; Jukema, JW; Kahn, RS; Kanai, R; Kloszewska, I; Knopman, DS; Kochunov, P; Kwok, JB; Lawrie, SM; Lemaître, H; Liu, X; Longo, DL; Longstreth, WT; Lopez, OL; Lovestone, S; Martinez, O; Martinot, JL; Mattay, VS; McDonald, C; McIntosh, AM; McMahon, KL; McMahon, FJ; Mecocci, P; Melle, I; Meyer-Lindenberg, A; Mohnke, S; Montgomery, GW; Morris, DW; Mosley, TH; Mühleisen, TW; Müller-Myhsok, B; Nalls, MA; Nauck, M; Nichols, TE; Niessen, WJ; Nöthen, MM; Nyberg, L; Ohi, K; Olvera, RL; Ophoff, RA; Pandolfo, M; Paus, T; Pausova, Z; Penninx, BW; Pike, GB; Potkin, SG; Psaty, BM; Reppermund, S; Rietschel, M; Roffman, JL; Romanczuk-Seiferth, N; Rotter, JI; Ryten, M ... Novel genetic loci underlying human intracranial volume identified through genome-wide association.
Nat Neurosci. 2016; 19(12):1569-1582 Doi: 10.1038/nn.4398 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Alesutan, I; Feger, M; Tuffaha, R; Castor, T; Musculus, K; Buehling, SS; Heine, CL; Kuro-O, M; Pieske, B; Schmidt, K; Tomaschitz, A; Maerz, W; Pilz, S; Meinitzer, A; Voelkl, J; Lang, F Augmentation of phosphate-induced osteo-/chondrogenic transformation of vascular smooth muscle cells by homoarginine.
Cardiovasc Res. 2016; 110(3):408-418 Doi: 10.1093/cvr/cvw062 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Al-Zoughbi, W; Pichler, M; Gorkiewicz, G; Guertl-Lackner, B; Haybaeck, J; Jahn, SW; Lackner, C; Liegl-Atzwanger, B; Popper, H; Schauer, S; Nusshold, E; Kindt, AS; Trajanoski, Z; Speicher, MR; Haemmerle, G; Zimmermann, R; Zechner, R; Vesely, PW; Hoefler, G Loss of adipose triglyceride lipase is associated with human cancer and induces mouse pulmonary neoplasia.
Oncotarget. 2016; 7(23):33832-33840 Doi: 10.18632/oncotarget.9418 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Beheshtian, M; Izadi, N; Kriegshauser, G; Kahrizi, K; Mehr, EP; Rostami, M; Hosseini, M; Azad, M; Montajabiniat, M; Kariminejad, A; Nemeth, S; Oberkanins, C; Najmabadi, H Prevalence of common MEFV mutations and carrier frequencies in a large cohort of Iranian populations.
J Genet. 2016; 95(3): 667-674. Doi: 10.1007/s12041-016-0682-6 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Friedrich, K; Smit, M; Brune, M; Giese, T; Rupp, C; Wannhoff, A; Kloeters, P; Leopold, Y; Denk, GU; Weiss, KH; Stremmel, W; Sauer, P; Hohenester, S; Schirmacher, P; Schemmer, P; Gotthardt, DN CD14 is associated with biliary stricture formation.
Hepatology. 2016; 64(3):843-852 Doi: 10.1002/hep.28543 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Iotchkova, V; Huang, J; Morris, JA; Jain, D; Barbieri, C; Walter, K; Min, JL; Chen, L; Astle, W; Cocca, M; Deelen, P; Elding, H; Farmaki, AE; Franklin, CS; Franberg, M; Gaunt, TR; Hofman, A; Jiang, T; Kleber, ME; Lachance, G; Luan, J; Malerba, G; Matchan, A; Mead, D; Memari, Y; Ntalla, I; Panoutsopoulou, K; Pazoki, R; Perry, JRB; Rivadeneira, F; Sabater-Lleal, M; Sennblad, B; Shin, SY; Southam, L; Traglia, M; van Dijk, F; van Leeuwen, EM; Zaza, G; Zhang, W; UK10K Consortium; Amin, N; Butterworth, A; Chambers, JC; Dedoussis, G; Dehghan, A; Franco, OH; Franke, L; Frontini, M; Gambaro, G; Gasparini, P; Hamsten, A; Issacs, A; Kooner, JS; Kooperberg, C; Langenberg, C; Marz, W; Scott, RA; Swertz, MA; Toniolo, D; Uitterlinden, AG; van Duijn, CM; Watkins, H; Zeggini, E; Maurano, MT; Timpson, NJ; Reiner, AP; Auer, PL; Soranzo, N Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.
Nat Genet. 2016; 48(11):1303-1312 Doi: 10.1038/ng.3668 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

