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

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Publikationen

Suchbegriffe: ASIAN CONTINENTAL ANCESTRY GROUP - GENETICS , . Treffer: 16

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 [OPEN ACCESS]
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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 [OPEN ACCESS]
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Li, JQ; Qiu, YL; Gong, JY; Dou, LM; Lu, Y; Knisely, AS; Zhang, MH; Luan, WS; Wang, JS Novel NBAS mutations and fever-related recurrent acute liver failure in Chinese children: a retrospective study.
BMC Gastroenterol. 2017; 17(1):77-77 [OPEN ACCESS]
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2016

Zhang, MH; Knisely, AS; Wang, NL; Gong, JY; Wang, JS Fibrinogen storage disease in a Chinese boy with de novo fibrinogen Aguadilla mutation: Incomplete response to carbamazepine and ursodeoxycholic acid.
BMC Gastroenterol. 2016; 16(1):92-92 (- Case Report) [OPEN ACCESS]
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2014

Khan, MA; Rupp, VM; Orpinell, M; Hussain, MS; Altmüller, J; Steinmetz, MO; Enzinger, C; Thiele, H; Höhne, W; Nürnberg, G; Baig, SM; Ansar, M; Nürnberg, P; Vincent, JB; Speicher, MR; Gönczy, P; Windpassinger, C A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family.
Hum Mol Genet. 2014; 23(22):5940-5949 [OPEN ACCESS]
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Lubitz, SA; Lunetta, KL; Lin, H; Arking, DE; Trompet, S; Li, G; Krijthe, BP; Chasman, DI; Barnard, J; Kleber, ME; Dörr, M; Ozaki, K; Smith, AV; Müller-Nurasyid, M; Walter, S; Agarwal, SK; Bis, JC; Brody, JA; Chen, LY; Everett, BM; Ford, I; Franco, OH; Harris, TB; Hofman, A; Kääb, S; Mahida, S; Kathiresan, S; Kubo, M; Launer, LJ; Macfarlane, PW; Magnani, JW; McKnight, B; McManus, DD; Peters, A; Psaty, BM; Rose, LM; Rotter, JI; Silbernagel, G; Smith, JD; Sotoodehnia, N; Stott, DJ; Taylor, KD; Tomaschitz, A; Tsunoda, T; Uitterlinden, AG; Van Wagoner, DR; Völker, U; Völzke, H; Murabito, JM; Sinner, MF; Gudnason, V; Felix, SB; März, W; Chung, M; Albert, CM; Stricker, BH; Tanaka, T; Heckbert, SR; Jukema, JW; Alonso, A; Benjamin, EJ; Ellinor, PT Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese.
J Am Coll Cardiol. 2014; 63(12):1200-1210 [OPEN ACCESS]
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2013

