Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Publikationen
Suchbegriffe: HERITABILITY, . Treffer: 40
2022
Hofer, E; Pirpamer, L; Langkammer, C; Tinauer, C; Seshadri, S; Schmidt, H; Schmidt, R
Heritability of R2* iron in the basal ganglia and cortex.
Aging (Albany NY). 2022; 14(16):6415-6426
Doi: 10.18632/aging.204212
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Hofer, E; Pirpamer, L; Langkammer, C; Tinauer, C; Seshadri, S; Schmidt, H; Schmidt, R
Heritability of R2*iron in the basal ganglia and cortex
AGING-US. 2022; 14(16): 6415-6426.
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Knol, MJ; Pawlak, MA; Lamballais, S; Terzikhan, N; Hofer, E; Xiong, Z; Klaver, CCW; Pirpamer, L; Vernooij, MW; Ikram, MA; Schmidt, R; Kayser, M; Evans, TE; Adams, HHH
Genetic architecture of orbital telorism.
Hum Mol Genet. 2021;
Doi: 10.1093/hmg/ddab334
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Pott, J; Gådin, JR; Theusch, E; Kleber, ME; Delgado, GE; Kirsten, H; Hauck, SM; Burkhardt, R; Scharnagl, H; Krauss, RM; Loeffler, M; März, W; Thiery, J; Silveira, A; Van't, Hooft, FM; Scholz, M
Meta-GWAS of PCSK9 levels detects two novel loci at APOB and TM6SF2.
Hum Mol Genet. 2022; 31(6):999-1011
Doi: 10.1093/hmg/ddab279
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Yengo, L; Vedantam, S; Marouli, E; Sidorenko, J; Bartell, E; Sakaue, S; Graff, M; Eliasen, AU; Jiang, Y; Raghavan, S; Miao, J; Arias, JD; Graham, SE; Mukamel, RE; Spracklen, CN; Yin, X; Chen, SH; Ferreira, T; Highland, HH; Ji, Y; Karaderi, T; Lin, K; Lüll, K; Malden, DE; Medina-Gomez, C; Machado, M; Moore, A; Rüeger, S; Sim, X; Vrieze, S; Ahluwalia, TS; Akiyama, M; Allison, MA; Alvarez, M; Andersen, MK; Ani, A; Appadurai, V; Arbeeva, L; Bhaskar, S; Bielak, LF; Bollepalli, S; Bonnycastle, LL; Bork-Jensen, J; Bradfield, JP; Bradford, Y; Braund, PS; Brody, JA; Burgdorf, KS; Cade, BE; Cai, H; Cai, Q; Campbell, A; Cañadas-Garre, M; Catamo, E; Chai, JF; Chai, X; Chang, LC; Chang, YC; Chen, CH; Chesi, A; Choi, SH; Chung, RH; Cocca, M; Concas, MP; Couture, C; Cuellar-Partida, G; Danning, R; Daw, EW; Degenhard, F; Delgado, GE; Delitala, A; Demirkan, A; Deng, X; Devineni, P; Dietl, A; Dimitriou, M; Dimitrov, L; Dorajoo, R; Ekici, AB; Engmann, JE; Fairhurst-Hunter, Z; Farmaki, AE; Faul, JD; Fernandez-Lopez, JC; Forer, L; Francescatto, M; Freitag-Wolf, S; Fuchsberger, C; Galesloot, TE; Gao, Y; Gao, Z; Geller, F; Giannakopoulou, O; Giulianini, F; Gjesing, AP; Goel, A; Gordon, SD; Gorski, M; Grove, J; Guo, X; Gustafsson, S; Haessler, J; Hansen, TF; Havulinna, AS; Haworth, SJ; He, J; Heard-Costa, N; Hebbar, P; Hindy, G; Ho, YA; Hofer, E; Holliday, E; Horn, K; Hornsby, WE; Hottenga, JJ; Huang, H; Huang, J; Huerta-Chagoya, A; Huffman, JE; Hung, YJ; Huo, S; Hwang, MY; Iha, H; Ikeda, DD; Isono, M; Jackson, AU; Jäger, S; Jansen, IE; Johansson, I; Jonas, JB; Jonsson, A; Jørgensen, T; Kalafati, IP; Kanai, M; Kanoni, S; Kårhus, LL; Kasturiratne, A; Katsuya, T; Kawaguchi, T; Kember, RL; Kentistou, KA; Kim, HN; Kim, YJ; Kleber, ME; Knol, MJ; Kurbasic, A; Lauzon, M; Le, P; Lea, R; Lee, JY; Leonard, HL; Li, SA; Li, X; Li, X; Liang, J; Lin, H; Lin, SY; Liu, J; Liu, X; Lo, KS; Long, J; Lores-Motta, L; Luan, J; Lyssenko, V; Lyytikäinen, LP; Mahajan, A; Mamakou, V; Mangino, M; Manichaikul, A; Marten, J; Mattheisen, M; Mavarani, L; McDaid, AF; Meidtner, K; Melendez, TL; Mercader, JM; Milaneschi, Y; Miller, JE; Millwood, IY; Mishra, PP; Mitchell, RE; Møllehave, LT; Morgan, A; Mucha, S; Munz, M; Nakatochi, M; Nelson, CP; Nethander, M; Nho, CW; Nielsen, AA; Nolte, IM; Nongmaithem, SS; Noordam, R; Ntalla, I; Nutile, T; Pandit, A; Christofidou, P; Pärna, K; Pauper, M; Petersen, ERB; Petersen, LV; Pitkänen, N; Polašek, O; Poveda, A; Preuss, MH; Pyarajan, S; Raffield, LM; Rakugi, H; Ramirez, J; Rasheed, A; Raven, D; Rayner, NW; Riveros, C; Rohde, R; Ruggiero, D; Ruotsalainen, SE; Ryan, KA; Sabater-Lleal, M; Saxena, R; Scholz, M; Sendamarai, A; Shen, B; Shi, J; Shin, JH; Sidore, C; Sitlani, CM; Slieker, RC; Smit, RAJ; Smith, AV; Smith, JA; Smyth, LJ; Southam, L; Steinthorsdottir, V; Sun, L; Takeuchi, F; Tallapragada, DSP; Taylor, KD; Tayo, BO; Tcheandjieu, C; Terzikhan, N; Tesolin, P; Teumer, A; Theusch, E; Thompson, DJ; Thorleifsson, G; Timmers, PRHJ; Trompet, S; Turman, C; Vaccargiu, S; van, der, Laan, SW; van, der, Most, PJ; van, Klinken, JB; van, Setten, J; Verma, SS; Verweij, N; Veturi, Y; Wang, CA; Wang, C; Wang, L; Wang, Z; Warren, HR; Bin, Wei, W; Wickremasinghe, AR; Wielscher, M; Wiggins, KL; Winsvold, BS; Wong, A; Wu, Y; Wuttke, M; Xia, R; Xie, T; Yamamoto, K; Yang, J; Yao, J; Young, H; Yousri, NA; Yu, L; Zeng, L; Zhang, W; Zhang, X; Zhao, JH; Zhao, W; Zhou, W; Zimmermann, ME; Zoledziewska, M; Adair, LS; Adams, HHH; Aguilar-Salinas, CA; Al-Mulla, F; Arnett, DK; Asse ...