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 Doi: 10.1111/ahg.12176 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

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 Doi: 10.1038/srep35371 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Moreno-Viedma, V; Amor, M; Sarabi, A; Bilban, M; Staffler, G; Zeyda, M; Stulnig, TM Common dysregulated pathways in obese adipose tissue and atherosclerosis.
Cardiovasc Diabetol. 2016; 15(1): 120-120. Doi: 10.1186/s12933-016-0441-2 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Nüesch, E; Dale, C; Palmer, TM; White, J; Keating, BJ; van Iperen, EP; Goel, A; Padmanabhan, S; Asselbergs, FW; EPIC-Netherland Investigators; Verschuren, WM; Wijmenga, C; Van der Schouw, YT; Onland-Moret, NC; Lange, LA; Hovingh, GK; Sivapalaratnam, S; Morris, RW; Whincup, PH; Wannamethe, GS; Gaunt, TR; Ebrahim, S; Steel, L; Nair, N; Reiner, AP; Kooperberg, C; Wilson, JF; Bolton, JL; McLachlan, S; Price, JF; Strachan, MW; Robertson, CM; Kleber, ME; Delgado, G; März, W; Melander, O; Dominiczak, AF; Farrall, M; Watkins, H; Leusink, M; Maitland-van der Zee, AH; de Groot, MC; Dudbridge, F; Hingorani, A; Ben-Shlomo, Y; Lawlor, DA; UCLEB Investigators; Amuzu, A; Caufield, M; Cavadino, A; Cooper, J; Davies, TL; IN Day; Drenos, F; Engmann, J; Finan, C; Giambartolomei, C; Hardy, R; Humphries, SE; Hypponen, E; Kivimaki, M; Kuh, D; Kumari, M; Ong, K; Plagnol, V; Power, C; Richards, M; Shah, S; Shah, T; Sofat, R; Talmud, PJ; Wareham, N; Warren, H; Whittaker, JC; Wong, A; Zabaneh, D; Davey Smith, G; Wells, JC; Leon, DA; Holmes, MV; Casas, JP Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis.
Int J Epidemiol. 2016; 45(6):1927-1937 Doi: 10.1093/ije/dyv074 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Pattaro, C; Teumer, A; Gorski, M; Chu, AY; Li, M; Mijatovic, V; Garnaas, M; Tin, A; Sorice, R; Li, Y; Taliun, D; Olden, M; Foster, M; Yang, Q; Chen, MH; Pers, TH; Johnson, AD; Ko, YA; Fuchsberger, C; Tayo, B; Nalls, M; Feitosa, MF; Isaacs, A; Dehghan, A; d'Adamo, P; Adeyemo, A; Dieffenbach, AK; Zonderman, AB; Nolte, IM; van der Most, PJ; Wright, AF; Shuldiner, AR; Morrison, AC; Hofman, A; Smith, AV; Dreisbach, AW; Franke, A; Uitterlinden, AG; Metspalu, A; Tonjes, A; Lupo, A; Robino, A; Johansson, Å; Demirkan, A; Kollerits, B; Freedman, BI; Ponte, B; Oostra, BA; Paulweber, B; Krämer, BK; Mitchell, BD; Buckley, BM; Peralta, CA; Hayward, C; Helmer, C; Rotimi, CN; Shaffer, CM; Müller, C; Sala, C; van Duijn, CM; Saint-Pierre, A; Ackermann, D; Shriner, D; Ruggiero, D; Toniolo, D; Lu, Y; Cusi, D; Czamara, D; Ellinghaus, D; Siscovick, DS; Ruderfer, D; Gieger, C; Grallert, H; Rochtchina, E; Atkinson, EJ; Holliday, EG; Boerwinkle, E; Salvi, E; Bottinger, EP; Murgia, F; Rivadeneira, F; Ernst, F; Kronenberg, F; Hu, FB; Navis, GJ; Curhan, GC; Ehret, GB; Homuth, G; Coassin, S; Thun, GA; Pistis, G; Gambaro, G; Malerba, G; Montgomery, GW; Eiriksdottir