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

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Publikationen

Suchbegriffe: EUROPEAN CONTINENTAL ANCESTRY GROUP - GENETICS , . Treffer: 55

2019

BIRTH-GENE (BIG) Study Working Group; Huang, T; Wang, T; Zheng, Y; Ellervik, C; Li, X; Gao, M; Fang, Z; Chai, JF; Ahluwalia, TVS; Wang, Y; Voortman, T; Noordam, R; Frazier-Wood, A; Scholz, M; Sonestedt, E; Akiyama, M; Dorajoo, R; Zhou, A; Kilpeläinen, TO; Kleber, ME; Crozier, SR; Godfrey, KM; Lemaitre, R; Felix, JF; Shi, Y; Gupta, P; Khor, CC; Lehtimäki, T; Wang, CA; Tiesler, CMT; Thiering, E; Standl, M; Rzehak, P; Marouli, E; He, M; Lecoeur, C; Corella, D; Lai, CQ; Moreno, LA; Pitkänen, N; Boreham, CA; Zhang, T; Saw, SM; Ridker, PM; Graff, M; van Rooij, FJA; Uitterlinden, AG; Hofman, A; van Heemst, D; Rosendaal, FR; de Mutsert, R; Burkhardt, R; Schulz, CA; Ericson, U; Kamatani, Y; Yuan, JM; Power, C; Hansen, T; Sørensen, TIA; Tjønneland, A; Overvad, K; Delgado, G; Cooper, C; Djousse, L; Rivadeneira, F; Jameson, K; Zhao, W; Liu, J; Lee, NR; Raitakari, O; Kähönen, M; Viikari, J; Grote, V; Langhendries, JP; Koletzko, B; Escribano, J; Verduci, E; Dedoussis, G; Yu, C; Tham, YC; Lim, B; Lim, SH; Froguel, P; Balkau, B; Fink, NR; Vinding, RK; Sevelsted, A; Bisgaard, H; Coltell, O; Dallongeville, J; Gottrand, F; Pahkala, K; Niinikoski, H; Hyppönen, E; Pedersen, O; März, W; Inskip, H; Jaddoe, VWV; Dennison, E; Wong, TY; Sabanayagam, C; Tai, ES; Mohlke, KL; Mackey, DA; Gruszfeld, D; Deloukas, P; Tucker, KL; Fumeron, F; Bønnelykke, K; Rossing, P; Estruch, R; Ordovas, JM; Arnett, DK; Meirhaeghe, A; Amouyel, P; Cheng, CY; Sim, X; Teo, YY; van Dam, RM; Koh, WP; Orho-Melander, M; Loeffler, M; Kubo, M; Thiery, J; Mook-Kanamori, DO; Mozaffarian, D; Psaty, BM; Franco, OH; Wu, T; North, KE; Davey Smith, G; Chavarro, JE; Chasman, DI; Qi, L Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study.
JAMA Netw Open. 2019; 2(9):e1910915-e1910915 Doi: 10.1001/jamanetworkopen.2019.10915 [OPEN ACCESS]
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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]
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2017

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]
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2016

Ibrahim-Verbaas, CA; Bressler, J; Debette, S; Schuur, M; Smith, AV; Bis, JC; Davies, G; Trompet, S; Smith, JA; Wolf, C; Chibnik, LB; Liu, Y; Vitart, V; Kirin, M; Petrovic, K; Polasek, O; Zgaga, L; Fawns-Ritchie, C; Hoffmann, P; Karjalainen, J; Lahti, J; Llewellyn, DJ; Schmidt, CO; Mather, KA; Chouraki, V; Sun, Q; Resnick, SM; Rose, LM; Oldmeadow, C; Stewart, M; Smith, BH; Gudnason, V; Yang, Q; Mirza, SS; Jukema, JW; deJager, PL; Harris, TB; Liewald, DC; Amin, N; Coker, LH; Stegle, O; Lopez, OL; Schmidt, R; Teumer, A; Ford, I; Karbalai, N; Becker, JT; Jonsdottir, MK; Au, R; Fehrmann, R; Herms, S; Nalls, M; Zhao, W; Turner, ST; Yaffe, K; Lohman, K; van Swieten, JC; Kardia, S; Knopman, DS; Meeks, WM; Heiss, G; Holliday, EG; Schofield, PW; Tanaka, T; Stott, DJ; Wang, J; Ridker, P; Gow, AJ; Pattie, A; Starr, JM; Hocking, LJ; Armstrong, NJ; McLachlan, S; Shulman, JM; Pilling, LC; Eiriksdottir, G; Scott, RJ; Kochan, NA; Palotie, A; Hsieh, YC; Eriksson, JG; Penman, A; Gottesman, RF; Oostra, BA; Yu, L; DeStefano, AL; Beiser, A; Garcia, M; Rotter, JI; Nöthen, MM; Hofman, A; Slagboom, PE; Westendorp, R; Buckley, BM; Wolf, PA; Uitterlinden, AG; Psaty, BM; Grabe, HJ; Bandinelli, S; Chasman, DI; Grodstein, F; Räikkönen, K; Lambert, JC; Porteous, DJ; Generation Scotland; Price, JF; Sachdev, PS; Ferrucci, L; Attia, JR; Rudan, I; Hayward, C; Wright, AF; Wilson, JF; Cichon, S; Franke, L; Schmidt, H; Ding, J; de Craen, A; Fornage, M; Bennett, DA; Deary, IJ; Ikram, MA; Launer, LJ; Fitzpatrick, AL; Seshadri, S; van Duijn, CM; Mosley, TH GWAS for executive function and processing speed suggests involvement of the CADM2 gene.
Mol Psychiatry. 2016; 21(2):189-197 Doi: 10.1038/mp.2015.37 [OPEN ACCESS]
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2015