A saturated map of common genetic variants associated with human height.
Nature. 2022; 610(7933):704-712
Doi: 10.1038/s41586-022-05275-y
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2021
Ahluwalia, TS; Prins, BP; Abdollahi, M; Armstrong, NJ; Aslibekyan, S; Bain, L; Jefferis, B; Baumert, J; Beekman, M; Ben-Shlomo, Y; Bis, JC; Mitchell, BD; de, Geus, E; Delgado, GE; Marek, D; Eriksson, J; Kajantie, E; Kanoni, S; Kemp, JP; Lu, C; Marioni, RE; McLachlan, S; Milaneschi, Y; Nolte, IM; Petrelis, AM; Porcu, E; Sabater-Lleal, M; Naderi, E; Seppälä, I; Shah, T; Singhal, G; Standl, M; Teumer, A; Thalamuthu, A; Thiering, E; Trompet, S; Ballantyne, CM; Benjamin, EJ; Casas, JP; Toben, C; Dedoussis, G; Deelen, J; Durda, P; Engmann, J; Feitosa, MF; Grallert, H; Hammarstedt, A; Harris, SE; Homuth, G; Hottenga, JJ; Jalkanen, S; Jamshidi, Y; Jawahar, MC; Jess, T; Kivimaki, M; Kleber, ME; Lahti, J; Liu, Y; Marques-Vidal, P; Mellström, D; Mooijaart, SP; Müller-Nurasyid, M; Penninx, B; Revez, JA; Rossing, P; Räikkönen, K; Sattar, N; Scharnagl, H; Sennblad, B; Silveira, A; Pourcain, BS; Timpson, NJ; Trollor, J; van, Dongen, J; Van, Heemst, D; Visvikis-Siest, S; Vollenweider, P; Völker, U; Waldenberger, M; Willemsen, G; Zabaneh, D; Morris, RW; Arnett, DK; Baune, BT; Boomsma, DI; Chang, YC; Deary, IJ; Deloukas, P; Eriksson, JG; Evans, DM; Ferreira, MA; Gaunt, T; Gudnason, V; Hamsten, A; Heinrich, J; Hingorani, A; Humphries, SE; Jukema, JW; Koenig, W; Kumari, M; Kutalik, Z; Lawlor, DA; Lehtimäki, T; März, W; Mather, KA; Naitza, S; Nauck, M; Ohlsson, C; Price, JF; Raitakari, O; Rice, K; Sachdev, PS; Slagboom, E; Sørensen, TIA; Spector, T; Stacey, D; Stathopoulou, MG; Tanaka, T; Wannamethee, SG; Whincup, P; Rotter, JI; Dehghan, A; Boerwinkle, E; Psaty, BM; Snieder, H; Alizadeh, BZ, , CHARGE, Inflammation, Working, Group
Genome-wide association study of circulating interleukin 6 levels identifies novel loci.
Hum Mol Genet. 2021; 30(5):393-409
Doi: 10.1093/hmg/ddab023
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Bressler, J; Davies, G; Smith, AV; Saba, Y; Bis, JC; Jian, X; Hayward, C; Yanek, L; Smith, JA; Mirza, SS; Wang, R; Adams, HHH; Becker, D; Boerwinkle, E; Campbell, A; Cox, SR; Eiriksdottir, G; Fawns-Ritchie, C; Gottesman, RF; Grove, ML; Guo, X; Hofer, E; Kardia, SLR; Knol, MJ; Koini, M; Lopez, OL; Marioni, RE; Nyquist, P; Pattie, A; Polasek, O; Porteous, DJ; Rudan, I; Satizabal, CL; Schmidt, H; Schmidt, R; Sidney, S; Simino, J; Smith, BH; Turner, ST; van, der, Lee, SJ; Ware, EB; Whitmer, RA; Yaffe, K; Yang, Q; Zhao, W; Gudnason, V; Launer, LJ; Fitzpatrick, AL; Psaty, BM; Fornage, M; Arfan, Ikram, M; van, Duijn, CM; Seshadri, S; Mosley, TH; Deary, IJ
Association of low-frequency and rare coding variants with information processing speed.