, G; Jacobs, G; Li, G; Wichmann, HE; Campbell, H; Schmidt, H; Wallaschofski, H; Völzke, H; Brenner, H; Kroemer, HK; Kramer, H; Lin, H; Leach, IM; Ford, I; Guessous, I; Rudan, I; Prokopenko, I; Borecki, I; Heid, IM; Kolcic, I; Persico, I; Jukema, JW; Wilson, JF; Felix, JF; Divers, J; Lambert, JC; Stafford, JM; Gaspoz, JM; Smith, JA; Faul, JD; Wang, JJ; Ding, J; Hirschhorn, JN; Attia, J; Whitfield, JB; Chalmers, J; Viikari, J; Coresh, J; Denny, JC; Karjalainen, J; Fernandes, JK; Endlich, K; Butterbach, K; Keene, KL; Lohman, K; Portas, L; Launer, LJ; Lyytikäinen, LP; Yengo, L; Franke, L; Ferrucci, L; Rose, LM; Kedenko, L; Rao, M; Struchalin, M; Kleber, ME; Cavalieri, M; Haun, M; Cornelis, MC; Ciullo, M; Pirastu, M; de Andrade, M; McEvoy, MA; Woodward, M; Adam, M; Cocca, M; Nauck, M; Imboden, M; Waldenberger, M; Pruijm, M; Metzger, M; Stumvoll, M; Evans, MK; Sale, MM; Kähönen, M; Boban, M; Bochud, M; Rheinberger, M; Verweij, N; Bouatia-Naji, N; Martin, NG; Hastie, N; Probst-Hensch, N; Soranzo, N; Devuyst, O; Raitakari, O; Gottesman, O; Franco, OH; Polasek, O; Gasparini, P; Munroe, PB; Ridker, PM; Mitchell, P; Muntner, P; Meisinger, C; Smit, JH; ICBP Consortium; AGEN Consortium; CARDIOGRAM; CHARGe-Heart Failure Group; ECHOGen Consortium; Kovacs, P; Wild, PS; Froguel, P; Rettig, R; Mägi, R; Biffar, R; Schmidt, R; Middelberg, RP; Carroll, RJ; Penninx, BW; Scott, RJ; Katz, R; Sedaghat, S; Wild, SH; Kardia, SL; Ulivi, S; Hwang, SJ; Enroth, S; Kloiber, S; Trompet, S; Stengel, B; Hancock, SJ; Turner, ST; Rosas, SE; Stracke, S; Harris, TB; Zeller, T; Zemunik, T; Lehtimäki, T; Illig, T; Aspelund, T; Nikopensius, T; Esko, T; Tanaka, T; Gyllensten, U; Völker, U; Emilsson, V; Vitart, V; Aalto, V; Gudnason, V; Chouraki, V; Chen, WM; Igl, W; März, W; Koenig, W; Lieb, W; Loos, RJ; Liu, Y; Snieder, H; Pramstaller, PP; Parsa, A; O'Connell, JR; Susztak, K; Hamet, P; Tremblay, J; de Boer, IH; Böger, CA; Goessling, W; Chasman, DI; Köttgen, A; Kao, WH; Fox, CS Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
Nat Commun. 2016; 7(1):10023-10023 Doi: 10.1038/ncomms10023 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Roeseler, E; Julius, U; Heigl, F; Spitthoever, R; Heutling, D; Breitenberger, P; Leebmann, J; Lehmacher, W; Kamstrup, PR; Nordestgaard, BG; Maerz, W; Noureen, A; Schmidt, K; Kronenberg, F; Heibges, A; Klingel, R; Pro(a)LiFe-Study Group Lipoprotein Apheresis for Lipoprotein(a)-Associated Cardiovascular Disease: Prospective 5 Years of Follow-Up and Apolipoprotein(a) Characterization.
Arterioscler Thromb Vasc Biol. 2016; 36(9):2019-2027 Doi: 10.1161/ATVBAHA.116.307983 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Scholl, HP; Strauss, RW; Singh, MS; Dalkara, D; Roska, B; Picaud, S; Sahel, JA Emerging therapies for inherited retinal degeneration.
Sci Transl Med. 2016; 8(368):368rv6-368rv6 Doi: 10.1126/scitranslmed.aaf2838
Web of Science PubMed FullText FullText_MUG