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 Doi: 10.1371/journal.pone.0135622 [OPEN ACCESS]
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Gorski, M; Tin, A; Garnaas, M; McMahon, GM; Chu, AY; Tayo, BO; Pattaro, C; Teumer, A; Chasman, DI; Chalmers, J; Hamet, P; Tremblay, J; Woodward, M; Aspelund, T; Eiriksdottir, G; Gudnason, V; Harris, TB; Launer, LJ; Smith, AV; Mitchell, BD; O'Connell, JR; Shuldiner, AR; Coresh, J; Li, M; Freudenberger, P; Hofer, E; Schmidt, H; Schmidt, R; Holliday, EG; Mitchell, P; Wang, JJ; de Boer, IH; Li, G; Siscovick, DS; Kutalik, Z; Corre, T; Vollenweider, P; Waeber, G; Gupta, J; Kanetsky, PA; Hwang, SJ; Olden, M; Yang, Q; de Andrade, M; Atkinson, EJ; Kardia, SL; Turner, ST; Stafford, JM; Ding, J; Liu, Y; Barlassina, C; Cusi, D; Salvi, E; Staessen, JA; Ridker, PM; Grallert, H; Meisinger, C; Müller-Nurasyid, M; Krämer, BK; Kramer, H; Rosas, SE; Nolte, IM; Penninx, BW; Snieder, H; Fabiola Del Greco, M; Franke, A; Nöthlings, U; Lieb, W; Bakker, SJ; Gansevoort, RT; van der Harst, P; Dehghan, A; Franco, OH; Hofman, A; Rivadeneira, F; Sedaghat, S; Uitterlinden, AG; Coassin, S; Haun, M; Kollerits, B; Kronenberg, F; Paulweber, B; Aumann, N; Endlich, K; Pietzner, M; Völker, U; Rettig, R; Chouraki, V; Helmer, C; Lambert, JC; Metzger, M; Stengel, B; Lehtimäki, T; Lyytikäinen, LP; Raitakari, O; Johnson, A; Parsa, A; Bochud, M; Heid, IM; Goessling, W; Köttgen, A; Kao, WH; Fox, CS; Böger, CA Genome-wide association study of kidney function decline in individuals of European descent.
Kidney Int. 2015; 87(5):1017-1029 Doi: 10.1038/ki.2014.361 [OPEN ACCESS]
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Heidari, A; Tongsook, C; Najafipour, R; Musante, L; Vasli, N; Garshasbi, M; Hu, H; Mittal, K; McNaughton, AJ; Sritharan, K; Hudson, M; Stehr, H; Talebi, S; Moradi, M; Darvish, H; Arshad Rafiq, M; Mozhdehipanah, H; Rashidinejad, A; Samiei, S; Ghadami, M; Windpassinger, C; Gillessen-Kaesbach, G; Tzschach, A; Ahmed, I; Mikhailov, A; Stavropoulos, DJ; Carter, MT; Keshavarz, S; Ayub, M; Najmabadi, H; Liu, X; Ropers, HH; Macheroux, P; Vincent, JB Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.
Hum Mol Genet. 2015; 24(20):5697-5710 Doi: 10.1093/hmg/ddv286 (- Case Report) [OPEN ACCESS]
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Iyengar, SK; Sedor, JR; Freedman, BI; Kao, WH; Kretzler, M; Keller, BJ; Abboud, HE; Adler, SG; Best, LG; Bowden, DW; Burlock, A; Chen, YD; Cole, SA; Comeau, ME; Curtis, JM; Divers, J; Drechsler, C; Duggirala, R; Elston, RC; Guo, X; Huang, H; Hoffmann, MM; Howard, BV; Ipp, E; Kimmel, PL; Klag, MJ; Knowler, WC; Kohn, OF; Leak, TS; Leehey, DJ; Li, M; Malhotra, A; März, W; Nair, V; Nelson, RG; Nicholas, SB; O'Brien, SJ; Pahl, MV; Parekh, RS; Pezzolesi, MG; Rasooly, RS; Rotimi, CN; Rotter, JI; Schelling, JR; Seldin, MF; Shah, VO; Smiles, AM; Smith, MW; Taylor, KD; Thameem, F; Thornley-Brown, DP; Truitt, BJ; Wanner, C; Weil, EJ; Winkler, CA; Zager, PG; Igo, RP; Hanson, RL; Langefeld, CD; Family Investigation of Nephropathy and Diabetes (FIND) Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND).
PLoS Genet. 2015; 11(8):e1005352-e1005352 Doi: 10.1371/journal.pgen.1005352 [OPEN ACCESS]
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Lindner, E; Glatz, W; Schwab, C; El-Shabrawi, Y; Mossböck, G Analysis of functional polymorphisms in apoptosis-related genes in primary open angle glaucoma.
Mol Vis. 2015; 21(7):1340-1344 [OPEN ACCESS]
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Matzhold, EM; Wagner, A; Drexler, C; Wagner, T Novel ABO gene variants caused by missense mutations in Exon 7 leading to discrepant ABO blood typing results.
Transfusion. 2015; 55(6 Pt 2):1589-1590 Doi: 10.1111/trf.13025 (- Case Report)
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Reinthaler, EM; Dejanovic, B; Lal, D; Semtner, M; Merkler, Y; Reinhold, A; Pittrich, DA; Hotzy, C; Feucht, M; Steinböck, H; Gruber-Sedlmayr, U; Ronen, GM; Neophytou, B; Geldner, J; Haberlandt, E; Muhle, H; Ikram, MA; van Duijn, CM; Uitterlinden, AG; Hofman, A; Altmüller, J; Kawalia, A; Toliat, MR; EuroEPINOMICS Consortium; Nürnberg, P; Lerche, H; Nothnagel, M; Thiele, H; Sander, T; Meier, JC; Schwarz, G; Neubauer, BA; Zimprich, F Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes.
Ann Neurol. 2015; 77(6):972-986 Doi: 10.1002/ana.24395
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2014