Transl Psychiatry. 2021; 11(1):613
Doi: 10.1038/s41398-021-01736-6
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Kalman, JL; Loohuis, LMO; Vreeker, A; McQuillin, A; Stahl, EA; Ruderfer, D; Grigoroiu-Serbanescu, M; Panagiotaropoulou, G; Ripke, S; Bigdeli, TB; Stein, F; Meller, T; Meinert, S; Pelin, H; Streit, F; Papiol, S; Adams, MJ; Adolfsson, R; Adorjan, K; Agartz, I; Aminoff, SR; Anderson-Schmidt, H; Andreassen, OA; Ardau, R; Aubry, JM; Balaban, C; Bass, N; Baune, BT; Bellivier, F; Benabarre, A; Bengesser, S; Berrettini, WH; Boks, MP; Bromet, EJ; Brosch, K; Budde, M; Byerley, W; Cervantes, P; Chillotti, C; Cichon, S; Clark, SR; Comes, AL; Corvin, A; Coryell, W; Craddock, N; Craig, DW; Croarkin, PE; Cruceanu, C; Czerski, PM; Dalkner, N; Dannlowski, U; Degenhardt, F; Del Zompo, M; DePaulo, JR; Djurovic, S; Edenberg, HJ; Al Eissa, M; Elvsashagen, T; Etain, B; Fanous, AH; Fellendorf, F; Fiorentino, A; Forstner, AJ; Frye, MA; Fullerton, JM; Gade, K; Garnham, J; Gershon, E; Gill, M; Goes, FS; Gordon-Smith, K; Grof, P; Guzman-Parra, J; Hahn, T; Hasler, R; Heilbronner, M; Heilbronner, U; Jamain, S; Jimenez, E; Jones, I; Jones, L; Jonsson, L; Kahn, RS; Kelsoe, JR; Kennedy, JL; Kircher, T; Kirov, G; Kittel-Schneider, S; Klohn-Saghatolislam, F; Knowles, JA; Kranz, TM; Lagerberg, TV; Landen, M; Lawson, WB; Leboyer, M; Li, QQS; Maj, M; Malaspina, D; Manchia, M; Mayoral, F; McElroy, SL; McInnis, MG; McIntosh, AM; Medeiros, H; Melle, I; Milanova, V; Mitchell, PB; Monteleone, P; Monteleone, AM; Nothen, MM; Novak, T; Nurnberger, JI; O'Brien, N; O'Connell, KS; O'Donovan, C; O'Donovan, MC; Opel, N; Ortiz, A; Owen, MJ; Palsson, E; Pato, C; Pato, MT; Pawlak, J; Pfarr, JK; Pisanu, C; Potash, JB; Rapaport, MH; Reich-Erkelenz, D; Reif, A; Reininghaus, E; Repple, J; Richard-Lepouriel, H; Rietschel, M; Ringwald, K; Roberts, G; Rouleau, G; Schaupp, S; Scheftner, WA; Schmitt, S; Schofield, PR; Schubert, KO; Schulte, EC; Schweizer, B; Senner, F; Severino, G; Sharp, S; Slaney, C; Smeland, OB; Sobell, JL; Squassina, A; Stopkova, P; Strauss, J; Tortorella, A; Turecki, G; Twarowska-Hauser, J; Veldic, M; Vieta, E; Vincent, JB; Xu, W; Zai, CC; Zandi, PP; Di Florio, A; Smoller, JW; Biernacka, JM; McMahon, FJ; Alda, M; Muller-Myhsok, B; Koutsouleris, N; Falkai, P; Freimer, NB; Andlauer, TFM; Schulze, TG; Ophoff, RA
Characterisation of age and polarity at onset in bipolar disorder
BRIT J PSYCHIAT. 2021; 219(6): 659-669.
Doi: 10.1192/bjp.2021.102
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2020
Hofer, E; Roshchupkin, GV; Adams, HHH; Knol, MJ; Lin, H; Li, S; Zare, H; Ahmad, S; Armstrong, NJ; Satizabal, CL; Bernard, M; Bis, JC; Gillespie, NA; Luciano, M; Mishra, A; Scholz, M; Teumer, A; Xia, R; Jian, X; Mosley, TH; Saba, Y; Pirpamer, L; Seiler, S; Becker, JT; Carmichael, O; Rotter, JI; Psaty, BM; Lopez, OL; Amin, N; van der Lee, SJ; Yang, Q; Himali, JJ; Maillard, P; Beiser, AS; DeCarli, C; Karama, S; Lewis, L; Harris, M; Bastin, ME; Deary, IJ; Veronica Witte, A; Beyer, F; Loeffler, M; Mather, KA; Schofield, PR; Thalamuthu, A; Kwok, JB; Wright, MJ; Ames, D; Trollor, J; Jiang, J; Brodaty, H; Wen, W; Vernooij, MW; Hofman, A; Uitterlinden, AG; Niessen, WJ; Wittfeld, K; Bülow, R; Völker, U; Pausova, Z; Bruce Pike, G; Maingault, S; Crivello, F; Tzourio, C; Amouyel, P; Mazoyer, B; Neale, MC; Franz, CE; Lyons, MJ; Panizzon, MS; Andreassen, OA; Dale, AM; Logue, M; Grasby, KL; Jahanshad, N; Painter, JN; Colodro-Conde, L; Bralten, J; Hibar, DP; Lind, PA; Pizzagalli, F; Stein, JL; Thompson, PM; Medland, SE; ENIGMA consortium; Sachdev, PS; Kremen, WS; Wardlaw, JM; Villringer, A; van Duijn, CM; Grabe, HJ; Longstreth, WT; Fornage, M; Paus, T; Debette, S; Arfan Ikram, M; Schmidt, H; Schmidt, R; Seshadri, S
Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.
Nat Commun. 2020; 11(1): 4796-4796.
Doi: 10.1038/s41467-020-18367-y
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Shah, S; Henry, A; Roselli, C; Lin, H; Sveinbjörnsson, G; Fatemifar, G; Hedman, ÅK; Wilk, JB; Morley, MP; Chaffin, MD; Helgadottir, A; Verweij, N; Dehghan, A; Almgren, P; Andersson, C; Aragam, KG; Ärnlöv, J; Backman, JD; Biggs, ML; Bloom, HL; Brandimarto, J; Brown, MR; Buckbinder, L; Carey, DJ; Chasman, DI; Chen, X; Chen, X; Chung, J; Chutkow, W; Cook, JP; Delgado, GE; Denaxas, S; Doney, AS; Dörr, M; Dudley, SC; Dunn, ME; Engström, G; Esko, T; Felix, SB; Finan, C; Ford, I; Ghanbari, M; Ghasemi, S; Giedraitis, V; Giulianini, F; Gottdiener, JS; Gross, S; Guðbjartsson, DF; Gutmann, R; Haggerty, CM; van der Harst, P; Hyde, CL; Ingelsson, E; Jukema, JW; Kavousi, M; Khaw, KT; Kleber, ME; Køber, L; Koekemoer, A; Langenberg, C; Lind, L; Lindgren, CM; London, B; Lotta, LA; Lovering, RC; Luan, J; Magnusson, P; Mahajan, A; Margulies, KB; März, W; Melander, O; Mordi, IR; Morgan, T; Morris, AD; Morris, AP; Morrison, AC; Nagle, MW; Nelson, CP; Niessner, A; Niiranen, T; O'Donoghue, ML; Owens, AT; Palmer, CNA; Parry, HM; Perola, M; Portilla-Fernandez, E; Psaty, BM; Regeneron Genetics Center; Rice, KM; Ridker, PM; Romaine, SPR; Rotter, JI; Salo, P; Salomaa, V; van Setten, J; Shalaby, AA; Smelser, DT; Smith, NL; Stender, S; Stott, DJ; Svensson, P; Tammesoo, ML; Taylor, KD; Teder-Laving, M; Teumer, A; Thorgeirsson, G; Thorsteinsdottir, U; Torp-Pedersen, C; Trompet, S; Tyl, B; Uitterlinden, AG; Veluchamy, A; Völker, U; Voors, AA; Wang, X; Wareham, NJ; Waterworth, D; Weeke, PE; Weiss, R; Wiggins, KL; Xing, H; Yerges-Armstrong, LM; Yu, B; Zannad, F; Zhao, JH; Hemingway, H; Samani, NJ; McMurray, JJV; Yang, J; Visscher, PM; Newton-Cheh, C; Malarstig, A; Holm, H; Lubitz, SA; Sattar, N; Holmes, MV; Cappola, TP; Asselbergs, FW; Hingorani, AD; Kuchenbaecker, K; Ellinor, PT; Lang, CC; Stefansson, K; Smith, JG; Vasan, RS; Swerdlow, DI; Lumbers, RT
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.