 

Tang, Y; Fickert, P; Trauner, M; Marcus, N; Blomenkamp, K; Teckman, J Autophagy induced by exogenous bile acids is therapeutic in a model of α-1-AT deficiency liver disease.
Am J Physiol Gastrointest Liver Physiol. 2016; 311(1):G156-G165 Doi: 10.1152/ajpgi.00143.2015 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Weber, ML; Schneider, DT; Offenmüller, S; Kaatsch, P; Einsiedel, HG; Benesch, M; Claviez, A; Ebinger, M; Kramm, C; Kratz, C; Lawlor, J; Leuschner, I; Merkel, S; Metzler, M; Nustede, R; Petsch, S; Seeger, KH; Schlegel, PG; Suttorp, M; Zolk, O; Brecht, IB Pediatric Colorectal Carcinoma is Associated With Excellent Outcome in the Context of Cancer Predisposition Syndromes.
Pediatr Blood Cancer. 2016; 63(4):611-617 Doi: 10.1002/pbc.25839
Web of Science PubMed FullText FullText_MUG

 

Wenzl, K; Hofer, S; Troppan, K; Lassnig, M; Steinbauer, E; Wiltgen, M; Zulus, B; Renner, W; Beham-Schmid, C; Neumeister, P; Deutsch, A Higher incidence of the SNP Met 788 Ile in the coding region of A20 in diffuse large B cell lymphomas.
Tumour Biol. 2016; 37(4):4785-4789 Doi: 10.1007/s13277-015-4322-1 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Woltsche, N; Schwab, C; Deinlein, T; Hofmann-Wellenhof, R; Zalaudek, I Dermoscopy in the era of dermato-oncology: from bed to bench side and retour.
Expert Rev Anticancer Ther. 2016; 16(5):531-541 Doi: 10.1586/14737140.2016.1168700
Web of Science PubMed FullText FullText_MUG

 

2015

Aoude, LG; Heitzer, E; Johansson, P; Gartside, M; Wadt, K; Pritchard, AL; Palmer, JM; Symmons, J; Gerdes, AM; Montgomery, GW; Martin, NG; Tomlinson, I; Kearsey, S; Hayward, NK POLE mutations in families predisposed to cutaneous melanoma.
Fam Cancer. 2015; 14(4):621-628 Doi: 10.1007/s10689-015-9826-8
Web of Science PubMed FullText FullText_MUG

 

Benke, K; Ágg, B; Mátyás, G; Szokolai, V; Harsányi, G; Szilveszter, B; Odler, B; Pólos, M; Maurovich-Horvat, P; Radovits, T; Merkely, B; Nagy, ZB; Szabolcs, Z Gene polymorphisms as risk factors for predicting the cardiovascular manifestations in Marfan syndrome. Role of folic acid metabolism enzyme gene polymorphisms in Marfan syndrome.
Thromb Haemost. 2015; 114(4): 748-756. Doi: 10.1160/TH15-02-0096
Web of Science PubMed FullText FullText_MUG

 

Ewald, L; Beate, LW; Stephanie, S; Wilfried, R; Yosuf, el-S Analysis of a Functional IL-6 Gene Polymorphism in HLAB27 Associated and Intermediate Uveitis Gives New Insight in Disease Pathogenesis and Commonality with Other Autoimmune Diseases.
J Immunol Res. 2015; 2015(7):174062-174062 Doi: 10.1155/2015/174062 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

International Genomics of Alzheimer's Disease Consortium (IGAP) Convergent genetic and expression data implicate immunity in Alzheimer's disease.
Alzheimers Dement. 2015; 11(6):658-671 Doi: 10.1016/j.jalz.2014.05.1757 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