Friedrich, K; Wannhoff, A; Kattner, S; Brune, M; Hov, JR; Weiss, KH; Antoni, C; Dollinger, M; Neumann-Haefelin, C; Seufferlein, T; Schemmer, P; Schirmacher, P; Stremmel, W; Gotthardt, DN PNPLA3 in end-stage liver disease: alcohol consumption, hepatocellular carcinoma development, and transplantation-free survival.
J Gastroenterol Hepatol. 2014; 29(7):1477-1484 Doi: 10.1111/jgh.12540
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Lam, UD; Lerchbaum, E; Schweighofer, N; Trummer, O; Eberhard, K; Genser, B; Pieber, TR; Obermayer-Pietsch, B Association of MEP1A gene variants with insulin metabolism in central European women with polycystic ovary syndrome.
Gene. 2014; 537(2):245-252 Doi: 10.1016/j.gene.2013.12.055
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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 Doi: 10.1016/j.jacc.2013.12.015 [OPEN ACCESS]
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Paar, C; Enko, D; Zahel, B; Mayr, R; Berg, J Reliable analysis of the single nucleotide polymorphism of lactase persistence LPH(-13910) C/T from saliva derived DNA: validation of a standardized saliva collection system.
Clin Lab. 2014; 60(12):1977-1982 Doi: 10.7754/Clin.Lab.2014.140406
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Tragante, V; Barnes, MR; Ganesh, SK; Lanktree, MB; Guo, W; Franceschini, N; Smith, EN; Johnson, T; Holmes, MV; Padmanabhan, S; Karczewski, KJ; Almoguera, B; Barnard, J; Baumert, J; Chang, YP; Elbers, CC; Farrall, M; Fischer, ME; Gaunt, TR; Gho, JM; Gieger, C; Goel, A; Gong, Y; Isaacs, A; Kleber, ME; Mateo Leach, I; McDonough, CW; Meijs, MF; Melander, O; Nelson, CP; Nolte, IM; Pankratz, N; Price, TS; Shaffer, J; Shah, S; Tomaszewski, M; van der Most, PJ; Van Iperen, EP; Vonk, JM; Witkowska, K; Wong, CO; Zhang, L; Beitelshees, AL; Berenson, GS; Bhatt, DL; Brown, M; Burt, A; Cooper-DeHoff, RM; Connell, JM; Cruickshanks, KJ; Curtis, SP; Davey-Smith, G; Delles, C; Gansevoort, RT; Guo, X; Haiqing, S; Hastie, CE; Hofker, MH; Hovingh, GK; Kim, DS; Kirkland, SA; Klein, BE; Klein, R; Li, YR; Maiwald, S; Newton-Cheh, C; O'Brien, ET; Onland-Moret, NC; Palmas, W; Parsa, A; Penninx, BW; Pettinger, M; Vasan, RS; Ranchalis, JE; M Ridker, P; Rose, LM; Sever, P; Shimbo, D; Steele, L; Stolk, RP; Thorand, B; Trip, MD; van Duijn, CM; Verschuren, WM; Wijmenga, C; Wyatt, S; Young, JH; Zwinderman, AH; Bezzina, CR; Boerwinkle, E; Casas, JP; Caulfield, MJ; Chakravarti, A; Chasman, DI; Davidson, KW; Doevendans, PA; Dominiczak, AF; FitzGerald, GA; Gums, JG; Fornage, M; Hakonarson, H; Halder, I; Hillege, HL; Illig, T; Jarvik, GP; Johnson, JA; Kastelein, JJ; Koenig, W; Kumari, M; März, W; Murray, SS; O'Connell, JR; Oldehinkel, AJ; Pankow, JS; Rader, DJ; Redline, S; Reilly, MP; Schadt, EE; Kottke-Marchant, K; Snieder, H; Snyder, M; Stanton, AV; Tobin, MD; Uitterlinden, AG; van der Harst, P; van der Schouw, YT; Samani, NJ; Watkins, H; Johnson, AD; Reiner, AP; Zhu, X; de Bakker, PI; Levy, D; Asselbergs, FW; Munroe, PB; Keating, BJ Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.
Am J Hum Genet. 2014; 94(3):349-360 Doi: 10.1016/j.ajhg.2013.12.016 [OPEN ACCESS]