Global Lipids Genetics Consortium; Willer, CJ; Schmidt, EM; Sengupta, S; Peloso, GM; Gustafsson, S; Kanoni, S; Ganna, A; Chen, J; Buchkovich, ML; Mora, S; Beckmann, JS; Bragg-Gresham, JL; Chang, HY; Demirkan, A; Den Hertog, HM; Do, R; Donnelly, LA; Ehret, GB; Esko, T; Feitosa, MF; Ferreira, T; Fischer, K; Fontanillas, P; Fraser, RM; Freitag, DF; Gurdasani, D; Heikkilä, K; Hyppönen, E; Isaacs, A; Jackson, AU; Johansson, A; Johnson, T; Kaakinen, M; Kettunen, J; Kleber, ME; Li, X; Luan, J; Lyytikäinen, LP; Magnusson, PK; Mangino, M; Mihailov, E; Montasser, ME; Müller-Nurasyid, M; Nolte, IM; O'Connell, JR; Palmer, CD; Perola, M; Petersen, AK; Sanna, S; Saxena, R; Service, SK; Shah, S; Shungin, D; Sidore, C; Song, C; Strawbridge, RJ; Surakka, I; Tanaka, T; Teslovich, TM; Thorleifsson, G; Van den Herik, EG; Voight, BF; Volcik, KA; Waite, LL; Wong, A; Wu, Y; Zhang, W; Absher, D; Asiki, G; Barroso, I; Been, LF; Bolton, JL; Bonnycastle, LL; Brambilla, P; Burnett, MS; Cesana, G; Dimitriou, M; Doney, AS; Döring, A; Elliott, P; Epstein, SE; Eyjolfsson, GI; Gigante, B; Goodarzi, MO; Grallert, H; Gravito, ML; Groves, CJ; Hallmans, G; Hartikainen, AL; Hayward, C; Hernandez, D; Hicks, AA; Holm, H; Hung, YJ; Illig, T; Jones, MR; Kaleebu, P; Kastelein, JJ; Khaw, KT; Kim, E; Klopp, N; Komulainen, P; Kumari, M; Langenberg, C; Lehtimäki, T; Lin, SY; Lindström, J; Loos, RJ; Mach, F; McArdle, WL; Meisinger, C; Mitchell, BD; Müller, G; Nagaraja, R; Narisu, N; Nieminen, TV; Nsubuga, RN; Olafsson, I; Ong, KK; Palotie, A; Papamarkou, T; Pomilla, C; Pouta, A; Rader, DJ; Reilly, MP; Ridker, PM; Rivadeneira, F; Rudan, I; Ruokonen, A; Samani, N; Scharnagl, H; Seeley, J; Silander, K; Stancáková, A; Stirrups, K; Swift, AJ; Tiret, L; Uitterlinden, AG; van Pelt, LJ; Vedantam, S; Wainwright, N; Wijmenga, C; Wild, SH; Willemsen, G; Wilsgaard, T; Wilson, JF; Young, EH; Zhao, JH; Adair, LS; Arveiler, D; Assimes, TL; Bandinelli, S; Bennett, F; Bochud, M; Boehm, BO; Boomsma, DI; Borecki, IB; Bornstein, SR; Bovet, P; Burnier, M; Campbell, H; Chakravarti, A; Chambers, JC; Chen, YD; Collins, FS; Cooper, RS; Danesh, J; Dedoussis, G; de Faire, U; Feranil, AB; Ferrières, J; Ferrucci, L; Freimer, NB; Gieger, C; Groop, LC; Gudnason, V; Gyllensten, U; Hamsten, A; Harris, TB; Hingorani, A; Hirschhorn, JN; Hofman, A; Hovingh, GK; Hsiung, CA; Humphries, SE; Hunt, SC; Hveem, K; Iribarren, C; Järvelin, MR; Jula, A; Kähönen, M; Kaprio, J; Kesäniemi, A; Kivimaki, M; Kooner, JS; Koudstaal, PJ; Krauss, RM; Kuh, D; Kuusisto, J; Kyvik, KO; Laakso, M; Lakka, TA; Lind, L; Lindgren, CM; Martin, NG; März, W; McCarthy, MI; McKenzie, CA; Meneton, P; Metspalu, A; Moilanen, L; Morris, AD; Munroe, PB; Njølstad, I; Pedersen, NL; Power, C; Pramstaller, PP; Price, JF; Psaty, BM; Quertermous, T; Rauramaa, R; Saleheen, D; Salomaa, V; Sanghera, DK; Saramies, J; Schwarz, PE; Sheu, WH; Shuldiner, AR; Siegbahn, A; Spector, TD; Stefansson, K; Strachan, DP; Tayo, BO; Tremoli, E; Tuomilehto, J; Uusitupa, M; van Duijn, CM; Vollenweider, P; Wallentin, L; Wareham, NJ; Whitfield, JB; Wolffenbuttel, BH; Ordovas, JM; Boerwinkle, E; Palmer, CN; Thorsteinsdottir, U; Chasman, DI; Rotter, JI; Franks, PW; Ripatti, S; Cupples, LA; Sandhu, MS; Rich, SS; Boehnke, M; Deloukas, P; Kathiresan, S; Mohlke, KL; Ingelsson, E; Abecasis, GR Discovery and refinement of loci associated with lipid levels.
Nat Genet. 2013; 45(11):1274-1283 [OPEN ACCESS]
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2012