Nat Commun. 2020; 11(1):163-163
Doi: 10.1038/s41467-019-13690-5
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Swietlik, EM; Greene, D; Zhu, N; Megy, K; Cogliano, M; Rajaram, S; Pandya, D; Tilly, T; Lutz, KA; Welch, CCL; Pauciulo, MW; Southgate, L; Martin, JM; Treacy, CM; Penkett, CJ; Stephens, JC; Bogaard, HJ; Church, C; Coghlan, G; Coleman, AW; Condliffe, R; Eichstaedt, CA; Eyries, M; Gall, H; Ghio, S; Girerd, B; Grünig, E; Holden, S; Howard, L; Humbert, M; Kiely, DG; Kovacs, G; Lordan, J; Machado, RD; Mackenzie, Ross, RV; McCabe, C; Moledina, S; Montani, D; Olschewski, H; Pepke-Zaba, J; Price, L; Rhodes, CJ; Seeger, W; Soubrier, F; Suntharalingam, J; Toshner, MR; Vonk, Noordegraaf, A; Wharton, J; Wild, JM; Wort, SJ; Lawrie, A; Wilkins, MR; Trembath, RC; Shen, Y; Chung, WK; Swift, AJ; Nichols, WC; Morrell, NW; Gräf, S
Bayesian Inference Associates Rare KDR Variants with Specific Phenotypes in Pulmonary Arterial Hypertension.
Circ Genom Precis Med. 2020; 14(1):e003155
Doi: 10.1161/CIRCGEN.120.003155
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Tsang, B; Pritišanac, I; Scherer, SW; Moses, AM; Forman-Kay, JD
Phase Separation as a Missing Mechanism for Interpretation of Disease Mutations.
Cell. 2020; 183(7):1742-1756
Doi: 10.1016/j.cell.2020.11.050
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2019
Patel, D; Mez, J; Vardarajan, BN; Staley, L; Chung, J; Zhang, X; Farrell, JJ; Rynkiewicz, MJ; Cannon-Albright, LA; Teerlink, CC; Stevens, J; Corcoran, C; Gonzalez Murcia, JD; Lopez, OL; Mayeux, R; Haines, JL; Pericak-Vance, MA; Schellenberg, G; Kauwe, JSK; Lunetta, KL; Farrer, LA; Alzheimer’s Disease Sequencing Project
Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.
JAMA Netw Open. 2019; 2(3):e191350-e191350
Doi: 10.1001/jamanetworkopen.2019.1350
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2018
Davies, G; Lam, M; Harris, SE; Trampush, JW; Luciano, M; Hill, WD; Hagenaars, SP; Ritchie, SJ; Marioni, RE; Fawns-Ritchie, C; Liewald, DCM; Okely, JA; Ahola-Olli, AV; Barnes, CLK; Bertram, L; Bis, JC; Burdick, KE; Christoforou, A; DeRosse, P; Djurovic, S; Espeseth, T; Giakoumaki, S; Giddaluru, S; Gustavson, DE; Hayward, C; Hofer, E; Ikram, MA; Karlsson, R; Knowles, E; Lahti, J; Leber, M; Li, S; Mather, KA; Melle, I; Morris, D; Oldmeadow, C; Palviainen, T; Payton, A; Pazoki, R; Petrovic, K; Reynolds, CA; Sargurupremraj, M; Scholz, M; Smith, JA; Smith, AV; Terzikhan, N; Thalamuthu, A; Trompet, S; van der Lee, SJ; Ware, EB; Windham, BG; Wright, MJ; Yang, J; Yu, J; Ames, D; Amin, N; Amouyel, P; Andreassen, OA; Armstrong, NJ; Assareh, AA; Attia, JR; Attix, D; Avramopoulos, D; Bennett, DA; Böhmer, AC; Boyle, PA; Brodaty, H; Campbell, H; Cannon, TD; Cirulli, ET; Congdon, E; Conley, ED; Corley, J; Cox, SR; Dale, AM; Dehghan, A; Dick, D; Dickinson, D; Eriksson, JG; Evangelou, E; Faul, JD; Ford, I; Freimer, NA; Gao, H; Giegling, I; Gillespie, NA; Gordon, SD; Gottesman, RF; Griswold, ME; Gudnason, V; Harris, TB; Hartmann, AM; Hatzimanolis, A; Heiss, G; Holliday, EG; Joshi, PK; Kähönen, M; Kardia, SLR; Karlsson, I; Kleineidam, L; Knopman, DS; Kochan, NA; Konte, B; Kwok, JB; Le Hellard, S; Lee, T; Lehtimäki, T; Li, SC; Liu, T; Koini, M; London, E; Longstreth, WT; Lopez, OL; Loukola, A; Luck, T; Lundervold, AJ; Lundquist, A; Lyytikäinen, LP; Martin, NG; Montgomery, GW; Murray, AD; Need, AC; Noordam, R; Nyberg, L; Ollier, W; Papenberg, G; Pattie, A; Polasek, O; Poldrack, RA; Psaty, BM; Reppermund, S; Riedel-Heller, SG; Rose, RJ; Rotter, JI; Roussos, P; Rovio, SP; Saba, Y; Sabb, FW; Sachdev, PS; Satizabal, CL; Schmid, M; Scott, RJ; Scult, MA; Simino, J; Slagboom, PE; Smyrnis, N; Soumaré, A; Stefanis, NC; Stott, DJ; Straub, RE; Sundet, K; Taylor, AM; Taylor, KD; Tzoulaki, I; Tzourio, C; Uitterlinden, A; Vitart, V; Voineskos, AN; Kaprio, J; Wagner, M; Wagner, H; Weinhold, L; Wen, KH; Widen, E; Yang, Q; Zhao, W; Adams, HHH; Arking, DE; Bilder, RM; Bitsios, P; Boerwinkle, E; Chiba-Falek, O; Corvin, A; De Jager, PL; Debette, S; Donohoe, G; Elliott, P; Fitzpatrick, AL; Gill, M; Glahn, DC; Hägg, S; Hansell, NK; Hariri, AR; Ikram, MK; Jukema, JW; Vuoksimaa, E; Keller, MC; Kremen, WS; Launer, L; Lindenberger, U; Palotie, A; Pedersen, NL; Pendleton, N; Porteous, DJ; Räikkönen, K; Raitakari, OT; Ramirez, A; Reinvang, I; Rudan, I; Dan Rujescu, I; Schmidt, R; Schmidt, H; Schofield, PW; Schofield, PR; Starr, JM; Steen, VM; Trollor, JN; Turner, ST; Van Duijn, CM; Villringer, A; Weinberger, DR; Weir, DR; Wilson, JF; Malhotra, A; McIntosh, AM; Gale, CR; Seshadri, S; Mosley, TH; Bressler, J; Lencz, T; Deary, IJ