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Wood, AR; Esko, T; Yang, J; Vedantam, S; Pers, TH; Gustafsson, S; Chu, AY; Estrada, K; Luan, J; Kutalik, Z; Amin, N; Buchkovich, ML; Croteau-Chonka, DC; Day, FR; Duan, Y; Fall, T; Fehrmann, R; Ferreira, T; Jackson, AU; Karjalainen, J; Lo, KS; Locke, AE; Mägi, R; Mihailov, E; Porcu, E; Randall, JC; Scherag, A; Vinkhuyzen, AA; Westra, HJ; Winkler, TW; Workalemahu, T; Zhao, JH; Absher, D; Albrecht, E; Anderson, D; Baron, J; Beekman, M; Demirkan, A; Ehret, GB; Feenstra, B; Feitosa, MF; Fischer, K; Fraser, RM; Goel, A; Gong, J; Justice, AE; Kanoni, S; Kleber, ME; Kristiansson, K; Lim, U; Lotay, V; Lui, JC; Mangino, M; Mateo Leach, I; Medina-Gomez, C; Nalls, MA; Nyholt, DR; Palmer, CD; Pasko, D; Pechlivanis, S; Prokopenko, I; Ried, JS; Ripke, S; Shungin, D; Stancáková, 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; Afzal, U; Arnlöv, J; Arscott, GM; Bandinelli, S; Barrett, A; Bellis, C; Bennett, AJ; Berne, C; Blüher, M; Bolton, JL; Böttcher, Y; Boyd, HA; Bruinenberg, M; Buckley, BM; Buyske, S; Caspersen, IH; Chines, PS; Clarke, R; Claudi-Boehm, S; Cooper, M; Daw, EW; De Jong, PA; Deelen, J; Delgado, G; Denny, JC; Dhonukshe-Rutten, R; Dimitriou, M; Doney, AS; Dörr, M; Eklund, N; Eury, E; Folkersen, L; Garcia, ME; Geller, F; Giedraitis, V; Go, AS; Grallert, H; Grammer, TB; Gräßler, J; Grönberg, H; de Groot, LC; Groves, CJ; Haessler, J; Hall, P; Haller, T; Hallmans, G; Hannemann, A; Hartman, CA; Hassinen, M; Hayward, C; Heard-Costa, NL; Helmer, Q; Hemani, G; Henders, AK; Hillege, HL; Hlatky, MA; Hoffmann, W; Hoffmann, P; Holmen, O; Houwing-Duistermaat, JJ; Illig, T; Isaacs, A; James, AL; Jeff, J; Johansen, B; Johansson, Å; Jolley, J; Juliusdottir, T; Junttila, J; Kho, AN; Kinnunen, L; Klopp, N; Kocher, T; Kratzer, W; Lichtner, P; Lind, L; Lindström, J; Lobbens, S; Lorentzon, M; Lu, Y; Lyssenko, V; Magnusson, PK; Mahajan, A; Maillard, M; McArdle, WL; McKenzie, CA; McLachlan, S; McLaren, PJ; Menni, C; Merger, S; Milani, L; Moayyeri, A; Monda, KL; Morken, MA; Müller, G; Müller-Nurasyid, M; Musk, AW; Narisu, N; Nauck, M; Nolte, IM; Nöthen, MM; Oozageer, L; Pilz, S; Rayner, NW; Renstrom, F; Robertson, NR; Rose, LM; Roussel, R; Sanna, S; Scharnagl, H; Scholtens, S; Schumacher, FR; Schunkert, H; Scott, RA; Sehmi, J; Seufferlein, T; Shi, J; Silventoinen, K; Smit, JH; Smith, AV; Smolonska, J; Stanton, AV; Stirrups, K; Stott, DJ; Stringham, HM; Sundström, J; Swertz, MA; Syvänen, AC; Tayo, BO; Thorleifsson, G; Tyrer, JP; van Dijk, S; van Schoor, NM; van der Velde, N; van Heemst, D; van Oort, FV; Vermeulen, SH; Verweij, N; Vonk, JM; Waite, LL; Waldenberger, M; Wennauer, R; Wilkens, LR; Willenborg, C; Wilsgaard, T; Wojczynski, MK; Wong, A; Wright, AF; Zhang, Q; Arveiler, D; Bakker, SJ; Beilby, J; Bergman, RN; Bergmann, S; Biffar, R; Blangero, J; Boomsma, DI; Bornstein, SR; Bovet, P; Brambilla, P; Brown, MJ; Campbell, H; Caulfield, MJ; Chakravarti, A; Collins, R; Collins, FS; Crawford, DC; Cupples, LA; Danesh, J; de Faire, U; den Ruijter, HM; Erbel, R; Erdmann, J; Eriksson, JG; Farrall, M; Ferrannini, E; Ferrières, J; Ford, I; Forouhi, NG; Forrester, T; Gansevoort, RT; Gejman, PV; Gieger, C; Golay, A; Gottesman, O; Gudnason, V; Gyllensten, U; Haas, DW; Hall, AS; Harris, TB; Hattersley, AT; Heath, AC; Hengstenberg, C; Hicks, AA; Hindorff, LA; Hingorani, AD; Hofman, A; Hovingh, GK; Humphries, SE; Hunt, SC; Hypponen, E; Jacobs, KB; Jarvelin, MR; Jousilahti, P ... Defining the role of common variation in the genomic and biological architecture of adult human height.
Nat Genet. 2014; 46(11):1173-1186 Doi: 10.1038/ng.3097 [OPEN ACCESS]
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2013