Khan, MA; Rafiq, MA; Noor, A; Hussain, S; Flores, JV; Rupp, V; Vincent, AK; Malli, R; Ali, G; Khan, FS; Ishak, GE; Doherty, D; Weksberg, R; Ayub, M; Windpassinger, C; Ibrahim, S; Frye, M; Ansar, M; Vincent, JB Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability.
Am J Hum Genet. 2012; 90(5):856-863 [OPEN ACCESS]
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Lu, X; Wang, L; Chen, S; He, L; Yang, X; Shi, Y; Cheng, J; Zhang, L; Gu, CC; Huang, J; Wu, T; Ma, Y; Li, J; Cao, J; Chen, J; Ge, D; Fan, Z; Li, Y; Zhao, L; Li, H; Zhou, X; Chen, L; Liu, D; Chen, J; Duan, X; Hao, Y; Wang, L; Lu, F; Liu, Z; Yao, C; Shen, C; Pu, X; Yu, L; Fang, X; Xu, L; Mu, J; Wu, X; Zheng, R; Wu, N; Zhao, Q; Li, Y; Liu, X; Wang, M; Yu, D; Hu, D; Ji, X; Guo, D; Sun, D; Wang, Q; Yang, Y; Liu, F; Mao, Q; Liang, X; Ji, J; Chen, P; Mo, X; Li, D; Chai, G; Tang, Y; Li, X; Du, Z; Liu, X; Dou, C; Yang, Z; Meng, Q; Wang, D; Wang, R; Yang, J; Schunkert, H; Samani, NJ; Kathiresan, S; Reilly, MP; Erdmann, J; Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium; Peng, X; Wu, X; Liu, D; Yang, Y; Chen, R; Qiang, B; Gu, D Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
Nat Genet. 2012; 44(8):890-894 [OPEN ACCESS]
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Okada, Y; Sim, X; Go, MJ; Wu, JY; Gu, D; Takeuchi, F; Takahashi, A; Maeda, S; Tsunoda, T; Chen, P; Lim, SC; Wong, TY; Liu, J; Young, TL; Aung, T; Seielstad, M; Teo, YY; Kim, YJ; Lee, JY; Han, BG; Kang, D; Chen, CH; Tsai, FJ; Chang, LC; Fann, SJ; Mei, H; Rao, DC; Hixson, JE; Chen, S; Katsuya, T; Isono, M; Ogihara, T; Chambers, JC; Zhang, W; Kooner, JS; KidneyGen Consortium; CKDGen Consortium; Albrecht, E; GUGC consortium; Yamamoto, K; Kubo, M; Nakamura, Y; Kamatani, N; Kato, N; He, J; Chen, YT; Cho, YS; Tai, ES; Tanaka, T Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.
Nat Genet. 2012; 44(8):904-909 [OPEN ACCESS]
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2011