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
Nat Commun. 2018; 9(1):2098-2098
Doi: 10.1038/s41467-018-04362-x
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Genetic Determinants of Circulating Estrogen Levels and Evidence of a Causal Effect of Estradiol on Bone Density in Men.
J CLIN ENDOCR METAB. 2018; 103(3): 991-1004.
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Gräf, S; Haimel, M; Bleda, M; Hadinnapola, C; Southgate, L; Li, W; Hodgson, J; Liu, B; Salmon, RM; Southwood, M; Machado, RD; Martin, JM; Treacy, CM; Yates, K; Daugherty, LC; Shamardina, O; Whitehorn, D; Holden, S; Aldred, M; Bogaard, HJ; Church, C; Coghlan, G; Condliffe, R; Corris, PA; Danesino, C; Eyries, M; Gall, H; Ghio, S; Ghofrani, HA; Gibbs, JSR; Girerd, B; Houweling, AC; Howard, L; Humbert, M; Kiely, DG; Kovacs, G; MacKenzie Ross, RV; Moledina, S; Montani, D; Newnham, M; Olschewski, A; Olschewski, H; Peacock, AJ; Pepke-Zaba, J; Prokopenko, I; Rhodes, CJ; Scelsi, L; Seeger, W; Soubrier, F; Stein, DF; Suntharalingam, J; Swietlik, EM; Toshner, MR; van Heel, DA; Vonk Noordegraaf, A; Waisfisz, Q; Wharton, J; Wort, SJ; Ouwehand, WH; Soranzo, N; Lawrie, A; Upton, PD; Wilkins, MR; Trembath, RC; Morrell, NW
Identification of rare sequence variation underlying heritable pulmonary arterial hypertension.
Nat Commun. 2018; 9(1): 1416-1416.
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Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels.
Nat Commun. 2018; 9(1): 260-260.
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Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
Nat Genet. 2018; 50(8):1112-1121
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Multi-ethnic genome-wide association study for atrial fibrillation.
NAT GENET. 2018; 50(9): 1225-1233.
Doi: 10.1038/s41588-018-0133-9
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Debette, S; Saba, Y; Vojinovic, D; Jian, X; Adams, H; Chauhan, G; Sargurupremraj, M; Kaffashian, S; Ding, J; Bis, JC; Nyquist, P; Mather, K; Van Duijn, C; Launer, LJ; Ikram, MA; Schmidt, H; Longstreth, WT; Fornage, M; Seshadri, S;
19th Workshop of the International Stroke Genetics Consortium, April 28-29, 2016, Boston, Massachusetts, USA: 2016.001 MRI-defined cerebrovascular genomics-The CHARGE consortium.
Neurol Genet. 2017; 3(1 Suppl 1):S2-S11.
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Hofer, P; Hagmann, M; Brezina, S; Dolejsi, E; Mach, K; Leeb, G; Baierl, A; Buch, S; Sutterlüty-Fall, H; Karner-Hanusch, J; Bergmann, MM; Bachleitner-Hofmann, T; Stift, A; Gerger, A; Rötzer, K; Karner, J; Stättner, S; Waldenberger, M; Meitinger, T; Strauch, K; Linseisen, J; Gieger, C; Frommlet, F; Gsur, A
Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas.
Oncotarget. 2017; 8(58):98623-98634
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Nelson, CP; Goel, A; Butterworth, AS; Kanoni, S; Webb, TR; Marouli, E; Zeng, L; Ntalla, I; Lai, FY; Hopewell, JC; Giannakopoulou, O; Jiang, T; Hamby, SE; Di Angelantonio, E; Assimes, TL; Bottinger, EP; Chambers, JC; Clarke, R; Palmer, CNA; Cubbon, RM; Ellinor, P; Ermel, R; Evangelou, E; Franks, PW; Grace, C; Gu, D; Hingorani, AD; Howson, JMM; Ingelsson, E; Kastrati, A; Kessler, T; Kyriakou, T; Lehtimäki, T; Lu, X; Lu, Y; März, W; McPherson, R; Metspalu, A; Pujades-Rodriguez, M; Ruusalepp, A; Schadt, EE; Schmidt, AF; Sweeting, MJ; Zalloua, PA; AlGhalayini, K; Keavney, BD; Kooner, JS; Loos, RJF; Patel, RS; Rutter, MK; Tomaszewski, M; Tzoulaki, I; Zeggini, E; Erdmann, J; Dedoussis, G; Björkegren, JLM; EPIC-CVD Consortium; CARDIoGRAMplusC4D; UK Biobank CardioMetabolic Consortium CHD working group; Schunkert, H; Farrall, M; Danesh, J; Samani, NJ; Watkins, H; Deloukas, P
Association analyses based on false discovery rate implicate new loci for coronary artery disease.