Ganesh, SK; Tragante, V; Guo, W; Guo, Y; Lanktree, MB; Smith, EN; Johnson, T; Castillo, BA; Barnard, J; Baumert, J; Chang, YP; Elbers, CC; Farrall, M; Fischer, ME; Franceschini, N; Gaunt, TR; Gho, JM; Gieger, C; Gong, Y; Isaacs, A; Kleber, ME; Mateo Leach, I; McDonough, CW; Meijs, MF; Mellander, O; Molony, CM; Nolte, IM; Padmanabhan, S; Price, TS; Rajagopalan, R; Shaffer, J; Shah, S; Shen, H; Soranzo, N; van der Most, PJ; Van Iperen, EP; Van Setten, J; Van Setten, JA; Vonk, JM; Zhang, L; Beitelshees, AL; Berenson, GS; Bhatt, DL; Boer, JM; Boerwinkle, E; Burkley, B; Burt, A; Chakravarti, A; Chen, W; Cooper-Dehoff, RM; Curtis, SP; Dreisbach, A; Duggan, D; Ehret, GB; Fabsitz, RR; Fornage, M; Fox, E; Furlong, CE; Gansevoort, RT; Hofker, MH; Hovingh, GK; Kirkland, SA; Kottke-Marchant, K; Kutlar, A; Lacroix, AZ; Langaee, TY; Li, YR; Lin, H; Liu, K; Maiwald, S; Malik, R; CARDIOGRAM, METASTROKE; Murugesan, G; Newton-Cheh, C; O'Connell, JR; Onland-Moret, NC; Ouwehand, WH; Palmas, W; Penninx, BW; Pepine, CJ; Pettinger, M; Polak, JF; Ramachandran, VS; Ranchalis, J; Redline, S; Ridker, PM; Rose, LM; Scharnag, H; Schork, NJ; Shimbo, D; Shuldiner, AR; Srinivasan, SR; Stolk, RP; Taylor, HA; Thorand, B; Trip, MD; van Duijn, CM; Verschuren, WM; Wijmenga, C; Winkelmann, BR; Wyatt, S; Young, JH; Boehm, BO; Caulfield, MJ; Chasman, DI; Davidson, KW; Doevendans, PA; Fitzgerald, GA; Gums, JG; Hakonarson, H; Hillege, HL; Illig, T; Jarvik, GP; Johnson, JA; Kastelein, JJ; Koenig, W; LifeLines Cohort Study; März, W; Mitchell, BD; Murray, SS; Oldehinkel, AJ; Rader, DJ; Reilly, MP; Reiner, AP; Schadt, EE; Silverstein, RL; Snieder, H; Stanton, AV; Uitterlinden, AG; van der Harst, P; van der Schouw, YT; Samani, NJ; Johnson, AD; Munroe, PB; de Bakker, PI; Zhu, X; Levy, D; Keating, BJ; Asselbergs, FW Loci influencing blood pressure identified using a cardiovascular gene-centric array.
Hum Mol Genet. 2013; 22(8):1663-1678 Doi: 10.1093/hmg/dds555 [OPEN ACCESS]
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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 Doi: 10.1038/ng.2797 [OPEN ACCESS]
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Parsa, A; Fuchsberger, C; Köttgen, A; O'Seaghdha, CM; Pattaro, C; de Andrade, M; Chasman, DI; Teumer, A; Endlich, K; Olden, M; Chen, MH; Tin, A; Kim, YJ; Taliun, D; Li, M; Feitosa, M; Gorski, M; Yang, Q; Hundertmark, C; Foster, MC; Glazer, N; Isaacs, A; Rao, M; Smith, AV; O'Connell, JR; Struchalin, M; Tanaka, T; Li, G; Hwang, SJ; Atkinson, EJ; Lohman, K; Cornelis, MC; Johansson, A; Tönjes, A; Dehghan, A; Couraki, V; Holliday, EG; Sorice, R; Kutalik, Z; Lehtimäki, T; Esko, T; Deshmukh, H; Ulivi, S; Chu, AY; Murgia, F; Trompet, S; Imboden, M; Kollerits, B; Pistis, G; Harris, TB; Launer, LJ; Aspelund, T; Eiriksdottir, G; Mitchell, BD; Boerwinkle, E; Schmidt, H; Hofer, E; Hu, F; Demirkan, A; Oostra, BA; Turner, ST; Ding, J; Andrews, JS; Freedman, BI; Giulianini, F; Koenig, W; Illig, T; Döring, A; Wichmann, HE; Zgaga, L; Zemunik, T; Boban, M; Minelli, C; Wheeler, HE; Igl, W; Zaboli, G; Wild, SH; Wright, AF; Campbell, H; Ellinghaus, D; Nöthlings, U; Jacobs, G; Biffar, R; Ernst, F; Homuth, G; Kroemer, HK; Nauck, M; Stracke, S; Völker, U; Völzke, H; Kovacs, P; Stumvoll, M; Mägi, R; Hofman, A; Uitterlinden, AG; Rivadeneira, F; Aulchenko, YS; Polasek, O; Hastie, N; Vitart, V; Helmer, C; Wang, JJ; Stengel, B; Ruggiero, D; Bergmann, S; Kähönen, M; Viikari, J; Nikopensius, T; Province, M; Colhoun, H; Doney, A; Robino, A; Krämer, BK; Portas, L; Ford, I; Buckley, BM; Adam, M; Thun, GA; Paulweber, B; Haun, M; Sala, C; Mitchell, P; Ciullo, M; Vollenweider, P; Raitakari, O; Metspalu, A; Palmer, C; Gasparini, P; Pirastu, M; Jukema, JW; Probst-Hensch, NM; Kronenberg, F; Toniolo, D; Gudnason, V; Shuldiner, AR; Coresh, J; Schmidt, R; Ferrucci, L; van Duijn, CM; Borecki, I; Kardia, SL; Liu, Y; Curhan, GC; Rudan, I; Gyllensten, U; Wilson, JF; Franke, A; Pramstaller, PP; Rettig, R; Prokopenko, I; Witteman, J; Hayward, C; Ridker, PM; Bochud, M; Heid, IM; Siscovick, DS; Fox, CS; Kao, WL; Böger, CA Common variants in Mendelian kidney disease genes and their association with renal function.
J Am Soc Nephrol. 2013; 24(12):2105-2117 Doi: 10.1681/ASN.2012100983 [OPEN ACCESS]
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Reiner, AP; Hartiala, J; Zeller, T; Bis, JC; Dupuis, J; Fornage, M; Baumert, J; Kleber, ME; Wild, PS; Baldus, S; Bielinski, SJ; Fontes, JD; Illig, T; Keating, BJ; Lange, LA; Ojeda, F; Müller-Nurasyid, M; Munzel, TF; Psaty, BM; Rice, K; Rotter, JI; Schnabel, RB; Tang, WH; Thorand, B; Erdmann, J; CARDIoGRAM Consortium; Jacobs, DR; Wilson, JG; Koenig, W; Tracy, RP; Blankenberg, S; März, W; Gross, MD; Benjamin, EJ; Hazen, SL; Allayee, H Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.
Hum Mol Genet. 2013; 22(16):3381-3393 Doi: 10.1093/hmg/ddt189 [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 Doi: 10.1161/CIRCULATIONAHA.113.002251 [OPEN ACCESS]
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Vimaleswaran, KS; Berry, DJ; Lu, C; Tikkanen, E; Pilz, S; Hiraki, LT; Cooper, JD; Dastani, Z; Li, R; Houston, DK; Wood, AR; Michaëlsson, K; Vandenput, L; Zgaga, L; Yerges-Armstrong, LM; McCarthy, MI; Dupuis, J; Kaakinen, M; Kleber, ME; Jameson, K; Arden, N; Raitakari, O; Viikari, J; Lohman, KK; Ferrucci, L; Melhus, H; Ingelsson, E; Byberg, L; Lind, L; Lorentzon, M; Salomaa, V; Campbell, H; Dunlop, M; Mitchell, BD; Herzig, KH; Pouta, A; Hartikainen, AL; Genetic Investigation of Anthropometric Traits (GIANT) consortium; Streeten, EA; Theodoratou, E; Jula, A; Wareham, NJ; Ohlsson, C; Frayling, TM; Kritchevsky, SB; Spector, TD; Richards, JB; Lehtimäki, T; Ouwehand, WH; Kraft, P; Cooper, C; März, W; Power, C; Loos, RJ; Wang, TJ; Järvelin, MR; Whittaker, JC; Hingorani, AD; Hyppönen, E Causal Relationship between Obesity and Vitamin D Status: Bi-Directional Mendelian Randomization Analysis of Multiple Cohorts.
PLoS Med. 2013; 10(2):e1001383-e1001383 Doi: 10.1371/journal.pmed.1001383 [OPEN ACCESS]
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2012