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 Doi: 10.1371/journal.pgen.1005352 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Lindner, E; Weger, M; Ardjomand, N; Renner, W; El-Shabrawi, Y Associations of Independent IL2RA Gene Variants with Intermediate Uveitis.
PLoS One. 2015; 10(7):e0130737-e0130737 Doi: 10.1371/journal.pone.0130737 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Neumann, M; Vosberg, S; Schlee, C; Heesch, S; Schwartz, S; Gökbuget, N; Hoelzer, D; Graf, A; Krebs, S; Bartram, I; Blum, H; Brüggemann, M; Hecht, J; Bohlander, SK; Greif, PA; Baldus, CD Mutational spectrum of adult T-ALL.
Oncotarget. 2015; 6(5): 2754-2766. Doi: 10.18632/oncotarget.2218 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Schulz, E; Kashofer, K; Heitzer, E; Mhatre, KN; Speicher, MR; Hoefler, G; Sill, H Preexisting TP53 mutation in therapy-related acute myeloid leukemia.
Ann Hematol. 2015; 94(3):527-529 Doi: 10.1007/s00277-014-2191-0 (- Case Report) [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Stättermayer, AF; Traussnigg, S; Dienes, HP; Aigner, E; Stauber, R; Lackner, K; Hofer, H; Stift, J; Wrba, F; Stadlmayr, A; Datz, C; Strasser, M; Maieron, A; Trauner, M; Ferenci, P Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations.
J Hepatol. 2015; 63(1):156-163 Doi: 10.1016/j.jhep.2015.01.034
Web of Science PubMed FullText FullText_MUG

 

Wiesner, T; Kiuru, M; Scott, SN; Arcila, M; Halpern, AC; Hollmann, T; Berger, MF; Busam, KJ NF1 Mutations Are Common in Desmoplastic Melanoma.
Am J Surg Pathol. 2015; 39(10): 1357-1362. Doi: 10.1097/PAS.0000000000000451 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

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 Doi: 10.1371/journal.pgen.1005378 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Wruck, W; Kashofer, K; Rehman, S; Daskalaki, A; Berg, D; Gralka, E; Jozefczuk, J; Drews, K; Pandey, V; Regenbrecht, C; Wierling, C; Turano, P; Korf, U; Zatloukal, K; Lehrach, H; Westerhoff, HV; Adjaye, J Multi-omic profiles of human non-alcoholic fatty liver disease tissue highlight heterogenic phenotypes.
Sci Data. 2015; 2(S 01):150068-150068 Doi: 10.1038/sdata.2015.68 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Zimmermann, E; Ängquist, LH; Mirza, SS; Zhao, JH; Chasman, DI; Fischer, K; Qi, Q; Smith, AV; Thinggaard, M; Jarczok, MN; Nalls, MA; Trompet, S; Timpson, NJ; Schmidt, B; Jackson, AU; Lyytikäinen, LP; Verweij, N; Mueller-Nurasyid, M; Vikström, M; Marques-Vidal, P; Wong, A; Meidtner, K; Middelberg, RP; Strawbridge, RJ; Christiansen, L; FTO-Mortality Collaborating Group; Kyvik, KO; Hamsten, A; Jääskeläinen, T; Tjønneland, A; Eriksson, JG; Whitfield, JB; Boeing, H; Hardy, R; Vollenweider, P; Leander, K; Peters, A; van der Harst, P; Kumari, M; Lehtimäki, T; Meirhaeghe, A; Tuomilehto, J; Jöckel, KH; Ben-Shlomo, Y; Sattar, N; Baumeister, SE; Smith, GD; Casas, JP; Houston, DK; März, W; Christensen, K; Gudnason, V; Hu, FB; Metspalu, A; Ridker, PM; Wareham, NJ; Loos, RJF; Tiemeier, H; Sonestedt, E; Sørensen, TIA Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults.
Obes Rev. 2015; 16(4):327-340 Doi: 10.1111/obr.12263 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

2014

Busam, KJ; Kutzner, H; Cerroni, L; Wiesner, T Clinical and pathologic findings of Spitz nevi and atypical Spitz tumors with ALK fusions.
Am J Surg Pathol. 2014; 38(7):925-933 Doi: 10.1097/PAS.0000000000000187 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Weitere 50 Treffer anzeigen

↑ Seitenanfang / Navigation

© Med Uni Graz • Impressum