Nat Genet. 2017; 49(9):1385-1391
Doi: 10.1038/ng.3913
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van der Lee, SJ; Roshchupkin, GV; Adams, HH; Schmidt, H; Hofer, E; Saba, Y; Schmidt, R; Hofman, A; Amin, N; van Duijn, CM; Vernooij, MW; Ikram, MA; Niessen, WJ
Gray matter heritability in family-based and population-based studies using voxel-based morphometry.
Hum Brain Mapp. 2017; 38(5):2408-2423
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Hou, L; Bergen, SE; Akula, N; Song, J; Hultman, CM; Landén, M; Adli, M; Alda, M; Ardau, R; Arias, B; Aubry, JM; Backlund, L; Badner, JA; Barrett, TB; Bauer, M; Baune, BT; Bellivier, F; Benabarre, A; Bengesser, S; Berrettini, WH; Bhattacharjee, AK; Biernacka, JM; Birner, A; Bloss, CS; Brichant-Petitjean, C; Bui, ET; Byerley, W; Cervantes, P; Chillotti, C; Cichon, S; Colom, F; Coryell, W; Craig, DW; Cruceanu, C; Czerski, PM; Davis, T; Dayer, A; Degenhardt, F; Del Zompo, M; DePaulo, JR; Edenberg, HJ; Étain, B; Falkai, P; Foroud, T; Forstner, AJ; Frisén, L; Frye, MA; Fullerton, JM; Gard, S; Garnham, JS; Gershon, ES; Goes, FS; Greenwood, TA; Grigoroiu-Serbanescu, M; Hauser, J; Heilbronner, U; Heilmann-Heimbach, S; Herms, S; Hipolito, M; Hitturlingappa, S; Hoffmann, P; Hofmann, A; Jamain, S; Jiménez, E; Kahn, JP; Kassem, L; Kelsoe, JR; Kittel-Schneider, S; Kliwicki, S; Koller, DL; König, B; Lackner, N; Laje, G; Lang, M; Lavebratt, C; Lawson, WB; Leboyer, M; Leckband, SG; Liu, C; Maaser, A; Mahon, PB; Maier, W; Maj, M; Manchia, M; Martinsson, L; McCarthy, MJ; McElroy, SL; McInnis, MG; McKinney, R; Mitchell, PB; Mitjans, M; Mondimore, FM; Monteleone, P; Mühleisen, TW; Nievergelt, CM; Nöthen, MM; Novák, T; Nurnberger, JI; Nwulia, EA; Ösby, U; Pfennig, A; Potash, JB; Propping, P; Reif, A; Reininghaus, E; Rice, J; Rietschel, M; Rouleau, GA; Rybakowski, JK; Schalling, M; Scheftner, WA; Schofield, PR; Schork, NJ; Schulze, TG; Schumacher, J; Schweizer, BW; Severino, G; Shekhtman, T; Shilling, PD; Simhandl, C; Slaney, CM; Smith, EN; Squassina, A; Stamm, T; Stopkova, P; Streit, F; Strohmaier, J; Szelinger, S; Tighe, SK; Tortorella, A; Turecki, G; Vieta, E; Volkert, J; Witt, SH; Wright, A; Zandi, PP; Zhang, P; Zollner, S; McMahon, FJ
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.
Hum Mol Genet. 2016; 25(15):3383-3394
Doi: 10.1093/hmg/ddw181
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Schweiger, R; Kaufman, S; Laaksonen, R; Kleber, ME; März, W; Eskin, E; Rosset, S; Halperin, E
Fast and Accurate Construction of Confidence Intervals for Heritability.
Am J Hum Genet. 2016; 98(6):1181-1192
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2015
Davies, G; Armstrong, N; Bis, JC; Bressler, J; Chouraki, V; Giddaluru, S; Hofer, E; Ibrahim-Verbaas, CA; Kirin, M; Lahti, J; van der Lee, SJ; Le Hellard, S; Liu, T; Marioni, RE; Oldmeadow, C; Postmus, I; Smith, AV; Smith, JA; Thalamuthu, A; Thomson, R; Vitart, V; Wang, J; Yu, L; Zgaga, L; Zhao, W; Boxall, R; Harris, SE; Hill, WD; Liewald, DC; Luciano, M; Adams, H; Ames, D; Amin, N; Amouyel, P; Assareh, AA; Au, R; Becker, JT; Beiser, A; Berr, C; Bertram, L; Boerwinkle, E; Buckley, BM; Campbell, H; Corley, J; De Jager, PL; Dufouil, C; Eriksson, JG; Espeseth, T; Faul, JD; Ford, I; Generation Scotland; Gottesman, RF; Griswold, ME; Gudnason, V; Harris, TB; Heiss, G; Hofman, A; Holliday, EG; Huffman, J; Kardia, SL; Kochan, N; Knopman, DS; Kwok, JB; Lambert, JC; Lee, T; Li, G; Li, SC; Loitfelder, M; Lopez, OL; Lundervold, AJ; Lundqvist, A; Mather, KA; Mirza, SS; Nyberg, L; Oostra, BA; Palotie, A; Papenberg, G; Pattie, A; Petrovic, K; Polasek, O; Psaty, BM; Redmond, P; Reppermund, S; Rotter, JI; Schmidt, H; Schuur, M; Schofield, PW; Scott, RJ; Steen, VM; Stott, DJ; van Swieten, JC; Taylor, KD; Trollor, J; Trompet, S; Uitterlinden, AG; Weinstein, G; Widen, E; Windham, BG; Jukema, JW; Wright, AF; Wright, MJ; Yang, Q; Amieva, H; Attia, JR; Bennett, DA; Brodaty, H; de Craen, AJ; Hayward, C; Ikram, MA; Lindenberger, U; Nilsson, LG; Porteous, DJ; Räikkönen, K; Reinvang, I; Rudan, I; Sachdev, PS; Schmidt, R; Schofield, PR; Srikanth, V; Starr, JM; Turner, ST; Weir, DR; Wilson, JF; van Duijn, C; Launer, L; Fitzpatrick, AL; Seshadri, S; Mosley, TH; Deary, IJ
Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).