Bachernegg, A; El-Shabrawi, Y; Weger, M; Mossböck, G Role of rs1533428 and rs12994401 in patients with Primary Open Angle Glaucoma in an European population.
Ophthalmic Genet. 2012; 34(1-2):48-51 Doi: 10.3109/13816810.2012.736592
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Demirkan, A; van Duijn, CM; Ugocsai, P; Isaacs, A; Pramstaller, PP; Liebisch, G; Wilson, JF; Johansson, Å; Rudan, I; Aulchenko, YS; Kirichenko, AV; Janssens, AC; Jansen, RC; Gnewuch, C; Domingues, FS; Pattaro, C; Wild, SH; Jonasson, I; Polasek, O; Zorkoltseva, IV; Hofman, A; Karssen, LC; Struchalin, M; Floyd, J; Igl, W; Biloglav, Z; Broer, L; Pfeufer, A; Pichler, I; Campbell, S; Zaboli, G; Kolcic, I; Rivadeneira, F; Huffman, J; Hastie, ND; Uitterlinden, A; Franke, L; Franklin, CS; Vitart, V; DIAGRAM Consortium; Nelson, CP; Preuss, M; CARDIoGRAM Consortium; Bis, JC; O'Donnell, CJ; Franceschini, N; CHARGE Consortium; Witteman, JC; Axenovich, T; Oostra, BA; Meitinger, T; Hicks, AA; Hayward, C; Wright, AF; Gyllensten, U; Campbell, H; Schmitz, G; EUROSPAN consortium Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
PLoS Genet. 2012; 8(2):e1002490-e1002490 Doi: 10.1371/journal.pgen.1002490 [OPEN ACCESS]
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Heitzer, E; Seidl, H; Bambach, I; Schmidbauer, U; Cerroni, L; Wolf, P Infrequent p53 gene mutation but UV gradient-like p53 protein positivity in keloids.
Exp Dermatol. 2012; 21(4):277-280 Doi: 10.1111/j.1600-0625.2012.01450.x
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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 Doi: 10.1038/ng.2337 [OPEN ACCESS]
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Meyer, WK; Arbeithuber, B; Ober, C; Ebner, T; Tiemann-Boege, I; Hudson, RR; Przeworski, M Evaluating the evidence for transmission distortion in human pedigrees.
Genetics. 2012; 191(1): 215-232. Doi: 10.1534/genetics.112.139576 [OPEN ACCESS]
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Pattaro, C; Köttgen, A; Teumer, A; Garnaas, M; Böger, CA; Fuchsberger, C; Olden, M; Chen, MH; Tin, A; Taliun, D; Li, M; Gao, X; Gorski, M; Yang, Q; Hundertmark, C; Foster, MC; O'Seaghdha, CM; Glazer, N; Isaacs, A; Liu, CT; Smith, AV; O'Connell, JR; Struchalin, M; Tanaka, T; Li, G; Johnson, AD; Gierman, HJ; Feitosa, M; Hwang, SJ; Atkinson, EJ; Lohman, K; Cornelis, MC; Johansson, Å; Tönjes, A; Dehghan, A; Chouraki, V; Holliday, EG; Sorice, R; Kutalik, Z; Lehtimäki, T; Esko, T; Deshmukh, H; Ulivi, S; Chu, AY; Murgia, F; Trompet, S; Imboden, M; Kollerits, B; Pistis, G; CARDIoGRAM Consortium; ICBP Consortium; CARe Consortium; Wellcome Trust Case Control Consortium 2 (WTCCC2); Harris, TB; Launer, LJ; Aspelund, T; Eiriksdottir, G; Mitchell, BD; Boerwinkle, E; Schmidt, H; Cavalieri, M; Rao, M; Hu, FB; Demirkan, A; Oostra, BA; de Andrade, M; Turner, ST; Ding, J; Andrews, JS; Freedman, BI; Koenig, W; Illig, T; Döring, A; Wichmann, HE; Kolcic, I; Zemunik, T; Boban, M; Minelli, C; Wheeler, HE; Igl, W; Zaboli, G; Wild, SH; Wright, AF; Campbell, H; Ellinghaus, D; Nöthlings, U; Jacobs, G; Biffar, R; Endlich, K; Ernst, F; Homuth, G; Kroemer, HK; Nauck, M; Stracke, S; Völker, U; Völzke, H; Kovacs, P; Stumvoll, M; Mägi, R; Hofman, A; Uitterlinden, AG; Rivadeneira, F; Aulchenko, YS; Polasek, O; Hastie, N; Vitart, V; Helmer, C; Wang, JJ; Ruggiero, D; Bergmann, S; Kähönen, M; Viikari, J; Nikopensius, T; Province, M; Ketkar, S; Colhoun, H; Doney, A; Robino, A; Giulianini, F; Krämer, BK; Portas, L; Ford, I; Buckley, BM; Adam, M; Thun, GA; Paulweber, B; Haun, M; Sala, C; Metzger, M; Mitchell, P; Ciullo, M; Kim, SK; Vollenweider, P; Raitakari, O; Metspalu, A; Palmer, C; Gasparini, P; Pirastu, M; Jukema, JW; Probst-Hensch, NM; Kronenberg, F; Toniolo, D; Gudnason, V; Shuldiner, AR; Coresh, J; Schmidt, R; Ferrucci, L; Siscovick, DS; van Duijn, CM; Borecki, I; Kardia, SL; Liu, Y; Curhan, GC; Rudan, I; Gyllensten, U; Wilson, JF; Franke, A; Pramstaller, PP; Rettig, R; Prokopenko, I; Witteman, JC; Hayward, C; Ridker, P; Parsa, A; Bochud, M; Heid, IM; Goessling, W; Chasman, DI; Kao, WH; Fox, CS Genome-wide association and functional follow-up reveals new loci for kidney function.
PLoS Genet. 2012; 8(3):e1002584-e1002584 Doi: 10.1371/journal.pgen.1002584 [OPEN ACCESS]
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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 Doi: 10.1038/ng.2238 [OPEN ACCESS]
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Tsoi, LC; Spain, SL; Knight, J; Ellinghaus, E; Stuart, PE; Capon, F; Ding, J; Li, Y; Tejasvi, T; Gudjonsson, JE; Kang, HM; Allen, MH; McManus, R; Novelli, G; Samuelsson, L; Schalkwijk, J; Ståhle, M; Burden, AD; Smith, CH; Cork, MJ; Estivill, X; Bowcock, AM; Krueger, GG; Weger, W; Worthington, J; Tazi-Ahnini, R; Nestle, FO; Hayday, A; Hoffmann, P; Winkelmann, J; Wijmenga, C; Langford, C; Edkins, S; Andrews, R; Blackburn, H; Strange, A; Band, G; Pearson, RD; Vukcevic, D; Spencer, CC; Deloukas, P; Mrowietz, U; Schreiber, S; Weidinger, S; Koks, S; Kingo, K; Esko, T; Metspalu, A; Lim, HW; Voorhees, JJ; Weichenthal, M; Wichmann, HE; Chandran, V; Rosen, CF; Rahman, P; Gladman, DD; Griffiths, CE; Reis, A; Kere, J; Collaborative Association Study of Psoriasis (CASP); Genetic Analysis of Psoriasis Consortium; Psoriasis Association Genetics Extension; Wellcome Trust Case Control Consortium 2; Nair, RP; Franke, A; Barker, JN; Abecasis, GR; Elder, JT; Trembath, RC Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.
Nat Genet. 2012; 44(12):1341-1348 Doi: 10.1038/ng.2467 [OPEN ACCESS]
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Wiesner, T; Fried, I; Ulz, P; Stacher, E; Popper, H; Murali, R; Kutzner, H; Lax, S; Smolle-Jüttner, F; Geigl, JB; Speicher, MR Toward an improved definition of the tumor spectrum associated with BAP1 germline mutations.
J Clin Oncol. 2012; 30(32):e337-e340 Doi: 10.1200/JCO.2011.41.2965 (- Case Report) [OPEN ACCESS]
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2011