IBC 50K CAD Consortium Large-scale gene-centric analysis identifies novel variants for coronary artery disease.
PLoS Genet. 2011; 7(9):e1002260-e1002260 [OPEN ACCESS]
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Lanktree, MB; Guo, Y; Murtaza, M; Glessner, JT; Bailey, SD; Onland-Moret, NC; Lettre, G; Ongen, H; Rajagopalan, R; Johnson, T; Shen, H; Nelson, CP; Klopp, N; Baumert, J; Padmanabhan, S; Pankratz, N; Pankow, JS; Shah, S; Taylor, K; Barnard, J; Peters, BJ; Maloney, CM; Lobmeyer, MT; Stanton, A; Zafarmand, MH; Romaine, SP; Mehta, A; van Iperen, EP; Gong, Y; Price, TS; Smith, EN; Kim, CE; Li, YR; Asselbergs, FW; Atwood, LD; Bailey, KM; Bhatt, D; Bauer, F; Behr, ER; Bhangale, T; Boer, JM; Boehm, BO; Bradfield, JP; Brown, M; Braund, PS; Burton, PR; Carty, C; Chandrupatla, HR; Chen, W; Connell, J; Dalgeorgou, C; Boer, Ad; Drenos, F; Elbers, CC; Fang, JC; Fox, CS; Frackelton, EC; Fuchs, B; Furlong, CE; Gibson, Q; Gieger, C; Goel, A; Grobbee, DE; Hastie, C; Howard, PJ; Huang, GH; Johnson, WC; Li, Q; Kleber, ME; Klein, BE; Klein, R; Kooperberg, C; Ky, B; Lacroix, A; Lanken, P; Lathrop, M; Li, M; Marshall, V; Melander, O; Mentch, FD; Meyer, NJ; Monda, KL; Montpetit, A; Murugesan, G; Nakayama, K; Nondahl, D; Onipinla, A; Rafelt, S; Newhouse, SJ; Otieno, FG; Patel, SR; Putt, ME; Rodriguez, S; Safa, RN; Sawyer, DB; Schreiner, PJ; Simpson, C; Sivapalaratnam, S; Srinivasan, SR; Suver, C; Swergold, G; Sweitzer, NK; Thomas, KA; Thorand, B; Timpson, NJ; Tischfield, S; Tobin, M; Tomaszewski, M; Tomaszweski, M; Verschuren, WM; Wallace, C; Winkelmann, B; Zhang, H; Zheng, D; Zhang, L; Zmuda, JM; Clarke, R; Balmforth, AJ; Danesh, J; Day, IN; Schork, NJ; de Bakker, PI; Delles, C; Duggan, D; Hingorani, AD; Hirschhorn, JN; Hofker, MH; Humphries, SE; Kivimaki, M; Lawlor, DA; Kottke-Marchant, K; Mega, JL; Mitchell, BD; Morrow, DA; Palmen, J; Redline, S; Shields, DC; Shuldiner, AR; Sleiman, PM; Smith, GD; Farrall, M; Jamshidi, Y; Christiani, DC; Casas, JP; Hall, AS; Doevendans, PA; Christie, JD; Berenson, GS; Murray, SS; Illig, T; Dorn, GW; Cappola, TP; Boerwinkle, E; Sever, P; Rader, DJ; Reilly, MP; Caulfield, M; Talmud, PJ; Topol, E; Engert, JC; Wang, K; Dominiczak, A; Hamsten, A; Curtis, SP; Silverstein, RL; Lange, LA; Sabatine, MS; Trip, M; Saleheen, D; Peden, JF; Cruickshanks, KJ; März, W; O'Connell, JR; Klungel, OH; Wijmenga, C; Maitland-van der Zee, AH; Schadt, EE; Johnson, JA; Jarvik, GP; Papanicolaou, GJ; Hugh Watkins on behalf of PROCARDIS; Grant, SF; Munroe, PB; North, KE; Samani, NJ; Koenig, W; Gaunt, TR; Anand, SS; van der Schouw, YT; Meena Kumari on behalf of the Whitehall II Study and the WHII 50K Group; Soranzo, N; Fitzgerald, GA; Reiner, A; Hegele, RA; Hakonarson, H; Keating, BJ Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.
Am J Hum Genet. 2011; 88(1):6-18 [OPEN ACCESS]
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2007

Mensah, AK; De Luca, V; Stachowiak, B; Noor, A; Windpassinger, C; Lam, ST; Kennedy, JL; Scherer, SW; Lo, IF; Vincent, JB Molecular analysis of a chromosome 4 inversion segregating in a large schizophrenia kindred from Hong Kong.
Schizophr Res. 2007; 95(1-3):228-235
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2004

Fröhlich, LF; Gensure, RC; Schipani, E; Jüppner, H; Bastepe, M Haplotype frequencies and linkage disequilibrium analysis of four frequent polymorphisms at the PTH/PTH-related peptide receptor gene locus.
Mol Cell Probes. 2004; 18(5): 353-357.
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2003

Lessig, R; Willuweit, S; Krawczak, M; Wu, FC; Pu, CE; Kim, W; Henke, L; Henke, J; Miranda, J; Hidding, M; Benecke, M; Schmitt, C; Magno, M; Calacal, G; Delfin, FC; de Ungria, MC; Elias, S; Augustin, C; Tun, Z; Honda, K; Kayser, M; Gusmao, L; Amorim, A; Alves, C; Hou, Y; Keyser, C; Ludes, B; Klintschar, M; Immel, UD; Reichenpfader, B; Zaharova, B; Roewer, L Asian online Y-STR Haplotype Reference Database.
Leg Med (Tokyo). 2003; 5 Suppl 1(Pt 3):S160-S163
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1990

Virgolini, I; O'Grady, J; Peskar, BA; Sinzinger, H Defects in the prostaglandin-system--heredity, prevalence and vascular risk analysis.
Prostaglandins Leukot Essent Fatty Acids. 1990; 40(3): 227-237.
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