Mol Psychiatry. 2015; 20(2):183-192
Doi: 10.1038/mp.2014.188
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Hernesniemi, JA; Lyytikäinen, LP; Oksala, N; Seppälä, I; Kleber, ME; Mononen, N; März, W; Mikkelsson, J; Pessi, T; Louhelainen, AM; Martiskainen, M; Nikus, K; Klopp, N; Waldenberger, M; Illig, T; Kähönen, M; Laaksonen, R; Karhunen, PJ; Lehtimäki, T
Predicting sudden cardiac death using common genetic risk variants for coronary artery disease.
Eur Heart J. 2015; 36(26):1669-1675
Doi: 10.1093/eurheartj/ehv106
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Hofer, E; Cavalieri, M; Bis, JC; DeCarli, C; Fornage, M; Sigurdsson, S; Srikanth, V; Trompet, S; Verhaaren, BF; Wolf, C; Yang, Q; Adams, HH; Amouyel, P; Beiser, A; Buckley, BM; Callisaya, M; Chauhan, G; de Craen, AJ; Dufouil, C; van Duijn, CM; Ford, I; Freudenberger, P; Gottesman, RF; Gudnason, V; Heiss, G; Hofman, A; Lumley, T; Martinez, O; Mazoyer, B; Moran, C; Niessen, WJ; Phan, T; Psaty, BM; Satizabal, CL; Sattar, N; Schilling, S; Shibata, DK; Slagboom, PE; Smith, A; Stott, DJ; Taylor, KD; Thomson, R; Töglhofer, AM; Tzourio, C; van Buchem, M; Wang, J; Westendorp, RG; Windham, BG; Vernooij, MW; Zijdenbos, A; Beare, R; Debette, S; Ikram, MA; Jukema, JW; Launer, LJ; Longstreth, WT; Mosley, TH; Seshadri, S; Schmidt, H; Schmidt, R; Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
White Matter Lesion Progression: Genome-Wide Search for Genetic Influences.
Stroke. 2015; 46(11):3048-3057
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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
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Lopez, LM; Hill, WD; Harris, SE; Valdes Hernandez, M; Munoz Maniega, S; Bastin, ME; Bailey, E; Smith, C; McBride, M; McClure, J; Graham, D; Dominiczak, A; Yang, Q; Fornage, M; Ikram, MA; Debette, S; Launer, L; Bis, JC; Schmidt, R; Seshadri, S; Porteous, DJ; Starr, J; Deary, IJ; Wardlaw, JM
Genes from a translational analysis support a multifactorial nature of white matter hyperintensities.
Stroke. 2015; 46(2):341-347
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Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.
PLoS One. 2014; 9(6):e94661-e94661
Doi: 10.1371/journal.pone.0094661
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Holliday, EG; Traylor, M; Malik, R; Bevan, S; Maguire, J; Koblar, SA; Sturm, J; Hankey, GJ; Oldmeadow, C; McEvoy, M; Sudlow, C; Rothwell, PM; Coresh, J; Hamet, P; Tremblay, J; Turner, ST; de Andrade, M; Rao, M; Schmidt, R; Crick, PA; Robino, A; Peralta, CA; Jukema, JW; Mitchell, P; Rosas, SE; Wang, JJ; Scott, RJ; Dichgans, M; Mitchell, BD; Kao, WH; Fox, CS; Levi, C; Attia, J; Markus, HS; CKDGen Consortium and the International Stroke Genetics Consortium
Polygenic overlap between kidney function and large artery atherosclerotic stroke.
Stroke. 2014; 45(12):3508-3513
Doi: 10.1161/STROKEAHA.114.006609
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Woo, D; Falcone, GJ; Devan, WJ; Brown, WM; Biffi, A; Howard, TD; Anderson, CD; Brouwers, HB; Valant, V; Battey, TW; Radmanesh, F; Raffeld, MR; Baedorf-Kassis, S; Deka, R; Woo, JG; Martin, LJ; Haverbusch, M; Moomaw, CJ; Sun, G; Broderick, JP; Flaherty, ML; Martini, SR; Kleindorfer, DO; Kissela, B; Comeau, ME; Jagiella, JM; Schmidt, H; Freudenberger, P; Pichler, A; Enzinger, C; Hansen, BM; Norrving, B; Jimenez-Conde, J; Giralt-Steinhauer, E; Elosua, R; Cuadrado-Godia, E; Soriano, C; Roquer, J; Kraft, P; Ayres, AM; Schwab, K; McCauley, JL; Pera, J; Urbanik, A; Rost, NS; Goldstein, JN; Viswanathan, A; Stögerer, EM; Tirschwell, DL; Selim, M; Brown, DL; Silliman, SL; Worrall, BB; Meschia, JF; Kidwell, CS; Montaner, J; Fernandez-Cadenas, I; Delgado, P; Malik, R; Dichgans, M; Greenberg, SM; Rothwell, PM; Lindgren, A; Slowik, A; Schmidt, R; Langefeld, CD; Rosand, J; International Stroke Genetics Consortium
Meta-analysis of Genome-wide Association Studies Identifies 1q22 as a Susceptibility Locus for Intracerebral Hemorrhage.
Am J Hum Genet. 2014; 94(4):511-521
Doi: 10.1016/j.ajhg.2014.02.012
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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
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2013
Devan, WJ; Falcone, GJ; Anderson, CD; Jagiella, JM; Schmidt, H; Hansen, BM; Jimenez-Conde, J; Giralt-Steinhauer, E; Cuadrado-Godia, E; Soriano, C; Ayres, AM; Schwab, K; Kassis, SB; Valant, V; Pera, J; Urbanik, A; Viswanathan, A; Rost, NS; Goldstein, JN; Freudenberger, P; Stögerer, EM; Norrving, B; Tirschwell, DL; Selim, M; Brown, DL; Silliman, SL; Worrall, BB; Meschia, JF; Kidwell, CS; Montaner, J; Fernandez-Cadenas, I; Delgado, P; Greenberg, SM; Roquer, J; Lindgren, A; Slowik, A; Schmidt, R; Woo, D; Rosand, J; Biffi, A; on behalf of the International Stroke Genetics Consortium
Heritability Estimates Identify a Substantial Genetic Contribution to Risk and Outcome of Intracerebral Hemorrhage.