Bis, JC; Kavousi, M; Franceschini, N; Isaacs, A; Abecasis, GR; Schminke, U; Post, WS; Smith, AV; Cupples, LA; Markus, HS; Schmidt, R; Huffman, JE; Lehtimäki, T; Baumert, J; Münzel, T; Heckbert, SR; Dehghan, A; North, K; Oostra, B; Bevan, S; Stoegerer, EM; Hayward, C; Raitakari, O; Meisinger, C; Schillert, A; Sanna, S; Völzke, H; Cheng, YC; Thorsson, B; Fox, CS; Rice, K; Rivadeneira, F; Nambi, V; Halperin, E; Petrovic, KE; Peltonen, L; Wichmann, HE; Schnabel, RB; Dörr, M; Parsa, A; Aspelund, T; Demissie, S; Kathiresan, S; Reilly, MP; Taylor, K; Uitterlinden, A; Couper, DJ; Sitzer, M; Kähönen, M; Illig, T; Wild, PS; Orru, M; Lüdemann, J; Shuldiner, AR; Eiriksdottir, G; White, CC; Rotter, JI; Hofman, A; Seissler, J; Zeller, T; Usala, G; Ernst, F; Launer, LJ; D'Agostino, RB; O'Leary, DH; Ballantyne, C; Thiery, J; Ziegler, A; Lakatta, EG; Chilukoti, RK; Harris, TB; Wolf, PA; Psaty, BM; Polak, JF; Li, X; Rathmann, W; Uda, M; Boerwinkle, E; Klopp, N; Schmidt, H; Wilson, JF; Viikari, J; Koenig, W; Blankenberg, S; Newman, AB; Witteman, J; Heiss, G; Duijn, Cv; Scuteri, A; Homuth, G; Mitchell, BD; Gudnason, V; O'Donnell, CJ; CARDIoGRAM Consortium Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.
Nat Genet. 2011; 43(10):940-947 Doi: 10.1038/ng.920 [OPEN ACCESS]
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IBC 50K CAD Consortium Large-scale gene-centric analysis identifies novel variants for coronary artery disease.
PLoS Genet. 2011; 7(9):e1002260-e1002260 Doi: 10.1371/journal.pgen.1002260 [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 Doi: 10.1016/j.ajhg.2010.11.007 [OPEN ACCESS]
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Morgan, TM; House, JA; Cresci, S; Jones, P; Allayee, H; Hazen, SL; Patel, Y; Patel, RS; Eapen, DJ; Waddy, SP; Quyyumi, AA; Kleber, ME; März, W; Winkelmann, BR; Boehm, BO; Krumholz, HM; Spertus, JA Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome.
BMC Med Genet. 2011; 12(4):127-127 Doi: 10.1186/1471-2350-12-127 [OPEN ACCESS]
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Mueller, EE; Eder, W; Ebner, S; Schwaiger, E; Santic, D; Kreindl, T; Stanger, O; Paulweber, B; Iglseder, B; Oberkofler, H; Maier, R; Mayr, JA; Krempler, F; Weitgasser, R; Patsch, W; Sperl, W; Kofler, B The Mitochondrial T16189C Polymorphism Is Associated with Coronary Artery Disease in Middle European Populations
PLOS ONE. 2011; 6(1): Doi: 10.1371/journal.pone.0016455 [OPEN ACCESS]
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Silbernagel, G; Renner, W; Grammer, TB; Hugl, SR; Bertram, J; Kleber, ME; Hoffmann, MM; Winkelmann, BR; Marz, W; Boehm, BO Association of TCF7L2 SNPs with age at onset of type 2 diabetes and proinsulin/insulin ratio but not with glucagon-like peptide 1
DIABETES-METAB RES. 2011; 27(5): 499-505. Doi: 10.1002/dmrr.1194 [OPEN ACCESS]
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2009