Stroke. 2013; 44(6):1578-1583
Doi: 10.1161/STROKEAHA.111.000089
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van der Loos, MJ; Rietveld, CA; Eklund, N; Koellinger, PD; Rivadeneira, F; Abecasis, GR; Ankra-Badu, GA; Baumeister, SE; Benjamin, DJ; Biffar, R; Blankenberg, S; Boomsma, DI; Cesarini, D; Cucca, F; de Geus, EJ; Dedoussis, G; Deloukas, P; Dimitriou, M; Eiriksdottir, G; Eriksson, J; Gieger, C; Gudnason, V; Höhne, B; Holle, R; Hottenga, JJ; Isaacs, A; Järvelin, MR; Johannesson, M; Kaakinen, M; Kähönen, M; Kanoni, S; Laaksonen, MA; Lahti, J; Launer, LJ; Lehtimäki, T; Loitfelder, M; Magnusson, PK; Naitza, S; Oostra, BA; Perola, M; Petrovic, K; Quaye, L; Raitakari, O; Ripatti, S; Scheet, P; Schlessinger, D; Schmidt, CO; Schmidt, H; Schmidt, R; Senft, A; Smith, AV; Spector, TD; Surakka, I; Svento, R; Terracciano, A; Tikkanen, E; van Duijn, CM; Viikari, J; Völzke, H; Wichmann, HE; Wild, PS; Willems, SM; Willemsen, G; van Rooij, FJ; Groenen, PJ; Uitterlinden, AG; Hofman, A; Thurik, AR
The molecular genetic architecture of self-employment.
PLoS One. 2013; 8(4):e60542-e60542
Doi: 10.1371/journal.pone.0060542
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2012
Asselbergs, FW; Guo, Y; van Iperen, EP; Sivapalaratnam, S; Tragante, V; Lanktree, MB; Lange, LA; Almoguera, B; Appelman, YE; Barnard, J; Baumert, J; Beitelshees, AL; Bhangale, TR; Chen, YD; Gaunt, TR; Gong, Y; Hopewell, JC; Johnson, T; Kleber, ME; Langaee, TY; Li, M; Li, YR; Liu, K; McDonough, CW; Meijs, MF; Middelberg, RP; Musunuru, K; Nelson, CP; O'Connell, JR; Padmanabhan, S; Pankow, JS; Pankratz, N; Rafelt, S; Rajagopalan, R; Romaine, SP; Schork, NJ; Shaffer, J; Shen, H; Smith, EN; Tischfield, SE; van der Most, PJ; van Vliet-Ostaptchouk, JV; Verweij, N; Volcik, KA; Zhang, L; Bailey, KR; Bailey, KM; Bauer, F; Boer, JM; Braund, PS; Burt, A; Burton, PR; Buxbaum, SG; Chen, W; Cooper-Dehoff, RM; Cupples, LA; deJong, JS; Delles, C; Duggan, D; Fornage, M; Furlong, CE; Glazer, N; Gums, JG; Hastie, C; Holmes, MV; Illig, T; Kirkland, SA; Kivimaki, M; Klein, R; Klein, BE; Kooperberg, C; Kottke-Marchant, K; Kumari, M; LaCroix, AZ; Mallela, L; Murugesan, G; Ordovas, J; Ouwehand, WH; Post, WS; Saxena, R; Scharnagl, H; Schreiner, PJ; Shah, T; Shields, DC; Shimbo, D; Srinivasan, SR; Stolk, RP; Swerdlow, DI; Taylor, HA; Topol, EJ; Toskala, E; van Pelt, JL; van Setten, J; Yusuf, S; Whittaker, JC; Zwinderman, AH; LifeLines Cohort Study; Anand, SS; Balmforth, AJ; Berenson, GS; Bezzina, CR; Boehm, BO; Boerwinkle, E; Casas, JP; Caulfield, MJ; Clarke, R; Connell, JM; Cruickshanks, KJ; Davidson, KW; Day, IN; de Bakker, PI; Doevendans, PA; Dominiczak, AF; Hall, AS; Hartman, CA; Hengstenberg, C; Hillege, HL; Hofker, MH; Humphries, SE; Jarvik, GP; Johnson, JA; Kaess, BM; Kathiresan, S; Koenig, W; Lawlor, DA; März, W; Melander, O; Mitchell, BD; Montgomery, GW; Munroe, PB; Murray, SS; Newhouse, SJ; Onland-Moret, NC; Poulter, N; Psaty, B; Redline, S; Rich, SS; Rotter, JI; Schunkert, H; Sever, P; Shuldiner, AR; Silverstein, RL; Stanton, A; Thorand, B; Trip, MD; Tsai, MY; van der Harst, P; van der Schoot, E; van der Schouw, YT; Verschuren, WM; Watkins, H; Wilde, AA; Wolffenbuttel, BH; Whitfield, JB; Hovingh, GK; Ballantyne, CM; Wijmenga, C; Reilly, MP; Martin, NG; Wilson, JG; Rader, DJ; Samani, NJ; Reiner, AP; Hegele, RA; Kastelein, JJ; Hingorani, AD; Talmud, PJ; Hakonarson, H; Elbers, CC; Keating, BJ; Drenos, F
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.
Am J Hum Genet. 2012; 91(5):823-838
Doi: 10.1016/j.ajhg.2012.08.032
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Freudenberger, P; Schmidt, R; Schmidt, H
Genetics of age-related white matter lesions from linkage to genome wide association studies.
J Neurol Sci. 2012; 322(1-2):82-86
Doi: 10.1016/j.jns.2012.06.016
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Schmidt, H; Freudenberger, P; Seiler, S; Schmidt, R
Genetics of subcortical vascular dementia.
Exp Gerontol. 2012; 47(11):873-877
Doi: 10.1016/j.exger.2012.06.003
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2010
Marzi, C; Albrecht, E; Hysi, PG; Lagou, V; Waldenberger, M; Tönjes, A; Prokopenko, I; Heim, K; Blackburn, H; Ried, JS; Kleber, ME; Mangino, M; Thorand, B; Peters, A; Hammond, CJ; Grallert, H; Boehm, BO; Kovacs, P; Geistlinger, L; Prokisch, H; Winkelmann, BR; Spector, TD; Wichmann, HE; Stumvoll, M; Soranzo, N; März, W; Koenig, W; Illig, T; Gieger, C
Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A.
PLoS Genet. 2010; 6(11):e1001213-e1001213
Doi: 10.1371/journal.pgen.1001213
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