Mossböck, G; Renner, W; El-Shabrawi, Y; Faschinger, C; Schmut, O; Wedrich, A; Zimmermann, C; Weger, M TNF-alpha -308 G>A and -238 G>A polymorphisms are not major risk factors in Caucasian patients with exfoliation glaucoma.
Mol Vis. 2009; 15(10): 518-522. [OPEN ACCESS]
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Müssig, K; Staiger, H; Machicao, F; Kirchhoff, K; Guthoff, M; Schäfer, SA; Kantartzis, K; Silbernagel, G; Stefan, N; Holst, JJ; Gallwitz, B; Häring, HU; Fritsche, A Association of type 2 diabetes candidate polymorphisms in KCNQ1 with incretin and insulin secretion.
Diabetes. 2009; 58(7):1715-1720 Doi: 10.2337/db08-1589 [OPEN ACCESS]
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2008

Mossböck, G; Renner, W; Faschinger, C; Schmut, O; Wedrich, A; Weger, M Lysyl oxidase-like protein 1 (LOXL1) gene polymorphisms and exfoliation glaucoma in a Central European population.
Mol Vis. 2008; 14(10): 857-861. [OPEN ACCESS]
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Staiger, H; Machicao, F; Kantartzis, K; Schäfer, SA; Kirchhoff, K; Guthoff, M; Silbernagel, G; Stefan, N; Fritsche, A; Häring, HU Novel meta-analysis-derived type 2 diabetes risk loci do not determine prediabetic phenotypes.
PLoS One. 2008; 3(8):e3019-e3019 Doi: 10.1371/journal.pone.0003019 [OPEN ACCESS]
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Weger, W; Hofer, A; Wolf, P; El-Shabrawi, Y; Renner, W; Kerl, H; Salmhofer, W Role of the interleukin 15 96516A>T and IL15 96330C>A gene polymorphisms in Caucasian patients with chronic plaque psoriasis.
J Dermatol Sci. 2008; 51(2): 147-149. Doi: 10.1016/j.jdermsci.2008.02.010
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2007

Weger, M; Renner, W; Steinbrugger, I; Köfer, K; Wedrich, A; Groselj-Strele, A; El-Shabrawi, Y; Schmut, O; Haas, A Association of the HTRA1 -625G>A promoter gene polymorphism with exudative age-related macular degeneration in a Central European population.
Mol Vis. 2007; 13(4): 1274-1279. [OPEN ACCESS]
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2006

Yazdani-Biuki, B; Brickmann, K; Wohlfahrt, K; Mueller, T; März, W; Renner, W; Gutjahr, M; Langsenlehner, U; Krippl, P; Wascher, TC; Paulweber, B; Graninger, W; Brezinschek, HP The MHC2TA -168A>G gene polymorphism is not associated with rheumatoid arthritis in Austrian patients.
Arthritis Res Ther. 2006; 8(4):R97-R97 Doi: 10.1186/ar1974 [OPEN ACCESS]
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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. Doi: 10.1016/j.mcp.2004.05.005
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2003

Ardigó, M; Borroni, G; Muscardin, L; Kerl, H; Cerroni, L Hypopigmented mycosis fungoides in Caucasian patients: a clinicopathologic study of 7 cases.
J Am Acad Dermatol. 2003; 49(2):264-270 Doi: 10.1067%2FS0190-9622%2803%2900907-1
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Reichenpfader, B; Immel, U; Klintschar, M Population data on the AmpFlSTR SGM plus PCR amplification kit in Germans and Austrians.
FORENSIC SCI INT 2003 132: 84-86. Doi: 10.1016%2FS0379-0738%2802%2900448-6
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Wascher, TC; Paulweber, B; Malaimare, L; Stadlmayr, A; Iglseder, B; Schmoelzer, I; Renner, W Associations of a human G protein beta3 subunit dimorphism with insulin resistance and carotid atherosclerosis.
Stroke. 2003; 34(3):605-609 Doi: 10.1161/01.STR.0000058159.63950.EA [OPEN ACCESS]
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2000

Obermayer-Pietsch, BM; Frühauf, GE; Chararas, K; Mikhail-Reinisch, S; Renner, W; Berghold, A; Kenner, L; Lackner, C Association of the vitamin D receptor genotype BB with low bone density in hyperthyroidism.
J Bone Miner Res. 2000; 15(10):1950-1955 Doi: 10.1359/jbmr.2000.15.10.1950 [OPEN ACCESS]
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